OR14J1 (olfactory receptor family 14 subfamily J member 1) - Rat Genome Database

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Gene: OR14J1 (olfactory receptor family 14 subfamily J member 1) Homo sapiens
Analyze
Symbol: OR14J1
Name: olfactory receptor family 14 subfamily J member 1
RGD ID: 1344262
HGNC Page HGNC:13971
Description: Predicted to enable odorant binding activity and olfactory receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway and detection of chemical stimulus involved in sensory perception of smell. Predicted to be located in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: bA150A6.4; hs6M1-28; olfactory receptor 14J1; olfactory receptor 5U1; olfactory receptor OR6-25; olfactory receptor, family 14, subfamily J, member 1; olfactory receptor, family 5, subfamily U member 1; olfactory receptor, family 5, subfamily U, member 1; OR5U1; OR6-25
RGD Orthologs
Mouse
Rat
Bonobo
Dog
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
GRCh38629,301,701 - 29,313,017 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl629,301,701 - 29,313,017 (+)EnsemblGRCh38hg38GRCh38
GRCh37629,269,478 - 29,280,794 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36629,382,446 - 29,383,411 (+)NCBINCBI36Build 36hg18NCBI36
Build 34629,382,445 - 29,383,411NCBI
Celera630,880,644 - 30,881,609 (+)NCBICelera
Cytogenetic Map6p22.1NCBI
HuRef629,082,076 - 29,083,041 (+)NCBIHuRef
CHM1_1629,276,729 - 29,277,694 (+)NCBICHM1_1
T2T-CHM13v2.0629,176,465 - 29,187,793 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
genetic disease  (IAGP)
megacolon  (IAGP)

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

Cellular Component
membrane  (IEA)
plasma membrane  (IEA,TAS)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14574404   PMID:14983052   PMID:19851445   PMID:21873635   PMID:33961781  


