GNG12-AS1 (GNG12, DIRAS3 and WLS antisense RNA 1) - Rat Genome Database

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Gene: GNG12-AS1 (GNG12, DIRAS3 and WLS antisense RNA 1) Homo sapiens
Analyze
Symbol: GNG12-AS1
Name: GNG12, DIRAS3 and WLS antisense RNA 1
RGD ID: 6769446
HGNC Page HGNC:43938
Description: ASSOCIATED WITH Zaki syndrome; INTERACTS WITH aflatoxin B1; benzo[a]pyrene; benzo[e]pyrene
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Previously known as: GNG12 antisense RNA 1; RP11-518D3.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38167,832,288 - 68,202,987 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl167,832,193 - 68,202,987 (+)EnsemblGRCh38hg38GRCh38
GRCh37168,297,971 - 68,668,670 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera166,588,675 - 66,959,303 (+)NCBICelera
Cytogenetic Map1p31.3NCBI
HuRef166,408,108 - 66,778,710 (+)NCBIHuRef
CHM1_1168,412,395 - 68,784,025 (+)NCBICHM1_1
T2T-CHM13v2.0167,709,732 - 68,080,405 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
Zaki syndrome  (IAGP)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
Additional References at PubMed
PMID:16344560   PMID:19801982   PMID:22504420   PMID:23648065   PMID:23871723   PMID:24249740   PMID:26760575   PMID:26832224   PMID:32735016   PMID:38277283  


Genomics

Variants

.
Variants in GNG12-AS1
84 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NR_040077.1(GNG12-AS1):n.149+52362T>G single nucleotide variant Lung cancer [RCV000090913] Chr1:67884798 [GRCh38]
Chr1:68350481 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_001002292.3(WLS):c.373+2757C>G single nucleotide variant Lung cancer [RCV000090914] Chr1:68191198 [GRCh38]
Chr1:68656881 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.2(DIRAS3):c.394G>A (p.Glu132Lys) single nucleotide variant Malignant melanoma [RCV000060239] Chr1:68046904 [GRCh38]
Chr1:68512587 [GRCh37]
Chr1:68285175 [NCBI36]
Chr1:1p31.3		 not provided
GRCh38/hg38 1p32.1-31.1(chr1:59760856-71578052)x1 copy number loss See cases [RCV000133710] Chr1:59760856..71578052 [GRCh38]
Chr1:60226528..72043735 [GRCh37]
Chr1:59999116..71816323 [NCBI36]
Chr1:1p32.1-31.1		 pathogenic
GRCh38/hg38 1p32.1-31.2(chr1:58819605-69107108)x1 copy number loss See cases [RCV000134142] Chr1:58819605..69107108 [GRCh38]
Chr1:59285277..69572791 [GRCh37]
Chr1:59057865..69345379 [NCBI36]
Chr1:1p32.1-31.2		 pathogenic
GRCh38/hg38 1p32.1-22.3(chr1:58819605-86098611)x1 copy number loss See cases [RCV000136913] Chr1:58819605..86098611 [GRCh38]
Chr1:59285277..86564294 [GRCh37]
Chr1:59057865..86336882 [NCBI36]
Chr1:1p32.1-22.3		 pathogenic
GRCh38/hg38 1p31.3-31.1(chr1:64072618-75518432)x3 copy number gain See cases [RCV000142452] Chr1:64072618..75518432 [GRCh38]
Chr1:64538290..75984117 [GRCh37]
Chr1:64310878..75756705 [NCBI36]
Chr1:1p31.3-31.1		 pathogenic
GRCh38/hg38 1p31.3-31.1(chr1:66865125-77123381)x1 copy number loss See cases [RCV000143129] Chr1:66865125..77123381 [GRCh38]
Chr1:67330808..77589066 [GRCh37]
Chr1:67103396..77361654 [NCBI36]
Chr1:1p31.3-31.1		 pathogenic
GRCh38/hg38 1p32.1-31.1(chr1:60473800-70944955)x1 copy number loss See cases [RCV000050703] Chr1:60473800..70944955 [GRCh38]
Chr1:60939472..71410638 [GRCh37]
Chr1:60712060..71183226 [NCBI36]
Chr1:1p32.1-31.1		 pathogenic
GRCh38/hg38 1p32.3-31.1(chr1:52595352-76767765)x3 copy number gain See cases [RCV000051822] Chr1:52595352..76767765 [GRCh38]
Chr1:53061024..77233450 [GRCh37]
Chr1:52833612..77006038 [NCBI36]
Chr1:1p32.3-31.1		 pathogenic
GRCh38/hg38 1p32.2-31.1(chr1:57350574-71325924)x1 copy number loss See cases [RCV000053841] Chr1:57350574..71325924 [GRCh38]
Chr1:57816246..71791607 [GRCh37]
Chr1:57588834..71564195 [NCBI36]
Chr1:1p32.2-31.1		 pathogenic
GRCh38/hg38 1p32.1-31.1(chr1:59632500-76730877)x1 copy number loss See cases [RCV000053842] Chr1:59632500..76730877 [GRCh38]
Chr1:60098172..77196562 [GRCh37]
Chr1:59870760..76969150 [NCBI36]
Chr1:1p32.1-31.1		 pathogenic
GRCh38/hg38 1p31.3-31.1(chr1:67239704-71924806)x1 copy number loss See cases [RCV000053843] Chr1:67239704..71924806 [GRCh38]
Chr1:67705387..72390489 [GRCh37]
Chr1:67477975..72163077 [NCBI36]
Chr1:1p31.3-31.1		 pathogenic
NM_004675.5(DIRAS3):c.142G>A (p.Val48Met) single nucleotide variant not specified [RCV004310991] Chr1:68047156 [GRCh38]
Chr1:68512839 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.650A>G (p.Asn217Ser) single nucleotide variant not specified [RCV004315861] Chr1:68046648 [GRCh38]
