Homo sapiens (human): 51308
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Entry
51308 CDS
T01001
Symbol
REEP2, C5orf19, SGC32445, SPG72, SPG72A, SPG72B, Yip2d
Name
(RefSeq) receptor accessory protein 2
KO
K17338
receptor expression-enhancing protein 1/2/3/4
Organism
hsa
Homo sapiens (human)
Disease
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99992 Structural proteins
51308 (REEP2)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TB2_DP1_HVA22
DUF2306
DUF6768
Motif
Other DBs
NCBI-GeneID:
51308
NCBI-ProteinID:
NP_057690
OMIM:
609347
HGNC:
17975
Ensembl:
ENSG00000132563
UniProt:
Q9BRK0
A8K3D2
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All DBs
Position
5:138439057..138446965
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AA seq
252 aa
AA seq
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MVSWIISRLVVLIFGTLYPAYSSYKAVKTKNVKEYVKWMMYWIVFAFFTTAETLTDIVLS
WFPFYFELKIAFVIWLLSPYTKGSSVLYRKFVHPTLSNKEKEIDEYITQARDKSYETMMR
VGKRGLNLAANAAVTAAAKGVLSEKLRSFSMQDLTLIRDEDALPLQRPDGRLRPSPGSLL
DTIEDLGDDPALSLRSSTNPADSRTEASEDDMGDKAPKRAKPIKKAPKAEPLASKTLKTR
PKKKTSGGGDSA
NT seq
759 nt
NT seq
+upstream
nt +downstream
nt
atggtgtcctggatcatctctcgcctggtggtgctcatctttggcaccctgtacccagcc
tattcttcctacaaggccgtgaagacaaaaaacgtgaaggaatatgtgaaatggatgatg
tactggatcgtctttgccttcttcaccacggccgagacgctcacggatatagtgctctcc
tggttccccttctactttgaactgaagatcgccttcgtgatatggctgctgtccccttac
accaagggctccagcgtgctctaccgcaagttcgtgcacccaacgctgtccaacaaggag
aaggagatcgacgagtacatcacgcaggcccgagacaagagctatgagaccatgatgagg
gtgggcaagaggggcctgaaccttgccgccaatgctgcagtcacagctgccgccaagggg
gtgctgtcagagaagctccgcagcttcagcatgcaggacctgaccctgatccgggacgag
gacgcactgcccctgcagaggcctgacggccgcctccgacccagccctggcagcctcctg
gacaccatcgaggacttaggagatgaccctgccctgagtctaaggtccagcacaaacccg
gcagattcccggacagaggcttctgaggatgacatgggagacaaagctcccaagagggcc
aaacccatcaaaaaagcgcccaaagctgagccactggcttccaagacactgaagacccgg
cccaagaagaagacctctggcgggggcgactcagcttga
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