GPRC5D-AS1 (GPRC5D and HEBP1 antisense RNA 1) - Rat Genome Database

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Gene: GPRC5D-AS1 (GPRC5D and HEBP1 antisense RNA 1) Homo sapiens
Analyze
Symbol: GPRC5D-AS1
Name: GPRC5D and HEBP1 antisense RNA 1
RGD ID: 13210648
HGNC Page HGNC:53599
Description: INTERACTS WITH Aflatoxin B2 alpha; bisphenol A; lipopolysaccharide
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381212,927,726 - 13,022,498 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1212,927,712 - 12,984,645 (+)EnsemblGRCh38hg38GRCh38
GRCh371213,080,660 - 13,175,432 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera1218,281,622 - 18,286,427 (+)NCBICelera
Cytogenetic Map12p13.1NCBI
HuRef1212,902,339 - 12,907,144 (+)NCBIHuRef
CHM1_11213,098,193 - 13,102,998 (+)NCBICHM1_1
T2T-CHM13v2.01212,801,331 - 12,896,717 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
References
Additional References at PubMed
PMID:7566098   PMID:8889548   PMID:12477932   PMID:14702039   PMID:16344560   PMID:28612367   PMID:37731844  


Genomics

Variants

.
Variants in GPRC5D-AS1
33 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12p13.2-13.1(chr12:11771233-13547775)x1 copy number loss See cases [RCV000050816] Chr12:11771233..13547775 [GRCh38]
Chr12:11924167..13700709 [GRCh37]
Chr12:11815434..13591976 [NCBI36]
Chr12:12p13.2-13.1		 pathogenic
NM_015987.5(HEBP1):c.562A>C (p.Lys188Gln) single nucleotide variant not specified [RCV004317231] Chr12:12975316 [GRCh38]
Chr12:13128250 [GRCh37]
Chr12:12p13.1		 uncertain significance
GRCh38/hg38 12p13.2-12.3(chr12:12388842-15540422)x1 copy number loss See cases [RCV000052780] Chr12:12388842..15540422 [GRCh38]
Chr12:12541776..15693356 [GRCh37]
Chr12:12433043..15584623 [NCBI36]
Chr12:12p13.2-12.3		 pathogenic
GRCh38/hg38 12p13.2-12.3(chr12:12363649-15280588)x1 copy number loss See cases [RCV000135331] Chr12:12363649..15280588 [GRCh38]
Chr12:12514722..15433522 [GRCh37]
Chr12:12405989..15324789 [NCBI36]
Chr12:12p13.2-12.3		 pathogenic
GRCh38/hg38 12p13.2-12.3(chr12:11121039-15908154)x1 copy number loss See cases [RCV000142882] Chr12:11121039..15908154 [GRCh38]
Chr12:11273638..16061088 [GRCh37]
Chr12:11164905..15952355 [NCBI36]
Chr12:12p13.2-12.3		 likely pathogenic
GRCh38/hg38 12p13.33-11.22(chr12:121055-28415184)x1 copy number loss See cases [RCV000052776] Chr12:121055..28415184 [GRCh38]
Chr12:282465..28568117 [GRCh37]
Chr12:100482..28459384 [NCBI36]
Chr12:12p13.33-11.22		 pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3 copy number gain See cases [RCV000053660] Chr12:77187..34380176 [GRCh38]
Chr12:282465..34533111 [GRCh37]
Chr12:56614..34424378 [NCBI36]
Chr12:12p13.33-11.1		 pathogenic
GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3 copy number gain See cases [RCV000053662] Chr12:80412..25470329 [GRCh38]
Chr12:282465..25623263 [GRCh37]
Chr12:59839..25514530 [NCBI36]
Chr12:12p13.33-12.1		 pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4 copy number gain See cases [RCV000053666] Chr12:212976..33926913 [GRCh38]
Chr12:322142..34079848 [GRCh37]
Chr12:192403..33971115 [NCBI36]
Chr12:12p13.33-11.1		 pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3 copy number gain See cases [RCV000136611] Chr12:121255..34603274 [GRCh38]
Chr12:282465..34756209 [GRCh37]
Chr12:100682..34647476 [NCBI36]
Chr12:12p13.33-11.1		 pathogenic
GRCh38/hg38 12p13.33-12.3(chr12:2871741-14987348)x3 copy number gain See cases [RCV000137694] Chr12:2871741..14987348 [GRCh38]
Chr12:2980907..15140282 [GRCh37]
Chr12:2851168..15031549 [NCBI36]
Chr12:12p13.33-12.3		 pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3 copy number gain See cases [RCV000139052] Chr12:121271..34603261 [GRCh38]