Chr1:68512331 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_001002292.4(WLS):c.1554del (p.Phe518fs) deletion WLS-related disorder [RCV003933183]|not provided [RCV000934204] Chr1:68098710 [GRCh38]
Chr1:68564393 [GRCh37]
Chr1:1p31.3		 benign|likely benign
NM_024911.7(WLS):c.1175A>G (p.Tyr392Cys) single nucleotide variant WLS syndrome [RCV001420501]|Zaki syndrome [RCV001788472] Chr1:68145972 [GRCh38]
Chr1:68611655 [GRCh37]
Chr1:1p31.3		 pathogenic
NM_024911.7(WLS):c.1433A>G (p.Tyr478Cys) single nucleotide variant WLS syndrome [RCV001420502]|Zaki syndrome [RCV001789704] Chr1:68137863 [GRCh38]
Chr1:68603546 [GRCh37]
Chr1:1p31.3		 pathogenic
NM_024911.7(WLS):c.1592T>C (p.Ile531Thr) single nucleotide variant WLS syndrome [RCV001420503]|Zaki syndrome [RCV001788473] Chr1:68126260 [GRCh38]
Chr1:68591943 [GRCh37]
Chr1:1p31.3		 pathogenic|likely pathogenic
NM_024911.7(WLS):c.1606C>T (p.Arg536Cys) single nucleotide variant WLS syndrome [RCV001420504]|Zaki syndrome [RCV001788474] Chr1:68126246 [GRCh38]
Chr1:68591929 [GRCh37]
Chr1:1p31.3		 pathogenic|likely pathogenic
Single allele duplication not specified [RCV002286371] Chr1:66885559..77949895 [GRCh38]
Chr1:1p31.3-31.1		 uncertain significance
NM_024911.7(WLS):c.961G>A (p.Glu321Lys) single nucleotide variant not specified [RCV004298608] Chr1:68150199 [GRCh38]
Chr1:68615882 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.547A>G (p.Lys183Glu) single nucleotide variant not specified [RCV004104115] Chr1:68046751 [GRCh38]
Chr1:68512434 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.659G>A (p.Arg220Gln) single nucleotide variant not specified [RCV004157585] Chr1:68155106 [GRCh38]
Chr1:68620789 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.554T>C (p.Met185Thr) single nucleotide variant not specified [RCV004162636] Chr1:68155211 [GRCh38]
Chr1:68620894 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1450T>C (p.Tyr484His) single nucleotide variant not specified [RCV004150399] Chr1:68137846 [GRCh38]
Chr1:68603529 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1496A>G (p.Tyr499Cys) single nucleotide variant not specified [RCV004084663] Chr1:68137800 [GRCh38]
Chr1:68603483 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1467G>A (p.Met489Ile) single nucleotide variant not specified [RCV004240552] Chr1:68137829 [GRCh38]
Chr1:68603512 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.401T>C (p.Met134Thr) single nucleotide variant not specified [RCV004145104] Chr1:68159226 [GRCh38]
Chr1:68624909 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1367C>T (p.Thr456Met) single nucleotide variant not specified [RCV004202570] Chr1:68137929 [GRCh38]
Chr1:68603612 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1501G>C (p.Glu501Gln) single nucleotide variant not specified [RCV004147672] Chr1:68137795 [GRCh38]
Chr1:68603478 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.35A>G (p.Lys12Arg) single nucleotide variant not specified [RCV004078436] Chr1:68047263 [GRCh38]
Chr1:68512946 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1514A>G (p.Asn505Ser) single nucleotide variant Zaki syndrome [RCV004763587]|not specified [RCV004229424] Chr1:68137782 [GRCh38]
Chr1:68603465 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.430G>A (p.Ala144Thr) single nucleotide variant not specified [RCV004092424] Chr1:68159197 [GRCh38]
Chr1:68624880 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.91C>T (p.Pro31Ser) single nucleotide variant not specified [RCV004122032] Chr1:68047207 [GRCh38]
Chr1:68512890 [GRCh37]
Chr1:1p31.3		 likely benign
NM_004675.5(DIRAS3):c.385G>A (p.Ala129Thr) single nucleotide variant not specified [RCV004099525] Chr1:68046913 [GRCh38]
Chr1:68512596 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.161G>A (p.Arg54His) single nucleotide variant not specified [RCV004133628] Chr1:68194173 [GRCh38]
Chr1:68659856 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1354G>A (p.Val452Ile) single nucleotide variant not specified [RCV004134613] Chr1:68144577 [GRCh38]
Chr1:68610260 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.296G>T (p.Arg99Leu) single nucleotide variant not specified [RCV004101300] Chr1:68047002 [GRCh38]
Chr1:68512685 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.725C>T (p.Thr242Met) single nucleotide variant not specified [RCV004134553] Chr1:68153595 [GRCh38]
Chr1:68619278 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1168T>G (p.Cys390Gly) single nucleotide variant not specified [RCV004130263] Chr1:68145979 [GRCh38]
