SLC39A1 (solute carrier family 39 member 1)

Gene: SLC39A1 (solute carrier family 39 member 1) Homo sapiens

Analyze

Symbol:

SLC39A1

Name:

solute carrier family 39 member 1

RGD ID:

1313154

HGNC Page

HGNC:12876

Description:

Enables zinc ion transmembrane transporter activity. Involved in zinc ion transmembrane transport. Located in plasma membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

hZIP1; solute carrier family 39 (zinc transporter), member 1; solute carrier family 39 (zinc transporter), member 3; zinc transporter 1; zinc transporter ZIP1; zinc-iron regulated transporter-like; zinc-iron-regulated transporter-like; zinc/iron regulated transporter-like; ZIP-1; ZIP1; ZIRTL; zrt- and Irt-like protein 1; ZRT/IRT-like protein 1

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):	Slc39a1 (solute carrier family 39 (zinc transporter), member 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Slc39a1 (solute carrier family 39 member 1)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Slc39a1 (solute carrier family 39 member 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	SLC39A1 (solute carrier family 39 member 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	SLC39A1 (solute carrier family 39 member 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Slc39a1 (solute carrier family 39 member 1)	NCBI	Ortholog
Sus scrofa (pig):	SLC39A1 (solute carrier family 39 member 1)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	SLC39A1 (solute carrier family 39 member 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Slc39a1 (solute carrier family 39 member 1)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Slc39a1 (solute carrier family 39 member 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Slc39a1 (solute carrier family 39 (zinc transporter), member 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	slc39a3 (solute carrier family 39 member 3)	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Danio rerio (zebrafish):	slc39a1 (solute carrier family 39 member 1)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoInspector\|SonicParanoid\|ZFIN)
Saccharomyces cerevisiae (baker's yeast):	ZRT1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid)
Drosophila melanogaster (fruit fly):	Zip42C.1	Alliance	DIOPT (InParanoid\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Zip42C.2	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Zip88E	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER)
Caenorhabditis elegans (roundworm):	zipt-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Caenorhabditis elegans (roundworm):	zipt-2.3	Alliance	DIOPT (OMA\|OrthoInspector\|PANTHER)
Saccharomyces cerevisiae (baker's yeast):	ZRT2	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid)
Caenorhabditis elegans (roundworm):	zipt-2.1	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoInspector\|PANTHER)
Caenorhabditis elegans (roundworm):	zipt-2.2	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoInspector\|PANTHER)
Xenopus laevis (African clawed frog):	slc39a1.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	slc39a1	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)

Related Pseudogenes:

SLC39A1P1

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	1	153,959,110 - 153,968,184 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	153,959,099 - 153,968,184 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	153,931,586 - 153,940,660 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	152,198,212 - 152,206,812 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	1	150,744,661 - 150,753,261	NCBI
Celera	1	127,003,339 - 127,011,938 (-)	NCBI		Celera
Cytogenetic Map	1	q21.3	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI		HuRef
CHM1_1	1	155,327,888 - 155,336,973 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	1	153,096,371 - 153,105,445 (-)	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

GAND syndrome (IAGP)

gastrointestinal stromal tumor (IAGP)

immunodeficiency 42 (IAGP)

MHC class II deficiency (IAGP)

parathyroid carcinoma (IAGP)

Prostatic Neoplasms (EXP)

respiratory allergy (EXP)

severe congenital neutropenia 3 (IAGP)

severe congenital neutropenia 5 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-epigallocatechin 3-gallate (EXP)

2,3',4,4',5-Pentachlorobiphenyl (ISO)

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

3,4-methylenedioxymethamphetamine (ISO)

4,4'-diaminodiphenylmethane (ISO)

4,4'-sulfonyldiphenol (ISO)

aflatoxin B1 (EXP)

aldosterone (ISO)

all-trans-retinoic acid (EXP)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

bisphenol F (ISO)

C60 fullerene (ISO)

cadmium atom (EXP)

cadmium dichloride (EXP,ISO)

calcitriol (EXP)

carbon nanotube (ISO)

chlorpyrifos (ISO)

cisplatin (EXP)

clobetasol (ISO)

cobalt dichloride (EXP,ISO)

dexamethasone (ISO)

diallyl trisulfide (EXP)

diuron (ISO)

elemental selenium (EXP)

epoxiconazole (ISO)

ethanol (ISO)

flavonoids (ISO)

iron dichloride (ISO)

N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (EXP)

nickel dichloride (ISO)

nickel subsulfide (ISO)

ochratoxin A (EXP)

oxaliplatin (ISO)

paracetamol (ISO)

selenium atom (EXP)

Soman (ISO)

spironolactone (ISO)

tetrachloromethane (ISO)

titanium dioxide (ISO)

topotecan (ISO)

vanadium atom (EXP)

vanadium(0) (EXP)

vitamin E (EXP)

zinc atom (EXP,ISO)

zinc dichloride (EXP)

zinc sulfate (EXP)

zinc(0) (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

embryonic cranial skeleton morphogenesis (IEA,ISO)

in utero embryonic development (IEA,ISO)

limb development (IEA,ISO)

metal ion transport (IEA)

monoatomic cation transport (TAS)

transmembrane transport (IEA)

zinc ion transmembrane transport (IBA,IDA,IEA,IMP,TAS)

zinc ion transport (IEA,ISO)

Cellular Component

endoplasmic reticulum (IEA)

endoplasmic reticulum membrane (IEA)

membrane (IEA,TAS)

plasma membrane (IBA,IDA,IEA,TAS)

Molecular Function

inorganic cation transmembrane transporter activity (TAS)

metal ion transmembrane transporter activity (IEA)

protein binding (IPI)

signaling receptor binding (IEA,ISO)

zinc ion transmembrane transporter activity (IBA,IDA,IEA,TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Gastrointestinal stroma tumor (IAGP)

Parathyroid carcinoma (IAGP)

References

References - curated

#	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

Additional References at PubMed

PMID:10477520	PMID:10610721	PMID:10681536	PMID:10810093	PMID:11301334	PMID:11696349	PMID:12477932	PMID:12888280	PMID:14525987	PMID:14702039	PMID:15489334	PMID:16153295
PMID:16169070	PMID:16203195	PMID:16303743	PMID:16344560	PMID:17635580	PMID:18279033	PMID:18765529	PMID:19026724	PMID:19644445	PMID:19802870	PMID:20471814	PMID:20705137
PMID:21053094	PMID:21103883	PMID:21360563	PMID:21873635	PMID:21988832	PMID:22349685	PMID:22658674	PMID:22903471	PMID:23839533	PMID:23921484	PMID:24488210	PMID:24878177
PMID:24922175	PMID:25356737	PMID:26081940	PMID:26186194	PMID:26760575	PMID:28298427	PMID:28514442	PMID:30581142	PMID:32296183	PMID:32513696	PMID:32814053	PMID:33144569
PMID:33961781	PMID:34615436	PMID:35696571	PMID:36057605

Genomics

Comparative Map Data

SLC39A1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	1	153,959,110 - 153,968,184 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	153,959,099 - 153,968,184 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	153,931,586 - 153,940,660 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	152,198,212 - 152,206,812 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	1	150,744,661 - 150,753,261	NCBI
Celera	1	127,003,339 - 127,011,938 (-)	NCBI		Celera
Cytogenetic Map	1	q21.3	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI		HuRef
CHM1_1	1	155,327,888 - 155,336,973 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	1	153,096,371 - 153,105,445 (-)	NCBI		T2T-CHM13v2.0

Slc39a1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	3	90,155,512 - 90,160,923 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	3	90,155,479 - 90,160,919 (+)	Ensembl		GRCm39 Ensembl
GRCm38	3	90,248,190 - 90,253,613 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	3	90,248,172 - 90,253,612 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	3	90,052,114 - 90,057,534 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	3	90,334,157 - 90,339,539 (+)	NCBI		MGSCv36	mm8
MGSCv36	3	91,093,484 - 91,099,116 (+)	NCBI		MGSCv36	mm8
Celera	3	90,285,048 - 90,290,812 (+)	NCBI		Celera
Cytogenetic Map	3	F1	NCBI
cM Map	3	39.21	NCBI

Slc39a1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	2	178,001,052 - 178,006,689 (+)	NCBI		GRCr8
mRatBN7.2	2	175,703,413 - 175,709,063 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	2	175,703,441 - 175,709,058 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	2	182,843,537 - 182,849,109 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	2	180,865,926 - 180,871,499 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	2	175,466,212 - 175,471,775 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	2	189,609,766 - 189,615,367 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	2	189,609,800 - 189,615,366 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	2	209,042,625 - 209,048,222 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	2	182,490,501 - 182,496,068 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	2	182,440,596 - 182,445,640 (+)	NCBI
Celera	2	169,638,848 - 169,644,414 (+)	NCBI		Celera
Cytogenetic Map	2	q34	NCBI

