RGS6 (regulator of G protein signaling 6) - Rat Genome Database

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Gene: RGS6 (regulator of G protein signaling 6) Homo sapiens
Analyze
Symbol: RGS6
Name: regulator of G protein signaling 6
RGD ID: 736970
HGNC Page HGNC:10002
Description: Enables GTPase activator activity. Predicted to be involved in regulation of G protein-coupled receptor signaling pathway. Located in cytosol; membrane; and nuclear lumen.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp313G1241; FLJ43552; G protein signaling 6 regulator; GAP; GTPase activating protein; H_DJ0283M22.1; H_DJ1108A12.1; HA117; MGC142132; regulator of G protein signalling 6; regulator of G-protein signaling 6; regulator of G-protein signalling 6; S914; WUGSC:H_DJ0283M22.1; WUGSC:H_DJ1108A12.1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381471,867,335 - 72,630,029 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1471,932,429 - 72,566,530 (+)EnsemblGRCh38hg38GRCh38
GRCh371472,398,888 - 73,033,238 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361471,469,539 - 72,102,991 (+)NCBINCBI36Build 36hg18NCBI36
Build 341471,469,585 - 72,100,407NCBI
Celera1452,462,976 - 53,096,417 (+)NCBICelera
Cytogenetic Map14q24.2NCBI
HuRef1452,565,478 - 53,199,765 (+)NCBIHuRef
CHM1_11472,336,952 - 72,971,253 (+)NCBICHM1_1
T2T-CHM13v2.01466,072,765 - 66,835,660 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. RGS Proteins in Heart: Brakes on the Vagus. Stewart A, etal., Front Physiol. 2012 Apr 13;3:95. doi: 10.3389/fphys.2012.00095. eCollection 2012.
Additional References at PubMed
PMID:7596406   PMID:10083744   PMID:10339615   PMID:10521509   PMID:12140291   PMID:12477932   PMID:12761220   PMID:12761221   PMID:14702039   PMID:14734556   PMID:15375002   PMID:16344560  
PMID:16691626   PMID:18676680   PMID:19170196   PMID:19435509   PMID:19625176   PMID:19692168   PMID:19834535   PMID:20379614   PMID:20453000   PMID:20635168   PMID:20642825   PMID:20811658  
PMID:21041304   PMID:21233807   PMID:21300955   PMID:21316428   PMID:21720420   PMID:21873635   PMID:21935397   PMID:22566634   PMID:22939624   PMID:23619123   PMID:24324551   PMID:24529757  
PMID:25056061   PMID:25120773   PMID:25120791   PMID:25525169   PMID:26097584   PMID:26340433   PMID:26653562   PMID:26987813   PMID:28090039   PMID:28514442   PMID:28665981   PMID:28731026  
PMID:30021884   PMID:31120439   PMID:33961781   PMID:35902557   PMID:35906200   PMID:36215168   PMID:38409136  


Genomics

Comparative Map Data
RGS6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381471,867,335 - 72,630,029 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1471,932,429 - 72,566,530 (+)EnsemblGRCh38hg38GRCh38
GRCh371472,398,888 - 73,033,238 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361471,469,539 - 72,102,991 (+)NCBINCBI36Build 36hg18NCBI36
Build 341471,469,585 - 72,100,407NCBI
Celera1452,462,976 - 53,096,417 (+)NCBICelera
Cytogenetic Map14q24.2NCBI
HuRef1452,565,478 - 53,199,765 (+)NCBIHuRef
CHM1_11472,336,952 - 72,971,253 (+)NCBICHM1_1
T2T-CHM13v2.01466,072,765 - 66,835,660 (+)NCBIT2T-CHM13v2.0
Rgs6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391282,663,325 - 83,208,835 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1282,635,066 - 83,208,830 (+)EnsemblGRCm39 Ensembl
GRCm381282,616,551 - 83,162,061 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1282,588,292 - 83,162,056 (+)EnsemblGRCm38mm10GRCm38
MGSCv371283,718,025 - 84,259,799 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361283,535,886 - 84,077,669 (+)NCBIMGSCv36mm8
Celera1284,069,722 - 84,604,177 (+)NCBICelera
Cytogenetic Map12D1NCBI
cM Map1238.14NCBI
Rgs6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr86107,875,883 - 108,527,472 (+)NCBIGRCr8
mRatBN7.26102,264,451 - 102,796,311 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl6102,264,447 - 102,824,753 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx6102,420,755 - 102,953,980 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.06102,719,975 - 103,253,217 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.06102,089,444 - 102,622,685 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.06106,310,442 - 106,598,668 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl6106,496,992 - 106,602,139 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06114,636,387 - 114,736,790 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46106,470,420 - 106,964,581 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.16106,940,142 - 106,967,896 (+)NCBI
Celera6100,100,895 - 100,625,650 (+)NCBICelera
Cytogenetic Map6q24-q31NCBI
Rgs6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555232,762,987 - 3,335,474 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555232,763,143 - 3,366,851 (-)NCBIChiLan1.0ChiLan1.0
RGS6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21573,042,379 - 73,677,406 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11472,258,892 - 72,893,920 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01452,511,846 - 53,146,872 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11471,377,567 - 72,012,766 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1471,409,701 - 72,008,988 (+)Ensemblpanpan1.1panPan2
RGS6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1845,392,246 - 45,975,073 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl845,438,239 - 46,009,049 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha845,077,684 - 45,656,669 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0845,630,187 - 46,197,033 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl845,654,256 - 46,194,458 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1845,301,232 - 45,866,115 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0845,329,999 - 45,882,332 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0845,692,998 - 46,272,644 (+)NCBIUU_Cfam_GSD_1.0
Rgs6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864030,144,323 - 30,732,878 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364881,361,310 - 1,921,353 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364881,336,075 - 1,924,635 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RGS6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl795,365,939 - 95,930,034 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1795,365,212 - 95,930,040 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
RGS6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12449,161,466 - 49,803,209 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2449,591,815 - 49,775,653 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605337,367,918 - 37,991,218 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Rgs6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473428,829,698 - 29,411,779 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473428,830,254 - 29,436,945 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in RGS6
148 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001204423.1(RGS6):c.-22+66736G>A single nucleotide variant Lung cancer [RCV000099028] Chr14:71998969 [GRCh38]
Chr14:72465686 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.-22+107125G>T single nucleotide variant Lung cancer [RCV000099029] Chr14:72039358 [GRCh38]
Chr14:72506075 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.-21-177662G>A single nucleotide variant Lung cancer [RCV000099030] Chr14:72174433 [GRCh38]
Chr14:72641141 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.-21-122450T>A single nucleotide variant Lung cancer [RCV000099031] Chr14:72229645 [GRCh38]
Chr14:72696353 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.-21-36432C>A single nucleotide variant Lung cancer [RCV000099032] Chr14:72315663 [GRCh38]
Chr14:72782371 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.80-34711C>A single nucleotide variant Lung cancer [RCV000099033] Chr14:72419817 [GRCh38]
Chr14:72886525 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.861-1430A>G single nucleotide variant Lung cancer [RCV000099034] Chr14:72508724 [GRCh38]
Chr14:72975432 [GRCh37]
Chr14:14q24.2		 uncertain significance
GRCh38/hg38 14q24.2(chr14:71647101-72567300)x3 copy number gain See cases [RCV000052082] Chr14:71647101..72567300 [GRCh38]
Chr14:72113818..73034008 [GRCh37]
Chr14:71183571..72103761 [NCBI36]
Chr14:14q24.2		 uncertain significance
NM_001204423.1(RGS6):c.159C>T (p.Ile53=) single nucleotide variant Malignant melanoma [RCV000070599] Chr14:72458299 [GRCh38]
Chr14:72925007 [GRCh37]
Chr14:71994760 [NCBI36]
Chr14:14q24.2		 not provided
NM_001204416.1(RGS6):c.10G>A (p.Gly4Arg) single nucleotide variant Malignant melanoma [RCV000062785] Chr14:71964801 [GRCh38]
Chr14:72431518 [GRCh37]
Chr14:71501271 [NCBI36]
Chr14:14q24.2		 not provided
GRCh38/hg38 14q24.1-31.1(chr14:69562099-81975384)x1 copy number loss See cases [RCV000134154] Chr14:69562099..81975384 [GRCh38]
Chr14:70028816..82441728 [GRCh37]
Chr14:69098569..81511481 [NCBI36]
Chr14:14q24.1-31.1		 pathogenic
GRCh38/hg38 14q24.2(chr14:72172189-72198910)x3 copy number gain See cases [RCV000134432] Chr14:72172189..72198910 [GRCh38]
Chr14:72638897..72665618 [GRCh37]
Chr14:71708650..71735371 [NCBI36]
Chr14:14q24.2		 benign
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q24.2(chr14:70752460-72490693)x3 copy number gain See cases [RCV000136584] Chr14:70752460..72490693 [GRCh38]
Chr14:71219177..72957401 [GRCh37]
Chr14:70288930..72027154 [NCBI36]
Chr14:14q24.2		 uncertain significance
GRCh38/hg38 14q24.2(chr14:72557579-72709419)x3 copy number gain See cases [RCV000139961] Chr14:72557579..72709419 [GRCh38]
Chr14:73024287..73176127 [GRCh37]
Chr14:72094040..72245880 [NCBI36]
Chr14:14q24.2		 uncertain significance
GRCh38/hg38 14q24.2(chr14:71864981-71952855)x3 copy number gain See cases [RCV000141268] Chr14:71864981..71952855 [GRCh38]
Chr14:72331698..72419572 [GRCh37]
Chr14:71401451..71489325 [NCBI36]
Chr14:14q24.2		 uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q24.1-24.2(chr14:68035240-73568130)x1 copy number loss See cases [RCV000512344] Chr14:68035240..73568130 [GRCh37]
Chr14:14q24.1-24.2		 likely pathogenic
NM_001204424.2(RGS6):c.1369-170A>G single nucleotide variant not provided [RCV001540275] Chr14:72539871 [GRCh38]
Chr14:73006579 [GRCh37]
Chr14:14q24.2		 benign
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q24.2(chr14:72818218-72875361)x1 copy number loss not provided [RCV000751050] Chr14:72818218..72875361 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.966-277T>C single nucleotide variant not provided [RCV001537330] Chr14:72509877 [GRCh38]
Chr14:72976585 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-164A>T single nucleotide variant not provided [RCV001691170] Chr14:72465594 [GRCh38]