Chr1:68611662 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.718T>C (p.Phe240Leu) single nucleotide variant not specified [RCV004276233] Chr1:68153602 [GRCh38]
Chr1:68619285 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.576T>A (p.His192Gln) single nucleotide variant not specified [RCV004259425] Chr1:68155189 [GRCh38]
Chr1:68620872 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.919T>C (p.Phe307Leu) single nucleotide variant Zaki syndrome [RCV003225911] Chr1:68150241 [GRCh38]
Chr1:68615924 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.605C>T (p.Pro202Leu) single nucleotide variant not specified [RCV004325299] Chr1:68155160 [GRCh38]
Chr1:68620843 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.702G>C (p.Trp234Cys) single nucleotide variant Zaki syndrome [RCV003340758] Chr1:68153618 [GRCh38]
Chr1:68619301 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.432G>A (p.Ala144=) single nucleotide variant Zaki syndrome [RCV003341584] Chr1:68159195 [GRCh38]
Chr1:68624878 [GRCh37]
Chr1:1p31.3		 benign
NM_004675.5(DIRAS3):c.513G>A (p.Met171Ile) single nucleotide variant not specified [RCV004336066] Chr1:68046785 [GRCh38]
Chr1:68512468 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.593A>G (p.Tyr198Cys) single nucleotide variant not specified [RCV004344238] Chr1:68046705 [GRCh38]
Chr1:68512388 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1414G>T (p.Ala472Ser) single nucleotide variant not specified [RCV004359789] Chr1:68137882 [GRCh38]
Chr1:68603565 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1214G>A (p.Arg405Gln) single nucleotide variant not specified [RCV004343867] Chr1:68145933 [GRCh38]
Chr1:68611616 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.227A>G (p.Asp76Gly) single nucleotide variant not specified [RCV004335392] Chr1:68194107 [GRCh38]
Chr1:68659790 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.520A>C (p.Asn174His) single nucleotide variant not specified [RCV004373881] Chr1:68046778 [GRCh38]
Chr1:68512461 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.291C>T (p.Pro97=) single nucleotide variant not provided [RCV003993388] Chr1:68194043 [GRCh38]
Chr1:68659726 [GRCh37]
Chr1:1p31.3		 likely benign
NM_004675.5(DIRAS3):c.207C>T (p.Thr69=) single nucleotide variant DIRAS3-related disorder [RCV003901973] Chr1:68047091 [GRCh38]
Chr1:68512774 [GRCh37]
Chr1:1p31.3		 likely benign
NM_024911.7(WLS):c.1363-3279C>A single nucleotide variant WLS-related disorder [RCV003896490] Chr1:68141212 [GRCh38]
Chr1:68606895 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.138_169dup (p.His57delinsArgArgTer) duplication WLS-related disorder [RCV003893998] Chr1:68194164..68194165 [GRCh38]
Chr1:68659847..68659848 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.505-10C>A single nucleotide variant WLS-related disorder [RCV003971716] Chr1:68155270 [GRCh38]
Chr1:68620953 [GRCh37]
Chr1:1p31.3		 likely benign
NM_024911.7(WLS):c.1298A>G (p.Lys433Arg) single nucleotide variant not specified [RCV004483012] Chr1:68144633 [GRCh38]
Chr1:68610316 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.254T>C (p.Ile85Thr) single nucleotide variant not specified [RCV004483013] Chr1:68194080 [GRCh38]
Chr1:68659763 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.403G>T (p.Asp135Tyr) single nucleotide variant not specified [RCV004483014] Chr1:68159224 [GRCh38]
Chr1:68624907 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.439G>A (p.Glu147Lys) single nucleotide variant not specified [RCV004483015] Chr1:68159188 [GRCh38]
Chr1:68624871 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.574C>T (p.His192Tyr) single nucleotide variant not specified [RCV004483016] Chr1:68155191 [GRCh38]
Chr1:68620874 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.598C>T (p.Arg200Trp) single nucleotide variant not specified [RCV004483017] Chr1:68155167 [GRCh38]
Chr1:68620850 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.802A>C (p.Lys268Gln) single nucleotide variant not specified [RCV004483018] Chr1:68153518 [GRCh38]
Chr1:68619201 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.916A>G (p.Ile306Val) single nucleotide variant not specified [RCV004483019] Chr1:68150244 [GRCh38]
Chr1:68615927 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.52C>T (p.Arg18Trp) single nucleotide variant not specified [RCV004616430] Chr1:68047246 [GRCh38]
Chr1:68512929 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1163G>C (p.Cys388Ser) single nucleotide variant not specified [RCV004678512] Chr1:68145984 [GRCh38]