Slc39a1
(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_004955545	554,947 - 560,336 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955545	556,210 - 559,732 (-)	NCBI	ChiLan1.0	ChiLan1.0

SLC39A1
(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	1	95,864,490 - 95,884,853 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	1	95,599,943 - 95,620,090 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	1	129,304,237 - 129,315,484 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	1	132,932,926 - 132,943,891 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	1	132,944,346 - 132,952,951 (-)	Ensembl	panpan1.1		panPan2
PanPan1.1 Ensembl	1	132,932,926 - 132,943,891 (-)	Ensembl	panpan1.1		panPan2

SLC39A1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	7	43,171,219 - 43,174,876 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	7	43,171,287 - 43,174,036 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	7	42,661,635 - 42,665,278 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	7	43,041,658 - 43,045,302 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	7	43,041,740 - 43,045,301 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	7	42,820,327 - 42,823,971 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	7	42,873,597 - 42,877,237 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	7	43,157,835 - 43,161,479 (+)	NCBI		UU_Cfam_GSD_1.0

Slc39a1
(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_024405058	24,674,699 - 24,678,289 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936580	3,704,723 - 3,708,677 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936580	3,704,738 - 3,708,671 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SLC39A1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	4	95,729,347 - 95,733,819 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	4	95,729,480 - 95,733,824 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	4	104,630,406 - 104,635,131 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SLC39A1
(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	20	9,847,928 - 9,852,998 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	20	9,847,968 - 9,853,413 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	9,218,019 - 9,223,131 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Slc39a1
(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_004624885	3,260,681 - 3,264,959 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624885	3,260,673 - 3,264,636 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in SLC39A1
16 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 1q21.3(chr1:153699434-153981614)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053212]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053212]\|See cases [RCV000053212]	Chr1:153699434..153981614 [GRCh38] Chr1:153671910..153954090 [GRCh37] Chr1:151938534..152220714 [NCBI36] Chr1:1q21.3	uncertain significance
GRCh38/hg38 1q21.3(chr1:153759563-154219803)x1	copy number loss	See cases [RCV000053883]	Chr1:153759563..154219803 [GRCh38] Chr1:153732039..154192279 [GRCh37] Chr1:151998663..152458903 [NCBI36] Chr1:1q21.3	pathogenic
GRCh38/hg38 1q21.3(chr1:153939571-153978276)x1	copy number loss	See cases [RCV000053884]	Chr1:153939571..153978276 [GRCh38] Chr1:153912047..153950752 [GRCh37] Chr1:152178671..152217376 [NCBI36] Chr1:1q21.3	pathogenic
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3	copy number gain	See cases [RCV000143515]	Chr1:149854269..180267197 [GRCh38] Chr1:149825831..180236332 [GRCh37] Chr1:148092455..178502955 [NCBI36] Chr1:1q21.2-25.2	pathogenic
Single allele	deletion	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome [RCV000677922]	Chr1:153887335..154062496 [GRCh38] Chr1:153859810..154034971 [GRCh37] Chr1:1q21.3	likely pathogenic
GRCh37/hg19 1q21.3-23.1(chr1:153751465-156660462)x3	copy number gain	not provided [RCV000585385]	Chr1:153751465..156660462 [GRCh37] Chr1:1q21.3-23.1	likely pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	copy number gain	See cases [RCV000510383]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	copy number gain	See cases [RCV000510926]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1q21.3(chr1:150853044-154647786)x3	copy number gain	not provided [RCV000684655]	Chr1:150853044..154647786 [GRCh37] Chr1:1q21.3	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3	copy number gain	not provided [RCV000736295]	Chr1:47851..249228449 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3	copy number gain	not provided [RCV000736305]	Chr1:82154..249218992 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1q21.3(chr1:153701504-154218584)	copy number loss	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome [RCV000767778]	Chr1:153701504..154218584 [GRCh37] Chr1:1q21.3	pathogenic
GRCh37/hg19 1q21.3(chr1:153659094-154307972)x3	copy number gain	not provided [RCV001005142]	Chr1:153659094..154307972 [GRCh37] Chr1:1q21.3	uncertain significance
NC_000001.10:g.(?_130980840)_(248900000_?)dup	duplication	Gastrointestinal stromal tumor [RCV001300221]\|Parathyroid carcinoma [RCV001341077]	Chr1:130980840..248900000 [GRCh37] Chr1:1q12-44	uncertain significance
GRCh37/hg19 1q21.3(chr1:153866956-154000766)x1	copy number loss	not provided [RCV001258472]	Chr1:153866956..154000766 [GRCh37] Chr1:1q21.3	uncertain significance
NC_000001.10:g.(?_149895434)_(156851434_?)dup	duplication	Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency [RCV001958273]\|Congenital neutropenia-myelofibrosis-nephromegaly syndrome [RCV001958271]\|Kostmann syndrome [RCV003120769]\|MHC class II deficiency [RCV001992607]	Chr1:149895434..156851434 [GRCh37] Chr1:1q21.2-23.1	uncertain significance
NC_000001.10:g.(?_153782653)_(153964569_?)del	deletion	not provided [RCV003109731]	Chr1:153782653..153964569 [GRCh37] Chr1:1q21.3	pathogenic
NM_001271958.2(SLC39A1):c.541T>C (p.Cys181Arg)	single nucleotide variant	not specified [RCV004164265]	Chr1:153960532 [GRCh38] Chr1:153933008 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.893G>C (p.Ser298Thr)	single nucleotide variant	not specified [RCV004105640]	Chr1:153960180 [GRCh38] Chr1:153932656 [GRCh37] Chr1:1q21.3	likely benign
NM_001271958.2(SLC39A1):c.13G>A (p.Gly5Arg)	single nucleotide variant	not specified [RCV004104399]	Chr1:153962703 [GRCh38] Chr1:153935179 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.83A>G (p.Glu28Gly)	single nucleotide variant	not specified [RCV004124021]	Chr1:153962633 [GRCh38] Chr1:153935109 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.131G>A (p.Cys44Tyr)	single nucleotide variant	not specified [RCV004160763]	Chr1:153962585 [GRCh38] Chr1:153935061 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.715G>T (p.Val239Leu)	single nucleotide variant	not specified [RCV004123503]	Chr1:153960358 [GRCh38] Chr1:153932834 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.910C>T (p.Leu304Phe)	single nucleotide variant	not specified [RCV004137172]	Chr1:153960163 [GRCh38] Chr1:153932639 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.584G>A (p.Gly195Glu)	single nucleotide variant	not specified [RCV004249076]	Chr1:153960489 [GRCh38] Chr1:153932965 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.856A>C (p.Ile286Leu)	single nucleotide variant	not specified [RCV004308976]	Chr1:153960217 [GRCh38] Chr1:153932693 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.751C>T (p.Pro251Ser)	single nucleotide variant	not specified [RCV004271725]	Chr1:153960322 [GRCh38] Chr1:153932798 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.467C>T (p.Pro156Leu)	single nucleotide variant	not specified [RCV004256080]	Chr1:153960606 [GRCh38] Chr1:153933082 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.19C>T (p.Pro7Ser)	single nucleotide variant	not specified [RCV004276646]	Chr1:153962697 [GRCh38] Chr1:153935173 [GRCh37] Chr1:1q21.3	uncertain significance
GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3	copy number gain	Chromosome 1q21.1 duplication syndrome [RCV003329522]	Chr1:142535935..157648813 [GRCh37] Chr1:1q12-23.1	pathogenic
NM_001271958.2(SLC39A1):c.616C>T (p.Arg206Trp)	single nucleotide variant	not specified [RCV004351048]	Chr1:153960457 [GRCh38] Chr1:153932933 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.175C>T (p.His59Tyr)	single nucleotide variant	not specified [RCV004357330]	Chr1:153962541 [GRCh38] Chr1:153935017 [GRCh37] Chr1:1q21.3	uncertain significance
GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3	copy number gain	not specified [RCV003986717]	Chr1:144368497..158992086 [GRCh37] Chr1:1q21.1-23.1	pathogenic
GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3	copy number gain	not specified [RCV003987261]	Chr1:146577511..157155587 [GRCh37] Chr1:1q21.1-23.1	pathogenic
NM_001271958.2(SLC39A1):c.634C>A (p.Leu212Met)	single nucleotide variant	not specified [RCV004461494]	Chr1:153960439 [GRCh38] Chr1:153932915 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.170C>A (p.Ala57Asp)	single nucleotide variant	not specified [RCV004461492]	Chr1:153962546 [GRCh38] Chr1:153935022 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.793G>A (p.Gly265Arg)	single nucleotide variant	not specified [RCV004461495]	Chr1:153960280 [GRCh38] Chr1:153932756 [GRCh37] Chr1:1q21.3	uncertain significance
NM_001271958.2(SLC39A1):c.532T>A (p.Leu178Met)	single nucleotide variant	not specified [RCV004461493]	Chr1:153960541 [GRCh38] Chr1:153933017 [GRCh37] Chr1:1q21.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3596
Count of miRNA genes:	851
Interacting mature miRNAs:	1023
Transcripts:	ENST00000310483, ENST00000356205, ENST00000368621, ENST00000368623, ENST00000413622, ENST00000417348, ENST00000429040, ENST00000461071, ENST00000537590
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.