Chr12:282465..34756196 [GRCh37]
Chr12:100698..34647463 [NCBI36]
Chr12:12p13.33-11.1		 pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33		 pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4 copy number gain See cases [RCV000139787] Chr12:54427..34608071 [GRCh38]
Chr12:282465..34761006 [GRCh37]
Chr12:33854..34652273 [NCBI36]
Chr12:12p13.33-11.1		 pathogenic
GRCh38/hg38 12p13.33-12.2(chr12:1258274-20657577)x3 copy number gain See cases [RCV000141905] Chr12:1258274..20657577 [GRCh38]
Chr12:1367440..20810511 [GRCh37]
Chr12:1237701..20701778 [NCBI36]
Chr12:12p13.33-12.2		 pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4 copy number gain See cases [RCV000142149] Chr12:64620..34682902 [GRCh38]
Chr12:173786..34835837 [GRCh37]
Chr12:44047..34727104 [NCBI36]
Chr12:12p13.33-11.1		 pathogenic
NM_018654.2(GPRC5D):c.775G>A (p.Val259Ile) single nucleotide variant not specified [RCV004331166] Chr12:12949610 [GRCh38]
Chr12:13102544 [GRCh37]
Chr12:12p13.1		 likely benign
NM_018654.2(GPRC5D):c.559G>A (p.Val187Ile) single nucleotide variant not specified [RCV004214222] Chr12:12949826 [GRCh38]
Chr12:13102760 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.578G>A (p.Cys193Tyr) single nucleotide variant not specified [RCV004165521] Chr12:12949807 [GRCh38]
Chr12:13102741 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.271G>A (p.Val91Ile) single nucleotide variant not specified [RCV004100756] Chr12:12950114 [GRCh38]
Chr12:13103048 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.365T>C (p.Ile122Thr) single nucleotide variant not specified [RCV004125280] Chr12:12987185 [GRCh38]
Chr12:13140119 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.468G>A (p.Met156Ile) single nucleotide variant not specified [RCV004200638] Chr12:12949917 [GRCh38]
Chr12:13102851 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.880C>G (p.Gln294Glu) single nucleotide variant not specified [RCV004093924] Chr12:12949505 [GRCh38]
Chr12:13102439 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.581G>A (p.Gly194Asp) single nucleotide variant not specified [RCV004185963] Chr12:12949804 [GRCh38]
Chr12:13102738 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.449G>A (p.Arg150His) single nucleotide variant not specified [RCV004197525] Chr12:12975429 [GRCh38]
Chr12:13128363 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.809G>A (p.Arg270Lys) single nucleotide variant not specified [RCV004102338] Chr12:12949576 [GRCh38]
Chr12:13102510 [GRCh37]
Chr12:12p13.1		 likely benign
NM_018654.2(GPRC5D):c.185C>T (p.Thr62Ile) single nucleotide variant not specified [RCV004176642] Chr12:12950200 [GRCh38]
Chr12:13103134 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.55G>A (p.Glu19Lys) single nucleotide variant not specified [RCV004186462] Chr12:12950330 [GRCh38]
Chr12:13103264 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.59T>G (p.Val20Gly) single nucleotide variant not specified [RCV004099234] Chr12:13000056 [GRCh38]
Chr12:13152990 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.188C>A (p.Ala63Glu) single nucleotide variant not specified [RCV004071041] Chr12:12989306 [GRCh38]
Chr12:13142240 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.227T>A (p.Met76Lys) single nucleotide variant not specified [RCV004141391] Chr12:12987323 [GRCh38]
Chr12:13140257 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.490G>A (p.Asp164Asn) single nucleotide variant not specified [RCV004191719] Chr12:12975388 [GRCh38]
Chr12:13128322 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.211G>T (p.Asp71Tyr) single nucleotide variant not specified [RCV004122061] Chr12:12989283 [GRCh38]