Chr1:68611667 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.10G>T (p.Ala4Ser) single nucleotide variant not specified [RCV004616428] Chr1:68047288 [GRCh38]
Chr1:68512971 [GRCh37]
Chr1:1p31.3		 likely benign
NM_004675.5(DIRAS3):c.356C>G (p.Thr119Ser) single nucleotide variant not specified [RCV004616431] Chr1:68046942 [GRCh38]
Chr1:68512625 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.79C>G (p.Arg27Gly) single nucleotide variant not specified [RCV004616432] Chr1:68047219 [GRCh38]
Chr1:68512902 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1213C>T (p.Arg405Trp) single nucleotide variant not specified [RCV004678506] Chr1:68145934 [GRCh38]
Chr1:68611617 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.122C>T (p.Thr41Met) single nucleotide variant not specified [RCV004678507] Chr1:68194212 [GRCh38]
Chr1:68659895 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.1150G>A (p.Val384Met) single nucleotide variant not specified [RCV004678508] Chr1:68145997 [GRCh38]
Chr1:68611680 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.453G>C (p.Met151Ile) single nucleotide variant not specified [RCV004678509] Chr1:68159174 [GRCh38]
Chr1:68624857 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.508C>T (p.Pro170Ser) single nucleotide variant not specified [RCV004678510] Chr1:68155257 [GRCh38]
Chr1:68620940 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_004675.5(DIRAS3):c.506G>A (p.Cys169Tyr) single nucleotide variant not specified [RCV004616426] Chr1:68046792 [GRCh38]
Chr1:68512475 [GRCh37]
Chr1:1p31.3		 likely benign
NM_004675.5(DIRAS3):c.305A>G (p.Gln102Arg) single nucleotide variant not specified [RCV004616429] Chr1:68046993 [GRCh38]
Chr1:68512676 [GRCh37]
Chr1:1p31.3		 uncertain significance
NM_024911.7(WLS):c.168C>T (p.Asn56=) single nucleotide variant not provided [RCV004722404] Chr1:68194166 [GRCh38]
Chr1:68659849 [GRCh37]
Chr1:1p31.3		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:334
Count of miRNA genes:262
Interacting mature miRNAs:274
Transcripts:ENST00000413628, ENST00000414904, ENST00000420587, ENST00000434072
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
406921024GWAS570000_Hunipolar depression, mood disorder QTL GWAS570000 (human)2e-09unipolar depression, mood disorder16790914567909146Human
407067586GWAS716562_Hheel bone mineral density QTL GWAS716562 (human)2e-11heel bone mineral densitybone mineral density (CMO:0001226)16813744868137449Human
407248455GWAS897431_Hbone density QTL GWAS897431 (human)5e-13bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16816895968168960Human
407206214GWAS855190_Hcortical surface area measurement QTL GWAS855190 (human)1e-19cerebral cortex morphology trait (VT:0000788)tibia-fibula cortical bone total cross-sectional area (CMO:0001721)16816226068162261Human
407216577GWAS865553_Hheel bone mineral density QTL GWAS865553 (human)7e-64heel bone mineral densitybone mineral density (CMO:0001226)16818780668187807Human
407089862GWAS738838_Hheel bone mineral density QTL GWAS738838 (human)7e-10heel bone mineral densitybone mineral density (CMO:0001226)16813744868137449Human
407216576GWAS865552_Hheel bone mineral density QTL GWAS865552 (human)2e-09heel bone mineral densitybone mineral density (CMO:0001226)16818495068184951Human
407013060GWAS662036_Hbone density QTL GWAS662036 (human)2e-12bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16816970768169708Human
407249100GWAS898076_Hosteoporosis QTL GWAS898076 (human)1e-09osteoporosis16816970768169708Human
407203022GWAS851998_Hspine bone mineral density QTL GWAS851998 (human)3e-21spine bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
406985934GWAS634910_Hresponse to antineoplastic agent, response to anthracycline-based chemotherapy QTL GWAS634910 (human)0.000005response to antineoplastic agent, response to anthracycline-based chemotherapy16816824168168242Human
407216584GWAS865560_Hheel bone mineral density QTL GWAS865560 (human)4e-73heel bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
407248456GWAS897432_Hbone density QTL GWAS897432 (human)4e-22bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16819101468191015Human
407062477GWAS711453_Hheel bone mineral density QTL GWAS711453 (human)3e-21heel bone mineral densitybone mineral density (CMO:0001226)16819659968196600Human
407216586GWAS865562_Hheel bone mineral density QTL GWAS865562 (human)2e-36heel bone mineral densitybone mineral density (CMO:0001226)16819934068199341Human
406915280GWAS564256_Hneuroimaging measurement QTL GWAS564256 (human)1e-10neuroimaging measurement16816226068162261Human
