ASIC4 (acid sensing ion channel subunit family member 4)

Gene: ASIC4 (acid sensing ion channel subunit family member 4) Homo sapiens

Analyze

Symbol:

ASIC4

Name:

acid sensing ion channel subunit family member 4

RGD ID:

1604616

HGNC Page

HGNC:21263

Description:

Predicted to enable ligand-gated sodium channel activity. Predicted to be involved in sodium ion transmembrane transport. Predicted to act upstream of or within behavioral fear response. Predicted to be located in plasma membrane.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

ACCN4; acid sensing (proton gated) ion channel family member 4; acid sensing ion channel family member 4; acid-sensing (proton-gated) ion channel family member 4; acid-sensing ion channel 4; amiloride-sensitive cation channel 4; amiloride-sensitive cation channel 4, pituitary; amiloride-sensitive cation channel family member 4, pituitary; BNAC4; brain sodium channel 4; MGC17248; MGC24860

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):	Asic4 (acid-sensing ion channel family member 4)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Asic4 (acid sensing ion channel subunit family member 4)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Asic4 (acid sensing ion channel subunit family member 4)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ASIC4 (acid sensing ion channel subunit family member 4)	NCBI	Ortholog
Canis lupus familiaris (dog):	ASIC4 (acid sensing ion channel subunit family member 4)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Asic4 (acid sensing ion channel subunit family member 4)	NCBI	Ortholog
Sus scrofa (pig):	ASIC4 (acid sensing ion channel subunit family member 4)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	ASIC4 (acid sensing ion channel subunit family member 4)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Asic4 (acid sensing ion channel subunit family member 4)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Asic4 (acid sensing ion channel subunit family member 4)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Asic4 (acid-sensing ion channel family member 4)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	asic4b (acid-sensing (proton-gated) ion channel family member 4b)	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Danio rerio (zebrafish):	asic4a (acid-sensing (proton-gated) ion channel family member 4a)	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	acd-1	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER)
Drosophila melanogaster (fruit fly):	ppk	Alliance	DIOPT (InParanoid\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ppk12	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ppk28	Alliance	DIOPT (Ensembl Compara\|InParanoid\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ppk8	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ppk26	Alliance	DIOPT (InParanoid\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	rpk	Alliance	DIOPT (InParanoid\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ppk16	Alliance	DIOPT (Ensembl Compara\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ppk5	Alliance	DIOPT (Ensembl Compara\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Nach	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER)
Drosophila melanogaster (fruit fly):	ppk21	Alliance	DIOPT (OMA\|PANTHER\|SonicParanoid)
Xenopus laevis (African clawed frog):	asic4.S	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	asic4.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	asic4	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)

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	2	219,507,093 - 219,538,772 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	219,514,170 - 219,538,772 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	220,379,204 - 220,403,494 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	220,087,296 - 220,111,738 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	214,148,884 - 214,173,457 (+)	NCBI		Celera
Cytogenetic Map	2	q35	NCBI
HuRef	2	212,231,962 - 212,256,523 (+)	NCBI		HuRef
CHM1_1	2	220,384,734 - 220,409,316 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	219,991,838 - 220,023,471 (+)	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

alacrima, achalasia, and impaired intellectual development syndrome (IAGP)

Neurodevelopmental Disorders (IAGP)

paroxysmal nonkinesigenic dyskinesia 1 (IAGP)

polydactyly (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

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

4,4'-sulfonyldiphenol (ISO)

all-trans-retinoic acid (EXP,ISO)

ammonium chloride (ISO)

aristolochic acid A (EXP)

atrazine (EXP,ISO)

benzo[a]pyrene (EXP,ISO)

bisphenol A (ISO)

bisphenol F (ISO)

C60 fullerene (ISO)

cisplatin (EXP)

Cuprizon (ISO)

dextran sulfate (ISO)

hydralazine (EXP)

ketamine (ISO)

Licochalcone B (EXP)

mono(2-ethylhexyl) phthalate (ISO)

morphine (ISO)

PCB138 (ISO)

pirinixic acid (EXP)

sodium arsenite (ISO)

Theaflavin 3,3'-digallate (EXP)

thioacetamide (ISO)

titanium dioxide (ISO)

toluene (EXP)

trichloroethene (ISO)

triclosan (EXP)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

behavioral fear response (IEA,ISO)

inorganic cation transmembrane transport (IEA)

monoatomic ion transmembrane transport (IEA)

sodium ion transmembrane transport (IBA,IEA)

sodium ion transport (IEA)

Cellular Component

membrane (IEA)

plasma membrane (IBA,TAS)

Molecular Function

ligand-gated sodium channel activity (IBA)

monoatomic ion channel activity (TAS)

protein binding (IPI)

sodium channel activity (IEA)

sodium ion transmembrane transporter activity (TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Polydactyly (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:9847074	PMID:10852210	PMID:11571555	PMID:12477932	PMID:15489334	PMID:15815621	PMID:17207965	PMID:18662336	PMID:21873635	PMID:24705354	PMID:26667795	PMID:28514442
PMID:32296183	PMID:32393512	PMID:33961781	PMID:35156780

Genomics

Comparative Map Data

ASIC4
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	219,507,093 - 219,538,772 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	219,514,170 - 219,538,772 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	220,379,204 - 220,403,494 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	220,087,296 - 220,111,738 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	214,148,884 - 214,173,457 (+)	NCBI		Celera
Cytogenetic Map	2	q35	NCBI
HuRef	2	212,231,962 - 212,256,523 (+)	NCBI		HuRef
CHM1_1	2	220,384,734 - 220,409,316 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	219,991,838 - 220,023,471 (+)	NCBI		T2T-CHM13v2.0

Asic4
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	1	75,426,467 - 75,450,984 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	1	75,427,080 - 75,450,987 (+)	Ensembl		GRCm39 Ensembl
GRCm38	1	75,450,510 - 75,474,340 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	1	75,450,436 - 75,474,343 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	1	75,447,085 - 75,470,915 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	1	75,333,847 - 75,357,488 (+)	NCBI		MGSCv36	mm8
Celera	1	75,941,575 - 75,963,693 (+)	NCBI		Celera
Cytogenetic Map	1	C4	NCBI
cM Map	1	39.08	NCBI

Asic4
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	9	84,389,610 - 84,411,545 (+)	NCBI		GRCr8
mRatBN7.2	9	76,941,532 - 76,962,900 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	9	76,941,532 - 76,962,900 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	9	85,385,842 - 85,407,158 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	9	90,514,723 - 90,536,037 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	9	88,900,898 - 88,922,216 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	9	82,647,071 - 82,668,920 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	9	82,647,071 - 82,668,920 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	9	82,412,948 - 82,438,181 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	9	74,728,291 - 74,749,661 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	9	74,875,294 - 74,896,710 (+)	NCBI
Celera	9	74,511,463 - 74,532,798 (+)	NCBI		Celera
Cytogenetic Map	9	q33	NCBI

Asic4
(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_004955453	13,935,826 - 13,961,664 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955453	13,937,745 - 13,961,664 (-)	NCBI	ChiLan1.0	ChiLan1.0

ASIC4
(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	13	122,142,061 - 122,168,942 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2B	122,157,383 - 122,183,950 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2B	106,770,714 - 106,796,044 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2B	225,361,131 - 225,386,087 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2B	225,361,477 - 225,386,081 (+)	Ensembl	panpan1.1		panPan2

ASIC4
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	37	26,024,136 - 26,048,060 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	37	26,024,947 - 26,048,077 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	37	26,849,461 - 26,873,031 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	37	26,039,062 - 26,062,668 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	37	26,039,987 - 26,063,158 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	37	25,942,213 - 25,966,226 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	37	25,879,090 - 25,902,650 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	37	25,899,663 - 25,923,239 (+)	NCBI		UU_Cfam_GSD_1.0