Chr14:72932302 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.537-85C>A single nucleotide variant not provided [RCV001648234] Chr14:72472787 [GRCh38]
Chr14:72939495 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1368+197G>A single nucleotide variant not provided [RCV001709021] Chr14:72536472 [GRCh38]
Chr14:73003180 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-135TGGA[11] microsatellite not provided [RCV001667311] Chr14:72465622..72465623 [GRCh38]
Chr14:72932330..72932331 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-160A>G single nucleotide variant not provided [RCV001678838] Chr14:72465598 [GRCh38]
Chr14:72932306 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.184+7C>T single nucleotide variant not provided [RCV000879110] Chr14:72352201 [GRCh38]
Chr14:72818909 [GRCh37]
Chr14:14q24.2		 benign|likely benign
NM_001204424.2(RGS6):c.444G>C (p.Leu148=) single nucleotide variant not provided [RCV000972509] Chr14:72465807 [GRCh38]
Chr14:72932515 [GRCh37]
Chr14:14q24.2		 benign|likely benign
NM_001204424.2(RGS6):c.249C>T (p.His83=) single nucleotide variant not provided [RCV000981521] Chr14:72458284 [GRCh38]
Chr14:72924992 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.93C>T (p.Asp31=) single nucleotide variant not provided [RCV000965274] Chr14:72352103 [GRCh38]
Chr14:72818811 [GRCh37]
Chr14:14q24.2		 benign|likely benign
NM_001204424.2(RGS6):c.84+7C>T single nucleotide variant not provided [RCV000965944] Chr14:71964882 [GRCh38]
Chr14:72431599 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.829T>C (p.Leu277=) single nucleotide variant not provided [RCV000836780] Chr14:72478304 [GRCh38]
Chr14:72945012 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1272C>T (p.Asp424=) single nucleotide variant not provided [RCV000841405] Chr14:72518531 [GRCh38]
Chr14:72985239 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1141G>T (p.Ala381Ser) single nucleotide variant Inborn genetic diseases [RCV003291133] Chr14:72518400 [GRCh38]
Chr14:72985108 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.619-126G>A single nucleotide variant not provided [RCV001617642] Chr14:72474499 [GRCh38]
Chr14:72941207 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.694-274T>C single nucleotide variant not provided [RCV001690283] Chr14:72476468 [GRCh38]
Chr14:72943176 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.793-33T>G single nucleotide variant not provided [RCV001615409] Chr14:72478235 [GRCh38]
Chr14:72944943 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+70C>G single nucleotide variant not provided [RCV001637788] Chr14:72510349 [GRCh38]
Chr14:72977057 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-207TGGA[11] microsatellite not provided [RCV001655245] Chr14:72465551..72465554 [GRCh38]
Chr14:72932259..72932262 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-136_395-133del deletion not provided [RCV001617955] Chr14:72465619..72465622 [GRCh38]
Chr14:72932327..72932330 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-135TGGA[12] microsatellite not provided [RCV001651644] Chr14:72465622..72465623 [GRCh38]
Chr14:72932330..72932331 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+202G>A single nucleotide variant not provided [RCV001639874] Chr14:72510481 [GRCh38]
Chr14:72977189 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1368+132G>T single nucleotide variant not provided [RCV001616926] Chr14:72536407 [GRCh38]
Chr14:73003115 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.855-262T>C single nucleotide variant not provided [RCV001716468] Chr14:72494890 [GRCh38]
Chr14:72961598 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+94A>C single nucleotide variant not provided [RCV001594615] Chr14:72510373 [GRCh38]
Chr14:72977081 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.459+279A>G single nucleotide variant not provided [RCV001614901] Chr14:72466101 [GRCh38]
Chr14:72932809 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.933C>T (p.Ser311=) single nucleotide variant not provided [RCV000924021] Chr14:72495230 [GRCh38]
Chr14:72961938 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.147C>G (p.Val49=) single nucleotide variant not provided [RCV000935887] Chr14:72352157 [GRCh38]
Chr14:72818865 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.395-207TGGA[8] microsatellite not provided [RCV001597854] Chr14:72465551..72465566 [GRCh38]
Chr14:72932259..72932274 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1092-180A>G single nucleotide variant not provided [RCV001682013] Chr14:72518171 [GRCh38]
Chr14:72984879 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+69TC[8] microsatellite not provided [RCV002255002] Chr14:72510347..72510348 [GRCh38]
Chr14:72977055..72977056 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1091+68_1091+69del deletion not provided [RCV001689395] Chr14:72510347..72510348 [GRCh38]
Chr14:72977055..72977056 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-77G>T single nucleotide variant not provided [RCV001594763] Chr14:72465681 [GRCh38]
Chr14:72932389 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-150G>A single nucleotide variant not provided [RCV001608264] Chr14:72465608 [GRCh38]
Chr14:72932316 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.343-199C>G single nucleotide variant not provided [RCV001618828] Chr14:72459433 [GRCh38]
Chr14:72926141 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.343-175A>G single nucleotide variant not provided [RCV001621840] Chr14:72459457 [GRCh38]
Chr14:72926165 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.235+131C>G single nucleotide variant not provided [RCV001637218] Chr14:72454709 [GRCh38]
Chr14:72921417 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.966-247T>C single nucleotide variant not provided [RCV001641339] Chr14:72509907 [GRCh38]
Chr14:72976615 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.966-232G>A single nucleotide variant not provided [RCV001715301] Chr14:72509922 [GRCh38]
Chr14:72976630 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+167C>T single nucleotide variant not provided [RCV001656479] Chr14:72510446 [GRCh38]
Chr14:72977154 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1369-251G>C single nucleotide variant not provided [RCV001617768] Chr14:72539790 [GRCh38]
Chr14:73006498 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-135TGGA[10] microsatellite not provided [RCV001677928] Chr14:72465622..72465623 [GRCh38]
Chr14:72932330..72932331 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+97A>G single nucleotide variant not provided [RCV001638468] Chr14:72510376 [GRCh38]
Chr14:72977084 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.618+74C>T single nucleotide variant not provided [RCV001720437] Chr14:72473027 [GRCh38]
Chr14:72939735 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-207TGGA[13] microsatellite not provided [RCV001710713] Chr14:72465550..72465551 [GRCh38]
Chr14:72932258..72932259 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.*3G>A single nucleotide variant not provided [RCV001665942] Chr14:72562470 [GRCh38]
Chr14:73029178 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.-20-34C>T single nucleotide variant not provided [RCV001649035] Chr14:71964738 [GRCh38]
Chr14:72431455 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-156T>A single nucleotide variant not provided [RCV001667463] Chr14:72465602 [GRCh38]
Chr14:72932310 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.342+86G>C single nucleotide variant not provided [RCV001710858] Chr14:72458463 [GRCh38]
Chr14:72925171 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.792+204C>T single nucleotide variant not provided [RCV001609433] Chr14:72477044 [GRCh38]
Chr14:72943752 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.*532T>C single nucleotide variant not provided [RCV001714203] Chr14:72562999 [GRCh38]
Chr14:73029707 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.-20-25A>G single nucleotide variant not provided [RCV001540523] Chr14:71964747 [GRCh38]
Chr14:72431464 [GRCh37]
Chr14:14q24.2		 benign
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3 copy number gain 14q22.2q24.3 duplication [RCV001506967] Chr14:54654001..75828024 [GRCh37]
Chr14:14q22.2-24.3		 likely pathogenic
NM_001204424.2(RGS6):c.*434C>T single nucleotide variant not provided [RCV001645743] Chr14:72562901 [GRCh38]
Chr14:73029609 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1278+151C>T single nucleotide variant not provided [RCV001688253] Chr14:72518688 [GRCh38]
Chr14:72985396 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.536+163T>C single nucleotide variant not provided [RCV001709972] Chr14:72470246 [GRCh38]
Chr14:72936954 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.343-254T>A single nucleotide variant not provided [RCV001674056] Chr14:72459378 [GRCh38]
Chr14:72926086 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.459+33G>A single nucleotide variant not provided [RCV001694919] Chr14:72465855 [GRCh38]
Chr14:72932563 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.619-127_619-126insA insertion not provided [RCV001696381] Chr14:72474498..72474499 [GRCh38]
Chr14:72941206..72941207 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1091+212G>A single nucleotide variant not provided [RCV001678771] Chr14:72510491 [GRCh38]
Chr14:72977199 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.395-155TGGGTGGA[2] microsatellite not provided [RCV001652790] Chr14:72465603..72465610 [GRCh38]
Chr14:72932311..72932318 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.966-63G>A single nucleotide variant not provided [RCV001768203] Chr14:72510091 [GRCh38]
Chr14:72976799 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.236-290A>G single nucleotide variant not provided [RCV001774974] Chr14:72457981 [GRCh38]
Chr14:72924689 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.*193G>T single nucleotide variant not provided [RCV001769918] Chr14:72562660 [GRCh38]
Chr14:73029368 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.460-254T>G single nucleotide variant not provided [RCV001774836] Chr14:72469753 [GRCh38]
Chr14:72936461 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.*469C>G single nucleotide variant not provided [RCV001757724] Chr14:72562936 [GRCh38]
Chr14:73029644 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.343-96G>A single nucleotide variant not provided [RCV001785993] Chr14:72459536 [GRCh38]
Chr14:72926244 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.395-207TGGA[14] microsatellite not provided [RCV001768022] Chr14:72465550..72465551 [GRCh38]
Chr14:72932258..72932259 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1422+77T>C single nucleotide variant not provided [RCV001769745] Chr14:72540171 [GRCh38]