Genomics

Comparative Map Data
OR14J1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38629,301,701 - 29,313,017 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl629,301,701 - 29,313,017 (+)EnsemblGRCh38hg38GRCh38
GRCh37629,269,478 - 29,280,794 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36629,382,446 - 29,383,411 (+)NCBINCBI36Build 36hg18NCBI36
Build 34629,382,445 - 29,383,411NCBI
Celera630,880,644 - 30,881,609 (+)NCBICelera
Cytogenetic Map6p22.1NCBI
HuRef629,082,076 - 29,083,041 (+)NCBIHuRef
CHM1_1629,276,729 - 29,277,694 (+)NCBICHM1_1
T2T-CHM13v2.0629,176,465 - 29,187,793 (+)NCBIT2T-CHM13v2.0
Or14j1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391738,145,802 - 38,146,919 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1738,143,840 - 38,149,381 (+)EnsemblGRCm39 Ensembl
GRCm381737,834,911 - 37,836,028 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1737,832,949 - 37,838,490 (+)EnsemblGRCm38mm10GRCm38
MGSCv371737,971,856 - 37,972,973 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361737,443,054 - 37,444,016 (+)NCBIMGSCv36mm8
Celera1741,274,402 - 41,275,519 (+)NCBICelera
Cytogenetic Map17B1NCBI
cM Map1719.16NCBI
Or14j1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr820694,951 - 695,913 (-)NCBIGRCr8
mRatBN7.220689,684 - 690,646 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl20685,475 - 692,605 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx20705,251 - 706,213 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.020708,716 - 709,678 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.020623,799 - 624,761 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.020830,485 - 831,447 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl20830,485 - 831,447 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.020814,959 - 815,921 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.420646,784 - 647,746 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.120646,783 - 647,746 (-)NCBI
Celera201,463,529 - 1,464,491 (-)NCBICelera
Cytogenetic Map20p12NCBI
LOC100970983
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2543,934,315 - 43,945,610 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1639,898,673 - 39,909,976 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0629,124,922 - 29,126,027 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1629,783,067 - 29,784,172 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl629,783,126 - 29,784,091 (+)Ensemblpanpan1.1panPan2
OR14J1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13526,143,651 - 26,144,616 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3526,143,651 - 26,144,616 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3525,954,903 - 25,955,868 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03526,448,330 - 26,449,295 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3526,448,330 - 26,449,295 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13526,103,742 - 26,104,707 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03526,161,971 - 26,162,936 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03527,633,094 - 27,634,059 (+)NCBIUU_Cfam_GSD_1.0
LOC103221890
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11743,256,772 - 43,261,237 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1743,257,284 - 43,258,246 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604428,976,538 - 28,977,642 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
LOC101726258
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624756111,415 - 112,377 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624756111,415 - 112,465 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in OR14J1
7 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6p22.3-21.33(chr6:18120520-30767516)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]|See cases [RCV000052180] Chr6:18120520..30767516 [GRCh38]
Chr6:18120751..30735293 [GRCh37]
Chr6:18228730..30843272 [NCBI36]
Chr6:6p22.3-21.33
pathogenic
GRCh38/hg38 6p22.1(chr6:28954915-29358240)x1 copy number loss See cases [RCV000138326] Chr6:28954915..29358240 [GRCh38]
Chr6:28922692..29326017 [GRCh37]
Chr6:29030671..29433996 [NCBI36]
Chr6:6p22.1
likely benign
GRCh38/hg38 6p22.1(chr6:28954920-29358310)x3 copy number gain See cases [RCV000139079] Chr6:28954920..29358310 [GRCh38]
Chr6:28922697..29326087 [GRCh37]
Chr6:29030676..29434066 [NCBI36]
Chr6:6p22.1
likely benign
GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3 copy number gain See cases [RCV000138956] Chr6:3224310..30657190 [GRCh38]
Chr6:3224544..30624967 [GRCh37]
Chr6:3169543..30732946 [NCBI36]
Chr6:6p25.2-21.33
pathogenic
GRCh38/hg38 6p22.1(chr6:28763187-29769828)x3 copy number gain See cases [RCV000141858] Chr6:28763187..29769828 [GRCh38]
Chr6:28730964..29737605 [GRCh37]
Chr6:28838943..29845584 [NCBI36]
Chr6:6p22.1
uncertain significance
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3 copy number gain See cases [RCV000143497] Chr6:156974..46789291 [GRCh38]
Chr6:156974..46757028 [GRCh37]
Chr6:101974..46864987 [NCBI36]
Chr6:6p25.3-12.3
pathogenic
NM_030946.2(OR14J1):c.92T>C (p.Val31Ala) single nucleotide variant Inborn genetic diseases [RCV003203336] Chr6:29306781 [GRCh38]
Chr6:29274558 [GRCh37]
Chr6:6p22.1
uncertain significance
GRCh37/hg19 6p22.1(chr6:28735761-29585573)x1 copy number loss See cases [RCV000445803] Chr6:28735761..29585573 [GRCh37]
Chr6:6p22.1
uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
NM_030946.2(OR14J1):c.922C>T (p.Leu308Phe) single nucleotide variant Inborn genetic diseases [RCV003248994] Chr6:29307611 [GRCh38]
Chr6:29275388 [GRCh37]
Chr6:6p22.1
likely benign
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p22.1-21.32(chr6:28130359-32108367)x3 copy number gain not provided [RCV000745592] Chr6:28130359..32108367 [GRCh37]
Chr6:6p22.1-21.32
uncertain significance
GRCh37/hg19 6p22.1(chr6:28920972-29348297)x3 copy number gain not provided [RCV000745599] Chr6:28920972..29348297 [GRCh37]
Chr6:6p22.1
benign
GRCh37/hg19 6p22.1(chr6:28920972-29354383)x3 copy number gain not provided [RCV000745600] Chr6:28920972..29354383 [GRCh37]
Chr6:6p22.1
benign
NC_000006.11:g.28005012_31683185del deletion Megacolon [RCV001290055] Chr6:28005012..31683185 [GRCh37]
Chr6:6p22.1-21.33
likely pathogenic
GRCh37/hg19 6p22.1(chr6:28735761-29585573) copy number loss not specified [RCV002053563] Chr6:28735761..29585573 [GRCh37]
Chr6:6p22.1
uncertain significance
GRCh37/hg19 6p22.1(chr6:29162783-30236331)x3 copy number gain not provided [RCV002472477] Chr6:29162783..30236331 [GRCh37]
Chr6:6p22.1
uncertain significance
NM_030946.2(OR14J1):c.652C>T (p.Arg218Cys) single nucleotide variant Inborn genetic diseases [RCV002855407] Chr6:29307341 [GRCh38]
Chr6:29275118 [GRCh37]
Chr6:6p22.1
uncertain significance
NM_030946.2(OR14J1):c.851A>G (p.Asn284Ser) single nucleotide variant Inborn genetic diseases [RCV003214477] Chr6:29307540 [GRCh38]
Chr6:29275317 [GRCh37]
Chr6:6p22.1
uncertain significance
NM_030946.2(OR14J1):c.629T>A (p.Ile210Asn) single nucleotide variant Inborn genetic diseases [RCV003384940] Chr6:29307318 [GRCh38]
Chr6:29275095 [GRCh37]
Chr6:6p22.1
uncertain significance
NM_030946.2(OR14J1):c.186G>T (p.Lys62Asn) single nucleotide variant Inborn genetic diseases [RCV003379097] Chr6:29306875 [GRCh38]
Chr6:29274652 [GRCh37]
Chr6:6p22.1
uncertain significance
GRCh37/hg19 6p22.1(chr6:29080457-29290402)x1 copy number loss not provided [RCV003485509] Chr6:29080457..29290402 [GRCh37]
Chr6:6p22.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:83
Count of miRNA genes:81
Interacting mature miRNAs:83
Transcripts:ENST00000377160
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.