Asic4
(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_024405303	175,553,612 - 175,576,041 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936569	1,896,395 - 1,918,847 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936569	1,894,631 - 1,918,822 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ASIC4
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	15	121,522,550 - 121,547,497 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	15	121,520,003 - 121,547,520 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	15	134,594,197 - 134,626,509 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ASIC4
(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	10	105,406,889 - 105,433,792 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666040	93,967,447 - 93,992,202 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Asic4
(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_004624823	5,523,185 - 5,544,956 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624823	5,523,166 - 5,544,982 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ASIC4
11 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3	copy number gain	See cases [RCV000051119]	Chr2:194898783..236473913 [GRCh38] Chr2:195763507..237382556 [GRCh37] Chr2:195471752..237047295 [NCBI36] Chr2:2q32.3-37.3	pathogenic
GRCh38/hg38 2q35-36.3(chr2:219081620-225430308)x1	copy number loss	See cases [RCV000052634]	Chr2:219081620..225430308 [GRCh38] Chr2:219946342..226295024 [GRCh37] Chr2:219654586..226003268 [NCBI36] Chr2:2q35-36.3	pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3	copy number gain	See cases [RCV000052958]	Chr2:188818195..242065208 [GRCh38] Chr2:189682921..243007359 [GRCh37] Chr2:189391166..242656032 [NCBI36] Chr2:2q32.2-37.3	pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	copy number gain	See cases [RCV000052959]	Chr2:190310736..241892770 [GRCh38] Chr2:191175462..242834921 [GRCh37] Chr2:190883707..242483594 [NCBI36] Chr2:2q32.2-37.3	pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:193122313-241074980)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]\|See cases [RCV000052960]	Chr2:193122313..241074980 [GRCh38] Chr2:193987039..242014395 [GRCh37] Chr2:193695284..241663068 [NCBI36] Chr2:2q32.3-37.3	pathogenic
GRCh38/hg38 2q34-36.3(chr2:212614422-227121230)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052964]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052964]\|See cases [RCV000052964]	Chr2:212614422..227121230 [GRCh38] Chr2:213479146..227985946 [GRCh37] Chr2:213187391..227694190 [NCBI36] Chr2:2q34-36.3	pathogenic
GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3	copy number gain	See cases [RCV000135934]	Chr2:210579676..242126245 [GRCh38] Chr2:211444400..243059659 [GRCh37] Chr2:211152645..242717069 [NCBI36] Chr2:2q34-37.3	pathogenic
GRCh38/hg38 2q35(chr2:219081620-219758878)x3	copy number gain	See cases [RCV000138093]	Chr2:219081620..219758878 [GRCh38] Chr2:219946342..220623600 [GRCh37] Chr2:219654586..220331844 [NCBI36] Chr2:2q35	uncertain significance
GRCh38/hg38 2q31.3-36.2(chr2:180513793-224302848)x3	copy number gain	See cases [RCV000139446]	Chr2:180513793..224302848 [GRCh38] Chr2:181378520..225167565 [GRCh37] Chr2:181086765..224875809 [NCBI36] Chr2:2q31.3-36.2	pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3	copy number gain	See cases [RCV000142307]	Chr2:189436149..241841232 [GRCh38] Chr2:190300875..242783384 [GRCh37] Chr2:190009120..242432057 [NCBI36] Chr2:2q32.2-37.3	pathogenic
GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3	copy number gain	See cases [RCV000143216]	Chr2:218101759..242126245 [GRCh38] Chr2:218966482..243059659 [GRCh37] Chr2:218674727..242717069 [NCBI36] Chr2:2q35-37.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q35-37.3(chr2:219966808-237815985)x3	copy number gain	See cases [RCV000448049]	Chr2:219966808..237815985 [GRCh37] Chr2:2q35-37.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q34-37.3(chr2:213518431-242783384)x3	copy number gain	See cases [RCV000512009]	Chr2:213518431..242783384 [GRCh37] Chr2:2q34-37.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q35-36.3(chr2:217374144-227643620)x1	copy number loss	not provided [RCV000585275]	Chr2:217374144..227643620 [GRCh37] Chr2:2q35-36.3	likely pathogenic
GRCh37/hg19 2q35-37.3(chr2:219225872-242016876)x3	copy number gain	not provided [RCV000682170]	Chr2:219225872..242016876 [GRCh37] Chr2:2q35-37.3	pathogenic
GRCh37/hg19 2q35-36.3(chr2:218813434-227450699)x1	copy number loss	not provided [RCV000682163]	Chr2:218813434..227450699 [GRCh37] Chr2:2q35-36.3	pathogenic
Single allele	deletion	Polydactyly [RCV000736029]	Chr2:219925666..220914504 [GRCh37] Chr2:2q35	pathogenic
Single allele	duplication	Neurodevelopmental disorder [RCV000787403]	Chr2:188926928..225298653 [GRCh37] Chr2:2q32.1-36.2	pathogenic
NM_018674.6(ASIC4):c.381A>G (p.Ala127=)	single nucleotide variant	not provided [RCV000946682]	Chr2:219515105 [GRCh38] Chr2:220379827 [GRCh37] Chr2:2q35	benign
NM_018674.6(ASIC4):c.1104G>A (p.Pro368=)	single nucleotide variant	not provided [RCV000908087]	Chr2:219535199 [GRCh38] Chr2:220399921 [GRCh37] Chr2:2q35	likely benign
NM_018674.6(ASIC4):c.98T>C (p.Val33Ala)	single nucleotide variant	not provided [RCV000964168]	Chr2:219514822 [GRCh38] Chr2:220379544 [GRCh37] Chr2:2q35	likely benign
GRCh37/hg19 2q34-37.3(chr2:210779657-239879183)x3	copy number gain	See cases [RCV000790568]	Chr2:210779657..239879183 [GRCh37] Chr2:2q34-37.3	pathogenic
NM_018674.6(ASIC4):c.735G>A (p.Thr245=)	single nucleotide variant	not provided [RCV000927248]	Chr2:219532008 [GRCh38] Chr2:220396730 [GRCh37] Chr2:2q35	likely benign
NM_018674.6(ASIC4):c.339G>A (p.Pro113=)	single nucleotide variant	not provided [RCV000887384]	Chr2:219515063 [GRCh38] Chr2:220379785 [GRCh37] Chr2:2q35	benign
NM_018674.6(ASIC4):c.892G>A (p.Ala298Thr)	single nucleotide variant	not provided [RCV000887385]	Chr2:219532351 [GRCh38] Chr2:220397073 [GRCh37] Chr2:2q35	benign
NM_018674.6(ASIC4):c.1425G>T (p.Arg475=)	single nucleotide variant	not provided [RCV000886435]	Chr2:219537655 [GRCh38] Chr2:220402377 [GRCh37] Chr2:2q35	benign
GRCh37/hg19 2q35(chr2:216883237-220953003)x3	copy number gain	not provided [RCV001007510]	Chr2:216883237..220953003 [GRCh37] Chr2:2q35	pathogenic
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3	copy number gain	See cases [RCV001263052]	Chr2:178397959..243007457 [GRCh37] Chr2:2q31.2-37.3	pathogenic
GRCh37/hg19 2q34-35(chr2:215122019-220397907)x1	copy number loss	not provided [RCV001259180]	Chr2:215122019..220397907 [GRCh37] Chr2:2q34-35	likely pathogenic
GRCh37/hg19 2q35-36.3(chr2:220056891-227164817)x1	copy number loss	not provided [RCV001537914]	Chr2:220056891..227164817 [GRCh37] Chr2:2q35-36.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2q35-37.3(chr2:219606537-239217703)	copy number loss	not specified [RCV002053285]	Chr2:219606537..239217703 [GRCh37] Chr2:2q35-37.3	pathogenic
GRCh37/hg19 2q34-36.1(chr2:215108009-221679980)	copy number gain	not specified [RCV002053282]	Chr2:215108009..221679980 [GRCh37] Chr2:2q34-36.1	pathogenic
NC_000002.11:g.(?_218999525)_(220435954_?)dup	duplication	Alacrima, achalasia, and intellectual disability syndrome [RCV001955103]\|Paroxysmal nonkinesigenic dyskinesia [RCV001962531]	Chr2:218999525..220435954 [GRCh37] Chr2:2q35	uncertain significance
GRCh37/hg19 2q32.1-36.1(chr2:186698504-223918111)x3	copy number gain	See cases [RCV003329558]	Chr2:186698504..223918111 [GRCh37] Chr2:2q32.1-36.1	pathogenic
GRCh37/hg19 2q35-37.3(chr2:218376403-242783384)x3	copy number gain	not provided [RCV003484087]	Chr2:218376403..242783384 [GRCh37] Chr2:2q35-37.3	pathogenic
GRCh37/hg19 2q35(chr2:220169575-220625221)x3	copy number gain	not provided [RCV003484089]	Chr2:220169575..220625221 [GRCh37] Chr2:2q35	uncertain significance
GRCh37/hg19 2q35(chr2:220368252-221475943)x3	copy number gain	not provided [RCV003484090]	Chr2:220368252..221475943 [GRCh37] Chr2:2q35	uncertain significance
GRCh37/hg19 2q35-37.3(chr2:216815496-242782258)x3	copy number gain	See cases [RCV004442836]	Chr2:216815496..242782258 [GRCh37] Chr2:2q35-37.3	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2332
Count of miRNA genes:	727
Interacting mature miRNAs:	877
Transcripts:	ENST00000347842, ENST00000358078, ENST00000461395, ENST00000473709, ENST00000474489
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.

Markers in Region

SHGC-79532

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,211 - 220,390,496	UniSTS	GRCh37
Build 36	2	220,098,455 - 220,098,740	RGD	NCBI36
Celera	2	214,160,194 - 214,160,479	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,243,253 - 212,243,538	UniSTS

ECD00429

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,353 - 220,391,260	UniSTS	GRCh37
Build 36	2	220,098,597 - 220,099,504	RGD	NCBI36
Celera	2	214,160,336 - 214,161,243	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,243,395 - 212,244,302	UniSTS

ECD00516

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,391,404 - 220,392,305	UniSTS	GRCh37
Build 36	2	220,099,648 - 220,100,549	RGD	NCBI36
Celera	2	214,161,387 - 214,162,288	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,244,446 - 212,245,347	UniSTS

ECD00921

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,403,069 - 220,403,953	UniSTS	GRCh37
Build 36	2	220,111,313 - 220,112,197	RGD	NCBI36
Celera	2	214,173,032 - 214,173,916	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,256,098 - 212,256,982	UniSTS

ECD01931

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,401,177 - 220,402,024	UniSTS	GRCh37
Build 36	2	220,109,421 - 220,110,268	RGD	NCBI36
Celera	2	214,171,140 - 214,171,987	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,254,206 - 212,255,053	UniSTS

ECD02440

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,132 - 220,402,961	UniSTS	GRCh37
Build 36	2	220,110,376 - 220,111,205	RGD	NCBI36
Celera	2	214,172,095 - 214,172,924	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,255,161 - 212,255,990	UniSTS

ECD02842

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,949 - 220,382,764	UniSTS	GRCh37
Build 36	2	220,090,193 - 220,091,008	RGD	NCBI36
Celera	2	214,151,941 - 214,152,756	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,235,019 - 212,235,834	UniSTS

ECD05191

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,377,557 - 220,378,299	UniSTS	GRCh37
Build 36	2	220,085,801 - 220,086,543	RGD	NCBI36
Celera	2	214,147,549 - 214,148,291	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,230,627 - 212,231,369	UniSTS

ECD05447

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,378,319 - 220,379,054	UniSTS	GRCh37
Build 36	2	220,086,563 - 220,087,298	RGD	NCBI36
Celera	2	214,148,311 - 214,149,046	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,231,389 - 212,232,124	UniSTS

ECD06448

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,015 - 220,380,723	UniSTS	GRCh37
Build 36	2	220,088,259 - 220,088,967	RGD	NCBI36
Celera	2	214,150,007 - 214,150,715	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,085 - 212,233,793	UniSTS

ECD07361

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,304 - 220,379,987	UniSTS	GRCh37
Build 36	2	220,087,548 - 220,088,231	RGD	NCBI36
Celera	2	214,149,296 - 214,149,979	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,232,374 - 212,233,057	UniSTS

ECD09490

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,394,482 - 220,395,109	UniSTS	GRCh37
Build 36	2	220,102,726 - 220,103,353	RGD	NCBI36
Celera	2	214,164,465 - 214,165,092	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,247,524 - 212,248,151	UniSTS

ECD11013

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,386,311 - 220,386,895	UniSTS	GRCh37
Build 36	2	220,094,555 - 220,095,139	RGD	NCBI36
Celera	2	214,156,303 - 214,156,878	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,239,381 - 212,239,938	UniSTS

ECD12036

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,385,739 - 220,386,293	UniSTS	GRCh37
Build 36	2	220,093,983 - 220,094,537	RGD	NCBI36
Celera	2	214,155,731 - 214,156,285	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,809 - 212,239,363	UniSTS

ECD13526

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,355 - 220,396,870	UniSTS	GRCh37
Build 36	2	220,104,599 - 220,105,114	RGD	NCBI36
Celera	2	214,166,338 - 214,166,853	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,397 - 212,249,912	UniSTS

ECD14175

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,456 - 220,384,955	UniSTS	GRCh37
Build 36	2	220,092,700 - 220,093,199	RGD	NCBI36
Celera	2	214,154,448 - 214,154,947	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,237,526 - 212,238,025	UniSTS

ECD14308

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,387,518 - 220,388,014	UniSTS	GRCh37
Build 36	2	220,095,762 - 220,096,258	RGD	NCBI36
Celera	2	214,157,501 - 214,157,997	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,240,561 - 212,241,057	UniSTS

ECD14536

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,399,550 - 220,400,041	UniSTS	GRCh37
Build 36	2	220,107,794 - 220,108,285	RGD	NCBI36
Celera	2	214,169,513 - 214,170,004	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,252,578 - 212,253,070	UniSTS

ECD15010

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,833 - 220,381,313	UniSTS	GRCh37
Build 36	2	220,089,077 - 220,089,557	RGD	NCBI36
Celera	2	214,150,825 - 214,151,305	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,903 - 212,234,383	UniSTS

ECD15141

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,030 - 220,388,507	UniSTS	GRCh37
Build 36	2	220,096,274 - 220,096,751	RGD	NCBI36
Celera	2	214,158,013 - 214,158,490	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,241,073 - 212,241,550	UniSTS