Markers in Region

RH186

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,931,606 - 153,931,745	UniSTS	GRCh37
Build 36	1	152,198,230 - 152,198,369	RGD	NCBI36
Celera	1	127,003,357 - 127,003,496	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,294,192 - 125,294,331	UniSTS
GeneMap99-GB4 RH Map	1	557.59	UniSTS
NCBI RH Map	1	1225.7	UniSTS

RH10553

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,931,642 - 153,931,834	UniSTS	GRCh37
Build 36	1	152,198,266 - 152,198,458	RGD	NCBI36
Celera	1	127,003,393 - 127,003,585	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,294,228 - 125,294,420	UniSTS

RH64708

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,932,566 - 153,932,651	UniSTS	GRCh37
Build 36	1	152,199,190 - 152,199,275	RGD	NCBI36
Celera	1	127,004,317 - 127,004,402	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,295,152 - 125,295,237	UniSTS

D1S2463

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,940,811 - 153,941,019	UniSTS	GRCh37
Build 36	1	152,207,435 - 152,207,643	RGD	NCBI36
Celera	1	127,012,561 - 127,012,769	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,303,397 - 125,303,605	UniSTS
Whitehead-RH Map	1	671.5	UniSTS
Whitehead-YAC Contig Map	1		UniSTS
NCBI RH Map	1	1294.3	UniSTS

PMC321570P9

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,932,574 - 153,933,152	UniSTS	GRCh37
Build 36	1	152,199,198 - 152,199,776	RGD	NCBI36
Celera	1	127,004,325 - 127,004,903	RGD
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,295,160 - 125,295,738	UniSTS

G19748

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,931,642 - 153,931,834	UniSTS	GRCh37
Build 36	1	152,198,266 - 152,198,458	RGD	NCBI36
Celera	1	127,003,393 - 127,003,585	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,294,228 - 125,294,420	UniSTS

RH16039

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,931,685 - 153,931,844	UniSTS	GRCh37
Build 36	1	152,198,309 - 152,198,468	RGD	NCBI36
Celera	1	127,003,436 - 127,003,595	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,294,271 - 125,294,430	UniSTS
GeneMap99-GB4 RH Map	1	557.59	UniSTS
NCBI RH Map	1	1222.2	UniSTS

WI-22571

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,939,116 - 153,939,292	UniSTS	GRCh37
Build 36	1	152,205,740 - 152,205,916	RGD	NCBI36
Celera	1	127,010,867 - 127,011,043	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,301,702 - 125,301,878	UniSTS
GeneMap99-GB4 RH Map	1	541.31	UniSTS
Whitehead-RH Map	1	673.1	UniSTS
NCBI RH Map	1	1114.2	UniSTS

D1S1830E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,931,677 - 153,931,783	UniSTS	GRCh37
Build 36	1	152,198,301 - 152,198,407	RGD	NCBI36
Celera	1	127,003,428 - 127,003,534	RGD
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	1	q21	UniSTS
HuRef	1	125,294,263 - 125,294,369	UniSTS
GeneMap99-GB4 RH Map	1	555.98	UniSTS
NCBI RH Map	1	1226.9	UniSTS

MARC_5745-5746:996690776:3

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	153,933,196 - 153,934,816	UniSTS	GRCh37
Build 36	1	152,199,820 - 152,201,440	RGD	NCBI36
Celera	1	127,004,947 - 127,006,567	RGD
HuRef	1	125,295,782 - 125,297,402	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

2431

2753

1696

596

1409

438

4335

2119

3293

398

1410

1604

171

1204

2768

Low

223

542

424

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001271957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001271958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001271959	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001271960	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001271961	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_014437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047418008	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054336011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF132942	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF151829	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ243649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ243650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ271671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK074943	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK075257	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293389	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297983	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300244	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL358472	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW571711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC002563	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC003152	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC007886	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC014303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047288	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG704399	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM807264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471121	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CQ783764	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR457217	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA052424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA354647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA711655	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA818910	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB001496	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY042960	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000310483 ⟹ ENSP00000309710

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,112 - 153,967,712 (-)	Ensembl

RefSeq Acc Id:

ENST00000356205 ⟹ ENSP00000348535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,110 - 153,963,537 (-)	Ensembl

RefSeq Acc Id:

ENST00000368621 ⟹ ENSP00000357610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,111 - 153,963,462 (-)	Ensembl

RefSeq Acc Id:

ENST00000368623 ⟹ ENSP00000357612

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,110 - 153,963,475 (-)	Ensembl

RefSeq Acc Id:

ENST00000413622 ⟹ ENSP00000392229

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,960,353 - 153,967,621 (-)	Ensembl

RefSeq Acc Id:

ENST00000417348 ⟹ ENSP00000407717

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,960,454 - 153,963,262 (-)	Ensembl

RefSeq Acc Id:

ENST00000429040 ⟹ ENSP00000392950

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,960,110 - 153,963,322 (-)	Ensembl

RefSeq Acc Id:

ENST00000461071

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,962,311 - 153,963,139 (-)	Ensembl

RefSeq Acc Id:

ENST00000537590 ⟹ ENSP00000443632

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,099 - 153,963,641 (-)	Ensembl

RefSeq Acc Id:

ENST00000617697 ⟹ ENSP00000479421

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,099 - 153,968,184 (-)	Ensembl

RefSeq Acc Id:

ENST00000621013 ⟹ ENSP00000484182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	153,959,099 - 153,963,492 (-)	Ensembl

RefSeq Acc Id:

NM_001271957 ⟹ NP_001258886

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,963,537 (-)	NCBI
GRCh37	1	153,931,575 - 153,940,660 (-)	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI
CHM1_1	1	155,327,888 - 155,332,157 (-)	NCBI
T2T-CHM13v2.0	1	153,096,371 - 153,100,798 (-)	NCBI

Sequence:

show sequence

AGGCCGGAAGCGCGCGGAGACCATGTAGTGAGACCCTCGCGAGGTGAGTGCGGGCTGTCTGGCA
GCGGGGTCCATGTCGGCTGCCCAGGCCTCCCCGGGCCCGGGAACAGGAGTCCCAGCTCACGCAT
TCTTCATCTGCTTCCCGCGACGCTTGGCGGCCTCGCACCCCGCCTCCTGGAGCCCGGACTTTCA
GGCACCGCCCTCAGTGTCGCCTCAGTCCGTCCCGGGACCGCAGACTCTTAGGGCCCCTCTCTTT
GGCCATCTGCCTCTAGGTCCCATCCTGGGGCCTGAAGCGCTTGTTCTCTGCGCTGGGAAAAGGG
GAACGATGGAGCGATCCAGCACCCAAACTTACCCTGTCCAGGTGGCCCACGAAGCTACCCAAGA
CATCTCTGCACAGCCCTAGCCTTTTTGGCTTCACCCACTCCGTTCGGGAGTTGGGGACCCGGCC
TCTACATTCCTTAGGGGAACTCCAGCTCCAGGTCTGAGAGTCACTGGAGCTACCAGAAGCATCA
TGGGGCCCTGGGGAGAGCCAGAGCTCCTGGTGTGGCGCCCCGAGGCGGTAGCTTCAGAGCCTCC
AGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGGTGCTCACCCTCCTC
TGCAGCCTGGTGCCCATCTGTGTGCTGCGCCGGCCAGGAGCTAACCATGAAGGCTCAGCTTCCC
GCCAGAAAGCCCTGAGCCTAGTAAGCTGTTTCGCGGGGGGCGTCTTTTTGGCCACTTGTCTCCT
GGACCTGCTGCCTGACTACCTGGCTGCCATAGATGAGGCCCTGGCAGCCTTGCACGTGACGCTC
CAGTTCCCACTGCAAGAGTTCATCCTGGCCATGGGCTTCTTCCTGGTCCTGGTGATGGAGCAGA
TCACACTGGCTTACAAGGAGCAGTCAGGGCCGTCACCTCTGGAGGAAACAAGGGCTCTGCTGGG
AACAGTGAATGGTGGGCCGCAGCATTGGCATGATGGGCCAGGGGTCCCACAGGCGAGTGGAGCC
CCAGCAACCCCCTCAGCCTTGCGTGCCTGTGTACTGGTGTTCTCCCTGGCCCTCCACTCCGTGT
TCGAGGGGCTGGCGGTAGGGCTGCAGCGAGACCGGGCTCGGGCCATGGAGCTGTGCCTGGCTTT
GCTGCTCCACAAGGGCATCCTGGCTGTCAGCCTGTCCCTGCGGCTGTTGCAGAGCCACCTTAGG
GCACAGGTGGTGGCTGGCTGTGGGATCCTCTTCTCATGCATGACACCTCTAGGCATCGGGCTGG
GTGCAGCTCTGGCAGAGTCGGCAGGACCTCTGCACCAGCTGGCCCAGTCTGTGCTAGAGGGCAT
GGCAGCTGGCACCTTTCTCTATATCACCTTTCTGGAAATCCTGCCCCAGGAGCTGGCCAGTTCT
GAGCAAAGGATCCTCAAGGTCATTCTGCTCCTAGCAGGCTTTGCCCTGCTCACTGGCCTGCTCT
TCATCCAAATCTAGGGGGCTTCAAGAGAGGGGCAGGGGAGATTGATGATCAGGTGCCCCTGTTC
TCCCTTCCCTCCCCCAGTTGTGGGGAATAGGAAGGAAAGGGGAAGGGAAATACTGAGGACCAAA
AAGTTCTCTGGGAGCTAAAGATAGAGCCTTTGGGGCTATCTGACTAATGAGAGGGAAGTGGGCA
GACAAGAGGCTGGCCCCAGTCCCAAGGAACAAGAGATGGTCAAGTCGCTAGAGACATATCAGGG
GACATTAGGATTGGGGAAGACACTTGACTGCTAGAATCAGAGGTTGGACACTATACATAAGGAC
AGGCTCACATGGGAGGCTGGAGGTGGGTACCCAGCTGCTGTGGAACGGGTATGGACAGGTCATA
AACCTAGAGTCAGTGTCCTGTTGGTCCTAGCCCATTTCAGCACCCTGCCACTTGGAGTGGACCC
CTCCTACTCTTCTTAGCGCCTACCCTCATACCTATCTCCCTCCTCCCATCTCCTAGGGGACTGG
CGCCAAATGGTCTCTCCCTGCCAATTTTGGTATCTTCTCTGGCCTCTCCAGTCCTGCTTACTCC
TCTATTTTTAAAGTGCCAAACAAATCCCCTTCCTCTTTCTCAAAGCACAGTAATGTGGCACTGA
GCCCTACCCAGCACCTCAGTGAAGGGGGCCTGCTTGCTCTTTATTTTGGTCCCGGATCCTGGGG
TGGGGCAGAAATATTTTCTGGGCTGGGGTAGGAGGAAGGTTGTTGCAGCCATCTACTGCTGCTG
TACCCTAGGAATATGGGGACATGGACATGGTGTCCCATGCCCAGATGATAAACACTGAGCTGCC
AAAACATTTTTTTAAATACACCCGAGGAGCCCAAGGGGGAAGGGCAATGCCTACCCCCAGCGTT
ATTTTTGGGGAGGGAGGGCTGTGCATAGGGACATATTCTTTAGAATCTATTTTATTAACTGACC
TGTTTTGGGACCTGTTACCCAAATAAAAGATGTTTCTAGACA

hide sequence

RefSeq Acc Id:

NM_001271958 ⟹ NP_001258887

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,963,537 (-)	NCBI
GRCh37	1	153,931,575 - 153,940,660 (-)	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI
CHM1_1	1	155,327,888 - 155,332,430 (-)	NCBI
T2T-CHM13v2.0	1	153,096,371 - 153,100,798 (-)	NCBI

Sequence:

show sequence

AGGCCGGAAGCGCGCGGAGACCATGTAGTGAGACCCTCGCGAGGTCTGAGAGTCACTGGAGCTA
CCAGAAGCATCATGGGGCCCTGGGGAGAGCCAGAGCTCCTGGTGTGGCGCCCCGAGGCGGTAGC
TTCAGAGCCTCCAGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGGTG
CTCACCCTCCTCTGCAGCCTGGTGCCCATCTGTGTGCTGCGCCGGCCAGGAGCTAACCATGAAG
GCTCAGCTTCCCGCCAGAAAGCCCTGAGCCTAGTAAGCTGTTTCGCGGGGGGCGTCTTTTTGGC
CACTTGTCTCCTGGACCTGCTGCCTGACTACCTGGCTGCCATAGATGAGGCCCTGGCAGCCTTG
CACGTGACGCTCCAGTTCCCACTGCAAGAGTTCATCCTGGCCATGGGCTTCTTCCTGGTCCTGG
TGATGGAGCAGATCACACTGGCTTACAAGGAGCAGTCAGGGCCGTCACCTCTGGAGGAAACAAG
GGCTCTGCTGGGAACAGTGAATGGTGGGCCGCAGCATTGGCATGATGGGCCAGGGGTCCCACAG
GCGAGTGGAGCCCCAGCAACCCCCTCAGCCTTGCGTGCCTGTGTACTGGTGTTCTCCCTGGCCC
TCCACTCCGTGTTCGAGGGGCTGGCGGTAGGGCTGCAGCGAGACCGGGCTCGGGCCATGGAGCT
GTGCCTGGCTTTGCTGCTCCACAAGGGCATCCTGGCTGTCAGCCTGTCCCTGCGGCTGTTGCAG
AGCCACCTTAGGGCACAGGTGGTGGCTGGCTGTGGGATCCTCTTCTCATGCATGACACCTCTAG
GCATCGGGCTGGGTGCAGCTCTGGCAGAGTCGGCAGGACCTCTGCACCAGCTGGCCCAGTCTGT
GCTAGAGGGCATGGCAGCTGGCACCTTTCTCTATATCACCTTTCTGGAAATCCTGCCCCAGGAG
CTGGCCAGTTCTGAGCAAAGGATCCTCAAGGTCATTCTGCTCCTAGCAGGCTTTGCCCTGCTCA
CTGGCCTGCTCTTCATCCAAATCTAGGGGGCTTCAAGAGAGGGGCAGGGGAGATTGATGATCAG
GTGCCCCTGTTCTCCCTTCCCTCCCCCAGTTGTGGGGAATAGGAAGGAAAGGGGAAGGGAAATA
CTGAGGACCAAAAAGTTCTCTGGGAGCTAAAGATAGAGCCTTTGGGGCTATCTGACTAATGAGA
GGGAAGTGGGCAGACAAGAGGCTGGCCCCAGTCCCAAGGAACAAGAGATGGTCAAGTCGCTAGA
GACATATCAGGGGACATTAGGATTGGGGAAGACACTTGACTGCTAGAATCAGAGGTTGGACACT
ATACATAAGGACAGGCTCACATGGGAGGCTGGAGGTGGGTACCCAGCTGCTGTGGAACGGGTAT
GGACAGGTCATAAACCTAGAGTCAGTGTCCTGTTGGTCCTAGCCCATTTCAGCACCCTGCCACT
TGGAGTGGACCCCTCCTACTCTTCTTAGCGCCTACCCTCATACCTATCTCCCTCCTCCCATCTC
CTAGGGGACTGGCGCCAAATGGTCTCTCCCTGCCAATTTTGGTATCTTCTCTGGCCTCTCCAGT
CCTGCTTACTCCTCTATTTTTAAAGTGCCAAACAAATCCCCTTCCTCTTTCTCAAAGCACAGTA
ATGTGGCACTGAGCCCTACCCAGCACCTCAGTGAAGGGGGCCTGCTTGCTCTTTATTTTGGTCC
CGGATCCTGGGGTGGGGCAGAAATATTTTCTGGGCTGGGGTAGGAGGAAGGTTGTTGCAGCCAT
CTACTGCTGCTGTACCCTAGGAATATGGGGACATGGACATGGTGTCCCATGCCCAGATGATAAA
CACTGAGCTGCCAAAACATTTTTTTAAATACACCCGAGGAGCCCAAGGGGGAAGGGCAATGCCT
ACCCCCAGCGTTATTTTTGGGGAGGGAGGGCTGTGCATAGGGACATATTCTTTAGAATCTATTT
TATTAACTGACCTGTTTTGGGACCTGTTACCCAAATAAAAGATGTTTCTAGACA

hide sequence

RefSeq Acc Id:

NM_001271959 ⟹ NP_001258888

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,963,537 (-)	NCBI
GRCh37	1	153,931,575 - 153,940,660 (-)	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI
CHM1_1	1	155,327,888 - 155,332,281 (-)	NCBI
T2T-CHM13v2.0	1	153,096,371 - 153,100,798 (-)	NCBI

Sequence:

show sequence

AGGCCGGAAGCGCGCGGAGACCATGTAGTGAGACCCTCGCGAGGTGAGTGCGGGCTGTCTGGCA
GCGGGGTCCATGTCGGCTGCCCAGGCCTCCCCGGGCCCGGGAACAGGAGTCCCAGCTCACGCAT
TCTTCATCTGCTTCCCGCGACGCTTGGCGGCCTCGCACCCCGCCTCCTGGAGCCCGGACTTTCA
GGCACCGCCCTCAGTGTCGCCTCAGTCCGTCCCGGGACCGCAGACTCTTAGGGCCCCTCTCTTT
GGCCATCTGCCTCTAGGTCCCATCCTGGGGCCTGAAGCGCTTGTTCTCTGCGCTGGGAAAAGGG
GAACGATGGAGCGATCCAGCACCCAAACTTACCCTGTCCAGGTCTGAGAGTCACTGGAGCTACC
AGAAGCATCATGGGGCCCTGGGGAGAGCCAGAGCTCCTGGTGTGGCGCCCCGAGGCGGTAGCTT
CAGAGCCTCCAGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGGTGCT
CACCCTCCTCTGCAGCCTGGTGCCCATCTGTGTGCTGCGCCGGCCAGGAGCTAACCATGAAGGC
TCAGCTTCCCGCCAGAAAGCCCTGAGCCTAGTAAGCTGTTTCGCGGGGGGCGTCTTTTTGGCCA
CTTGTCTCCTGGACCTGCTGCCTGACTACCTGGCTGCCATAGATGAGGCCCTGGCAGCCTTGCA
CGTGACGCTCCAGTTCCCACTGCAAGAGTTCATCCTGGCCATGGGCTTCTTCCTGGTCCTGGTG
ATGGAGCAGATCACACTGGCTTACAAGGAGCAGTCAGGGCCGTCACCTCTGGAGGAAACAAGGG
CTCTGCTGGGAACAGTGAATGGTGGGCCGCAGCATTGGCATGATGGGCCAGGGGTCCCACAGGC
GAGTGGAGCCCCAGCAACCCCCTCAGCCTTGCGTGCCTGTGTACTGGTGTTCTCCCTGGCCCTC
CACTCCGTGTTCGAGGGGCTGGCGGTAGGGCTGCAGCGAGACCGGGCTCGGGCCATGGAGCTGT
GCCTGGCTTTGCTGCTCCACAAGGGCATCCTGGCTGTCAGCCTGTCCCTGCGGCTGTTGCAGAG
CCACCTTAGGGCACAGGTGGTGGCTGGCTGTGGGATCCTCTTCTCATGCATGACACCTCTAGGC
ATCGGGCTGGGTGCAGCTCTGGCAGAGTCGGCAGGACCTCTGCACCAGCTGGCCCAGTCTGTGC
TAGAGGGCATGGCAGCTGGCACCTTTCTCTATATCACCTTTCTGGAAATCCTGCCCCAGGAGCT
GGCCAGTTCTGAGCAAAGGATCCTCAAGGTCATTCTGCTCCTAGCAGGCTTTGCCCTGCTCACT
GGCCTGCTCTTCATCCAAATCTAGGGGGCTTCAAGAGAGGGGCAGGGGAGATTGATGATCAGGT
GCCCCTGTTCTCCCTTCCCTCCCCCAGTTGTGGGGAATAGGAAGGAAAGGGGAAGGGAAATACT
GAGGACCAAAAAGTTCTCTGGGAGCTAAAGATAGAGCCTTTGGGGCTATCTGACTAATGAGAGG
GAAGTGGGCAGACAAGAGGCTGGCCCCAGTCCCAAGGAACAAGAGATGGTCAAGTCGCTAGAGA
CATATCAGGGGACATTAGGATTGGGGAAGACACTTGACTGCTAGAATCAGAGGTTGGACACTAT
ACATAAGGACAGGCTCACATGGGAGGCTGGAGGTGGGTACCCAGCTGCTGTGGAACGGGTATGG
ACAGGTCATAAACCTAGAGTCAGTGTCCTGTTGGTCCTAGCCCATTTCAGCACCCTGCCACTTG
GAGTGGACCCCTCCTACTCTTCTTAGCGCCTACCCTCATACCTATCTCCCTCCTCCCATCTCCT
AGGGGACTGGCGCCAAATGGTCTCTCCCTGCCAATTTTGGTATCTTCTCTGGCCTCTCCAGTCC
TGCTTACTCCTCTATTTTTAAAGTGCCAAACAAATCCCCTTCCTCTTTCTCAAAGCACAGTAAT
GTGGCACTGAGCCCTACCCAGCACCTCAGTGAAGGGGGCCTGCTTGCTCTTTATTTTGGTCCCG
GATCCTGGGGTGGGGCAGAAATATTTTCTGGGCTGGGGTAGGAGGAAGGTTGTTGCAGCCATCT
ACTGCTGCTGTACCCTAGGAATATGGGGACATGGACATGGTGTCCCATGCCCAGATGATAAACA
CTGAGCTGCCAAAACATTTTTTTAAATACACCCGAGGAGCCCAAGGGGGAAGGGCAATGCCTAC
CCCCAGCGTTATTTTTGGGGAGGGAGGGCTGTGCATAGGGACATATTCTTTAGAATCTATTTTA
TTAACTGACCTGTTTTGGGACCTGTTACCCAAATAAAAGATGTTTCTAGACA

hide sequence

RefSeq Acc Id:

NM_001271960 ⟹ NP_001258889

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,968,184 (-)	NCBI
GRCh37	1	153,931,575 - 153,940,660 (-)	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI
CHM1_1	1	155,327,888 - 155,336,973 (-)	NCBI
T2T-CHM13v2.0	1	153,096,371 - 153,105,445 (-)	NCBI

Sequence:

show sequence

ACTACAAAAGTGGATGCCACCTTGCCAGGAGCCACGGTAGGGCCGCTGTATCTGGGAGTAGGGG
ACTAAGAGTCTGAGGGTCCACAAACGGAATTTAAGAAGTCGCCTGCTCCGCCCGCTCCCGCTCC
CGATCTCTGATTGCTCCTAACTGACGTCACTCCCGGTCTGTCCCCGCCCACTCGGTGCTGCCAT
TGGCAGTCGGTCGTGGGTCTGAGAGTCACTGGAGCTACCAGAAGCATCATGGGGCCCTGGGGAG
AGCCAGAGCTCCTGGTGTGGCGCCCCGAGGCGGTAGCTTCAGAGCCTCCAGTGCCTGTGGGGCT
GGAGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGGTGCTCACCCTCCTCTGCAGCCTGGTGCCC
ATCTGTGTGCTGCGCCGGCCAGGAGCTAACCATGAAGGCTCAGCTTCCCGCCAGAAAGCCCTGA
GCCTAGTAAGCTGTTTCGCGGGGGGCGTCTTTTTGGCCACTTGTCTCCTGGACCTGCTGCCTGA
CTACCTGGCTGCCATAGATGAGGCCCTGGCAGCCTTGCACGTGACGCTCCAGTTCCCACTGCAA
GAGTTCATCCTGGCCATGGGCTTCTTCCTGGTCCTGGTGATGGAGCAGATCACACTGGCTTACA
AGGAGCAGTCAGGGCCGTCACCTCTGGAGGAAACAAGGGCTCTGCTGGGAACAGTGAATGGTGG
GCCGCAGCATTGGCATGATGGGCCAGGGGTCCCACAGGCGAGTGGAGCCCCAGCAACCCCCTCA
GCCTTGCGTGCCTGTGTACTGGTGTTCTCCCTGGCCCTCCACTCCGTGTTCGAGGGGCTGGCGG
TAGGGCTGCAGCGAGACCGGGCTCGGGCCATGGAGCTGTGCCTGGCTTTGCTGCTCCACAAGGG
CATCCTGGCTGTCAGCCTGTCCCTGCGGCTGTTGCAGAGCCACCTTAGGGCACAGGTGGTGGCT
GGCTGTGGGATCCTCTTCTCATGCATGACACCTCTAGGCATCGGGCTGGGTGCAGCTCTGGCAG
AGTCGGCAGGACCTCTGCACCAGCTGGCCCAGTCTGTGCTAGAGGGCATGGCAGCTGGCACCTT
TCTCTATATCACCTTTCTGGAAATCCTGCCCCAGGAGCTGGCCAGTTCTGAGCAAAGGATCCTC
AAGGTCATTCTGCTCCTAGCAGGCTTTGCCCTGCTCACTGGCCTGCTCTTCATCCAAATCTAGG
GGGCTTCAAGAGAGGGGCAGGGGAGATTGATGATCAGGTGCCCCTGTTCTCCCTTCCCTCCCCC
AGTTGTGGGGAATAGGAAGGAAAGGGGAAGGGAAATACTGAGGACCAAAAAGTTCTCTGGGAGC
TAAAGATAGAGCCTTTGGGGCTATCTGACTAATGAGAGGGAAGTGGGCAGACAAGAGGCTGGCC
CCAGTCCCAAGGAACAAGAGATGGTCAAGTCGCTAGAGACATATCAGGGGACATTAGGATTGGG
GAAGACACTTGACTGCTAGAATCAGAGGTTGGACACTATACATAAGGACAGGCTCACATGGGAG
GCTGGAGGTGGGTACCCAGCTGCTGTGGAACGGGTATGGACAGGTCATAAACCTAGAGTCAGTG
TCCTGTTGGTCCTAGCCCATTTCAGCACCCTGCCACTTGGAGTGGACCCCTCCTACTCTTCTTA
GCGCCTACCCTCATACCTATCTCCCTCCTCCCATCTCCTAGGGGACTGGCGCCAAATGGTCTCT
CCCTGCCAATTTTGGTATCTTCTCTGGCCTCTCCAGTCCTGCTTACTCCTCTATTTTTAAAGTG
CCAAACAAATCCCCTTCCTCTTTCTCAAAGCACAGTAATGTGGCACTGAGCCCTACCCAGCACC
TCAGTGAAGGGGGCCTGCTTGCTCTTTATTTTGGTCCCGGATCCTGGGGTGGGGCAGAAATATT
TTCTGGGCTGGGGTAGGAGGAAGGTTGTTGCAGCCATCTACTGCTGCTGTACCCTAGGAATATG
GGGACATGGACATGGTGTCCCATGCCCAGATGATAAACACTGAGCTGCCAAAACATTTTTTTAA
ATACACCCGAGGAGCCCAAGGGGGAAGGGCAATGCCTACCCCCAGCGTTATTTTTGGGGAGGGA
GGGCTGTGCATAGGGACATATTCTTTAGAATCTATTTTATTAACTGACCTGTTTTGGGACCTGT
TACCCAAATAAAAGATGTTTCTAGACA

hide sequence

RefSeq Acc Id:

NM_001271961 ⟹ NP_001258890

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,963,537 (-)	NCBI
GRCh37	1	153,931,575 - 153,940,660 (-)	NCBI
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI
CHM1_1	1	155,327,888 - 155,332,430 (-)	NCBI
T2T-CHM13v2.0	1	153,096,371 - 153,100,798 (-)	NCBI

Sequence:

show sequence

AGGCCGGAAGCGCGCGGAGACCATGTAGTGAGACCCTCGCGAGGTCTGAGAGTCACTGGAGCTA
CCAGAAGCATCATGGGGCCCTGGGGAGAGCCAGAGCTCCTGGTGTGGCGCCCCGAGGCGGTAGC
TTCAGAGCCTCCAGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGGTG
CTCACCCTCCTCTGCAGCCTGGTGCCCATCTGTGTGCTGCGCCGGCCAGGAGCTAACCATGAAG
GCTCAGCTCCAGTTCCCACTGCAAGAGTTCATCCTGGCCATGGGCTTCTTCCTGGTCCTGGTGA
TGGAGCAGATCACACTGGCTTACAAGGAGCAGTCAGGGCCGTCACCTCTGGAGGAAACAAGGGC
TCTGCTGGGAACAGTGAATGGTGGGCCGCAGCATTGGCATGATGGGCCAGGGGTCCCACAGGCG
AGTGGAGCCCCAGCAACCCCCTCAGCCTTGCGTGCCTGTGTACTGGTGTTCTCCCTGGCCCTCC
ACTCCGTGTTCGAGGGGCTGGCGGTAGGGCTGCAGCGAGACCGGGCTCGGGCCATGGAGCTGTG
CCTGGCTTTGCTGCTCCACAAGGGCATCCTGGCTGTCAGCCTGTCCCTGCGGCTGTTGCAGAGC
CACCTTAGGGCACAGGTGGTGGCTGGCTGTGGGATCCTCTTCTCATGCATGACACCTCTAGGCA
TCGGGCTGGGTGCAGCTCTGGCAGAGTCGGCAGGACCTCTGCACCAGCTGGCCCAGTCTGTGCT
AGAGGGCATGGCAGCTGGCACCTTTCTCTATATCACCTTTCTGGAAATCCTGCCCCAGGAGCTG
GCCAGTTCTGAGCAAAGGATCCTCAAGGTCATTCTGCTCCTAGCAGGCTTTGCCCTGCTCACTG
GCCTGCTCTTCATCCAAATCTAGGGGGCTTCAAGAGAGGGGCAGGGGAGATTGATGATCAGGTG
CCCCTGTTCTCCCTTCCCTCCCCCAGTTGTGGGGAATAGGAAGGAAAGGGGAAGGGAAATACTG
AGGACCAAAAAGTTCTCTGGGAGCTAAAGATAGAGCCTTTGGGGCTATCTGACTAATGAGAGGG
AAGTGGGCAGACAAGAGGCTGGCCCCAGTCCCAAGGAACAAGAGATGGTCAAGTCGCTAGAGAC
ATATCAGGGGACATTAGGATTGGGGAAGACACTTGACTGCTAGAATCAGAGGTTGGACACTATA
CATAAGGACAGGCTCACATGGGAGGCTGGAGGTGGGTACCCAGCTGCTGTGGAACGGGTATGGA
CAGGTCATAAACCTAGAGTCAGTGTCCTGTTGGTCCTAGCCCATTTCAGCACCCTGCCACTTGG
AGTGGACCCCTCCTACTCTTCTTAGCGCCTACCCTCATACCTATCTCCCTCCTCCCATCTCCTA
GGGGACTGGCGCCAAATGGTCTCTCCCTGCCAATTTTGGTATCTTCTCTGGCCTCTCCAGTCCT
GCTTACTCCTCTATTTTTAAAGTGCCAAACAAATCCCCTTCCTCTTTCTCAAAGCACAGTAATG
TGGCACTGAGCCCTACCCAGCACCTCAGTGAAGGGGGCCTGCTTGCTCTTTATTTTGGTCCCGG
ATCCTGGGGTGGGGCAGAAATATTTTCTGGGCTGGGGTAGGAGGAAGGTTGTTGCAGCCATCTA
CTGCTGCTGTACCCTAGGAATATGGGGACATGGACATGGTGTCCCATGCCCAGATGATAAACAC
TGAGCTGCCAAAACATTTTTTTAAATACACCCGAGGAGCCCAAGGGGGAAGGGCAATGCCTACC
CCCAGCGTTATTTTTGGGGAGGGAGGGCTGTGCATAGGGACATATTCTTTAGAATCTATTTTAT
TAACTGACCTGTTTTGGGACCTGTTACCCAAATAAAAGATGTTTCTAGACA

hide sequence

RefSeq Acc Id:

NM_014437 ⟹ NP_055252

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,967,725 (-)	NCBI
GRCh37	1	153,931,575 - 153,940,660 (-)	NCBI
Build 36	1	152,198,212 - 152,206,812 (-)	NCBI Archive
HuRef	1	125,294,161 - 125,303,246 (-)	NCBI
CHM1_1	1	155,327,888 - 155,336,521 (-)	NCBI
T2T-CHM13v2.0	1	153,096,371 - 153,104,986 (-)	NCBI