407203028GWAS852004_Hspine bone mineral density QTL GWAS852004 (human)1e-19spine bone mineral densitybone mineral density (CMO:0001226)16819934068199341Human
406960213GWAS609189_Haging QTL GWAS609189 (human)3e-10aging16807088568070886Human
406899029GWAS548005_Hmosquito bite reaction itch intensity measurement QTL GWAS548005 (human)0.000002mosquito bite reaction itch intensity measurement16797946467979465Human
406958932GWAS607908_Hbone density QTL GWAS607908 (human)3e-45bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16818203368182034Human
407135571GWAS784547_HQT interval QTL GWAS784547 (human)0.000002QT intervalQT interval (CMO:0000235)16813456468134565Human
407062484GWAS711460_Hheel bone mineral density QTL GWAS711460 (human)2e-10heel bone mineral densitybone mineral density (CMO:0001226)16819822168198222Human
407145308GWAS794284_Hbone density QTL GWAS794284 (human)7e-31bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16819101468191015Human
407175133GWAS824109_Hneuroticism measurement QTL GWAS824109 (human)3e-08neuroticism measurement16790516867905169Human
407188447GWAS837423_Hcortical surface area measurement QTL GWAS837423 (human)1e-17cerebral cortex morphology trait (VT:0000788)tibia-fibula cortical bone total cross-sectional area (CMO:0001721)16816226068162261Human
407013084GWAS662060_Hheel bone mineral density QTL GWAS662060 (human)5e-43heel bone mineral densitybone mineral density (CMO:0001226)16813744868137449Human
407112044GWAS761020_Hfemoral neck bone mineral density QTL GWAS761020 (human)5e-20femoral neck bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
407178476GWAS827452_Hcortical thickness QTL GWAS827452 (human)1e-09cortical thickness16811626468116265Human
407051240GWAS700216_Hcortical surface area measurement QTL GWAS700216 (human)2e-12cerebral cortex morphology trait (VT:0000788)tibia-fibula cortical bone total cross-sectional area (CMO:0001721)16816226068162261Human
407175018GWAS823994_Hbrain measurement, neuroimaging measurement QTL GWAS823994 (human)2e-10brain measurement, neuroimaging measurementbrain measurement (CMO:0000911)16816226068162261Human
407112042GWAS761018_Hspine bone mineral density QTL GWAS761018 (human)4e-23spine bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
407324008GWAS972984_Heducational attainment QTL GWAS972984 (human)0.000006educational attainment16801416068014161Human
407242358GWAS891334_Hcarotid artery intima media thickness QTL GWAS891334 (human)0.000004carotid artery intima media thickness16789702967897030Human
407195637GWAS844613_Hfemoral neck bone mineral density QTL GWAS844613 (human)7e-17femoral neck bone mineral densitybone mineral density (CMO:0001226)16819934068199341Human
406886770GWAS535746_Hmosquito bite reaction itch intensity measurement, mosquito bite reaction size measurement QTL GWAS535746 (human)0.000009mosquito bite reaction itch intensity measurement, mosquito bite reaction size measurement16793863767938638Human
406909047GWAS558023_Hmosquito bite reaction itch intensity measurement, mosquito bite reaction size measurement QTL GWAS558023 (human)0.000004mosquito bite reaction itch intensity measurement, mosquito bite reaction size measurement16795649167956492Human
407170172GWAS819148_Hneuroticism measurement QTL GWAS819148 (human)3e-08neuroticism measurement16790426767904268Human
407081338GWAS730314_Hinformation processing speed QTL GWAS730314 (human)0.000009information processing speed16808327068083271Human
407062649GWAS711625_Hretinal vasculature measurement QTL GWAS711625 (human)3e-10retina blood vessel morphology trait (VT:0002792)16784928467849285Human
407268860GWAS917836_HDrugs affecting bone structure and mineralization use measurement QTL GWAS917836 (human)2e-09Drugs affecting bone structure and mineralization use measurement16819816468198165Human
406928257GWAS577233_Hcigarettes per day measurement QTL GWAS577233 (human)1e-09cigarettes per day measurement16783634167836342Human
406906882GWAS555858_Hsmoking initiation QTL GWAS555858 (human)5e-11smoking initiation16801489768014898Human
407195394GWAS844370_Hfemoral neck bone mineral density QTL GWAS844370 (human)4e-17femoral neck bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
407414017GWAS1062993_HDrugs affecting bone structure and mineralization use measurement QTL GWAS1062993 (human)6e-10Drugs affecting bone structure and mineralization use measurement16816939268169393Human