Chr14:73006879 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.965+185G>A single nucleotide variant not provided [RCV001769808] Chr14:72495447 [GRCh38]
Chr14:72962155 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.236-264C>T single nucleotide variant not provided [RCV001769693] Chr14:72458007 [GRCh38]
Chr14:72924715 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.184+66C>T single nucleotide variant not provided [RCV001759147] Chr14:72352260 [GRCh38]
Chr14:72818968 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.*113G>A single nucleotide variant not provided [RCV001758956] Chr14:72562580 [GRCh38]
Chr14:73029288 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.85-188G>T single nucleotide variant not provided [RCV001768140] Chr14:72351907 [GRCh38]
Chr14:72818615 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.536+17G>A single nucleotide variant not provided [RCV001769798] Chr14:72470100 [GRCh38]
Chr14:72936808 [GRCh37]
Chr14:14q24.2		 benign|likely benign
NM_001204424.2(RGS6):c.618+261T>C single nucleotide variant not provided [RCV001769929] Chr14:72473214 [GRCh38]
Chr14:72939922 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.236-214T>C single nucleotide variant not provided [RCV001757692] Chr14:72458057 [GRCh38]
Chr14:72924765 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1423-128G>T single nucleotide variant not provided [RCV001769611] Chr14:72562289 [GRCh38]
Chr14:73028997 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.792+203C>T single nucleotide variant not provided [RCV001799909] Chr14:72477043 [GRCh38]
Chr14:72943751 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1369-274G>A single nucleotide variant not provided [RCV001759077] Chr14:72539767 [GRCh38]
Chr14:73006475 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1368+171C>G single nucleotide variant not provided [RCV001759078] Chr14:72536446 [GRCh38]
Chr14:73003154 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1422+77del deletion not provided [RCV001758957] Chr14:72540158 [GRCh38]
Chr14:73006866 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.-20-279C>T single nucleotide variant not provided [RCV001752950] Chr14:71964493 [GRCh38]
Chr14:72431210 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1368+20G>C single nucleotide variant not provided [RCV001806499] Chr14:72536295 [GRCh38]
Chr14:73003003 [GRCh37]
Chr14:14q24.2		 benign|likely benign
GRCh37/hg19 14q24.2(chr14:72452471-72759904)x3 copy number gain not provided [RCV001832884] Chr14:72452471..72759904 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.771A>G (p.Thr257=) single nucleotide variant not provided [RCV002078664] Chr14:72476819 [GRCh38]
Chr14:72943527 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.966-10C>T single nucleotide variant not provided [RCV002153290] Chr14:72510144 [GRCh38]
Chr14:72976852 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.1281G>A (p.Glu427=) single nucleotide variant not provided [RCV002119785] Chr14:72536188 [GRCh38]
Chr14:73002896 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.394+108G>C single nucleotide variant not provided [RCV002285727] Chr14:72459791 [GRCh38]
Chr14:72926499 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.536+147C>T single nucleotide variant not provided [RCV002286210] Chr14:72470230 [GRCh38]
Chr14:72936938 [GRCh37]
Chr14:14q24.2		 likely benign
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
NM_001204424.2(RGS6):c.932G>A (p.Ser311Asn) single nucleotide variant Inborn genetic diseases [RCV002684194] Chr14:72495229 [GRCh38]
Chr14:72961937 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.1250G>A (p.Gly417Glu) single nucleotide variant Inborn genetic diseases [RCV002879476] Chr14:72518509 [GRCh38]
Chr14:72985217 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.706G>A (p.Val236Met) single nucleotide variant Inborn genetic diseases [RCV002992173] Chr14:72476754 [GRCh38]
Chr14:72943462 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.445G>A (p.Ala149Thr) single nucleotide variant Inborn genetic diseases [RCV002993037]|not provided [RCV003669351] Chr14:72465808 [GRCh38]
Chr14:72932516 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.934G>A (p.Asp312Asn) single nucleotide variant Inborn genetic diseases [RCV002981401] Chr14:72495231 [GRCh38]
Chr14:72961939 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.532G>C (p.Val178Leu) single nucleotide variant Inborn genetic diseases [RCV002761730] Chr14:72470079 [GRCh38]
Chr14:72936787 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.1368+17C>T single nucleotide variant not provided [RCV002781075] Chr14:72536292 [GRCh38]
Chr14:73003000 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.118A>G (p.Lys40Glu) single nucleotide variant Inborn genetic diseases [RCV003170605]|not provided [RCV002910219] Chr14:72352128 [GRCh38]
Chr14:72818836 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.870G>A (p.Thr290=) single nucleotide variant not provided [RCV002627261] Chr14:72495167 [GRCh38]
Chr14:72961875 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.134C>T (p.Pro45Leu) single nucleotide variant Inborn genetic diseases [RCV002893772] Chr14:72352144 [GRCh38]
Chr14:72818852 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.837G>A (p.Met279Ile) single nucleotide variant Inborn genetic diseases [RCV002788980] Chr14:72478312 [GRCh38]
Chr14:72945020 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.265G>T (p.Ala89Ser) single nucleotide variant Inborn genetic diseases [RCV002963957] Chr14:72458300 [GRCh38]
Chr14:72925008 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.250T>C (p.Leu84=) single nucleotide variant not provided [RCV002600347] Chr14:72458285 [GRCh38]
Chr14:72924993 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.1136A>G (p.Asp379Gly) single nucleotide variant not provided [RCV002962952] Chr14:72518395 [GRCh38]
Chr14:72985103 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.73G>A (p.Val25Ile) single nucleotide variant Inborn genetic diseases [RCV002652569] Chr14:71964864 [GRCh38]
Chr14:72431581 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.885A>C (p.Glu295Asp) single nucleotide variant Inborn genetic diseases [RCV003196217] Chr14:72495182 [GRCh38]
Chr14:72961890 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.1040G>A (p.Arg347Gln) single nucleotide variant Inborn genetic diseases [RCV003173990]|not provided [RCV003549007] Chr14:72510228 [GRCh38]
Chr14:72976936 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.94A>C (p.Ile32Leu) single nucleotide variant Inborn genetic diseases [RCV003198080] Chr14:72352104 [GRCh38]
Chr14:72818812 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.1055G>A (p.Arg352Gln) single nucleotide variant Inborn genetic diseases [RCV003196102] Chr14:72510243 [GRCh38]
Chr14:72976951 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.172A>G (p.Ser58Gly) single nucleotide variant Inborn genetic diseases [RCV003175644] Chr14:72352182 [GRCh38]
Chr14:72818890 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.581G>C (p.Ser194Thr) single nucleotide variant Inborn genetic diseases [RCV003179344] Chr14:72472916 [GRCh38]
Chr14:72939624 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.1414C>T (p.Arg472Cys) single nucleotide variant Inborn genetic diseases [RCV003362049] Chr14:72540086 [GRCh38]
Chr14:73006794 [GRCh37]
Chr14:14q24.2		 uncertain significance
GRCh37/hg19 14q24.2-24.3(chr14:72984321-73975604)x3 copy number gain not provided [RCV003485041] Chr14:72984321..73975604 [GRCh37]
Chr14:14q24.2-24.3		 uncertain significance
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
NM_001204424.2(RGS6):c.85-17_85-13del microsatellite not provided [RCV003879706] Chr14:72352072..72352076 [GRCh38]
Chr14:72818780..72818784 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.854+11C>T single nucleotide variant not provided [RCV003882155] Chr14:72478340 [GRCh38]
Chr14:72945048 [GRCh37]
Chr14:14q24.2		 benign
NM_001204424.2(RGS6):c.697G>A (p.Val233Met) single nucleotide variant not provided [RCV003819134] Chr14:72476745 [GRCh38]
Chr14:72943453 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.235+6T>C single nucleotide variant not provided [RCV003846595] Chr14:72454584 [GRCh38]
Chr14:72921292 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.1431G>A (p.Ser477=) single nucleotide variant not provided [RCV003735756] Chr14:72562425 [GRCh38]
Chr14:73029133 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.693+4C>T single nucleotide variant not provided [RCV003871191] Chr14:72474703 [GRCh38]
Chr14:72941411 [GRCh37]
Chr14:14q24.2		 uncertain significance
NM_001204424.2(RGS6):c.185-7G>A single nucleotide variant not provided [RCV003730860] Chr14:72454521 [GRCh38]
Chr14:72921229 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.460-5A>C single nucleotide variant not provided [RCV003677392] Chr14:72470002 [GRCh38]
Chr14:72936710 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.793-283C>T single nucleotide variant not provided [RCV001758889] Chr14:72477985 [GRCh38]
Chr14:72944693 [GRCh37]
Chr14:14q24.2		 likely benign
NM_001204424.2(RGS6):c.224T>C (p.Ile75Thr) single nucleotide variant Inborn genetic diseases [RCV003246260] Chr14:72454567 [GRCh38]
Chr14:72921275 [GRCh37]
Chr14:14q24.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4998
Count of miRNA genes:1064
Interacting mature miRNAs:1345
Transcripts:ENST00000343854, ENST00000355512, ENST00000402788, ENST00000404301, ENST00000406236, ENST00000407322, ENST00000434263, ENST00000553519, ENST00000553525, ENST00000553530, ENST00000553690, ENST00000554300, ENST00000554474, ENST00000554734, ENST00000554782, ENST00000555368, ENST00000555571, ENST00000556437
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
D14S277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,027,458 - 73,027,609UniSTSGRCh37
Build 361472,097,211 - 72,097,362RGDNCBI36
Celera1453,090,637 - 53,090,788RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,193,985 - 53,194,136UniSTS
Marshfield Genetic Map1479.07UniSTS
Marshfield Genetic Map1479.07RGD
Genethon Genetic Map1468.0UniSTS
deCODE Assembly Map1471.02UniSTS
Whitehead-RH Map14255.2UniSTS
Whitehead-YAC Contig Map14 UniSTS
NCBI RH Map14734.8UniSTS
SHGC-37117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,845,020 - 72,845,151UniSTSGRCh37
Build 361471,914,773 - 71,914,904RGDNCBI36
Celera1452,908,196 - 52,908,327RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,011,429 - 53,011,560UniSTS
GeneMap99-G3 RH Map142654.0UniSTS
G38061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,830,554 - 72,830,705UniSTSGRCh37
Build 361471,900,307 - 71,900,458RGDNCBI36
Celera1452,893,730 - 52,893,881RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,996,963 - 52,997,114UniSTS
