SLC22A12 (solute carrier family 22 member 12) - Rat Genome Database

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Gene: SLC22A12 (solute carrier family 22 member 12) Homo sapiens
Analyze
Symbol: SLC22A12
Name: solute carrier family 22 member 12
RGD ID: 1323543
HGNC Page HGNC:17989
Description: Enables PDZ domain binding activity and urate transmembrane transporter activity. Involved in response to xenobiotic stimulus; urate metabolic process; and urate transport. Located in apical plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: OAT4L; organic anion transporter 4-like protein; renal-specific transporter; RST; solute carrier family 22 (organic anion/cation transporter), member 12; solute carrier family 22 (organic anion/urate transporter), member 12; URAT1; urate anion exchanger 1; urate transporter 1; urate:anion antiporter SLC22A12
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
GRCh381164,591,220 - 64,602,344 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1164,590,641 - 64,602,353 (+)EnsemblGRCh38hg38GRCh38
GRCh371164,358,692 - 64,369,816 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361164,114,858 - 64,126,396 (+)NCBINCBI36Build 36hg18NCBI36
Build 341164,114,857 - 64,126,396NCBI
Celera1161,684,540 - 61,696,078 (+)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1160,685,738 - 60,696,371 (+)NCBIHuRef
CHM1_11164,241,496 - 64,253,033 (+)NCBICHM1_1
T2T-CHM13v2.01164,583,912 - 64,595,327 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,1-dichloroethene  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-D  (ISO)
2-hydroxypropanoic acid  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
5-azaorotic acid  (ISO)
6-propyl-2-thiouracil  (ISO)
7,9-dihydro-1H-purine-2,6,8(3H)-trione  (EXP,ISO)
acrylamide  (ISO)
allopurinol  (ISO)
alloxanthine  (EXP)
ammonium chloride  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
barium(0)  (ISO)
benzarone  (EXP)
benzbromarone  (EXP,ISO)
benzo[a]pyrene  (ISO)
benzylpenicillin  (ISO)
bisphenol A  (EXP,ISO)
buta-1,3-diene  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
CGP 52608  (EXP)
D-gluconic acid  (ISO)
decabromodiphenyl ether  (ISO)
dehydroepiandrosterone sulfate  (ISO)
dichlorine  (EXP)
dichloroacetic acid  (ISO)
diethyl pyrocarbonate  (ISO)
E3040  (EXP)
enalapril  (EXP)
estrone 3-sulfate  (EXP)
fructose  (ISO)
hypoxanthine  (ISO)
imperatorin  (ISO)
indometacin  (EXP)
isoimperatorin  (ISO)
losartan  (EXP)
mangiferin  (ISO)
methylmercury chloride  (ISO)
ochratoxin A  (ISO)
ouabain  (ISO)
p-aminohippuric acid  (ISO)
paracetamol  (ISO)
perfluorodecanoic acid  (EXP)
perfluoroheptanoic acid  (EXP)
perfluorohexanoic acid  (EXP)
perfluorononanoic acid  (EXP)
perfluorooctanoic acid  (EXP)
phenobarbital  (ISO)
phenylbutazone  (EXP)
pirinixic acid  (ISO)
Potassium 2,6-dihydroxytriazinecarboxylate  (ISO)
potassium atom  (ISO)
probenecid  (EXP,ISO)
psoralen  (ISO)
pterostilbene  (ISO)
pyrazine-2-carboxylic acid  (ISO)
pyrazinecarboxamide  (EXP)
quercetin  (ISO)
rac-lactic acid  (ISO)
rutin  (ISO)
salicylates  (EXP)
sodium arsenite  (EXP)
stilben-4-ol  (ISO)
sulfinpyrazone  (EXP)
trans-piceid  (ISO)
trichloroethene  (ISO)
triptonide  (ISO)
valproic acid  (EXP,ISO)
vancomycin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
apical plasma membrane  (IDA,IEA,ISO)
brush border membrane  (ISS,NAS)
extracellular exosome  (HDA)
membrane  (IDA,IEA)
plasma membrane  (IDA,IEA,IMP,TAS)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Insulin stimulates uric acid reabsorption via regulating urate transporter 1 and ATP-binding cassette subfamily G member 2. null
2. Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Enomoto A, etal., Nature. 2002 May 23;417(6887):447-52. Epub 2002 Apr 14.
3. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
4. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
7. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
8. Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia. Wakida N, etal., J Clin Endocrinol Metab. 2005 Apr;90(4):2169-74. Epub 2005 Jan 5.
Additional References at PubMed
PMID:12477932   PMID:12975309   PMID:14531806   PMID:14694169   PMID:14702039   PMID:15304510   PMID:15327384   PMID:15338274   PMID:15772301   PMID:15772829   PMID:16059895   PMID:16344560  
PMID:16385546   PMID:16775029   PMID:16837472   PMID:16920156   PMID:17445045   PMID:17567994   PMID:17891408   PMID:17891652   PMID:18409511   PMID:18492088   PMID:18670416   PMID:18701466  
PMID:18824160   PMID:18936980   PMID:19019168   PMID:19056867   PMID:19503597   PMID:19762362   PMID:19833602   PMID:19890391   PMID:20139978   PMID:20162742   PMID:20162743   PMID:20714133  
PMID:21148271   PMID:21154327   PMID:21211204   PMID:21350910   PMID:21366895   PMID:21544634   PMID:21614936   PMID:21722610   PMID:21768215   PMID:21873635   PMID:22000646   PMID:22132991  
PMID:22194875   PMID:22564045   PMID:22688828   PMID:22797727   PMID:22841915   PMID:22942308   PMID:22971602   PMID:23043931   PMID:23129426   PMID:23148994   PMID:23152669   PMID:23238572  
PMID:23263486   PMID:23291366   PMID:23386035   PMID:23544272   PMID:23981340   PMID:24107611   PMID:24344204   PMID:24360580   PMID:24723238   PMID:25268603   PMID:25275768   PMID:25739858  
PMID:26033041   PMID:26086348   PMID:26290326   PMID:26418379   PMID:26500098   PMID:26821810   PMID:27225847   PMID:27713539   PMID:27899376   PMID:27906637   PMID:28514442   PMID:28870626  
PMID:29126251   PMID:29215084   PMID:29352852   PMID:29486147   PMID:29958533   PMID:30097038   PMID:30315176   PMID:30621105   PMID:30920107   PMID:31131560   PMID:31257523   PMID:31478104  
PMID:31591475   PMID:31841133   PMID:32005656   PMID:32183743   PMID:32271837   PMID:32283759   PMID:32375679   PMID:33008107   PMID:33011794   PMID:33132325   PMID:33368618   PMID:33821957  
PMID:33961781   PMID:34255816   PMID:34498315   PMID:34631016  


Genomics

Comparative Map Data
SLC22A12
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381164,591,220 - 64,602,344 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1164,590,641 - 64,602,353 (+)EnsemblGRCh38hg38GRCh38
GRCh371164,358,692 - 64,369,816 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361164,114,858 - 64,126,396 (+)NCBINCBI36Build 36hg18NCBI36
Build 341164,114,857 - 64,126,396NCBI
Celera1161,684,540 - 61,696,078 (+)NCBICelera
Cytogenetic Map11q13.1NCBI
HuRef1160,685,738 - 60,696,371 (+)NCBIHuRef
CHM1_11164,241,496 - 64,253,033 (+)NCBICHM1_1
T2T-CHM13v2.01164,583,912 - 64,595,327 (+)NCBIT2T-CHM13v2.0
Slc22a12
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39196,585,884 - 6,593,100 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl196,585,875 - 6,593,062 (-)EnsemblGRCm39 Ensembl
GRCm38196,535,854 - 6,543,070 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl196,535,845 - 6,543,032 (-)EnsemblGRCm38mm10GRCm38
MGSCv37196,535,854 - 6,543,070 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36196,535,854 - 6,543,006 (-)NCBIMGSCv36mm8
Celera196,408,578 - 6,415,794 (-)NCBICelera
Cytogenetic Map19ANCBI
Slc22a12
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21203,845,039 - 203,852,496 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1203,845,048 - 203,853,555 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1212,194,211 - 212,201,339 (-)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.01219,290,324 - 219,297,440 (-)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.01211,981,381 - 211,988,497 (-)NCBIRnor_WKY
Rnor_6.01221,910,787 - 221,919,277 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1221,910,767 - 221,919,301 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01228,902,080 - 228,910,569 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41209,320,804 - 209,327,918 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11209,479,477 - 209,480,301 (-)NCBI
Celera1201,379,795 - 201,386,875 (-)NCBICelera
Cytogenetic Map1q43NCBI
Slc22a12
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542220,556,098 - 20,596,012 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542220,555,458 - 20,561,818 (-)NCBIChiLan1.0ChiLan1.0