ECD15304

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,904 - 220,397,377	UniSTS	GRCh37
Build 36	2	220,105,148 - 220,105,621	RGD	NCBI36
Celera	2	214,166,887 - 214,167,360	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,946 - 212,250,419	UniSTS

ECD15550

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,340 - 220,381,807	UniSTS	GRCh37
Build 36	2	220,089,584 - 220,090,051	RGD	NCBI36
Celera	2	214,151,332 - 214,151,799	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,234,410 - 212,234,877	UniSTS

ECD16096

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,382,986 - 220,383,439	UniSTS	GRCh37
Build 36	2	220,091,230 - 220,091,683	RGD	NCBI36
Celera	2	214,152,978 - 214,153,431	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,236,056 - 212,236,509	UniSTS

ECD16623

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,385,059 - 220,385,491	UniSTS	GRCh37
Build 36	2	220,093,303 - 220,093,735	RGD	NCBI36
Celera	2	214,155,051 - 214,155,483	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,129 - 212,238,561	UniSTS

ECD18409

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,393,973 - 220,394,333	UniSTS	GRCh37
Build 36	2	220,102,217 - 220,102,577	RGD	NCBI36
Celera	2	214,163,956 - 214,164,316	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,247,015 - 212,247,375	UniSTS

ECD19807

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,555 - 220,397,863	UniSTS	GRCh37
Build 36	2	220,105,799 - 220,106,107	RGD	NCBI36
Celera	2	214,167,538 - 214,167,846	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,250,597 - 212,250,905	UniSTS

ECD21993

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,796 - 220,401,028	UniSTS	GRCh37
Build 36	2	220,109,040 - 220,109,272	RGD	NCBI36
Celera	2	214,170,759 - 214,170,991	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,253,825 - 212,254,057	UniSTS

ECD22356

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,389,453 - 220,389,674	UniSTS	GRCh37
Build 36	2	220,097,697 - 220,097,918	RGD	NCBI36
Celera	2	214,159,436 - 214,159,657	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,242,495 - 212,242,716	UniSTS

ECD22554

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,392,715 - 220,392,930	UniSTS	GRCh37
Build 36	2	220,100,959 - 220,101,174	RGD	NCBI36
Celera	2	214,162,698 - 214,162,913	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,245,757 - 212,245,972	UniSTS

ECD22625

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,038 - 220,384,251	UniSTS	GRCh37
Build 36	2	220,092,282 - 220,092,495	RGD	NCBI36
Celera	2	214,154,030 - 214,154,243	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,237,108 - 212,237,321	UniSTS

ECD22746

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,398,787 - 220,398,996	UniSTS	GRCh37
Build 36	2	220,107,031 - 220,107,240	RGD	NCBI36
Celera	2	214,168,770 - 214,168,979	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,251,831 - 212,252,040	UniSTS

REN53156

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,376,988 - 220,377,239	UniSTS	GRCh37
Build 36	2	220,085,232 - 220,085,483	RGD	NCBI36
Celera	2	214,146,980 - 214,147,231	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,230,058 - 212,230,309	UniSTS

REN53157

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,377,237 - 220,377,486	UniSTS	GRCh37
Build 36	2	220,085,481 - 220,085,730	RGD	NCBI36
Celera	2	214,147,229 - 214,147,478	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,230,307 - 212,230,556	UniSTS

REN53158

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,377,461 - 220,377,700	UniSTS	GRCh37
Build 36	2	220,085,705 - 220,085,944	RGD	NCBI36
Celera	2	214,147,453 - 214,147,692	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,230,531 - 212,230,770	UniSTS

REN53159

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,377,690 - 220,377,939	UniSTS	GRCh37
Build 36	2	220,085,934 - 220,086,183	RGD	NCBI36
Celera	2	214,147,682 - 214,147,931	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,230,760 - 212,231,009	UniSTS

REN53160

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,377,918 - 220,378,168	UniSTS	GRCh37
Build 36	2	220,086,162 - 220,086,412	RGD	NCBI36
Celera	2	214,147,910 - 214,148,160	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,230,988 - 212,231,238	UniSTS

REN53161

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,378,134 - 220,378,381	UniSTS	GRCh37
Build 36	2	220,086,378 - 220,086,625	RGD	NCBI36
Celera	2	214,148,126 - 214,148,373	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,231,204 - 212,231,451	UniSTS

REN53162

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,378,350 - 220,378,610	UniSTS	GRCh37
Build 36	2	220,086,594 - 220,086,854	RGD	NCBI36
Celera	2	214,148,342 - 214,148,602	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,231,420 - 212,231,680	UniSTS

REN53163

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,378,584 - 220,378,837	UniSTS	GRCh37
Build 36	2	220,086,828 - 220,087,081	RGD	NCBI36
Celera	2	214,148,576 - 214,148,829	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,231,654 - 212,231,907	UniSTS

REN53164

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,378,812 - 220,379,049	UniSTS	GRCh37
Build 36	2	220,087,056 - 220,087,293	RGD	NCBI36
Celera	2	214,148,804 - 214,149,041	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,231,882 - 212,232,119	UniSTS

REN53165

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,016 - 220,379,284	UniSTS	GRCh37
Build 36	2	220,087,260 - 220,087,528	RGD	NCBI36
Celera	2	214,149,008 - 214,149,276	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,232,086 - 212,232,354	UniSTS

REN53166

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,265 - 220,379,514	UniSTS	GRCh37
Build 36	2	220,087,509 - 220,087,758	RGD	NCBI36
Celera	2	214,149,257 - 214,149,506	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,232,335 - 212,232,584	UniSTS

REN53167

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,468 - 220,379,737	UniSTS	GRCh37
Build 36	2	220,087,712 - 220,087,981	RGD	NCBI36
Celera	2	214,149,460 - 214,149,729	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,232,538 - 212,232,807	UniSTS

REN53168

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,733 - 220,379,992	UniSTS	GRCh37
Build 36	2	220,087,977 - 220,088,236	RGD	NCBI36
Celera	2	214,149,725 - 214,149,984	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,232,803 - 212,233,062	UniSTS

REN53169

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,973 - 220,380,235	UniSTS	GRCh37
Build 36	2	220,088,217 - 220,088,479	RGD	NCBI36
Celera	2	214,149,965 - 214,150,227	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,043 - 212,233,305	UniSTS

REN53170

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,204 - 220,380,436	UniSTS	GRCh37
Build 36	2	220,088,448 - 220,088,680	RGD	NCBI36
Celera	2	214,150,196 - 214,150,428	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,274 - 212,233,506	UniSTS

REN53171

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,421 - 220,380,645	UniSTS	GRCh37
Build 36	2	220,088,665 - 220,088,889	RGD	NCBI36
Celera	2	214,150,413 - 214,150,637	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,491 - 212,233,715	UniSTS

REN53172

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,629 - 220,380,879	UniSTS	GRCh37
Build 36	2	220,088,873 - 220,089,123	RGD	NCBI36
Celera	2	214,150,621 - 214,150,871	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,699 - 212,233,949	UniSTS

REN53173

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,867 - 220,381,120	UniSTS	GRCh37
Build 36	2	220,089,111 - 220,089,364	RGD	NCBI36
Celera	2	214,150,859 - 214,151,112	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,233,937 - 212,234,190	UniSTS

REN53174

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,063 - 220,381,313	UniSTS	GRCh37
Build 36	2	220,089,307 - 220,089,557	RGD	NCBI36
Celera	2	214,151,055 - 214,151,305	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,234,133 - 212,234,383	UniSTS

REN53175

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,290 - 220,381,545	UniSTS	GRCh37
Build 36	2	220,089,534 - 220,089,789	RGD	NCBI36
Celera	2	214,151,282 - 214,151,537	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,234,360 - 212,234,615	UniSTS

REN53176

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,522 - 220,381,778	UniSTS	GRCh37
Build 36	2	220,089,766 - 220,090,022	RGD	NCBI36
Celera	2	214,151,514 - 214,151,770	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,234,592 - 212,234,848	UniSTS

REN53177

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,717 - 220,381,979	UniSTS	GRCh37
Build 36	2	220,089,961 - 220,090,223	RGD	NCBI36
Celera	2	214,151,709 - 214,151,971	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,234,787 - 212,235,049	UniSTS

REN53178

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,976 - 220,382,229	UniSTS	GRCh37
Build 36	2	220,090,220 - 220,090,473	RGD	NCBI36
Celera	2	214,151,968 - 214,152,221	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,235,046 - 212,235,299	UniSTS

REN53179

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,382,209 - 220,382,457	UniSTS	GRCh37
Build 36	2	220,090,453 - 220,090,701	RGD	NCBI36
Celera	2	214,152,201 - 214,152,449	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,235,279 - 212,235,527	UniSTS

REN53180

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,382,450 - 220,382,674	UniSTS	GRCh37
Build 36	2	220,090,694 - 220,090,918	RGD	NCBI36
Celera	2	214,152,442 - 214,152,666	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,235,520 - 212,235,744	UniSTS

REN53181

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,382,671 - 220,382,939	UniSTS	GRCh37
Build 36	2	220,090,915 - 220,091,183	RGD	NCBI36
Celera	2	214,152,663 - 214,152,931	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,235,741 - 212,236,009	UniSTS

REN53182

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,382,927 - 220,383,160	UniSTS	GRCh37
Build 36	2	220,091,171 - 220,091,404	RGD	NCBI36
Celera	2	214,152,919 - 214,153,152	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,235,997 - 212,236,230	UniSTS

REN53183

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,383,131 - 220,383,378	UniSTS	GRCh37
Build 36	2	220,091,375 - 220,091,622	RGD	NCBI36
Celera	2	214,153,123 - 214,153,370	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,236,201 - 212,236,448	UniSTS

REN53184

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,383,332 - 220,383,580	UniSTS	GRCh37
Build 36	2	220,091,576 - 220,091,824	RGD	NCBI36
Celera	2	214,153,324 - 214,153,572	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,236,402 - 212,236,650	UniSTS

REN53185

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,383,420 - 220,383,670	UniSTS	GRCh37
Build 36	2	220,091,664 - 220,091,914	RGD	NCBI36
Celera	2	214,153,412 - 214,153,662	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,236,490 - 212,236,740	UniSTS

REN53186

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,383,887 - 220,384,124	UniSTS	GRCh37
Build 36	2	220,092,131 - 220,092,368	RGD	NCBI36
Celera	2	214,153,879 - 214,154,116	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,236,957 - 212,237,194	UniSTS

REN53187

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,100 - 220,384,342	UniSTS	GRCh37
Build 36	2	220,092,344 - 220,092,586	RGD	NCBI36
Celera	2	214,154,092 - 214,154,334	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,237,170 - 212,237,412	UniSTS

REN53188

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,312 - 220,384,579	UniSTS	GRCh37
Build 36	2	220,092,556 - 220,092,823	RGD	NCBI36
Celera	2	214,154,304 - 214,154,571	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,237,382 - 212,237,649	UniSTS

REN53189

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,576 - 220,384,801	UniSTS	GRCh37
Build 36	2	220,092,820 - 220,093,045	RGD	NCBI36
Celera	2	214,154,568 - 214,154,793	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,237,646 - 212,237,871	UniSTS

