ZFAND6 (zinc finger AN1-type containing 6)

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Gene: ZFAND6 (zinc finger AN1-type containing 6) Homo sapiens

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Symbol:

ZFAND6

Name:

zinc finger AN1-type containing 6

RGD ID:

1345898

HGNC Page

HGNC:30164

Description:

Predicted to enable polyubiquitin modification-dependent protein binding activity. Involved in cellular response to tumor necrosis factor; negative regulation of apoptotic process; and regulation of canonical NF-kappaB signal transduction. Predicted to be located in cytosol.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

AN1-type zinc finger protein 6; associated with PRK1 protein; AWP1; protein associated with PRK1; ZA20D3; ZFAND5B; zinc finger A20 domain-containing protein 3; zinc finger, A20 domain containing 3; zinc finger, AN1-type domain 6

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Zfand6 (zinc finger, AN1-type domain 6)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Zfand6 (zinc finger AN1-type containing 6)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Zfand6 (zinc finger AN1-type containing 6)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ZFAND6 (zinc finger AN1-type containing 6)	NCBI	Ortholog
Canis lupus familiaris (dog):	ZFAND6 (zinc finger AN1-type containing 6)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Zfand6 (zinc finger AN1-type containing 6)	NCBI	Ortholog
Sus scrofa (pig):	ZFAND6 (zinc finger AN1-type containing 6)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	ZFAND6 (zinc finger AN1-type containing 6)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Zfand6 (zinc finger AN1-type containing 6)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Man1c1 (mannosidase, alpha, class 1C, member 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Zfand6 (zinc finger AN1-type containing 6)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Zfand6 (zinc finger, AN1-type domain 6)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	zfand6 (zinc finger, AN1-type domain 6)	Alliance	DIOPT (Hieranoid\|OMA\|OrthoFinder\|PANTHER\|ZFIN)
Drosophila melanogaster (fruit fly):	CG15368	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Caenorhabditis elegans (roundworm):	F22D6.2	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG45050	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus tropicalis (tropical clawed frog):	zfand6	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	zfand6.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	zfand6.L	Alliance	DIOPT (Xenbase)

Related Pseudogenes:

ZFAND6P1

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	15	80,058,951 - 80,138,393 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	15	80,059,568 - 80,140,292 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	15	80,352,018 - 80,430,735 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	15	78,139,076 - 78,217,767 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	15	78,139,075 - 78,217,765	NCBI
Celera	15	57,289,219 - 57,367,921 (+)	NCBI		Celera
Cytogenetic Map	15	q25.1	NCBI
HuRef	15	57,109,927 - 57,188,777 (+)	NCBI		HuRef
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Arsenic Poisoning (EXP)

Bloom syndrome (IAGP)

colorectal cancer (IAGP)

Delayed Emergence from Anesthesia (EXP)

skin disease (EXP)

tyrosinemia type I (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (EXP)

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

3,4-methylenedioxymethamphetamine (ISO)

3H-1,2-dithiole-3-thione (ISO)

all-trans-retinoic acid (EXP)

arsane (EXP)

arsenic atom (EXP)

arsenite(3-) (EXP)

benzo[a]pyrene (EXP,ISO)

beta-lapachone (EXP)

bisphenol A (EXP,ISO)

chromium(6+) (EXP)

clofibrate (ISO)

copper(II) sulfate (EXP)

diazinon (EXP)

dicrotophos (EXP)

dioxygen (ISO)

ethanol (ISO)

folic acid (ISO)

formaldehyde (EXP)

gold atom (EXP)

gold(0) (EXP)

lead diacetate (ISO)

lead(0) (EXP)

levonorgestrel (EXP)

p-chloromercuribenzoic acid (EXP)

paracetamol (EXP,ISO)

pirinixic acid (ISO)

potassium chromate (EXP)

propiconazole (ISO)

resveratrol (EXP)

rotenone (ISO)

sodium arsenate (ISO)

sodium arsenite (EXP)

testosterone undecanoate (EXP)

thiram (EXP)

trichloroethene (ISO)

trichostatin A (EXP)

triphenyl phosphate (EXP)

triptonide (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

apoptotic process (IEA)

cellular response to tumor necrosis factor (IMP)

negative regulation of apoptotic process (IMP)

protein targeting to peroxisome (IBA,IEA,ISS)

protein transport (IEA)

regulation of canonical NF-kappaB signal transduction (IMP)

signal transduction (ISO)

Cellular Component

cytoplasm (IEA)

cytosol (TAS)

Molecular Function

DNA binding (IEA)

metal ion binding (IEA)

polyubiquitin modification-dependent protein binding (IBA,IEA,ISS)

protein binding (IPI)

zinc ion binding (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
2.	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.	Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.

Additional References at PubMed

PMID:11054541	PMID:11230166	PMID:11256614	PMID:14702039	PMID:15146197	PMID:15342556	PMID:15489334	PMID:15698998	PMID:16169070	PMID:16189514	PMID:16344560	PMID:19285159
PMID:20379614	PMID:20549515	PMID:20581827	PMID:20889853	PMID:21810480	PMID:21873635	PMID:22939629	PMID:23314748	PMID:23443559	PMID:25416956	PMID:26344197	PMID:28190767
PMID:28514442	PMID:28580277	PMID:29351065	PMID:30232004	PMID:30561431	PMID:31494268	PMID:32296183	PMID:33961781	PMID:34672954	PMID:35563538	PMID:35831314	PMID:36980809
PMID:37127184	PMID:37738238	PMID:38803224	PMID:39098523

Genomics

Comparative Map Data

ZFAND6
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	15	80,058,951 - 80,138,393 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	15	80,059,568 - 80,140,292 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	15	80,352,018 - 80,430,735 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	15	78,139,076 - 78,217,767 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	15	78,139,075 - 78,217,765	NCBI
Celera	15	57,289,219 - 57,367,921 (+)	NCBI		Celera
Cytogenetic Map	15	q25.1	NCBI
HuRef	15	57,109,927 - 57,188,777 (+)	NCBI		HuRef
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI		T2T-CHM13v2.0

Zfand6
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	84,264,253 - 84,339,224 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	84,262,974 - 84,339,167 (-)	Ensembl		GRCm39 Ensembl
GRCm38	7	84,615,045 - 84,690,016 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	84,613,766 - 84,689,959 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	91,763,564 - 91,827,861 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	84,491,239 - 84,555,536 (-)	NCBI		MGSCv36	mm8
Celera	7	82,017,675 - 82,086,800 (-)	NCBI		Celera
Cytogenetic Map	7	D3	NCBI
cM Map	7	48.36	NCBI

Zfand6
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	147,990,099 - 148,061,221 (-)	NCBI		GRCr8
mRatBN7.2	1	138,581,002 - 138,652,052 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	138,581,002 - 138,651,939 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	146,533,717 - 146,604,324 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	153,702,718 - 153,773,333 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	146,577,924 - 146,648,533 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	146,745,850 - 146,823,762 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	146,745,859 - 146,823,762 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	147,672,431 - 147,750,196 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	140,885,701 - 140,960,486 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	140,964,112 - 141,038,892 (-)	NCBI
Celera	1	130,599,032 - 130,612,301 (-)	NCBI		Celera
Cytogenetic Map	1	q31	NCBI

Zfand6
(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_004955533	877,985 - 894,934 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955533	823,883 - 895,713 (+)	NCBI	ChiLan1.0	ChiLan1.0

ZFAND6
(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	16	69,306,795 - 69,392,607 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	15	73,471,591 - 73,557,324 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	15	59,023,678 - 59,107,270 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	15	77,996,265 - 78,067,171 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	15	78,048,571 - 78,115,098 (+)	Ensembl	panpan1.1		panPan2

ZFAND6
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	3	57,341,757 - 57,406,205 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	3	57,342,448 - 57,406,182 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	3	60,000,188 - 60,064,463 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	3	57,768,504 - 57,833,026 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	3	57,768,543 - 57,823,947 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	3	57,274,102 - 57,338,400 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	3	57,480,865 - 57,545,311 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	3	57,827,874 - 57,892,235 (-)	NCBI		UU_Cfam_GSD_1.0