SLC22A12
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11163,289,393 - 63,300,742 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1163,290,329 - 63,299,047 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01159,944,311 - 59,956,102 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
SLC22A12
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11852,541,820 - 52,550,037 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1852,542,497 - 52,549,655 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1851,149,805 - 51,156,963 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01853,587,392 - 53,595,590 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1853,587,387 - 53,595,227 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11852,678,526 - 52,685,694 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01852,264,797 - 52,271,967 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01853,048,889 - 53,056,060 (-)NCBIUU_Cfam_GSD_1.0
Slc22a12
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049478,250,573 - 8,258,303 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365994,693,352 - 4,698,721 (-)EnsemblSpeTri2.0
SpeTri2.0NW_0049365994,693,493 - 4,698,556 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLC22A12
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl27,558,535 - 7,565,751 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.127,557,822 - 7,565,801 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.226,688,333 - 6,696,292 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SLC22A12
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.119,633,589 - 9,644,519 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl19,632,645 - 9,643,664 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038107,023,694 - 107,035,578 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Slc22a12
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476721,772,744 - 21,779,230 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476721,771,137 - 21,780,305 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SLC22A12
133 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2898
Count of miRNA genes:551
Interacting mature miRNAs:616
Transcripts:ENST00000336464, ENST00000377567, ENST00000377572, ENST00000377574, ENST00000473690
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
RH98949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,639 - 64,369,799UniSTSGRCh37
Build 361164,126,215 - 64,126,375RGDNCBI36
Celera1161,695,897 - 61,696,057RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,696,185 - 60,696,345UniSTS
ECD00270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,357,712 - 64,358,629UniSTSGRCh37
Build 361164,114,288 - 64,115,205RGDNCBI36
Celera1161,683,970 - 61,684,887RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,685,168 - 60,686,085UniSTS
ECD00836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,673 - 64,359,561UniSTSGRCh37
Build 361164,115,249 - 64,116,137RGDNCBI36
Celera1161,684,931 - 61,685,819RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,129 - 60,687,017UniSTS
ECD01395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,359,667 - 64,360,533UniSTSGRCh37
Build 361164,116,243 - 64,117,109RGDNCBI36
Celera1161,685,925 - 61,686,791RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,687,123 - 60,687,989UniSTS
ECD01422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,360,588 - 64,361,453UniSTSGRCh37
Build 361164,117,164 - 64,118,029RGDNCBI36
Celera1161,686,846 - 61,687,711RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,688,044 - 60,688,909UniSTS
ECD04909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,894 - 64,366,644UniSTSGRCh37
Build 361164,122,470 - 64,123,220RGDNCBI36
Celera1161,692,152 - 61,692,902RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,692,295 - 60,693,045UniSTS
ECD06038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,087 - 64,365,806UniSTSGRCh37
Build 361164,121,663 - 64,122,382RGDNCBI36
Celera1161,691,345 - 61,692,064RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,691,488 - 60,692,207UniSTS
ECD10161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,368,641 - 64,369,250UniSTSGRCh37
Build 361164,125,217 - 64,125,826RGDNCBI36
Celera1161,694,899 - 61,695,508RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,695,187 - 60,695,796UniSTS
ECD10338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,154 - 64,367,758UniSTSGRCh37
Build 361164,123,730 - 64,124,334RGDNCBI36
Celera1161,693,412 - 61,694,016RGD
Cytogenetic Map11q13.1UniSTS
ECD10558  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,821 - 64,368,419UniSTSGRCh37
Build 361164,124,397 - 64,124,995RGDNCBI36
Celera1161,694,079 - 61,694,677RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,694,367 - 60,694,965UniSTS
ECD10646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,332 - 64,369,927UniSTSGRCh37
Build 361164,125,908 - 64,126,503RGDNCBI36
Celera1161,695,590 - 61,696,185RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,695,878 - 60,696,473UniSTS
ECD17261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,363,961 - 64,364,367UniSTSGRCh37
Build 361164,120,537 - 64,120,943RGDNCBI36
Celera1161,690,219 - 61,690,625RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,690,362 - 60,690,768UniSTS
ECD18162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,356,885 - 64,357,255UniSTSGRCh37
Build 361164,113,461 - 64,113,831RGDNCBI36
Celera1161,683,143 - 61,683,513RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,684,341 - 60,684,711UniSTS
ECD20376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,361,578 - 64,361,864UniSTSGRCh37
Build 361164,118,154 - 64,118,440RGDNCBI36
Celera1161,687,836 - 61,688,122RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,689,034 - 60,689,320UniSTS
REN55621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,356,444 - 64,356,693UniSTSGRCh37
Build 361164,113,020 - 64,113,269RGDNCBI36
Celera1161,682,702 - 61,682,951RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,683,900 - 60,684,149UniSTS
REN55622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,356,668 - 64,356,921UniSTSGRCh37
Build 361164,113,244 - 64,113,497RGDNCBI36
Celera1161,682,926 - 61,683,179RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,684,124 - 60,684,377UniSTS
REN55623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,356,883 - 64,357,139UniSTSGRCh37
Build 361164,113,459 - 64,113,715RGDNCBI36
Celera1161,683,141 - 61,683,397RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,684,339 - 60,684,595UniSTS
REN55624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,357,114 - 64,357,351UniSTSGRCh37
Build 361164,113,690 - 64,113,927RGDNCBI36
Celera1161,683,372 - 61,683,609RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,684,570 - 60,684,807UniSTS
REN55625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,357,336 - 64,357,560UniSTSGRCh37
Build 361164,113,912 - 64,114,136RGDNCBI36
Celera1161,683,594 - 61,683,818RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,684,792 - 60,685,016UniSTS
REN55626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,357,520 - 64,357,761UniSTSGRCh37
Build 361164,114,096 - 64,114,337RGDNCBI36
Celera1161,683,778 - 61,684,019RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,684,976 - 60,685,217UniSTS
REN55627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,357,730 - 64,357,957UniSTSGRCh37
Build 361164,114,306 - 64,114,533RGDNCBI36
Celera1161,683,988 - 61,684,215RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,685,186 - 60,685,413UniSTS
REN55628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,357,934 - 64,358,163UniSTSGRCh37
Build 361164,114,510 - 64,114,739RGDNCBI36
Celera1161,684,192 - 61,684,421RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,685,390 - 60,685,619UniSTS
REN55629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,158 - 64,358,397UniSTSGRCh37
Build 361164,114,734 - 64,114,973RGDNCBI36
Celera1161,684,416 - 61,684,655RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,685,614 - 60,685,853UniSTS
