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Gene: FNDC3A (fibronectin type III domain containing 3A) Homo sapiens

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Symbol:

FNDC3A

Name:

fibronectin type III domain containing 3A

RGD ID:

1354235

HGNC Page

HGNC:20296

Description:

Enables RNA binding activity. Predicted to be involved in spermatid development. Predicted to act upstream of or within Sertoli cell development; cell-cell adhesion; and fertilization. Located in Golgi apparatus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

bA203I16.1; bA203I16.5; fibronectin type-III domain-containing protein 3A; FLJ31509; FNDC3; HUGO; human gene expressed in odontoblasts; KIAA0970; RP11-203I16.5

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Related Pseudogenes:

FNDC3CP

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	13	48,975,291 - 49,209,779 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	13	48,975,912 - 49,209,779 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	13	49,550,048 - 49,783,915 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	13	48,448,049 - 48,681,916 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	13	48,448,939 - 48,681,729	NCBI
Celera	13	30,605,901 - 30,839,799 (+)	NCBI		Celera
Cytogenetic Map	13	q14.2	NCBI
HuRef	13	30,344,082 - 30,577,725 (+)	NCBI		HuRef
CHM1_1	13	49,517,625 - 49,751,465 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	13	48,193,984 - 48,431,085 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
FNDC3A	Human	chromosome 13q14 deletion syndrome		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome	ClinVar
FNDC3A	Human	intellectual disability		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
FNDC3A	Human	(-)-epigallocatechin 3-gallate	multiple interactions	EXP		6480464	[potassium chromate(VI) co-treated with epigallocatechin gallate] results in decreased expression of FNDC3A mRNA	CTD	PMID:22079256
FNDC3A	Human	1,2-dimethylhydrazine	decreases expression	ISO	Fndc3a (Mus musculus)	6480464	1 and 2-Dimethylhydrazine results in decreased expression of FNDC3A mRNA	CTD	PMID:22206623
FNDC3A	Human	17alpha-ethynylestradiol	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Ethinyl Estradiol results in increased expression of FNDC3A mRNA	CTD	PMID:29097150
FNDC3A	Human	17beta-estradiol	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Estradiol results in increased expression of FNDC3A mRNA	CTD	PMID:32145629
FNDC3A	Human	17beta-estradiol	increases expression	ISO	Fndc3a (Mus musculus)	6480464	Estradiol results in increased expression of FNDC3A mRNA	CTD	PMID:39298647
FNDC3A	Human	2-bromohexadecanoic acid	multiple interactions	EXP		6480464	2-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in increased palmitoylation of FNDC3A protein]	CTD	PMID:38195004
FNDC3A	Human	3,4-methylenedioxymethamphetamine	increases expression	ISO	Fndc3a (Mus musculus)	6480464	N-Methyl-3 and 4-methylenedioxyamphetamine results in increased expression of FNDC3A mRNA	CTD	PMID:20188158
FNDC3A	Human	3,4-methylenedioxymethamphetamine	decreases expression	ISO	Fndc3a (Mus musculus)	6480464	N-Methyl-3 and 4-methylenedioxyamphetamine results in decreased expression of FNDC3A mRNA	CTD	PMID:26251327
FNDC3A	Human	4,4'-sulfonyldiphenol	increases expression	ISO	Fndc3a (Mus musculus)	6480464	bisphenol S results in increased expression of FNDC3A mRNA	CTD	PMID:39298647
FNDC3A	Human	5-aza-2'-deoxycytidine	decreases methylation	ISO	Fndc3a (Mus musculus)	6480464	Decitabine results in decreased methylation of FNDC3A gene	CTD	PMID:27923600
FNDC3A	Human	acetamide	decreases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	acetamide results in decreased expression of FNDC3A mRNA	CTD	PMID:31881176
FNDC3A	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of FNDC3A gene	CTD	PMID:27153756
FNDC3A	Human	Aflatoxin B2 alpha	decreases methylation	EXP		6480464	aflatoxin B2 results in decreased methylation of FNDC3A intron	CTD	PMID:30157460
FNDC3A	Human	all-trans-retinoic acid	increases expression	EXP		6480464	Tretinoin results in increased expression of FNDC3A mRNA	CTD	PMID:33167477
FNDC3A	Human	amitrole	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Amitrole results in increased expression of FNDC3A mRNA	CTD	PMID:38685447
FNDC3A	Human	aristolochic acid A	decreases expression	EXP		6480464	aristolochic acid I results in decreased expression of FNDC3A mRNA	CTD	PMID:33212167
FNDC3A	Human	arsane	multiple interactions	EXP		6480464	[sodium arsenite results in increased abundance of Arsenic] which results in increased expression of FNDC3A mRNA	CTD	PMID:39836092
FNDC3A	Human	arsenic atom	multiple interactions	EXP		6480464	[sodium arsenite results in increased abundance of Arsenic] which results in increased expression of FNDC3A mRNA	CTD	PMID:39836092
FNDC3A	Human	benzo[a]pyrene	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Benzo(a)pyrene results in increased expression of FNDC3A mRNA	CTD	PMID:21839799
FNDC3A	Human	benzo[a]pyrene	decreases methylation	EXP		6480464	Benzo(a)pyrene results in decreased methylation of FNDC3A promoter	CTD	PMID:27901495
FNDC3A	Human	benzo[a]pyrene diol epoxide I	decreases expression	EXP		6480464	7 more ...	CTD	PMID:19150397
FNDC3A	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of FNDC3A mRNA	CTD	PMID:25047013
FNDC3A	Human	bisphenol A	affects methylation	EXP		6480464	bisphenol A affects the methylation of FNDC3A gene	CTD	PMID:31601247
FNDC3A	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] affects the methylation of FNDC3A gene	CTD	PMID:31601247
FNDC3A	Human	bisphenol A	decreases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of FNDC3A mRNA	CTD	PMID:30816183 and PMID:34947998
FNDC3A	Human	bisphenol A	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	bisphenol A results in increased expression of FNDC3A mRNA	CTD	PMID:25181051 and PMID:32145629
FNDC3A	Human	cadmium atom	multiple interactions	EXP		6480464	2-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in increased palmitoylation of FNDC3A protein] and [Cadmium Chloride results in increased abundance of Cadmium] which results in increased palmitoylation of FNDC3A protein	CTD	PMID:38195004
FNDC3A	Human	cadmium dichloride	decreases expression	ISO	Fndc3a (Mus musculus)	6480464	Cadmium Chloride results in decreased expression of FNDC3A mRNA	CTD	PMID:24982889
FNDC3A	Human	cadmium dichloride	multiple interactions	EXP		6480464	2-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in increased palmitoylation of FNDC3A protein] and [Cadmium Chloride results in increased abundance of Cadmium] which results in increased palmitoylation of FNDC3A protein	CTD	PMID:38195004
FNDC3A	Human	cadmium dichloride	increases expression	EXP		6480464	Cadmium Chloride results in increased expression of FNDC3A mRNA	CTD	PMID:38568856
FNDC3A	Human	caffeine	decreases phosphorylation	EXP		6480464	Caffeine results in decreased phosphorylation of FNDC3A protein	CTD	PMID:35688186
FNDC3A	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to FNDC3A gene]	CTD	PMID:28238834
FNDC3A	Human	chlorpyrifos	decreases expression	ISO	Fndc3a (Mus musculus)	6480464	Chlorpyrifos results in decreased expression of FNDC3A mRNA	CTD	PMID:37019170
FNDC3A	Human	chromium(6+)	multiple interactions	EXP		6480464	[zinc chromate results in increased abundance of chromium hexavalent ion] which results in increased expression of FNDC3A mRNA	CTD	PMID:38479592
FNDC3A	Human	cyclosporin A	increases expression	ISO	Fndc3a (Mus musculus)	6480464	Cyclosporine results in increased expression of FNDC3A mRNA	CTD	PMID:19770486
FNDC3A	Human	cyclosporin A	increases expression	EXP		6480464	Cyclosporine results in increased expression of FNDC3A mRNA	CTD	PMID:20106945 more ...
FNDC3A	Human	Dibutyl phosphate	affects expression	EXP		6480464	di-n-butylphosphoric acid affects the expression of FNDC3A mRNA	CTD	PMID:37042841
FNDC3A	Human	dorsomorphin	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
FNDC3A	Human	doxorubicin	decreases expression	EXP		6480464	Doxorubicin results in decreased expression of FNDC3A mRNA	CTD	PMID:29803840
FNDC3A	Human	entinostat	decreases expression	EXP		6480464	entinostat results in decreased expression of FNDC3A mRNA	CTD	PMID:27188386
FNDC3A	Human	ethanol	affects splicing	ISO	Fndc3a (Mus musculus)	6480464	Ethanol affects the splicing of FNDC3A mRNA	CTD	PMID:30319688
FNDC3A	Human	flutamide	decreases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Flutamide results in decreased expression of FNDC3A mRNA	CTD	PMID:24136188
FNDC3A	Human	folic acid	decreases expression	EXP		6480464	Folic Acid results in decreased expression of FNDC3A mRNA	CTD	PMID:21867686
FNDC3A	Human	FR900359	affects phosphorylation	EXP		6480464	FR900359 affects the phosphorylation of FNDC3A protein	CTD	PMID:37730182
FNDC3A	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] affects the methylation of FNDC3A gene	CTD	PMID:31601247
FNDC3A	Human	hydrogen peroxide	affects expression	EXP		6480464	Hydrogen Peroxide affects the expression of FNDC3A mRNA	CTD	PMID:20044591
FNDC3A	Human	ivermectin	decreases expression	EXP		6480464	Ivermectin results in decreased expression of FNDC3A protein	CTD	PMID:32959892
FNDC3A	Human	lead diacetate	increases expression	ISO	Fndc3a (Mus musculus)	6480464	lead acetate results in increased expression of FNDC3A mRNA	CTD	PMID:22609695
FNDC3A	Human	menadione	affects expression	EXP		6480464	Vitamin K 3 affects the expression of FNDC3A mRNA	CTD	PMID:20044591
FNDC3A	Human	methapyrilene	decreases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Methapyrilene results in decreased expression of FNDC3A mRNA	CTD	PMID:30467583
FNDC3A	Human	mitoxantrone	affects response to substance	EXP		6480464	FNDC3A protein affects the susceptibility to Mitoxantrone	CTD	PMID:16217747
FNDC3A	Human	nickel sulfate	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	nickel sulfate results in increased expression of FNDC3A mRNA	CTD	PMID:11114790
FNDC3A	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of FNDC3A mRNA	CTD	PMID:21420995
FNDC3A	Human	pentachlorophenol	increases expression	ISO	Fndc3a (Mus musculus)	6480464	Pentachlorophenol results in increased expression of FNDC3A mRNA	CTD	PMID:23892564
FNDC3A	Human	perfluorooctane-1-sulfonic acid	decreases expression	EXP		6480464	perfluorooctane sulfonic acid results in decreased expression of FNDC3A mRNA	CTD	PMID:27153767
FNDC3A	Human	phenytoin	increases expression	ISO	Fndc3a (Rattus norvegicus)	6480464	Phenytoin results in increased expression of FNDC3A mRNA	CTD	PMID:20345932
FNDC3A	Human	pirinixic acid	decreases expression	ISO	Fndc3a (Mus musculus)	6480464	pirinixic acid results in decreased expression of FNDC3A mRNA	CTD	PMID:18445702
FNDC3A	Human	potassium chromate	decreases expression	EXP		6480464	potassium chromate(VI) results in decreased expression of FNDC3A mRNA	CTD	PMID:22079256
FNDC3A	Human	potassium chromate	multiple interactions	EXP		6480464	[potassium chromate(VI) co-treated with epigallocatechin gallate] results in decreased expression of FNDC3A mRNA	CTD	PMID:22079256
FNDC3A	Human	progesterone	increases expression	EXP		6480464	Progesterone results in increased expression of FNDC3A mRNA	CTD	PMID:18037150
FNDC3A	Human	resveratrol	multiple interactions	EXP		6480464	[Plant Extracts co-treated with Resveratrol] results in increased expression of FNDC3A mRNA	CTD	PMID:23557933
FNDC3A	Human	SB 431542	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...	CTD	PMID:27188386
FNDC3A	Human	silicon dioxide	increases expression	EXP		6480464	Silicon Dioxide analog results in increased expression of FNDC3A mRNA	CTD	PMID:25895662
FNDC3A	Human	sodium arsenite	decreases expression	EXP		6480464	sodium arsenite results in decreased expression of FNDC3A mRNA	CTD	PMID:28595984 and PMID:34032870
FNDC3A	Human	sodium arsenite	multiple interactions	EXP		6480464	[sodium arsenite results in increased abundance of Arsenic] which results in increased expression of FNDC3A mRNA and sodium arsenite promotes the reaction [FNDC3A protein binds to CAPRIN1 protein]	CTD	PMID:33939924 and PMID:39836092
FNDC3A	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of FNDC3A mRNA	CTD	PMID:38568856
FNDC3A	Human	tacrolimus hydrate	increases expression	ISO	Fndc3a (Mus musculus)	6480464	Tacrolimus results in increased expression of FNDC3A mRNA	CTD	PMID:25270620
FNDC3A	Human	testosterone	decreases expression	EXP		6480464	Testosterone results in decreased expression of FNDC3A mRNA	CTD	PMID:33359661
FNDC3A	Human	tetrachloromethane	increases expression	ISO	Fndc3a (Mus musculus)	6480464	Carbon Tetrachloride results in increased expression of FNDC3A mRNA	CTD	PMID:31919559
FNDC3A	Human	thiram	increases expression	EXP		6480464	Thiram results in increased expression of FNDC3A mRNA	CTD	PMID:38568856
FNDC3A	Human	titanium dioxide	increases methylation	ISO	Fndc3a (Mus musculus)	6480464	titanium dioxide results in increased methylation of FNDC3A gene	CTD	PMID:35295148
FNDC3A	Human	titanium dioxide	decreases methylation	ISO	Fndc3a (Mus musculus)	6480464	titanium dioxide results in decreased methylation of FNDC3A enhancer	CTD	PMID:35295148
FNDC3A	Human	titanium dioxide	affects methylation	ISO	Fndc3a (Mus musculus)	6480464	titanium dioxide affects the methylation of FNDC3A promoter	CTD	PMID:35295148
FNDC3A	Human	trichostatin A	decreases expression	EXP		6480464	trichostatin A results in decreased expression of FNDC3A mRNA	CTD	PMID:24935251 and PMID:26272509
FNDC3A	Human	trichostatin A	multiple interactions	EXP		6480464	[NOG protein co-treated with trichostatin A co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of FNDC3A mRNA	CTD	PMID:27188386
FNDC3A	Human	valproic acid	affects expression	EXP		6480464	Valproic Acid affects the expression of FNDC3A mRNA	CTD	PMID:25979313
FNDC3A	Human	valproic acid	multiple interactions	EXP		6480464	[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of FNDC3A mRNA	CTD	PMID:27188386
FNDC3A	Human	valproic acid	decreases expression	EXP		6480464	Valproic Acid results in decreased expression of FNDC3A mRNA	CTD	PMID:23179753 more ...
FNDC3A	Human	valproic acid	decreases methylation	EXP		6480464	Valproic Acid results in decreased methylation of FNDC3A gene	CTD	PMID:29154799
FNDC3A	Human	vinclozolin	increases methylation	ISO	Fndc3a (Rattus norvegicus)	6480464	vinclozolin results in increased methylation of FNDC3A gene	CTD	PMID:31079544

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
FNDC3A	Human	cell-cell adhesion	acts_upstream_of_or_within	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107
FNDC3A	Human	fertilization	acts_upstream_of_or_within	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107
FNDC3A	Human	Sertoli cell development	acts_upstream_of_or_within	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107
FNDC3A	Human	spermatid development	involved_in	IBA	MGI:1196463 and PANTHER:PTN008605752	150520179		GO_Central	GO_REF:0000033
FNDC3A	Human	spermatid development	acts_upstream_of_or_within	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
FNDC3A	Human	acrosomal vesicle	located_in	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107
FNDC3A	Human	cytoplasm	is_active_in	IBA	MGI:1196463 more ...	150520179		GO_Central	GO_REF:0000033
FNDC3A	Human	cytoplasmic vesicle	located_in	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107
FNDC3A	Human	cytosol	located_in	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107
FNDC3A	Human	Golgi apparatus	located_in	IDA		150520179	PMID:18218838	UniProt	PMID:18218838
FNDC3A	Human	Golgi apparatus	located_in	IEA	UniProtKB-KW:KW-0333	150520179		UniProt	GO_REF:0000043
FNDC3A	Human	Golgi membrane	located_in	IEA	UniProtKB-SubCell:SL-0134	150520179		UniProt	GO_REF:0000044
FNDC3A	Human	intracellular membrane-bounded organelle	is_active_in	IBA	MGI:1196463 more ...	150520179		GO_Central	GO_REF:0000033
FNDC3A	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
FNDC3A	Human	membrane	is_active_in	IBA	MGI:1196463 and PANTHER:PTN008605752	150520179		GO_Central	GO_REF:0000033
FNDC3A	Human	membrane	located_in	HDA		150520179	PMID:19946888	UniProt	PMID:19946888
FNDC3A	Human	vesicle membrane	located_in	IEA	UniProtKB:Q8BX90 and ensembl:ENSMUSP00000086411	150520179		Ensembl	GO_REF:0000107

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
FNDC3A	Human	RNA binding	enables	HDA		150520179	PMID:22658674	UniProt	PMID:22658674

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
FNDC3A	Human	Intellectual disability		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:8889548	PMID:10231032	PMID:12168954	PMID:12477932	PMID:14702039	PMID:15057823	PMID:15489334	PMID:17081983	PMID:18029348	PMID:18218838	PMID:19322201	PMID:19946888
PMID:21832049	PMID:21873635	PMID:22658674	PMID:23639254	PMID:25476789	PMID:26186194	PMID:26496610	PMID:26638075	PMID:28380382	PMID:28514442	PMID:29117863	PMID:29180619
PMID:29395067	PMID:29568061	PMID:29955894	PMID:30021884	PMID:31056421	PMID:31073040	PMID:31177093	PMID:31871319	PMID:32235678	PMID:32344865	PMID:32788342	PMID:32877691
PMID:32878247	PMID:32963011	PMID:32966780	PMID:33957083	PMID:33961781	PMID:34079125	PMID:34273398	PMID:34432599	PMID:34672954	PMID:34709727	PMID:35211260	PMID:35271311
PMID:35384245	PMID:35906200	PMID:35944360	PMID:36215168	PMID:37774976	PMID:37931956	PMID:38334954	PMID:38569033	PMID:39231216

FNDC3A
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	13	48,975,291 - 49,209,779 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	13	48,975,912 - 49,209,779 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	13	49,550,048 - 49,783,915 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	13	48,448,049 - 48,681,916 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	13	48,448,939 - 48,681,729	NCBI
Celera	13	30,605,901 - 30,839,799 (+)	NCBI		Celera
Cytogenetic Map	13	q14.2	NCBI
HuRef	13	30,344,082 - 30,577,725 (+)	NCBI		HuRef
CHM1_1	13	49,517,625 - 49,751,465 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	13	48,193,984 - 48,431,085 (+)	NCBI		T2T-CHM13v2.0

Fndc3a
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	14	72,775,388 - 72,948,141 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	14	72,775,386 - 72,947,443 (-)	Ensembl		GRCm39 Ensembl
GRCm38	14	72,537,948 - 72,710,701 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	14	72,537,946 - 72,710,003 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	14	72,937,760 - 73,109,810 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	14	71,273,033 - 71,445,085 (-)	NCBI		MGSCv36	mm8
Celera	14	70,075,554 - 70,248,633 (-)	NCBI		Celera
Cytogenetic Map	14	D2	NCBI
cM Map	14	37.62	NCBI

Fndc3a
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	15	54,099,510 - 54,276,963 (-)	NCBI		GRCr8
mRatBN7.2	15	47,689,909 - 47,867,354 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	15	47,689,919 - 47,866,784 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	15	51,826,854 - 51,970,141 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	15	52,938,415 - 53,081,704 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	15	49,780,815 - 49,921,305 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	15	54,378,865 - 54,582,954 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	15	54,381,044 - 54,528,480 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	15	58,102,190 - 58,306,554 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	15	53,124,740 - 53,312,367 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	15	53,140,516 - 53,328,793 (-)	NCBI
Celera	15	47,348,000 - 47,488,015 (-)	NCBI		Celera
Cytogenetic Map	15	p11	NCBI

Fndc3a
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955431	2,553,892 - 2,696,744 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955431	2,553,311 - 2,696,596 (+)	NCBI	ChiLan1.0	ChiLan1.0

FNDC3A
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	14	50,419,146 - 50,647,201 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	13	49,070,446 - 49,298,260 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	13	30,119,740 - 30,347,544 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	13	48,820,120 - 49,047,770 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	13	48,820,018 - 49,049,274 (+)	Ensembl	panpan1.1		panPan2