REN53190

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,776 - 220,385,003	UniSTS	GRCh37
Build 36	2	220,093,020 - 220,093,247	RGD	NCBI36
Celera	2	214,154,768 - 214,154,995	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,237,846 - 212,238,073	UniSTS

REN53191

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,986 - 220,385,211	UniSTS	GRCh37
Build 36	2	220,093,230 - 220,093,455	RGD	NCBI36
Celera	2	214,154,978 - 214,155,203	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,056 - 212,238,281	UniSTS

REN53192

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,385,188 - 220,385,456	UniSTS	GRCh37
Build 36	2	220,093,432 - 220,093,700	RGD	NCBI36
Celera	2	214,155,180 - 214,155,448	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,258 - 212,238,526	UniSTS

REN53193

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,385,445 - 220,385,690	UniSTS	GRCh37
Build 36	2	220,093,689 - 220,093,934	RGD	NCBI36
Celera	2	214,155,437 - 214,155,682	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,515 - 212,238,760	UniSTS

REN53194

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,385,667 - 220,385,922	UniSTS	GRCh37
Build 36	2	220,093,911 - 220,094,166	RGD	NCBI36
Celera	2	214,155,659 - 214,155,914	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,737 - 212,238,992	UniSTS

REN53195

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,385,906 - 220,386,179	UniSTS	GRCh37
Build 36	2	220,094,150 - 220,094,423	RGD	NCBI36
Celera	2	214,155,898 - 214,156,171	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,238,976 - 212,239,249	UniSTS

REN53196

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,386,159 - 220,386,401	UniSTS	GRCh37
Build 36	2	220,094,403 - 220,094,645	RGD	NCBI36
Celera	2	214,156,151 - 214,156,393	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,239,229 - 212,239,471	UniSTS

REN53197

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,386,380 - 220,386,642	UniSTS	GRCh37
Build 36	2	220,094,624 - 220,094,886	RGD	NCBI36
Celera	2	214,156,372 - 214,156,625	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,239,450 - 212,239,685	UniSTS

REN53198

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,386,616 - 220,386,840	UniSTS	GRCh37
Build 36	2	220,094,860 - 220,095,084	RGD	NCBI36
Celera	2	214,156,599 - 214,156,823	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,239,659 - 212,239,883	UniSTS

REN53199

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,386,822 - 220,387,077	UniSTS	GRCh37
Build 36	2	220,095,066 - 220,095,321	RGD	NCBI36
Celera	2	214,156,805 - 214,157,060	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,239,865 - 212,240,120	UniSTS

REN53200

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,387,054 - 220,387,299	UniSTS	GRCh37
Build 36	2	220,095,298 - 220,095,543	RGD	NCBI36
Celera	2	214,157,037 - 214,157,282	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,240,097 - 212,240,342	UniSTS

REN53201

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,387,277 - 220,387,537	UniSTS	GRCh37
Build 36	2	220,095,521 - 220,095,781	RGD	NCBI36
Celera	2	214,157,260 - 214,157,520	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,240,320 - 212,240,580	UniSTS

REN53202

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,387,343 - 220,387,580	UniSTS	GRCh37
Build 36	2	220,095,587 - 220,095,824	RGD	NCBI36
Celera	2	214,157,326 - 214,157,563	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,240,386 - 212,240,623	UniSTS

REN53203

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,387,574 - 220,387,834	UniSTS	GRCh37
Build 36	2	220,095,818 - 220,096,078	RGD	NCBI36
Celera	2	214,157,557 - 214,157,817	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,240,617 - 212,240,877	UniSTS

REN53204

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,387,811 - 220,388,051	UniSTS	GRCh37
Build 36	2	220,096,055 - 220,096,295	RGD	NCBI36
Celera	2	214,157,794 - 214,158,034	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,240,854 - 212,241,094	UniSTS

REN53205

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,030 - 220,388,289	UniSTS	GRCh37
Build 36	2	220,096,274 - 220,096,533	RGD	NCBI36
Celera	2	214,158,013 - 214,158,272	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,241,073 - 212,241,332	UniSTS

REN53206

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,252 - 220,388,494	UniSTS	GRCh37
Build 36	2	220,096,496 - 220,096,738	RGD	NCBI36
Celera	2	214,158,235 - 214,158,477	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,241,295 - 212,241,537	UniSTS

REN53207

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,319 - 220,388,548	UniSTS	GRCh37
Build 36	2	220,096,563 - 220,096,792	RGD	NCBI36
Celera	2	214,158,302 - 214,158,531	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,241,362 - 212,241,591	UniSTS

REN53208

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,522 - 220,388,776	UniSTS	GRCh37
Build 36	2	220,096,766 - 220,097,020	RGD	NCBI36
Celera	2	214,158,505 - 214,158,759	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,241,565 - 212,241,818	UniSTS

REN53209

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,735 - 220,388,994	UniSTS	GRCh37
Build 36	2	220,096,979 - 220,097,238	RGD	NCBI36
Celera	2	214,158,718 - 214,158,977	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,241,777 - 212,242,036	UniSTS

REN53210

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,988 - 220,389,221	UniSTS	GRCh37
Build 36	2	220,097,232 - 220,097,465	RGD	NCBI36
Celera	2	214,158,971 - 214,159,204	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,242,030 - 212,242,263	UniSTS

REN53211

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,389,195 - 220,389,445	UniSTS	GRCh37
Build 36	2	220,097,439 - 220,097,689	RGD	NCBI36
Celera	2	214,159,178 - 214,159,428	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,242,237 - 212,242,487	UniSTS

REN53212

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,389,432 - 220,389,680	UniSTS	GRCh37
Build 36	2	220,097,676 - 220,097,924	RGD	NCBI36
Celera	2	214,159,415 - 214,159,663	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,242,474 - 212,242,722	UniSTS

REN53213

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,389,665 - 220,389,903	UniSTS	GRCh37
Build 36	2	220,097,909 - 220,098,147	RGD	NCBI36
Celera	2	214,159,648 - 214,159,886	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,242,707 - 212,242,945	UniSTS

REN53214

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,389,901 - 220,390,139	UniSTS	GRCh37
Build 36	2	220,098,145 - 220,098,383	RGD	NCBI36
Celera	2	214,159,884 - 214,160,122	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,242,943 - 212,243,181	UniSTS

REN53215

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,137 - 220,390,408	UniSTS	GRCh37
Build 36	2	220,098,381 - 220,098,652	RGD	NCBI36
Celera	2	214,160,120 - 214,160,391	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,243,179 - 212,243,450	UniSTS

REN53216

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,395 - 220,390,637	UniSTS	GRCh37
Build 36	2	220,098,639 - 220,098,881	RGD	NCBI36
Celera	2	214,160,378 - 214,160,620	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,243,437 - 212,243,679	UniSTS

REN53217

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,626 - 220,390,891	UniSTS	GRCh37
Build 36	2	220,098,870 - 220,099,135	RGD	NCBI36
Celera	2	214,160,609 - 214,160,874	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,243,668 - 212,243,933	UniSTS

REN53218

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,879 - 220,391,117	UniSTS	GRCh37
Build 36	2	220,099,123 - 220,099,361	RGD	NCBI36
Celera	2	214,160,862 - 214,161,100	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,243,921 - 212,244,159	UniSTS

REN53219

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,391,103 - 220,391,347	UniSTS	GRCh37
Build 36	2	220,099,347 - 220,099,591	RGD	NCBI36
Celera	2	214,161,086 - 214,161,330	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,244,145 - 212,244,389	UniSTS

REN53220

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,391,338 - 220,391,604	UniSTS	GRCh37
Build 36	2	220,099,582 - 220,099,848	RGD	NCBI36
Celera	2	214,161,321 - 214,161,587	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,244,380 - 212,244,646	UniSTS

REN53221

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,391,582 - 220,391,832	UniSTS	GRCh37
Build 36	2	220,099,826 - 220,100,076	RGD	NCBI36
Celera	2	214,161,565 - 214,161,815	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,244,624 - 212,244,874	UniSTS

REN53222

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,391,812 - 220,392,068	UniSTS	GRCh37
Build 36	2	220,100,056 - 220,100,312	RGD	NCBI36
Celera	2	214,161,795 - 214,162,051	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,244,854 - 212,245,110	UniSTS

REN53223

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,392,045 - 220,392,294	UniSTS	GRCh37
Build 36	2	220,100,289 - 220,100,538	RGD	NCBI36
Celera	2	214,162,028 - 214,162,277	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,245,087 - 212,245,336	UniSTS

REN53224

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,392,291 - 220,392,541	UniSTS	GRCh37
Build 36	2	220,100,535 - 220,100,785	RGD	NCBI36
Celera	2	214,162,274 - 214,162,524	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,245,333 - 212,245,583	UniSTS

REN53225

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,392,497 - 220,392,751	UniSTS	GRCh37
Build 36	2	220,100,741 - 220,100,995	RGD	NCBI36
Celera	2	214,162,480 - 214,162,734	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,245,539 - 212,245,793	UniSTS

REN53226

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,392,715 - 220,392,952	UniSTS	GRCh37
Build 36	2	220,100,959 - 220,101,196	RGD	NCBI36
Celera	2	214,162,698 - 214,162,935	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,245,757 - 212,245,994	UniSTS

REN53227

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,393,493 - 220,393,727	UniSTS	GRCh37
Build 36	2	220,101,737 - 220,101,971	RGD	NCBI36
Celera	2	214,163,476 - 214,163,710	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,246,535 - 212,246,769	UniSTS

REN53228

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,393,701 - 220,393,938	UniSTS	GRCh37
Build 36	2	220,101,945 - 220,102,182	RGD	NCBI36
Celera	2	214,163,684 - 214,163,921	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,246,743 - 212,246,980	UniSTS

REN53229

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,393,924 - 220,394,168	UniSTS	GRCh37
Build 36	2	220,102,168 - 220,102,412	RGD	NCBI36
Celera	2	214,163,907 - 214,164,151	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,246,966 - 212,247,210	UniSTS

REN53230

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,394,160 - 220,394,417	UniSTS	GRCh37
Build 36	2	220,102,404 - 220,102,661	RGD	NCBI36
Celera	2	214,164,143 - 214,164,400	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,247,202 - 212,247,459	UniSTS

REN53231

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,394,407 - 220,394,660	UniSTS	GRCh37
Build 36	2	220,102,651 - 220,102,904	RGD	NCBI36
Celera	2	214,164,390 - 214,164,643	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,247,449 - 212,247,702	UniSTS

REN53232

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,394,626 - 220,394,873	UniSTS	GRCh37
Build 36	2	220,102,870 - 220,103,117	RGD	NCBI36
Celera	2	214,164,609 - 214,164,856	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,247,668 - 212,247,915	UniSTS

REN53233

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,394,847 - 220,395,111	UniSTS	GRCh37
Build 36	2	220,103,091 - 220,103,355	RGD	NCBI36
Celera	2	214,164,830 - 214,165,094	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,247,889 - 212,248,153	UniSTS

REN53234

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,395,088 - 220,395,315	UniSTS	GRCh37
Build 36	2	220,103,332 - 220,103,559	RGD	NCBI36
Celera	2	214,165,071 - 214,165,298	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,248,130 - 212,248,357	UniSTS