REN55630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,375 - 64,358,631UniSTSGRCh37
Build 361164,114,951 - 64,115,207RGDNCBI36
Celera1161,684,633 - 61,684,889RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,685,831 - 60,686,087UniSTS
REN55631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,629 - 64,358,869UniSTSGRCh37
Build 361164,115,205 - 64,115,445RGDNCBI36
Celera1161,684,887 - 61,685,127RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,085 - 60,686,325UniSTS
REN55632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,849 - 64,359,100UniSTSGRCh37
Build 361164,115,425 - 64,115,676RGDNCBI36
Celera1161,685,107 - 61,685,358RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,305 - 60,686,556UniSTS
REN55633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,359,024 - 64,359,253UniSTSGRCh37
Build 361164,115,600 - 64,115,829RGDNCBI36
Celera1161,685,282 - 61,685,511RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,480 - 60,686,709UniSTS
REN55634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,359,236 - 64,359,489UniSTSGRCh37
Build 361164,115,812 - 64,116,065RGDNCBI36
Celera1161,685,494 - 61,685,747RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,692 - 60,686,945UniSTS
REN55635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,359,465 - 64,359,689UniSTSGRCh37
Build 361164,116,041 - 64,116,265RGDNCBI36
Celera1161,685,723 - 61,685,947RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,921 - 60,687,145UniSTS
REN55636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,359,675 - 64,359,927UniSTSGRCh37
Build 361164,116,251 - 64,116,503RGDNCBI36
Celera1161,685,933 - 61,686,185RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,687,131 - 60,687,383UniSTS
REN55637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,359,925 - 64,360,149UniSTSGRCh37
Build 361164,116,501 - 64,116,725RGDNCBI36
Celera1161,686,183 - 61,686,407RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,687,381 - 60,687,605UniSTS
REN55638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,360,120 - 64,360,365UniSTSGRCh37
Build 361164,116,696 - 64,116,941RGDNCBI36
Celera1161,686,378 - 61,686,623RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,687,576 - 60,687,821UniSTS
REN55639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,360,342 - 64,360,570UniSTSGRCh37
Build 361164,116,918 - 64,117,146RGDNCBI36
Celera1161,686,600 - 61,686,828RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,687,798 - 60,688,026UniSTS
REN55640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,360,545 - 64,360,812UniSTSGRCh37
Build 361164,117,121 - 64,117,388RGDNCBI36
Celera1161,686,803 - 61,687,070RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,688,001 - 60,688,268UniSTS
REN55641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,360,790 - 64,361,046UniSTSGRCh37
Build 361164,117,366 - 64,117,622RGDNCBI36
Celera1161,687,048 - 61,687,304RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,688,246 - 60,688,502UniSTS
REN55642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,361,022 - 64,361,284UniSTSGRCh37
Build 361164,117,598 - 64,117,860RGDNCBI36
Celera1161,687,280 - 61,687,542RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,688,478 - 60,688,740UniSTS
REN55643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,361,263 - 64,361,514UniSTSGRCh37
Build 361164,117,839 - 64,118,090RGDNCBI36
Celera1161,687,521 - 61,687,772RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,688,719 - 60,688,970UniSTS
REN55644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,361,491 - 64,361,741UniSTSGRCh37
Build 361164,118,067 - 64,118,317RGDNCBI36
Celera1161,687,749 - 61,687,999RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,688,947 - 60,689,197UniSTS
REN55645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,361,637 - 64,361,868UniSTSGRCh37
Build 361164,118,213 - 64,118,444RGDNCBI36
Celera1161,687,895 - 61,688,126RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,689,093 - 60,689,324UniSTS
REN55646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,361,840 - 64,362,083UniSTSGRCh37
Build 361164,118,416 - 64,118,659RGDNCBI36
Celera1161,688,098 - 61,688,341RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,689,296 - 60,689,531UniSTS
REN55648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,363,663 - 64,363,914UniSTSGRCh37
Build 361164,120,239 - 64,120,490RGDNCBI36
Celera1161,689,921 - 61,690,172RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,690,038 - 60,690,315UniSTS
REN55649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,363,898 - 64,364,151UniSTSGRCh37
Build 361164,120,474 - 64,120,727RGDNCBI36
Celera1161,690,156 - 61,690,409RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,690,299 - 60,690,552UniSTS
REN55650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,364,148 - 64,364,404UniSTSGRCh37
Build 361164,120,724 - 64,120,980RGDNCBI36
Celera1161,690,406 - 61,690,662RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,690,549 - 60,690,805UniSTS
REN55651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,364,384 - 64,364,640UniSTSGRCh37
Build 361164,120,960 - 64,121,216RGDNCBI36
Celera1161,690,642 - 61,690,898RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,690,785 - 60,691,041UniSTS
REN55652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,364,623 - 64,364,886UniSTSGRCh37
Build 361164,121,199 - 64,121,462RGDNCBI36
Celera1161,690,881 - 61,691,144RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,691,024 - 60,691,287UniSTS
REN55653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,364,863 - 64,365,102UniSTSGRCh37
Build 361164,121,439 - 64,121,678RGDNCBI36
Celera1161,691,121 - 61,691,360RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,691,264 - 60,691,503UniSTS
REN55654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,063 - 64,365,311UniSTSGRCh37
Build 361164,121,639 - 64,121,887RGDNCBI36
Celera1161,691,321 - 61,691,569RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,691,464 - 60,691,712UniSTS
REN55655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,288 - 64,365,540UniSTSGRCh37
Build 361164,121,864 - 64,122,116RGDNCBI36
Celera1161,691,546 - 61,691,798RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,691,689 - 60,691,941UniSTS
REN55656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,536 - 64,365,794UniSTSGRCh37
Build 361164,122,112 - 64,122,370RGDNCBI36
Celera1161,691,794 - 61,692,052RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,691,937 - 60,692,195UniSTS
REN55657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,772 - 64,366,026UniSTSGRCh37
Build 361164,122,348 - 64,122,602RGDNCBI36
Celera1161,692,030 - 61,692,284RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,692,173 - 60,692,427UniSTS
REN55658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,366,019 - 64,366,265UniSTSGRCh37
Build 361164,122,595 - 64,122,841RGDNCBI36
Celera1161,692,277 - 61,692,523RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,692,420 - 60,692,666UniSTS
REN55659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,366,211 - 64,366,441UniSTSGRCh37
Build 361164,122,787 - 64,123,017RGDNCBI36
Celera1161,692,469 - 61,692,699RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,692,612 - 60,692,842UniSTS
REN55660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,366,423 - 64,366,679UniSTSGRCh37
Build 361164,122,999 - 64,123,255RGDNCBI36
Celera1161,692,681 - 61,692,937RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,692,824 - 60,693,080UniSTS
REN55661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,366,670 - 64,366,920UniSTSGRCh37
Build 361164,123,246 - 64,123,496RGDNCBI36
Celera1161,692,928 - 61,693,178RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,693,071 - 60,693,321UniSTS
REN55662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,366,893 - 64,367,140UniSTSGRCh37
Build 361164,123,469 - 64,123,716RGDNCBI36
Celera1161,693,151 - 61,693,398RGD
Cytogenetic Map11q13.1UniSTS
REN55663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,117 - 64,367,348UniSTSGRCh37