G38088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,958,830 - 72,959,073UniSTSGRCh37
Build 361472,028,583 - 72,028,826RGDNCBI36
Celera1453,021,997 - 53,022,240RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,125,348 - 53,125,591UniSTS
G38069  
Human AssemblyChrPosition (strand)SourceJBrowse
Celera1452,779,587 - 52,779,858RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,882,824 - 52,883,095UniSTS
WI-18648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,033,102 - 73,033,208UniSTSGRCh37
Build 361472,102,855 - 72,102,961RGDNCBI36
Celera1453,096,281 - 53,096,387RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,199,629 - 53,199,735UniSTS
GeneMap99-GB4 RH Map14185.59UniSTS
Whitehead-RH Map14255.2UniSTS
NCBI RH Map14733.8UniSTS
G38263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,664,417 - 72,664,565UniSTSGRCh37
Build 361471,734,170 - 71,734,318RGDNCBI36
Celera1452,727,618 - 52,727,766RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,830,864 - 52,831,012UniSTS
WI-11724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,008,590 - 73,008,739UniSTSGRCh37
Build 361472,078,343 - 72,078,492RGDNCBI36
Celera1453,071,762 - 53,071,911RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,175,110 - 53,175,259UniSTS
GeneMap99-GB4 RH Map14183.07UniSTS
Whitehead-RH Map14252.7UniSTS
G38075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,960,833 - 72,961,276UniSTSGRCh37
Build 361472,030,586 - 72,031,029RGDNCBI36
Celera1453,023,999 - 53,024,442RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,127,350 - 53,127,793UniSTS
RH44624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,478,077 - 72,478,241UniSTSGRCh37
Build 361471,547,830 - 71,547,994RGDNCBI36
Celera1452,541,292 - 52,541,456RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,644,640 - 52,644,804UniSTS
GeneMap99-GB4 RH Map14181.75UniSTS
NCBI RH Map14692.6UniSTS
RH66044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,844,988 - 72,845,148UniSTSGRCh37
Build 361471,914,741 - 71,914,901RGDNCBI36
Celera1452,908,164 - 52,908,324RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,011,397 - 53,011,557UniSTS
GeneMap99-GB4 RH Map14183.17UniSTS
G38275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,515,976 - 72,516,265UniSTSGRCh37
Build 361471,585,729 - 71,586,018RGDNCBI36
Celera1452,579,181 - 52,579,470RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,682,433 - 52,682,722UniSTS
SHGC-34891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,478,170 - 72,478,295UniSTSGRCh37
Build 361471,547,923 - 71,548,048RGDNCBI36
Celera1452,541,385 - 52,541,510RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,644,733 - 52,644,858UniSTS
GeneMap99-GB4 RH Map14180.27UniSTS
Whitehead-RH Map14255.4UniSTS
GeneMap99-G3 RH Map142661.0UniSTS
RH93225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,712,966 - 72,713,085UniSTSGRCh37
Build 361471,782,719 - 71,782,838RGDNCBI36
Celera1452,776,129 - 52,776,248RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,879,366 - 52,879,485UniSTS
GeneMap99-GB4 RH Map14180.59UniSTS
RH76013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,414,507 - 72,414,685UniSTSGRCh37
Build 361471,484,260 - 71,484,438RGDNCBI36
Celera1452,477,711 - 52,477,889RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,581,182 - 52,581,360UniSTS
SHGC-77937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,633,304 - 72,633,600UniSTSGRCh37
Build 361471,703,057 - 71,703,353RGDNCBI36
Celera1452,696,506 - 52,696,802RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,799,742 - 52,800,038UniSTS
TNG Radiation Hybrid Map1425353.0UniSTS
RH104242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,533,286 - 72,533,406UniSTSGRCh37
Build 361471,603,039 - 71,603,159RGDNCBI36
Celera1452,596,486 - 52,596,606RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,699,742 - 52,699,862UniSTS
GeneMap99-GB4 RH Map14182.06UniSTS
SHGC-77849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,621,325 - 72,621,612UniSTSGRCh37
Build 361471,691,078 - 71,691,365RGDNCBI36
Celera1452,684,530 - 52,684,817RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,787,775 - 52,788,062UniSTS
TNG Radiation Hybrid Map1425381.0UniSTS
SHGC-80729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,576,482 - 72,576,755UniSTSGRCh37
Build 361471,646,235 - 71,646,508RGDNCBI36
Celera1452,639,679 - 52,639,952RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,742,931 - 52,743,204UniSTS
RH119814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,797,519 - 72,797,793UniSTSGRCh37
Build 361471,867,272 - 71,867,546RGDNCBI36
Celera1452,860,693 - 52,860,967RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,963,900 - 52,964,174UniSTS
TNG Radiation Hybrid Map1425920.0UniSTS
RH121567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,425,752 - 72,426,047UniSTSGRCh37
Build 361471,495,505 - 71,495,800RGDNCBI36
Celera1452,488,965 - 52,489,260RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,592,434 - 52,592,729UniSTS
TNG Radiation Hybrid Map1425451.0UniSTS
G60076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,030,369 - 73,030,467UniSTSGRCh37
Build 361472,100,122 - 72,100,220RGDNCBI36
Celera1453,093,548 - 53,093,646RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,196,896 - 53,196,994UniSTS
TNG Radiation Hybrid Map1425992.0UniSTS
D14S787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,033,268 - 73,033,418UniSTSGRCh37
Build 361472,103,021 - 72,103,171RGDNCBI36
Celera1453,096,447 - 53,096,597RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,199,795 - 53,199,939UniSTS
D14S1181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,976,982 - 72,977,147UniSTSGRCh37
Build 361472,046,735 - 72,046,900RGDNCBI36
Celera1453,040,156 - 53,040,321RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,143,503 - 53,143,668UniSTS
D14S1182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,822,787 - 72,822,914UniSTSGRCh37
Build 361471,892,540 - 71,892,667RGDNCBI36
Celera1452,885,963 - 52,886,090RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,989,193 - 52,989,320UniSTS
GDB:681455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,710,731 - 72,710,814UniSTSGRCh37
Build 361471,780,484 - 71,780,567RGDNCBI36
Celera1452,773,897 - 52,773,980RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,877,134 - 52,877,217UniSTS
SHGC-107399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,487,632 - 72,487,948UniSTSGRCh37
Build 361471,557,385 - 71,557,701RGDNCBI36
Celera1452,550,845 - 52,551,161RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,654,193 - 52,654,509UniSTS
TNG Radiation Hybrid Map1425439.0UniSTS
SHGC-151129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,027,367 - 73,027,641UniSTSGRCh37
Build 361472,097,120 - 72,097,394RGDNCBI36
Celera1453,090,546 - 53,090,820RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,193,894 - 53,194,168UniSTS
TNG Radiation Hybrid Map1426013.0UniSTS
TNG Radiation Hybrid Map102041.0UniSTS
TNG Radiation Hybrid Map1441817.0UniSTS
G38266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,999,845 - 73,000,091UniSTSGRCh37
Build 361472,069,598 - 72,069,844RGDNCBI36
Celera1453,063,017 - 53,063,263RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,166,365 - 53,166,611UniSTS
G38060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,527,428 - 72,527,639UniSTSGRCh37
Build 361471,597,181 - 71,597,392RGDNCBI36
Celera1452,590,630 - 52,590,841RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,693,886 - 52,694,097UniSTS
RGS6_788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,030,006 - 73,030,813UniSTSGRCh37
Build 361472,099,759 - 72,100,566RGDNCBI36
Celera1453,093,185 - 53,093,992RGD
HuRef1453,196,533 - 53,197,340UniSTS
A005E46  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,030,367 - 73,030,485UniSTSGRCh37
Build 361472,100,120 - 72,100,238RGDNCBI36
Celera1453,093,546 - 53,093,664RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,196,894 - 53,197,012UniSTS
GeneMap99-GB4 RH Map14185.49UniSTS
Whitehead-RH Map14255.2UniSTS
NCBI RH Map14734.8UniSTS
G38141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,813,067 - 72,813,316UniSTSGRCh37
Build 361471,882,820 - 71,883,069RGDNCBI36
Celera1452,876,241 - 52,876,490RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,979,473 - 52,979,722UniSTS
D14S1371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,032,205 - 73,032,305UniSTSGRCh37
Build 361472,101,958 - 72,102,058RGDNCBI36
Celera1453,095,384 - 53,095,484RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,198,732 - 53,198,832UniSTS
RH78916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,030,440 - 73,030,581UniSTSGRCh37
Build 361472,100,193 - 72,100,334RGDNCBI36
Celera1453,093,619 - 53,093,760RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,196,967 - 53,197,108UniSTS
GeneMap99-GB4 RH Map14183.36UniSTS
NCBI RH Map14709.0UniSTS
D14S912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,770,262 - 72,770,414UniSTSGRCh37
Build 361471,840,015 - 71,840,167RGDNCBI36
Celera1452,833,427 - 52,833,579RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,936,644 - 52,936,796UniSTS
TNG Radiation Hybrid Map1425908.0UniSTS
Stanford-G3 RH Map142613.0UniSTS
NCBI RH Map14743.8UniSTS
G36235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,971,281 - 72,971,409UniSTSGRCh37
Build 361472,041,034 - 72,041,162RGDNCBI36
Celera1453,034,450 - 53,034,578RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,137,801 - 53,137,929UniSTS
G38259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,412,480 - 72,412,804UniSTSGRCh37
Build 361471,482,233 - 71,482,557RGDNCBI36
Celera1452,475,684 - 52,476,008RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,579,155 - 52,579,479UniSTS
G35548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,969,515 - 72,969,614UniSTSGRCh37
Build 361472,039,268 - 72,039,367RGDNCBI36
Celera1453,032,684 - 53,032,783RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,136,035 - 53,136,134UniSTS
G35605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,997,669 - 72,997,839UniSTSGRCh37
Build 361472,067,422 - 72,067,592RGDNCBI36
Celera1453,060,840 - 53,061,011RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,164,188 - 53,164,359UniSTS
D12S831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,793,351 - 72,793,589UniSTSGRCh37
Build 361471,863,104 - 71,863,342RGDNCBI36
Celera1452,856,525 - 52,856,763RGD
HuRef11100,581,384 - 100,581,776UniSTS
HuRef1452,959,732 - 52,959,970UniSTS
HuRef6105,153,540 - 105,153,791UniSTS
G38073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,653,440 - 72,653,584UniSTSGRCh37
Build 361471,723,193 - 71,723,337RGDNCBI36
Celera1452,716,644 - 52,716,788RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,819,889 - 52,820,033UniSTS
RH45686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,468,664 - 72,468,830UniSTSGRCh37
