GNA15 (G protein subunit alpha 15) - Rat Genome Database
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Gene: GNA15 (G protein subunit alpha 15) Homo sapiens
Analyze
Symbol: GNA15
Name: G protein subunit alpha 15
RGD ID: 732130
HGNC Page HGNC
Description: Exhibits G protein-coupled receptor binding activity. Involved in positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G protein-coupled signaling pathway. Predicted to localize to plasma membrane; PARTICIPATES IN eicosanoid signaling pathway; endothelin signaling pathway; sphingosine 1-phosphate signaling pathway; INTERACTS WITH (-)-demecolcine; 17beta-estradiol; 2,4-Nonadienal.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: epididymis tissue protein Li 17E; g alpha-15; g alpha-16; G-protein subunit alpha-15; G-protein subunit alpha-16; GNA16; guanine nucleotide binding protein (G protein), alpha 15 (Gq class); guanine nucleotide-binding protein subunit alpha-15; guanine nucleotide-binding protein subunit alpha-16
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
GRCh38.p13 Ensembl193,136,033 - 3,163,749 (+)EnsemblGRCh38hg38GRCh38
GRCh38193,136,033 - 3,163,749 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37193,136,031 - 3,163,747 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36193,087,191 - 3,114,766 (+)NCBINCBI36hg18NCBI36
Build 34193,087,229 - 3,114,741NCBI
Celera193,072,520 - 3,100,641 (+)NCBI
Cytogenetic Map19p13.3NCBI
HuRef192,905,020 - 2,932,757 (+)NCBIHuRef
CHM1_1193,135,905 - 3,163,646 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

References

Additional References at PubMed
PMID:1302014   PMID:1322796   PMID:1905813   PMID:7608160   PMID:7703490   PMID:7797501   PMID:7937899   PMID:8415674   PMID:8863838   PMID:9572309   PMID:9742207   PMID:9843397  
PMID:9988720   PMID:10571060   PMID:10644723   PMID:10973974   PMID:11118617   PMID:11686331   PMID:12095632   PMID:12401211   PMID:12477932   PMID:12647293   PMID:12670499   PMID:12748287  
PMID:12885252   PMID:14535952   PMID:14551213   PMID:15057824   PMID:15489334   PMID:16102047   PMID:16218966   PMID:17207965   PMID:18240029   PMID:18755267   PMID:19275934   PMID:19687291  
PMID:20150327   PMID:20445134   PMID:20736409   PMID:21486497   PMID:21832049   PMID:21873635   PMID:22227248   PMID:23200847   PMID:24204697   PMID:25701539   PMID:28514442  


Genomics

Comparative Map Data
GNA15
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl193,136,033 - 3,163,749 (+)EnsemblGRCh38hg38GRCh38
GRCh38193,136,033 - 3,163,749 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37193,136,031 - 3,163,747 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36193,087,191 - 3,114,766 (+)NCBINCBI36hg18NCBI36
Build 34193,087,229 - 3,114,741NCBI
Celera193,072,520 - 3,100,641 (+)NCBI
Cytogenetic Map19p13.3NCBI
HuRef192,905,020 - 2,932,757 (+)NCBIHuRef
CHM1_1193,135,905 - 3,163,646 (+)NCBICHM1_1
Gna15
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391081,338,147 - 81,360,283 (-)NCBIGRCm39mm39
GRCm39 Ensembl1081,338,140 - 81,360,059 (-)Ensembl
GRCm381081,502,313 - 81,524,447 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1081,502,306 - 81,524,225 (-)EnsemblGRCm38mm10GRCm38
MGSCv371080,965,058 - 80,986,970 (-)NCBIGRCm37mm9NCBIm37
MGSCv361080,905,442 - 80,927,354 (-)NCBImm8
Celera1082,525,696 - 82,547,406 (-)NCBICelera
Cytogenetic Map10C1NCBI
cM Map1039.72NCBI
Gna15
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.278,184,632 - 8,205,508 (+)NCBI
Rnor_6.0 Ensembl711,054,333 - 11,077,251 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0711,054,249 - 11,075,152 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0711,221,467 - 11,242,341 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.479,669,956 - 9,689,442 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.179,669,955 - 9,689,442 (+)NCBI