407233545GWAS882521_Hbone density QTL GWAS882521 (human)1e-30bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16798865267988653Human
407054227GWAS703203_Hresponse to surgery, post-operative sign or symptom QTL GWAS703203 (human)0.000006response to surgery, post-operative sign or symptom16817655768176558Human
407199383GWAS848359_Hbrain measurement QTL GWAS848359 (human)2e-24brain measurementbrain measurement (CMO:0000911)16816226068162261Human
407147799GWAS796775_Hbone density QTL GWAS796775 (human)2e-14bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16819101468191015Human
407172497GWAS821473_Hneuroticism measurement QTL GWAS821473 (human)2e-08neuroticism measurement16790516867905169Human
407190291GWAS839267_Hcortical thickness QTL GWAS839267 (human)3e-12cortical thickness16816226068162261Human
406912663GWAS561639_Hdiastolic blood pressure, systolic blood pressure QTL GWAS561639 (human)3e-08diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)16789379967893800Human
407147795GWAS796771_Hbone density QTL GWAS796771 (human)1e-11bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16819101468191015Human
406889625GWAS538601_Hheel bone mineral density QTL GWAS538601 (human)2e-75heel bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
407173657GWAS822633_Hneuroticism measurement QTL GWAS822633 (human)4e-08neuroticism measurement16789249467892495Human
407175065GWAS824041_Hcortical surface area measurement, neuroimaging measurement QTL GWAS824041 (human)1e-08cerebral cortex morphology trait (VT:0000788)tibia-fibula cortical bone total cross-sectional area (CMO:0001721)16816226068162261Human
2314561GLUCO47_HGlucose level QTL 47 (human)1.1Glucose level14477336070773360Human
407044768GWAS693744_Hheel bone mineral density QTL GWAS693744 (human)1e-13heel bone mineral densitybone mineral density (CMO:0001226)16793852067938521Human
407393067GWAS1042043_Hfemoral neck bone mineral density QTL GWAS1042043 (human)3e-11femoral neck bone mineral densitybone mineral density (CMO:0001226)16816939268169393Human
1578620LDLPS20_HLow density lipoprotein particle size QTL 21 (human)2.040.00046LDL particle size15253110578531105Human
406946471GWAS595447_Hbone density QTL GWAS595447 (human)3e-13bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16816939268169393Human
406990506GWAS639482_Hcigarettes per day measurement QTL GWAS639482 (human)3e-10cigarettes per day measurement16786225667862257Human
407058347GWAS707323_Hheel bone mineral density QTL GWAS707323 (human)2e-14heel bone mineral densitybone mineral density (CMO:0001226)16793870867938709Human
407201581GWAS850557_Hspine bone mineral density QTL GWAS850557 (human)5e-17spine bone mineral densitybone mineral density (CMO:0001226)16817460368174604Human
406993960GWAS642936_Hbody height QTL GWAS642936 (human)2e-08body height (VT:0001253)body height (CMO:0000106)16791899167918992Human
407193643GWAS842619_Hspine bone mineral density QTL GWAS842619 (human)1e-10spine bone mineral densitybone mineral density (CMO:0001226)16817740868177409Human
407072428GWAS721404_Hheel bone mineral density QTL GWAS721404 (human)6e-20heel bone mineral densitybone mineral density (CMO:0001226)16813744868137449Human
407362743GWAS1011719_HHMG CoA reductase inhibitor use measurement QTL GWAS1011719 (human)9e-09HMG CoA reductase inhibitor use measurement16801242268012423Human
407079347GWAS728323_Hheel bone mineral density QTL GWAS728323 (human)2e-31heel bone mineral densitybone mineral density (CMO:0001226)16813790368137904Human
1578602LDLPS21_HLow density lipoprotein particle size QTL 21 (human)2.050.00037LDL particle size15253110578531105Human
407275188GWAS924164_Hbody height QTL GWAS924164 (human)2e-18body height (VT:0001253)body height (CMO:0000106)16816970768169708Human
407275186GWAS924162_Hbody height QTL GWAS924162 (human)9e-28body height (VT:0001253)body height (CMO:0000106)16785404067854041Human
407275187GWAS924163_Hbody height QTL GWAS924163 (human)4e-22body height (VT:0001253)body height (CMO:0000106)16814556068145561Human
407147324GWAS796300_Hbone density QTL GWAS796300 (human)2e-34bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16819101468191015Human
1578594LDLPS19_HLow density lipoprotein particle size QTL 19 (human)2.560.00009LDL particle size15253110578531105Human
407171902GWAS820878_Hneuroticism measurement QTL GWAS820878 (human)5e-08neuroticism measurement16790516867905169Human
407216575GWAS865551_Hheel bone mineral density QTL GWAS865551 (human)8e-45heel bone mineral densitybone mineral density (CMO:0001226)16813790368137904Human