Build 361471,538,417 - 71,538,583RGDNCBI36
Celera1452,531,854 - 52,532,020RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,635,202 - 52,635,368UniSTS
GeneMap99-GB4 RH Map14181.75UniSTS
NCBI RH Map14692.6UniSTS
G38279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,002,260 - 73,002,677UniSTSGRCh37
Build 361472,072,013 - 72,072,430RGDNCBI36
Celera1453,065,432 - 53,065,849RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,168,780 - 53,169,197UniSTS
SHGC-52498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,441,260 - 72,441,460UniSTSGRCh37
Build 361471,511,013 - 71,511,213RGDNCBI36
Celera1452,504,468 - 52,504,668RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,607,939 - 52,608,139UniSTS
TNG Radiation Hybrid Map1425459.0UniSTS
GeneMap99-G3 RH Map142654.0UniSTS
G35709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,695,254 - 72,695,381UniSTSGRCh37
Build 361471,765,007 - 71,765,134RGDNCBI36
Celera1452,758,424 - 52,758,551RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,861,674 - 52,861,801UniSTS
G38337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,727,313 - 72,727,430UniSTSGRCh37
Build 361471,797,066 - 71,797,183RGDNCBI36
Celera1452,790,479 - 52,790,596RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,893,716 - 52,893,833UniSTS
G38140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,902,258 - 72,902,411UniSTSGRCh37
Build 361471,972,011 - 71,972,164RGDNCBI36
Celera1452,965,433 - 52,965,586RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,068,636 - 53,068,789UniSTS
G38274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,430,643 - 72,430,748UniSTSGRCh37
Build 361471,500,396 - 71,500,501RGDNCBI36
Celera1452,493,856 - 52,493,961RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,597,325 - 52,597,430UniSTS
G38270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,550,307 - 72,550,575UniSTSGRCh37
Build 361471,620,060 - 71,620,328RGDNCBI36
Celera1452,613,508 - 52,613,776RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,716,765 - 52,717,033UniSTS
G38071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,518,748 - 72,519,097UniSTSGRCh37
Build 361471,588,501 - 71,588,850RGDNCBI36
Celera1452,581,953 - 52,582,302RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,685,205 - 52,685,554UniSTS
G38278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,965,827 - 72,966,128UniSTSGRCh37
Build 361472,035,580 - 72,035,881RGDNCBI36
Celera1453,028,996 - 53,029,297RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,132,347 - 53,132,648UniSTS
A047WF5  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,033,268 - 73,033,420UniSTSGRCh37
Build 361472,103,021 - 72,103,173RGDNCBI36
Celera1453,096,447 - 53,096,599RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,199,795 - 53,199,941UniSTS
Whitehead-YAC Contig Map9 UniSTS
RH15747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,899,903 - 72,900,028UniSTSGRCh37
Build 361471,969,656 - 71,969,781RGDNCBI36
Celera1452,963,078 - 52,963,203RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,066,281 - 53,066,406UniSTS
GeneMap99-GB4 RH Map14185.59UniSTS
NCBI RH Map14709.0UniSTS
RH70438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,516,683 - 72,516,815UniSTSGRCh37
Build 361471,586,436 - 71,586,568RGDNCBI36
Celera1452,579,888 - 52,580,020RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,683,140 - 52,683,272UniSTS
GeneMap99-GB4 RH Map14180.54UniSTS
D9S1990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,554,357 - 72,554,466UniSTSGRCh37
Build 361471,624,110 - 71,624,219RGDNCBI36
Celera1452,617,559 - 52,617,668RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,720,816 - 52,720,925UniSTS
Whitehead-YAC Contig Map9 UniSTS
G38264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,891,155 - 72,891,428UniSTSGRCh37
Build 361471,960,908 - 71,961,181RGDNCBI36
Celera1452,954,330 - 52,954,603RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,057,533 - 53,057,806UniSTS
RH45338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,606,128 - 72,606,246UniSTSGRCh37
Build 361471,675,881 - 71,675,999RGDNCBI36
Celera1452,669,335 - 52,669,453RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,772,581 - 52,772,699UniSTS
GeneMap99-GB4 RH Map14182.06UniSTS
G38070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371472,807,334 - 72,807,610UniSTSGRCh37
Build 361471,877,087 - 71,877,363RGDNCBI36
Celera1452,870,508 - 52,870,784RGD
Cytogenetic Map14q24.3UniSTS
HuRef1452,973,739 - 52,974,015UniSTS
G31413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371473,033,271 - 73,033,429UniSTSGRCh37
Build 361472,103,024 - 72,103,182RGDNCBI36
Celera1453,096,450 - 53,096,608RGD
Cytogenetic Map14q24.3UniSTS
HuRef1453,199,798 - 53,199,950UniSTS


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 1 118 11 2 13 2 335 468 18 15 13 328
Low 1043 1889 983 130 780 21 2781 1092 2948 128 958 1164 116 1 1189 1682 4 1
Below cutoff 1315 977 587 360 993 309 1159 1069 259 191 406 285 56 2 778 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021831 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017021834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449759 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449761 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047431990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054377115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001750613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF073920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF073921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF107619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF107620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF156932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH011570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY230154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY309097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY309098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY309099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY309100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC104877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC113572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX096120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA386861 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC317315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC343081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L40394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000343854   ⟹   ENSP00000341199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,352,093 - 72,566,529 (+)Ensembl
RefSeq Acc Id: ENST00000355512   ⟹   ENSP00000347699
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,964,792 - 72,537,713 (+)Ensembl
RefSeq Acc Id: ENST00000402788   ⟹   ENSP00000383953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,352,092 - 72,566,529 (+)Ensembl
RefSeq Acc Id: ENST00000404301   ⟹   ENSP00000385243
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,964,792 - 72,540,324 (+)Ensembl
RefSeq Acc Id: ENST00000406236   ⟹   ENSP00000384218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,964,792 - 72,540,324 (+)Ensembl
RefSeq Acc Id: ENST00000407322   ⟹   ENSP00000384612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,964,792 - 72,540,333 (+)Ensembl
RefSeq Acc Id: ENST00000434263   ⟹   ENSP00000412144
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,454,520 - 72,550,674 (+)Ensembl
RefSeq Acc Id: ENST00000553519
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,511,607 - 72,515,847 (+)Ensembl
RefSeq Acc Id: ENST00000553525   ⟹   ENSP00000451030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,932,429 - 72,566,530 (+)Ensembl
RefSeq Acc Id: ENST00000553530   ⟹   ENSP00000452331
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,933,116 - 72,566,526 (+)Ensembl
RefSeq Acc Id: ENST00000553690
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,420,979 - 72,474,069 (+)Ensembl
RefSeq Acc Id: ENST00000554300
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,540,062 - 72,562,837 (+)Ensembl
RefSeq Acc Id: ENST00000554474   ⟹   ENSP00000450858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,933,145 - 72,562,864 (+)Ensembl
RefSeq Acc Id: ENST00000554734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,473,987 - 72,477,260 (+)Ensembl
RefSeq Acc Id: ENST00000554782   ⟹   ENSP00000451912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,459,669 - 72,562,754 (+)Ensembl
RefSeq Acc Id: ENST00000555368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,454,520 - 72,478,331 (+)Ensembl
RefSeq Acc Id: ENST00000555571   ⟹   ENSP00000450936
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,932,617 - 72,562,467 (+)Ensembl
RefSeq Acc Id: ENST00000556437   ⟹   ENSP00000451855
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1471,933,232 - 72,562,592 (+)Ensembl
RefSeq Acc Id: ENST00000622468   ⟹   ENSP00000478186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,352,093 - 72,566,529 (+)Ensembl
RefSeq Acc Id: ENST00000644463   ⟹   ENSP00000496764
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1472,540,041 - 72,562,589 (+)Ensembl
RefSeq Acc Id: NM_001204416   ⟹   NP_001191345
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204417   ⟹   NP_001191346
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,967,477 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204418   ⟹   NP_001191347
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,967,477 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204419   ⟹   NP_001191348
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204420   ⟹   NP_001191349
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204421   ⟹   NP_001191350
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,967,477 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204422   ⟹   NP_001191351
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,967,477 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204423   ⟹   NP_001191352
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,171 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,336,952 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,137,624 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204424   ⟹   NP_001191353
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,291 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370270   ⟹   NP_001357199
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,171 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,624 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370271   ⟹   NP_001357200
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,527 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,980 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370272   ⟹   NP_001357201