Celera76,375,600 - 6,396,028 (+)NCBICelera
Cytogenetic Map7q11NCBI
Gna15
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554955,252,547 - 5,270,894 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554955,254,546 - 5,270,864 (-)NCBIChiLan1.0ChiLan1.0
GNA15
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1193,116,969 - 3,146,118 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl193,116,969 - 3,146,118 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0192,163,773 - 2,191,985 (+)NCBIMhudiblu_PPA_v0panPan3
GNA15
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl2056,118,067 - 56,126,502 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.12056,117,398 - 56,129,251 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Gna15
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_0049365881,802,576 - 1,816,772 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GNA15
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl275,408,722 - 75,433,814 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1275,408,723 - 75,433,809 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2275,928,409 - 75,949,083 (-)NCBISscrofa10.2Sscrofa10.2susScr3
GNA15
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.162,901,502 - 2,930,567 (+)NCBI
ChlSab1.1 Ensembl62,901,762 - 2,932,138 (+)Ensembl
Gna15
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248286,048,697 - 6,062,851 (-)NCBI

Position Markers
D19S247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37193,139,982 - 3,140,202UniSTSGRCh37
Build 36193,090,982 - 3,091,202RGDNCBI36
Celera193,076,311 - 3,076,539RGD
Cytogenetic Map19p13.3UniSTS
HuRef192,908,753 - 2,909,009UniSTS
Marshfield Genetic Map199.84UniSTS
Marshfield Genetic Map199.84RGD
RH11456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37193,163,410 - 3,163,613UniSTSGRCh37
Build 36193,114,410 - 3,114,613RGDNCBI36
Celera193,100,285 - 3,100,488RGD
Cytogenetic Map19p13.3UniSTS
HuRef192,932,401 - 2,932,604UniSTS
GeneMap99-GB4 RH Map1927.61UniSTS
GNA15__7519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37193,163,086 - 3,163,875UniSTSGRCh37
Build 36193,114,086 - 3,114,875RGDNCBI36
Celera193,099,961 - 3,100,750RGD
HuRef192,932,077 - 2,932,866UniSTS
G13205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37193,163,597 - 3,163,740UniSTSGRCh37
Build 36193,114,597 - 3,114,740RGDNCBI36
Celera193,100,472 - 3,100,615RGD
Cytogenetic Map19p13.3UniSTS
HuRef192,932,588 - 2,932,731UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:908
Count of miRNA genes:621
Interacting mature miRNAs:688
Transcripts:ENST00000262958, ENST00000586082, ENST00000592455
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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 128 901 46 126 1386 14 1563 28 130 73 474 742 124 378 780 1
Low 2248 1934 1512 364 452 318 2143 1519 3324 289 913 749 49 1 826 1509 3 1
Below cutoff 47 152 160 127 68 126 613 639 259 44 60 95 1 499 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000262958   ⟹   ENSP00000262958
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl193,136,033 - 3,163,749 (+)Ensembl
RefSeq Acc Id: ENST00000586082
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl193,149,840 - 3,155,826 (+)Ensembl
RefSeq Acc Id: ENST00000592455   ⟹   ENSP00000467256
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl193,136,442 - 3,151,822 (+)Ensembl
RefSeq Acc Id: NM_002068   ⟹   NP_002059
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38193,136,033 - 3,163,749 (+)NCBI
GRCh37193,136,191 - 3,163,766 (+)ENTREZGENE
Build 36193,087,191 - 3,114,766 (+)NCBI Archive
HuRef192,905,020 - 2,932,757 (+)ENTREZGENE