FNDC3A
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	22	2,524,173 - 2,700,223 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	22	2,526,381 - 2,700,780 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	22	2,553,053 - 2,728,963 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	22	2,513,419 - 2,688,986 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	22	2,513,429 - 2,688,514 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	22	2,423,463 - 2,599,487 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	22	2,470,964 - 2,646,132 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	22	2,491,255 - 2,667,301 (-)	NCBI		UU_Cfam_GSD_1.0

Fndc3a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404945	158,670,041 - 158,828,620 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936565	2,154,599 - 2,312,862 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936565	2,154,672 - 2,312,670 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

FNDC3A
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	11	18,564,280 - 18,757,869 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	11	18,564,280 - 18,757,742 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	11	18,971,020 - 19,002,968 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

FNDC3A
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	3	26,902,353 - 27,121,248 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	3	26,902,353 - 27,121,008 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666057	16,770,535 - 16,992,110 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Fndc3a
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624748	5,501,411 - 5,716,737 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624748	5,503,053 - 5,716,734 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in FNDC3A
87 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3	copy number gain	See cases [RCV000050293]	Chr13:31363472..90575292 [GRCh38] Chr13:31937609..91227546 [GRCh37] Chr13:30835609..90025547 [NCBI36] Chr13:13q12.3-31.3	pathogenic
GRCh38/hg38 13q14.12-31.3(chr13:44967523-92738168)x1	copy number loss	See cases [RCV000050891]	Chr13:44967523..92738168 [GRCh38] Chr13:45541658..93390421 [GRCh37] Chr13:44439658..92188422 [NCBI36] Chr13:13q14.12-31.3	pathogenic
GRCh38/hg38 13q12.3-21.33(chr13:30697728-69471973)x1	copy number loss	See cases [RCV000051373]	Chr13:30697728..69471973 [GRCh38] Chr13:31271865..70046105 [GRCh37] Chr13:30169865..68944106 [NCBI36] Chr13:13q12.3-21.33	pathogenic
GRCh38/hg38 13q14.11-14.2(chr13:43505396-49983668)x1	copy number loss	See cases [RCV000051378]	Chr13:43505396..49983668 [GRCh38] Chr13:44079532..50557804 [GRCh37] Chr13:42977532..49455805 [NCBI36] Chr13:13q14.11-14.2	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	copy number gain	See cases [RCV000053731]	Chr13:19837395..114327173 [GRCh38] Chr13:20411535..115085141 [GRCh37] Chr13:19309535..114110750 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q12.3-31.1(chr13:30318913-83610426)x3	copy number gain	See cases [RCV000053737]	Chr13:30318913..83610426 [GRCh38] Chr13:30893050..84184561 [GRCh37] Chr13:29791050..83082562 [NCBI36] Chr13:13q12.3-31.1	pathogenic
GRCh38/hg38 13q11-34(chr13:18565048-114327173)x3	copy number gain	See cases [RCV000053719]	Chr13:18565048..114327173 [GRCh38] Chr13:19139188..115085141 [GRCh37] Chr13:18037188..114110750 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q11-34(chr13:18850545-114327173)x3	copy number gain	See cases [RCV000053723]	Chr13:18850545..114327173 [GRCh38] Chr13:19296527..115085141 [GRCh37] Chr13:18194527..114110750 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q12.11-34(chr13:18946182-114304628)x3	copy number gain	See cases [RCV000053726]	Chr13:18946182..114304628 [GRCh38] Chr13:19520322..115070103 [GRCh37] Chr13:18418322..114088205 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q13.2-34(chr13:33528097-114327173)x3	copy number gain	See cases [RCV000053759]	Chr13:33528097..114327173 [GRCh38] Chr13:34102234..115085141 [GRCh37] Chr13:33000234..114110750 [NCBI36] Chr13:13q13.2-34	pathogenic
GRCh38/hg38 13q14.11-34(chr13:43219125-114327314)x3	copy number gain	See cases [RCV000053762]	Chr13:43219125..114327314 [GRCh38] Chr13:43793261..115085141 [GRCh37] Chr13:42691261..114110891 [NCBI36] Chr13:13q14.11-34	pathogenic
GRCh38/hg38 13q14.11-34(chr13:44164751-114327173)x3	copy number gain	See cases [RCV000053764]	Chr13:44164751..114327173 [GRCh38] Chr13:44738887..115085141 [GRCh37] Chr13:43636887..114110750 [NCBI36] Chr13:13q14.11-34	pathogenic
GRCh38/hg38 13q14.12-34(chr13:44733046-114327173)x3	copy number gain	See cases [RCV000053767]	Chr13:44733046..114327173 [GRCh38] Chr13:45307182..115085141 [GRCh37] Chr13:44205182..114110750 [NCBI36] Chr13:13q14.12-34	pathogenic
NM_001079673.1(FNDC3A):c.2002C>T (p.Pro668Ser)	single nucleotide variant	Malignant melanoma [RCV000070383]	Chr13:49191072 [GRCh38] Chr13:49765208 [GRCh37] Chr13:48663209 [NCBI36] Chr13:13q14.2	not provided
NM_001079673.1(FNDC3A):c.2798G>A (p.Ser933Asn)	single nucleotide variant	Malignant melanoma [RCV000070384]	Chr13:49198385 [GRCh38] Chr13:49772521 [GRCh37] Chr13:48670522 [NCBI36] Chr13:13q14.2	not provided
GRCh38/hg38 13q13.3-21.31(chr13:36777318-62955876)x1	copy number loss	See cases [RCV000133696]	Chr13:36777318..62955876 [GRCh38] Chr13:37351455..63530009 [GRCh37] Chr13:36249455..62428010 [NCBI36] Chr13:13q13.3-21.31	pathogenic
GRCh38/hg38 13q14.11-31.1(chr13:41288493-85137552)x3	copy number gain	See cases [RCV000133944]	Chr13:41288493..85137552 [GRCh38] Chr13:41862629..85711687 [GRCh37] Chr13:40760629..84609688 [NCBI36] Chr13:13q14.11-31.1	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19833130-114298614)x3	copy number gain	See cases [RCV000134104]	Chr13:19833130..114298614 [GRCh38] Chr13:20407270..115064089 [GRCh37] Chr13:19305270..114082191 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q12.3-21.32(chr13:31553608-65470367)x3	copy number gain	See cases [RCV000135808]	Chr13:31553608..65470367 [GRCh38] Chr13:32127745..66044499 [GRCh37] Chr13:31025745..64942500 [NCBI36] Chr13:13q12.3-21.32	pathogenic
GRCh38/hg38 13q11-34(chr13:18445862-114327173)x1	copy number loss	See cases [RCV000135610]	Chr13:18445862..114327173 [GRCh38] Chr13:19020001..115085141 [GRCh37] Chr13:10098739..114110750 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q14.11-31.1(chr13:41143820-85137552)x1	copy number loss	See cases [RCV000136526]	Chr13:41143820..85137552 [GRCh38] Chr13:41717956..85711687 [GRCh37] Chr13:40615956..84609688 [NCBI36] Chr13:13q14.11-31.1	pathogenic
GRCh38/hg38 13q14.2-14.3(chr13:48307302-50927473)x1	copy number loss	See cases [RCV000136624]	Chr13:48307302..50927473 [GRCh38] Chr13:48881438..51501609 [GRCh37] Chr13:47779439..50399610 [NCBI36] Chr13:13q14.2-14.3	pathogenic
GRCh38/hg38 13q14.2-31.1(chr13:47117587-84300935)x1	copy number loss	See cases [RCV000136647]	Chr13:47117587..84300935 [GRCh38] Chr13:47691722..84875070 [GRCh37] Chr13:46589723..83773071 [NCBI36] Chr13:13q14.2-31.1	pathogenic
GRCh38/hg38 13q14.11-34(chr13:40942298-114340331)x1	copy number loss	See cases [RCV000137893]	Chr13:40942298..114340331 [GRCh38] Chr13:41516434..115085141 [GRCh37] Chr13:40414434..114123908 [NCBI36] Chr13:13q14.11-34	pathogenic
GRCh38/hg38 13q13.1-31.1(chr13:32531486-86757044)x3	copy number gain	See cases [RCV000138339]	Chr13:32531486..86757044 [GRCh38] Chr13:33105623..87409299 [GRCh37] Chr13:32003623..86207300 [NCBI36] Chr13:13q13.1-31.1	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19833130-114327106)x3	copy number gain	See cases [RCV000139078]	Chr13:19833130..114327106 [GRCh38] Chr13:20407270..115085141 [GRCh37] Chr13:19305270..114110683 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q11-34(chr13:18456040-114340285)x3	copy number gain	See cases [RCV000140004]	Chr13:18456040..114340285 [GRCh38] Chr13:19030180..115105760 [GRCh37] Chr13:17928180..114123862 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q13.3-21.32(chr13:37864226-67963788)x1	copy number loss	See cases [RCV000140744]	Chr13:37864226..67963788 [GRCh38] Chr13:38438363..68537920 [GRCh37] Chr13:37336363..67435921 [NCBI36] Chr13:13q13.3-21.32	pathogenic
GRCh38/hg38 13q13.3-14.3(chr13:38514177-51425214)x1	copy number loss	See cases [RCV000140788]	Chr13:38514177..51425214 [GRCh38] Chr13:39088314..51999350 [GRCh37] Chr13:37986314..50897351 [NCBI36] Chr13:13q13.3-14.3	pathogenic
GRCh38/hg38 13q14.2-21.31(chr13:47765202-62058520)x1	copy number loss	See cases [RCV000142223]	Chr13:47765202..62058520 [GRCh38] Chr13:48339337..62632653 [GRCh37] Chr13:47237338..61530654 [NCBI36] Chr13:13q14.2-21.31	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19671934-114340331)x3	copy number gain	See cases [RCV000142924]	Chr13:19671934..114340331 [GRCh38] Chr13:20246074..115085141 [GRCh37] Chr13:19144074..114123908 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q11-34(chr13:18862146-114342258)x3	copy number gain	See cases [RCV000143462]	Chr13:18862146..114342258 [GRCh38] Chr13:19436286..115107733 [GRCh37] Chr13:18334286..114125835 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q14.2(chr13:48591738-50064488)x3	copy number gain	See cases [RCV000143577]	Chr13:48591738..50064488 [GRCh38] Chr13:49165874..50638624 [GRCh37] Chr13:48063875..49536625 [NCBI36] Chr13:13q14.2	uncertain significance
GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3	copy number gain	See cases [RCV000148244]	Chr13:31363472..90575292 [GRCh38] Chr13:31937609..91227546 [GRCh37] Chr13:30835609..90025547 [NCBI36] Chr13:13q12.3-31.3	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	copy number gain	See cases [RCV000148126]	Chr13:19837395..114327173 [GRCh38] Chr13:20411535..115085141 [GRCh37] Chr13:19309535..114110750 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	copy number gain	See cases [RCV000240150]	Chr13:19571503..115092569 [GRCh37] Chr13:13q12.11-34	pathogenic
GRCh37/hg19 13q12.11-34(chr13:19571503-115092510)	copy number gain	See cases [RCV000449142]	Chr13:19571503..115092510 [GRCh37] Chr13:13q12.11-34	pathogenic
GRCh37/hg19 13q14.11-31.3(chr13:42457841-91796698)x1	copy number loss	See cases [RCV000446747]	Chr13:42457841..91796698 [GRCh37] Chr13:13q14.11-31.3	pathogenic
GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217)x1	copy number loss	See cases [RCV000446067]	Chr13:32946120..62698217 [GRCh37] Chr13:13q13.1-21.31	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	copy number gain	See cases [RCV000445886]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q14.2-14.3(chr13:48906943-52778614)x1	copy number loss	See cases [RCV000448535]	Chr13:48906943..52778614 [GRCh37] Chr13:13q14.2-14.3	pathogenic
GRCh37/hg19 13q14.2(chr13:49726336-50158142)x1	copy number loss	See cases [RCV000448039]	Chr13:49726336..50158142 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13q11-34(chr13:19436287-115107733)	copy number gain	See cases [RCV000510405]	Chr13:19436287..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q14.2-14.3(chr13:47312129-51342279)x1	copy number loss	See cases [RCV000511479]	Chr13:47312129..51342279 [GRCh37] Chr13:13q14.2-14.3	pathogenic
GRCh37/hg19 13q11-34(chr13:19436287-115107733)x3	copy number gain	See cases [RCV000511880]	Chr13:19436287..115107733 [GRCh37] Chr13:13q11-34	pathogenic
NM_001079673.2(FNDC3A):c.59T>G (p.Leu20Arg)	single nucleotide variant	not specified [RCV004318796]	Chr13:49006249 [GRCh38] Chr13:49580385 [GRCh37] Chr13:13q14.2	uncertain significance
Single allele	deletion	Intellectual disability [RCV000684766]	Chr13:48225451..58070399 [GRCh37] Chr13:13q14.2-21.1	likely pathogenic
GRCh37/hg19 13q14.2(chr13:49638092-50045664)x3	copy number gain	not provided [RCV000683525]	Chr13:49638092..50045664 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13q14.2(chr13:48292731-50577868)x3	copy number gain	not provided [RCV000683557]	Chr13:48292731..50577868 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13q11-22.1(chr13:19436286-74045459)x3	copy number gain	not provided [RCV000683572]	Chr13:19436286..74045459 [GRCh37] Chr13:13q11-22.1	pathogenic
NC_000013.11:g.46968080_87381985del40413906	deletion	Chromosome 13q14 deletion syndrome [RCV000721955]	Chr13:46968080..87381985 [GRCh38] Chr13:13q14.2-31.2	pathogenic
GRCh37/hg19 13q11-34(chr13:19058717-115103529)x3	copy number gain	not provided [RCV000738115]	Chr13:19058717..115103529 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19031237-115107157)x3	copy number gain	not provided [RCV000750643]	Chr13:19031237..115107157 [GRCh37] Chr13:13q11-34	pathogenic
NM_001079673.2(FNDC3A):c.1752C>T (p.Thr584=)	single nucleotide variant	FNDC3A-related disorder [RCV003916079]\|not provided [RCV000962477]	Chr13:49186098 [GRCh38] Chr13:49760234 [GRCh37] Chr13:13q14.2	benign
NM_001079673.2(FNDC3A):c.319A>G (p.Ser107Gly)	single nucleotide variant	not provided [RCV000967312]	Chr13:49131203 [GRCh38] Chr13:49705339 [GRCh37] Chr13:13q14.2	benign
NM_001079673.2(FNDC3A):c.825C>T (p.Ser275=)	single nucleotide variant	not provided [RCV000947526]	Chr13:49145783 [GRCh38] Chr13:49719919 [GRCh37] Chr13:13q14.2	benign
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	copy number gain	not provided [RCV000849129]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q14.2-21.2(chr13:49586017-61311845)x1	copy number loss	not provided [RCV000846575]	Chr13:49586017..61311845 [GRCh37] Chr13:13q14.2-21.2	uncertain significance
NM_001079673.2(FNDC3A):c.679G>C (p.Ala227Pro)	single nucleotide variant	not specified [RCV004299367]	Chr13:49136520 [GRCh38] Chr13:49710656 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13p13-q34(chr13:1-115169878)	copy number gain	Complete trisomy 13 syndrome [RCV002280659]	Chr13:1..115169878 [GRCh37] Chr13:13p13-q34	pathogenic
GRCh37/hg19 13q14.12-14.3(chr13:45487628-52639336)x3	copy number gain	not provided [RCV001258545]	Chr13:45487628..52639336 [GRCh37] Chr13:13q14.12-14.3	likely pathogenic
GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3	copy number gain	See cases [RCV001353184]	Chr13:19053605..115108528 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13p13-q34(chr13:1-115169878)x3	copy number gain	See cases [RCV001780076]	Chr13:1..115169878 [GRCh37] Chr13:13p13-q34	pathogenic
GRCh37/hg19 13q14.13-21.31(chr13:45819046-63910212)x1	copy number loss	not provided [RCV001795546]	Chr13:45819046..63910212 [GRCh37] Chr13:13q14.13-21.31	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-114981726)	copy number gain	not specified [RCV002053035]	Chr13:19436286..114981726 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q14.11-33.3(chr13:42504540-108206269)x3	copy number gain	not provided [RCV001829235]	Chr13:42504540..108206269 [GRCh37] Chr13:13q14.11-33.3	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)	copy number gain	not specified [RCV002053036]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217)	copy number loss	not specified [RCV002053048]	Chr13:32946120..62698217 [GRCh37] Chr13:13q13.1-21.31	pathogenic
GRCh37/hg19 13q14.11-31.3(chr13:42457841-91796698)	copy number loss	not specified [RCV002053057]	Chr13:42457841..91796698 [GRCh37] Chr13:13q14.11-31.3	pathogenic
GRCh37/hg19 13q14.11-14.3(chr13:44573371-53324137)	copy number loss	not specified [RCV002053058]	Chr13:44573371..53324137 [GRCh37] Chr13:13q14.11-14.3	pathogenic
GRCh37/hg19 13q13.3-31.1(chr13:36376204-80681753)	copy number loss	not specified [RCV002053052]	Chr13:36376204..80681753 [GRCh37] Chr13:13q13.3-31.1	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	copy number gain	not provided [RCV001834436]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3	copy number gain	not provided [RCV002291540]	Chr13:19253848..115108937 [GRCh37] Chr13:13q11-34	pathogenic
NM_001079673.2(FNDC3A):c.3113A>G (p.Tyr1038Cys)	single nucleotide variant	not specified [RCV004329185]	Chr13:49201925 [GRCh38] Chr13:49776061 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1579G>T (p.Val527Leu)	single nucleotide variant	not specified [RCV004323660]	Chr13:49178616 [GRCh38] Chr13:49752752 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3494G>A (p.Arg1165Gln)	single nucleotide variant	not specified [RCV004204890]	Chr13:49207292 [GRCh38] Chr13:49781428 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2816T>C (p.Phe939Ser)	single nucleotide variant	not specified [RCV004151199]	Chr13:49198403 [GRCh38] Chr13:49772539 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3310C>T (p.Arg1104Trp)	single nucleotide variant	not specified [RCV004238272]	Chr13:49207108 [GRCh38] Chr13:49781244 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1178C>T (p.Ala393Val)	single nucleotide variant	not specified [RCV004161702]	Chr13:49172044 [GRCh38] Chr13:49746180 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2210C>T (p.Ala737Val)	single nucleotide variant	not specified [RCV004224207]	Chr13:49191368 [GRCh38] Chr13:49765504 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.881A>G (p.Asn294Ser)	single nucleotide variant	not specified [RCV004144160]	Chr13:49145839 [GRCh38] Chr13:49719975 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3425T>C (p.Leu1142Pro)	single nucleotide variant	not specified [RCV004093101]	Chr13:49207223 [GRCh38] Chr13:49781359 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.538A>T (p.Ser180Cys)	single nucleotide variant	not specified [RCV004097420]	Chr13:49136379 [GRCh38] Chr13:49710515 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.165G>C (p.Gln55His)	single nucleotide variant	not specified [RCV004240152]	Chr13:49075354 [GRCh38] Chr13:49649490 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1136T>C (p.Ile379Thr)	single nucleotide variant	not specified [RCV004104420]	Chr13:49168711 [GRCh38] Chr13:49742847 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.584G>A (p.Gly195Glu)	single nucleotide variant	not specified [RCV004140310]	Chr13:49136425 [GRCh38] Chr13:49710561 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1142A>G (p.Asn381Ser)	single nucleotide variant	not specified [RCV004077232]	Chr13:49168717 [GRCh38] Chr13:49742853 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.766G>C (p.Asp256His)	single nucleotide variant	not specified [RCV004229181]	Chr13:49138752 [GRCh38] Chr13:49712888 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.355C>G (p.Leu119Val)	single nucleotide variant	not specified [RCV004188558]	Chr13:49131239 [GRCh38] Chr13:49705375 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.46A>G (p.Ser16Gly)	single nucleotide variant	not specified [RCV004211336]	Chr13:49006236 [GRCh38] Chr13:49580372 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2289G>C (p.Lys763Asn)	single nucleotide variant	not specified [RCV004147222]	Chr13:49196939 [GRCh38] Chr13:49771075 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3506G>A (p.Ser1169Asn)	single nucleotide variant	not specified [RCV004175284]	Chr13:49207304 [GRCh38] Chr13:49781440 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1712C>T (p.Ser571Leu)	single nucleotide variant	not provided [RCV004695396]\|not specified [RCV004091729]	Chr13:49186058 [GRCh38] Chr13:49760194 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.742G>A (p.Val248Ile)	single nucleotide variant	not specified [RCV004081129]	Chr13:49136583 [GRCh38] Chr13:49710719 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.100-8T>C	single nucleotide variant	not provided [RCV003393316]	Chr13:49075281 [GRCh38] Chr13:49649417 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.3320G>A (p.Ser1107Asn)	single nucleotide variant	not specified [RCV004251964]	Chr13:49207118 [GRCh38] Chr13:49781254 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1507T>G (p.Leu503Val)	single nucleotide variant	not specified [RCV004276405]	Chr13:49175518 [GRCh38] Chr13:49749654 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1006G>A (p.Asp336Asn)	single nucleotide variant	not specified [RCV004286933]	Chr13:49167272 [GRCh38] Chr13:49741408 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1879C>G (p.Arg627Gly)	single nucleotide variant	not specified [RCV004278636]	Chr13:49188568 [GRCh38] Chr13:49762704 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.404A>C (p.His135Pro)	single nucleotide variant	not specified [RCV004268277]	Chr13:49131288 [GRCh38] Chr13:49705424 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2590G>A (p.Asp864Asn)	single nucleotide variant	not specified [RCV004343432]	Chr13:49198081 [GRCh38] Chr13:49772217 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3548T>G (p.Phe1183Cys)	single nucleotide variant	not specified [RCV004350960]	Chr13:49207346 [GRCh38] Chr13:49781482 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.536C>G (p.Ser179Cys)	single nucleotide variant	not specified [RCV004355910]	Chr13:49136377 [GRCh38] Chr13:49710513 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2206C>T (p.Arg736Cys)	single nucleotide variant	not specified [RCV004353053]	Chr13:49191364 [GRCh38] Chr13:49765500 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.115G>A (p.Val39Ile)	single nucleotide variant	not specified [RCV004353052]	Chr13:49075304 [GRCh38] Chr13:49649440 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2100A>C (p.Glu700Asp)	single nucleotide variant	not specified [RCV004344605]	Chr13:49191258 [GRCh38] Chr13:49765394 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.481G>A (p.Gly161Arg)	single nucleotide variant	not specified [RCV004351581]	Chr13:49131365 [GRCh38] Chr13:49705501 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13q14.11-21.2(chr13:44076923-60520078)x1	copy number loss	not specified [RCV003987012]	Chr13:44076923..60520078 [GRCh37] Chr13:13q14.11-21.2	pathogenic
GRCh37/hg19 13q13.2-21.1(chr13:35015723-59553519)x3	copy number gain	not specified [RCV003987040]	Chr13:35015723..59553519 [GRCh37] Chr13:13q13.2-21.1	pathogenic
GRCh37/hg19 13q14.2-32.2(chr13:49547974-98214905)x1	copy number loss	not specified [RCV003987008]	Chr13:49547974..98214905 [GRCh37] Chr13:13q14.2-32.2	pathogenic
GRCh37/hg19 13q13.2-21.2(chr13:34884647-61309742)x1	copy number loss	not provided [RCV003885457]	Chr13:34884647..61309742 [GRCh37] Chr13:13q13.2-21.2	pathogenic
NM_001079673.2(FNDC3A):c.2589C>T (p.Ser863=)	single nucleotide variant	FNDC3A-related disorder [RCV003977169]	Chr13:49198080 [GRCh38] Chr13:49772216 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.761-3A>T	single nucleotide variant	FNDC3A-related disorder [RCV003936799]	Chr13:49138744 [GRCh38] Chr13:49712880 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.3132A>G (p.Lys1044=)	single nucleotide variant	FNDC3A-related disorder [RCV003916910]	Chr13:49201944 [GRCh38] Chr13:49776080 [GRCh37] Chr13:13q14.2	benign
NM_001079673.2(FNDC3A):c.1653A>G (p.Pro551=)	single nucleotide variant	FNDC3A-related disorder [RCV003934080]	Chr13:49185999 [GRCh38] Chr13:49760135 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.2043A>G (p.Leu681=)	single nucleotide variant	FNDC3A-related disorder [RCV003941986]	Chr13:49191113 [GRCh38] Chr13:49765249 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.1221A>G (p.Glu407=)	single nucleotide variant	FNDC3A-related disorder [RCV003934605]	Chr13:49172087 [GRCh38] Chr13:49746223 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.3049A>G (p.Thr1017Ala)	single nucleotide variant	FNDC3A-related disorder [RCV003974691]	Chr13:49201861 [GRCh38] Chr13:49775997 [GRCh37] Chr13:13q14.2	benign
NM_001079673.2(FNDC3A):c.2366T>C (p.Val789Ala)	single nucleotide variant	not specified [RCV004391931]	Chr13:49197750 [GRCh38] Chr13:49771886 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2751T>G (p.Asn917Lys)	single nucleotide variant	not specified [RCV004391933]	Chr13:49198242 [GRCh38] Chr13:49772378 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3206G>C (p.Cys1069Ser)	single nucleotide variant	not specified [RCV004391938]	Chr13:49203208 [GRCh38] Chr13:49777344 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.496C>T (p.His166Tyr)	single nucleotide variant	not specified [RCV004391939]	Chr13:49136337 [GRCh38] Chr13:49710473 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.244G>A (p.Ala82Thr)	single nucleotide variant	not specified [RCV004391932]	Chr13:49114723 [GRCh38] Chr13:49688859 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2941A>G (p.Thr981Ala)	single nucleotide variant	not specified [RCV004391934]	Chr13:49198528 [GRCh38] Chr13:49772664 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.1378T>C (p.Tyr460His)	single nucleotide variant	not specified [RCV004391928]	Chr13:49175389 [GRCh38] Chr13:49749525 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2053C>T (p.Pro685Ser)	single nucleotide variant	not specified [RCV004391929]	Chr13:49191211 [GRCh38] Chr13:49765347 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1144C>T (p.Arg382Trp)	single nucleotide variant	not specified [RCV004391925]	Chr13:49168719 [GRCh38] Chr13:49742855 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1366G>C (p.Glu456Gln)	single nucleotide variant	not specified [RCV004391927]	Chr13:49175377 [GRCh38] Chr13:49749513 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.499T>G (p.Ser167Ala)	single nucleotide variant	not specified [RCV004391940]	Chr13:49136340 [GRCh38] Chr13:49710476 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3122C>G (p.Thr1041Ser)	single nucleotide variant	not specified [RCV004391935]	Chr13:49201934 [GRCh38] Chr13:49776070 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.769G>A (p.Glu257Lys)	single nucleotide variant	not specified [RCV004391941]	Chr13:49138755 [GRCh38] Chr13:49712891 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2168G>A (p.Ser723Asn)	single nucleotide variant	not specified [RCV004626023]	Chr13:49191326 [GRCh38] Chr13:49765462 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3382C>G (p.Leu1128Val)	single nucleotide variant	not specified [RCV004626024]	Chr13:49207180 [GRCh38] Chr13:49781316 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.1936C>G (p.Gln646Glu)	single nucleotide variant	not specified [RCV004626025]	Chr13:49188625 [GRCh38] Chr13:49762761 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2944G>A (p.Asp982Asn)	single nucleotide variant	not specified [RCV004626026]	Chr13:49198531 [GRCh38] Chr13:49772667 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.965A>G (p.Lys322Arg)	single nucleotide variant	not specified [RCV004626027]	Chr13:49145923 [GRCh38] Chr13:49720059 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.578G>T (p.Arg193Leu)	single nucleotide variant	not specified [RCV004626028]	Chr13:49136419 [GRCh38] Chr13:49710555 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2509G>A (p.Ala837Thr)	single nucleotide variant	not specified [RCV004626029]	Chr13:49198000 [GRCh38] Chr13:49772136 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2750A>G (p.Asn917Ser)	single nucleotide variant	not specified [RCV004626030]	Chr13:49198241 [GRCh38] Chr13:49772377 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2452G>A (p.Gly818Arg)	single nucleotide variant	not specified [RCV004919122]	Chr13:49197836 [GRCh38] Chr13:49771972 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.826G>A (p.Asp276Asn)	single nucleotide variant	not specified [RCV004916632]	Chr13:49145784 [GRCh38] Chr13:49719920 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2189C>T (p.Thr730Ile)	single nucleotide variant	not specified [RCV004916636]	Chr13:49191347 [GRCh38] Chr13:49765483 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.841A>G (p.Thr281Ala)	single nucleotide variant	not specified [RCV004916639]	Chr13:49145799 [GRCh38] Chr13:49719935 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.928G>A (p.Val310Ile)	single nucleotide variant	not specified [RCV004916629]	Chr13:49145886 [GRCh38] Chr13:49720022 [GRCh37] Chr13:13q14.2	likely benign
NM_001079673.2(FNDC3A):c.821C>T (p.Ala274Val)	single nucleotide variant	not specified [RCV004916633]	Chr13:49145779 [GRCh38] Chr13:49719915 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2130A>T (p.Arg710Ser)	single nucleotide variant	not specified [RCV004916638]	Chr13:49191288 [GRCh38] Chr13:49765424 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.2275C>A (p.Pro759Thr)	single nucleotide variant	not specified [RCV004919121]	Chr13:49196925 [GRCh38] Chr13:49771061 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1910G>A (p.Arg637Gln)	single nucleotide variant	not specified [RCV004916630]	Chr13:49188599 [GRCh38] Chr13:49762735 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3115A>G (p.Ile1039Val)	single nucleotide variant	not specified [RCV004916635]	Chr13:49201927 [GRCh38] Chr13:49776063 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1927G>T (p.Asp643Tyr)	single nucleotide variant	not specified [RCV004916637]	Chr13:49188616 [GRCh38] Chr13:49762752 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.1145G>A (p.Arg382Gln)	single nucleotide variant	not specified [RCV004916631]	Chr13:49168720 [GRCh38] Chr13:49742856 [GRCh37] Chr13:13q14.2	uncertain significance
NM_001079673.2(FNDC3A):c.3067A>C (p.Ile1023Leu)	single nucleotide variant	not specified [RCV004916634]	Chr13:49201879 [GRCh38] Chr13:49776015 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13q12.3-14.3(chr13:32076445-54495559)x1	copy number loss	not provided [RCV004819377]	Chr13:32076445..54495559 [GRCh37] Chr13:13q12.3-14.3	pathogenic
NM_001079673.2(FNDC3A):c.53T>C (p.Ile18Thr)	single nucleotide variant	not specified [RCV004919120]	Chr13:49006243 [GRCh38] Chr13:49580379 [GRCh37] Chr13:13q14.2	uncertain significance
GRCh37/hg19 13q11-31.3(chr13:19436287-92292639)x3	copy number gain	not provided [RCV004819310]	Chr13:19436287..92292639 [GRCh37] Chr13:13q11-31.3	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	3141
Count of miRNA genes:	878
Interacting mature miRNAs:	1020
Transcripts:	ENST00000378383, ENST00000398316, ENST00000484074, ENST00000492622, ENST00000497644, ENST00000541916
Prediction methods:	Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
406959045	GWAS608021_H	ankylosing spondylitis, psoriasis, ulcerative colitis, Crohn's disease, sclerosing cholangitis QTL GWAS608021 (human)		0.0000001	intestine integrity trait (VT:0010554)		13	49021195	49021196	Human
597285747	GWAS1381821_H	inflammatory bowel disease QTL GWAS1381821 (human)		4e-08	inflammatory bowel disease		13	49021195	49021196	Human
597275730	GWAS1371804_H	insomnia QTL GWAS1371804 (human)		7e-10	insomnia		13	49066537	49066538	Human
407086120	GWAS735096_H	preterm premature rupture of the membranes, spontaneous preterm birth QTL GWAS735096 (human)		0.000007	preterm premature rupture of the membranes, spontaneous preterm birth		13	49071567	49071568	Human
597050266	GWAS1146340_H	uterine fibroid QTL GWAS1146340 (human)		0.000006	uterine fibroid		13	49209079	49209080	Human
597224501	GWAS1320575_H	cystatin C measurement QTL GWAS1320575 (human)		9e-35	cystatin C measurement	blood cystatin C level (CMO:0002777)	13	49174144	49174145	Human
597286902	GWAS1382976_H	Crohn's disease QTL GWAS1382976 (human)		0.000007	intestine integrity trait (VT:0010554)		13	49021195	49021196	Human
597050265	GWAS1146339_H	uterine fibroid QTL GWAS1146339 (human)		0.000005	uterine fibroid		13	49037911	49037912	Human
596959972	GWAS1079491_H	glomerular filtration rate QTL GWAS1079491 (human)		2e-31	glomerular filtration rate		13	49096917	49096918	Human
596960262	GWAS1079781_H	glomerular filtration rate QTL GWAS1079781 (human)		2e-62	glomerular filtration rate		13	49096917	49096918	Human
2292823	PRSTS88_H	Prostate tumor susceptibility QTL 88 (human)			Prostate tumor susceptibility		13	41532058	67532058	Human
597318863	GWAS1414937_H	N-acetylmethionine measurement QTL GWAS1414937 (human)		0.0000008	N-acetylmethionine measurement		13	49118944	49118945	Human
1643298	BW212_H	Body weight QTL 212 (human)	2.67	0.0002	Body weight	BMI	13	41532058	67532058	Human
596979049	GWAS1098568_H	Crohn's disease QTL GWAS1098568 (human)		0.000007	Crohn's disease		13	49021195	49021196	Human
597067017	GWAS1163091_H	susceptibility to common cold measurement QTL GWAS1163091 (human)		0.000009	susceptibility to common cold measurement		13	49004804	49004805	Human