Zfand6
(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_024408640	120,215,856 - 120,279,115 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936471	38,063,981 - 38,127,191 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936471	38,063,932 - 38,127,190 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZFAND6
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	7	48,967,579 - 49,034,703 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	7	48,967,402 - 49,034,711 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	7	54,475,829 - 54,542,954 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZFAND6
(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	26	3,274,721 - 3,356,873 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	26	3,274,194 - 3,314,527 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666048	138,518,274 - 138,601,371 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zfand6
(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_004624941	967,345 - 1,027,018 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624941	953,407 - 1,025,082 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZFAND6
14 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 15q24.2-26.3(chr15:75307767-101723215)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]\|See cases [RCV000052346]	Chr15:75307767..101723215 [GRCh38] Chr15:75600108..102263418 [GRCh37] Chr15:73387161..100080941 [NCBI36] Chr15:15q24.2-26.3	pathogenic
GRCh38/hg38 15q24.3-26.3(chr15:77543797-101843411)x3	copy number gain	See cases [RCV000052347]	Chr15:77543797..101843411 [GRCh38] Chr15:77836139..102383614 [GRCh37] Chr15:75623194..100201137 [NCBI36] Chr15:15q24.3-26.3	pathogenic
GRCh38/hg38 15q25.1(chr15:79552851-80526230)x3	copy number gain	See cases [RCV000052107]	Chr15:79552851..80526230 [GRCh38] Chr15:79845193..80818571 [GRCh37] Chr15:77632248..78605626 [NCBI36] Chr15:15q25.1	uncertain significance
GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	copy number gain	See cases [RCV000142915]	Chr15:59828460..101920998 [GRCh38] Chr15:60120659..102461201 [GRCh37] Chr15:57907951..100278724 [NCBI36] Chr15:15q22.2-26.3	pathogenic
GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	copy number gain	See cases [RCV000143019]	Chr15:72154949..101920998 [GRCh38] Chr15:72447290..102461201 [GRCh37] Chr15:70234344..100278724 [NCBI36] Chr15:15q23-26.3	pathogenic
GRCh37/hg19 15q24.2-26.3(chr15:76061144-102429112)x3	copy number gain	See cases [RCV000511332]	Chr15:76061144..102429112 [GRCh37] Chr15:15q24.2-26.3	pathogenic
GRCh37/hg19 15q22.31-26.3(chr15:64637227-102509910)x3	copy number gain	See cases [RCV000240602]	Chr15:64637227..102509910 [GRCh37] Chr15:15q22.31-26.3	pathogenic
GRCh37/hg19 15q22.1-26.3(chr15:59297293-102480888)x3	copy number gain	not provided [RCV000415836]	Chr15:59297293..102480888 [GRCh37] Chr15:15q22.1-26.3	likely pathogenic
GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4	copy number gain	See cases [RCV000447123]	Chr15:41745084..102354798 [GRCh37] Chr15:15q15.1-26.3	pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	copy number gain	See cases [RCV000510717]	Chr15:22770422..102429112 [GRCh37] Chr15:15q11.2-26.3	pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4	copy number gain	See cases [RCV000447765]	Chr15:20733395..102511616 [GRCh37] Chr15:15q11.2-26.3	pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	copy number gain	See cases [RCV000512019]	Chr15:22770422..102429112 [GRCh37] Chr15:15q11.2-26.3	pathogenic
NM_019006.4(ZFAND6):c.451A>T (p.Met151Leu)	single nucleotide variant	not specified [RCV004327682]	Chr15:80131266 [GRCh38] Chr15:80423608 [GRCh37] Chr15:15q25.1	uncertain significance
Single allele	duplication	not provided [RCV000677926]	Chr15:31115047..102354857 [GRCh37] Chr15:15q13.2-26.3	pathogenic
GRCh37/hg19 15q25.1-25.3(chr15:79023343-87158823)x1,2	copy number gain	not provided [RCV000683712]	Chr15:79023343..87158823 [GRCh37] Chr15:15q25.1-25.3	pathogenic
GRCh37/hg19 15q23-26.3(chr15:71329220-102270758)x3	copy number gain	not provided [RCV000683703]	Chr15:71329220..102270758 [GRCh37] Chr15:15q23-26.3	pathogenic
GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3	copy number gain	not provided [RCV000683710]	Chr15:77479244..102429112 [GRCh37] Chr15:15q24.3-26.3	pathogenic
GRCh37/hg19 15q25.1(chr15:80137560-80443036)x3	copy number gain	not provided [RCV000738849]	Chr15:80137560..80443036 [GRCh37] Chr15:15q25.1	benign
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3	copy number gain	not provided [RCV000751156]	Chr15:20071673..102461162 [GRCh37] Chr15:15q11.1-26.3	pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3	copy number gain	not provided [RCV000751155]	Chr15:20016811..102493540 [GRCh37] Chr15:15q11.1-26.3	pathogenic
NC_000015.9:g.(?_80403807)_(81274523_?)dup	duplication	Tyrosinemia type I [RCV001031622]	Chr15:80403807..81274523 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.348A>C (p.Glu116Asp)	single nucleotide variant	not specified [RCV004288741]	Chr15:80122784 [GRCh38] Chr15:80415126 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.304T>G (p.Ser102Ala)	single nucleotide variant	not provided [RCV000895763]	Chr15:80122740 [GRCh38] Chr15:80415082 [GRCh37] Chr15:15q25.1	likely benign
GRCh37/hg19 15q25.1-25.2(chr15:79996626-82097796)x1	copy number loss	not provided [RCV002472703]	Chr15:79996626..82097796 [GRCh37] Chr15:15q25.1-25.2	uncertain significance
GRCh37/hg19 15q25.1(chr15:79679772-80383301)x3	copy number gain	not provided [RCV001259713]	Chr15:79679772..80383301 [GRCh37] Chr15:15q25.1	uncertain significance
NC_000015.9:g.(?_32964879)_(91358519_?)dup	duplication	Bloom syndrome [RCV001343104]\|Familial colorectal cancer [RCV001325176]	Chr15:32964879..91358519 [GRCh37] Chr15:15q13.3-26.1	uncertain significance
NC_000015.9:g.(?_78857986)_(81282132_?)dup	duplication	not provided [RCV003116793]	Chr15:78857986..81282132 [GRCh37] Chr15:15q25.1	uncertain significance
GRCh37/hg19 15q24.3-26.3(chr15:77512817-102035027)x3	copy number gain	not provided [RCV002475797]	Chr15:77512817..102035027 [GRCh37] Chr15:15q24.3-26.3	pathogenic
NM_019006.4(ZFAND6):c.268G>A (p.Val90Ile)	single nucleotide variant	not specified [RCV004167825]	Chr15:80122704 [GRCh38] Chr15:80415046 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.425C>T (p.Pro142Leu)	single nucleotide variant	not specified [RCV004131526]	Chr15:80131240 [GRCh38] Chr15:80423582 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.539A>G (p.Asn180Ser)	single nucleotide variant	not specified [RCV004138417]	Chr15:80137540 [GRCh38] Chr15:80429882 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.304T>C (p.Ser102Pro)	single nucleotide variant	not specified [RCV004103524]	Chr15:80122740 [GRCh38] Chr15:80415082 [GRCh37] Chr15:15q25.1	uncertain significance
GRCh37/hg19 15q22.33-26.1(chr15:67358491-91644328)x3	copy number gain	not provided [RCV003222839]	Chr15:67358491..91644328 [GRCh37] Chr15:15q22.33-26.1	pathogenic
NM_019006.4(ZFAND6):c.296C>T (p.Ser99Phe)	single nucleotide variant	not specified [RCV004259818]	Chr15:80122732 [GRCh38] Chr15:80415074 [GRCh37] Chr15:15q25.1	uncertain significance
GRCh37/hg19 15q24.1-26.3(chr15:75165490-102520892)x3	copy number gain	See cases [RCV003329502]	Chr15:75165490..102520892 [GRCh37] Chr15:15q24.1-26.3	pathogenic
GRCh37/hg19 15q25.1(chr15:80208164-81551831)x3	copy number gain	not provided [RCV003485073]	Chr15:80208164..81551831 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.172C>G (p.Leu58Val)	single nucleotide variant	not specified [RCV004483788]	Chr15:80121729 [GRCh38] Chr15:80414071 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.253A>G (p.Met85Val)	single nucleotide variant	not specified [RCV004483789]	Chr15:80121810 [GRCh38] Chr15:80414152 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.424C>A (p.Pro142Thr)	single nucleotide variant	not specified [RCV004483790]	Chr15:80131239 [GRCh38] Chr15:80423581 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.239C>G (p.Ser80Cys)	single nucleotide variant	not specified [RCV004686340]	Chr15:80121796 [GRCh38] Chr15:80414138 [GRCh37] Chr15:15q25.1	uncertain significance
NM_019006.4(ZFAND6):c.421A>C (p.Lys141Gln)	single nucleotide variant	not specified [RCV004686339]	Chr15:80131236 [GRCh38] Chr15:80423578 [GRCh37] Chr15:15q25.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2634
Count of miRNA genes:	750
Interacting mature miRNAs:	867
Transcripts:	ENST00000261749, ENST00000557793, ENST00000557983, ENST00000558087, ENST00000558272, ENST00000558390, ENST00000558494, ENST00000558688, ENST00000558724, ENST00000558997, ENST00000559157, ENST00000559775, ENST00000559835, ENST00000560228, ENST00000560392, ENST00000560470, ENST00000560976, ENST00000561012, ENST00000561017, ENST00000561060, ENST00000564367
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
406999392	GWAS648368_H	reticulocyte measurement QTL GWAS648368 (human)		4e-17	reticulocyte morphology trait (VT:0002424)	red blood cell measurement (CMO:0001356)	15	80090739	80090740	Human
406990736	GWAS639712_H	reticulocyte measurement QTL GWAS639712 (human)		2e-29	reticulocyte morphology trait (VT:0002424)	red blood cell measurement (CMO:0001356)	15	80106556	80106557	Human
407099751	GWAS748727_H	reticulocyte measurement QTL GWAS748727 (human)		2e-24	reticulocyte morphology trait (VT:0002424)	red blood cell measurement (CMO:0001356)	15	80106556	80106557	Human
406981863	GWAS630839_H	reticulocyte count QTL GWAS630839 (human)		3e-33	reticulocyte count	total reticulocyte count (CMO:0003020)	15	80106556	80106557	Human
406965017	GWAS613993_H	reticulocyte count QTL GWAS613993 (human)		8e-14	reticulocyte count	total reticulocyte count (CMO:0003020)	15	80070911	80070912	Human
407113389	GWAS762365_H	reticulocyte count QTL GWAS762365 (human)		2e-28	reticulocyte count	total reticulocyte count (CMO:0003020)	15	80106556	80106557	Human
407254682	GWAS903658_H	brain measurement QTL GWAS903658 (human)		1e-13	brain measurement	brain measurement (CMO:0000911)	15	80105157	80105158	Human
406977182	GWAS626158_H	reticulocyte count QTL GWAS626158 (human)		3e-12	reticulocyte count	total reticulocyte count (CMO:0003020)	15	80070911	80070912	Human