Sequence:

show sequence

AGTTTGGCTGTTCAGGAGAGTCAGGCCAATGGGGCCGCAGTTCTTTCTTTTTTTTTTCTTTATT
CTTATTTTTGGAGACAGGGTCTCGCTCTGTTGCCCAGGCTGGAGTGCGGTGGTGCGATCACGGT
TCCATGCAGCCCCCGACCTCCCGGGCTCAGGTGATTCTCCCGCCTCAGCACCGCGAGCAGCTAG
GACCACAGGCGCGAGCCACTGCGTCCGGCCGGCGGGACTTATTTGTCAGGCGGGGATTGGGTTC
CGCCAGCCTAAAGGGAGGGGTAAGCGCCAGAATATGAATCGCCGGGAAGCTGGGAGAAAGCTCC
GGGAAACCCTGAGCAGCCAGGTCGCCTGCTCCGCCCGCTCCCGCTCCCGATCTCTGATTGCTCC
TAACTGACGTCACTCCCGGTCTGTCCCCGCCCACTCGGTGCTGCCATTGGCAGTCGGTCGTGGG
TCTGAGAGTCACTGGAGCTACCAGAAGCATCATGGGGCCCTGGGGAGAGCCAGAGCTCCTGGTG
TGGCGCCCCGAGGCGGTAGCTTCAGAGCCTCCAGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGG
CCCTGGTGCTGCTGCTGGTGCTCACCCTCCTCTGCAGCCTGGTGCCCATCTGTGTGCTGCGCCG
GCCAGGAGCTAACCATGAAGGCTCAGCTTCCCGCCAGAAAGCCCTGAGCCTAGTAAGCTGTTTC
GCGGGGGGCGTCTTTTTGGCCACTTGTCTCCTGGACCTGCTGCCTGACTACCTGGCTGCCATAG
ATGAGGCCCTGGCAGCCTTGCACGTGACGCTCCAGTTCCCACTGCAAGAGTTCATCCTGGCCAT
GGGCTTCTTCCTGGTCCTGGTGATGGAGCAGATCACACTGGCTTACAAGGAGCAGTCAGGGCCG
TCACCTCTGGAGGAAACAAGGGCTCTGCTGGGAACAGTGAATGGTGGGCCGCAGCATTGGCATG
ATGGGCCAGGGGTCCCACAGGCGAGTGGAGCCCCAGCAACCCCCTCAGCCTTGCGTGCCTGTGT
ACTGGTGTTCTCCCTGGCCCTCCACTCCGTGTTCGAGGGGCTGGCGGTAGGGCTGCAGCGAGAC
CGGGCTCGGGCCATGGAGCTGTGCCTGGCTTTGCTGCTCCACAAGGGCATCCTGGCTGTCAGCC
TGTCCCTGCGGCTGTTGCAGAGCCACCTTAGGGCACAGGTGGTGGCTGGCTGTGGGATCCTCTT
CTCATGCATGACACCTCTAGGCATCGGGCTGGGTGCAGCTCTGGCAGAGTCGGCAGGACCTCTG
CACCAGCTGGCCCAGTCTGTGCTAGAGGGCATGGCAGCTGGCACCTTTCTCTATATCACCTTTC
TGGAAATCCTGCCCCAGGAGCTGGCCAGTTCTGAGCAAAGGATCCTCAAGGTCATTCTGCTCCT
AGCAGGCTTTGCCCTGCTCACTGGCCTGCTCTTCATCCAAATCTAGGGGGCTTCAAGAGAGGGG
CAGGGGAGATTGATGATCAGGTGCCCCTGTTCTCCCTTCCCTCCCCCAGTTGTGGGGAATAGGA
AGGAAAGGGGAAGGGAAATACTGAGGACCAAAAAGTTCTCTGGGAGCTAAAGATAGAGCCTTTG
GGGCTATCTGACTAATGAGAGGGAAGTGGGCAGACAAGAGGCTGGCCCCAGTCCCAAGGAACAA
GAGATGGTCAAGTCGCTAGAGACATATCAGGGGACATTAGGATTGGGGAAGACACTTGACTGCT
AGAATCAGAGGTTGGACACTATACATAAGGACAGGCTCACATGGGAGGCTGGAGGTGGGTACCC
AGCTGCTGTGGAACGGGTATGGACAGGTCATAAACCTAGAGTCAGTGTCCTGTTGGTCCTAGCC
CATTTCAGCACCCTGCCACTTGGAGTGGACCCCTCCTACTCTTCTTAGCGCCTACCCTCATACC
TATCTCCCTCCTCCCATCTCCTAGGGGACTGGCGCCAAATGGTCTCTCCCTGCCAATTTTGGTA
TCTTCTCTGGCCTCTCCAGTCCTGCTTACTCCTCTATTTTTAAAGTGCCAAACAAATCCCCTTC
CTCTTTCTCAAAGCACAGTAATGTGGCACTGAGCCCTACCCAGCACCTCAGTGAAGGGGGCCTG
CTTGCTCTTTATTTTGGTCCCGGATCCTGGGGTGGGGCAGAAATATTTTCTGGGCTGGGGTAGG
AGGAAGGTTGTTGCAGCCATCTACTGCTGCTGTACCCTAGGAATATGGGGACATGGACATGGTG
TCCCATGCCCAGATGATAAACACTGAGCTGCCAAAACATTTTTTTAAATACACCCGAGGAGCCC
AAGGGGGAAGGGCAATGCCTACCCCCAGCGTTATTTTTGGGGAGGGAGGGCTGTGCATAGGGAC
ATATTCTTTAGAATCTATTTTATTAACTGACCTGTTTTGGGACCTGTTACCCAAATAAAAGATG
TTTCTAGACA

hide sequence

RefSeq Acc Id:

XM_047418008 ⟹ XP_047273964

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,959,110 - 153,967,725 (-)	NCBI

RefSeq Acc Id:

XM_054336011 ⟹ XP_054191986

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	153,096,371 - 153,104,986 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001258886	(Get FASTA)	NCBI Sequence Viewer
	NP_001258887	(Get FASTA)	NCBI Sequence Viewer
	NP_001258888	(Get FASTA)	NCBI Sequence Viewer
	NP_001258889	(Get FASTA)	NCBI Sequence Viewer
	NP_001258890	(Get FASTA)	NCBI Sequence Viewer
	NP_055252	(Get FASTA)	NCBI Sequence Viewer
	XP_047273964	(Get FASTA)	NCBI Sequence Viewer
	XP_054191986	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD27717	(Get FASTA)	NCBI Sequence Viewer
	AAD34066	(Get FASTA)	NCBI Sequence Viewer
	AAH02563	(Get FASTA)	NCBI Sequence Viewer
	AAH03152	(Get FASTA)	NCBI Sequence Viewer
	AAH07886	(Get FASTA)	NCBI Sequence Viewer
	AAH14303	(Get FASTA)	NCBI Sequence Viewer
	BAC11502	(Get FASTA)	NCBI Sequence Viewer
	BAG52035	(Get FASTA)	NCBI Sequence Viewer
	BAG56898	(Get FASTA)	NCBI Sequence Viewer
	BAG60292	(Get FASTA)	NCBI Sequence Viewer
	BAG62011	(Get FASTA)	NCBI Sequence Viewer
	CAB59979	(Get FASTA)	NCBI Sequence Viewer
	CAB59980	(Get FASTA)	NCBI Sequence Viewer
	CAB82784	(Get FASTA)	NCBI Sequence Viewer
	CAF86850	(Get FASTA)	NCBI Sequence Viewer
	CAG33498	(Get FASTA)	NCBI Sequence Viewer
	EAW53259	(Get FASTA)	NCBI Sequence Viewer
	EAW53261	(Get FASTA)	NCBI Sequence Viewer
	EAW53264	(Get FASTA)	NCBI Sequence Viewer
	EAW53265	(Get FASTA)	NCBI Sequence Viewer
	EAW53267	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000309710
	ENSP00000309710.6
	ENSP00000348535
	ENSP00000348535.4
	ENSP00000357610
	ENSP00000357610.1
	ENSP00000357612.3
	ENSP00000392229.1
	ENSP00000407717.1
	ENSP00000443632
	ENSP00000443632.2
	ENSP00000479421
	ENSP00000479421.1
	ENSP00000484182
	ENSP00000484182.1
GenBank Protein	Q9NY26	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_055252 ⟸ NM_014437
- Peptide Label:	isoform a
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q6IAD8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHEGSAS RQKALSLVSCFAGGVFLATCLLDLLPDYLAAIDEALAALHVTLQFPLQEFILAMGFFLVLVMEQ ITLAYKEQSGPSPLEETRALLGTVNGGPQHWHDGPGVPQASGAPATPSALRACVLVFSLALHSV FEGLAVGLQRDRARAMELCLALLLHKGILAVSLSLRLLQSHLRAQVVAGCGILFSCMTPLGIGL GAALAESAGPLHQLAQSVLEGMAAGTFLYITFLEILPQELASSEQRILKVILLLAGFALLTGLL FIQI hide sequence