REN53235

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,395,302 - 220,395,569	UniSTS	GRCh37
Build 36	2	220,103,546 - 220,103,813	RGD	NCBI36
Celera	2	214,165,285 - 214,165,552	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,248,344 - 212,248,611	UniSTS

REN53236

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,395,558 - 220,395,789	UniSTS	GRCh37
Build 36	2	220,103,802 - 220,104,033	RGD	NCBI36
Celera	2	214,165,541 - 214,165,772	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,248,600 - 212,248,831	UniSTS

REN53237

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,395,766 - 220,395,998	UniSTS	GRCh37
Build 36	2	220,104,010 - 220,104,242	RGD	NCBI36
Celera	2	214,165,749 - 214,165,981	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,248,808 - 212,249,040	UniSTS

REN53238

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,395,964 - 220,396,202	UniSTS	GRCh37
Build 36	2	220,104,208 - 220,104,446	RGD	NCBI36
Celera	2	214,165,947 - 214,166,185	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,006 - 212,249,244	UniSTS

REN53239

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,166 - 220,396,395	UniSTS	GRCh37
Build 36	2	220,104,410 - 220,104,639	RGD	NCBI36
Celera	2	214,166,149 - 214,166,378	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,208 - 212,249,437	UniSTS

REN53240

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,368 - 220,396,630	UniSTS	GRCh37
Build 36	2	220,104,612 - 220,104,874	RGD	NCBI36
Celera	2	214,166,351 - 214,166,613	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,410 - 212,249,672	UniSTS

REN53241

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,623 - 220,396,871	UniSTS	GRCh37
Build 36	2	220,104,867 - 220,105,115	RGD	NCBI36
Celera	2	214,166,606 - 214,166,854	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,665 - 212,249,913	UniSTS

REN53242

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,857 - 220,397,129	UniSTS	GRCh37
Build 36	2	220,105,101 - 220,105,373	RGD	NCBI36
Celera	2	214,166,840 - 214,167,112	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,249,899 - 212,250,171	UniSTS

REN53243

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,107 - 220,397,349	UniSTS	GRCh37
Build 36	2	220,105,351 - 220,105,593	RGD	NCBI36
Celera	2	214,167,090 - 214,167,332	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,250,149 - 212,250,391	UniSTS

REN53244

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,327 - 220,397,579	UniSTS	GRCh37
Build 36	2	220,105,571 - 220,105,823	RGD	NCBI36
Celera	2	214,167,310 - 214,167,562	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,250,369 - 212,250,621	UniSTS

REN53245

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,556 - 220,397,805	UniSTS	GRCh37
Build 36	2	220,105,800 - 220,106,049	RGD	NCBI36
Celera	2	214,167,539 - 214,167,788	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,250,598 - 212,250,847	UniSTS

REN53246

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,781 - 220,398,024	UniSTS	GRCh37
Build 36	2	220,106,025 - 220,106,268	RGD	NCBI36
Celera	2	214,167,764 - 214,168,007	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,250,823 - 212,251,066	UniSTS

REN53247

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,964 - 220,398,230	UniSTS	GRCh37
Build 36	2	220,106,208 - 220,106,474	RGD	NCBI36
Celera	2	214,167,947 - 214,168,213	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,251,006 - 212,251,272	UniSTS

REN53248

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,398,201 - 220,398,462	UniSTS	GRCh37
Build 36	2	220,106,445 - 220,106,706	RGD	NCBI36
Celera	2	214,168,184 - 214,168,445	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,251,243 - 212,251,504	UniSTS

REN53249

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,398,439 - 220,398,682	UniSTS	GRCh37
Build 36	2	220,106,683 - 220,106,926	RGD	NCBI36
Celera	2	214,168,422 - 214,168,665	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,251,481 - 212,251,724	UniSTS

REN53250

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,398,656 - 220,398,906	UniSTS	GRCh37
Build 36	2	220,106,900 - 220,107,150	RGD	NCBI36
Celera	2	214,168,639 - 214,168,889	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,251,698 - 212,251,950	UniSTS

REN53251

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,398,892 - 220,399,144	UniSTS	GRCh37
Build 36	2	220,107,136 - 220,107,388	RGD	NCBI36
Celera	2	214,168,875 - 214,169,127	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,251,936 - 212,252,188	UniSTS

REN53252

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,399,143 - 220,399,391	UniSTS	GRCh37
Build 36	2	220,107,387 - 220,107,635	RGD	NCBI36
Celera	2	214,169,126 - 214,169,374	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,252,187 - 212,252,435	UniSTS

REN53253

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,399,362 - 220,399,610	UniSTS	GRCh37
Build 36	2	220,107,606 - 220,107,854	RGD	NCBI36
Celera	2	214,169,345 - 214,169,573	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,252,406 - 212,252,638	UniSTS

REN53254

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,399,607 - 220,399,878	UniSTS	GRCh37
Build 36	2	220,107,851 - 220,108,122	RGD	NCBI36
Celera	2	214,169,570 - 214,169,841	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,252,635 - 212,252,907	UniSTS

REN53255

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,399,852 - 220,400,140	UniSTS	GRCh37
GRCh37	2	220,399,852 - 220,400,103	UniSTS	GRCh37
Build 36	2	220,108,096 - 220,108,347	RGD	NCBI36
Celera	2	214,169,815 - 214,170,103	UniSTS
Celera	2	214,169,815 - 214,170,066	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,252,881 - 212,253,132	UniSTS
HuRef	2	212,252,881 - 212,253,169	UniSTS

REN53256

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,018 - 220,400,268	UniSTS	GRCh37
Build 36	2	220,108,262 - 220,108,512	RGD	NCBI36
Celera	2	214,169,981 - 214,170,231	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,253,047 - 212,253,297	UniSTS

REN53257

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,244 - 220,400,488	UniSTS	GRCh37
Build 36	2	220,108,488 - 220,108,732	RGD	NCBI36
Celera	2	214,170,207 - 214,170,451	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,253,273 - 212,253,517	UniSTS

REN53258

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,434 - 220,400,665	UniSTS	GRCh37
Build 36	2	220,108,678 - 220,108,909	RGD	NCBI36
Celera	2	214,170,397 - 214,170,628	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,253,463 - 212,253,694	UniSTS

REN53259

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,630 - 220,400,898	UniSTS	GRCh37
Build 36	2	220,108,874 - 220,109,142	RGD	NCBI36
Celera	2	214,170,593 - 214,170,861	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,253,659 - 212,253,927	UniSTS

REN53260

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,873 - 220,401,131	UniSTS	GRCh37
Build 36	2	220,109,117 - 220,109,375	RGD	NCBI36
Celera	2	214,170,836 - 214,171,094	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,253,902 - 212,254,160	UniSTS

REN53261

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,401,124 - 220,401,374	UniSTS	GRCh37
Build 36	2	220,109,368 - 220,109,618	RGD	NCBI36
Celera	2	214,171,087 - 214,171,337	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,254,153 - 212,254,403	UniSTS

REN53262

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,401,361 - 220,401,620	UniSTS	GRCh37
Build 36	2	220,109,605 - 220,109,864	RGD	NCBI36
Celera	2	214,171,324 - 214,171,583	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,254,390 - 212,254,649	UniSTS

REN53263

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,401,606 - 220,401,845	UniSTS	GRCh37
Build 36	2	220,109,850 - 220,110,089	RGD	NCBI36
Celera	2	214,171,569 - 214,171,808	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,254,635 - 212,254,874	UniSTS

REN53264

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,401,843 - 220,402,074	UniSTS	GRCh37
Build 36	2	220,110,087 - 220,110,318	RGD	NCBI36
Celera	2	214,171,806 - 214,172,037	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,254,872 - 212,255,103	UniSTS

REN53265

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,056 - 220,402,321	UniSTS	GRCh37
Build 36	2	220,110,300 - 220,110,565	RGD	NCBI36
Celera	2	214,172,019 - 214,172,284	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,255,085 - 212,255,350	UniSTS

REN53266

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,297 - 220,402,537	UniSTS	GRCh37
Build 36	2	220,110,541 - 220,110,781	RGD	NCBI36
Celera	2	214,172,260 - 214,172,500	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,255,326 - 212,255,566	UniSTS

REN53267

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,503 - 220,402,765	UniSTS	GRCh37
Build 36	2	220,110,747 - 220,111,009	RGD	NCBI36
Celera	2	214,172,466 - 214,172,728	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,255,532 - 212,255,794	UniSTS

REN53268

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,746 - 220,402,972	UniSTS	GRCh37
Build 36	2	220,110,990 - 220,111,216	RGD	NCBI36
Celera	2	214,172,709 - 214,172,935	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,255,775 - 212,256,001	UniSTS

REN53269

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,936 - 220,403,169	UniSTS	GRCh37
Build 36	2	220,111,180 - 220,111,413	RGD	NCBI36
Celera	2	214,172,899 - 214,173,132	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,255,965 - 212,256,198	UniSTS

REN53270

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,403,148 - 220,403,394	UniSTS	GRCh37
Build 36	2	220,111,392 - 220,111,638	RGD	NCBI36
Celera	2	214,173,111 - 214,173,357	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,256,177 - 212,256,423	UniSTS

REN53271

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,403,379 - 220,403,630	UniSTS	GRCh37
Build 36	2	220,111,623 - 220,111,874	RGD	NCBI36
Celera	2	214,173,342 - 214,173,593	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,256,408 - 212,256,659	UniSTS

REN53272

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,403,611 - 220,403,859	UniSTS	GRCh37
Build 36	2	220,111,855 - 220,112,103	RGD	NCBI36
Celera	2	214,173,574 - 214,173,822	RGD
Cytogenetic Map	2	q35	UniSTS
HuRef	2	212,256,640 - 212,256,888	UniSTS