RH45056

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,680,635 - 49,680,871	UniSTS	GRCh37
Build 36	13	48,578,636 - 48,578,872	RGD	NCBI36
Celera	13	30,736,506 - 30,736,742	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,474,425 - 30,474,661	UniSTS
GeneMap99-GB4 RH Map	13	151.97	UniSTS

D13S1171

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,688,182 - 49,688,285	UniSTS	GRCh37
Build 36	13	48,586,183 - 48,586,286	RGD	NCBI36
Celera	13	30,744,054 - 30,744,157	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,481,974 - 30,482,077	UniSTS
Whitehead-RH Map	13	140.8	UniSTS
Whitehead-YAC Contig Map	13		UniSTS

WI-18286

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,666,737 - 49,666,861	UniSTS	GRCh37
Build 36	13	48,564,738 - 48,564,862	RGD	NCBI36
Celera	13	30,722,617 - 30,722,741	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,460,536 - 30,460,660	UniSTS
GeneMap99-GB4 RH Map	13	151.97	UniSTS
Whitehead-RH Map	13	140.6	UniSTS

G28207

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,549,705 - 49,549,851	UniSTS	GRCh37
Build 36	13	48,447,706 - 48,447,852	RGD	NCBI36
Celera	13	30,605,558 - 30,605,704	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,343,739 - 30,343,885	UniSTS

RH69432

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,761,746 - 49,761,827	UniSTS	GRCh37
GRCh37	1	202,736,488 - 202,736,569	UniSTS	GRCh37
Build 36	1	201,003,111 - 201,003,192	RGD	NCBI36
Celera	13	30,817,623 - 30,817,704	UniSTS
Celera	1	175,864,368 - 175,864,449	RGD
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	13	q14-q21	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,555,551 - 30,555,632	UniSTS

RH98674

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,653,250 - 49,653,415	UniSTS	GRCh37
Build 36	13	48,551,251 - 48,551,416	RGD	NCBI36
Celera	13	30,709,131 - 30,709,296	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,447,050 - 30,447,215	UniSTS
GeneMap99-GB4 RH Map	13	151.97	UniSTS

RH47134

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,783,117 - 49,783,305	UniSTS	GRCh37
Build 36	13	48,681,118 - 48,681,306	RGD	NCBI36
Celera	13	30,839,001 - 30,839,189	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,576,927 - 30,577,115	UniSTS
GeneMap99-GB4 RH Map	13	149.17	UniSTS

RH44749

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,781,500 - 49,781,657	UniSTS	GRCh37
Build 36	13	48,679,501 - 48,679,658	RGD	NCBI36
Celera	13	30,837,384 - 30,837,541	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,575,310 - 30,575,467	UniSTS
GeneMap99-GB4 RH Map	13	148.39	UniSTS

A006G05

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,783,685 - 49,783,852	UniSTS	GRCh37
Build 36	13	48,681,686 - 48,681,853	RGD	NCBI36
Celera	13	30,839,569 - 30,839,736	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,577,495 - 30,577,662	UniSTS
GeneMap99-GB4 RH Map	13	153.75	UniSTS

A005T12

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,549,571 - 49,549,748	UniSTS	GRCh37
Build 36	13	48,447,572 - 48,447,749	RGD	NCBI36
Celera	13	30,605,424 - 30,605,601	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,343,605 - 30,343,782	UniSTS
GeneMap99-GB4 RH Map	13	148.07	UniSTS

RH45787

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,714,993 - 49,715,150	UniSTS	GRCh37
Build 36	13	48,612,994 - 48,613,151	RGD	NCBI36
Celera	13	30,770,866 - 30,771,023	RGD
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,508,788 - 30,508,945	UniSTS
GeneMap99-GB4 RH Map	13	151.97	UniSTS

D15S1477

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	4	q32-q35	UniSTS
Cytogenetic Map	5	q11	UniSTS
Cytogenetic Map	10	p12.1	UniSTS
Cytogenetic Map	10	p12.1-p11.2	UniSTS
Cytogenetic Map	15	q13	UniSTS
Cytogenetic Map	21	q21.3	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	3	p24.3	UniSTS
Cytogenetic Map	5	q14	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	7	p21.3	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	14	q31-q32	UniSTS
Cytogenetic Map	10	q25.2	UniSTS
Cytogenetic Map	16	p13.13-p13.12	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	2	p22.1	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	15	q21.1	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	1	q41	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	1	q42.11	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	6	q16.2	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	X	q26.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	7	q21.2	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	11	q14.2	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	5	q23	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	13	q12.1	UniSTS
Cytogenetic Map	6	p21.32	UniSTS
Cytogenetic Map	2	q31	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	3	p21.2	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	4	q28.2	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	22	q12.3	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	19	p	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	q11.21	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	10	q23.2	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	9	q34.13	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	1	q31.3	UniSTS
Cytogenetic Map	4	q35	UniSTS
Cytogenetic Map	9	p13	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	6	q25.2-q25.3	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	7	q22.3	UniSTS
Cytogenetic Map	9	q34.2	UniSTS
Cytogenetic Map	17	q24	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	20	q13	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	17	q22-q23	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	7	p15.2	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	16	q12.2	UniSTS
Cytogenetic Map	13	q11	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	3	p25-p24	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	3	p12	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	X	p11.2	UniSTS
Cytogenetic Map	11	q13.1-q13.2	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	3	q26.2	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	6	p21.1-p12.2	UniSTS
Cytogenetic Map	12	q14.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	1	p35	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	8	q23.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	14	q11.1	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	3	p14.1	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	1	p36.11-p34.2	UniSTS
Cytogenetic Map	9	p22	UniSTS
Cytogenetic Map	1	q42.12	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	9	p22.1	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	20	p11.23	UniSTS
Cytogenetic Map	15	q15.2	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	8	q12.1	UniSTS
Cytogenetic Map	14	q21.2	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	18	q12.3	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	12	q11-q12	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	2	p24	UniSTS
Cytogenetic Map	8	q24.21	UniSTS
Cytogenetic Map	12	q22-q23.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	15	q21-q22	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	10	q24	UniSTS
Cytogenetic Map	8	q11.2	UniSTS
Cytogenetic Map	7	p14-p13	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	6	q22-q23	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	4	q21.22	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	16	p12.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	11	q24.3	UniSTS
Cytogenetic Map	11	q13.1-q13.3	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	2	q24	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	15	q21-q23	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	3	p22.1	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	6	p21	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	14	q23.1	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	11	q12	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	10	q21.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	4	q31.1	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	18	q21.3	UniSTS
Cytogenetic Map	11	q21	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	11	q23.2	UniSTS
Cytogenetic Map	8	q12	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	12	q24.11	UniSTS
Cytogenetic Map	9	q21.12	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	20	p11.22-p11.1	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	16	q23.1	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	9	q31-q33	UniSTS
Cytogenetic Map	6	p24.1	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	5	q35.2	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	3	q26.1-q26.2	UniSTS
Cytogenetic Map	5	q11.2-q13.2	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	X	q13.3	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	5	q35.1	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	4	q21.21	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	X	q21.1	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	5	q34	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	12	q21	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	7	q22-q31	UniSTS
Cytogenetic Map	22	q12	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	12	q14	UniSTS
Cytogenetic Map	11	q23.1-q23.2	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	17	q	UniSTS
Cytogenetic Map	2	q33	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	5	q21.3	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	6	p24.2	UniSTS