Markers in Region

D15S969

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	80,383,345 - 80,383,626	UniSTS	GRCh37
Build 36	15	78,170,400 - 78,170,681	RGD	NCBI36
Celera	15	57,320,543 - 57,320,824	RGD
Cytogenetic Map	15	q25.1	UniSTS
HuRef	15	57,141,366 - 57,141,655	UniSTS
Marshfield Genetic Map	15	75.27	RGD
Marshfield Genetic Map	15	75.27	UniSTS
Genethon Genetic Map	15	74.6	UniSTS
Whitehead-YAC Contig Map	15		UniSTS

RH94373

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	80,430,139 - 80,430,261	UniSTS	GRCh37
Build 36	15	78,217,194 - 78,217,316	RGD	NCBI36
Celera	15	57,367,350 - 57,367,472	RGD
Cytogenetic Map	15	q25.1	UniSTS
HuRef	15	57,188,181 - 57,188,303	UniSTS
GeneMap99-GB4 RH Map	15	282.71	UniSTS

WI-11220

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	80,380,170 - 80,380,295	UniSTS	GRCh37
Build 36	15	78,167,225 - 78,167,350	RGD	NCBI36
Celera	15	57,317,368 - 57,317,493	RGD
Cytogenetic Map	15	q25.1	UniSTS
HuRef	15	57,138,191 - 57,138,316	UniSTS
Whitehead-YAC Contig Map	15		UniSTS

WI-15537

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	80,425,125 - 80,425,274	UniSTS	GRCh37
GRCh37	11	84,949,901 - 84,950,026	UniSTS	GRCh37
Build 36	11	84,627,549 - 84,627,674	RGD	NCBI36
Celera	11	82,259,192 - 82,259,317	RGD
Celera	15	57,362,336 - 57,362,485	UniSTS
Cytogenetic Map	15	q25.1	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
HuRef	11	81,246,716 - 81,246,841	UniSTS
HuRef	15	57,183,163 - 57,183,312	UniSTS
GeneMap99-GB4 RH Map	15	281.92	UniSTS
Whitehead-RH Map	15	306.8	UniSTS
NCBI RH Map	15	537.2	UniSTS

Expression

RNA-SEQ Expression

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	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001242911	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242912	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242913	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242914	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242915	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242916	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242917	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242918	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242919	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_019006	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011521684	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449955	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449959	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449960	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449961	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449963	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047432694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047432695	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047432696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047432697	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054378222	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054378223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054378224	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054378225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054378226	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC092701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF061739	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF261138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ251095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK055881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK312646	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL136598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW571396	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC005283	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG720174	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI562073	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP231220	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP234517	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX363429	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN428457	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR533476	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA091136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB050060	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DR762914	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF456103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000261749 ⟹ ENSP00000261749

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,676 - 80,138,393 (+)	Ensembl

Ensembl Acc Id:

ENST00000557793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,591 - 80,120,802 (+)	Ensembl

Ensembl Acc Id:

ENST00000557983

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,129,600 - 80,138,379 (+)	Ensembl

Ensembl Acc Id:

ENST00000558087 ⟹ ENSP00000453888

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,075,161 - 80,137,811 (+)	Ensembl

Ensembl Acc Id:

ENST00000558272 ⟹ ENSP00000456973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,590 - 80,121,750 (+)	Ensembl

Ensembl Acc Id:

ENST00000558390 ⟹ ENSP00000453308

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,590 - 80,131,241 (+)	Ensembl

Ensembl Acc Id:

ENST00000558494 ⟹ ENSP00000454137

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,714 - 80,138,360 (+)	Ensembl

Ensembl Acc Id:

ENST00000558688 ⟹ ENSP00000452664

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,587 - 80,131,517 (+)	Ensembl

Ensembl Acc Id:

ENST00000558724 ⟹ ENSP00000452625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,075,191 - 80,131,294 (+)	Ensembl

Ensembl Acc Id:

ENST00000558997 ⟹ ENSP00000453571

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,075,161 - 80,131,294 (+)	Ensembl

Ensembl Acc Id:

ENST00000559157 ⟹ ENSP00000454152

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,635 - 80,140,292 (+)	Ensembl

Ensembl Acc Id:

ENST00000559775 ⟹ ENSP00000453709

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,583 - 80,138,358 (+)	Ensembl

Ensembl Acc Id:

ENST00000559835 ⟹ ENSP00000453291

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,578 - 80,138,360 (+)	Ensembl

Ensembl Acc Id:

ENST00000560228 ⟹ ENSP00000454409

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,564 - 80,120,440 (+)	Ensembl

Ensembl Acc Id:

ENST00000560392 ⟹ ENSP00000455146

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,588 - 80,121,820 (+)	Ensembl

Ensembl Acc Id:

ENST00000560470 ⟹ ENSP00000455515

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,060,424 - 80,120,405 (+)	Ensembl

Ensembl Acc Id:

ENST00000560976 ⟹ ENSP00000453710

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,072,588 - 80,131,233 (+)	Ensembl

Ensembl Acc Id:

ENST00000561012 ⟹ ENSP00000453590

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,676 - 80,120,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000561017

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,121,719 - 80,123,067 (+)	Ensembl

Ensembl Acc Id:

ENST00000561060 ⟹ ENSP00000452735

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,613 - 80,137,678 (+)	Ensembl

Ensembl Acc Id:

ENST00000564367 ⟹ ENSP00000454273

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,690 - 80,137,560 (+)	Ensembl

Ensembl Acc Id:

ENST00000613266 ⟹ ENSP00000479071

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,059,568 - 80,138,392 (+)	Ensembl

Ensembl Acc Id:

ENST00000616533 ⟹ ENSP00000478129

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,075,161 - 80,138,392 (+)	Ensembl

Ensembl Acc Id:

ENST00000618205 ⟹ ENSP00000484971

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	80,060,160 - 80,138,392 (+)	Ensembl

RefSeq Acc Id:

NM_001242911 ⟹ NP_001229840

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,676 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI

Sequence:

show sequence

AATAAACAGCGGACGGAGGGGCCGGCGGTGGCGGAGCCGGAGCAAGCAGGGGTTCGGCGGCATT
ACCTGTACCCATTCACCGGCGGCTACCGGCGGCGGCGCGCAGCGTGTCAGGCGGAGAGACCCGC
CGCCAGGTGTGCAACTGAGGAACATGGCTCAAGAAACTAATCACAGCCAAGTGCCTATGCTTTG
TTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAAATGGCATGTGTTCAGTATGCTATAAA
GAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAATAAGCCCACCTGCAACCTCTGTCAGTA
GTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGCAGTGTGCCAGAAGCCCAGTCAGCATT
AGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAATCAGTCACTTTTATCAGAATCT
GTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCAGTACCTGAAACAGAAGATGTGC
AGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGCAAAGCAAGTCTCTTGAAAAACC
GAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTTACTGGGTTTGAATGC
CGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACACAATTGCTCTTACAATT
ACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTTGGTGAAAAGATCCA
AAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAACTAAAAATTGACTTGA
GGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATGTCATCGGAAGAATA
GATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTCCATTGCAATTTCTGTG
GCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTTAATTTTAGTTGAGTGC
AGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTTCCAGTATTAAACAT
GCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATCGCTTTTCTCTGCAGCA
CGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTAACTGAATGTATCTTAA
TCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGTTAGCATATAGTTTCTT
TGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTGATGAGATTGTAAGT
TTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCATTTCATTGCTGTCTA
CAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGAAGAATGATCTGAAGTA
ATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGAAAACCAGAATGCTC
CCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242912 ⟹ NP_001229841

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,676 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI

Sequence:

show sequence

AATAAACAGCGGACGGAGGGGCCGGCGGTGGCGGAGCCGGAGCAAGCAGGGGTTCGGCGGCATT
ACCTGTACCCATTCACCGGCGGCTACCGGCGGCGGCGCGCAGCGTGTCAGGCGGAGAGACCCGC
CGCCAGATACTTTGGTGTTGAACATTTGGGATAGAAGAGAGAAATTTAAAATTAAAAATTTTCC
ATATTTCTATCACAAATATTGGTGTGCAACTGAGGAACATGGCTCAAGAAACTAATCACAGCCA
AGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAAATGGCATGTGT
TCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAATAAGCCCACCTG
CAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGCAGTGTGCCAGA
AGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAATCAGTCA
CTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCAGTACCTG
AAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGCAAAGCAA
GTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTT
ACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACACA
ATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGT
TGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAAC
TAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCAT
GTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTCC
ATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTTA
ATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTT
TCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATCG
CTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTAA
CTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGTT
AGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCT
GATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCA
TTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGAA
GAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAGG
AAAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242913 ⟹ NP_001229842

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,922 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,470,222 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,338 - 78,001,808 (+)	NCBI

Sequence:

show sequence

GCCCGAGAGCCGGAAGCGGAGGGCGGCCGGCCGGCGCAGCAGATACTTTGGTGTTGAACATTTG
GGATAGAAGAGAGAAATTTAAAATTAAAAATTTTCCATATTTCTATCACAAATATTGGAATGAA
TCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTTAAAATGTTTTCTTGCATAAAATTCAAAAC
TTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAGAAAGCTAATGTCTGTCTCAAGATACAGGA
CAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCAACTGAGGAACATGGCTCAAGAAACTAATC
ACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAAATGG
CATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAATAAGC
CCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGCAGTG
TGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAA
TCAGTCACTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCA
GTACCTGAAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGC
AAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGT
GGGACTTACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGAT
GTACACAATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAG
TAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATC
TGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTAT
CTTGCATGTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATT
TATTTCCATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGAT
CATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTG
TGATTTTTCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTA
TATATCGCTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTA
TCAGTAACTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTC
ATATGTTAGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGT
GTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCT
GTATGCATTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACA
ATATGAAGAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAAT
AAAAAGGAAAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242914 ⟹ NP_001229843

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,060,119 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,470,452 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,535 - 78,001,808 (+)	NCBI

Sequence:

show sequence

AGTTCTTCAGGGCCGCGGAGGCCGCGACGCGCGCCGCCCCGAGCGGGTTGCGAGCGGTTGGCTG
GCGGGGGTCGGAAGGGCCCCGGGCACACTGGGGCGCGTCAGTTCCCCGCCTCCTCCGAGTCTCA
GGAATGAATCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTTAAAATGTTTTCTTGCATAAAA
TTCAAAACTTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAGAAAGCTAATGTCTGTCTCAAG
ATACAGGACAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCAACTGAGGAACATGGCTCAAGA
AACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGT
ACAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTA
GAATAAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGA
TGGCAGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCT
GTATCAAATCAGTCACTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGG
ACAAAGCAGTACCTGAAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATC
TGAAGAGCAAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGG
AAGAAAGTGGGACTTACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTT
ACTCAGATGTACACAATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGA
AAATCCAGTAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCT
TGAGCATCTGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAG
CAGTGTATCTTGCATGTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTC
TGAACATTTATTTCCATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCT
TTTAAGATCATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTG
GAGGGCTGTGATTTTTCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTG
TGTATGTATATATCGCTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACA
ACTAGTTATCAGTAACTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAA
GGTTATTCATATGTTAGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCAC
AAGAGAGTGTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAG
AAAAAGCTGTATGCATTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTG
TGTATACAATATGAAGAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTT
GATTAAATAAAAAGGAAAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242915 ⟹ NP_001229844

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,072,562 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,482,851 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,935,979 - 78,001,808 (+)	NCBI

Sequence:

show sequence

GTATTCAGGTTTGGTTGCTTTGGAGTACAGCTTCAAGTGAAGTTAATCTGAGGTGAAGCAAACA
GAAAATTGTGGAGGTTTTGTTGGTGTGCAACTGAGGAACATGGCTCAAGAAACTAATCACAGCC
AAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAAATGGCATGTG
TTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAATAAGCCCACCT
GCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGCAGTGTGCCAG
AAGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAATCAGTC
ACTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCAGTACCT
GAAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGCAAAGCA
AGTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACT
TACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACAC
AATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTG
TTGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAA
CTAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCA
TGTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTC
CATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTT
AATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTT
TTCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATC
GCTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTA
ACTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGT
TAGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGC
TGATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGC
ATTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGA
AGAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAG
GAAAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242916 ⟹ NP_001229845

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,072,562 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,482,851 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,935,979 - 78,001,808 (+)	NCBI