CHM1_1193,135,905 - 3,163,646 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002059   ⟸   NM_002068
- UniProtKB: P30679 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000262958   ⟸   ENST00000262958
RefSeq Acc Id: ENSP00000467256   ⟸   ENST00000592455
Protein Domains
G-alpha

Promoters
RGD ID:6795606
Promoter ID:HG_KWN:28505
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid,   NB4
Transcripts:NM_002068
Position:
Human AssemblyChrPosition (strand)Source
Build 36193,086,981 - 3,087,481 (+)MPROMDB
RGD ID:7237993
Promoter ID:EPDNEW_H24742
Type:initiation region
Name:GNA15_1
Description:G protein subunit alpha 15
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
GRCh38193,136,242 - 3,136,302EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.3(chr19:1565575-4108128)x3 copy number gain See cases [RCV000052878] Chr19:1565575..4108128 [GRCh38]
Chr19:1565574..4108126 [GRCh37]
Chr19:1516574..4059126 [NCBI36]
Chr19:19p13.3
pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3 copy number gain See cases [RCV000052879] Chr19:1972245..9648879 [GRCh38]
Chr19:1972244..9759555 [GRCh37]
Chr19:1923244..9620555 [NCBI36]
Chr19:19p13.3-13.2
pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:265917-8564134)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|See cases [RCV000052876] Chr19:265917..8564134 [GRCh38]
Chr19:265917..8629018 [GRCh37]
Chr19:216917..8535018 [NCBI36]
Chr19:19p13.3-13.2
pathogenic
GRCh38/hg38 19p13.3(chr19:233565-4699472)x3 copy number gain See cases [RCV000052575] Chr19:233565..4699472 [GRCh38]
Chr19:233565..4699484 [GRCh37]
Chr19:184565..4650484 [NCBI36]
Chr19:19p13.3
pathogenic
GRCh38/hg38 19p13.3(chr19:3080621-3730716)x3 copy number gain See cases [RCV000054107] Chr19:3080621..3730716 [GRCh38]
Chr19:3080619..3730714 [GRCh37]
Chr19:3031619..3681714 [NCBI36]
Chr19:19p13.3
uncertain significance
GRCh38/hg38 19p13.3(chr19:2926238-4051635)x1 copy number loss See cases [RCV000053942] Chr19:2926238..4051635 [GRCh38]
Chr19:2926236..4051633 [GRCh37]
Chr19:2877236..4002633 [NCBI36]
Chr19:19p13.3
pathogenic
NM_002068.3(GNA15):c.517G>A (p.Glu173Lys) single nucleotide variant Malignant melanoma [RCV000063488] Chr19:3151738 [GRCh38]
Chr19:3151736 [GRCh37]
Chr19:3102736 [NCBI36]
Chr19:19p13.3
not provided
NM_002068.3(GNA15):c.1096C>T (p.Arg366Cys) single nucleotide variant Malignant melanoma [RCV000063489] Chr19:3162990 [GRCh38]
Chr19:3162988 [GRCh37]
Chr19:3113988 [NCBI36]
Chr19:19p13.3
not provided
GRCh38/hg38 19p13.3(chr19:1549144-4288720)x1 copy number loss See cases [RCV000134795] Chr19:1549144..4288720 [GRCh38]
Chr19:1549143..4288717 [GRCh37]
Chr19:1500143..4239717 [NCBI36]
Chr19:19p13.3
pathogenic
GRCh38/hg38 19p13.3(chr19:3080621-4912622)x3 copy number gain See cases [RCV000137713] Chr19:3080621..4912622 [GRCh38]
Chr19:3080619..4912634 [GRCh37]
Chr19:3031619..4863634 [NCBI36]
Chr19:19p13.3
likely pathogenic
GRCh38/hg38 19p13.3(chr19:3020573-3482611)x3 copy number gain See cases [RCV000139774] Chr19:3020573..3482611 [GRCh38]
Chr19:3020571..3482609 [GRCh37]
Chr19:2971571..3433609 [NCBI36]
Chr19:19p13.3
uncertain significance
GRCh38/hg38 19p13.3(chr19:2884401-3451078)x3 copy number gain See cases [RCV000143086] Chr19:2884401..3451078 [GRCh38]
Chr19:2884399..3451076 [GRCh37]
Chr19:2835399..3402076 [NCBI36]
Chr19:19p13.3
uncertain significance
GRCh38/hg38 19p13.3(chr19:259395-6795611)x3 copy number gain See cases [RCV000142627] Chr19:259395..6795611 [GRCh38]
Chr19:259395..6795622 [GRCh37]
Chr19:210395..6746622 [NCBI36]
Chr19:19p13.3
pathogenic
GRCh37/hg19 19p13.3(chr19:259395-3152419) copy number gain Global developmental delay [RCV000626520] Chr19:259395..3152419 [GRCh37]
Chr19:19p13.3
likely pathogenic