Build 361164,123,693 - 64,123,924RGDNCBI36
Celera1161,693,375 - 61,693,606RGD
Cytogenetic Map11q13.1UniSTS
REN55664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,329 - 64,367,579UniSTSGRCh37
Build 361164,123,905 - 64,124,155RGDNCBI36
Celera1161,693,587 - 61,693,837RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,693,875 - 60,694,125UniSTS
REN55665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,556 - 64,367,803UniSTSGRCh37
Build 361164,124,132 - 64,124,379RGDNCBI36
Celera1161,693,814 - 61,694,061RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,694,102 - 60,694,349UniSTS
REN55666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,715 - 64,367,949UniSTSGRCh37
Build 361164,124,291 - 64,124,525RGDNCBI36
Celera1161,693,973 - 61,694,207RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,694,261 - 60,694,495UniSTS
REN55667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,367,926 - 64,368,188UniSTSGRCh37
Build 361164,124,502 - 64,124,764RGDNCBI36
Celera1161,694,184 - 61,694,446RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,694,472 - 60,694,734UniSTS
REN55668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,368,181 - 64,368,417UniSTSGRCh37
Build 361164,124,757 - 64,124,993RGDNCBI36
Celera1161,694,439 - 61,694,675RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,694,727 - 60,694,963UniSTS
REN55669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,368,394 - 64,368,624UniSTSGRCh37
Build 361164,124,970 - 64,125,200RGDNCBI36
Celera1161,694,652 - 61,694,882RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,694,940 - 60,695,170UniSTS
REN55670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,368,601 - 64,368,844UniSTSGRCh37
Build 361164,125,177 - 64,125,420RGDNCBI36
Celera1161,694,859 - 61,695,102RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,695,147 - 60,695,390UniSTS
REN55671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,368,825 - 64,369,089UniSTSGRCh37
Build 361164,125,401 - 64,125,665RGDNCBI36
Celera1161,695,083 - 61,695,347RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,695,371 - 60,695,635UniSTS
REN55672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,056 - 64,369,310UniSTSGRCh37
Build 361164,125,632 - 64,125,886RGDNCBI36
Celera1161,695,314 - 61,695,568RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,695,602 - 60,695,856UniSTS
REN55673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,283 - 64,369,529UniSTSGRCh37
Build 361164,125,859 - 64,126,105RGDNCBI36
Celera1161,695,541 - 61,695,787RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,695,829 - 60,696,075UniSTS
REN55674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,466 - 64,369,726UniSTSGRCh37
Build 361164,126,042 - 64,126,302RGDNCBI36
Celera1161,695,724 - 61,695,984RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,696,012 - 60,696,272UniSTS
REN55675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,705 - 64,369,969UniSTSGRCh37
Build 361164,126,281 - 64,126,545RGDNCBI36
Celera1161,695,963 - 61,696,227RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,696,251 - 60,696,515UniSTS
REN55676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,369,948 - 64,370,194UniSTSGRCh37
Build 361164,126,524 - 64,126,770RGDNCBI36
Celera1161,696,206 - 61,696,452RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,696,494 - 60,696,740UniSTS
stSG635523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,673 - 64,358,856UniSTSGRCh37
Build 361164,115,249 - 64,115,432RGDNCBI36
Celera1161,684,931 - 61,685,114RGD
Cytogenetic Map11q13.1UniSTS
HuRef1160,686,129 - 60,686,312UniSTS
stSG635524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,358,857 - 64,360,038UniSTSGRCh37
Build 361164,115,433 - 64,116,614RGDNCBI36
Celera1161,685,115 - 61,686,296RGD
HuRef1160,686,313 - 60,687,494UniSTS
stSG635528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,364,002 - 64,365,305UniSTSGRCh37
Build 361164,120,578 - 64,121,881RGDNCBI36
Celera1161,690,260 - 61,691,563RGD
HuRef1160,690,403 - 60,691,706UniSTS
stSG635529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371164,365,286 - 64,366,389UniSTSGRCh37
Build 361164,121,862 - 64,122,965RGDNCBI36
Celera1161,691,544 - 61,692,647RGD
HuRef1160,691,687 - 60,692,790UniSTS


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 adipose tissue appendage
High
Medium 9 9 9 1 199 1
Low 3 46 47 46 114 2 10 69 10 2 1 208
Below cutoff 1147 1608 986 351 618 235 2459 1116 2172 36 881 756 116 871 1634

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_008110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001276326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001276327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_144585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_153378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB050269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB071863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC044790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK122599 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX191499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY639400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX104022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA631511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ514592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ514593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ514594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ514595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ514596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ655911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ655912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000336464   ⟹   ENSP00000336836
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1164,591,263 - 64,601,551 (+)Ensembl
RefSeq Acc Id: ENST00000377567   ⟹   ENSP00000366790
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1164,590,641 - 64,602,348 (+)Ensembl
RefSeq Acc Id: ENST00000377572   ⟹   ENSP00000366795
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1164,590,810 - 64,602,353 (+)Ensembl
RefSeq Acc Id: ENST00000377574   ⟹   ENSP00000366797
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1164,591,220 - 64,602,344 (+)Ensembl
RefSeq Acc Id: ENST00000473690   ⟹   ENSP00000438437
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1164,591,228 - 64,602,348 (+)Ensembl
RefSeq Acc Id: NM_001276326   ⟹   NP_001263255
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,602,344 (+)NCBI
GRCh371164,358,113 - 64,369,825 (+)NCBI
HuRef1160,685,738 - 60,696,371 (+)NCBI
CHM1_11164,241,496 - 64,253,033 (+)NCBI
T2T-CHM13v2.01164,583,912 - 64,595,327 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001276327   ⟹   NP_001263256
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,602,344 (+)NCBI
GRCh371164,358,113 - 64,369,825 (+)NCBI
HuRef1160,685,738 - 60,696,371 (+)NCBI
CHM1_11164,241,496 - 64,253,033 (+)NCBI
T2T-CHM13v2.01164,583,912 - 64,595,327 (+)NCBI
Sequence:
RefSeq Acc Id: NM_144585   ⟹   NP_653186
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,602,344 (+)NCBI
GRCh371164,358,113 - 64,369,825 (+)NCBI
Build 361164,114,858 - 64,126,396 (+)NCBI Archive
HuRef1160,685,738 - 60,696,371 (+)NCBI
CHM1_11164,241,496 - 64,253,033 (+)NCBI
T2T-CHM13v2.01164,583,912 - 64,595,327 (+)NCBI
Sequence:
RefSeq Acc Id: NM_153378   ⟹   NP_700357
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,602,344 (+)NCBI
GRCh371164,358,113 - 64,369,825 (+)NCBI
Build 361164,114,858 - 64,126,396 (+)NCBI Archive
HuRef1160,685,738 - 60,696,371 (+)NCBI
CHM1_11164,241,496 - 64,253,033 (+)NCBI
T2T-CHM13v2.01164,583,912 - 64,595,327 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006718430   ⟹   XP_006718493
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,602,344 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006718431   ⟹   XP_006718494
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,602,344 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_653186   ⟸   NM_144585
- Peptide Label: isoform a