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370273   ⟹   NP_001357202
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370274   ⟹   NP_001357203
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370275   ⟹   NP_001357204
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370276   ⟹   NP_001357205
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370277   ⟹   NP_001357206
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,527 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,980 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370278   ⟹   NP_001357207
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370279   ⟹   NP_001357208
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370280   ⟹   NP_001357209
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370281   ⟹   NP_001357210
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370282   ⟹   NP_001357211
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370283   ⟹   NP_001357212
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370284   ⟹   NP_001357213
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,527 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,980 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370286   ⟹   NP_001357215
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370287   ⟹   NP_001357216
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370288   ⟹   NP_001357217
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,527 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,980 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370289   ⟹   NP_001357218
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,171 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,624 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370290   ⟹   NP_001357219
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370291   ⟹   NP_001357220
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370292   ⟹   NP_001357221
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370293   ⟹   NP_001357222
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,527 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,138,980 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370294   ⟹   NP_001357223
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NM_004296   ⟹   NP_004287
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
GRCh371472,398,817 - 73,033,238 (+)ENTREZGENE
Build 361471,469,539 - 72,102,991 (+)NCBI Archive
HuRef1452,565,478 - 53,199,765 (+)ENTREZGENE
CHM1_11472,337,890 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: NR_135235
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 72,566,530 (+)NCBI
CHM1_11472,337,890 - 72,971,253 (+)NCBI
T2T-CHM13v2.01466,138,675 - 66,772,163 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537397   ⟹   XP_011535699
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381472,458,363 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021820   ⟹   XP_016877309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021822   ⟹   XP_016877311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,581,899 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021825   ⟹   XP_016877314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,630,029 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021826   ⟹   XP_016877315
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,541,568 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021827   ⟹   XP_016877316
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,579,483 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021828   ⟹   XP_016877317
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,538,411 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021830   ⟹   XP_016877319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,541,568 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021831   ⟹   XP_016877320
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,526,943 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021832   ⟹   XP_016877321
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,538,208 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017021833   ⟹   XP_016877322
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,518,412 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449759   ⟹   XP_024305527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449760   ⟹   XP_024305528
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,527 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449761   ⟹   XP_024305529
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,867,335 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449763   ⟹   XP_024305531
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381472,421,305 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449764   ⟹   XP_024305532
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381472,420,621 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449776   ⟹   XP_024305544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,566,530 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047431985   ⟹   XP_047287941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381472,454,528 - 72,566,530 (+)NCBI
RefSeq Acc Id: XM_047431987   ⟹   XP_047287943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,541,762 (+)NCBI
RefSeq Acc Id: XM_047431988   ⟹   XP_047287944
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381472,473,957 - 72,566,530 (+)NCBI
RefSeq Acc Id: XM_047431990   ⟹   XP_047287946
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,429 - 72,538,411 (+)NCBI
RefSeq Acc Id: XM_054377095   ⟹   XP_054233070
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,624 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377096   ⟹   XP_054233071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,072,765 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377097   ⟹   XP_054233072
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,138,980 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377098   ⟹   XP_054233073
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,546,225 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377099   ⟹   XP_054233074
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377100   ⟹   XP_054233075
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377101   ⟹   XP_054233076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377102   ⟹   XP_054233077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,138,675 - 66,747,291 (+)NCBI
RefSeq Acc Id: XM_054377103   ⟹   XP_054233078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,792,171 (+)NCBI
RefSeq Acc Id: XM_054377104   ⟹   XP_054233079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,747,291 (+)NCBI
RefSeq Acc Id: XM_054377105   ⟹   XP_054233080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,835,660 (+)NCBI
RefSeq Acc Id: XM_054377106   ⟹   XP_054233081
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,747,194 (+)NCBI
RefSeq Acc Id: XM_054377107   ⟹   XP_054233082
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,785,112 (+)NCBI
RefSeq Acc Id: XM_054377108   ⟹   XP_054233083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,745,600 (+)NCBI
RefSeq Acc Id: XM_054377109   ⟹   XP_054233084
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,747,194 (+)NCBI
RefSeq Acc Id: XM_054377110   ⟹   XP_054233085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,747,246 (+)NCBI
RefSeq Acc Id: XM_054377111   ⟹   XP_054233086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,733,794 (+)NCBI
RefSeq Acc Id: XM_054377112   ⟹   XP_054233087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,743,834 (+)NCBI
RefSeq Acc Id: XM_054377113   ⟹   XP_054233088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,772,163 (+)NCBI
RefSeq Acc Id: XM_054377114   ⟹   XP_054233089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,745,720 (+)NCBI
RefSeq Acc Id: XM_054377115   ⟹   XP_054233090
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01466,137,882 - 66,724,035 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001191345 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191346 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191347 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191348 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191349 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191350 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191351 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191352 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191353 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357199 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357200 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357201 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357202 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357203 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357204 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357205 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357206 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357207 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357208 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357209 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357210 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357211 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357212 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357213 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357215 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357216 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357217 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357218 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357219 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357220 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357221 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357222 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357223 (Get FASTA)   NCBI Sequence Viewer  
  NP_004287 (Get FASTA)   NCBI Sequence Viewer  
  XP_011535699 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877309 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877311 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877314 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877315 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877316 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877317 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877319 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877320 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877321 (Get FASTA)   NCBI Sequence Viewer  