Chr12:13142217 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.819C>G (p.Cys273Trp) single nucleotide variant not specified [RCV004193178] Chr12:12949566 [GRCh38]
Chr12:13102500 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.395T>C (p.Ile132Thr) single nucleotide variant not specified [RCV004360000] Chr12:12949990 [GRCh38]
Chr12:13102924 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.373C>T (p.Arg125Trp) single nucleotide variant not specified [RCV004334757] Chr12:12987177 [GRCh38]
Chr12:13140111 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.229G>A (p.Ala77Thr) single nucleotide variant not specified [RCV004339166] Chr12:12950156 [GRCh38]
Chr12:13103090 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.665C>T (p.Ser222Phe) single nucleotide variant not specified [RCV004352510] Chr12:12949720 [GRCh38]
Chr12:13102654 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.679G>A (p.Gly227Ser) single nucleotide variant not specified [RCV004391320] Chr12:12949706 [GRCh38]
Chr12:13102640 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.684C>A (p.Asn228Lys) single nucleotide variant not specified [RCV004391321] Chr12:12949701 [GRCh38]
Chr12:13102635 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.719C>T (p.Pro240Leu) single nucleotide variant not specified [RCV004391323] Chr12:12949666 [GRCh38]
Chr12:13102600 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.959C>T (p.Pro320Leu) single nucleotide variant not specified [RCV004391324] Chr12:12942265 [GRCh38]
Chr12:13095199 [GRCh37]
Chr12:12p13.1		 likely benign
NM_018654.2(GPRC5D):c.438G>T (p.Glu146Asp) single nucleotide variant not specified [RCV004391315] Chr12:12949947 [GRCh38]
Chr12:13102881 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.275G>A (p.Arg92His) single nucleotide variant not specified [RCV004391314] Chr12:12950110 [GRCh38]
Chr12:13103044 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.73G>A (p.Asp25Asn) single nucleotide variant not specified [RCV004401761] Chr12:13000042 [GRCh38]
Chr12:13152976 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.487C>T (p.Pro163Ser) single nucleotide variant not specified [RCV004391316] Chr12:12949898 [GRCh38]
Chr12:13102832 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.708G>T (p.Gln236His) single nucleotide variant not specified [RCV004391322] Chr12:12949677 [GRCh38]
Chr12:13102611 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.500A>G (p.Asn167Ser) single nucleotide variant not specified [RCV004391317] Chr12:12949885 [GRCh38]
Chr12:13102819 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_018654.2(GPRC5D):c.605A>G (p.His202Arg) single nucleotide variant not specified [RCV004391318] Chr12:12949780 [GRCh38]
Chr12:13102714 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.142G>C (p.Asp48His) single nucleotide variant not specified [RCV004401758] Chr12:12989352 [GRCh38]
Chr12:13142286 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.499T>C (p.Phe167Leu) single nucleotide variant not specified [RCV004401760] Chr12:12975379 [GRCh38]
Chr12:13128313 [GRCh37]
Chr12:12p13.1		 uncertain significance
NM_015987.5(HEBP1):c.194A>G (p.Tyr65Cys) single nucleotide variant not specified [RCV004401759] Chr12:12989300 [GRCh38]
Chr12:13142234 [GRCh37]
Chr12:12p13.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1399
Count of miRNA genes:780
Interacting mature miRNAs:924
Transcripts:ENST00000394742, ENST00000499948, ENST00000536029, ENST00000538231, ENST00000540198, ENST00000542078, ENST00000543515, ENST00000545914, ENST00000607894
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.