- UniProtKB: Q96DT2 (UniProtKB/Swiss-Prot),   Q96S37 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_700357   ⟸   NM_153378
- Peptide Label: isoform b
- UniProtKB: Q96S37 (UniProtKB/Swiss-Prot),   B3KP53 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001263255   ⟸   NM_001276326
- Peptide Label: isoform c
- UniProtKB: Q96S37 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001263256   ⟸   NM_001276327
- Peptide Label: isoform d
- UniProtKB: Q96S37 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006718493   ⟸   XM_006718430
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_006718494   ⟸   XM_006718431
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000336836   ⟸   ENST00000336464
RefSeq Acc Id: ENSP00000366790   ⟸   ENST00000377567
RefSeq Acc Id: ENSP00000366795   ⟸   ENST00000377572
RefSeq Acc Id: ENSP00000366797   ⟸   ENST00000377574
RefSeq Acc Id: ENSP00000438437   ⟸   ENST00000473690
Protein Domains
MFS

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96S37-F1-model_v2 AlphaFold Q96S37 1-553 view protein structure

Promoters
RGD ID:7220901
Promoter ID:EPDNEW_H16196
Type:initiation region
Name:SLC22A12_1
Description:solute carrier family 22 member 12
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381164,591,220 - 64,591,280EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_144585.4(SLC22A12):c.774G>A (p.Trp258Ter) single nucleotide variant Dalmatian hypouricemia [RCV000003689]|not provided [RCV001851624] Chr11:64593747 [GRCh38]
Chr11:64361219 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.650C>T (p.Thr217Met) single nucleotide variant Dalmatian hypouricemia [RCV000003690]|not provided [RCV001851625] Chr11:64593548 [GRCh38]
Chr11:64361020 [GRCh37]
Chr11:11q13.1
pathogenic|likely pathogenic
NM_144585.4(SLC22A12):c.894G>T (p.Glu298Asp) single nucleotide variant Dalmatian hypouricemia [RCV000003691] Chr11:64598579 [GRCh38]
Chr11:64366051 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.1253T>G (p.Leu418Arg) single nucleotide variant Dalmatian hypouricemia [RCV000003692] Chr11:64599858 [GRCh38]
Chr11:64367330 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.269G>A (p.Arg90His) single nucleotide variant Dalmatian hypouricemia [RCV000003693]|Familial renal hypouricemia [RCV000826151] Chr11:64591825 [GRCh38]
Chr11:64359297 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.1082G>T (p.Gly361Val) single nucleotide variant Dalmatian hypouricemia [RCV000003694] Chr11:64599687 [GRCh38]
Chr11:64367159 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.*517G>A single nucleotide variant Dalmatian hypouricemia [RCV000395041] Chr11:64602068 [GRCh38]
Chr11:64369540 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.831-4T>C single nucleotide variant Dalmatian hypouricemia [RCV000396962]|not provided [RCV000956954] Chr11:64598512 [GRCh38]
Chr11:64365984 [GRCh37]
Chr11:11q13.1
benign|likely benign
NM_144585.3(SLC22A12):c.-417C>T single nucleotide variant Dalmatian hypouricemia [RCV000397475] Chr11:64591140 [GRCh38]
Chr11:64358612 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.-45C>G single nucleotide variant Dalmatian hypouricemia [RCV000371107] Chr11:64591512 [GRCh38]
Chr11:64358984 [GRCh37]
Chr11:11q13.1
likely benign|uncertain significance
NM_144585.4(SLC22A12):c.1612G>A (p.Ala538Thr) single nucleotide variant Dalmatian hypouricemia [RCV000267049]|not provided [RCV001850620] Chr11:64601501 [GRCh38]
Chr11:64368973 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.3(SLC22A12):c.-466C>G single nucleotide variant Dalmatian hypouricemia [RCV000285040] Chr11:64591091 [GRCh38]
Chr11:64358563 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.3(SLC22A12):c.-354G>A single nucleotide variant Dalmatian hypouricemia [RCV000303967] Chr11:64591203 [GRCh38]
Chr11:64358675 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1145A>T (p.Gln382Leu) single nucleotide variant Dalmatian hypouricemia [RCV000348762] Chr11:64599750 [GRCh38]
Chr11:64367222 [GRCh37]
Chr11:11q13.1
likely pathogenic
NM_144585.3(SLC22A12):c.-718C>T single nucleotide variant Dalmatian hypouricemia [RCV000373468]|not provided [RCV001642950] Chr11:64590839 [GRCh38]
Chr11:64358311 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.426T>C (p.His142=) single nucleotide variant Dalmatian hypouricemia [RCV000286659]|not provided [RCV001518722]|not specified [RCV000611294] Chr11:64592802 [GRCh38]
Chr11:64360274 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1626G>A (p.Thr542=) single nucleotide variant Dalmatian hypouricemia [RCV000326890]|not provided [RCV001503728] Chr11:64601515 [GRCh38]
Chr11:64368987 [GRCh37]
Chr11:11q13.1
likely benign|uncertain significance
NM_144585.4(SLC22A12):c.402+13C>T single nucleotide variant Dalmatian hypouricemia [RCV000377928] Chr11:64591971 [GRCh38]
Chr11:64359443 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1254C>T (p.Leu418=) single nucleotide variant Dalmatian hypouricemia [RCV000354125] Chr11:64599859 [GRCh38]
Chr11:64367331 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*397C>T single nucleotide variant Dalmatian hypouricemia [RCV000292900] Chr11:64601948 [GRCh38]
Chr11:64369420 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*70G>A single nucleotide variant Dalmatian hypouricemia [RCV000291554] Chr11:64601621 [GRCh38]
Chr11:64369093 [GRCh37]
Chr11:11q13.1
likely benign|uncertain significance
NM_144585.4(SLC22A12):c.1005C>T (p.Ala335=) single nucleotide variant Dalmatian hypouricemia [RCV000293887] Chr11:64598858 [GRCh38]
Chr11:64366330 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.-220G>A single nucleotide variant Dalmatian hypouricemia [RCV000275434]|not provided [RCV001672453] Chr11:64591337 [GRCh38]
Chr11:64358809 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.-10A>C single nucleotide variant Dalmatian hypouricemia [RCV000276551] Chr11:64591547 [GRCh38]
Chr11:64359019 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.3(SLC22A12):c.-424T>C single nucleotide variant Dalmatian hypouricemia [RCV000339005]|not provided [RCV001612965] Chr11:64591133 [GRCh38]
Chr11:64358605 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1460G>A (p.Arg487Gln) single nucleotide variant Dalmatian hypouricemia [RCV000265459]|not provided [RCV001303330] Chr11:64600800 [GRCh38]
Chr11:64368272 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.564G>A (p.Thr188=) single nucleotide variant Dalmatian hypouricemia [RCV000341648] Chr11:64593462 [GRCh38]
Chr11:64360934 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.-234C>T single nucleotide variant Dalmatian hypouricemia [RCV000365350]|not provided [RCV001636874] Chr11:64591323 [GRCh38]
Chr11:64358795 [GRCh37]
Chr11:11q13.1
benign|likely benign
NM_144585.4(SLC22A12):c.1309T>C (p.Leu437=) single nucleotide variant Dalmatian hypouricemia [RCV000300784]|not provided [RCV001517190] Chr11:64600390 [GRCh38]
Chr11:64367862 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1509G>A (p.Thr503=) single nucleotide variant Dalmatian hypouricemia [RCV000320589] Chr11:64600849 [GRCh38]
Chr11:64368321 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.258C>T (p.His86=) single nucleotide variant Dalmatian hypouricemia [RCV000372062]|not provided [RCV001518721]|not specified [RCV000607529] Chr11:64591814 [GRCh38]
Chr11:64359286 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.*249GCCCT[3] microsatellite Dalmatian hypouricemia [RCV000327878]|not provided [RCV001672454] Chr11:64601795..64601796 [GRCh38]
Chr11:64369267..64369268 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1230C>T (p.Ala410=) single nucleotide variant Dalmatian hypouricemia [RCV000399608] Chr11:64599835 [GRCh38]
Chr11:64367307 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.3(SLC22A12):c.-469G>A single nucleotide variant Dalmatian hypouricemia [RCV000374746] Chr11:64591088 [GRCh38]
Chr11:64358560 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.-310A>C single nucleotide variant Dalmatian hypouricemia [RCV000401787] Chr11:64591247 [GRCh38]
Chr11:64358719 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1285+6G>C single nucleotide variant Dalmatian hypouricemia [RCV000402354] Chr11:64599896 [GRCh38]