RefSeq Acc Id:	NP_001258889 ⟸ NM_001271960
- Peptide Label:	isoform a
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q6IAD8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHEGSAS RQKALSLVSCFAGGVFLATCLLDLLPDYLAAIDEALAALHVTLQFPLQEFILAMGFFLVLVMEQ ITLAYKEQSGPSPLEETRALLGTVNGGPQHWHDGPGVPQASGAPATPSALRACVLVFSLALHSV FEGLAVGLQRDRARAMELCLALLLHKGILAVSLSLRLLQSHLRAQVVAGCGILFSCMTPLGIGL GAALAESAGPLHQLAQSVLEGMAAGTFLYITFLEILPQELASSEQRILKVILLLAGFALLTGLL FIQI hide sequence

RefSeq Acc Id:	NP_001258890 ⟸ NM_001271961
- Peptide Label:	isoform b
- UniProtKB:	A0A0A0MTL8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHEGSAP VPTARVHPGHGLLPGPGDGADHTGLQGAVRAVTSGGNKGSAGNSEWWAAALA hide sequence

RefSeq Acc Id:	NP_001258887 ⟸ NM_001271958
- Peptide Label:	isoform a
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q6IAD8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHEGSAS RQKALSLVSCFAGGVFLATCLLDLLPDYLAAIDEALAALHVTLQFPLQEFILAMGFFLVLVMEQ ITLAYKEQSGPSPLEETRALLGTVNGGPQHWHDGPGVPQASGAPATPSALRACVLVFSLALHSV FEGLAVGLQRDRARAMELCLALLLHKGILAVSLSLRLLQSHLRAQVVAGCGILFSCMTPLGIGL GAALAESAGPLHQLAQSVLEGMAAGTFLYITFLEILPQELASSEQRILKVILLLAGFALLTGLL FIQI hide sequence

RefSeq Acc Id:	NP_001258888 ⟸ NM_001271959
- Peptide Label:	isoform a
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q6IAD8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHEGSAS RQKALSLVSCFAGGVFLATCLLDLLPDYLAAIDEALAALHVTLQFPLQEFILAMGFFLVLVMEQ ITLAYKEQSGPSPLEETRALLGTVNGGPQHWHDGPGVPQASGAPATPSALRACVLVFSLALHSV FEGLAVGLQRDRARAMELCLALLLHKGILAVSLSLRLLQSHLRAQVVAGCGILFSCMTPLGIGL GAALAESAGPLHQLAQSVLEGMAAGTFLYITFLEILPQELASSEQRILKVILLLAGFALLTGLL FIQI hide sequence

RefSeq Acc Id:	NP_001258886 ⟸ NM_001271957
- Peptide Label:	isoform a
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q6IAD8 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPWGEPELLVWRPEAVASEPPVPVGLEVKLGALVLLLVLTLLCSLVPICVLRRPGANHEGSAS RQKALSLVSCFAGGVFLATCLLDLLPDYLAAIDEALAALHVTLQFPLQEFILAMGFFLVLVMEQ ITLAYKEQSGPSPLEETRALLGTVNGGPQHWHDGPGVPQASGAPATPSALRACVLVFSLALHSV FEGLAVGLQRDRARAMELCLALLLHKGILAVSLSLRLLQSHLRAQVVAGCGILFSCMTPLGIGL GAALAESAGPLHQLAQSVLEGMAAGTFLYITFLEILPQELASSEQRILKVILLLAGFALLTGLL FIQI hide sequence

RefSeq Acc Id:

ENSP00000484182 ⟸ ENST00000621013

RefSeq Acc Id:

ENSP00000392229 ⟸ ENST00000413622

RefSeq Acc Id:

ENSP00000392950 ⟸ ENST00000429040

RefSeq Acc Id:

ENSP00000407717 ⟸ ENST00000417348

RefSeq Acc Id:

ENSP00000309710 ⟸ ENST00000310483

RefSeq Acc Id:

ENSP00000443632 ⟸ ENST00000537590

RefSeq Acc Id:

ENSP00000479421 ⟸ ENST00000617697

RefSeq Acc Id:

ENSP00000357610 ⟸ ENST00000368621

RefSeq Acc Id:

ENSP00000357612 ⟸ ENST00000368623

RefSeq Acc Id:

ENSP00000348535 ⟸ ENST00000356205

RefSeq Acc Id:	XP_047273964 ⟸ XM_047418008
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054191986 ⟸ XM_054336011
- Peptide Label:	isoform X1
- UniProtKB:	Q9Y2Z7 (UniProtKB/Swiss-Prot), Q9UBI7 (UniProtKB/Swiss-Prot), Q9NY26 (UniProtKB/Swiss-Prot), Q9BTV0 (UniProtKB/Swiss-Prot), Q8N2H7 (UniProtKB/Swiss-Prot), Q5T4K1 (UniProtKB/Swiss-Prot), B4DDY7 (UniProtKB/Swiss-Prot), Q9Y380 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9NY26-F1-model_v2	AlphaFold	Q9NY26	1-324	view protein structure

Promoters

RGD ID:

6786880

Promoter ID:

HG_KWN:5242

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:

ENST00000368621, ENST00000368623, OTTHUMT00000090283, OTTHUMT00000090289, OTTHUMT00000098817, UC001FDH.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	152,201,746 - 152,203,272 (-)	MPROMDB

RGD ID:

6786878

Promoter ID:

HG_KWN:5243

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell

Transcripts:

NM_014437, OTTHUMT00000090287

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	152,206,266 - 152,206,766 (-)	MPROMDB

RGD ID:

6857292

Promoter ID:

EPDNEW_H1811

Type:

initiation region

Name:

SLC39A1_1

Description:

solute carrier family 39 member 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H1814

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,963,537 - 153,963,597	EPDNEW

RGD ID:

6857298

Promoter ID:

EPDNEW_H1814

Type:

initiation region

Name:

SLC39A1_2

Description:

solute carrier family 39 member 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H1811

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	153,967,725 - 153,967,785	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12876	AgrOrtholog
COSMIC	SLC39A1	COSMIC
Ensembl Genes	ENSG00000143570	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000310483	ENTREZGENE
	ENST00000310483.10	UniProtKB/Swiss-Prot
	ENST00000356205	ENTREZGENE
	ENST00000356205.9	UniProtKB/Swiss-Prot
	ENST00000368621	ENTREZGENE
	ENST00000368621.5	UniProtKB/Swiss-Prot
	ENST00000368623.7	UniProtKB/Swiss-Prot
	ENST00000413622.5	UniProtKB/TrEMBL
	ENST00000417348.2	UniProtKB/TrEMBL
	ENST00000537590	ENTREZGENE
	ENST00000537590.5	UniProtKB/TrEMBL
	ENST00000617697	ENTREZGENE
	ENST00000617697.4	UniProtKB/Swiss-Prot
	ENST00000621013	ENTREZGENE
	ENST00000621013.4	UniProtKB/Swiss-Prot
GTEx	ENSG00000143570	GTEx
HGNC ID	HGNC:12876	ENTREZGENE
Human Proteome Map	SLC39A1	Human Proteome Map
InterPro	ZIP	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:27173	UniProtKB/Swiss-Prot
NCBI Gene	27173	ENTREZGENE
OMIM	604740	OMIM
PANTHER	ZINC TRANSPORTER ZIP1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC/IRON TRANSPORTER	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Zip	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37465	PharmGKB
UniProt	A0A0A0MTL8	ENTREZGENE, UniProtKB/TrEMBL
	B4DDY7	ENTREZGENE
	L8ECE7_HUMAN	UniProtKB/TrEMBL
	Q5T4K1	ENTREZGENE
	Q5T4K2_HUMAN	UniProtKB/TrEMBL
	Q5T4K4_HUMAN	UniProtKB/TrEMBL
	Q6IAD8	ENTREZGENE, UniProtKB/TrEMBL
	Q8N2H7	ENTREZGENE
	Q9BTV0	ENTREZGENE
	Q9NY26	ENTREZGENE
	Q9UBI7	ENTREZGENE
	Q9Y2Z7	ENTREZGENE
	Q9Y380	ENTREZGENE
	S39A1_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DDY7	UniProtKB/Swiss-Prot
	Q5T4K1	UniProtKB/Swiss-Prot
	Q8N2H7	UniProtKB/Swiss-Prot
	Q9BTV0	UniProtKB/Swiss-Prot
	Q9UBI7	UniProtKB/Swiss-Prot
	Q9Y2Z7	UniProtKB/Swiss-Prot
	Q9Y380	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-03-08	SLC39A1	solute carrier family 39 member 1		solute carrier family 39 (zinc transporter), member 1	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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