GRCh37/hg19 19p13.3(chr19:2652901-4342179)x3 copy number gain See cases [RCV000448078] Chr19:2652901..4342179 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3(chr19:260911-3200875)x3 copy number gain not provided [RCV000684094] Chr19:260911..3200875 [GRCh37]
Chr19:19p13.3
pathogenic
GRCh37/hg19 19p13.3-13.2(chr19:3120160-9732820)x3 copy number gain not provided [RCV000684096] Chr19:3120160..9732820 [GRCh37]
Chr19:19p13.3-13.2
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3(chr19:3015481-3543109)x3 copy number gain not provided [RCV000740000] Chr19:3015481..3543109 [GRCh37]
Chr19:19p13.3
benign
Single allele deletion Internal malformations [RCV000787421] Chr19:2229488..4004142 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_002068.4(GNA15):c.813C>T (p.Ser271=) single nucleotide variant not provided [RCV000970345] Chr19:3157796 [GRCh38]
Chr19:3157794 [GRCh37]
Chr19:19p13.3
benign
NM_002068.4(GNA15):c.561G>A (p.Met187Ile) single nucleotide variant not provided [RCV000973222] Chr19:3151782 [GRCh38]
Chr19:3151780 [GRCh37]
Chr19:19p13.3
benign
NM_002068.4(GNA15):c.341G>A (p.Ser114Asn) single nucleotide variant not provided [RCV000969111] Chr19:3150141 [GRCh38]
Chr19:3150139 [GRCh37]
Chr19:19p13.3
benign
GRCh37/hg19 19p13.3(chr19:3076808-4796782) copy number loss not provided [RCV000767742] Chr19:3076808..4796782 [GRCh37]
Chr19:19p13.3
pathogenic
GRCh37/hg19 19p13.3(chr19:3132909-3907470)x3 copy number gain not provided [RCV000847631] Chr19:3132909..3907470 [GRCh37]
Chr19:19p13.3
uncertain significance
NC_000019.9:g.1406030_3597207dup duplication Neurodevelopmental disorder [RCV000787423] Chr19:1406030..3597207 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3(chr19:3134686-3501127)x3 copy number gain not provided [RCV000847642] Chr19:3134686..3501127 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3(chr19:260911-4788357)x3 copy number gain not provided [RCV000846988] Chr19:260911..4788357 [GRCh37]
Chr19:19p13.3
pathogenic
GRCh37/hg19 19p13.3(chr19:260911-3501271)x3 copy number gain not provided [RCV001007025] Chr19:260911..3501271 [GRCh37]
Chr19:19p13.3
pathogenic
GRCh37/hg19 19p13.3(chr19:260912-4384674)x3 copy number gain See cases [RCV001007443] Chr19:260912..4384674 [GRCh37]
Chr19:19p13.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:4383 AgrOrtholog
COSMIC GNA15 COSMIC
Ensembl Genes ENSG00000060558 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000262958 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000467256 UniProtKB/TrEMBL
Ensembl Transcript ENST00000262958 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000592455 UniProtKB/TrEMBL
Gene3D-CATH 1.10.400.10 UniProtKB/Swiss-Prot
GTEx ENSG00000060558 GTEx
HGNC ID HGNC:4383 ENTREZGENE
Human Proteome Map GNA15 Human Proteome Map
InterPro Gprotein_alpha_Q UniProtKB/Swiss-Prot
  Gprotein_alpha_su UniProtKB/Swiss-Prot
  GproteinA_insert UniProtKB/Swiss-Prot
  P-loop_NTPase UniProtKB/Swiss-Prot
KEGG Report hsa:2769 UniProtKB/Swiss-Prot
NCBI Gene 2769 ENTREZGENE
OMIM 139314 OMIM
PANTHER PTHR10218 UniProtKB/Swiss-Prot
Pfam G-alpha UniProtKB/Swiss-Prot
PharmGKB PA28768 PharmGKB
PRINTS GPROTEINA UniProtKB/Swiss-Prot
  GPROTEINAQ UniProtKB/Swiss-Prot
PROSITE G_ALPHA UniProtKB/Swiss-Prot
SMART G_alpha UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47895 UniProtKB/Swiss-Prot
  SSF52540 UniProtKB/Swiss-Prot
UniProt GNA15_HUMAN UniProtKB/Swiss-Prot
  K7EP74_HUMAN UniProtKB/TrEMBL
  P30679 ENTREZGENE
UniProt Secondary E9KL40 UniProtKB/Swiss-Prot
  E9KL47 UniProtKB/Swiss-Prot
  O75247 UniProtKB/Swiss-Prot
  Q53XK2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-14 GNA15  G protein subunit alpha 15    guanine nucleotide binding protein (G protein), alpha 15 (Gq class)  Symbol and/or name change 5135510 APPROVED