Chr11:64367368 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.-248G>A single nucleotide variant Dalmatian hypouricemia [RCV000310670] Chr11:64591309 [GRCh38]
Chr11:64358781 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1329C>T (p.Gly443=) single nucleotide variant Dalmatian hypouricemia [RCV000355584] Chr11:64600410 [GRCh38]
Chr11:64367882 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.570T>C (p.Ala190=) single nucleotide variant Dalmatian hypouricemia [RCV000382188]|not provided [RCV002056216] Chr11:64593468 [GRCh38]
Chr11:64360940 [GRCh37]
Chr11:11q13.1
benign|uncertain significance
NM_144585.4(SLC22A12):c.1248A>G (p.Ala416=) single nucleotide variant Dalmatian hypouricemia [RCV000313264]|not provided [RCV001518723]|not specified [RCV000599779] Chr11:64599853 [GRCh38]
Chr11:64367325 [GRCh37]
Chr11:11q13.1
benign
NM_144585.3(SLC22A12):c.-556G>A single nucleotide variant Dalmatian hypouricemia [RCV000338930] Chr11:64591001 [GRCh38]
Chr11:64358473 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1572C>T (p.Pro524=) single nucleotide variant Dalmatian hypouricemia [RCV000361744]|not provided [RCV000910957] Chr11:64600912 [GRCh38]
Chr11:64368384 [GRCh37]
Chr11:11q13.1
likely benign|uncertain significance
NM_144585.3(SLC22A12):c.-563A>G single nucleotide variant Dalmatian hypouricemia [RCV000279160] Chr11:64590994 [GRCh38]
Chr11:64358466 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.246C>T (p.Asn82=) single nucleotide variant Dalmatian hypouricemia [RCV000317584]|not provided [RCV001512958]|not specified [RCV000825089] Chr11:64591802 [GRCh38]
Chr11:64359274 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.*294del deletion Dalmatian hypouricemia [RCV000387098]|not provided [RCV001642951] Chr11:64601842 [GRCh38]
Chr11:64369314 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.*553A>T single nucleotide variant Dalmatian hypouricemia [RCV000280120] Chr11:64602104 [GRCh38]
Chr11:64369576 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.327C>T (p.Ser109=) single nucleotide variant Dalmatian hypouricemia [RCV000318578]|not provided [RCV000915664] Chr11:64591883 [GRCh38]
Chr11:64359355 [GRCh37]
Chr11:11q13.1
likely benign|uncertain significance
NM_144585.4(SLC22A12):c.-332A>G single nucleotide variant Dalmatian hypouricemia [RCV000344878] Chr11:64591225 [GRCh38]
Chr11:64358697 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*43TCT[1] microsatellite Dalmatian hypouricemia [RCV000381478] Chr11:64601592..64601594 [GRCh38]
Chr11:64369064..64369066 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*626G>A single nucleotide variant Dalmatian hypouricemia [RCV000401401] Chr11:64602177 [GRCh38]
Chr11:64369649 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*616T>C single nucleotide variant Dalmatian hypouricemia [RCV000335204] Chr11:64602167 [GRCh38]
Chr11:64369639 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.103_104del (p.Ser35fs) microsatellite not provided [RCV000585202] Chr11:64591657..64591658 [GRCh38]
Chr11:64359129..64359130 [GRCh37]
Chr11:11q13.1
likely pathogenic
NM_144585.4(SLC22A12):c.*476del deletion Dalmatian hypouricemia [RCV000352704] Chr11:64602027 [GRCh38]
Chr11:64369499 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.603G>C (p.Leu201=) single nucleotide variant Dalmatian hypouricemia [RCV000287786] Chr11:64593501 [GRCh38]
Chr11:64360973 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.-93C>T single nucleotide variant Dalmatian hypouricemia [RCV000311717] Chr11:64591464 [GRCh38]
Chr11:64358936 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*643A>G single nucleotide variant Dalmatian hypouricemia [RCV000300197] Chr11:64602194 [GRCh38]
Chr11:64369666 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.3(SLC22A12):c.*795G>A single nucleotide variant Dalmatian hypouricemia [RCV000359750] Chr11:64602346 [GRCh38]
Chr11:64369818 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.361del (p.Val121fs) deletion not provided [RCV000722787] Chr11:64591915 [GRCh38]
Chr11:64359387 [GRCh37]
Chr11:11q13.1
uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
NM_144585.4(SLC22A12):c.502G>A (p.Asp168Asn) single nucleotide variant Dalmatian hypouricemia [RCV001533016] Chr11:64592878 [GRCh38]
Chr11:64360350 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.615G>A (p.Leu205=) single nucleotide variant Dalmatian hypouricemia [RCV001108038]|not provided [RCV000902182] Chr11:64593513 [GRCh38]
Chr11:64360985 [GRCh37]
Chr11:11q13.1
benign|likely benign
NM_144585.4(SLC22A12):c.850C>T (p.Arg284Ter) single nucleotide variant Dalmatian hypouricemia [RCV000779070] Chr11:64598535 [GRCh38]
Chr11:64366007 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1216C>T (p.Arg406Cys) single nucleotide variant Dalmatian hypouricemia [RCV000779071] Chr11:64599821 [GRCh38]
Chr11:64367293 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1654_1655del (p.Gln552fs) microsatellite Dalmatian hypouricemia [RCV000779072] Chr11:64601539..64601540 [GRCh38]
Chr11:64369011..64369012 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.661+1G>A single nucleotide variant Dalmatian hypouricemia [RCV000778334]|not provided [RCV001378102] Chr11:64593560 [GRCh38]
Chr11:64361032 [GRCh37]
Chr11:11q13.1
likely pathogenic|uncertain significance
dup(11)(q13.1q13.1) duplication Ependymoma [RCV000785872] Chr11:63533279..65429676 [GRCh37]
Chr11:11q13.1
likely pathogenic
NM_144585.4(SLC22A12):c.1301G>A (p.Arg434His) single nucleotide variant Dalmatian hypouricemia [RCV001104752]|not provided [RCV000894068] Chr11:64600382 [GRCh38]
Chr11:64367854 [GRCh37]
Chr11:11q13.1
benign|uncertain significance
NM_144585.4(SLC22A12):c.374G>A (p.Ser125Asn) single nucleotide variant Dalmatian hypouricemia [RCV001107385] Chr11:64591930 [GRCh38]
Chr11:64359402 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.224T>C (p.Ile75Thr) single nucleotide variant Dalmatian hypouricemia [RCV001104638]|not provided [RCV001759873] Chr11:64591780 [GRCh38]
Chr11:64359252 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*129C>T single nucleotide variant Dalmatian hypouricemia [RCV001108139] Chr11:64601680 [GRCh38]
Chr11:64369152 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.798G>A (p.Ser266=) single nucleotide variant Dalmatian hypouricemia [RCV001102823] Chr11:64593771 [GRCh38]
Chr11:64361243 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1071-33C>T single nucleotide variant not provided [RCV001671147] Chr11:64599643 [GRCh38]
Chr11:64367115 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.507-254G>A single nucleotide variant not provided [RCV001617661] Chr11:64593151 [GRCh38]
Chr11:64360623 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1599-17G>C single nucleotide variant not provided [RCV001549724] Chr11:64601471 [GRCh38]
Chr11:64368943 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.1285+65C>G single nucleotide variant not provided [RCV001616871] Chr11:64599955 [GRCh38]
Chr11:64367427 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1071-98A>G single nucleotide variant not provided [RCV001721563] Chr11:64599578 [GRCh38]
Chr11:64367050 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1070+224A>G single nucleotide variant not provided [RCV001695983] Chr11:64599147 [GRCh38]
Chr11:64366619 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.831-192C>A single nucleotide variant not provided [RCV001721610] Chr11:64598324 [GRCh38]
Chr11:64365796 [GRCh37]
Chr11:11q13.1
benign
Single allele single nucleotide variant not provided [RCV001681659] Chr11:64590769 [GRCh38]
Chr11:64358241 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1286-103A>G single nucleotide variant not provided [RCV001669805] Chr11:64600264 [GRCh38]
Chr11:64367736 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.507-247G>A single nucleotide variant not provided [RCV001643916] Chr11:64593158 [GRCh38]
Chr11:64360630 [GRCh37]
Chr11:11q13.1
benign
Single allele single nucleotide variant not provided [RCV001724692] Chr11:64590793 [GRCh38]