  XP_016877322 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305527 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305528 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305529 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305531 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305532 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305544 (Get FASTA)   NCBI Sequence Viewer  
  XP_047287941 (Get FASTA)   NCBI Sequence Viewer  
  XP_047287943 (Get FASTA)   NCBI Sequence Viewer  
  XP_047287944 (Get FASTA)   NCBI Sequence Viewer  
  XP_047287946 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233070 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233071 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233072 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233073 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233074 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233075 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233076 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233077 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233078 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233079 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233080 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233081 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233082 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233083 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233084 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233085 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233086 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233087 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233088 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233089 (Get FASTA)   NCBI Sequence Viewer  
  XP_054233090 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC26049 (Get FASTA)   NCBI Sequence Viewer  
  AAC26050 (Get FASTA)   NCBI Sequence Viewer  
  AAC42001 (Get FASTA)   NCBI Sequence Viewer  
  AAC83180 (Get FASTA)   NCBI Sequence Viewer  
  AAD05031 (Get FASTA)   NCBI Sequence Viewer  
  AAD34717 (Get FASTA)   NCBI Sequence Viewer  
  AAD34718 (Get FASTA)   NCBI Sequence Viewer  
  AAD40183 (Get FASTA)   NCBI Sequence Viewer  
  AAI04878 (Get FASTA)   NCBI Sequence Viewer  
  AAI13573 (Get FASTA)   NCBI Sequence Viewer  
  AAM03010 (Get FASTA)   NCBI Sequence Viewer  
  AAM03012 (Get FASTA)   NCBI Sequence Viewer  
  AAP74386 (Get FASTA)   NCBI Sequence Viewer  
  AAP74387 (Get FASTA)   NCBI Sequence Viewer  
  AAP74388 (Get FASTA)   NCBI Sequence Viewer  
  AAP74389 (Get FASTA)   NCBI Sequence Viewer  
  BAD92699 (Get FASTA)   NCBI Sequence Viewer  
  BAG36265 (Get FASTA)   NCBI Sequence Viewer  
  BAH11786 (Get FASTA)   NCBI Sequence Viewer  
  BAH11917 (Get FASTA)   NCBI Sequence Viewer  
  BAH13671 (Get FASTA)   NCBI Sequence Viewer  
  EAW81062 (Get FASTA)   NCBI Sequence Viewer  
  EAW81063 (Get FASTA)   NCBI Sequence Viewer  
  EAW81064 (Get FASTA)   NCBI Sequence Viewer  
  EAW81065 (Get FASTA)   NCBI Sequence Viewer  
  EAW81066 (Get FASTA)   NCBI Sequence Viewer  
  EAW81067 (Get FASTA)   NCBI Sequence Viewer  
  EAW81068 (Get FASTA)   NCBI Sequence Viewer  
  EAW81069 (Get FASTA)   NCBI Sequence Viewer  
  EAW81070 (Get FASTA)   NCBI Sequence Viewer  
  EAW81071 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000341199
  ENSP00000341199.7
  ENSP00000347699
  ENSP00000347699.6
  ENSP00000383953
  ENSP00000383953.3
  ENSP00000384218
  ENSP00000384218.4
  ENSP00000384612
  ENSP00000384612.4
  ENSP00000385243.2
  ENSP00000412144
  ENSP00000412144.2
  ENSP00000450858
  ENSP00000450858.1
  ENSP00000450936
  ENSP00000450936.1
  ENSP00000451030
  ENSP00000451030.1
  ENSP00000451855
  ENSP00000451855.1
  ENSP00000451912.1
  ENSP00000452331
  ENSP00000452331.1
  ENSP00000478186.1
  ENSP00000496764.1
GenBank Protein P49758 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001191352   ⟸   NM_001204423
- Peptide Label: isoform 9
- UniProtKB: B7Z2N1 (UniProtKB/TrEMBL),   A0A087WTW9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191353   ⟸   NM_001204424
- Peptide Label: isoform 1
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191345   ⟸   NM_001204416
- Peptide Label: isoform 1
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_004287   ⟸   NM_004296
- Peptide Label: isoform 2
- UniProtKB: Q9Y245 (UniProtKB/Swiss-Prot),   Q9UDT0 (UniProtKB/Swiss-Prot),   Q9UDS8 (UniProtKB/Swiss-Prot),   Q8TE22 (UniProtKB/Swiss-Prot),   Q8TE21 (UniProtKB/Swiss-Prot),   Q8TE20 (UniProtKB/Swiss-Prot),   Q8TE19 (UniProtKB/Swiss-Prot),   Q8TE18 (UniProtKB/Swiss-Prot),   Q8TE17 (UniProtKB/Swiss-Prot),   Q8TE16 (UniProtKB/Swiss-Prot),   Q8TE15 (UniProtKB/Swiss-Prot),   Q8TE14 (UniProtKB/Swiss-Prot),   Q8TE13 (UniProtKB/Swiss-Prot),   Q7Z4K6 (UniProtKB/Swiss-Prot),   Q7Z4K5 (UniProtKB/Swiss-Prot),   Q7Z4K4 (UniProtKB/Swiss-Prot),   Q7Z4K3 (UniProtKB/Swiss-Prot),   O75577 (UniProtKB/Swiss-Prot),   O75576 (UniProtKB/Swiss-Prot),   F8W7W5 (UniProtKB/Swiss-Prot),   C9JE95 (UniProtKB/Swiss-Prot),   Q9Y647 (UniProtKB/Swiss-Prot),   P49758 (UniProtKB/Swiss-Prot),   Q2M3K2 (UniProtKB/TrEMBL),   B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191348   ⟸   NM_001204419
- Peptide Label: isoform 5
- UniProtKB: A0A0A0MRA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191349   ⟸   NM_001204420
- Peptide Label: isoform 6
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191346   ⟸   NM_001204417
- Peptide Label: isoform 3
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191347   ⟸   NM_001204418
- Peptide Label: isoform 4
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191350   ⟸   NM_001204421
- Peptide Label: isoform 7
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191351   ⟸   NM_001204422
- Peptide Label: isoform 8
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011535699   ⟸   XM_011537397
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016877314   ⟸   XM_017021825
- Peptide Label: isoform X8
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877311   ⟸   XM_017021822
- Peptide Label: isoform X6
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877316   ⟸   XM_017021827
- Peptide Label: isoform X10
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877309   ⟸   XM_017021820
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016877319   ⟸   XM_017021830
- Peptide Label: isoform X13
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877315   ⟸   XM_017021826
- Peptide Label: isoform X9
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877317   ⟸   XM_017021828
- Peptide Label: isoform X12
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877321   ⟸   XM_017021832
- Peptide Label: isoform X15
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877320   ⟸   XM_017021831
- Peptide Label: isoform X14
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016877322   ⟸   XM_017021833
- Peptide Label: isoform X18
- Sequence:
RefSeq Acc Id: XP_024305529   ⟸   XM_024449761
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024305527   ⟸   XM_024449759
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024305544   ⟸   XM_024449776
- Peptide Label: isoform X16
- UniProtKB: A0A0A0MRA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024305528   ⟸   XM_024449760
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024305532   ⟸   XM_024449764
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_024305531   ⟸   XM_024449763
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: NP_001357199   ⟸   NM_001370270
- Peptide Label: isoform 10
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357218   ⟸   NM_001370289
- Peptide Label: isoform 2
- UniProtKB: Q9Y245 (UniProtKB/Swiss-Prot),   Q9UDT0 (UniProtKB/Swiss-Prot),   Q9UDS8 (UniProtKB/Swiss-Prot),   Q8TE22 (UniProtKB/Swiss-Prot),   Q8TE21 (UniProtKB/Swiss-Prot),   Q8TE20 (UniProtKB/Swiss-Prot),   Q8TE19 (UniProtKB/Swiss-Prot),   Q8TE18 (UniProtKB/Swiss-Prot),   Q8TE17 (UniProtKB/Swiss-Prot),   Q8TE16 (UniProtKB/Swiss-Prot),   Q8TE15 (UniProtKB/Swiss-Prot),   Q8TE14 (UniProtKB/Swiss-Prot),   Q8TE13 (UniProtKB/Swiss-Prot),   Q7Z4K6 (UniProtKB/Swiss-Prot),   Q7Z4K5 (UniProtKB/Swiss-Prot),   Q7Z4K4 (UniProtKB/Swiss-Prot),   Q7Z4K3 (UniProtKB/Swiss-Prot),   P49758 (UniProtKB/Swiss-Prot),   O75577 (UniProtKB/Swiss-Prot),   O75576 (UniProtKB/Swiss-Prot),   F8W7W5 (UniProtKB/Swiss-Prot),   C9JE95 (UniProtKB/Swiss-Prot),   Q9Y647 (UniProtKB/Swiss-Prot),   Q2M3K2 (UniProtKB/TrEMBL),   B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357211   ⟸   NM_001370282
- Peptide Label: isoform 17
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357202   ⟸   NM_001370273
- Peptide Label: isoform 10
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357204   ⟸   NM_001370275
- Peptide Label: isoform 11
RefSeq Acc Id: NP_001357220   ⟸   NM_001370291
- Peptide Label: isoform 20
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357216   ⟸   NM_001370287
- Peptide Label: isoform 2
- UniProtKB: Q9Y245 (UniProtKB/Swiss-Prot),   Q9UDT0 (UniProtKB/Swiss-Prot),   Q9UDS8 (UniProtKB/Swiss-Prot),   Q8TE22 (UniProtKB/Swiss-Prot),   Q8TE21 (UniProtKB/Swiss-Prot),   Q8TE20 (UniProtKB/Swiss-Prot),   Q8TE19 (UniProtKB/Swiss-Prot),   Q8TE18 (UniProtKB/Swiss-Prot),   Q8TE17 (UniProtKB/Swiss-Prot),   Q8TE16 (UniProtKB/Swiss-Prot),   Q8TE15 (UniProtKB/Swiss-Prot),   Q8TE14 (UniProtKB/Swiss-Prot),   Q8TE13 (UniProtKB/Swiss-Prot),   Q7Z4K6 (UniProtKB/Swiss-Prot),   Q7Z4K5 (UniProtKB/Swiss-Prot),   Q7Z4K4 (UniProtKB/Swiss-Prot),   Q7Z4K3 (UniProtKB/Swiss-Prot),   P49758 (UniProtKB/Swiss-Prot),   O75577 (UniProtKB/Swiss-Prot),   O75576 (UniProtKB/Swiss-Prot),   F8W7W5 (UniProtKB/Swiss-Prot),   C9JE95 (UniProtKB/Swiss-Prot),   Q9Y647 (UniProtKB/Swiss-Prot),   Q2M3K2 (UniProtKB/TrEMBL),   B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357209   ⟸   NM_001370280
- Peptide Label: isoform 15
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357221   ⟸   NM_001370292
- Peptide Label: isoform 6
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357223   ⟸   NM_001370294
- Peptide Label: isoform 21
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357215   ⟸   NM_001370286
- Peptide Label: isoform 19
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357207   ⟸   NM_001370278
- Peptide Label: isoform 13
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357210   ⟸   NM_001370281
- Peptide Label: isoform 16
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357203   ⟸   NM_001370274
- Peptide Label: isoform 10
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357201   ⟸   NM_001370272
- Peptide Label: isoform 10
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357205   ⟸   NM_001370276