407102648GWAS751624_Hspine bone mineral density QTL GWAS751624 (human)3e-09spine bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human
407222590GWAS871566_Hbone density QTL GWAS871566 (human)1e-11bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)16819182768191828Human
407083453GWAS732429_Hfeeling "fed-up" measurement QTL GWAS732429 (human)9e-10feeling "fed-up" measurement16790914567909146Human
407079357GWAS728333_Hheel bone mineral density QTL GWAS728333 (human)2e-13heel bone mineral densitybone mineral density (CMO:0001226)16819934068199341Human
407079356GWAS728332_Hheel bone mineral density QTL GWAS728332 (human)3e-54heel bone mineral densitybone mineral density (CMO:0001226)16819101468191015Human

Markers in Region
G09848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,598,713 - 68,598,854UniSTSGRCh37
Build 36168,371,301 - 68,371,442RGDNCBI36
Celera166,889,375 - 66,889,501RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,708,765 - 66,708,906UniSTS
A004O04  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,584,823 - 68,585,006UniSTSGRCh37
Build 36168,357,411 - 68,357,594RGDNCBI36
Celera166,875,486 - 66,875,669RGD
Cytogenetic Map1p31.3UniSTS
GeneMap99-GB4 RH Map1184.91UniSTS
NCBI RH Map1459.5UniSTS
RH28305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711124,502,453 - 124,502,557UniSTSGRCh37
GRCh37168,484,076 - 68,484,182UniSTSGRCh37
Build 36168,256,664 - 68,256,770RGDNCBI36
Celera11121,662,629 - 121,662,733UniSTS
Celera166,774,779 - 66,774,885RGD
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map11q24.2UniSTS
HuRef11120,444,912 - 120,445,016UniSTS
HuRef166,594,171 - 66,594,277UniSTS
RH92980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,584,960 - 68,585,111UniSTSGRCh37
Build 36168,357,548 - 68,357,699RGDNCBI36
Celera166,875,623 - 66,875,774RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,695,012 - 66,695,163UniSTS
AL034314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,511,437 - 68,511,625UniSTSGRCh37
Build 36168,284,025 - 68,284,213RGDNCBI36
Celera166,802,140 - 66,802,328RGD
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1p31UniSTS
HuRef166,621,539 - 66,621,727UniSTS
SHGC-79685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,349,180 - 68,349,466UniSTSGRCh37
Build 36168,121,768 - 68,122,054RGDNCBI36
Celera166,639,880 - 66,640,166RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,459,323 - 66,459,609UniSTS
TNG Radiation Hybrid Map138986.0UniSTS
RH120114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,453,567 - 68,453,763UniSTSGRCh37
Build 36168,226,155 - 68,226,351RGDNCBI36
Celera166,744,260 - 66,744,456RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,563,650 - 66,563,846UniSTS
TNG Radiation Hybrid Map139023.0UniSTS
RH122086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,417,807 - 68,418,119UniSTSGRCh37
Build 36168,190,395 - 68,190,707RGDNCBI36
Celera166,708,496 - 66,708,808RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,528,034 - 66,528,347UniSTS
TNG Radiation Hybrid Map138975.0UniSTS
G60301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,591,041 - 68,591,377UniSTSGRCh37
Build 36168,363,629 - 68,363,965RGDNCBI36
Celera166,881,704 - 66,882,040RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,701,094 - 66,701,430UniSTS
TNG Radiation Hybrid Map138941.0UniSTS
SHGC-57898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,511,960 - 68,512,137UniSTSGRCh37
Build 36168,284,548 - 68,284,725RGDNCBI36
Celera166,802,663 - 66,802,840RGD
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1p31UniSTS
HuRef166,622,062 - 66,622,239UniSTS
RH64518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,599,042 - 68,599,174UniSTSGRCh37
Build 36168,371,630 - 68,371,762RGDNCBI36
Celera166,889,689 - 66,889,821RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,709,094 - 66,709,226UniSTS
GeneMap99-GB4 RH Map1185.64UniSTS
D1S3040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,511,698 - 68,511,848UniSTSGRCh37
Build 36168,284,286 - 68,284,436RGDNCBI36
Celera166,802,401 - 66,802,551RGD
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1p31UniSTS
HuRef166,621,800 - 66,621,950UniSTS
GeneMap99-GB4 RH Map1183.66UniSTS
Whitehead-RH Map1210.0UniSTS
Whitehead-YAC Contig Map1 UniSTS
NCBI RH Map1476.3UniSTS
A006M39  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,586,074 - 68,586,290UniSTSGRCh37
Build 36168,358,662 - 68,358,878RGDNCBI36
Celera166,876,737 - 66,876,953RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,696,126 - 66,696,342UniSTS
GeneMap99-GB4 RH Map1184.86UniSTS