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 7 2 40 2 1 2 4 2 2 376 96 1 1
Low 2028 1602 1658 599 756 441 3034 804 1289 378 1011 1490 170 1037 1733 5 2
Below cutoff 399 1344 27 23 956 22 1260 1318 2406 34 71 20 4 1 167 1007

Sequence

Nucleotide Sequences
RefSeq Transcripts NR_038920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA362711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AA412641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC023790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC042978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF976135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ951575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU684530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR746233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA768922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY076286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA986094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA986095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000394742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,947,151 - 12,953,957 (+)Ensembl
RefSeq Acc Id: ENST00000499948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,979,837 - 12,984,645 (+)Ensembl
RefSeq Acc Id: ENST00000536029
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,927,764 - 12,980,094 (+)Ensembl
RefSeq Acc Id: ENST00000538231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,947,165 - 12,948,577 (+)Ensembl
RefSeq Acc Id: ENST00000540198
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,927,727 - 12,952,750 (+)Ensembl
RefSeq Acc Id: ENST00000542078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,927,734 - 12,984,081 (+)Ensembl
RefSeq Acc Id: ENST00000543515
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,927,712 - 12,980,566 (+)Ensembl
RefSeq Acc Id: ENST00000545914
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,927,726 - 12,980,307 (+)Ensembl
RefSeq Acc Id: ENST00000607894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,979,837 - 12,984,012 (+)Ensembl
RefSeq Acc Id: ENST00000660059
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1212,927,727 - 12,980,562 (+)Ensembl
RefSeq Acc Id: NR_038920
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,979,837 - 12,984,642 (+)NCBI
CHM1_11213,098,193 - 13,102,998 (+)NCBI
T2T-CHM13v2.01212,853,499 - 12,858,304 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149062
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,927,726 - 12,984,642 (+)NCBI
T2T-CHM13v2.01212,801,331 - 12,858,304 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149063
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,927,726 - 12,980,562 (+)NCBI
T2T-CHM13v2.01212,801,331 - 12,854,224 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149064
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,927,726 - 12,980,562 (+)NCBI
T2T-CHM13v2.01212,801,331 - 12,854,224 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149065
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,927,726 - 12,980,562 (+)NCBI
T2T-CHM13v2.01212,801,331 - 12,854,224 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149066
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,927,726 - 12,980,562 (+)NCBI
T2T-CHM13v2.01212,801,331 - 12,854,224 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149067
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381212,927,726 - 13,022,498 (+)NCBI
T2T-CHM13v2.01212,801,331 - 12,896,717 (+)NCBI
Sequence:
Promoters
RGD ID:15096569
Promoter ID:EPDNEWNC_H1412
Type:multiple initiation site
Name:GPRC5D-AS1_1
Description:GPRC5D and HEBP1 antisense RNA 1 [Source:HGNCSymbol;Acc:HGNC:53599]
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
GRCh381212,927,724 - 12,927,784EPDNEWNC

Additional Information

Database Acc Id Source(s)
COSMIC GPRC5D-AS1 COSMIC
Ensembl Genes ENSG00000247498 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000499948 ENTREZGENE
  ENST00000543515 ENTREZGENE
GTEx ENSG00000247498 GTEx
HGNC ID HGNC:53599 ENTREZGENE
Human Proteome Map GPRC5D-AS1 Human Proteome Map
NCBI Gene GPRC5D-AS1 ENTREZGENE
RNAcentral URS000075B988 RNACentral
  URS0000BC43C2 RNACentral
  URS0000BC43D8 RNACentral
  URS0000BC4476 RNACentral
  URS0000BC44AA RNACentral
  URS0000BC450E RNACentral
  URS0000BC45B8 RNACentral