Homo sapiens (human): 92840
Help
Entry
92840 CDS
T01001
Symbol
REEP6, C19orf32, DP1L1, REEP6.1, REEP6.2, RP77, TB1, TB2L1, Yip2f
Name
(RefSeq) receptor expression-enhancing protein 6 isoform 1
KO
K17279
receptor expression-enhancing protein 5/6
Organism
hsa
Homo sapiens (human)
Disease
H00527
Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
92840 (REEP6)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of hepatic cells
92840 (REEP6)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
TB2_DP1_HVA22
Motif
Other DBs
NCBI-GeneID:
92840
NCBI-ProteinID:
NP_001316485
OMIM:
609346
HGNC:
30078
Ensembl:
ENSP00000378861.5
UniProt:
Q96HR9
LinkDB
All DBs
Position
19:1491181..1497927
Genome browser
AA seq
211 aa
AA seq
DB search
MDGLRQRVEHFLEQRNLVTEVLGALEAKTGVEKRYLAAGAVTLLSLYLLFGYGASLLCNL
IGFVYPAYASIKAIESPSKDDDTVWLTYWVVYALFGLAEFFSDLLLSWFPFYYVGKCAFL
LFCMAPRPWNGALMLYQRVVRPLFLRHHGAVDRIMNDLSGRALDAAAGITRNVLQVLARS
RAGITPVAVAGPSTPLEADLKPSQTPQPKDK
NT seq
636 nt
NT seq
+upstream
nt +downstream
nt
atggacggcctgaggcagcgcgtggagcacttcctggagcaaaggaacctggtcaccgaa
gtgctgggggcgctggaggccaagaccggggtggagaagcggtatctggctgcaggagcc
gtcactctgctaagcctgtatctgctgttcggctacggagcgtctctgctgtgcaatctc
atcggatttgtgtaccccgcatatgcctcaatcaaagctatcgagagcccaagcaaggac
gacgacactgtgtggctcacctactgggtggtgtacgccctgtttgggctggccgagttc
ttcagcgatctactcctgtcctggttccctttctactacgtgggcaagtgcgccttcctg
ttgttctgcatggctcccaggccctggaacggggctctcatgctgtatcagcgcgtcgtg
cgtccgctgttcctaaggcaccacggggccgtagacagaatcatgaacgacctcagcggg
cgagccctggacgcggcggccggaataaccaggaacgtcttgcaggtcctggcccgtagc
cgggcaggcatcaccccggtggctgtggccgggccctccactcccctggaagctgacctc
aagccaagccagaccccgcagccgaaggacaagtga
DBGET
integrated database retrieval system