Homo sapiens (human): 56246
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Entry
56246 CDS
T01001
Symbol
MRAP, B27, C21orf61, FALP, FGD2, GCCD2, MRAP1
Name
(RefSeq) melanocortin 2 receptor accessory protein
KO
K22398
melanocortin-2 receptor accessory protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04927
Cortisol synthesis and secretion
hsa04934
Cushing syndrome
Network
nt06310
CRH-ACTH-cortisol signaling
nt06360
Cushing syndrome
Element
N00297
ACTH-cortisol signaling pathway
N00298
CYP11B1-CYP11B2 fusion to ACTH-cortisol signaling pathway
Disease
H00256
Familial glucocorticoid deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04927 Cortisol synthesis and secretion
56246 (MRAP)
09160 Human Diseases
09167 Endocrine and metabolic disease
04934 Cushing syndrome
56246 (MRAP)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MRAP
Motif
Other DBs
NCBI-GeneID:
56246
NCBI-ProteinID:
NP_848932
OMIM:
609196
HGNC:
1304
Ensembl:
ENSG00000170262
Pharos:
Q8TCY5
(Tbio)
UniProt:
Q8TCY5
Structure
PDB
PDBj
LinkDB
All DBs
Position
21:32291813..32314784
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AA seq
172 aa
AA seq
DB search
MANGTNASAPYYSYEYYLDYLDLIPVDEKKLKAHKHSIVIAFWVSLAAFVVLLFLILLYM
SWSASPQMRNSPKHHQTCPWSHGLNLHLCIQKCLPCHREPLATSQAQASSVEPGSRTGPD
QPLRQESSSTLPLGGFQTHPTLLWELTLNGGPLVRSKPSEPPPGDRTSQLQS
NT seq
519 nt
NT seq
+upstream
nt +downstream
nt
atggccaacgggaccaacgcctctgccccatactacagctatgaatactacctggactat
ctggacctcattcccgtggacgagaagaagctgaaagcccacaaacattccatcgtgatc
gcattctgggtgagcctggctgccttcgtggtgctgctcttcctcatcttgctctacatg
tcctggtccgcctccccgcagatgaggaacagccccaagcaccaccaaacatgcccctgg
agtcacggcctcaacctccacctctgcatccagaagtgcctgccgtgccacagggaaccc
ctggcaacctcacaggctcaggcgagctcagtggagccagggagcagaactggccctgac
cagccgctacgacaggagagctcctccaccttgcccctcgggggtttccagacccacccc
actctcctctgggaactgaccctcaatgggggtcccctcgtcaggagcaagcccagcgag
cctccccctggagacaggacctctcaattgcagagctga
DBGET
integrated database retrieval system