ACCN4_8063

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,746 - 220,403,666	UniSTS	GRCh37
Build 36	2	220,110,990 - 220,111,910	RGD	NCBI36
Celera	2	214,172,709 - 214,173,629	RGD
HuRef	2	212,255,775 - 212,256,695	UniSTS

stSG633053

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,377,379 - 220,378,435	UniSTS	GRCh37
Build 36	2	220,085,623 - 220,086,679	RGD	NCBI36
Celera	2	214,147,371 - 214,148,427	RGD
HuRef	2	212,230,449 - 212,231,505	UniSTS

stSG633054

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,378,416 - 220,379,513	UniSTS	GRCh37
Build 36	2	220,086,660 - 220,087,757	RGD	NCBI36
Celera	2	214,148,408 - 214,149,505	RGD
HuRef	2	212,231,486 - 212,232,583	UniSTS

stSG633055

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,379,494 - 220,380,723	UniSTS	GRCh37
Build 36	2	220,087,738 - 220,088,967	RGD	NCBI36
Celera	2	214,149,486 - 214,150,715	RGD
HuRef	2	212,232,564 - 212,233,793	UniSTS

stSG633056

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,380,704 - 220,381,787	UniSTS	GRCh37
Build 36	2	220,088,948 - 220,090,031	RGD	NCBI36
Celera	2	214,150,696 - 214,151,779	RGD
HuRef	2	212,233,774 - 212,234,857	UniSTS

stSG633057

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,381,768 - 220,383,260	UniSTS	GRCh37
Build 36	2	220,090,012 - 220,091,504	RGD	NCBI36
Celera	2	214,151,760 - 214,153,252	RGD
HuRef	2	212,234,838 - 212,236,330	UniSTS

stSG633058

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,383,315 - 220,384,582	UniSTS	GRCh37
Build 36	2	220,091,559 - 220,092,826	RGD	NCBI36
Celera	2	214,153,307 - 214,154,574	RGD
HuRef	2	212,236,385 - 212,237,652	UniSTS

stSG633059

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,384,660 - 220,385,923	UniSTS	GRCh37
Build 36	2	220,092,904 - 220,094,167	RGD	NCBI36
Celera	2	214,154,652 - 214,155,915	RGD
HuRef	2	212,237,730 - 212,238,993	UniSTS

stSG633062

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,388,343 - 220,389,463	UniSTS	GRCh37
Build 36	2	220,096,587 - 220,097,707	RGD	NCBI36
Celera	2	214,158,326 - 214,159,446	RGD
HuRef	2	212,241,386 - 212,242,505	UniSTS

stSG633063

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,389,444 - 220,390,549	UniSTS	GRCh37
Build 36	2	220,097,688 - 220,098,793	RGD	NCBI36
Celera	2	214,159,427 - 214,160,532	RGD
HuRef	2	212,242,486 - 212,243,591	UniSTS

stSG633064

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,390,626 - 220,391,678	UniSTS	GRCh37
Build 36	2	220,098,870 - 220,099,922	RGD	NCBI36
Celera	2	214,160,609 - 214,161,661	RGD
HuRef	2	212,243,668 - 212,244,720	UniSTS

stSG633065

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,391,812 - 220,392,821	UniSTS	GRCh37
Build 36	2	220,100,056 - 220,101,065	RGD	NCBI36
Celera	2	214,161,795 - 214,162,804	RGD
HuRef	2	212,244,854 - 212,245,863	UniSTS

stSG633066

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,392,802 - 220,394,092	UniSTS	GRCh37
Build 36	2	220,101,046 - 220,102,336	RGD	NCBI36
Celera	2	214,162,785 - 214,164,075	RGD
HuRef	2	212,245,844 - 212,247,134	UniSTS

stSG633067

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,394,074 - 220,395,109	UniSTS	GRCh37
Build 36	2	220,102,318 - 220,103,353	RGD	NCBI36
Celera	2	214,164,057 - 214,165,092	RGD
HuRef	2	212,247,116 - 212,248,151	UniSTS

stSG633068

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,395,090 - 220,396,465	UniSTS	GRCh37
Build 36	2	220,103,334 - 220,104,709	RGD	NCBI36
Celera	2	214,165,073 - 214,166,448	RGD
HuRef	2	212,248,132 - 212,249,507	UniSTS

stSG633069

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,396,446 - 220,397,746	UniSTS	GRCh37
Build 36	2	220,104,690 - 220,105,990	RGD	NCBI36
Celera	2	214,166,429 - 214,167,729	RGD
HuRef	2	212,249,488 - 212,250,788	UniSTS

stSG633070

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,397,729 - 220,398,846	UniSTS	GRCh37
Build 36	2	220,105,973 - 220,107,090	RGD	NCBI36
Celera	2	214,167,712 - 214,168,829	RGD
HuRef	2	212,250,771 - 212,251,890	UniSTS

stSG633071

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,398,827 - 220,399,976	UniSTS	GRCh37
Build 36	2	220,107,071 - 220,108,220	RGD	NCBI36
Celera	2	214,168,810 - 214,169,939	RGD
HuRef	2	212,251,871 - 212,253,005	UniSTS

stSG633072

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,400,019 - 220,401,465	UniSTS	GRCh37
Build 36	2	220,108,263 - 220,109,709	RGD	NCBI36
Celera	2	214,169,982 - 214,171,428	RGD
HuRef	2	212,253,048 - 212,254,494	UniSTS

stSG633073

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,401,517 - 220,402,517	UniSTS	GRCh37
Build 36	2	220,109,761 - 220,110,761	RGD	NCBI36
Celera	2	214,171,480 - 214,172,480	RGD
HuRef	2	212,254,546 - 212,255,546	UniSTS

stSG633074

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	220,402,496 - 220,403,524	UniSTS	GRCh37
Build 36	2	220,110,740 - 220,111,768	RGD	NCBI36
Celera	2	214,172,459 - 214,173,487	RGD
HuRef	2	212,255,525 - 212,256,553	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

High

Medium

264

848

Low

372

479

1099

242

2704

739

313

237

817

Below cutoff

1925

2212

976

364

1130

222

3188

1891

173

208

589

1074

151

934

1956

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_018674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_182847	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047444915	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047444916	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047444917	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342837	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342838	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054342840	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC009955	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC053503	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC139723	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ271643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ408881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ408882	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ408883	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ408884	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK308804	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309373	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC010439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC073912	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EL736952	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000347842 ⟹ ENSP00000326627

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	219,514,482 - 219,538,772 (+)	Ensembl

RefSeq Acc Id:

ENST00000358078 ⟹ ENSP00000350786

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	219,514,482 - 219,538,772 (+)	Ensembl

RefSeq Acc Id:

ENST00000461395

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	219,514,170 - 219,534,058 (+)	Ensembl

RefSeq Acc Id:

ENST00000473709

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	219,517,241 - 219,533,031 (+)	Ensembl

RefSeq Acc Id:

ENST00000474489

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	219,517,136 - 219,538,772 (+)	Ensembl

RefSeq Acc Id:

ENST00000693692 ⟹ ENSP00000508764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	219,514,344 - 219,538,772 (+)	Ensembl

RefSeq Acc Id:

NM_018674 ⟹ NP_061144

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,514,482 - 219,538,772 (+)	NCBI
Build 36	2	220,087,296 - 220,111,738 (+)	NCBI Archive
Celera	2	214,148,884 - 214,173,457 (+)	RGD
T2T-CHM13v2.0	2	219,999,227 - 220,023,471 (+)	NCBI

Sequence:

show sequence

GAGGAGAGAGACAAGCGGCAGCAGAGGCAGCAGCGGCAGAGGCAGCACCAGGGCTGCGGAGCTG
CTGGGAGTGGGAGTGACTCCCCCACCTCGGGCCCCCACCCTGTCCCTGTCCTCTTCCCGCTTGC
CCTGAGTTTAGAAGAGCAGCCGCTGCCACCACTGCCACTCGGGAGGGCACCAGGGCTGCTGGCT
AGGGAGGGACAGGGCAGGGAGGCTCTGGCCAGTCCCAGCAGCCGGGGACAGATGCCGATCGAGA
TTGTGTGCAAAATCAAATTTGCTGAGGAGGATGCGAAACCCAAGGAGAAGGAGGCAGGGGATGA
GCAGAGCCTCCTCGGGGCTGTTGCCCCTGGAGCAGCCCCCCGAGACCTGGCCACCTTTGCCAGC
ACCAGCACCCTGCATGGACTGGGCCGGGCCTGTGGCCCAGGCCCCCACGGACTGCGCAGAACCC
TGTGGGCACTGGCCCTACTCACCTCGCTGGCTGCCTTCCTGTACCAGGCGGCTGGCCTGGCCCG
GGGCTACCTGACCCGGCCTCACCTGGTGGCAATGGACCCCGCTGCCCCAGCCCCAGTGGCGGGC
TTCCCGGCTGTCACCCTCTGCAATATCAACCGCTTCCGGCATTCGGCACTCAGCGATGCCGACA
TCTTCCACCTGGCCAATCTGACAGGGCTGCCCCCCAAAGACCGGGATGGGCACCGTGCGGCTGG
CCTGCGCTACCCAGAGCCTGACATGGTAGACATCCTCAACCGCACTGGCCACCAGCTCGCCGAC
ATGCTTAAGAGCTGCAACTTCAGTGGGCATCACTGCTCCGCCAGCAACTTCTCTGTGGTCTATA
CTCGCTATGGGAAGTGTTACACCTTCAACGCGGACCCGCGGAGCTCGCTGCCCAGCCGGGCAGG
GGGCATGGGCAGTGGCCTGGAGATCATGCTGGACATCCAGCAGGAGGAGTACCTGCCCATCTGG
AGGGAGACAAATGAGACGTCGTTTGAGGCAGGTATTCGGGTGCAGATCCACAGCCAGGAGGAGC
CGCCCTACATCCACCAGCTGGGGTTCGGGGTGTCCCCAGGCTTCCAGACCTTTGTGTCCTGCCA
GGAACAGCGGCTGACCTACCTGCCCCAGCCCTGGGGCAACTGCCGCGCAGAGAGTGAGCTCAGG
GAGCCTGAGCTTCAGGGCTACTCGGCCTACAGTGTGTCTGCCTGCCGGCTGCGCTGTGAAAAGG
AGGCCGTGCTTCAGCGCTGCCACTGCCGGATGGTGCACATGCCAGGCAATGAGACCATCTGCCC
ACCAAATATCTACATCGAGTGTGCAGACCACACACTGGACTCCCTGGGTGGGGGCCCTGAGGGC
CCGTGCTTCTGCCCCACCCCCTGCAACCTGACACGCTATGGGAAAGAGATCTCCATGGTCAGGA
TCCCCAACAGGGGCTCAGCCCGGTACCTGGCGAGGAAGTACAACCGCAACGAGACCTACATACG
GGAGAACTTCCTGGTCCTAGATGTCTTCTTTGAGGCCCTGACCTCTGAAGCCATGGAGCAGCGA
GCAGCCTATGGCCTGTCAGCCCTGCTGGGAGACCTCGGGGGACAGATGGGCCTGTTCATTGGGG
CCAGCATCCTCACGTTGCTGGAGATCCTCGACTACATCTATGAGGTGTCCTGGGATCGACTGAA
GCGGGTATGGAGGCGTCCCAAGACCCCCCTGCGGACCTCCACTGGGGGCATCTCCACTTTGGGG
CTTCAGGAGCTGAAGGAACAGAGTCCCTGCCCGAGCCGGGGCCGAGTGGAGGGTGGGGGGGTCA
GCAGTCTGCTCCCCAATCACCACCACCCCCACGGTCCCCCAGGAGGTCTCTTTGAAGATTTTGC
TTGCTAGGACGGTGCTGTGACTGAAAGGACCCAGGAGTCTGGGACCCCTCCTGGGATCCCCAGC
ACATTCTCCTGCTCCTGGGAGAGGCCTGGGGGCGGTGCTCACTGGGAGGGCCAGGACTCAGTTC
CTGCTCTCATCCTCCCCTGCCCTGATGTCAGCTGCTTTGCACAAAGGTCCTTCTTGTCCACACC
CCTTATCCCCAGGCTGGTGCCCCGGGAGGGCTGGAGACCAGGCCATGGGCCCTCACGGAGAGGA
AGGGAAGGAAGGAGAGGGAGGGGGAGGATAGAGCCCATCCCAGCCGGGGAGGGGGAGCCCTCTG
TACATTTGTAAATATTTAGGGAAAGCCGGGTGGGGGGAGGGGATACAGATGTAGAAGGTGGGTA
GGGCTACAGGGGTGGGTGATTTAGGGACAGCCAGGGTCCCAGCCCCAATGTCAGCAGGATAGGG
AGAGCCCCAGGACTCAGGAGTGCTGGGCTGGTCCTACTTCCTGCCCCTCTCCAGGCCCAGCTCC
CCTCTTGGCAGGGGGAGAGGATGGCCCAGCAGGCCTGGCCCAGCTCCCAGTTCCCCCTGCACCA
GCCCCACCCCTAGAGTCCCTTCTATAGGGAGGGGGCAGGAGACCTTCCAGACTTCGGCTGAGCT
TGGAGGGTGGGAAGGGAGCCTTCTCAGTCCTCTCTCCCTCCAGTCTGATTTTATAAAGTGCTGA
CGAGATTGGGAATAAAGAGGCATAAAGAA

hide sequence

RefSeq Acc Id:

NM_182847 ⟹ NP_878267

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,514,482 - 219,538,772 (+)	NCBI
GRCh37	2	220,378,892 - 220,403,494 (+)	RGD
Build 36	2	220,087,296 - 220,111,738 (+)	NCBI Archive
Celera	2	214,148,884 - 214,173,457 (+)	RGD
HuRef	2	212,231,962 - 212,256,523 (+)	ENTREZGENE
CHM1_1	2	220,384,734 - 220,409,316 (+)	NCBI
T2T-CHM13v2.0	2	219,999,227 - 220,023,471 (+)	NCBI

Sequence:

show sequence

GAGGAGAGAGACAAGCGGCAGCAGAGGCAGCAGCGGCAGAGGCAGCACCAGGGCTGCGGAGCTG
CTGGGAGTGGGAGTGACTCCCCCACCTCGGGCCCCCACCCTGTCCCTGTCCTCTTCCCGCTTGC
CCTGAGTTTAGAAGAGCAGCCGCTGCCACCACTGCCACTCGGGAGGGCACCAGGGCTGCTGGCT
AGGGAGGGACAGGGCAGGGAGGCTCTGGCCAGTCCCAGCAGCCGGGGACAGATGCCGATCGAGA
TTGTGTGCAAAATCAAATTTGCTGAGGAGGATGCGAAACCCAAGGAGAAGGAGGCAGGGGATGA
GCAGAGCCTCCTCGGGGCTGTTGCCCCTGGAGCAGCCCCCCGAGACCTGGCCACCTTTGCCAGC
ACCAGCACCCTGCATGGACTGGGCCGGGCCTGTGGCCCAGGCCCCCACGGACTGCGCAGAACCC
TGTGGGCACTGGCCCTACTCACCTCGCTGGCTGCCTTCCTGTACCAGGCGGCTGGCCTGGCCCG
GGGCTACCTGACCCGGCCTCACCTGGTGGCAATGGACCCCGCTGCCCCAGCCCCAGTGGCGGGC
TTCCCGGCTGTCACCCTCTGCAATATCAACCGCTTCCGGCATTCGGCACTCAGCGATGCCGACA
TCTTCCACCTGGCCAATCTGACAGGGCTGCCCCCCAAAGACCGGGATGGGCACCGTGCGGCTGG
CCTGCGCTACCCAGAGCCTGACATGGTAGACATCCTCAACCGCACTGGCCACCAGCTCGCCGAC
ATGCTTAAGAGCTGCAACTTCAGTGGGCATCACTGCTCCGCCAGCAACTTCTCTGTGGTCTATA
CTCGCTATGGGAAGTGTTACACCTTCAACGCGGACCCGCGGAGCTCGCTGCCCAGCCGGGCAGG
GGGCATGGGCAGTGGCCTGGAGATCATGCTGGACATCCAGCAGGAGGAGTACCTGCCCATCTGG
AGGGAGACAAATGAGACGTCGTTTGAGGCAGGTATTCGGGTGCAGATCCACAGCCAGGAGGAGC
CGCCCTACATCCACCAGCTGGGGTTCGGGGTGTCCCCAGGCTTCCAGACCTTTGTGTCCTGCCA
GGAACAGCGGCTGACCTACCTGCCCCAGCCCTGGGGCAACTGCCGCGCAGAGAGTGAGCTCAGG
GAGCCTGAGCTTCAGGGCTACTCGGCCTACAGTGTGTCTGCCTGCCGGCTGCGCTGTGAAAAGG
AGGCCGTGCTTCAGCGCTGCCACTGCCGGATGGTGCACATGCCAGACTCCCTGGGTGGGGGCCC
TGAGGGCCCGTGCTTCTGCCCCACCCCCTGCAACCTGACACGCTATGGGAAAGAGATCTCCATG
GTCAGGATCCCCAACAGGGGCTCAGCCCGGTACCTGGCGAGGAAGTACAACCGCAACGAGACCT
ACATACGGGAGAACTTCCTGGTCCTAGATGTCTTCTTTGAGGCCCTGACCTCTGAAGCCATGGA
GCAGCGAGCAGCCTATGGCCTGTCAGCCCTGCTGGGAGACCTCGGGGGACAGATGGGCCTGTTC
ATTGGGGCCAGCATCCTCACGTTGCTGGAGATCCTCGACTACATCTATGAGGTGTCCTGGGATC
GACTGAAGCGGGTATGGAGGCGTCCCAAGACCCCCCTGCGGACCTCCACTGGGGGCATCTCCAC
TTTGGGGCTTCAGGAGCTGAAGGAACAGAGTCCCTGCCCGAGCCGGGGCCGAGTGGAGGGTGGG
GGGGTCAGCAGTCTGCTCCCCAATCACCACCACCCCCACGGTCCCCCAGGAGGTCTCTTTGAAG
ATTTTGCTTGCTAGGACGGTGCTGTGACTGAAAGGACCCAGGAGTCTGGGACCCCTCCTGGGAT
CCCCAGCACATTCTCCTGCTCCTGGGAGAGGCCTGGGGGCGGTGCTCACTGGGAGGGCCAGGAC
TCAGTTCCTGCTCTCATCCTCCCCTGCCCTGATGTCAGCTGCTTTGCACAAAGGTCCTTCTTGT
CCACACCCCTTATCCCCAGGCTGGTGCCCCGGGAGGGCTGGAGACCAGGCCATGGGCCCTCACG
GAGAGGAAGGGAAGGAAGGAGAGGGAGGGGGAGGATAGAGCCCATCCCAGCCGGGGAGGGGGAG
CCCTCTGTACATTTGTAAATATTTAGGGAAAGCCGGGTGGGGGGAGGGGATACAGATGTAGAAG
GTGGGTAGGGCTACAGGGGTGGGTGATTTAGGGACAGCCAGGGTCCCAGCCCCAATGTCAGCAG
GATAGGGAGAGCCCCAGGACTCAGGAGTGCTGGGCTGGTCCTACTTCCTGCCCCTCTCCAGGCC
CAGCTCCCCTCTTGGCAGGGGGAGAGGATGGCCCAGCAGGCCTGGCCCAGCTCCCAGTTCCCCC
TGCACCAGCCCCACCCCTAGAGTCCCTTCTATAGGGAGGGGGCAGGAGACCTTCCAGACTTCGG
CTGAGCTTGGAGGGTGGGAAGGGAGCCTTCTCAGTCCTCTCTCCCTCCAGTCTGATTTTATAAA
GTGCTGACGAGATTGGGAATAAAGAGGCATAAAGAA

hide sequence

RefSeq Acc Id:

XM_017004439 ⟹ XP_016859928

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,517,205 - 219,538,772 (+)	NCBI

Sequence:

show sequence

GGAAGGGTGATGAGACCTCAGTGAGAGGAAAGGAGAGGAAGAGCTGGAGGGGGTGAGGAAGTAA
GGGGAGGGAGGCAGAGGGTTCTGCTTGGTCTCCAGGCTAGGAGGCGGTGCCTGGAGGATACAGG
AACGGGGATCCTCTGATCAAGGCTGGTCTATACTCGCTATGGGAAGTGTTACACCTTCAACGCG
GACCCGCGGAGCTCGCTGCCCAGCCGGGCAGGGGGCATGGGCAGTGGCCTGGAGATCATGCTGG
ACATCCAGCAGGAGGAGTACCTGCCCATCTGGAGGGAGACAAATGAGACGTCGTTTGAGGCAGG
TATTCGGGTGCAGATCCACAGCCAGGAGGAGCCGCCCTACATCCACCAGCTGGGGTTCGGGGTG
TCCCCAGGCTTCCAGACCTTTGTGTCCTGCCAGGAACAGCGGCTGACCTACCTGCCCCAGCCCT
GGGGCAACTGCCGCGCAGAGAGTGAGCTCAGGGAGCCTGAGCTTCAGGGCTACTCGGCCTACAG
TGTGTCTGCCTGCCGGCTGCGCTGTGAAAAGGAGGCCGTGCTTCAGCGCTGCCACTGCCGGATG
GTGCACATGCCAGGCAATGAGACCATCTGCCCACCAAATATCTACATCGAGTGTGCAGACCACA
CACTGGACTCCCTGGGTGGGGGCCCTGAGGGCCCGTGCTTCTGCCCCACCCCCTGCAACCTGAC
ACGCTATGGGAAAGAGATCTCCATGGTCAGGATCCCCAACAGGGGCTCAGCCCGGTACCTGGCG
AGGAAGTACAACCGCAACGAGACCTACATACGGGAGAACTTCCTGGTCCTAGATGTCTTCTTTG
AGGCCCTGACCTCTGAAGCCATGGAGCAGCGAGCAGCCTATGGCCTGTCAGCCCTGCTGGGAGA
CCTCGGGGGACAGATGGGCCTGTTCATTGGGGCCAGCATCCTCACGTTGCTGGAGATCCTCGAC
TACATCTATGAGGTGTCCTGGGATCGACTGAAGCGGGTATGGAGGCGTCCCAAGACCCCCCTGC
GGACCTCCACTGGGGGCATCTCCACTTTGGGGCTTCAGGAGCTGAAGGAACAGAGTCCCTGCCC
GAGCCGGGGCCGAGTGGAGGGTGGGGGGGTCAGCAGTCTGCTCCCCAATCACCACCACCCCCAC
GGTCCCCCAGGAGGTCTCTTTGAAGATTTTGCTTGCTAGGACGGTGCTGTGACTGAAAGGACCC
AGGAGTCTGGGACCCCTCCTGGGATCCCCAGCACATTCTCCTGCTCCTGGGAGAGGCCTGGGGG
CGGTGCTCACTGGGAGGGCCAGGACTCAGTTCCTGCTCTCATCCTCCCCTGCCCTGATGTCAGC
TGCTTTGCACAAAGGTCCTTCTTGTCCACACCCCTTATCCCCAGGCTGGTGCCCCGGGAGGGCT
GGAGACCAGGCCATGGGCCCTCACGGAGAGGAAGGGAAGGAAGGAGAGGGAGGGGGAGGATAGA
GCCCATCCCAGCCGGGGAGGGGGAGCCCTCTGTACATTTGTAAATATTTAGGGAAAGCCGGGTG
GGGGGAGGGGATACAGATGTAGAAGGTGGGTAGGGCTACAGGGGTGGGTGATTTAGGGACAGCC
AGGGTCCCAGCCCCAATGTCAGCAGGATAGGGAGAGCCCCAGGACTCAGGAGTGCTGGGCTGGT
CCTACTTCCTGCCCCTCTCCAGGCCCAGCTCCCCTCTTGGCAGGGGGAGAGGATGGCCCAGCAG
GCCTGGCCCAGCTCCCAGTTCCCCCTGCACCAGCCCCACCCCTAGAGTCCCTTCTATAGGGAGG
GGGCAGGAGACCTTCCAGACTTCGGCTGAGCTTGGAGGGTGGGAAGGGAGCCTTCTCAGTCCTC
TCTCCCTCCAGTCTGATTTTATAAAGTGCTGACGAGATTGGGAATAAAGAGGCATAAAGAA

hide sequence

RefSeq Acc Id:

XM_047444915 ⟹ XP_047300871

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,514,482 - 219,535,264 (+)	NCBI

RefSeq Acc Id:

XM_047444916 ⟹ XP_047300872

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,514,482 - 219,535,318 (+)	NCBI

RefSeq Acc Id:

XM_047444917 ⟹ XP_047300873

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,507,093 - 219,534,032 (+)	NCBI

RefSeq Acc Id:

XM_054342837 ⟹ XP_054198812

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	219,991,838 - 220,023,471 (+)	NCBI

RefSeq Acc Id:

XM_054342838 ⟹ XP_054198813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	219,991,838 - 220,019,963 (+)	NCBI

RefSeq Acc Id:

XM_054342839 ⟹ XP_054198814

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	219,991,838 - 220,020,017 (+)	NCBI

RefSeq Acc Id:

XM_054342840 ⟹ XP_054198815

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	220,001,950 - 220,023,471 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_061144	(Get FASTA)	NCBI Sequence Viewer
	NP_878267	(Get FASTA)	NCBI Sequence Viewer
	XP_016859928	(Get FASTA)	NCBI Sequence Viewer
	XP_047300871	(Get FASTA)	NCBI Sequence Viewer
	XP_047300872	(Get FASTA)	NCBI Sequence Viewer
	XP_047300873	(Get FASTA)	NCBI Sequence Viewer
	XP_054198812	(Get FASTA)	NCBI Sequence Viewer
	XP_054198813	(Get FASTA)	NCBI Sequence Viewer
	XP_054198814	(Get FASTA)	NCBI Sequence Viewer
	XP_054198815	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH10439	(Get FASTA)	NCBI Sequence Viewer
	AAH31812	(Get FASTA)	NCBI Sequence Viewer
	AAY15054	(Get FASTA)	NCBI Sequence Viewer
	CAB93980	(Get FASTA)	NCBI Sequence Viewer
	CAC51338	(Get FASTA)	NCBI Sequence Viewer
	EAW70760	(Get FASTA)	NCBI Sequence Viewer
	EAW70761	(Get FASTA)	NCBI Sequence Viewer
	EAW70762	(Get FASTA)	NCBI Sequence Viewer
	EAW70763	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000326627
	ENSP00000326627.4
	ENSP00000350786
	ENSP00000350786.5
	ENSP00000508764.1
GenBank Protein	Q96FT7	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_061144 ⟸ NM_018674
- Peptide Label:	isoform 1
- UniProtKB:	Q96FT7 (UniProtKB/Swiss-Prot), Q6PIN9 (UniProtKB/Swiss-Prot), Q6GMS1 (UniProtKB/Swiss-Prot), Q53SB7 (UniProtKB/Swiss-Prot), Q9NQA4 (UniProtKB/Swiss-Prot), A0A8I5KPF5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLSGAAGAARRGGAALAPSLTRSLAGTHAGADSCAGADKGSHKETIEERDKRQQRQQRQRQHQG CGAAGSGSDSPTSGPHPVPVLFPLALSLEEQPLPPLPLGRAPGLLAREGQGREALASPSSRGQM PIEIVCKIKFAEEDAKPKEKEAGDEQSLLGAVAPGAAPRDLATFASTSTLHGLGRACGPGPHGL RRTLWALALLTSLAAFLYQAAGLARGYLTRPHLVAMDPAAPAPVAGFPAVTLCNINRFRHSALS DADIFHLANLTGLPPKDRDGHRAAGLRYPEPDMVDILNRTGHQLADMLKSCNFSGHHCSASNFS VVYTRYGKCYTFNADPRSSLPSRAGGMGSGLEIMLDIQQEEYLPIWRETNETSFEAGIRVQIHS QEEPPYIHQLGFGVSPGFQTFVSCQEQRLTYLPQPWGNCRAESELREPELQGYSAYSVSACRLR CEKEAVLQRCHCRMVHMPGNETICPPNIYIECADHTLDSLGGGPEGPCFCPTPCNLTRYGKEIS MVRIPNRGSARYLARKYNRNETYIRENFLVLDVFFEALTSEAMEQRAAYGLSALLGDLGGQMGL FIGASILTLLEILDYIYEVSWDRLKRVWRRPKTPLRTSTGGISTLGLQELKEQSPCPSRGRVEG GGVSSLLPNHHHPHGPPGGLFEDFAC hide sequence

RefSeq Acc Id:

NP_878267 ⟸ NM_182847

- Peptide Label:

isoform 2

- Sequence:

show sequence

MLSGAAGAARRGGAALAPSLTRSLAGTHAGADSCAGADKGSHKETIEERDKRQQRQQRQRQHQG
CGAAGSGSDSPTSGPHPVPVLFPLALSLEEQPLPPLPLGRAPGLLAREGQGREALASPSSRGQM
PIEIVCKIKFAEEDAKPKEKEAGDEQSLLGAVAPGAAPRDLATFASTSTLHGLGRACGPGPHGL
RRTLWALALLTSLAAFLYQAAGLARGYLTRPHLVAMDPAAPAPVAGFPAVTLCNINRFRHSALS
DADIFHLANLTGLPPKDRDGHRAAGLRYPEPDMVDILNRTGHQLADMLKSCNFSGHHCSASNFS
VVYTRYGKCYTFNADPRSSLPSRAGGMGSGLEIMLDIQQEEYLPIWRETNETSFEAGIRVQIHS
QEEPPYIHQLGFGVSPGFQTFVSCQEQRLTYLPQPWGNCRAESELREPELQGYSAYSVSACRLR
CEKEAVLQRCHCRMVHMPDSLGGGPEGPCFCPTPCNLTRYGKEISMVRIPNRGSARYLARKYNR
NETYIRENFLVLDVFFEALTSEAMEQRAAYGLSALLGDLGGQMGLFIGASILTLLEILDYIYEV
SWDRLKRVWRRPKTPLRTSTGGISTLGLQELKEQSPCPSRGRVEGGGVSSLLPNHHHPHGPPGG
LFEDFAC

hide sequence

RefSeq Acc Id:

XP_016859928 ⟸ XM_017004439

- Peptide Label:

isoform X4

- Sequence:

show sequence

MGSGLEIMLDIQQEEYLPIWRETNETSFEAGIRVQIHSQEEPPYIHQLGFGVSPGFQTFVSCQE
QRLTYLPQPWGNCRAESELREPELQGYSAYSVSACRLRCEKEAVLQRCHCRMVHMPGNETICPP
NIYIECADHTLDSLGGGPEGPCFCPTPCNLTRYGKEISMVRIPNRGSARYLARKYNRNETYIRE
NFLVLDVFFEALTSEAMEQRAAYGLSALLGDLGGQMGLFIGASILTLLEILDYIYEVSWDRLKR
VWRRPKTPLRTSTGGISTLGLQELKEQSPCPSRGRVEGGGVSSLLPNHHHPHGPPGGLFEDFAC

hide sequence

RefSeq Acc Id:

ENSP00000326627 ⟸ ENST00000347842

RefSeq Acc Id:

ENSP00000350786 ⟸ ENST00000358078

RefSeq Acc Id:

ENSP00000508764 ⟸ ENST00000693692

RefSeq Acc Id:	XP_047300873 ⟸ XM_047444917
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047300872 ⟸ XM_047444916
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047300871 ⟸ XM_047444915
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054198812 ⟸ XM_054342837
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054198814 ⟸ XM_054342839
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054198813 ⟸ XM_054342838
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054198815 ⟸ XM_054342840
- Peptide Label:	isoform X4

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96FT7-F1-model_v2	AlphaFold	Q96FT7	1-539	view protein structure

Promoters

RGD ID:

6862920

Promoter ID:

EPDNEW_H4625

Type:

initiation region

Name:

ASIC4_1

Description:

acid sensing ion channel subunit family member 4

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	219,514,404 - 219,514,464	EPDNEW

RGD ID:

6796739

Promoter ID:

HG_KWN:37384

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

OTTHUMT00000130263, OTTHUMT00000130264, OTTHUMT00000130266, UC010FWI.1, UC010FWJ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	2	220,087,166 - 220,087,666 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:21263	AgrOrtholog
COSMIC	ASIC4	COSMIC
Ensembl Genes	ENSG00000072182	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000347842	ENTREZGENE
	ENST00000347842.8	UniProtKB/Swiss-Prot
	ENST00000358078	ENTREZGENE
	ENST00000358078.5	UniProtKB/Swiss-Prot
	ENST00000693692.1	UniProtKB/TrEMBL
Gene3D-CATH	Acid-sensing ion channels like domains	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	YojJ-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000072182	GTEx
HGNC ID	HGNC:21263	ENTREZGENE
Human Proteome Map	ASIC4	Human Proteome Map
InterPro	ENaC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ENaC_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:55515	UniProtKB/Swiss-Prot
NCBI Gene	55515	ENTREZGENE
OMIM	606715	OMIM
PANTHER	ACID-SENSING ION CHANNEL 4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR11690	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	ASC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134956731	PharmGKB
PRINTS	AMINACHANNEL	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	ASC	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A8I5KPF5	ENTREZGENE, UniProtKB/TrEMBL
	ASIC4_HUMAN	UniProtKB/Swiss-Prot
	Q53SB7	ENTREZGENE
	Q6GMS1	ENTREZGENE
	Q6PIN9	ENTREZGENE
	Q96FT7	ENTREZGENE
	Q9NQA4	ENTREZGENE
UniProt Secondary	Q53SB7	UniProtKB/Swiss-Prot
	Q6GMS1	UniProtKB/Swiss-Prot
	Q6PIN9	UniProtKB/Swiss-Prot
	Q9NQA4	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-12-22	ASIC4	acid sensing ion channel subunit family member 4	ASIC4	acid sensing ion channel family member 4	Symbol and/or name change	5135510	APPROVED
2015-12-08	ASIC4	acid sensing ion channel family member 4	ASIC4	acid sensing (proton gated) ion channel family member 4	Symbol and/or name change	5135510	APPROVED
2015-01-20	ASIC4	acid sensing (proton gated) ion channel family member 4	ASIC4	acid-sensing (proton-gated) ion channel family member 4	Symbol and/or name change	5135510	APPROVED
2012-03-01	ASIC4	acid-sensing (proton-gated) ion channel family member 4	ACCN4	amiloride-sensitive cation channel 4, pituitary	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 - ClinVar

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