- Peptide Label: isoform 11
RefSeq Acc Id: NP_001357219   ⟸   NM_001370290
- Peptide Label: isoform 20
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357212   ⟸   NM_001370283
- Peptide Label: isoform 18
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357208   ⟸   NM_001370279
- Peptide Label: isoform 14
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357206   ⟸   NM_001370277
- Peptide Label: isoform 12
- UniProtKB: B7Z7N5 (UniProtKB/TrEMBL),   C9J109 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357200   ⟸   NM_001370271
- Peptide Label: isoform 10
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357213   ⟸   NM_001370284
- Peptide Label: isoform 1
- UniProtKB: B7Z2A0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357217   ⟸   NM_001370288
- Peptide Label: isoform 2
- UniProtKB: Q9Y245 (UniProtKB/Swiss-Prot),   Q9UDT0 (UniProtKB/Swiss-Prot),   Q9UDS8 (UniProtKB/Swiss-Prot),   Q8TE22 (UniProtKB/Swiss-Prot),   Q8TE21 (UniProtKB/Swiss-Prot),   Q8TE20 (UniProtKB/Swiss-Prot),   Q8TE19 (UniProtKB/Swiss-Prot),   Q8TE18 (UniProtKB/Swiss-Prot),   Q8TE17 (UniProtKB/Swiss-Prot),   Q8TE16 (UniProtKB/Swiss-Prot),   Q8TE15 (UniProtKB/Swiss-Prot),   Q8TE14 (UniProtKB/Swiss-Prot),   Q8TE13 (UniProtKB/Swiss-Prot),   Q7Z4K6 (UniProtKB/Swiss-Prot),   Q7Z4K5 (UniProtKB/Swiss-Prot),   Q7Z4K4 (UniProtKB/Swiss-Prot),   Q7Z4K3 (UniProtKB/Swiss-Prot),   P49758 (UniProtKB/Swiss-Prot),   O75577 (UniProtKB/Swiss-Prot),   O75576 (UniProtKB/Swiss-Prot),   F8W7W5 (UniProtKB/Swiss-Prot),   C9JE95 (UniProtKB/Swiss-Prot),   Q9Y647 (UniProtKB/Swiss-Prot),   Q2M3K2 (UniProtKB/TrEMBL),   B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357222   ⟸   NM_001370293
- Peptide Label: isoform 6
- UniProtKB: B2R8R8 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000450936   ⟸   ENST00000555571
RefSeq Acc Id: ENSP00000451855   ⟸   ENST00000556437
RefSeq Acc Id: ENSP00000478186   ⟸   ENST00000622468
RefSeq Acc Id: ENSP00000383953   ⟸   ENST00000402788
RefSeq Acc Id: ENSP00000385243   ⟸   ENST00000404301
RefSeq Acc Id: ENSP00000384218   ⟸   ENST00000406236
RefSeq Acc Id: ENSP00000384612   ⟸   ENST00000407322
RefSeq Acc Id: ENSP00000347699   ⟸   ENST00000355512
RefSeq Acc Id: ENSP00000496764   ⟸   ENST00000644463
RefSeq Acc Id: ENSP00000412144   ⟸   ENST00000434263
RefSeq Acc Id: ENSP00000452331   ⟸   ENST00000553530
RefSeq Acc Id: ENSP00000451030   ⟸   ENST00000553525
RefSeq Acc Id: ENSP00000341199   ⟸   ENST00000343854
RefSeq Acc Id: ENSP00000450858   ⟸   ENST00000554474
RefSeq Acc Id: ENSP00000451912   ⟸   ENST00000554782
RefSeq Acc Id: XP_047287943   ⟸   XM_047431987
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047287946   ⟸   XM_047431990
- Peptide Label: isoform X17
RefSeq Acc Id: XP_047287941   ⟸   XM_047431985
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047287944   ⟸   XM_047431988
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054233071   ⟸   XM_054377096
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054233070   ⟸   XM_054377095
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054233080   ⟸   XM_054377105
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054233078   ⟸   XM_054377103
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054233082   ⟸   XM_054377107
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054233076   ⟸   XM_054377101
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054233075   ⟸   XM_054377100
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054233088   ⟸   XM_054377113
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054233074   ⟸   XM_054377099
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054233079   ⟸   XM_054377104
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054233085   ⟸   XM_054377110
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054233081   ⟸   XM_054377106
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054233084   ⟸   XM_054377109
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054233089   ⟸   XM_054377114
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054233083   ⟸   XM_054377108
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054233087   ⟸   XM_054377112
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054233086   ⟸   XM_054377111
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054233090   ⟸   XM_054377115
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054233077   ⟸   XM_054377102
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054233072   ⟸   XM_054377097
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054233073   ⟸   XM_054377098
- Peptide Label: isoform X20
Protein Domains
DEP   G protein gamma   RGS

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P49758-F1-model_v2 AlphaFold P49758 1-472 view protein structure

Promoters
RGD ID:6791836
Promoter ID:HG_KWN:19704
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:NM_004296,   UC001XMY.2,   UC001XNA.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361471,468,951 - 71,469,652 (+)MPROMDB
RGD ID:7228061
Promoter ID:EPDNEW_H19776
Type:initiation region
Name:RGS6_4
Description:regulator of G protein signaling 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19775  EPDNEW_H19777  EPDNEW_H19778  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,092 - 71,932,152EPDNEW
RGD ID:7228063
Promoter ID:EPDNEW_H19777
Type:initiation region
Name:RGS6_2
Description:regulator of G protein signaling 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19775  EPDNEW_H19776  EPDNEW_H19778  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,932,580 - 71,932,640EPDNEW
RGD ID:7228065
Promoter ID:EPDNEW_H19778
Type:initiation region
Name:RGS6_1
Description:regulator of G protein signaling 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19775  EPDNEW_H19776  EPDNEW_H19777  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381471,933,222 - 71,933,282EPDNEW
RGD ID:6791838
Promoter ID:HG_KWN:19707
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell
Transcripts:UC010ARG.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361471,957,186 - 71,957,686 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10002 AgrOrtholog
COSMIC RGS6 COSMIC
Ensembl Genes ENSG00000182732 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000343854 ENTREZGENE
  ENST00000343854.10 UniProtKB/TrEMBL
  ENST00000355512 ENTREZGENE
  ENST00000355512.10 UniProtKB/Swiss-Prot
  ENST00000402788 ENTREZGENE
  ENST00000402788.6 UniProtKB/TrEMBL
  ENST00000404301.6 UniProtKB/Swiss-Prot
  ENST00000406236 ENTREZGENE
  ENST00000406236.8 UniProtKB/Swiss-Prot
  ENST00000407322 ENTREZGENE
  ENST00000407322.8 UniProtKB/Swiss-Prot
  ENST00000434263 ENTREZGENE
  ENST00000434263.6 UniProtKB/TrEMBL
  ENST00000553525 ENTREZGENE
  ENST00000553525.6 UniProtKB/Swiss-Prot
  ENST00000553530 ENTREZGENE
  ENST00000553530.5 UniProtKB/Swiss-Prot
  ENST00000554474 ENTREZGENE
  ENST00000554474.5 UniProtKB/Swiss-Prot
  ENST00000554782.1 UniProtKB/Swiss-Prot
  ENST00000555571 ENTREZGENE
  ENST00000555571.5 UniProtKB/Swiss-Prot
  ENST00000556437 ENTREZGENE
  ENST00000556437.5 UniProtKB/Swiss-Prot
  ENST00000622468.4 UniProtKB/TrEMBL
  ENST00000644463.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.10.1240.60 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.10.167.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.10.196.10 UniProtKB/TrEMBL
  4.10.260.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000182732 GTEx
HGNC ID HGNC:10002 ENTREZGENE
Human Proteome Map RGS6 Human Proteome Map
InterPro DEP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G-protein_gamma-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GGL_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS6/7/9/11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS6/7/9/11_DHEX_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS6_RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS_DHEX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS_subdom1/3 UniProtKB/TrEMBL
  RGS_subdomain_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH-like_DNA-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH_DNA-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9628 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 9628 ENTREZGENE
OMIM 603894 OMIM
PANTHER LP21163P UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  REGULATOR OF G-PROTEIN SIGNALING 6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DEP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G-gamma UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS_DHEX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34377 PharmGKB
PRINTS RGSPROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE DEP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DEP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_gamma UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GGL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF46785 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48097 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48670 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WTW9 ENTREZGENE, UniProtKB/TrEMBL
  A0A0A0MRA9 ENTREZGENE, UniProtKB/TrEMBL
  A0A2R8Y8A2_HUMAN UniProtKB/TrEMBL
  B2R8R8 ENTREZGENE, UniProtKB/TrEMBL
  B7Z2A0 ENTREZGENE, UniProtKB/TrEMBL
  B7Z2N1 ENTREZGENE, UniProtKB/TrEMBL
  B7Z7N5 ENTREZGENE, UniProtKB/TrEMBL
  C9J109 ENTREZGENE
  C9JE95 ENTREZGENE
  F8W7W5 ENTREZGENE
  O75576 ENTREZGENE
  O75577 ENTREZGENE
  P49758 ENTREZGENE
  Q2M3K2 ENTREZGENE, UniProtKB/TrEMBL
  Q7Z4K3 ENTREZGENE
  Q7Z4K4 ENTREZGENE
  Q7Z4K5 ENTREZGENE
  Q7Z4K6 ENTREZGENE
  Q8TE13 ENTREZGENE
  Q8TE14 ENTREZGENE
  Q8TE15 ENTREZGENE
  Q8TE16 ENTREZGENE
  Q8TE17 ENTREZGENE
  Q8TE18 ENTREZGENE
  Q8TE19 ENTREZGENE
  Q8TE20 ENTREZGENE
  Q8TE21 ENTREZGENE
  Q8TE22 ENTREZGENE
  Q9UDS8 ENTREZGENE
  Q9UDT0 ENTREZGENE
  Q9Y245 ENTREZGENE
  Q9Y647 ENTREZGENE
  RGS6_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary C9J109 UniProtKB/TrEMBL
  C9JE95 UniProtKB/Swiss-Prot
  F8W7W5 UniProtKB/Swiss-Prot
  O75576 UniProtKB/Swiss-Prot
  O75577 UniProtKB/Swiss-Prot
  Q7Z4K3 UniProtKB/Swiss-Prot
  Q7Z4K4 UniProtKB/Swiss-Prot
  Q7Z4K5 UniProtKB/Swiss-Prot
  Q7Z4K6 UniProtKB/Swiss-Prot
  Q8TE13 UniProtKB/Swiss-Prot
  Q8TE14 UniProtKB/Swiss-Prot
  Q8TE15 UniProtKB/Swiss-Prot
  Q8TE16 UniProtKB/Swiss-Prot
  Q8TE17 UniProtKB/Swiss-Prot
  Q8TE18 UniProtKB/Swiss-Prot
  Q8TE19 UniProtKB/Swiss-Prot
  Q8TE20 UniProtKB/Swiss-Prot
  Q8TE21 UniProtKB/Swiss-Prot
  Q8TE22 UniProtKB/Swiss-Prot
  Q9UDS8 UniProtKB/Swiss-Prot
  Q9UDT0 UniProtKB/Swiss-Prot
  Q9Y245 UniProtKB/Swiss-Prot
  Q9Y647 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-04-18 RGS6  regulator of G protein signaling 6    regulator of G-protein signaling 6  Symbol and/or name change 5135510 APPROVED