Sequence:

show sequence

GTATTCAGGTTTGGTTGCTTTGGAGTACAGCTTCAAGTGAAGTTAATCTGAGGTGAAGCAAACA
GAAAATTGTGGAGGTTTTGTTGGAATGAATCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTT
AAAATGTTTTCTTGCATAAAATTCAAAACTTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAG
AAAGCTAATGTCTGTCTCAAGATACAGGACAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCA
ACTGAGGAACATGGCTCAAGAAACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGT
GGATTTTATGGAAACCCTCGTACAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAA
GACAGAATAGTAGTAATGGTAGAATAAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATC
TTTACCAGTTCAATGCACAGATGGCAGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCT
TCATCTATGCAGCCCAGCCCTGTATCAAATCAGTCACTTTTATCAGAATCTGTAGCATCTTCTC
AATTGGACAGTACATCTGTGGACAAAGCAGTACCTGAAACAGAAGATGTGCAGGCTTCAGTATC
AGACACAGCACAGCAGCCATCTGAAGAGCAAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAG
AATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTTACTGGGTTTGAATGCCGGTGTGGAAATG
TTTACTGTGGTGTACACCGTTACTCAGATGTACACAATTGCTCTTACAATTACAAAGCCGATGC
TGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACT
CCTGCTGGAATACAAAATTCTTGAGCATCTGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTC
CTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATGTCATCGGAAGAATAGATTTTTGTTTTG
GTTTTGTTTTGAAAATGACTCTGAACATTTATTTCCATTGCAATTTCTGTGGCTGAGGAGACTT
AAACTTTACAAGTATTATCCTTTTAAGATCATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTAT
AACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTTCCAGTATTAAACATGCATGCATTAATC
TTGCAGTTTATTTTCTCATTGTGTATGTATATATCGCTTTTCTCTGCAGCACGATTTCTCTTTT
GATAATGCCCTTTAGGGCACAACTAGTTATCAGTAACTGAATGTATCTTAATCATTATGGCTGC
TTCTGTTTTTTCATTAACAAAGGTTATTCATATGTTAGCATATAGTTTCTTTGCACCCACTATT
TATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAA
CTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCATTTCATTGCTGTCTACAGGTTTCTTTCA
GATTATGTTCATGGGTTTGTGTGTATACAATATGAAGAATGATCTGAAGTAATTGTGCTGTATT
TATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGAAAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242917 ⟹ NP_001229846

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,676 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI

Sequence:

show sequence

AATAAACAGCGGACGGAGGGGCCGGCGGTGGCGGAGCCGGAGCAAGCAGGGGTTCGGCGGCATT
ACCTGTACCCATTCACCGGCGGCTACCGGCGGCGGCGCGCAGCGTGTCAGGCGGAGAGACCCGC
CGCCAGATCAAAAGACACTGACTTAGCTGCTTACCAGAAGGGGAACTTGGGTGTGCAACTGAGG
AACATGGCTCAAGAAACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTT
ATGGAAACCCTCGTACAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAA
TAGTAGTAATGGTAGAATAAGCCCACCTGTTCAATGCACAGATGGCAGTGTGCCAGAAGCCCAG
TCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAATCAGTCACTTTTAT
CAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCAGTACCTGAAACAGA
AGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGCAAAGCAAGTCTCTT
GAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTTACTGGGT
TTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACACAATTGCTC
TTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTTGGTGAA
AAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAACTAAAAAT
TGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATGTCATCG
GAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTCCATTGCAA
TTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTTAATTTTAG
TTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTTCCAGTA
TTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATCGCTTTTCT
CTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTAACTGAATG
TATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGTTAGCATAT
AGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTGATGAGA
TTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCATTTCATT
GCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGAAGAATGAT
CTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGAAAACCA
GAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242918 ⟹ NP_001229847

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,676 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI

Sequence:

show sequence

AATAAACAGCGGACGGAGGGGCCGGCGGTGGCGGAGCCGGAGCAAGCAGGGGTTCGGCGGCATT
ACCTGTACCCATTCACCGGCGGCTACCGGCGGCGGCGCGCAGCGTGTCAGGCGGAGAGACCCGC
CGCCAGGTGTGCAACTGAGGAACATGGCTCAAGAAACTAATCACAGCCAAGTGCCTATGCTTTG
TTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAAATGGCATGTGTTCAGTATGCTATAAA
GAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAATAAGCCCACCTGCAACCTCTGTCAGTA
GTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGCAGTGTGCCAGAAGCCCAGTCAGCATT
AGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAATCAGTCACTTTTATCAGAATCT
GTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCAGTACCTGAAACAGAAGATGTGC
AGGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACACAA
TTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTT
GGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAACT
AAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATG
TCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTCCA
TTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTTAA
TTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTT
CCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATCGC
TTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTAAC
TGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGTTA
GCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTG
ATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCAT
TTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGAAG
AATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGA
AAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

NM_001242919 ⟹ NP_001229848

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,098,416 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,508,718 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,961,831 - 78,001,808 (+)	NCBI

Sequence:

show sequence

GAATGAATCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTTAAAATGTTTTCTTGCATAAAAT
TCAAAACTTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAGAAAGCTAATGTCTGTCTCAAGA
TACAGGACAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCAACTGAGGAACATGGCTCAAGAA
ACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGTA
CAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTAG
AATAAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGAT
GGCAGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTGTGGACAAAGCAGTACCTGAAA
CAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGCAAAGCAAGTC
TCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTTACT
GGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACACAATT
GCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTTGG
TGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAACTAA
AAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATGTC
ATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTCCATT
GCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTTAATT
TTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTTCC
AGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATCGCTT
TTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTAACTG
AATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGTTAGC
ATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTGAT
GAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCATTT
CATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGAAGAA
TGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGAAA
ACCAGAATGCTCCCTTGTAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_019006 ⟹ NP_061879

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,676 - 80,138,393 (+)	NCBI
GRCh37	15	80,351,910 - 80,430,735 (+)	ENTREZGENE
Build 36	15	78,139,076 - 78,217,767 (+)	NCBI Archive
Celera	15	57,289,219 - 57,367,921 (+)	RGD
HuRef	15	57,109,927 - 57,188,777 (+)	ENTREZGENE
CHM1_1	15	80,469,860 - 80,548,702 (+)	NCBI
T2T-CHM13v2.0	15	77,923,092 - 78,001,808 (+)	NCBI

Sequence:

show sequence

AATAAACAGCGGACGGAGGGGCCGGCGGTGGCGGAGCCGGAGCAAGCAGGGGTTCGGCGGCATT
ACCTGTACCCATTCACCGGCGGCTACCGGCGGCGGCGCGCAGCGTGTCAGGCGGAGAGACCCGC
CGCCAGGAATGAATCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTTAAAATGTTTTCTTGCA
TAAAATTCAAAACTTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAGAAAGCTAATGTCTGTC
TCAAGATACAGGACAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCAACTGAGGAACATGGCT
CAAGAAACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACC
CTCGTACAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAA
TGGTAGAATAAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGC
ACAGATGGCAGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCA
GCCCTGTATCAAATCAGTCACTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATC
TGTGGACAAAGCAGTACCTGAAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAG
CCATCTGAAGAGCAAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGT
GCAGGAAGAAAGTGGGACTTACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACA
CCGTTACTCAGATGTACACAATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGA
AAAGAAAATCCAGTAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAA
ATTCTTGAGCATCTGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATG
TAGAGCAGTGTATCTTGCATGTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAAT
GACTCTGAACATTTATTTCCATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATT
ATCCTTTTAAGATCATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAA
TTTTGGAGGGCTGTGATTTTTCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCT
CATTGTGTATGTATATATCGCTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGG
GCACAACTAGTTATCAGTAACTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTA
ACAAAGGTTATTCATATGTTAGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTT
GTCACAAGAGAGTGTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAG
GGAAGAAAAAGCTGTATGCATTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGT
TTGTGTGTATACAATATGAAGAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAG
TCTTTGATTAAATAAAAAGGAAAACCAGAATGCTCCCTTGTA

hide sequence

RefSeq Acc Id:

XM_011521684 ⟹ XP_011519986

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,072,562 - 80,138,393 (+)	NCBI

