Homo sapiens (human): 2861
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Entry
2861 CDS
T01001
Symbol
GPR37, EDNRBL, PAELR, hET(B)R-LP
Name
(RefSeq) G protein-coupled receptor 37
KO
K04243
prosaposin receptor
Organism
hsa
Homo sapiens (human)
Pathway
hsa05012
Parkinson disease
hsa05022
Pathways of neurodegeneration - multiple diseases
Network
nt06463
Parkinson disease
nt06466
Pathways of neurodegeneration
Element
N01021
Parkin-mediated ubiquitination
N01022
Mutation-inactivated PRKN to Parkin-mediated ubiquitination
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09164 Neurodegenerative disease
05012 Parkinson disease
2861 (GPR37)
05022 Pathways of neurodegeneration - multiple diseases
2861 (GPR37)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
hsa04030
]
2861 (GPR37)
G protein-coupled receptors [BR:
hsa04030
]
Rhodopsin family
Peptide
Prosaposin
2861 (GPR37)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
7tm_1
Motif
Other DBs
NCBI-GeneID:
2861
NCBI-ProteinID:
NP_005293
OMIM:
602583
HGNC:
4494
Ensembl:
ENSG00000170775
UniProt:
O15354
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All DBs
Position
7:complement(124743885..124765792)
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AA seq
613 aa
AA seq
DB search
MRAPGALLARMSRLLLLLLLKVSASSALGVAPASRNETCLGESCAPTVIQRRGRDAWGPG
NSARDVLRARAPREEQGAAFLAGPSWDLPAAPGRDPAAGRGAEASAAGPPGPPTRPPGPW
RWKGARGQEPSETLGRGNPTALQLFLQISEEEEKGPRGAGISGRSQEQSVKTVPGASDLF
YWPRRAGKLQGSHHKPLSKTANGLAGHEGWTIALPGRALAQNGSLGEGIHEPGGPRRGNS
TNRRVRLKNPFYPLTQESYGAYAVMCLSVVIFGTGIIGNLAVMCIVCHNYYMRSISNSLL
ANLAFWDFLIIFFCLPLVIFHELTKKWLLEDFSCKIVPYIEVASLGVTTFTLCALCIDRF
RAATNVQMYYEMIENCSSTTAKLAVIWVGALLLALPEVVLRQLSKEDLGFSGRAPAERCI
IKISPDLPDTIYVLALTYDSARLWWYFGCYFCLPTLFTITCSLVTARKIRKAEKACTRGN
KRQIQLESQMNCTVVALTILYGFCIIPENICNIVTAYMATGVSQQTMDLLNIISQFLLFF
KSCVTPVLLFCLCKPFSRAFMECCCCCCEECIQKSSTVTSDDNDNEYTTELELSPFSTIR
REMSTFASVGTHC
NT seq
1842 nt
NT seq
+upstream
nt +downstream
nt
atgcgagccccgggcgcgcttctcgcccgcatgtcgcggctactgcttctgctactgctc
aaggtgtctgcctcttctgccctcggggtcgcccctgcgtccagaaacgaaacttgtctg
ggggagagctgtgcacctacagtgatccagcgccgcggcagggacgcctggggaccggga
aattctgcaagagacgttctgcgagcccgagcacccagggaggagcagggggcagcgttt
cttgcgggaccctcctgggacctgccggcggccccgggccgtgacccggctgcaggcaga
ggggcggaggcgtcggcagccggacccccgggacctccaaccaggccacctggcccctgg
aggtggaaaggtgctcggggtcaggagccttctgaaactttggggagagggaaccccacg
gccctccagctcttccttcagatctcagaggaggaagagaagggtcccagaggcgctggc
atttccgggcgtagccaggagcagagtgtgaagacagtccccggagccagcgatcttttt
tactggccaaggagagccgggaaactccagggttcccaccacaagcccctgtccaagacg
gccaatggactggcggggcacgaagggtggacaattgcactcccgggccgggcgctggcc
cagaatggatccttgggtgaaggaatccatgagcctgggggtccccgccggggaaacagc
acgaaccggcgtgtgagactgaagaaccccttctacccgctgacccaggagtcctatgga
gcctacgcggtcatgtgtctgtccgtggtgatcttcgggaccggcatcattggcaacctg
gcggtgatgtgcatcgtgtgccacaactactacatgcggagcatctccaactccctcttg
gccaacctggccttctgggactttctcatcatcttcttctgccttccgctggtcatcttc
cacgagctgaccaagaagtggctgctggaggacttctcctgcaagatcgtgccctatata
gaggtcgcttctctgggagtcaccactttcaccttatgtgctctgtgcatagaccgcttc
cgtgctgccaccaacgtacagatgtactacgaaatgatcgaaaactgttcctcaacaact
gccaaacttgctgttatatgggtgggagctctattgttagcacttccagaagttgttctc
cgccagctgagcaaggaggatttggggtttagtggccgagctccggcagaaaggtgcatt
attaagatctctcctgatttaccagacaccatctatgttctagccctcacctacgacagt
gcgagactgtggtggtattttggctgttacttttgtttgcccacgcttttcaccatcacc
tgctctctagtgactgcgaggaaaatccgcaaagcagagaaagcctgtacccgagggaat
aaacggcagattcaactagagagtcagatgaactgtacagtagtggcactgaccatttta
tatggattttgcattattcctgaaaatatctgcaacattgttactgcctacatggctaca
ggggtttcacagcagacaatggacctccttaatatcatcagccagttccttttgttcttt
aagtcctgtgtcaccccagtcctccttttctgtctctgcaaacccttcagtcgggccttc
atggagtgctgctgctgttgctgtgaggaatgcattcagaagtcttcaacggtgaccagt
gatgacaatgacaacgagtacaccacggaactcgaactctcgcctttcagtaccatacgc
cgtgaaatgtccacttttgcttctgtcggaactcattgctga
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