L18426

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	18	q12.1-q21.1	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	5	q31.3	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	14	q21	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	10	p11	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	9	p13.2	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	9	q34.1	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	2	p23.1	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	9	q21.32	UniSTS
Cytogenetic Map	1	p34-p33	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	17	q21.1	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	20	q11.2-q13.2	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	8	p23-p22	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	17	q21-q22	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	13	q11	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	7	p12.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	X	p22	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	2	p25	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	1	p21.3	UniSTS
Cytogenetic Map	19	q13.13	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	1	p35-p34.3	UniSTS
Cytogenetic Map	5	q35.1	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	4	q22.1-q23	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	17	q22-q23.2	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	18	q22.3	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	12	q24.1-q24.3	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	9	p24.2	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	3	p22.1	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	1	p32	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	6	q25.1-q26	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	17	q23.1	UniSTS
Cytogenetic Map	X	q13-q21	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	10	q22.1	UniSTS
Cytogenetic Map	1	q41	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	3	q28-q29	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	1	q41-q42.2	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	11	p11.11	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	1	q43	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	8	q11.2	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	13	q12-q14	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	14	q31	UniSTS
Cytogenetic Map	8	p12-p11	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	17	q23.2	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	21	q22.1	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	2	p15-p13	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	3	p14.1	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	13	q11-q12	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	3	q12	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	16	p13.11	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	1	p21	UniSTS
Cytogenetic Map	7	p14.2	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	18	p11.22	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	1	q22-q23	UniSTS
Cytogenetic Map	4	q21.22	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	9	q31-q33	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	9	q22.1-q22.2	UniSTS
Cytogenetic Map	4	q26	UniSTS
Cytogenetic Map	4	q28.1	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	21	q21.1	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	12	p12.3	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	12	q13.11	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	4	q35.2	UniSTS
Cytogenetic Map	4	q28.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	11	q24.3	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	8	q23.3	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	X	p21.1	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	X	p11.23	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	5	p15.3	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	22	q12	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	19	q13.1-q13.2	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	7	q31.3	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	1	p13-p12	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	14	q32.2	UniSTS
Cytogenetic Map	15	q24.1	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	10	q21.1	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	1	p36	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	20	p11.21	UniSTS
Cytogenetic Map	12	q24.1	UniSTS
Cytogenetic Map	5	q31.2	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	1	q12	UniSTS
Cytogenetic Map	22	q11.22	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	14	q32.3	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	16	p13.13-p13.12	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	3	q27	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	1	p13.1	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	16	q13	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	13	q14.3	UniSTS
Cytogenetic Map	14	q24	UniSTS
Cytogenetic Map	14	q22-q24	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	10	q11	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	20	q12	UniSTS
Cytogenetic Map	2	q13	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	12	q21.31	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	19	q12	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	11	q14.2	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	X	q21.1	UniSTS
Cytogenetic Map	9	p21.1	UniSTS

G32341

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	49,783,685 - 49,783,852	UniSTS	GRCh37
Celera	13	30,839,569 - 30,839,736	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
HuRef	13	30,577,495 - 30,577,662	UniSTS

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2253	4973	1726	2351	5	624	1949	465	2269	7301	6468	51	3734	1	852	1744	1616	175	1


RefSeq Transcripts	NM_001079673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001278438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_014923	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_103528	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011534997	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020440	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020441	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020443	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054374243	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054374244	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054374245	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB023187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ749706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ749707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056071	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK172814	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302415	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL137000	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL161421	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL359184	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC036010	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC051029	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC060816	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC070072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC107793	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC132812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC136617	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC144301	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM973827	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX640739	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471075	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB460317	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000378383 ⟹ ENSP00000484320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	48,976,069 - 49,146,847 (+)	Ensembl

Ensembl Acc Id:

ENST00000398316 ⟹ ENSP00000381362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	49,110,313 - 49,209,593 (+)	Ensembl

Ensembl Acc Id:

ENST00000484074 ⟹ ENSP00000420275

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	48,976,673 - 49,209,607 (+)	Ensembl

Ensembl Acc Id:

ENST00000492622 ⟹ ENSP00000417257

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	48,975,912 - 49,209,779 (+)	Ensembl

Ensembl Acc Id:

ENST00000497644 ⟹ ENSP00000418703

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	49,198,210 - 49,203,205 (+)	Ensembl

Ensembl Acc Id:

ENST00000541916 ⟹ ENSP00000441831

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	48,976,609 - 49,209,778 (+)	Ensembl

RefSeq Acc Id:

NM_001079673 ⟹ NP_001073141

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,975,912 - 49,209,779 (+)	NCBI
GRCh37	13	49,550,048 - 49,783,915 (+)	RGD
Build 36	13	48,448,049 - 48,681,916 (+)	NCBI Archive
Celera	13	30,605,901 - 30,839,799 (+)	RGD
HuRef	13	30,344,082 - 30,577,725 (+)	RGD
CHM1_1	13	49,517,625 - 49,751,465 (+)	NCBI
T2T-CHM13v2.0	13	48,197,201 - 48,431,085 (+)	NCBI

Sequence:

show sequence

CTCCCGGCTCCGTAGTAAGCATGGCGGCGGCGGCGTTCGTGGTCCCTCGGGTGAAACAGAAAGCGGGAGCTACGCGGAGAGGGAGCGAAGAGCGGGGCTGAGGCGGCGGCGTCACTGCCAGGAAACAA
CCCCAACAGTCAGCGCGCCGGCGGCCGCGGCGGCCCTGAGAGCTGACTCTGCAGCTGAGGTAGAGAGACAACGATCAGGAACCCTAAGAAGAGGCGCCAGAGGAGCCGCCTTCTGCCTCAGAACGGCG
TGACTCGGAGAATTGGAGCGTTATTCAGTATATTAATGTCTTATTGATAATGGCAGAACATCCACCACTACTGGATACAACTCAGATCTTAAGTAGTGATATTTCTCTTTTGTCTGCCCCTATTGTAA
GTGCAGATGGAACACAACAGGTTATTCTGGTACAAGTTAACCCAGGAGAAGCATTTACAATAAGAAGAGAAGATGGACAGTTTCAGTGCATTACAGGTCCTGCTCAGGTTCCAATGATGTCCCCAAAT
GGTTCTGTGCCTCCTATCTATGTGCCTCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGTTGTCGTGGTCCCTCAGGCACCAGAGTTTCACCCTGGTAGTCACACAGTTCTCCA
CCGTTCTCCACATCCTCCTCTACCTGGTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGTACTCACCCGTGACTGGAGCTGGAGACATGACAACACAGTATATGCCACAGTATC
AGTCTTCACAAGTCTATGGAGATGTAGATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCTAGTAAAACATATGAACGTTTGCAGAAAAAATTGAAGGATCGCCAAGGAACACAG
AAAGATAAAATGAGCAGTCCACCATCATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTATAAAAGGACAAATTGCTGGTGGTATAAACACAGGATCAGCAAAAATCAAGTCTGG
GAAGGGGAAAGGTGGTACACAAGTTGATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCACTTCTTTCCAACATTGTCAAACCAGTGGCCTCCGACATCCAGGCAAGGACAGTAG
TACTTACCTGGTCACCACCTTCCAGCCTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGTTATGAAGTTCTGATCTCAAGTACTGGAAAAGATGGGAAATACAAAAGTGTATAT
GTAGGAGAAGAAACAAATATCACTTTAAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGAATATAATTCTATAAAGGGAACTCCTTCAGAGGCTGAAATCTTTACCACCTTGAG
CTGTGAACCTGATATACCTAATCCACCAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGGCACCTAGTGACAATGGTTCTAAAATCCAAAACTTTGTATTAGAATGGGATGAAG
GAAAAGGAAATGGAGAATTTTGTCAGTGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCAGCAATGGGCTGTAAATTCAGACTATCGGCCAGAAATGACTATGGTACAAGTGGT
TTTAGTGAAGAAGTCTTATATTACACCTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGCTGGAATTACTTGGTTATCCTTACAATGGAGTAAGCCCTCAGGAACACCATCAGA
TGAAGGAATTTCTTACATTTTAGAGATGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAGAAGATCTTGCTTACACAGTGAAAAATCTCAGACGTAGTACTAAGTATAAATTTA
AGGTTATTGCTTACAACTCAGAAGGTAAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAACCAGGCATACCTGTAAAGCCTTCAGTGAAAGGAAAGATACATTCACACAGTTTT
AAAATAACCTGGGATCCACCAAAAGACAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGGTTCTAACGGAAACAAATGGGAAATGATATACAGTGGTGCTACCAGGGAACATCT
TTGTGATCGACTGAATCCAGGCTGTTTCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGGTCTCTGAATCTTTACTTGTGCAGACTCCAGCTGTGCCTCCTGGCCCATGCCTCC
CTCCCAGATTACAGGGTAGACCCAAAGCAAAAGAAATACAGTTACGATGGGGACCCCCTCTGGTTGATGGTGGATCACCCATTTCCTGTTACAGTGTGGAAATGTCTCCTATAGAAAAAGATGAACCT
AGAGAAGTTTACCAAGGTTCTGAAGTAGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAGACTACGTGCAGCTAACAAAATGGGGTTTGGACCATTTTCAGAAAAATGTGATAT
TACTACAGCCCCTGGGCCACCAGATCAGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAGTGAATTGGGAGGTTCCTTTGAGTAATGGAACAGATGTCACTGAATATCGACTGG
AGTGGGGAGGAGTTGAAGGAAGTATGCAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTTTCACCAGCAACTACCTATTATTGCAGGGTCCAGGCTCTGAGTGTTGTGGGTGCA
GGCCCTTTCAGTGAAGTAGTAGCCTGTGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAATAAGCGATGATGAGATAGAAAATCCCCATTATTCACCTTCTACATGCCTTGCAAT
AAGCTGGGAAAAGCCTTGTGATCATGGTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCCTAACAGTGGGAAAGGTTACAAGCTATATTATCAACAATTTGCAACCAGATACAA
CATACAGAATACGAATTCAAGCCTTGAATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACTAAGCCTCTCCCTCCTGATCCACCTCGTCTGGAATGTGTTGCCTTTAGCCACCAG
AACCTTAAGCTGAAATGGGGAGAAGGAACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGATGGAGGATAAGAATGGACGGTTTGTATCCCTATACAGAGGACCATGTCATACATA
CAAAGTACAAAGACTTAATGAGTCAACATCCTATAAATTCTGTATTCAAGCTTGTAATGAAGCTGGGGAAGGTCCCCTCTCCCAAGAATATATTTTCACTACTCCAAAATCTGTCCCAGCTGCCTTGA
AAGCCCCCAAAATAGAGAAAGTAAATGATCACATTTGTGAAATTACATGGGAGTGTTTACAGCCAATGAAAGGTGATCCAGTTATTTACAGTCTTCAAGTTATGTTGGGAAAAGATTCAGAATTCAAA
CAGATTTACAAGGGTCCCGACTCTTCCTTCCGGTATTCCAGCCTTCAGCTGAACTGTGAATATCGCTTCCGTGTATGTGCCATTCGCCAGTGCCAAGACTCTCTGGGACACCAGGACCTCGTAGGTCC
CTACAGCACCACAGTGCTCTTCATCTCTCAGAGGACTGAACCACCAGCCAGCACCAACAGAGACACTGTGGAAAGCACAAGGACCCGACGGGCACTGAGTGACGAGCAGTGTGCTGCCGTCATCCTTG
TGCTGTTTGCTTTCTTTTCCATTTTGATTGCCTTTATCATTCAGTACTTTGTAATCAAGTGAAAATATAACTTTATTTTTTAACTCTATTACATTTTATTTTGTCATGTACTAAAATTATTTCTGTAT
TGCTTTTATAAAAAACAGTGGCATTTAGCACTGGCATTGAGACTATAGCACATCATTTTTGCCATTTTCAGTGCTTATATTGTTAGGTAGAGGCTGGCACTTTATTAGAATGCAAGCCACAAAAATAT
CAATTTTGTTTTTTTTGTTAGGGTGGGTCTTCTTTTTTTCTTTCCCTCTCTCTTTTTTTAACAAATGCCTTCTTATAGAAAAACTTTCTAAGAGGCAACAATTTAGAATGGATATTTTGACGAATCGG
CATGAGTGTAACAGTGATAACCTGATCTGTTTGTTTTAAAGATTATTACCAAGTGAAAAATTCAGAATGAATAGAATTTACACTAACATGCTATATAAAATGTTAAAGTCTGATGCTGTGAAAGCAAT
CTAGTGCTATATTTCTACCTCCTCATTTGTCTTAATTATTTGGTAAGTGGGATTATGATGAGTAACTGGAGGGGCTTAGAAACAAAAACTGGATGAAAGAGTATGCATGAAGAAAAGCTTCTTTGATA
AATGTGGAGTTCTTCATTATAAATATATATTCATGAATTCACAGATAAGTACTTAAAGAACAGACAGTTTACTTGGCCTAAAAATATTTTGATGTTTACTCAAAAAGTACCTCTTCAGGTCTTGAGAA
CATGGAAAAGAATTGAGTGCTTTTAAATACTTTTTAGAAAGTAATCATAAAAGTAAATTGAATTTCAAACCTATTTGGCTTCTGTTTTGTGAACCTTTGAACTATATGTATGTGTATAAGGGTATACA
CATACATATATGGCATATAACAAGTGTACACATATACACATAACAAGTGTAGAAGTATATATTACATACATACACTCACTCTGTCTGGTATAGGCTAATTTTGAAGAACTCCCATAAGTTTCTGCTGC
TTCTCCCATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGTTTGGGGCACCAAATCTGAAGACAAAATTAATTTGCACCAGTAAACTTCAAGCTGCTTTCTTTCTTGAAAA
CTAAACGTTTAACGTATAATGTCTGTTTGGATACTGTTCCAAATTGTTGATTGCATGTGGTTAATGTTGCATTAGAGCACTTTGCAATTGCATAATTCATTAATGTTTTGTGAGCTTGCATTTGTGAG
TTATTGGATGATCAGACTGAATTTTGTCAAGTATCACATTGTACATCTTGCCTAGATGTCGATGACTGCAAGTAATAATACAGTTTATAATGAAACTATCTACAATTCTTGTTTTAGCACATCTGTTA
TCCGTAAAACACCTGTAACTAGCTTTTTTAATTTATTATTTGAATTTTAGGATAGCGAATCACTAATTTTTAGTTGCTGAGGTTGGCATTTTAGTGATTATTAAGCACTTCTGTCAGTCTTTGAAAAA
AGAACGTATTTTTTGTGCTTTGAAGATCTCTGAAGAATTTCTTTTATAATAGAATGGGCATGTATTGTAACAGTTTTATGTCAAATGATCTGTGCTGTAGAAAAACATTAACCCTTGTTCAAAAAAGA
AATGGATAAACTTGGCCTTTCTAAGTGGTAAGAATGACCTGTCACTATAATATACTGTATGTTTACATTTTATTTAAATTTAATCTCTTATGTATAGGGTGATAACCTTCCCCAGAAACAACAGTGAT
TGCGATTGTTTTCTAGAAACTTCTTTAAAGTGCCACATTTGGCAGTACAAATGAGTCTGAGTGTAATAGCCCAGAGATTTATATATAGTTGAATGTCTAAAATGGTAAAATGTGCCACTGTGTCAAGT
TACAGTGGCTTATGTTTTTCATAGTAATTCAAATGAACTTCCTATTTTTGATAGTAAATGTCATTTAATAGTATACTTGCCATTTGAGCCTCACTGCAAAATTAGTGCAGAGGAGAAAACAATTTTTA
ATGTAATCTTGATTTTACCTCATATACTGTACATTCCAAAAACTCTAAACTTTTTAAAGATTATAGATACACTACCAAACATATCACCTTAAAATTGTATAAGGCTGAATGAACTTCATACAAATGAA
AAAAATCTCATAAAAATACATAAACTATGTAGCAAAAGTATCTGTAAAATCCATGGAAAATAAAAGTTGTATCATTCTTTTTGAGATACGTTTATTGTATTCATATATATTCATTATTTGCTACCTGT
TTAAGAAAGTGAAATGTTATGGTCTCCCCTCTTCCAATGAGCTTAAAACATTTTTCCCAACAGTATATAAATCTTCAACATGAGAGGATGTATATTTATTATATAAAGCCCAGTAAAGAATAAAATTA
GAAGTTTTATCCTA

hide sequence

RefSeq Acc Id:

NM_001278438 ⟹ NP_001265367

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,976,662 - 49,209,779 (+)	NCBI
GRCh37	13	49,550,048 - 49,783,915 (+)	NCBI
HuRef	13	30,344,082 - 30,577,725 (+)	NCBI
CHM1_1	13	49,518,322 - 49,751,465 (+)	NCBI
T2T-CHM13v2.0	13	48,197,951 - 48,431,085 (+)	NCBI

Sequence:

