KEGG   Homo sapiens (human): 54112
Entry
54112             CDS       T01001                                 
Symbol
GPR88, COCPMR, STRG
Name
(RefSeq) G protein-coupled receptor 88
  KO
K08422  G protein-coupled receptor 88
Organism
hsa  Homo sapiens (human)
Disease
H02367  Chorea, childhood-onset, with psychomotor retardation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04030 G protein-coupled receptors [BR:hsa04030]
    54112 (GPR88)
G protein-coupled receptors [BR:hsa04030]
 Rhodopsin family
  Others
   Orphan GPCRs / unclassified GPCRs
    54112 (GPR88)
SSDB
Motif
Pfam: 7tm_1 7TM_GPCR_Srx
Other DBs
NCBI-GeneID: 54112
NCBI-ProteinID: NP_071332
OMIM: 607468
HGNC: 4539
Ensembl: ENSG00000181656
UniProt: Q9GZN0
Structure
Position
1:100538139..100542021
AA seq 384 aa
MTNSSSTSTSSTTGGSLLLLCEEEESWAGRRIPVSLLYSGLAIGGTLANGMVIYLVSSFR
KLQTTSNAFIVNGCAADLSVCALWMPQEAVLGLLPTGSAEPPADWDGAGGSYRLLRGGLL
GLGLTVSLLSHCLVALNRYLLITRAPATYQALYQRRHTAGMLALSWALALGLVLLLPPWA
PRPGAAPPRVHYPALLAAAALLAQTALLLHCYLGIVRRVRVSVKRVSVLNFHLLHQLPGC
AAAAAAFPGAQHAPGPGGAAHPAQAQPLPPALHPRRAQRRLSGLSVLLLCCVFLLATQPL
VWVSLASGFSLPVPWGVQAASWLLCCALSALNPLLYTWRNEEFRRSVRSVLPGVGDAAAA
AVAATAVPAVSQAQLGTRAAGQHW
NT seq 1155 nt   +upstreamnt  +downstreamnt
atgaccaactcctcctccacatccacctcctccaccaccggtggctcgctgctgctgctc
tgcgaggaagaggagtcgtgggcgggccggcgcatcccggtgtcactcctgtattcgggc
ctggccatcgggggcacgctggccaacggcatggtcatctatctcgtgtcgtccttccga
aagctgcagaccaccagcaacgccttcatcgtgaacggctgcgccgccgacctcagcgtc
tgcgccctctggatgccgcaggaggcggtgctcgggctcctgcccaccggctctgcggag
ccccccgcagactgggacggcgctgggggcagctaccgcctgctacggggtgggctgctg
ggcctcggactcacggtgtccctcctctcccactgcctcgtggccctgaaccgctacctg
ctcatcacccgggcgcccgccacctaccaggcgctgtaccagaggcgccacacggcgggc
atgctggcgctgtcctgggcgctcgccctgggcctcgtgctgctgctcccgccctgggca
ccgcggcccggcgccgcgccaccgcgagtccactacccggcgctgctggccgccgcggcg
ctgctggcgcagacagctctgctgctgcactgctacctgggcatcgtgcgccgcgtgcgt
gtcagcgtcaagcgggtcagcgtgctcaacttccacctgctgcaccagttgcccggctgc
gccgccgccgccgccgccttcccgggcgcccagcacgcgccgggccccggtggcgccgcg
cacccggcgcaggcccagcccctgccgcccgcgctgcacccgcggcgggcacagcggcgt
ctcagcggcctgtcggtgctgctgctctgctgcgtcttcctgctggccacgcagccactg
gtgtgggtgagcctggccagcggcttctcgctgccggtgccctggggagtgcaggcggcc
agctggctcctgtgctgcgccctgtccgcgctcaatccgctgctctacacgtggaggaac
gaggagttccgccgctccgtgcgctcagtcctgccgggcgtcggcgacgcggcggccgct
gccgttgccgccacagccgtgcccgcagtgtcccaggcgcaactgggcacccgcgccgcg
ggccagcactggtaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (11)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (9)   
   RefSeq(nuc) (1)   
   GenBank (4)   
   EMBL (4)   
3D Structure (2)   
   PDB (2)   
Protein domain (2)   
   Pfam (2)   
All databases (33)   

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