Homo sapiens (human): 65055
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Entry
65055 CDS
T01001
Symbol
REEP1, C2orf23, DSMA6, HMN5B, HMND12, HMNR6, SPG31, Yip2a
Name
(RefSeq) receptor accessory protein 1
KO
K17338
receptor expression-enhancing protein 1/2/3/4
Organism
hsa
Homo sapiens (human)
Disease
H00266
Hereditary spastic paraplegia
H00856
Distal hereditary motor neuropathies
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99992 Structural proteins
65055 (REEP1)
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Paralog
Gene cluster
GFIT
Motif
Pfam:
TB2_DP1_HVA22
DUF6768
Motif
Other DBs
NCBI-GeneID:
65055
NCBI-ProteinID:
NP_075063
OMIM:
609139
HGNC:
25786
Ensembl:
ENSG00000068615
UniProt:
Q9H902
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Position
2:complement(86213993..86338083)
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AA seq
201 aa
AA seq
DB search
MVSWIISRLVVLIFGTLYPAYYSYKAVKSKDIKEYVKWMMYWIIFALFTTAETFTDIFLC
WFPFYYELKIAFVAWLLSPYTKGSSLLYRKFVHPTLSSKEKEIDDCLVQAKDRSYDALVH
FGKRGLNVAATAAVMAASKGQGALSERLRSFSMQDLTTIRGDGAPAPSGPPPPGSGRASG
KHGQPKMSRSASESASSSGTA
NT seq
606 nt
NT seq
+upstream
nt +downstream
nt
atggtgtcatggatcatctccaggctggtggtgcttatatttggcaccctttaccctgcg
tattattcctacaaggctgtgaaatcaaaggacattaaggaatatgtcaaatggatgatg
tactggattatatttgcacttttcaccacagcagagacattcacagacatcttcctttgt
tggtttccattctattatgaactaaaaatagcatttgtagcctggctgctgtctccctac
acaaaaggctccagcctcctgtacaggaagtttgtacatcccacgctatcttcaaaagaa
aaggaaatcgatgattgtctggtccaagcaaaagaccgaagttacgatgcccttgtgcac
ttcgggaagcggggcttgaacgtggccgccacagcggctgtgatggctgcttccaaggga
cagggtgccttatcggagagactgcggagcttcagcatgcaggacctcaccaccatcagg
ggagacggcgcccctgctccctcgggccccccaccaccggggtctgggcgggccagcggc
aaacacggccagcctaagatgtccaggagtgcttctgagagcgctagcagctcaggcacc
gcctag
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