show sequence

GGCCGCCCGGCAGCCGCCGAACTTGAACGCTTTTCTGAAGAGAGTTTTCCCCGCTCATCTTGGG
GTTAAAACCTCGAAAACCCGCCCTCTGTTTGATCCTGCGTGGCTGCTTCCAGTACCTGGCAGTTCCTCTCCCCGGGCGAGTTAACCACCTGTTCAGTCGGGAGGTGGACTCGAGGCTGCAGTCCTCGC
CCGGTTTTAACAACCTGGATCTTCGAACTTTTGACACGGCTTTGGAAACGACGTCATGTGTTAGAATTGGAGCGTTATTCAGTATATTAATGTCTTATTGATAATGGCAGAACATCCACCACTACTGG
ATACAACTCAGATCTTAAGTAGTGATATTTCTCTTTTGTCTGCCCCTATTGTAAGTGCAGATGGAACACAACAGGTTATTCTGGTACAAGTTAACCCAGGAGAAGCATTTACAATAAGAAGAGAAGAT
GGACAGTTTCAGTGCATTACAGGTCCTGCTCAGGTTCCAATGATGTCCCCAAATGGTTCTGTGCCTCCTATCTATGTGCCTCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGT
TGTCGTGGTCCCTCAGGCACCAGAGTTTCACCCTGGTAGTCACACAGTTCTCCACCGTTCTCCACATCCTCCTCTACCTGGTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGT
ACTCACCCGTGACTGGAGCTGGAGACATGACAACACAGTATATGCCACAGTATCAGTCTTCACAAGTCTATGGAGATGTAGATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCT
AGTAAAACATATGAACGTTTGCAGAAAAAATTGAAGGATCGCCAAGGAACACAGAAAGATAAAATGAGCAGTCCACCATCATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTAT
AAAAGGACAAATTGCTGGTGGTATAAACACAGGATCAGCAAAAATCAAGTCTGGGAAGGGGAAAGGTGGTACACAAGTTGATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCAC
TTCTTTCCAACATTGTCAAACCAGTGGCCTCCGACATCCAGGCAAGGACAGTAGTACTTACCTGGTCACCACCTTCCAGCCTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGT
TATGAAGTTCTGATCTCAAGTACTGGAAAAGATGGGAAATACAAAAGTGTATATGTAGGAGAAGAAACAAATATCACTTTAAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGA
ATATAATTCTATAAAGGGAACTCCTTCAGAGGCTGAAATCTTTACCACCTTGAGCTGTGAACCTGATATACCTAATCCACCAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGG
CACCTAGTGACAATGGTTCTAAAATCCAAAACTTTGTATTAGAATGGGATGAAGGAAAAGGAAATGGAGAATTTTGTCAGTGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCA
GCAATGGGCTGTAAATTCAGACTATCGGCCAGAAATGACTATGGTACAAGTGGTTTTAGTGAAGAAGTCTTATATTACACCTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGC
TGGAATTACTTGGTTATCCTTACAATGGAGTAAGCCCTCAGGAACACCATCAGATGAAGGAATTTCTTACATTTTAGAGATGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAG
AAGATCTTGCTTACACAGTGAAAAATCTCAGACGTAGTACTAAGTATAAATTTAAGGTTATTGCTTACAACTCAGAAGGTAAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAA
CCAGGCATACCTGTAAAGCCTTCAGTGAAAGGAAAGATACATTCACACAGTTTTAAAATAACCTGGGATCCACCAAAAGACAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGG
TTCTAACGGAAACAAATGGGAAATGATATACAGTGGTGCTACCAGGGAACATCTTTGTGATCGACTGAATCCAGGCTGTTTCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGG
TCTCTGAATCTTTACTTGTGCAGACTCCAGCTGTGCCTCCTGGCCCATGCCTCCCTCCCAGATTACAGGGTAGACCCAAAGCAAAAGAAATACAGTTACGATGGGGACCCCCTCTGGTTGATGGTGGA
TCACCCATTTCCTGTTACAGTGTGGAAATGTCTCCTATAGAAAAAGATGAACCTAGAGAAGTTTACCAAGGTTCTGAAGTAGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAG
ACTACGTGCAGCTAACAAAATGGGGTTTGGACCATTTTCAGAAAAATGTGATATTACTACAGCCCCTGGGCCACCAGATCAGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAG
TGAATTGGGAGGTTCCTTTGAGTAATGGAACAGATGTCACTGAATATCGACTGGAGTGGGGAGGAGTTGAAGGAAGTATGCAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTT
TCACCAGCAACTACCTATTATTGCAGGGTCCAGGCTCTGAGTGTTGTGGGTGCAGGCCCTTTCAGTGAAGTAGTAGCCTGTGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAAT
AAGCGATGATGAGATAGAAAATCCCCATTATTCACCTTCTACATGCCTTGCAATAAGCTGGGAAAAGCCTTGTGATCATGGTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCC
TAACAGTGGGAAAGGTTACAAGCTATATTATCAACAATTTGCAACCAGATACAACATACAGAATACGAATTCAAGCCTTGAATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACT
AAGCCTCTCCCTCCTGATCCACCTCGTCTGGAATGTGTTGCCTTTAGCCACCAGAACCTTAAGCTGAAATGGGGAGAAGGAACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGAT
GGAGGATAAGAATGGACGGTTTGTATCCCTATACAGAGGACCATGTCATACATACAAAGTACAAAGACTTAATGAGTCAACATCCTATAAATTCTGTATTCAAGCTTGTAATGAAGCTGGGGAAGGTC
CCCTCTCCCAAGAATATATTTTCACTACTCCAAAATCTGTCCCAGCTGCCTTGAAAGCCCCCAAAATAGAGAAAGTAAATGATCACATTTGTGAAATTACATGGGAGTGTTTACAGCCAATGAAAGGT
GATCCAGTTATTTACAGTCTTCAAGTTATGTTGGGAAAAGATTCAGAATTCAAACAGATTTACAAGGGTCCCGACTCTTCCTTCCGGTATTCCAGCCTTCAGCTGAACTGTGAATATCGCTTCCGTGT
ATGTGCCATTCGCCAGTGCCAAGACTCTCTGGGACACCAGGACCTCGTAGGTCCCTACAGCACCACAGTGCTCTTCATCTCTCAGAGGACTGAACCACCAGCCAGCACCAACAGAGACACTGTGGAAA
GCACAAGGACCCGACGGGCACTGAGTGACGAGCAGTGTGCTGCCGTCATCCTTGTGCTGTTTGCTTTCTTTTCCATTTTGATTGCCTTTATCATTCAGTACTTTGTAATCAAGTGAAAATATAACTTT
ATTTTTTAACTCTATTACATTTTATTTTGTCATGTACTAAAATTATTTCTGTATTGCTTTTATAAAAAACAGTGGCATTTAGCACTGGCATTGAGACTATAGCACATCATTTTTGCCATTTTCAGTGC
TTATATTGTTAGGTAGAGGCTGGCACTTTATTAGAATGCAAGCCACAAAAATATCAATTTTGTTTTTTTTGTTAGGGTGGGTCTTCTTTTTTTCTTTCCCTCTCTCTTTTTTTAACAAATGCCTTCTT
ATAGAAAAACTTTCTAAGAGGCAACAATTTAGAATGGATATTTTGACGAATCGGCATGAGTGTAACAGTGATAACCTGATCTGTTTGTTTTAAAGATTATTACCAAGTGAAAAATTCAGAATGAATAG
AATTTACACTAACATGCTATATAAAATGTTAAAGTCTGATGCTGTGAAAGCAATCTAGTGCTATATTTCTACCTCCTCATTTGTCTTAATTATTTGGTAAGTGGGATTATGATGAGTAACTGGAGGGG
CTTAGAAACAAAAACTGGATGAAAGAGTATGCATGAAGAAAAGCTTCTTTGATAAATGTGGAGTTCTTCATTATAAATATATATTCATGAATTCACAGATAAGTACTTAAAGAACAGACAGTTTACTT
GGCCTAAAAATATTTTGATGTTTACTCAAAAAGTACCTCTTCAGGTCTTGAGAACATGGAAAAGAATTGAGTGCTTTTAAATACTTTTTAGAAAGTAATCATAAAAGTAAATTGAATTTCAAACCTAT
TTGGCTTCTGTTTTGTGAACCTTTGAACTATATGTATGTGTATAAGGGTATACACATACATATATGGCATATAACAAGTGTACACATATACACATAACAAGTGTAGAAGTATATATTACATACATACA
CTCACTCTGTCTGGTATAGGCTAATTTTGAAGAACTCCCATAAGTTTCTGCTGCTTCTCCCATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGTTTGGGGCACCAAATCT
GAAGACAAAATTAATTTGCACCAGTAAACTTCAAGCTGCTTTCTTTCTTGAAAACTAAACGTTTAACGTATAATGTCTGTTTGGATACTGTTCCAAATTGTTGATTGCATGTGGTTAATGTTGCATTA
GAGCACTTTGCAATTGCATAATTCATTAATGTTTTGTGAGCTTGCATTTGTGAGTTATTGGATGATCAGACTGAATTTTGTCAAGTATCACATTGTACATCTTGCCTAGATGTCGATGACTGCAAGTA
ATAATACAGTTTATAATGAAACTATCTACAATTCTTGTTTTAGCACATCTGTTATCCGTAAAACACCTGTAACTAGCTTTTTTAATTTATTATTTGAATTTTAGGATAGCGAATCACTAATTTTTAGT
TGCTGAGGTTGGCATTTTAGTGATTATTAAGCACTTCTGTCAGTCTTTGAAAAAAGAACGTATTTTTTGTGCTTTGAAGATCTCTGAAGAATTTCTTTTATAATAGAATGGGCATGTATTGTAACAGT
TTTATGTCAAATGATCTGTGCTGTAGAAAAACATTAACCCTTGTTCAAAAAAGAAATGGATAAACTTGGCCTTTCTAAGTGGTAAGAATGACCTGTCACTATAATATACTGTATGTTTACATTTTATT
TAAATTTAATCTCTTATGTATAGGGTGATAACCTTCCCCAGAAACAACAGTGATTGCGATTGTTTTCTAGAAACTTCTTTAAAGTGCCACATTTGGCAGTACAAATGAGTCTGAGTGTAATAGCCCAG
AGATTTATATATAGTTGAATGTCTAAAATGGTAAAATGTGCCACTGTGTCAAGTTACAGTGGCTTATGTTTTTCATAGTAATTCAAATGAACTTCCTATTTTTGATAGTAAATGTCATTTAATAGTAT
ACTTGCCATTTGAGCCTCACTGCAAAATTAGTGCAGAGGAGAAAACAATTTTTAATGTAATCTTGATTTTACCTCATATACTGTACATTCCAAAAACTCTAAACTTTTTAAAGATTATAGATACACTA
CCAAACATATCACCTTAAAATTGTATAAGGCTGAATGAACTTCATACAAATGAAAAAAATCTCATAAAAATACATAAACTATGTAGCAAAAGTATCTGTAAAATCCATGGAAAATAAAAGTTGTATCA
TTCTTTTTGAGATACGTTTATTGTATTCATATATATTCATTATTTGCTACCTGTTTAAGAAAGTGAAATGTTATGGTCTCCCCTCTTCCAATGAGCTTAAAACATTTTTCCCAACAGTATATAAATCT
TCAACATGAGAGGATGTATATTTATTATATAAAGCCCAGTAAAGAATAAAATTAGAAGTTTTATCCTA

hide sequence

RefSeq Acc Id:

NM_014923 ⟹ NP_055738

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	49,110,317 - 49,209,779 (+)	NCBI
GRCh37	13	49,550,048 - 49,783,915 (+)	RGD
Build 36	13	48,582,450 - 48,681,916 (+)	NCBI Archive
Celera	13	30,605,901 - 30,839,799 (+)	RGD
HuRef	13	30,344,082 - 30,577,725 (+)	RGD
CHM1_1	13	49,651,985 - 49,751,465 (+)	NCBI
T2T-CHM13v2.0	13	48,331,613 - 48,431,085 (+)	NCBI

Sequence:

show sequence

GTTCTCCAATTAAAGCTGTTAACGTGTACTACGCTGTTTCCTTGTTGGATTTTCTTGTTCTCTGCTGCTACTGTAAAAACGAAATGAGTGGTCCTGCTCAGGTTCCAATGATGTCCCCAAATGGTTCT
GTGCCTCCTATCTATGTGCCTCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGTTGTCGTGGTCCCTCAGGCACCAGAGTTTCACCCTGGTAGTCACACAGTTCTCCACCGTTC
TCCACATCCTCCTCTACCTGGTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGTACTCACCCGTGACTGGAGCTGGAGACATGACAACACAGTATATGCCACAGTATCAGTCTT
CACAAGTCTATGGAGATGTAGATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCTAGTAAAACATATGAACGTTTGCAGAAAAAATTGAAGGATCGCCAAGGAACACAGAAAGAT
AAAATGAGCAGTCCACCATCATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTATAAAAGGACAAATTGCTGGTGGTATAAACACAGGATCAGCAAAAATCAAGTCTGGGAAGGG
GAAAGGTGGTACACAAGTTGATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCACTTCTTTCCAACATTGTCAAACCAGTGGCCTCCGACATCCAGGCAAGGACAGTAGTACTTA
CCTGGTCACCACCTTCCAGCCTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGTTATGAAGTTCTGATCTCAAGTACTGGAAAAGATGGGAAATACAAAAGTGTATATGTAGGA
GAAGAAACAAATATCACTTTAAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGAATATAATTCTATAAAGGGAACTCCTTCAGAGGCTGAAATCTTTACCACCTTGAGCTGTGA
ACCTGATATACCTAATCCACCAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGGCACCTAGTGACAATGGTTCTAAAATCCAAAACTTTGTATTAGAATGGGATGAAGGAAAAG
GAAATGGAGAATTTTGTCAGTGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCAGCAATGGGCTGTAAATTCAGACTATCGGCCAGAAATGACTATGGTACAAGTGGTTTTAGT
GAAGAAGTCTTATATTACACCTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGCTGGAATTACTTGGTTATCCTTACAATGGAGTAAGCCCTCAGGAACACCATCAGATGAAGG
AATTTCTTACATTTTAGAGATGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAGAAGATCTTGCTTACACAGTGAAAAATCTCAGACGTAGTACTAAGTATAAATTTAAGGTTA
TTGCTTACAACTCAGAAGGTAAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAACCAGGCATACCTGTAAAGCCTTCAGTGAAAGGAAAGATACATTCACACAGTTTTAAAATA
ACCTGGGATCCACCAAAAGACAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGGTTCTAACGGAAACAAATGGGAAATGATATACAGTGGTGCTACCAGGGAACATCTTTGTGA
TCGACTGAATCCAGGCTGTTTCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGGTCTCTGAATCTTTACTTGTGCAGACTCCAGCTGTGCCTCCTGGCCCATGCCTCCCTCCCA
GATTACAGGGTAGACCCAAAGCAAAAGAAATACAGTTACGATGGGGACCCCCTCTGGTTGATGGTGGATCACCCATTTCCTGTTACAGTGTGGAAATGTCTCCTATAGAAAAAGATGAACCTAGAGAA
GTTTACCAAGGTTCTGAAGTAGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAGACTACGTGCAGCTAACAAAATGGGGTTTGGACCATTTTCAGAAAAATGTGATATTACTAC
AGCCCCTGGGCCACCAGATCAGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAGTGAATTGGGAGGTTCCTTTGAGTAATGGAACAGATGTCACTGAATATCGACTGGAGTGGG
GAGGAGTTGAAGGAAGTATGCAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTTTCACCAGCAACTACCTATTATTGCAGGGTCCAGGCTCTGAGTGTTGTGGGTGCAGGCCCT
TTCAGTGAAGTAGTAGCCTGTGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAATAAGCGATGATGAGATAGAAAATCCCCATTATTCACCTTCTACATGCCTTGCAATAAGCTG
GGAAAAGCCTTGTGATCATGGTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCCTAACAGTGGGAAAGGTTACAAGCTATATTATCAACAATTTGCAACCAGATACAACATACA
GAATACGAATTCAAGCCTTGAATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACTAAGCCTCTCCCTCCTGATCCACCTCGTCTGGAATGTGTTGCCTTTAGCCACCAGAACCTT
AAGCTGAAATGGGGAGAAGGAACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGATGGAGGATAAGAATGGACGGTTTGTATCCCTATACAGAGGACCATGTCATACATACAAAGT
ACAAAGACTTAATGAGTCAACATCCTATAAATTCTGTATTCAAGCTTGTAATGAAGCTGGGGAAGGTCCCCTCTCCCAAGAATATATTTTCACTACTCCAAAATCTGTCCCAGCTGCCTTGAAAGCCC
CCAAAATAGAGAAAGTAAATGATCACATTTGTGAAATTACATGGGAGTGTTTACAGCCAATGAAAGGTGATCCAGTTATTTACAGTCTTCAAGTTATGTTGGGAAAAGATTCAGAATTCAAACAGATT
TACAAGGGTCCCGACTCTTCCTTCCGGTATTCCAGCCTTCAGCTGAACTGTGAATATCGCTTCCGTGTATGTGCCATTCGCCAGTGCCAAGACTCTCTGGGACACCAGGACCTCGTAGGTCCCTACAG
CACCACAGTGCTCTTCATCTCTCAGAGGACTGAACCACCAGCCAGCACCAACAGAGACACTGTGGAAAGCACAAGGACCCGACGGGCACTGAGTGACGAGCAGTGTGCTGCCGTCATCCTTGTGCTGT
TTGCTTTCTTTTCCATTTTGATTGCCTTTATCATTCAGTACTTTGTAATCAAGTGAAAATATAACTTTATTTTTTAACTCTATTACATTTTATTTTGTCATGTACTAAAATTATTTCTGTATTGCTTT
TATAAAAAACAGTGGCATTTAGCACTGGCATTGAGACTATAGCACATCATTTTTGCCATTTTCAGTGCTTATATTGTTAGGTAGAGGCTGGCACTTTATTAGAATGCAAGCCACAAAAATATCAATTT
TGTTTTTTTTGTTAGGGTGGGTCTTCTTTTTTTCTTTCCCTCTCTCTTTTTTTAACAAATGCCTTCTTATAGAAAAACTTTCTAAGAGGCAACAATTTAGAATGGATATTTTGACGAATCGGCATGAG
TGTAACAGTGATAACCTGATCTGTTTGTTTTAAAGATTATTACCAAGTGAAAAATTCAGAATGAATAGAATTTACACTAACATGCTATATAAAATGTTAAAGTCTGATGCTGTGAAAGCAATCTAGTG
CTATATTTCTACCTCCTCATTTGTCTTAATTATTTGGTAAGTGGGATTATGATGAGTAACTGGAGGGGCTTAGAAACAAAAACTGGATGAAAGAGTATGCATGAAGAAAAGCTTCTTTGATAAATGTG
GAGTTCTTCATTATAAATATATATTCATGAATTCACAGATAAGTACTTAAAGAACAGACAGTTTACTTGGCCTAAAAATATTTTGATGTTTACTCAAAAAGTACCTCTTCAGGTCTTGAGAACATGGA
AAAGAATTGAGTGCTTTTAAATACTTTTTAGAAAGTAATCATAAAAGTAAATTGAATTTCAAACCTATTTGGCTTCTGTTTTGTGAACCTTTGAACTATATGTATGTGTATAAGGGTATACACATACA
TATATGGCATATAACAAGTGTACACATATACACATAACAAGTGTAGAAGTATATATTACATACATACACTCACTCTGTCTGGTATAGGCTAATTTTGAAGAACTCCCATAAGTTTCTGCTGCTTCTCC
CATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGTTTGGGGCACCAAATCTGAAGACAAAATTAATTTGCACCAGTAAACTTCAAGCTGCTTTCTTTCTTGAAAACTAAAC
GTTTAACGTATAATGTCTGTTTGGATACTGTTCCAAATTGTTGATTGCATGTGGTTAATGTTGCATTAGAGCACTTTGCAATTGCATAATTCATTAATGTTTTGTGAGCTTGCATTTGTGAGTTATTG
GATGATCAGACTGAATTTTGTCAAGTATCACATTGTACATCTTGCCTAGATGTCGATGACTGCAAGTAATAATACAGTTTATAATGAAACTATCTACAATTCTTGTTTTAGCACATCTGTTATCCGTA
AAACACCTGTAACTAGCTTTTTTAATTTATTATTTGAATTTTAGGATAGCGAATCACTAATTTTTAGTTGCTGAGGTTGGCATTTTAGTGATTATTAAGCACTTCTGTCAGTCTTTGAAAAAAGAACG
TATTTTTTGTGCTTTGAAGATCTCTGAAGAATTTCTTTTATAATAGAATGGGCATGTATTGTAACAGTTTTATGTCAAATGATCTGTGCTGTAGAAAAACATTAACCCTTGTTCAAAAAAGAAATGGA
TAAACTTGGCCTTTCTAAGTGGTAAGAATGACCTGTCACTATAATATACTGTATGTTTACATTTTATTTAAATTTAATCTCTTATGTATAGGGTGATAACCTTCCCCAGAAACAACAGTGATTGCGAT
TGTTTTCTAGAAACTTCTTTAAAGTGCCACATTTGGCAGTACAAATGAGTCTGAGTGTAATAGCCCAGAGATTTATATATAGTTGAATGTCTAAAATGGTAAAATGTGCCACTGTGTCAAGTTACAGT
GGCTTATGTTTTTCATAGTAATTCAAATGAACTTCCTATTTTTGATAGTAAATGTCATTTAATAGTATACTTGCCATTTGAGCCTCACTGCAAAATTAGTGCAGAGGAGAAAACAATTTTTAATGTAA
TCTTGATTTTACCTCATATACTGTACATTCCAAAAACTCTAAACTTTTTAAAGATTATAGATACACTACCAAACATATCACCTTAAAATTGTATAAGGCTGAATGAACTTCATACAAATGAAAAAAAT
CTCATAAAAATACATAAACTATGTAGCAAAAGTATCTGTAAAATCCATGGAAAATAAAAGTTGTATCATTCTTTTTGAGATACGTTTATTGTATTCATATATATTCATTATTTGCTACCTGTTTAAGA
AAGTGAAATGTTATGGTCTCCCCTCTTCCAATGAGCTTAAAACATTTTTCCCAACAGTATATAAATCTTCAACATGAGAGGATGTATATTTATTATATAAAGCCCAGTAAAGAATAAAATTAGAAGTT
TTATCCTA

hide sequence

RefSeq Acc Id:

NR_103528

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,976,662 - 49,209,779 (+)	NCBI
GRCh37	13	49,550,048 - 49,783,915 (+)	NCBI
HuRef	13	30,344,082 - 30,577,725 (+)	NCBI
CHM1_1	13	49,518,322 - 49,751,465 (+)	NCBI
T2T-CHM13v2.0	13	48,197,951 - 48,431,085 (+)	NCBI

Sequence:

show sequence

GGCCGCCCGGCAGCCGCCGAACTTGAACGCTTTTCTGAAGAGAGTTTTCCCCGCTCATCTTGGG
GTTAAAACCTCGAAAACCCGCCCTCTGTTTGATCCTGCGTGGCTGCTTCCAGTACCTGGCAGTTCCTCTCCCCGGGCGAGTTAACCACCTGTTCAGTCGGGAGGTGGACTCGAGGCTGCAGTCCTCGC
CCGGTTTTAACAACCTGGATCTTCGAACTTTTGACACGGCTTTGGAAACGACGTCATGTGTTAGAATTGGAGCGTTATTCAGTATATTAATGTCTTATTGATAATGGCAGAACATCCACCACTACTGG
ATACAACTCAGATCTTAAGTAGTGATATTTCTCTTTTGTCTGCCCCTATTGTAAGTGCAGATGGAACACAACAGGTTATTCTGGTACAAGTTAACCCAGGAGAAGCATTTACAATAAGAAGAGAAGAT
GGACAGTTTCAGTGCATTACAGGTCCTGCTCAGGTTCCAATGATGTCCCCAAATGGTTCTGTGCCTCCTATCTATGTGCCTCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGT
TGTCGTGGTCCCTCAGGCACCAGAGTTTCACCCTGGTAGTCACACAGTTCTCCACCGTTCTCCACATCCTCCTCTACCTGGTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGT
ACTCACCCGTGACTGGAGCTGGAGACATGACAACACAGTATATGCCACAGTATCAGTCTTCACAAGTCTATGGAGATGTAGATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCT
AGTAAAACATATGAACGTTTGCAGAAAAAATTGAAGGATCGCCAAGGAACACAGAAAGATAAAATGAGCAGTCCACCATCATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTAT
AAAAGGACAAATTGCTGGTGGTATAAACACAGGATCAGCAAAAATCAAGTCTGGGAAGGGGAAAGGTGGTACACAAGTTGATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCAC
TTCTTTCCAACATTGTCAAACCAGTGGCCTCCGACATCCAGGCAAGGACAGTAGTACTTACCTGGTCACCACCTTCCAGCCTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGT
TATGAAGTTCTGATCTCAAGTACTGGAAAAGATGGGAAATACAAAAGTGTATATGTAGGAGAAGAAACAAATATCACTTTAAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGA
ATATAATTCTATAAAGGGAACTCCTTCAGAGGCTGAAATCTTTACCACCTTGAGCTGTGAACCTGATATACCTAATCCACCAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGG
CACCTAGTGACAATGGTTCTAAAATCCAAAACTTTGTATTAGAATGGGATGAAGGAAAAGGAAATGGAGAATTTTGTCAGTGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCA
GCAATGGGCTGTAAATTCAGACTATCGGCCAGAAATGACTATGGTACAAGTGGTTTTAGTGAAGAAGTCTTATATTACACCTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGC
TGGAATTACTTGGTTATCCTTACAATGGAGTAAGCCCTCAGGAACACCATCAGATGAAGGAATTTCTTACATTTTAGAGATGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAG
AAGATCTTGCTTACACAGTGAAAAATCTCAGACGTAGTACTAAGTATAAATTTAAGGTTATTGCTTACAACTCAGAAGGTAAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAA
CCAGGCATACCTGTAAAGCCTTCAGTGAAAGGAAAGATACATTCACACAGTTTTAAAATAACCTGGGATCCACCAAAAGACAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGG
TTCTAACGGAAACAAATGGGAAATGATATACAGTGGTGCTACCAGGGAACATCTTTGTGATCGACTGAATCCAGGCTGTTTCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGG
TCTCTGAATCTTTACTTGTGCAGACTCCAGCTGTGCCTCCTGGCCCATGCCTCCCTCCCAGATTACAGGGTAGACCCAAAGCAAAAGAAATACAGACCCCCTCTGGTTGATGGTGGATCACCCATTTC
CTGTTACAGTGTGGAAATGTCTCCTATAGAAAAAGATGAACCTAGAGAAGTTTACCAAGGTTCTGAAGTAGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAGACTACGTGCAG
CTAACAAAATGGGGTTTGGACCATTTTCAGAAAAATGTGATATTACTACAGCCCCTGGGCCACCAGATCAGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAGTGAATTGGGAG
GTTCCTTTGAGTAATGGAACAGATGTCACTGAATATCGACTGGAGTGGGGAGGAGTTGAAGGAAGTATGCAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTTTCACCAGCAAC
TACCTATTATTGCAGGGTCCAGGCTCTGAGTGTTGTGGGTGCAGGCCCTTTCAGTGAAGTAGTAGCCTGTGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAATAAGCGATGATG
AGATAGAAAATCCCCATTATTCACCTTCTACATGCCTTGCAATAAGCTGGGAAAAGCCTTGTGATCATGGTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCCTAACAGTGGGA
AAGGTTACAAGCTATATTATCAACAATTTGCAACCAGATACAACATACAGAATACGAATTCAAGCCTTGAATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACTAAGCCTCTCCC
TCCTGATCCACCTCGTCTGGAATGTGTTGCCTTTAGCCACCAGAACCTTAAGCTGAAATGGGGAGAAGGAACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGATGGAGGATAAGA
ATGGACGGTTTGTATCCCTATACAGAGGACCATGTCATACATACAAAGTACAAAGACTTAATGAGTCAACATCCTATAAATTCTGTATTCAAGCTTGTAATGAAGCTGGGGAAGGTCCCCTCTCCCAA
GAATATATTTTCACTACTCCAAAATCTGTCCCAGCTGCCTTGAAAGCCCCCAAAATAGAGAAAGTAAATGATCACATTTGTGAAATTACATGGGAGTGTTTACAGCCAATGAAAGGTGATCCAGTTAT
TTACAGTCTTCAAGTTATGTTGGGAAAAGATTCAGAATTCAAACAGATTTACAAGGGTCCCGACTCTTCCTTCCGGTATTCCAGCCTTCAGCTGAACTGTGAATATCGCTTCCGTGTATGTGCCATTC
GCCAGTGCCAAGACTCTCTGGGACACCAGGACCTCGTAGGTCCCTACAGCACCACAGTGCTCTTCATCTCTCAGAGGACTGAACCACCAGCCAGCACCAACAGAGACACTGTGGAAAGCACAAGGACC
CGACGGGCACTGAGTGACGAGCAGTGTGCTGCCGTCATCCTTGTGCTGTTTGCTTTCTTTTCCATTTTGATTGCCTTTATCATTCAGTACTTTGTAATCAAGTGAAAATATAACTTTATTTTTTAACT
CTATTACATTTTATTTTGTCATGTACTAAAATTATTTCTGTATTGCTTTTATAAAAAACAGTGGCATTTAGCACTGGCATTGAGACTATAGCACATCATTTTTGCCATTTTCAGTGCTTATATTGTTA
GGTAGAGGCTGGCACTTTATTAGAATGCAAGCCACAAAAATATCAATTTTGTTTTTTTTGTTAGGGTGGGTCTTCTTTTTTTCTTTCCCTCTCTCTTTTTTTAACAAATGCCTTCTTATAGAAAAACT
TTCTAAGAGGCAACAATTTAGAATGGATATTTTGACGAATCGGCATGAGTGTAACAGTGATAACCTGATCTGTTTGTTTTAAAGATTATTACCAAGTGAAAAATTCAGAATGAATAGAATTTACACTA
ACATGCTATATAAAATGTTAAAGTCTGATGCTGTGAAAGCAATCTAGTGCTATATTTCTACCTCCTCATTTGTCTTAATTATTTGGTAAGTGGGATTATGATGAGTAACTGGAGGGGCTTAGAAACAA
AAACTGGATGAAAGAGTATGCATGAAGAAAAGCTTCTTTGATAAATGTGGAGTTCTTCATTATAAATATATATTCATGAATTCACAGATAAGTACTTAAAGAACAGACAGTTTACTTGGCCTAAAAAT
ATTTTGATGTTTACTCAAAAAGTACCTCTTCAGGTCTTGAGAACATGGAAAAGAATTGAGTGCTTTTAAATACTTTTTAGAAAGTAATCATAAAAGTAAATTGAATTTCAAACCTATTTGGCTTCTGT
TTTGTGAACCTTTGAACTATATGTATGTGTATAAGGGTATACACATACATATATGGCATATAACAAGTGTACACATATACACATAACAAGTGTAGAAGTATATATTACATACATACACTCACTCTGTC
TGGTATAGGCTAATTTTGAAGAACTCCCATAAGTTTCTGCTGCTTCTCCCATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGTTTGGGGCACCAAATCTGAAGACAAAAT
TAATTTGCACCAGTAAACTTCAAGCTGCTTTCTTTCTTGAAAACTAAACGTTTAACGTATAATGTCTGTTTGGATACTGTTCCAAATTGTTGATTGCATGTGGTTAATGTTGCATTAGAGCACTTTGC
AATTGCATAATTCATTAATGTTTTGTGAGCTTGCATTTGTGAGTTATTGGATGATCAGACTGAATTTTGTCAAGTATCACATTGTACATCTTGCCTAGATGTCGATGACTGCAAGTAATAATACAGTT
TATAATGAAACTATCTACAATTCTTGTTTTAGCACATCTGTTATCCGTAAAACACCTGTAACTAGCTTTTTTAATTTATTATTTGAATTTTAGGATAGCGAATCACTAATTTTTAGTTGCTGAGGTTG
GCATTTTAGTGATTATTAAGCACTTCTGTCAGTCTTTGAAAAAAGAACGTATTTTTTGTGCTTTGAAGATCTCTGAAGAATTTCTTTTATAATAGAATGGGCATGTATTGTAACAGTTTTATGTCAAA
TGATCTGTGCTGTAGAAAAACATTAACCCTTGTTCAAAAAAGAAATGGATAAACTTGGCCTTTCTAAGTGGTAAGAATGACCTGTCACTATAATATACTGTATGTTTACATTTTATTTAAATTTAATC
TCTTATGTATAGGGTGATAACCTTCCCCAGAAACAACAGTGATTGCGATTGTTTTCTAGAAACTTCTTTAAAGTGCCACATTTGGCAGTACAAATGAGTCTGAGTGTAATAGCCCAGAGATTTATATA
TAGTTGAATGTCTAAAATGGTAAAATGTGCCACTGTGTCAAGTTACAGTGGCTTATGTTTTTCATAGTAATTCAAATGAACTTCCTATTTTTGATAGTAAATGTCATTTAATAGTATACTTGCCATTT
GAGCCTCACTGCAAAATTAGTGCAGAGGAGAAAACAATTTTTAATGTAATCTTGATTTTACCTCATATACTGTACATTCCAAAAACTCTAAACTTTTTAAAGATTATAGATACACTACCAAACATATC
ACCTTAAAATTGTATAAGGCTGAATGAACTTCATACAAATGAAAAAAATCTCATAAAAATACATAAACTATGTAGCAAAAGTATCTGTAAAATCCATGGAAAATAAAAGTTGTATCATTCTTTTTGAG
ATACGTTTATTGTATTCATATATATTCATTATTTGCTACCTGTTTAAGAAAGTGAAATGTTATGGTCTCCCCTCTTCCAATGAGCTTAAAACATTTTTCCCAACAGTATATAAATCTTCAACATGAGA
GGATGTATATTTATTATATAAAGCCCAGTAAAGAATAAAATTAGAAGTTTTATCCTA

hide sequence

RefSeq Acc Id:

XM_011534997 ⟹ XP_011533299

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	49,097,617 - 49,209,779 (+)	NCBI

Sequence:

show sequence

CATGTCACCATTAACCATAAGAATCACAAAATAACATAATGGTTGCAGGACAGGATTTCTTTAC
AGTTCCCCTGGGAAGTGCCAGTCTTACAACATAAACTAACAGGAAGGGTAATGCTTTAAGTGTACAGGCCTAGTTTCTTTTTGGGAGAACCTACAGCAGGATGTGAACATTCTGTGCCAAGCCTCCAG
GGGTCCTGCTCAGGTTCCAATGATGTCCCCAAATGGTTCTGTGCCTCCTATCTATGTGCCTCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGTTGTCGTGGTCCCTCAGGCAC
CAGAGTTTCACCCTGGTAGTCACACAGTTCTCCACCGTTCTCCACATCCTCCTCTACCTGGTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGTACTCACCCGTGACTGGAGCT
GGAGACATGACAACACAGTATATGCCACAGTATCAGTCTTCACAAGTCTATGGAGATGTAGATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCTAGTAAAACATATGAACGTTT
GCAGAAAAAATTGAAGGATCGCCAAGGAACACAGAAAGATAAAATGAGCAGTCCACCATCATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTATAAAAGGACAAATTGCTGGTG
GTATAAACACAGGATCAGCAAAAATCAAGTCTGGGAAGGGGAAAGGTGGTACACAAGTTGATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCACTTCTTTCCAACATTGTCAAA
CCAGTGGCCTCCGACATCCAGGCAAGGACAGTAGTACTTACCTGGTCACCACCTTCCAGCCTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGTTATGAAGTTCTGATCTCAAG
TACTGGAAAAGATGGGAAATACAAAAGTGTATATGTAGGAGAAGAAACAAATATCACTTTAAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGAATATAATTCTATAAAGGGAA
CTCCTTCAGAGGCTGAAATCTTTACCACCTTGAGCTGTGAACCTGATATACCTAATCCACCAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGGCACCTAGTGACAATGGTTCT
AAAATCCAAAACTTTGTATTAGAATGGGATGAAGGAAAAGGAAATGGAGAATTTTGTCAGTGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCAGCAATGGGCTGTAAATTCAG
ACTATCGGCCAGAAATGACTATGGTACAAGTGGTTTTAGTGAAGAAGTCTTATATTACACCTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGCTGGAATTACTTGGTTATCCT
TACAATGGAGTAAGCCCTCAGGAACACCATCAGATGAAGGAATTTCTTACATTTTAGAGATGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAGAAGATCTTGCTTACACAGTG
AAAAATCTCAGACGTAGTACTAAGTATAAATTTAAGGTTATTGCTTACAACTCAGAAGGTAAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAACCAGGCATACCTGTAAAGCC
TTCAGTGAAAGGAAAGATACATTCACACAGTTTTAAAATAACCTGGGATCCACCAAAAGACAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGGTTCTAACGGAAACAAATGGG
AAATGATATACAGTGGTGCTACCAGGGAACATCTTTGTGATCGACTGAATCCAGGCTGTTTCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGGTCTCTGAATCTTTACTTGTG
CAGACTCCAGCTGTGCCTCCTGGCCCATGCCTCCCTCCCAGATTACAGGGTAGACCCAAAGCAAAAGAAATACAGTTACGATGGGGACCCCCTCTGGTTGATGGTGGATCACCCATTTCCTGTTACAG
TGTGGAAATGTCTCCTATAGAAAAAGATGAACCTAGAGAAGTTTACCAAGGTTCTGAAGTAGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAGACTACGTGCAGCTAACAAAA
TGGGGTTTGGACCATTTTCAGAAAAATGTGATATTACTACAGCCCCTGGGCCACCAGATCAGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAGTGAATTGGGAGGTTCCTTTG
AGTAATGGAACAGATGTCACTGAATATCGACTGGAGTGGGGAGGAGTTGAAGGAAGTATGCAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTTTCACCAGCAACTACCTATTA
TTGCAGGGTCCAGGCTCTGAGTGTTGTGGGTGCAGGCCCTTTCAGTGAAGTAGTAGCCTGTGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAATAAGCGATGATGAGATAGAAA
ATCCCCATTATTCACCTTCTACATGCCTTGCAATAAGCTGGGAAAAGCCTTGTGATCATGGTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCCTAACAGTGGGAAAGGTTACA
AGCTATATTATCAACAATTTGCAACCAGATACAACATACAGAATACGAATTCAAGCCTTGAATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACTAAGCCTCTCCCTCCTGATCC
ACCTCGTCTGGAATGTGTTGCCTTTAGCCACCAGAACCTTAAGCTGAAATGGGGAGAAGGAACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGATGGAGGATAAGAATGGACGGT
TTGTATCCCTATACAGAGGACCATGTCATACATACAAAGTACAAAGACTTAATGAGTCAACATCCTATAAATTCTGTATTCAAGCTTGTAATGAAGCTGGGGAAGGTCCCCTCTCCCAAGAATATATT
TTCACTACTCCAAAATCTGTCCCAGCTGCCTTGAAAGCCCCCAAAATAGAGAAAGTAAATGATCACATTTGTGAAATTACATGGGAGTGTTTACAGCCAATGAAAGGTGATCCAGTTATTTACAGTCT
TCAAGTTATGTTGGGAAAAGATTCAGAATTCAAACAGATTTACAAGGGTCCCGACTCTTCCTTCCGGTATTCCAGCCTTCAGCTGAACTGTGAATATCGCTTCCGTGTATGTGCCATTCGCCAGTGCC
AAGACTCTCTGGGACACCAGGACCTCGTAGGTCCCTACAGCACCACAGTGCTCTTCATCTCTCAGAGGACTGAACCACCAGCCAGCACCAACAGAGACACTGTGGAAAGCACAAGGACCCGACGGGCA
CTGAGTGACGAGCAGTGTGCTGCCGTCATCCTTGTGCTGTTTGCTTTCTTTTCCATTTTGATTGCCTTTATCATTCAGTACTTTGTAATCAAGTGAAAATATAACTTTATTTTTTAACTCTATTACAT
TTTATTTTGTCATGTACTAAAATTATTTCTGTATTGCTTTTATAAAAAACAGTGGCATTTAGCACTGGCATTGAGACTATAGCACATCATTTTTGCCATTTTCAGTGCTTATATTGTTAGGTAGAGGC
TGGCACTTTATTAGAATGCAAGCCACAAAAATATCAATTTTGTTTTTTTTGTTAGGGTGGGTCTTCTTTTTTTCTTTCCCTCTCTCTTTTTTTAACAAATGCCTTCTTATAGAAAAACTTTCTAAGAG
GCAACAATTTAGAATGGATATTTTGACGAATCGGCATGAGTGTAACAGTGATAACCTGATCTGTTTGTTTTAAAGATTATTACCAAGTGAAAAATTCAGAATGAATAGAATTTACACTAACATGCTAT
ATAAAATGTTAAAGTCTGATGCTGTGAAAGCAATCTAGTGCTATATTTCTACCTCCTCATTTGTCTTAATTATTTGGTAAGTGGGATTATGATGAGTAACTGGAGGGGCTTAGAAACAAAAACTGGAT
GAAAGAGTATGCATGAAGAAAAGCTTCTTTGATAAATGTGGAGTTCTTCATTATAAATATATATTCATGAATTCACAGATAAGTACTTAAAGAACAGACAGTTTACTTGGCCTAAAAATATTTTGATG
TTTACTCAAAAAGTACCTCTTCAGGTCTTGAGAACATGGAAAAGAATTGAGTGCTTTTAAATACTTTTTAGAAAGTAATCATAAAAGTAAATTGAATTTCAAACCTATTTGGCTTCTGTTTTGTGAAC
CTTTGAACTATATGTATGTGTATAAGGGTATACACATACATATATGGCATATAACAAGTGTACACATATACACATAACAAGTGTAGAAGTATATATTACATACATACACTCACTCTGTCTGGTATAGG
CTAATTTTGAAGAACTCCCATAAGTTTCTGCTGCTTCTCCCATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGTTTGGGGCACCAAATCTGAAGACAAAATTAATTTGCA
CCAGTAAACTTCAAGCTGCTTTCTTTCTTGAAAACTAAACGTTTAACGTATAATGTCTGTTTGGATACTGTTCCAAATTGTTGATTGCATGTGGTTAATGTTGCATTAGAGCACTTTGCAATTGCATA
ATTCATTAATGTTTTGTGAGCTTGCATTTGTGAGTTATTGGATGATCAGACTGAATTTTGTCAAGTATCACATTGTACATCTTGCCTAGATGTCGATGACTGCAAGTAATAATACAGTTTATAATGAA
ACTATCTACAATTCTTGTTTTAGCACATCTGTTATCCGTAAAACACCTGTAACTAGCTTTTTTAATTTATTATTTGAATTTTAGGATAGCGAATCACTAATTTTTAGTTGCTGAGGTTGGCATTTTAG
TGATTATTAAGCACTTCTGTCAGTCTTTGAAAAAAGAACGTATTTTTTGTGCTTTGAAGATCTCTGAAGAATTTCTTTTATAATAGAATGGGCATGTATTGTAACAGTTTTATGTCAAATGATCTGTG
CTGTAGAAAAACATTAACCCTTGTTCAAAAAAGAAATGGATAAACTTGGCCTTTCTAAGTGGTAAGAATGACCTGTCACTATAATATACTGTATGTTTACATTTTATTTAAATTTAATCTCTTATGTA
TAGGGTGATAACCTTCCCCAGAAACAACAGTGATTGCGATTGTTTTCTAGAAACTTCTTTAAAGTGCCACATTTGGCAGTACAAATGAGTCTGAGTGTAATAGCCCAGAGATTTATATATAGTTGAAT
GTCTAAAATGGTAAAATGTGCCACTGTGTCAAGTTACAGTGGCTTATGTTTTTCATAGTAATTCAAATGAACTTCCTATTTTTGATAGTAAATGTCATTTAATAGTATACTTGCCATTTGAGCCTCAC
TGCAAAATTAGTGCAGAGGAGAAAACAATTTTTAATGTAATCTTGATTTTACCTCATATACTGTACATTCCAAAAACTCTAAACTTTTTAAAGATTATAGATACACTACCAAACATATCACCTTAAAA
TTGTATAAGGCTGAATGAACTTCATACAAATGAAAAAAATCTCATAAAAATACATAAACTATGTAGCAAAAGTATCTGTAAAATCCATGGAAAATAAAAGTTGTATCATTCTTTTTGA

hide sequence

RefSeq Acc Id:

XM_017020440 ⟹ XP_016875929

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,975,291 - 49,209,779 (+)	NCBI

Sequence:

show sequence

ATTGCAGCGTCCCACATTGTTTGAGGTTCCAGGAAGTCGCTGCTACGCTCACTTGTAAGTCTTCGTGCTGTTGTAAAAATTGAGGTCGTGGTTTTCCACGCGATTTGGCTGGCGAAGAGACCACGAAG
CCACCCCCCACGTTTTCAACTGAAATTGGAGCGTTATTCAGTATATTAATGTCTTATTGATAATGGCAGAACATCCACCACTACTGGATACAACTCAGATCTTAAGTAGTGATATTTCTCTTTTGTCT
GCCCCTATTGTAAGTGCAGATGGAACACAACAGGTTATTCTGGTACAAGTTAACCCAGGAGAAGCATTTACAATAAGAAGAGAAGATGGACAGTTTCAGTGCATTACAGGTCCTGCTCAGGTTCCAAT
GATGTCCCCAAATGGTTCTGTGCCTCCTATCTATGTGCCTCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGTTGTCGTGGTCCCTCAGGCACCAGAGTTTCACCCTGGTAGTC
ACACAGTTCTCCACCGTTCTCCACATCCTCCTCTACCTGGTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGTACTCACCCGTGACTGGAGCTGGAGACATGACAACACAGTAT
ATGCCACAGTATCAGTCTTCACAAGTCTATGGAGATGTAGATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCTAGTAAAACATATGAACGTTTGCAGAAAAAATTGAAGGATCG
CCAAGGAACACAGAAAGATAAAATGAGCAGTCCACCATCATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTATAAAAGGACAAATTGCTGGTGGTATAAACACAGGATCAGCAA
AAATCAAGTCTGGGAAGGGGAAAGGTGGTACACAAGTTGATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCACTTCTTTCCAACATTGTCAAACCAGTGGCCTCCGACATCCAG
GCAAGGACAGTAGTACTTACCTGGTCACCACCTTCCAGCCTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGTTATGAAGTTCTGATCTCAAGTACTGGAAAAGATGGGAAATA
CAAAAGTGTATATGTAGGAGAAGAAACAAATATCACTTTAAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGAATATAATTCTATAAAGGGAACTCCTTCAGAGGCTGAAATCT
TTACCACCTTGAGCTGTGAACCTGATATACCTAATCCACCAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGGCACCTAGTGACAATGGTTCTAAAATCCAAAACTTTGTATTA
GAATGGGATGAAGGAAAAGGAAATGGAGAATTTTGTCAGTGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCAGCAATGGGCTGTAAATTCAGACTATCGGCCAGAAATGACTA
TGGTACAAGTGGTTTTAGTGAAGAAGTCTTATATTACACCTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGCTGGAATTACTTGGTTATCCTTACAATGGAGTAAGCCCTCAG
GAACACCATCAGATGAAGGAATTTCTTACATTTTAGAGATGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAGAAGATCTTGCTTACACAGTGAAAAATCTCAGACGTAGTACT
AAGTATAAATTTAAGGTTATTGCTTACAACTCAGAAGGTAAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAACCAGGCATACCTGTAAAGCCTTCAGTGAAAGGAAAGATACA
TTCACACAGTTTTAAAATAACCTGGGATCCACCAAAAGACAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGGTTCTAACGGAAACAAATGGGAAATGATATACAGTGGTGCTA
CCAGGGAACATCTTTGTGATCGACTGAATCCAGGCTGTTTCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGGTCTCTGAATCTTTACTTGTGCAGACTCCAGCTGTGCCTCCT
GGCCCATGCCTCCCTCCCAGATTACAGGGTAGACCCAAAGCAAAAGAAATACAGTTACGATGGGGACCCCCTCTGGTTGATGGTGGATCACCCATTTCCTGTTACAGTGTGGAAATGTCTCCTATAGA
AAAAGATGAACCTAGAGAAGTTTACCAAGGTTCTGAAGTAGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAGACTACGTGCAGCTAACAAAATGGGGTTTGGACCATTTTCAG
AAAAATGTGATATTACTACAGCCCCTGGGCCACCAGATCAGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAGTGAATTGGGAGGTTCCTTTGAGTAATGGAACAGATGTCACT
GAATATCGACTGGAGTGGGGAGGAGTTGAAGGAAGTATGCAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTTTCACCAGCAACTACCTATTATTGCAGGGTCCAGGCTCTGAG
TGTTGTGGGTGCAGGCCCTTTCAGTGAAGTAGTAGCCTGTGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAATAAGCGATGATGAGATAGAAAATCCCCATTATTCACCTTCTA
CATGCCTTGCAATAAGCTGGGAAAAGCCTTGTGATCATGGTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCCTAACAGTGGGAAAGGTTACAAGCTATATTATCAACAATTTG
CAACCAGATACAACATACAGAATACGAATTCAAGCCTTGAATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACTAAGCCTCTCCCTCCTGATCCACCTCGTCTGGAATGTGTTGC
CTTTAGCCACCAGAACCTTAAGCTGAAATGGGGAGAAGGAACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGATGGAGGATAAGAATGGACGGTTTGTATCCCTATACAGAGGAC
CATGTCATACATACAAAGTACAAAGACTTAATGAGTCAACATCCTATAAATTCTGTATTCAAGCTTGTAATGAAGCTGGGGAAGGTCCCCTCTCCCAAGAATATATTTTCACTACTCCAAAATCTGTC
CCAGCTGCCTTGAAAGCCCCCAAAATAGAGAAAGTAAATGATCACATTTGTGAAATTACATGGGAGTGTTTACAGCCAATGAAAGGTGATCCAGTTATTTACAGTCTTCAAGTTATGTTGGGAAAAGA
TTCAGAATTCAAACAGATTTACAAGGGTCCCGACTCTTCCTTCCGGTATTCCAGCCTTCAGCTGAACTGTGAATATCGCTTCCGTGTATGTGCCATTCGCCAGTGCCAAGACTCTCTGGGACACCAGG
ACCTCGTAGGTCCCTACAGCACCACAGTGCTCTTCATCTCTCAGAGGACTGAACCACCAGCCAGCACCAACAGAGACACTGTGGAAAGCACAAGGACCCGACGGGCACTGAGTGACGAGCAGTGTGCT
GCCGTCATCCTTGTGCTGTTTGCTTTCTTTTCCATTTTGATTGCCTTTATCATTCAGTACTTTGTAATCAAGTGAAAATATAACTTTATTTTTTAACTCTATTACATTTTATTTTGTCATGTACTAAA
ATTATTTCTGTATTGCTTTTATAAAAAACAGTGGCATTTAGCACTGGCATTGAGACTATAGCACATCATTTTTGCCATTTTCAGTGCTTATATTGTTAGGTAGAGGCTGGCACTTTATTAGAATGCAA
GCCACAAAAATATCAATTTTGTTTTTTTTGTTAGGGTGGGTCTTCTTTTTTTCTTTCCCTCTCTCTTTTTTTAACAAATGCCTTCTTATAGAAAAACTTTCTAAGAGGCAACAATTTAGAATGGATAT
TTTGACGAATCGGCATGAGTGTAACAGTGATAACCTGATCTGTTTGTTTTAAAGATTATTACCAAGTGAAAAATTCAGAATGAATAGAATTTACACTAACATGCTATATAAAATGTTAAAGTCTGATG
CTGTGAAAGCAATCTAGTGCTATATTTCTACCTCCTCATTTGTCTTAATTATTTGGTAAGTGGGATTATGATGAGTAACTGGAGGGGCTTAGAAACAAAAACTGGATGAAAGAGTATGCATGAAGAAA
AGCTTCTTTGATAAATGTGGAGTTCTTCATTATAAATATATATTCATGAATTCACAGATAAGTACTTAAAGAACAGACAGTTTACTTGGCCTAAAAATATTTTGATGTTTACTCAAAAAGTACCTCTT
CAGGTCTTGAGAACATGGAAAAGAATTGAGTGCTTTTAAATACTTTTTAGAAAGTAATCATAAAAGTAAATTGAATTTCAAACCTATTTGGCTTCTGTTTTGTGAACCTTTGAACTATATGTATGTGT
ATAAGGGTATACACATACATATATGGCATATAACAAGTGTACACATATACACATAACAAGTGTAGAAGTATATATTACATACATACACTCACTCTGTCTGGTATAGGCTAATTTTGAAGAACTCCCAT
AAGTTTCTGCTGCTTCTCCCATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGTTTGGGGCACCAAATCTGAAGACAAAATTAATTTGCACCAGTAAACTTCAAGCTGCTT
TCTTTCTTGAAAACTAAACGTTTAACGTATAATGTCTGTTTGGATACTGTTCCAAATTGTTGATTGCATGTGGTTAATGTTGCATTAGAGCACTTTGCAATTGCATAATTCATTAATGTTTTGTGAGC
TTGCATTTGTGAGTTATTGGATGATCAGACTGAATTTTGTCAAGTATCACATTGTACATCTTGCCTAGATGTCGATGACTGCAAGTAATAATACAGTTTATAATGAAACTATCTACAATTCTTGTTTT
AGCACATCTGTTATCCGTAAAACACCTGTAACTAGCTTTTTTAATTTATTATTTGAATTTTAGGATAGCGAATCACTAATTTTTAGTTGCTGAGGTTGGCATTTTAGTGATTATTAAGCACTTCTGTC
AGTCTTTGAAAAAAGAACGTATTTTTTGTGCTTTGAAGATCTCTGAAGAATTTCTTTTATAATAGAATGGGCATGTATTGTAACAGTTTTATGTCAAATGATCTGTGCTGTAGAAAAACATTAACCCT
TGTTCAAAAAAGAAATGGATAAACTTGGCCTTTCTAAGTGGTAAGAATGACCTGTCACTATAATATACTGTATGTTTACATTTTATTTAAATTTAATCTCTTATGTATAGGGTGATAACCTTCCCCAG
AAACAACAGTGATTGCGATTGTTTTCTAGAAACTTCTTTAAAGTGCCACATTTGGCAGTACAAATGAGTCTGAGTGTAATAGCCCAGAGATTTATATATAGTTGAATGTCTAAAATGGTAAAATGTGC
CACTGTGTCAAGTTACAGTGGCTTATGTTTTTCATAGTAATTCAAATGAACTTCCTATTTTTGATAGTAAATGTCATTTAATAGTATACTTGCCATTTGAGCCTCACTGCAAAATTAGTGCAGAGGAG
AAAACAATTTTTAATGTAATCTTGATTTTACCTCATATACTGTACATTCCAAAAACTCTAAACTTTTTAAAGATTATAGATACACTACCAAACATATCACCTTAAAATTGTATAAGGCTGAATGAACT
TCATACAAATGAAAAAAATCTCATAAAAATACATAAACTATGTAGCAAAAGTATCTGTAAAATCCATGGAAAATAAAAGTTGTATCATTCTTTTTGA

hide sequence

RefSeq Acc Id:

XM_017020443 ⟹ XP_016875932

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,976,662 - 49,201,793 (+)	NCBI

Sequence:

show sequence

CTCTCCAGGGCTCGGCCCCGTCGAGGGGCGCGGACCACCCCCTTCTGTGGGCGCGCTGTGGGCAGAGGTGCAGAGGGGCAGTGGGGCCGGGGACAGGACCGGTCTACTAGTCGGGCACCTGCCGGGGC
CGAGCCTAGCCAGGACACGCTTGCGGGGGCGCGGCCGGGGGCGCCATCCAGCCCAAGAGGAGGCGGCATCTAGCCCGAGGGAGGTGGCGCTGGTGCGCGGGCGGCCCTTCTCTCTGTCCCCCGCCTCC
TCCCCGCGGCGAGCCGCGTAGCTCCGGAGGGCTCGGGGGCGGGGGCGGGGGCGGGGGCTGGGGCGGAATCCTCCTGAGAGGATCGCCCAGCACCCGCGGCGCCTTCGGCTTTGGCCGCCCGGCAGCCG
CCGAACTTGAACGCTTTTCTGAAGAGAGTTTTCCCCGCTCATCTTGGGGTTAAAACCTCGAAAACCCGCCCTCTGTTTGATCCTGCGTGGCTGCTTCCAGTACCTGGCAGTTCCTCTCCCCGGGCGAG
TTAACCACCTGTTCAGTCGGGAGGTGGACTCGAGGCTGCAGTCCTCGCCCGGTTTTAACAACCTGGATCTTCGAACTTTTGACACGGCTTTGGAAACGACGTCATGTGTTAGAATTGGAGCGTTATTC
AGTATATTAATGTCTTATTGATAATGGCAGAACATCCACCACTACTGGATACAACTCAGATCTTAAGTAGTGATATTTCTCTTTTGTCTGCCCCTATTGTAAGTGCAGATGGAACACAACAGGTTATT
CTGGTACAAGTTAACCCAGGAGAAGCATTTACAATAAGAAGAGAAGATGGACAGTTTCAGTGCATTACAGGTCCTGCTCAGGTTCCAATGATGTCCCCAAATGGTTCTGTGCCTCCTATCTATGTGCC
TCCTGGATATGCCCCACAGGTTATTGAAGACAATGGTGTTCGAAGAGTTGTCGTGGTCCCTCAGGCACCAGAGTTTCACCCTGGTAGTCACACAGTTCTCCACCGTTCTCCACATCCTCCTCTACCTG
GTTTCATTCCTGTCCCAACTATGATGCCGCCTCCACCACGTCATATGTACTCACCCGTGACTGGAGCTGGAGACATGACAACACAGTATATGCCACAGTATCAGTCTTCACAAGTCTATGGAGATGTA
GATGCTCACTCTACACATGGAAGGTCCAACTTTAGAGATGAACGATCTAGTAAAACATATGAACGTTTGCAGAAAAAATTGAAGGATCGCCAAGGAACACAGAAAGATAAAATGAGCAGTCCACCATC
ATCACCCCAGAAATGCCCTTCTCCCATTAATGAACATAATGGACTTATAAAAGGACAAATTGCTGGTGGTATAAACACAGGATCAGCAAAAATCAAGTCTGGGAAGGGGAAAGGTGGTACACAAGTTG
ATACAGAAATTGAAGAAAAAGATGAAGAAACTAAAGCATTTGAAGCACTTCTTTCCAACATTGTCAAACCAGTGGCCTCCGACATCCAGGCAAGGACAGTAGTACTTACCTGGTCACCACCTTCCAGC
CTCATTAATGGTGAAACAGATGAAAGTAGTGTACCAGAGCTCTATGGTTATGAAGTTCTGATCTCAAGTACTGGAAAAGATGGGAAATACAAAAGTGTATATGTAGGAGAAGAAACAAATATCACTTT
AAATGATCTCAAGCCAGCCATGGATTACCATGCAAAAGTCCAGGCAGAATATAATTCTATAAAGGGAACTCCTTCAGAGGCTGAAATCTTTACCACCTTGAGCTGTGAACCTGATATACCTAATCCAC
CAAGGATAGCCAATCGGACCAAAAATTCACTCACTTTGCAATGGAAGGCACCTAGTGACAATGGTTCTAAAATCCAAAACTTTGTATTAGAATGGGATGAAGGAAAAGGAAATGGAGAATTTTGTCAG
TGTTACATGGGCTCACAGAAACAATTTAAAATTACTAAACTTTCACCAGCAATGGGCTGTAAATTCAGACTATCGGCCAGAAATGACTATGGTACAAGTGGTTTTAGTGAAGAAGTCTTATATTACAC
CTCAGGCTGTGCTCCTTCTATGCCAGCAAGTCCTGTATTAACCAAGGCTGGAATTACTTGGTTATCCTTACAATGGAGTAAGCCCTCAGGAACACCATCAGATGAAGGAATTTCTTACATTTTAGAGA
TGGAGGAAGAAACTTCAGGATATGGTTTTAAGCCTAAATATGATGGAGAAGATCTTGCTTACACAGTGAAAAATCTCAGACGTAGTACTAAGTATAAATTTAAGGTTATTGCTTACAACTCAGAAGGT
AAAAGTAATCCAAGTGAAGTAGTAGAATTTACTACTTGCCCTGATAAACCAGGCATACCTGTAAAGCCTTCAGTGAAAGGAAAGATACATTCACACAGTTTTAAAATAACCTGGGATCCACCAAAAGA
CAATGGCGGAGCAACCATCAATAAATATGTAGTGGAGATGGCAGAAGGTTCTAACGGAAACAAATGGGAAATGATATACAGTGGTGCTACCAGGGAACATCTTTGTGATCGACTGAATCCAGGCTGTT
TCTATCGTTTACGAGTTTACTGCATCAGTGATGGAGGACAGAGTGCGGTCTCTGAATCTTTACTTGTGCAGACTCCAGCTGTGCCTCCTGGCCCATGCCTCCCTCCCAGATTACAGGGTAGACCCAAA
GCAAAAGAAATACAGTTACGATGGGGACCCCCTCTGGTTGATGGTGGATCACCCATTTCCTGTTACAGTGTGGAAATGTCTCCTATAGAAAAAGATGAACCTAGAGAAGTTTACCAAGGTTCTGAAGT
AGAATGTACAGTGAGCAGCCTTCTTCCTGGAAAGACATACAGCTTCAGACTACGTGCAGCTAACAAAATGGGGTTTGGACCATTTTCAGAAAAATGTGATATTACTACAGCCCCTGGGCCACCAGATC
AGTGCAAGCCCCCTCAAGTGACATGTAGATCTGCAACTTGTGCACAAGTGAATTGGGAGGTTCCTTTGAGTAATGGAACAGATGTCACTGAATATCGACTGGAGTGGGGAGGAGTTGAAGGAAGTATG
CAGATATGTTACTGTGGGCCTGGTCTCAGTTATGAAATAAAAGGACTTTCACCAGCAACTACCTATTATTGCAGGGTCCAGGCTCTGAGTGTTGTGGGTGCAGGCCCTTTCAGTGAAGTAGTAGCCTG
TGTGACTCCACCATCAGTTCCTGGCATTGTGACCTGTCTTCAAGAAATAAGCGATGATGAGATAGAAAATCCCCATTATTCACCTTCTACATGCCTTGCAATAAGCTGGGAAAAGCCTTGTGATCATG
GTTCGGAAATCCTTGCCTACAGCATAGACTTTGGAGATAAACAATCCCTAACAGTGGGAAAGGTTACAAGCTATATTATCAACAATTTGCAACCAGATACAACATACAGAATACGAATTCAAGCCTTG
AATAGCCTTGGAGCTGGTCCTTTCAGCCATATGATAAAATTAAAAACTAAGCCTCTCCCTCCTGATCCACCTCGTCTGGAATGTGTTGCCTTTAGCCACCAGAACCTTAAGCTGAAATGGGGAGAAGG
AACTCCAAAGACATTGTCAACCGATTCTATTCAGTACCACCTTCAGATGGAGGATAAGAATGGACGAAACATCCAATCAAAAATAATGGGATGCATTCAACTTATAGATAACATATTAGGAGAAATAT
GTATGATATTCAACTTCATTGAACAGTTCAAGTGGGTAATGTATTGGAAATTTTATATTATCATACTGCTTTTGTAAATCTCTAAAAAAACGTCACCAAGTCAACTAAAAATCTGCCTGGGAATTGAG
AATTCTCTTTTTTCCAGATAAAGACAAGGAAGATTAAAATAGAAACTTAATCTCATAGCTCAGGTCTCTATGCCATACTTGGCAAATTTTATCAATATGACTTTAGTTAGAAATAATTTGTAATGAAA
ATTGTGATGTTCTGAGCATCTTTTAAAATGTACATTAACAAAACAGTATTCAGAAACAAAGCTAAACCGGAAGCCTGAGAAGAAACAGTTATGGTCGGACATGAAATTTAGTAACAGACTTTTGGTAA
ATCATGTCAAATTGGGAAATTTACCAAATATCCTATTTTTCTTAATCTGATGAAAAACAGATTTATTTTAAGTGACATAGAGTTCCTGGCATCAAACTTTTGGGGTAACTTATCACTCCTAAATAATG
TTCATAACTGTGTTTTTATACTAGTTTGTAAAACACTTTAATAAGGTATCATAAGGTAGTATAAGGTTTATCTAATAGTTATTTCCA

hide sequence

RefSeq Acc Id:

XM_054374243 ⟹ XP_054230218

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	13	48,193,984 - 48,431,085 (+)	NCBI

RefSeq Acc Id:

XM_054374244 ⟹ XP_054230219

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	13	48,318,872 - 48,431,085 (+)	NCBI

RefSeq Acc Id:

XM_054374245 ⟹ XP_054230220

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	13	48,197,951 - 48,423,094 (+)	NCBI


Protein RefSeqs	NP_001073141	(Get FASTA)	NCBI Sequence Viewer
	NP_001265367	(Get FASTA)	NCBI Sequence Viewer
	NP_055738	(Get FASTA)	NCBI Sequence Viewer
	XP_011533299	(Get FASTA)	NCBI Sequence Viewer
	XP_016875929	(Get FASTA)	NCBI Sequence Viewer
	XP_016875932	(Get FASTA)	NCBI Sequence Viewer
	XP_054230218	(Get FASTA)	NCBI Sequence Viewer
	XP_054230219	(Get FASTA)	NCBI Sequence Viewer
	XP_054230220	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH60816	(Get FASTA)	NCBI Sequence Viewer
	AAH70072	(Get FASTA)	NCBI Sequence Viewer
	AAI32813	(Get FASTA)	NCBI Sequence Viewer
	AAI36618	(Get FASTA)	NCBI Sequence Viewer
	AAI44302	(Get FASTA)	NCBI Sequence Viewer
	BAA76814	(Get FASTA)	NCBI Sequence Viewer
	BAD18784	(Get FASTA)	NCBI Sequence Viewer
	BAG63723	(Get FASTA)	NCBI Sequence Viewer
	CAE45852	(Get FASTA)	NCBI Sequence Viewer
	CAG44602	(Get FASTA)	NCBI Sequence Viewer
	CAG44603	(Get FASTA)	NCBI Sequence Viewer
	CAI45989	(Get FASTA)	NCBI Sequence Viewer
	EAX08803	(Get FASTA)	NCBI Sequence Viewer
	EAX08804	(Get FASTA)	NCBI Sequence Viewer
	EAX08805	(Get FASTA)	NCBI Sequence Viewer
	EAX08806	(Get FASTA)	NCBI Sequence Viewer
	EAX08807	(Get FASTA)	NCBI Sequence Viewer
	EAX08808	(Get FASTA)	NCBI Sequence Viewer
	EAX08809	(Get FASTA)	NCBI Sequence Viewer
	EAX08810	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000381362
	ENSP00000381362.3
	ENSP00000417257
	ENSP00000417257.1
	ENSP00000441831
	ENSP00000441831.1
GenBank Protein	Q9Y2H6	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001073141 ⟸ NM_001079673
- Peptide Label:	isoform 1
- UniProtKB:	Q6ZME4 (UniProtKB/Swiss-Prot), Q6P9D5 (UniProtKB/Swiss-Prot), Q6N020 (UniProtKB/Swiss-Prot), Q6EVH4 (UniProtKB/Swiss-Prot), Q6EVH3 (UniProtKB/Swiss-Prot), Q5JVF9 (UniProtKB/Swiss-Prot), Q5JVF8 (UniProtKB/Swiss-Prot), Q5HYC9 (UniProtKB/Swiss-Prot), B4DYG1 (UniProtKB/Swiss-Prot), Q9H1W1 (UniProtKB/Swiss-Prot), Q9Y2H6 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAEHPPLLDTTQILSSDISLLSAPIVSADGTQQVILVQVNPGEAFTIRREDGQFQCITGPAQVPMMSPNGSVPPIYVPPGYAPQVIEDNGVRRVVVVPQAPEFHPGSHTVLHRSPHPPLPGFIPVPTM MPPPPRHMYSPVTGAGDMTTQYMPQYQSSQVYGDVDAHSTHGRSNFRDERSSKTYERLQKKLKDRQGTQKDKMSSPPSSPQKCPSPINEHNGLIKGQIAGGINTGSAKIKSGKGKGGTQVDTEIEEKD EETKAFEALLSNIVKPVASDIQARTVVLTWSPPSSLINGETDESSVPELYGYEVLISSTGKDGKYKSVYVGEETNITLNDLKPAMDYHAKVQAEYNSIKGTPSEAEIFTTLSCEPDIPNPPRIANRTK NSLTLQWKAPSDNGSKIQNFVLEWDEGKGNGEFCQCYMGSQKQFKITKLSPAMGCKFRLSARNDYGTSGFSEEVLYYTSGCAPSMPASPVLTKAGITWLSLQWSKPSGTPSDEGISYILEMEEETSGY GFKPKYDGEDLAYTVKNLRRSTKYKFKVIAYNSEGKSNPSEVVEFTTCPDKPGIPVKPSVKGKIHSHSFKITWDPPKDNGGATINKYVVEMAEGSNGNKWEMIYSGATREHLCDRLNPGCFYRLRVYC ISDGGQSAVSESLLVQTPAVPPGPCLPPRLQGRPKAKEIQLRWGPPLVDGGSPISCYSVEMSPIEKDEPREVYQGSEVECTVSSLLPGKTYSFRLRAANKMGFGPFSEKCDITTAPGPPDQCKPPQVT CRSATCAQVNWEVPLSNGTDVTEYRLEWGGVEGSMQICYCGPGLSYEIKGLSPATTYYCRVQALSVVGAGPFSEVVACVTPPSVPGIVTCLQEISDDEIENPHYSPSTCLAISWEKPCDHGSEILAYS IDFGDKQSLTVGKVTSYIINNLQPDTTYRIRIQALNSLGAGPFSHMIKLKTKPLPPDPPRLECVAFSHQNLKLKWGEGTPKTLSTDSIQYHLQMEDKNGRFVSLYRGPCHTYKVQRLNESTSYKFCIQ ACNEAGEGPLSQEYIFTTPKSVPAALKAPKIEKVNDHICEITWECLQPMKGDPVIYSLQVMLGKDSEFKQIYKGPDSSFRYSSLQLNCEYRFRVCAIRQCQDSLGHQDLVGPYSTTVLFISQRTEPPA STNRDTVESTRTRRALSDEQCAAVILVLFAFFSILIAFIIQYFVIK hide sequence

RefSeq Acc Id:

NP_055738 ⟸ NM_014923

- Peptide Label:

isoform 2

- Sequence:

show sequence

MSGPAQVPMMSPNGSVPPIYVPPGYAPQVIEDNGVRRVVVVPQAPEFHPGSHTVLHRSPHPPLP
GFIPVPTMMPPPPRHMYSPVTGAGDMTTQYMPQYQSSQVYGDVDAHSTHGRSNFRDERSSKTYERLQKKLKDRQGTQKDKMSSPPSSPQKCPSPINEHNGLIKGQIAGGINTGSAKIKSGKGKGGTQV
DTEIEEKDEETKAFEALLSNIVKPVASDIQARTVVLTWSPPSSLINGETDESSVPELYGYEVLISSTGKDGKYKSVYVGEETNITLNDLKPAMDYHAKVQAEYNSIKGTPSEAEIFTTLSCEPDIPNP
PRIANRTKNSLTLQWKAPSDNGSKIQNFVLEWDEGKGNGEFCQCYMGSQKQFKITKLSPAMGCKFRLSARNDYGTSGFSEEVLYYTSGCAPSMPASPVLTKAGITWLSLQWSKPSGTPSDEGISYILE
MEEETSGYGFKPKYDGEDLAYTVKNLRRSTKYKFKVIAYNSEGKSNPSEVVEFTTCPDKPGIPVKPSVKGKIHSHSFKITWDPPKDNGGATINKYVVEMAEGSNGNKWEMIYSGATREHLCDRLNPGC
FYRLRVYCISDGGQSAVSESLLVQTPAVPPGPCLPPRLQGRPKAKEIQLRWGPPLVDGGSPISCYSVEMSPIEKDEPREVYQGSEVECTVSSLLPGKTYSFRLRAANKMGFGPFSEKCDITTAPGPPD
QCKPPQVTCRSATCAQVNWEVPLSNGTDVTEYRLEWGGVEGSMQICYCGPGLSYEIKGLSPATTYYCRVQALSVVGAGPFSEVVACVTPPSVPGIVTCLQEISDDEIENPHYSPSTCLAISWEKPCDH
GSEILAYSIDFGDKQSLTVGKVTSYIINNLQPDTTYRIRIQALNSLGAGPFSHMIKLKTKPLPPDPPRLECVAFSHQNLKLKWGEGTPKTLSTDSIQYHLQMEDKNGRFVSLYRGPCHTYKVQRLNES
TSYKFCIQACNEAGEGPLSQEYIFTTPKSVPAALKAPKIEKVNDHICEITWECLQPMKGDPVIYSLQVMLGKDSEFKQIYKGPDSSFRYSSLQLNCEYRFRVCAIRQCQDSLGHQDLVGPYSTTVLFI
SQRTEPPASTNRDTVESTRTRRALSDEQCAAVILVLFAFFSILIAFIIQYFVIK

hide sequence

RefSeq Acc Id:	NP_001265367 ⟸ NM_001278438
- Peptide Label:	isoform 1
- UniProtKB:	Q6ZME4 (UniProtKB/Swiss-Prot), Q6P9D5 (UniProtKB/Swiss-Prot), Q6N020 (UniProtKB/Swiss-Prot), Q6EVH4 (UniProtKB/Swiss-Prot), Q6EVH3 (UniProtKB/Swiss-Prot), Q5JVF9 (UniProtKB/Swiss-Prot), Q5JVF8 (UniProtKB/Swiss-Prot), Q5HYC9 (UniProtKB/Swiss-Prot), B4DYG1 (UniProtKB/Swiss-Prot), Q9H1W1 (UniProtKB/Swiss-Prot), Q9Y2H6 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAEHPPLLDTTQILSSDISLLSAPIVSADGTQQVILVQVNPGEAFTIRREDGQFQCITGPAQVP MMSPNGSVPPIYVPPGYAPQVIEDNGVRRVVVVPQAPEFHPGSHTVLHRSPHPPLPGFIPVPTMMPPPPRHMYSPVTGAGDMTTQYMPQYQSSQVYGDVDAHSTHGRSNFRDERSSKTYERLQKKLKD RQGTQKDKMSSPPSSPQKCPSPINEHNGLIKGQIAGGINTGSAKIKSGKGKGGTQVDTEIEEKDEETKAFEALLSNIVKPVASDIQARTVVLTWSPPSSLINGETDESSVPELYGYEVLISSTGKDGK YKSVYVGEETNITLNDLKPAMDYHAKVQAEYNSIKGTPSEAEIFTTLSCEPDIPNPPRIANRTKNSLTLQWKAPSDNGSKIQNFVLEWDEGKGNGEFCQCYMGSQKQFKITKLSPAMGCKFRLSARND YGTSGFSEEVLYYTSGCAPSMPASPVLTKAGITWLSLQWSKPSGTPSDEGISYILEMEEETSGYGFKPKYDGEDLAYTVKNLRRSTKYKFKVIAYNSEGKSNPSEVVEFTTCPDKPGIPVKPSVKGKI HSHSFKITWDPPKDNGGATINKYVVEMAEGSNGNKWEMIYSGATREHLCDRLNPGCFYRLRVYCISDGGQSAVSESLLVQTPAVPPGPCLPPRLQGRPKAKEIQLRWGPPLVDGGSPISCYSVEMSPI EKDEPREVYQGSEVECTVSSLLPGKTYSFRLRAANKMGFGPFSEKCDITTAPGPPDQCKPPQVTCRSATCAQVNWEVPLSNGTDVTEYRLEWGGVEGSMQICYCGPGLSYEIKGLSPATTYYCRVQAL SVVGAGPFSEVVACVTPPSVPGIVTCLQEISDDEIENPHYSPSTCLAISWEKPCDHGSEILAYSIDFGDKQSLTVGKVTSYIINNLQPDTTYRIRIQALNSLGAGPFSHMIKLKTKPLPPDPPRLECV AFSHQNLKLKWGEGTPKTLSTDSIQYHLQMEDKNGRFVSLYRGPCHTYKVQRLNESTSYKFCIQACNEAGEGPLSQEYIFTTPKSVPAALKAPKIEKVNDHICEITWECLQPMKGDPVIYSLQVMLGK DSEFKQIYKGPDSSFRYSSLQLNCEYRFRVCAIRQCQDSLGHQDLVGPYSTTVLFISQRTEPPASTNRDTVESTRTRRALSDEQCAAVILVLFAFFSILIAFIIQYFVIK hide sequence

RefSeq Acc Id:	XP_011533299 ⟸ XM_011534997
- Peptide Label:	isoform X2
- UniProtKB:	Q9Y2H6 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMSPNGSVPPIYVPPGYAPQVIEDNGVRRVVVVPQAPEFHPGSHTVLHRSPHPPLPGFIPVPTMMPPPPRHMYSPVTGAGDMTTQYMPQYQSSQVYGDVDAHSTHGRSNFRDERSSKTYERLQKKLKD RQGTQKDKMSSPPSSPQKCPSPINEHNGLIKGQIAGGINTGSAKIKSGKGKGGTQVDTEIEEKDEETKAFEALLSNIVKPVASDIQARTVVLTWSPPSSLINGETDESSVPELYGYEVLISSTGKDGK YKSVYVGEETNITLNDLKPAMDYHAKVQAEYNSIKGTPSEAEIFTTLSCEPDIPNPPRIANRTKNSLTLQWKAPSDNGSKIQNFVLEWDEGKGNGEFCQCYMGSQKQFKITKLSPAMGCKFRLSARND YGTSGFSEEVLYYTSGCAPSMPASPVLTKAGITWLSLQWSKPSGTPSDEGISYILEMEEETSGYGFKPKYDGEDLAYTVKNLRRSTKYKFKVIAYNSEGKSNPSEVVEFTTCPDKPGIPVKPSVKGKI HSHSFKITWDPPKDNGGATINKYVVEMAEGSNGNKWEMIYSGATREHLCDRLNPGCFYRLRVYCISDGGQSAVSESLLVQTPAVPPGPCLPPRLQGRPKAKEIQLRWGPPLVDGGSPISCYSVEMSPI EKDEPREVYQGSEVECTVSSLLPGKTYSFRLRAANKMGFGPFSEKCDITTAPGPPDQCKPPQVTCRSATCAQVNWEVPLSNGTDVTEYRLEWGGVEGSMQICYCGPGLSYEIKGLSPATTYYCRVQAL SVVGAGPFSEVVACVTPPSVPGIVTCLQEISDDEIENPHYSPSTCLAISWEKPCDHGSEILAYSIDFGDKQSLTVGKVTSYIINNLQPDTTYRIRIQALNSLGAGPFSHMIKLKTKPLPPDPPRLECV AFSHQNLKLKWGEGTPKTLSTDSIQYHLQMEDKNGRFVSLYRGPCHTYKVQRLNESTSYKFCIQACNEAGEGPLSQEYIFTTPKSVPAALKAPKIEKVNDHICEITWECLQPMKGDPVIYSLQVMLGK DSEFKQIYKGPDSSFRYSSLQLNCEYRFRVCAIRQCQDSLGHQDLVGPYSTTVLFISQRTEPPASTNRDTVESTRTRRALSDEQCAAVILVLFAFFSILIAFIIQYFVIK hide sequence

RefSeq Acc Id:	XP_016875929 ⟸ XM_017020440
- Peptide Label:	isoform X1
- UniProtKB:	Q6ZME4 (UniProtKB/Swiss-Prot), Q6P9D5 (UniProtKB/Swiss-Prot), Q6N020 (UniProtKB/Swiss-Prot), Q6EVH4 (UniProtKB/Swiss-Prot), Q6EVH3 (UniProtKB/Swiss-Prot), Q5JVF9 (UniProtKB/Swiss-Prot), Q5JVF8 (UniProtKB/Swiss-Prot), Q5HYC9 (UniProtKB/Swiss-Prot), B4DYG1 (UniProtKB/Swiss-Prot), Q9H1W1 (UniProtKB/Swiss-Prot), Q9Y2H6 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAEHPPLLDTTQILSSDISLLSAPIVSADGTQQVILVQVNPGEAFTIRREDGQFQCITGPAQVPMMSPNGSVPPIYVPPGYAPQVIEDNGVRRVVVVPQAPEFHPGSHTVLHRSPHPPLPGFIPVPTM MPPPPRHMYSPVTGAGDMTTQYMPQYQSSQVYGDVDAHSTHGRSNFRDERSSKTYERLQKKLKDRQGTQKDKMSSPPSSPQKCPSPINEHNGLIKGQIAGGINTGSAKIKSGKGKGGTQVDTEIEEKD EETKAFEALLSNIVKPVASDIQARTVVLTWSPPSSLINGETDESSVPELYGYEVLISSTGKDGKYKSVYVGEETNITLNDLKPAMDYHAKVQAEYNSIKGTPSEAEIFTTLSCEPDIPNPPRIANRTK NSLTLQWKAPSDNGSKIQNFVLEWDEGKGNGEFCQCYMGSQKQFKITKLSPAMGCKFRLSARNDYGTSGFSEEVLYYTSGCAPSMPASPVLTKAGITWLSLQWSKPSGTPSDEGISYILEMEEETSGY GFKPKYDGEDLAYTVKNLRRSTKYKFKVIAYNSEGKSNPSEVVEFTTCPDKPGIPVKPSVKGKIHSHSFKITWDPPKDNGGATINKYVVEMAEGSNGNKWEMIYSGATREHLCDRLNPGCFYRLRVYC ISDGGQSAVSESLLVQTPAVPPGPCLPPRLQGRPKAKEIQLRWGPPLVDGGSPISCYSVEMSPIEKDEPREVYQGSEVECTVSSLLPGKTYSFRLRAANKMGFGPFSEKCDITTAPGPPDQCKPPQVT CRSATCAQVNWEVPLSNGTDVTEYRLEWGGVEGSMQICYCGPGLSYEIKGLSPATTYYCRVQALSVVGAGPFSEVVACVTPPSVPGIVTCLQEISDDEIENPHYSPSTCLAISWEKPCDHGSEILAYS IDFGDKQSLTVGKVTSYIINNLQPDTTYRIRIQALNSLGAGPFSHMIKLKTKPLPPDPPRLECVAFSHQNLKLKWGEGTPKTLSTDSIQYHLQMEDKNGRFVSLYRGPCHTYKVQRLNESTSYKFCIQ ACNEAGEGPLSQEYIFTTPKSVPAALKAPKIEKVNDHICEITWECLQPMKGDPVIYSLQVMLGKDSEFKQIYKGPDSSFRYSSLQLNCEYRFRVCAIRQCQDSLGHQDLVGPYSTTVLFISQRTEPPA STNRDTVESTRTRRALSDEQCAAVILVLFAFFSILIAFIIQYFVIK hide sequence

Protein Domains

Fibronectin type-III

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9Y2H6-F1-model_v2	AlphaFold	Q9Y2H6	1-1198	view protein structure

RGD ID:

6790926

Promoter ID:

HG_KWN:17839

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

NM_001079673, UC001VCL.1, UC001VCN.1, UC001VCO.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	13	48,447,451 - 48,448,957 (+)	MPROMDB

RGD ID:

6790880

Promoter ID:

HG_KWN:17843

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

NM_014923, UC001VCP.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	13	48,582,169 - 48,582,669 (+)	MPROMDB

RGD ID:

7226417

Promoter ID:

EPDNEW_H18954

Type:

initiation region

Name:

FNDC3A_5

Description:

fibronectin type III domain containing 3A

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H18955 EPDNEW_H18956 EPDNEW_H18957 EPDNEW_H18958

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,975,291 - 48,975,351	EPDNEW

RGD ID:

7226419

Promoter ID:

EPDNEW_H18955

Type:

initiation region

Name:

FNDC3A_2

Description:

fibronectin type III domain containing 3A

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H18954 EPDNEW_H18956 EPDNEW_H18957 EPDNEW_H18958

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,975,912 - 48,975,972	EPDNEW

RGD ID:

7226421

Promoter ID:

EPDNEW_H18956

Type:

initiation region

Name:

FNDC3A_3

Description:

fibronectin type III domain containing 3A

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H18954 EPDNEW_H18955 EPDNEW_H18957 EPDNEW_H18958

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,976,662 - 48,976,722	EPDNEW

RGD ID:

7226423

Promoter ID:

EPDNEW_H18957

Type:

initiation region

Name:

FNDC3A_4

Description:

fibronectin type III domain containing 3A

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H18954 EPDNEW_H18955 EPDNEW_H18956 EPDNEW_H18958

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	48,976,820 - 48,976,880	EPDNEW

RGD ID:

7226427

Promoter ID:

EPDNEW_H18958

Type:

initiation region

Name:

FNDC3A_1

Description:

fibronectin type III domain containing 3A

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H18954 EPDNEW_H18955 EPDNEW_H18956 EPDNEW_H18957

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	49,110,317 - 49,110,377	EPDNEW

Database	Acc Id	Source(s)
COSMIC	FNDC3A	COSMIC
Ensembl Genes	ENSG00000102531	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000398316	ENTREZGENE
	ENST00000398316.7	UniProtKB/Swiss-Prot
	ENST00000484074	ENTREZGENE
	ENST00000492622	ENTREZGENE
	ENST00000492622.6	UniProtKB/Swiss-Prot
	ENST00000541916	ENTREZGENE
	ENST00000541916.5	UniProtKB/Swiss-Prot
Gene3D-CATH	2.60.40.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000102531	GTEx
HGNC ID	HGNC:20296	ENTREZGENE
Human Proteome Map	FNDC3A	Human Proteome Map
InterPro	E3_ligase_FN3/SPRY	UniProtKB/Swiss-Prot
	FN3_dom	UniProtKB/Swiss-Prot
	FN3_sf	UniProtKB/Swiss-Prot
	Ig-like_fold	UniProtKB/Swiss-Prot
KEGG Report	hsa:22862	UniProtKB/Swiss-Prot
NCBI Gene	22862	ENTREZGENE
OMIM	615794	OMIM
PANTHER	E3 UBIQUITIN-PROTEIN LIGASE TRIM36-RELATED	UniProtKB/Swiss-Prot
	FIBRONECTIN TYPE III DOMAIN CONTAINING 3C2-RELATED	UniProtKB/Swiss-Prot
Pfam	fn3	UniProtKB/Swiss-Prot
PharmGKB	PA128394588	PharmGKB
PRINTS	FNTYPEIII	UniProtKB/Swiss-Prot
PROSITE	FN3	UniProtKB/Swiss-Prot
SMART	FN3	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF49265	UniProtKB/Swiss-Prot
UniProt	A0A087X1M6_HUMAN	UniProtKB/TrEMBL
	B4DYG1	ENTREZGENE
	FND3A_HUMAN	UniProtKB/Swiss-Prot
	G5E9X3_HUMAN	UniProtKB/TrEMBL
	H7C507_HUMAN	UniProtKB/TrEMBL
	Q5HYC9	ENTREZGENE
	Q5JVF8	ENTREZGENE
	Q5JVF9	ENTREZGENE
	Q6EVH3	ENTREZGENE
	Q6EVH4	ENTREZGENE
	Q6N020	ENTREZGENE
	Q6P9D5	ENTREZGENE
	Q6ZME4	ENTREZGENE
	Q9H1W1	ENTREZGENE
	Q9Y2H6	ENTREZGENE
UniProt Secondary	B4DYG1	UniProtKB/Swiss-Prot
	Q5HYC9	UniProtKB/Swiss-Prot
	Q5JVF8	UniProtKB/Swiss-Prot
	Q5JVF9	UniProtKB/Swiss-Prot
	Q6EVH3	UniProtKB/Swiss-Prot
	Q6EVH4	UniProtKB/Swiss-Prot
	Q6N020	UniProtKB/Swiss-Prot
	Q6P9D5	UniProtKB/Swiss-Prot
	Q6ZME4	UniProtKB/Swiss-Prot
	Q9H1W1	UniProtKB/Swiss-Prot

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailable


InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailable


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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