NCBI RH Map1459.5UniSTS
G20702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,591,125 - 68,591,231UniSTSGRCh37
Build 36168,363,713 - 68,363,819RGDNCBI36
Celera166,881,788 - 66,881,894RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,701,178 - 66,701,284UniSTS
A006C26  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,591,125 - 68,591,231UniSTSGRCh37
Build 36168,363,713 - 68,363,819RGDNCBI36
Celera166,881,788 - 66,881,894RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,701,178 - 66,701,284UniSTS
GeneMap99-GB4 RH Map1191.64UniSTS
D1S1583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,585,633 - 68,585,868UniSTSGRCh37
Build 36168,358,221 - 68,358,456RGDNCBI36
Celera166,876,296 - 66,876,531RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,695,685 - 66,695,920UniSTS
TNG Radiation Hybrid Map138949.0UniSTS
G16188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,411,006 - 68,411,178UniSTSGRCh37
Build 36168,183,594 - 68,183,766RGDNCBI36
Celera166,701,695 - 66,701,867RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,521,196 - 66,521,368UniSTS
HSC2OB072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,584,743 - 68,584,900UniSTSGRCh37
Build 36168,357,331 - 68,357,488RGDNCBI36
Celera166,875,406 - 66,875,563RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,694,795 - 66,694,952UniSTS
GeneMap99-GB4 RH Map1191.46UniSTS
GeneMap99-GB4 RH Map1184.86UniSTS
Whitehead-RH Map1210.6UniSTS
NCBI RH Map1459.5UniSTS
RH68355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37168,564,262 - 68,564,441UniSTSGRCh37
Build 36168,336,850 - 68,337,029RGDNCBI36
Celera166,854,963 - 66,855,142RGD
Cytogenetic Map1p31.3UniSTS
HuRef166,674,364 - 66,674,543UniSTS
GeneMap99-GB4 RH Map1191.33UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2433 2785 2221 4886 1700 2306 5 604 1295 444 2265 6625 5820 44 3651 1 848 1736 1592 174 1

Sequence


Ensembl Acc Id: ENST00000413628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,832,309 - 68,202,987 (+)Ensembl
Ensembl Acc Id: ENST00000414904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,955,405 - 68,026,762 (+)Ensembl
Ensembl Acc Id: ENST00000420587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,832,303 - 68,202,987 (+)Ensembl
Ensembl Acc Id: ENST00000434072
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl168,138,357 - 68,141,788 (+)Ensembl
Ensembl Acc Id: ENST00000688125
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,832,193 - 67,873,650 (+)Ensembl
Ensembl Acc Id: ENST00000786419
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl168,071,800 - 68,122,706 (+)Ensembl
Ensembl Acc Id: ENST00000786420
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl168,199,831 - 68,202,190 (+)Ensembl
Ensembl Acc Id: ENST00000786421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl168,199,831 - 68,202,190 (+)Ensembl
Ensembl Acc Id: ENST00000826363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,946,157 - 68,034,871 (+)Ensembl
Ensembl Acc Id: ENST00000826364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,946,157 - 68,034,815 (+)Ensembl
Ensembl Acc Id: ENST00000826365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl167,955,405 - 67,975,692 (+)Ensembl
RefSeq Acc Id: NR_040077
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38167,832,288 - 68,202,987 (+)NCBI
GRCh37168,297,917 - 68,668,670 (+)NCBI
HuRef166,408,108 - 66,778,710 (+)NCBI
CHM1_1168,412,395 - 68,784,025 (+)NCBI
T2T-CHM13v2.0167,709,732 - 68,080,405 (+)NCBI
Sequence:
Protein Sequences
GenBank Protein BAC85755 (Get FASTA)   NCBI Sequence Viewer  

Promoters
RGD ID:15095240
Promoter ID:EPDNEWNC_H69
Type:initiation region
Name:GNG12-AS1_1
Description:GNG12, DIRAS3 and WLS antisense RNA 1 [Source:HGNCSymbol;Acc:HGNC:43938]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38167,832,303 - 67,832,363EPDNEWNC

Additional Information

Database Acc Id Source(s)
COSMIC GNG12-AS1 COSMIC
Ensembl Genes ENSG00000232284 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000420587 ENTREZGENE
GTEx ENSG00000232284 GTEx
HGNC ID HGNC:43938 ENTREZGENE
Human Proteome Map GNG12-AS1 Human Proteome Map
NCBI Gene GNG12-AS1 ENTREZGENE
OMIM 615406 OMIM
RNAcentral URS0000759D5C RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-08-28 GNG12-AS1  GNG12, DIRAS3 and WLS antisense RNA 1    GNG12 antisense RNA 1  Symbol and/or name change 5135510 APPROVED
2012-08-21 GNG12-AS1  GNG12 antisense RNA 1  GNG12-AS1  GNG12 antisense RNA 1 (non-protein coding)  Symbol and/or name change 5135510 APPROVED