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
Low 1 2 1 1 1 3 2 2 1 332 1 2
Below cutoff 118 145 75 26 111 17 164 81 192 12 99 85 9 65 96

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_030946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AL096770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL662781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL662857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC136905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX005432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX908738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX927232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR753509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR759808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR933842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR936918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000377160   ⟹   ENSP00000366365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl629,306,626 - 29,307,742 (+)Ensembl
RefSeq Acc Id: ENST00000641895   ⟹   ENSP00000492893
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl629,301,701 - 29,313,017 (+)Ensembl
RefSeq Acc Id: NM_030946   ⟹   NP_112208
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38629,301,701 - 29,313,017 (+)NCBI
GRCh37629,274,467 - 29,275,432 (+)RGD
Build 36629,382,446 - 29,383,411 (+)NCBI Archive
Celera630,880,644 - 30,881,609 (+)RGD
HuRef629,082,076 - 29,083,041 (+)RGD
CHM1_1629,276,729 - 29,277,694 (+)NCBI
T2T-CHM13v2.0629,176,465 - 29,187,793 (+)NCBI
Sequence:
RefSeq Acc Id: NP_112208   ⟸   NM_030946
- UniProtKB: B0V078 (UniProtKB/Swiss-Prot),   A2BEC2 (UniProtKB/Swiss-Prot),   Q5ST27 (UniProtKB/Swiss-Prot),   Q9UGF5 (UniProtKB/Swiss-Prot),   A0A126GW10 (UniProtKB/TrEMBL),   A0A126GWP1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000366365   ⟸   ENST00000377160
RefSeq Acc Id: ENSP00000492893   ⟸   ENST00000641895
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9UGF5-F1-model_v2 AlphaFold Q9UGF5 1-321 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13971 AgrOrtholog
COSMIC OR14J1 COSMIC
Ensembl Genes ENSG00000112459 UniProtKB/Swiss-Prot
  ENSG00000204695 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000225291 UniProtKB/Swiss-Prot
  ENSG00000234100 UniProtKB/Swiss-Prot
  ENSG00000234195 UniProtKB/Swiss-Prot
  ENSG00000236927 UniProtKB/Swiss-Prot
  ENSG00000237777 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000230221.5 UniProtKB/Swiss-Prot
  ENST00000377160.4 UniProtKB/Swiss-Prot
  ENST00000420495.4 UniProtKB/Swiss-Prot
  ENST00000421489.4 UniProtKB/Swiss-Prot
  ENST00000434778.4 UniProtKB/Swiss-Prot
  ENST00000435798.4 UniProtKB/Swiss-Prot
  ENST00000451272.4 UniProtKB/Swiss-Prot
  ENST00000641895 ENTREZGENE
  ENST00000641895.1 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000112459 GTEx
  ENSG00000204695 GTEx
  ENSG00000225291 GTEx
  ENSG00000234100 GTEx
  ENSG00000234195 GTEx
  ENSG00000236927 GTEx
  ENSG00000237777 GTEx
HGNC ID HGNC:13971 ENTREZGENE
Human Proteome Map OR14J1 Human Proteome Map
InterPro GPCR_Rhodpsn UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_Rhodpsn_7TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Olfact_rcpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:442191 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 442191 ENTREZGENE
PANTHER OLFACTORY RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR 14J1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162398444 PharmGKB
PRINTS GPCRRHODOPSN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORYR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE G_PROTEIN_RECEP_F1_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_PROTEIN_RECEP_F1_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A126GVW3_HUMAN UniProtKB/TrEMBL
  A0A126GW10 ENTREZGENE, UniProtKB/TrEMBL
  A0A126GWP1 ENTREZGENE, UniProtKB/TrEMBL
  A0A126GWQ8_HUMAN UniProtKB/TrEMBL
  A2BEC2 ENTREZGENE
  B0V078 ENTREZGENE
  O14J1_HUMAN UniProtKB/Swiss-Prot
  Q5ST27 ENTREZGENE
  Q9UGF5 ENTREZGENE
UniProt Secondary A2BEC2 UniProtKB/Swiss-Prot
  B0V078 UniProtKB/Swiss-Prot
  Q5ST27 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR14J1  olfactory receptor family 14 subfamily J member 1  OR14J1  olfactory receptor, family 14, subfamily J, member 1  Symbol and/or name change 5135510 APPROVED