Sequence:

show sequence

ACAGCTTCAAGTGAAGTTAATCTGAGGTGAAGCAAACAGAAAATTGTGGAGGTTTTGTTGGTGG
AGATAAGTAATTAACATTTCGAAACAGGAAATGAAAGGATTTATATTTTTAAAAGCTATAGGAA
TGAATCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTTAAAATGTTTTCTTGCATAAAATTCA
AAACTTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAGAAAGCTAATGTCTGTCTCAAGATAC
AGGACAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCAACTGAGGAACATGGCTCAAGAAACT
AATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAA
ATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAAT
AAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGC
AGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTAT
CAAATCAGTCACTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAA
AGCAGTACCTGAAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAA
GAGCAAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGA
AAGTGGGACTTACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTC
AGATGTACACAATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAAT
CCAGTAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAG
CATCTGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGT
GTATCTTGCATGTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAA
CATTTATTTCCATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTA
AGATCATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGG
GCTGTGATTTTTCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTA
TGTATATATCGCTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTA
GTTATCAGTAACTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTT
ATTCATATGTTAGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGA
GAGTGTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAA
AGCTGTATGCATTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTA
TACAATATGAAGAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATT
AAATAAAAAGGAAAACCAGAATGC

hide sequence

RefSeq Acc Id:

XM_024449956 ⟹ XP_024305724

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,922 - 80,138,393 (+)	NCBI

Sequence:

show sequence

GCCCGAGAGCCGGAAGCGGAGGGCGGCCGGCCGGCGCAGCAGGAATGAATCTGAAGTCTGCTGC
AGTAAAACACAGAAGGCTTTAAAATGTTTTCTTGCATAAAATTCAAAACTTTTAAGTAGCTGCT
TATGAGAATAGGGAAGGCAGAAAGCTAATGTCTGTCTCAAGATACAGGACAGCTGTTTGCTCAT
CAACCTCAACTGTGTGTGCAACTGAGGAACATGGCTCAAGAAACTAATCACAGCCAAGTGCCTA
TGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCTCGTACAAATGGCATGTGTTCAGTATG
CTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATGGTAGAATAAGCCCACCTGCAACCTCT
GTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCACAGATGGCAGTGTGCCAGAAGCCCAGT
CAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGCCCTGTATCAAATCAGTCACTTTTATC
AGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTGTGGACAAAGCAGTACCTGAAACAGAA
GATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCCATCTGAAGAGCAAAGCAAGTCTCTTG
AAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTTACTGGGTT
TGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACCGTTACTCAGATGTACACAATTGCTCT
TACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTTGGTGAAA
AGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAATTCTTGAGCATCTGCAAACTAAAAATT
GACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATGTCATCGG
AAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGACTCTGAACATTTATTTCCATTGCAAT
TTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTATCCTTTTAAGATCATTTTAATTTTAGT
TGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTTCCAGTAT
TAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCATTGTGTATGTATATATCGCTTTTCTC
TGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGCACAACTAGTTATCAGTAACTGAATGT
ATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAACAAAGGTTATTCATATGTTAGCATATA
GTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTGATGAGAT
TGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCATTTCATTG
CTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTTGTGTGTATACAATATGAAGAATGATC
TGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGAAAACCAG
AATGC

hide sequence

RefSeq Acc Id:

XM_024449959 ⟹ XP_024305727

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,922 - 80,138,393 (+)	NCBI

Sequence:

show sequence

GCGGCCGGCCGGCGCAGCAGGTGGAGATAAGTAATTAACATTTCGAAACAGGAAATGAAAGGAT
TTATATTTTTAAAAGCTATAGGAATGAATCTGAAGTCTGCTGCAGTAAAACACAGAAGGCTTTA
AAATGTTTTCTTGCATAAAATTCAAAACTTTTAAGTAGCTGCTTATGAGAATAGGGAAGGCAGA
AAGCTAATGTCTGTCTCAAGATACAGGACAGCTGTTTGCTCATCAACCTCAACTGTGTGTGCAA
CTGAGGAACATGGCTCAAGAAACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTG
GATTTTATGGAAACCCTCGTACAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAG
ACAGAATAGTAGTAATGGTAGAATAAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCT
TTACCAGTTCAATGCACAGATGGCAGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTT
CATCTATGCAGCCCAGCCCTGTATCAAATCAGTCACTTTTATCAGAATCTGTAGCATCTTCTCA
ATTGGACAGTACATCTGTGGACAAAGCAGTACCTGAAACAGAAGATGTGCAGGCTTCAGTATCA
GACACAGCACAGCAGCCATCTGAAGAGCAAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAGA
ATCGCTGTTTCATGTGCAGGAAGAAAGTGGGACTTACTGGGTTTGAATGCCGGTGTGGAAATGT
TTACTGTGGTGTACACCGTTACTCAGATGTACACAATTGCTCTTACAATTACAAAGCCGATGCT
GCTGAGAAAATCAGAAAAGAAAATCCAGTAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACTC
CTGCTGGAATACAAAATTCTTGAGCATCTGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTCC
TAGTCATTGGGAATGTAGAGCAGTGTATCTTGCATGTCATCGGAAGAATAGATTTTTGTTTTGG
TTTTGTTTTGAAAATGACTCTGAACATTTATTTCCATTGCAATTTCTGTGGCTGAGGAGACTTA
AACTTTACAAGTATTATCCTTTTAAGATCATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTATA
ACAAACGTGCAGAAATTTTGGAGGGCTGTGATTTTTCCAGTATTAAACATGCATGCATTAATCT
TGCAGTTTATTTTCTCATTGTGTATGTATATATCGCTTTTCTCTGCAGCACGATTTCTCTTTTG
ATAATGCCCTTTAGGGCACAACTAGTTATCAGTAACTGAATGTATCTTAATCATTATGGCTGCT
TCTGTTTTTTCATTAACAAAGGTTATTCATATGTTAGCATATAGTTTCTTTGCACCCACTATTT
ATGTCTGAATCATTTGTCACAAGAGAGTGTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAAC
TTTTTTTTGAGCGAGGGAAGAAAAAGCTGTATGCATTTCATTGCTGTCTACAGGTTTCTTTCAG
ATTATGTTCATGGGTTTGTGTGTATACAATATGAAGAATGATCTGAAGTAATTGTGCTGTATTT
ATGTTTATTCACCAGTCTTTGATTAAATAAAAAGGAAAACCAGAATGC

hide sequence

RefSeq Acc Id:

XM_024449963 ⟹ XP_024305731

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,922 - 80,138,393 (+)	NCBI

Sequence:

show sequence

CGAGAGCCGGAAGCGGAGGGCGGCCGGCCGGCGCAGCAGGTGTGCAACTGAGGAACATGGCTCA
AGAAACTAATCACAGCCAAGTGCCTATGCTTTGTTCCACTGGCTGTGGATTTTATGGAAACCCT
CGTACAAATGGCATGTGTTCAGTATGCTATAAAGAACATCTTCAAAGACAGAATAGTAGTAATG
GTAGAATAAGCCCACCTGCAACCTCTGTCAGTAGTCTGTCTGAATCTTTACCAGTTCAATGCAC
AGATGGCAGTGTGCCAGAAGCCCAGTCAGCATTAGACTCTACATCTTCATCTATGCAGCCCAGC
CCTGTATCAAATCAGTCACTTTTATCAGAATCTGTAGCATCTTCTCAATTGGACAGTACATCTG
TGGACAAAGCAGTACCTGAAACAGAAGATGTGCAGGCTTCAGTATCAGACACAGCACAGCAGCC
ATCTGAAGAGCAAAGCAAGTCTCTTGAAAAACCGAAACAAAAAAAGAATCGCTGTTTCATGTGC
AGGAAGAAAGTGGGACTTACTGGGTTTGAATGCCGGTGTGGAAATGTTTACTGTGGTGTACACC
GTTACTCAGATGTACACAATTGCTCTTACAATTACAAAGCCGATGCTGCTGAGAAAATCAGAAA
AGAAAATCCAGTAGTTGTTGGTGAAAAGATCCAAAAGATTTGAACTCCTGCTGGAATACAAAAT
TCTTGAGCATCTGCAAACTAAAAATTGACTTGAGGTTTTTTTTTTCCTAGTCATTGGGAATGTA
GAGCAGTGTATCTTGCATGTCATCGGAAGAATAGATTTTTGTTTTGGTTTTGTTTTGAAAATGA
CTCTGAACATTTATTTCCATTGCAATTTCTGTGGCTGAGGAGACTTAAACTTTACAAGTATTAT
CCTTTTAAGATCATTTTAATTTTAGTTGAGTGCAGAGGGCTTTTATAACAAACGTGCAGAAATT
TTGGAGGGCTGTGATTTTTCCAGTATTAAACATGCATGCATTAATCTTGCAGTTTATTTTCTCA
TTGTGTATGTATATATCGCTTTTCTCTGCAGCACGATTTCTCTTTTGATAATGCCCTTTAGGGC
ACAACTAGTTATCAGTAACTGAATGTATCTTAATCATTATGGCTGCTTCTGTTTTTTCATTAAC
AAAGGTTATTCATATGTTAGCATATAGTTTCTTTGCACCCACTATTTATGTCTGAATCATTTGT
CACAAGAGAGTGTGTGCTGATGAGATTGTAAGTTTGTGTGTTTAAACTTTTTTTTGAGCGAGGG
AAGAAAAAGCTGTATGCATTTCATTGCTGTCTACAGGTTTCTTTCAGATTATGTTCATGGGTTT
GTGTGTATACAATATGAAGAATGATCTGAAGTAATTGTGCTGTATTTATGTTTATTCACCAGTC
TTTGATTAAATAAAAAGGAAAACCAGAATGC

hide sequence

RefSeq Acc Id:

XM_047432694 ⟹ XP_047288650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,111,538 - 80,138,393 (+)	NCBI

RefSeq Acc Id:

XM_047432695 ⟹ XP_047288651

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,072,562 - 80,138,393 (+)	NCBI

RefSeq Acc Id:

XM_047432696 ⟹ XP_047288652

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,060,119 - 80,138,393 (+)	NCBI

RefSeq Acc Id:

XM_047432697 ⟹ XP_047288653

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,058,951 - 80,138,393 (+)	NCBI

RefSeq Acc Id:

XM_054378222 ⟹ XP_054234197

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	15	77,974,953 - 78,001,808 (+)	NCBI

RefSeq Acc Id:

XM_054378223 ⟹ XP_054234198

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	15	77,923,331 - 78,001,808 (+)	NCBI

RefSeq Acc Id:

XM_054378224 ⟹ XP_054234199

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	15	77,935,979 - 78,001,808 (+)	NCBI

RefSeq Acc Id:

XM_054378225 ⟹ XP_054234200

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	15	77,935,979 - 78,001,808 (+)	NCBI

RefSeq Acc Id:

XM_054378226 ⟹ XP_054234201

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	15	77,923,535 - 78,001,808 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001229840	(Get FASTA)	NCBI Sequence Viewer
	NP_001229841	(Get FASTA)	NCBI Sequence Viewer
	NP_001229842	(Get FASTA)	NCBI Sequence Viewer
	NP_001229843	(Get FASTA)	NCBI Sequence Viewer
	NP_001229844	(Get FASTA)	NCBI Sequence Viewer
	NP_001229845	(Get FASTA)	NCBI Sequence Viewer
	NP_001229846	(Get FASTA)	NCBI Sequence Viewer
	NP_001229847	(Get FASTA)	NCBI Sequence Viewer
	NP_001229848	(Get FASTA)	NCBI Sequence Viewer
	NP_061879	(Get FASTA)	NCBI Sequence Viewer
	XP_011519986	(Get FASTA)	NCBI Sequence Viewer
	XP_024305724	(Get FASTA)	NCBI Sequence Viewer
	XP_024305727	(Get FASTA)	NCBI Sequence Viewer
	XP_024305731	(Get FASTA)	NCBI Sequence Viewer
	XP_047288650	(Get FASTA)	NCBI Sequence Viewer
	XP_047288651	(Get FASTA)	NCBI Sequence Viewer
	XP_047288652	(Get FASTA)	NCBI Sequence Viewer
	XP_047288653	(Get FASTA)	NCBI Sequence Viewer
	XP_054234197	(Get FASTA)	NCBI Sequence Viewer
	XP_054234198	(Get FASTA)	NCBI Sequence Viewer
	XP_054234199	(Get FASTA)	NCBI Sequence Viewer
	XP_054234200	(Get FASTA)	NCBI Sequence Viewer
	XP_054234201	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD17528	(Get FASTA)	NCBI Sequence Viewer
	AAG44674	(Get FASTA)	NCBI Sequence Viewer
	AAH05283	(Get FASTA)	NCBI Sequence Viewer
	BAG35530	(Get FASTA)	NCBI Sequence Viewer
	CAB66533	(Get FASTA)	NCBI Sequence Viewer
	CAC14876	(Get FASTA)	NCBI Sequence Viewer
	CAG38507	(Get FASTA)	NCBI Sequence Viewer
	EAW99122	(Get FASTA)	NCBI Sequence Viewer
	EAW99123	(Get FASTA)	NCBI Sequence Viewer
	EAW99124	(Get FASTA)	NCBI Sequence Viewer
	EAW99125	(Get FASTA)	NCBI Sequence Viewer
	EAW99126	(Get FASTA)	NCBI Sequence Viewer
	EAW99127	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000261749
	ENSP00000261749.6
	ENSP00000452625.1
	ENSP00000452664.1
	ENSP00000452735.1
	ENSP00000453291
	ENSP00000453291.1
	ENSP00000453308.1
	ENSP00000453571.1
	ENSP00000453590.1
	ENSP00000453709
	ENSP00000453709.1
	ENSP00000453710.1
	ENSP00000453888.1
	ENSP00000454137
	ENSP00000454137.1
	ENSP00000454152
	ENSP00000454152.1
	ENSP00000454273
	ENSP00000454273.1
	ENSP00000454409.1
	ENSP00000455146.1
	ENSP00000455515.1
	ENSP00000456973.1
	ENSP00000478129
	ENSP00000478129.1
	ENSP00000479071
	ENSP00000479071.1
	ENSP00000484971
	ENSP00000484971.1
GenBank Protein	Q6FIF0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_061879 ⟸ NM_019006
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229841 ⟸ NM_001242912
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229846 ⟸ NM_001242917
- Peptide Label:	isoform b
- UniProtKB:	B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPVQCTDGSVPEAQS ALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTAQQPSEEQSKSLE KPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEKIRKENPVVVGEK IQKI hide sequence

RefSeq Acc Id:	NP_001229840 ⟸ NM_001242911
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229847 ⟸ NM_001242918
- Peptide Label:	isoform c
- UniProtKB:	H3BM82 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQGFECRCG NVYCGVHRYSDVHNCSYNYKADAAEKIRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229842 ⟸ NM_001242913
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229843 ⟸ NM_001242914
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229845 ⟸ NM_001242916
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229844 ⟸ NM_001242915
- Peptide Label:	isoform a
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	NP_001229848 ⟸ NM_001242919
- Peptide Label:	isoform d
- UniProtKB:	B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSVDKAVPETEDVQASVSDTAQQPSEEQSKSLEKPKQKKNRCFMCRKK VGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEKIRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	XP_011519986 ⟸ XM_011521684
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	XP_024305724 ⟸ XM_024449956
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	XP_024305731 ⟸ XM_024449963
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

RefSeq Acc Id:	XP_024305727 ⟸ XM_024449959
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot), B2R6N3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQETNHSQVPMLCSTGCGFYGNPRTNGMCSVCYKEHLQRQNSSNGRISPPATSVSSLSESLPV QCTDGSVPEAQSALDSTSSSMQPSPVSNQSLLSESVASSQLDSTSVDKAVPETEDVQASVSDTA QQPSEEQSKSLEKPKQKKNRCFMCRKKVGLTGFECRCGNVYCGVHRYSDVHNCSYNYKADAAEK IRKENPVVVGEKIQKI hide sequence