Chr11:64358265 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1285+227A>G single nucleotide variant not provided [RCV001724693] Chr11:64600117 [GRCh38]
Chr11:64367589 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1598+260G>C single nucleotide variant not provided [RCV001716667] Chr11:64601198 [GRCh38]
Chr11:64368670 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.677C>T (p.Ala226Val) single nucleotide variant Dalmatian hypouricemia [RCV001108040]|not provided [RCV001856442] Chr11:64593650 [GRCh38]
Chr11:64361122 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1271C>T (p.Thr424Met) single nucleotide variant not provided [RCV001064891] Chr11:64599876 [GRCh38]
Chr11:64367348 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.831-320C>A single nucleotide variant not provided [RCV001720781] Chr11:64598196 [GRCh38]
Chr11:64365668 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.830+109G>T single nucleotide variant not provided [RCV001720792] Chr11:64593912 [GRCh38]
Chr11:64361384 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.831-45T>C single nucleotide variant Dalmatian hypouricemia [RCV001807436]|not provided [RCV001598244] Chr11:64598471 [GRCh38]
Chr11:64365943 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1070+134G>C single nucleotide variant not provided [RCV001658522] Chr11:64599057 [GRCh38]
Chr11:64366529 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.403-237T>C single nucleotide variant not provided [RCV001620029] Chr11:64592542 [GRCh38]
Chr11:64360014 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1598+254C>A single nucleotide variant not provided [RCV001590629] Chr11:64601192 [GRCh38]
Chr11:64368664 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.507-172C>T single nucleotide variant not provided [RCV001721660] Chr11:64593233 [GRCh38]
Chr11:64360705 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1071-42del deletion not provided [RCV001621093] Chr11:64599626 [GRCh38]
Chr11:64367098 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1195C>T (p.Leu399=) single nucleotide variant Dalmatian hypouricemia [RCV001102827] Chr11:64599800 [GRCh38]
Chr11:64367272 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.551C>A (p.Ala184Asp) single nucleotide variant Dalmatian hypouricemia [RCV001108037] Chr11:64593449 [GRCh38]
Chr11:64360921 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.682C>T (p.Arg228Trp) single nucleotide variant Dalmatian hypouricemia [RCV001108041] Chr11:64593655 [GRCh38]
Chr11:64361127 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1289T>C (p.Met430Thr) single nucleotide variant Dalmatian hypouricemia [RCV001104751] Chr11:64600370 [GRCh38]
Chr11:64367842 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*741G>A single nucleotide variant Dalmatian hypouricemia [RCV001104839] Chr11:64602292 [GRCh38]
Chr11:64369764 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*750C>T single nucleotide variant Dalmatian hypouricemia [RCV001104840] Chr11:64602301 [GRCh38]
Chr11:64369773 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1469G>C (p.Gly490Ala) single nucleotide variant Dalmatian hypouricemia [RCV001105889] Chr11:64600809 [GRCh38]
Chr11:64368281 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1096G>C (p.Gly366Arg) single nucleotide variant not provided [RCV001091627] Chr11:64599701 [GRCh38]
Chr11:64367173 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.1044C>T (p.Phe348=) single nucleotide variant Dalmatian hypouricemia [RCV001102824]|not provided [RCV001462298] Chr11:64598897 [GRCh38]
Chr11:64366369 [GRCh37]
Chr11:11q13.1
likely benign|uncertain significance
NM_144585.4(SLC22A12):c.1062G>A (p.Thr354=) single nucleotide variant Dalmatian hypouricemia [RCV001102825] Chr11:64598915 [GRCh38]
Chr11:64366387 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*151G>A single nucleotide variant Dalmatian hypouricemia [RCV001108140] Chr11:64601702 [GRCh38]
Chr11:64369174 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.402+197C>T single nucleotide variant not provided [RCV001611993] Chr11:64592155 [GRCh38]
Chr11:64359627 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1071-42_1071-41insCA insertion not provided [RCV001586492] Chr11:64599634..64599635 [GRCh38]
Chr11:64367106..64367107 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.507-248C>T single nucleotide variant not provided [RCV001609343] Chr11:64593157 [GRCh38]
Chr11:64360629 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1286-188G>A single nucleotide variant not provided [RCV001645295] Chr11:64600179 [GRCh38]
Chr11:64367651 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1071-42_1071-41insCCA insertion not provided [RCV001693095] Chr11:64599634..64599635 [GRCh38]
Chr11:64367106..64367107 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1400C>T (p.Thr467Met) single nucleotide variant Dalmatian hypouricemia [RCV001105887]|not provided [RCV001306138] Chr11:64600740 [GRCh38]
Chr11:64368212 [GRCh37]
Chr11:11q13.1
conflicting interpretations of pathogenicity|uncertain significance
NM_144585.4(SLC22A12):c.1427C>A (p.Ala476Asp) single nucleotide variant Dalmatian hypouricemia [RCV001105888]|not provided [RCV001238782] Chr11:64600767 [GRCh38]
Chr11:64368239 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.730G>A (p.Gly244Ser) single nucleotide variant Dalmatian hypouricemia [RCV001102822] Chr11:64593703 [GRCh38]
Chr11:64361175 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.*268G>A single nucleotide variant Dalmatian hypouricemia [RCV001102921] Chr11:64601819 [GRCh38]
Chr11:64369291 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.-37A>C single nucleotide variant Dalmatian hypouricemia [RCV001104636] Chr11:64591520 [GRCh38]
Chr11:64358992 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.123G>A (p.Ser41=) single nucleotide variant Dalmatian hypouricemia [RCV001104637]|not provided [RCV001523674] Chr11:64591679 [GRCh38]
Chr11:64359151 [GRCh37]
Chr11:11q13.1
benign|likely benign
NM_144585.4(SLC22A12):c.233C>T (p.Pro78Leu) single nucleotide variant Dalmatian hypouricemia [RCV001104639] Chr11:64591789 [GRCh38]
Chr11:64359261 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1075G>A (p.Ala359Thr) single nucleotide variant Dalmatian hypouricemia [RCV001102826] Chr11:64599680 [GRCh38]
Chr11:64367152 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.274C>T (p.Arg92Cys) single nucleotide variant Dalmatian hypouricemia [RCV001107384] Chr11:64591830 [GRCh38]
Chr11:64359302 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.661+11G>A single nucleotide variant Dalmatian hypouricemia [RCV001108039]|not provided [RCV002069766] Chr11:64593570 [GRCh38]
Chr11:64361042 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.*240C>T single nucleotide variant Dalmatian hypouricemia [RCV001108141] Chr11:64601791 [GRCh38]
Chr11:64369263 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.122C>T (p.Ser41Leu) single nucleotide variant not provided [RCV001213329] Chr11:64591678 [GRCh38]
Chr11:64359150 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.334G>A (p.Asp112Asn) single nucleotide variant Dalmatian hypouricemia [RCV001328619] Chr11:64591890 [GRCh38]
Chr11:64359362 [GRCh37]
Chr11:11q13.1
uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic
NC_000011.9:g.(?_59596957)_(68707199_?)dup duplication Familial temporal lobe epilepsy 8 [RCV001372442] Chr11:59596957..68707199 [GRCh37]
Chr11:11q12.1-13.3
uncertain significance
NM_144585.4(SLC22A12):c.151del (p.Ala51fs) deletion Familial renal hypouricemia [RCV001334548] Chr11:64591705 [GRCh38]
Chr11:64359177 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.391A>G (p.Ile131Val) single nucleotide variant not provided [RCV001337526] Chr11:64591947 [GRCh38]
Chr11:64359419 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.679G>A (p.Ala227Thr) single nucleotide variant not provided [RCV001403953] Chr11:64593652 [GRCh38]
Chr11:64361124 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.662-7C>T single nucleotide variant not provided [RCV001493481] Chr11:64593628 [GRCh38]
Chr11:64361100 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.412G>C (p.Val138Leu) single nucleotide variant Dalmatian hypouricemia [RCV001533015] Chr11:64592788 [GRCh38]
Chr11:64360260 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.1607_1624dup (p.Lys536_Gly541dup) duplication not provided [RCV001444401] Chr11:64601494..64601495 [GRCh38]
Chr11:64368966..64368967 [GRCh37]
Chr11:11q13.1
likely benign
Single allele single nucleotide variant not provided [RCV001590553] Chr11:64590628 [GRCh38]
Chr11:64358100 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.1071-34A>C single nucleotide variant not provided [RCV001530700] Chr11:64599642 [GRCh38]
Chr11:64367114 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1428C>T (p.Ala476=) single nucleotide variant not provided [RCV001519233] Chr11:64600768 [GRCh38]
Chr11:64368240 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1598+18C>T single nucleotide variant Dalmatian hypouricemia [RCV001807403]|not provided [RCV001511852] Chr11:64600956 [GRCh38]
Chr11:64368428 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.661+20C>T single nucleotide variant not provided [RCV001513839] Chr11:64593579 [GRCh38]
Chr11:64361051 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.1024C>T (p.Arg342Cys) single nucleotide variant not provided [RCV001450387] Chr11:64598877 [GRCh38]
Chr11:64366349 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.1071-42dup duplication not provided [RCV001732497] Chr11:64599625..64599626 [GRCh38]
Chr11:64367097..64367098 [GRCh37]
Chr11:11q13.1
benign
NM_144585.4(SLC22A12):c.85A>G (p.Met29Val) single nucleotide variant not provided [RCV001774743] Chr11:64591641 [GRCh38]
Chr11:64359113 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1534G>A (p.Ala512Thr) single nucleotide variant not provided [RCV002044784] Chr11:64600874 [GRCh38]
Chr11:64368346 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.587T>G (p.Phe196Cys) single nucleotide variant not provided [RCV002025341] Chr11:64593485 [GRCh38]
Chr11:64360957 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.880T>G (p.Trp294Gly) single nucleotide variant not provided [RCV001896686] Chr11:64598565 [GRCh38]
Chr11:64366037 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.408C>A (p.Asn136Lys) single nucleotide variant not provided [RCV001894304] Chr11:64592784 [GRCh38]
Chr11:64360256 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.973C>T (p.Arg325Trp) single nucleotide variant not provided [RCV002039698] Chr11:64598826 [GRCh38]
Chr11:64366298 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.507-8_511del deletion not provided [RCV002023505] Chr11:64593391..64593403 [GRCh38]
Chr11:64360863..64360875 [GRCh37]
Chr11:11q13.1
likely pathogenic
NC_000011.9:g.(?_64367819)_(64369023_?)del deletion not provided [RCV001912110] Chr11:64367819..64369023 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1096G>A (p.Gly366Ser) single nucleotide variant not provided [RCV001908865] Chr11:64599701 [GRCh38]
Chr11:64367173 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1376T>G (p.Leu459Arg) single nucleotide variant not provided [RCV002038515] Chr11:64600457 [GRCh38]
Chr11:64367929 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.476G>A (p.Gly159Glu) single nucleotide variant not provided [RCV001886797] Chr11:64592852 [GRCh38]
Chr11:64360324 [GRCh37]
Chr11:11q13.1
uncertain significance
NC_000011.9:g.(?_64359029)_(64359450_?)del deletion not provided [RCV001959039] Chr11:64359029..64359450 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.743del (p.Thr248fs) deletion not provided [RCV001870028] Chr11:64593716 [GRCh38]
Chr11:64361188 [GRCh37]
Chr11:11q13.1
pathogenic
NM_144585.4(SLC22A12):c.1039C>T (p.Arg347Cys) single nucleotide variant not provided [RCV002030300] Chr11:64598892 [GRCh38]
Chr11:64366364 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.797C>T (p.Ser266Leu) single nucleotide variant not provided [RCV001905730] Chr11:64593770 [GRCh38]
Chr11:64361242 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1453C>G (p.Leu485Val) single nucleotide variant not provided [RCV001957135] Chr11:64600793 [GRCh38]
Chr11:64368265 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.700A>G (p.Met234Val) single nucleotide variant not provided [RCV001922377] Chr11:64593673 [GRCh38]
Chr11:64361145 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.802C>T (p.Pro268Ser) single nucleotide variant not provided [RCV001993738] Chr11:64593775 [GRCh38]
Chr11:64361247 [GRCh37]
Chr11:11q13.1
uncertain significance
NM_144585.4(SLC22A12):c.1464G>T (p.Leu488=) single nucleotide variant not provided [RCV002133653] Chr11:64600804 [GRCh38]
Chr11:64368276 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.12T>C (p.Ser4=) single nucleotide variant not provided [RCV002097188] Chr11:64591568 [GRCh38]
Chr11:64359040 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.591C>G (p.Pro197=) single nucleotide variant not provided [RCV002153850] Chr11:64593489 [GRCh38]
Chr11:64360961 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.955-11C>T single nucleotide variant not provided [RCV002121002] Chr11:64598797 [GRCh38]
Chr11:64366269 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.955-19C>T single nucleotide variant not provided [RCV002121683] Chr11:64598789 [GRCh38]
Chr11:64366261 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.1311G>A (p.Leu437=) single nucleotide variant not provided [RCV002177920] Chr11:64600392 [GRCh38]
Chr11:64367864 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.729C>T (p.Phe243=) single nucleotide variant not provided [RCV002176379] Chr11:64593702 [GRCh38]
Chr11:64361174 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.336C>T (p.Asp112=) single nucleotide variant not provided [RCV002219516] Chr11:64591892 [GRCh38]
Chr11:64359364 [GRCh37]
Chr11:11q13.1
likely benign
NM_144585.4(SLC22A12):c.1599-17G>A single nucleotide variant not provided [RCV002136699] Chr11:64601471 [GRCh38]
Chr11:64368943 [GRCh37]
Chr11:11q13.1
benign
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17989 AgrOrtholog
COSMIC SLC22A12 COSMIC
Ensembl Genes ENSG00000197891 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000336836 ENTREZGENE
  ENSP00000336836.7 UniProtKB/Swiss-Prot
  ENSP00000366790.2 UniProtKB/Swiss-Prot
  ENSP00000366795 ENTREZGENE
  ENSP00000366795.1 UniProtKB/Swiss-Prot
  ENSP00000366797 ENTREZGENE
  ENSP00000366797.1 UniProtKB/Swiss-Prot
  ENSP00000438437 ENTREZGENE
  ENSP00000438437.1 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000336464 ENTREZGENE
  ENST00000336464.7 UniProtKB/Swiss-Prot
  ENST00000377567.6 UniProtKB/Swiss-Prot
  ENST00000377572 ENTREZGENE
  ENST00000377572.5 UniProtKB/Swiss-Prot
  ENST00000377574 ENTREZGENE
  ENST00000377574.6 UniProtKB/Swiss-Prot
  ENST00000473690 ENTREZGENE
  ENST00000473690.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.1250.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000197891 GTEx
HGNC ID HGNC:17989 ENTREZGENE
Human Proteome Map SLC22A12 Human Proteome Map
InterPro MFS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_sugar_transport-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:116085 UniProtKB/Swiss-Prot
NCBI Gene 116085 ENTREZGENE
OMIM 220150 OMIM
  607096 OMIM
Pfam Sugar_tr UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38478 PharmGKB
PROSITE MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B3KP53 ENTREZGENE, UniProtKB/TrEMBL
  Q05CF4_HUMAN UniProtKB/TrEMBL
  Q19PG1_HUMAN UniProtKB/TrEMBL
  Q96DT2 ENTREZGENE
  Q96S37 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B7WPG1 UniProtKB/Swiss-Prot
  G3XAN7 UniProtKB/Swiss-Prot
  Q19PF7 UniProtKB/Swiss-Prot
  Q19PF8 UniProtKB/Swiss-Prot
  Q19PF9 UniProtKB/Swiss-Prot
  Q19PG0 UniProtKB/Swiss-Prot
  Q6UXW3 UniProtKB/Swiss-Prot
  Q96DT2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-08 SLC22A12  solute carrier family 22 member 12  SLC22A12  solute carrier family 22 (organic anion/urate transporter), member 12  Symbol and/or name change 5135510 APPROVED