Ensembl Acc Id:

ENSP00000456973 ⟸ ENST00000558272

Ensembl Acc Id:

ENSP00000453888 ⟸ ENST00000558087

Ensembl Acc Id:

ENSP00000452664 ⟸ ENST00000558688

Ensembl Acc Id:

ENSP00000454137 ⟸ ENST00000558494

Ensembl Acc Id:

ENSP00000453308 ⟸ ENST00000558390

Ensembl Acc Id:

ENSP00000453571 ⟸ ENST00000558997

Ensembl Acc Id:

ENSP00000452625 ⟸ ENST00000558724

Ensembl Acc Id:

ENSP00000453291 ⟸ ENST00000559835

Ensembl Acc Id:

ENSP00000453709 ⟸ ENST00000559775

Ensembl Acc Id:

ENSP00000454152 ⟸ ENST00000559157

Ensembl Acc Id:

ENSP00000479071 ⟸ ENST00000613266

Ensembl Acc Id:

ENSP00000455515 ⟸ ENST00000560470

Ensembl Acc Id:

ENSP00000455146 ⟸ ENST00000560392

Ensembl Acc Id:

ENSP00000454409 ⟸ ENST00000560228

Ensembl Acc Id:

ENSP00000453710 ⟸ ENST00000560976

Ensembl Acc Id:

ENSP00000453590 ⟸ ENST00000561012

Ensembl Acc Id:

ENSP00000452735 ⟸ ENST00000561060

Ensembl Acc Id:

ENSP00000478129 ⟸ ENST00000616533

Ensembl Acc Id:

ENSP00000454273 ⟸ ENST00000564367

Ensembl Acc Id:

ENSP00000484971 ⟸ ENST00000618205

Ensembl Acc Id:

ENSP00000261749 ⟸ ENST00000261749

RefSeq Acc Id:	XP_047288653 ⟸ XM_047432697
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047288652 ⟸ XM_047432696
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047288651 ⟸ XM_047432695
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047288650 ⟸ XM_047432694
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054234198 ⟸ XM_054378223
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054234201 ⟸ XM_054378226
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054234200 ⟸ XM_054378225
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054234199 ⟸ XM_054378224
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054234197 ⟸ XM_054378222
- Peptide Label:	isoform X1
- UniProtKB:	Q9BQF7 (UniProtKB/Swiss-Prot), Q6FIF0 (UniProtKB/Swiss-Prot), O95792 (UniProtKB/Swiss-Prot), D3DW94 (UniProtKB/Swiss-Prot), D3DW92 (UniProtKB/Swiss-Prot), Q9GZY3 (UniProtKB/Swiss-Prot)

Protein Domains

A20-type AN1-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6FIF0-F1-model_v2	AlphaFold	Q6FIF0	1-208	view protein structure

Promoters

RGD ID:

6792721

Promoter ID:

HG_KWN:22079

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:

OTTHUMT00000291368, UC002BFF.1, UC002BFG.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	15	78,138,751 - 78,139,367 (+)	MPROMDB

RGD ID:

6792722

Promoter ID:

HG_KWN:22080

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3, Lymphoblastoid, NB4

Transcripts:

UC002BFH.1, UC002BFI.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	15	78,151,741 - 78,152,241 (+)	MPROMDB

RGD ID:

7230283

Promoter ID:

EPDNEW_H20887

Type:

initiation region

Name:

ZFAND6_1

Description:

zinc finger AN1-type containing 6

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H20889

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,059,676 - 80,059,736	EPDNEW

RGD ID:

7230287

Promoter ID:

EPDNEW_H20889

Type:

initiation region

Name:

ZFAND6_2

Description:

zinc finger AN1-type containing 6

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H20887

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	80,072,596 - 80,072,656	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:30164	AgrOrtholog
COSMIC	ZFAND6	COSMIC
Ensembl Genes	ENSG00000086666	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000261749	ENTREZGENE
	ENST00000261749.11	UniProtKB/Swiss-Prot
	ENST00000558087.5	UniProtKB/Swiss-Prot
	ENST00000558272.5	UniProtKB/TrEMBL
	ENST00000558390.5	UniProtKB/TrEMBL
	ENST00000558494	ENTREZGENE
	ENST00000558494.5	UniProtKB/Swiss-Prot
	ENST00000558688.5	UniProtKB/TrEMBL
	ENST00000558724.1	UniProtKB/TrEMBL
	ENST00000558997.5	UniProtKB/TrEMBL
	ENST00000559157	ENTREZGENE
	ENST00000559157.5	UniProtKB/Swiss-Prot
	ENST00000559775	ENTREZGENE
	ENST00000559775.5	UniProtKB/Swiss-Prot
	ENST00000559835	ENTREZGENE
	ENST00000559835.5	UniProtKB/Swiss-Prot
	ENST00000560228.5	UniProtKB/TrEMBL
	ENST00000560392.5	UniProtKB/TrEMBL
	ENST00000560470.5	UniProtKB/TrEMBL
	ENST00000560976.5	UniProtKB/TrEMBL
	ENST00000561012.5	UniProtKB/TrEMBL
	ENST00000561060.5	UniProtKB/Swiss-Prot
	ENST00000564367	ENTREZGENE
	ENST00000564367.5	UniProtKB/TrEMBL
	ENST00000613266	ENTREZGENE
	ENST00000613266.4	UniProtKB/Swiss-Prot
	ENST00000616533	ENTREZGENE
	ENST00000616533.4	UniProtKB/Swiss-Prot
	ENST00000618205	ENTREZGENE
	ENST00000618205.4	UniProtKB/Swiss-Prot
Gene3D-CATH	1.20.5.4770	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	4.10.1110.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000086666	GTEx
HGNC ID	HGNC:30164	ENTREZGENE
Human Proteome Map	ZFAND6	Human Proteome Map
InterPro	AN1-like_Znf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	AN1_A20_ZnFinger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_A20	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_AN1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:54469	UniProtKB/Swiss-Prot
NCBI Gene	54469	ENTREZGENE
OMIM	610183	OMIM
PANTHER	AN1-TYPE ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	AN1-TYPE ZINC FINGER PROTEIN 6	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	zf-A20	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	zf-AN1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134883256	PharmGKB
PROSITE	ZF_A20	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZF_AN1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	ZnF_A20	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_AN1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Glucocorticoid receptor-like (DNA-binding domain)	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF118310	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B2R6N3	ENTREZGENE, UniProtKB/TrEMBL
	D3DW92	ENTREZGENE
	D3DW94	ENTREZGENE
	H0YK21_HUMAN	UniProtKB/TrEMBL
	H0YK54_HUMAN	UniProtKB/TrEMBL
	H0YLR2_HUMAN	UniProtKB/TrEMBL
	H0YME2_HUMAN	UniProtKB/TrEMBL
	H0YMG0_HUMAN	UniProtKB/TrEMBL
	H0YMR5_HUMAN	UniProtKB/TrEMBL
	H3BM82	ENTREZGENE, UniProtKB/TrEMBL
	H3BMJ5_HUMAN	UniProtKB/TrEMBL
	H3BP46_HUMAN	UniProtKB/TrEMBL
	H3BPX9_HUMAN	UniProtKB/TrEMBL
	H3BT16_HUMAN	UniProtKB/TrEMBL
	O95792	ENTREZGENE
	Q6FIF0	ENTREZGENE
	Q9BQF7	ENTREZGENE
	Q9GZY3	ENTREZGENE
	ZFAN6_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	D3DW92	UniProtKB/Swiss-Prot
	D3DW94	UniProtKB/Swiss-Prot
	O95792	UniProtKB/Swiss-Prot
	Q9BQF7	UniProtKB/Swiss-Prot
	Q9GZY3	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-02-16	ZFAND6	zinc finger AN1-type containing 6		zinc finger, AN1-type domain 6	Symbol and/or name change	5135510	APPROVED

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

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

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

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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Imported Disease Annotations - CTD

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD