Homo sapiens (human): 387733
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Entry
387733 CDS
T01001
Symbol
IFITM5, BRIL, DSPA1, Hrmp1, OI5, fragilis4
Name
(RefSeq) interferon induced transmembrane protein 5
KO
K06566
interferon induced transmembrane protein
Organism
hsa
Homo sapiens (human)
Disease
H00506
Osteogenesis imperfecta
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
387733 (IFITM5)
04147 Exosome [BR:
hsa04147
]
387733 (IFITM5)
Transporters [BR:
hsa02000
]
Other transporters
Accessory factors involved in transport [TC:
8
]
387733 (IFITM5)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of colorectal cancer cells
387733 (IFITM5)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CD225
DUF3708
Motif
Other DBs
NCBI-GeneID:
387733
NCBI-ProteinID:
NP_001020466
OMIM:
614757
HGNC:
16644
Ensembl:
ENSG00000206013
UniProt:
A6NNB3
LinkDB
All DBs
Position
11:complement(298200..299526)
Genome browser
AA seq
132 aa
AA seq
DB search
MDTAYPREDTRAPTPSKAGAHTALTLGAPHPPPRDHLIWSVFSTLYLNLCCLGFLALAYS
IKARDQKVVGDLEAARRFGSKAKCYNILAAMWTLVPPLLLLGLVVTGALHLARLAKDSAA
FFSTKFDDADYD
NT seq
399 nt
NT seq
+upstream
nt +downstream
nt
atggacacggcgtatccccgcgaggacacccgggcccccacgcccagcaaggccggtgcc
cacacagccctcacactgggggccccgcaccccccgcctcgagaccacttgatctggtcg
gtgttcagcaccctctacctgaatctgtgttgcctcggcttcctggcgctggcctactcc
atcaaggcccgagatcagaaggtggttggtgacctggaagcggcccggcgttttggctcc
aaagccaagtgctacaacatcctggccgcgatgtggacgctggtgccgccactgctgctc
ctggggctggtggtgactggtgccctgcacctggcccggctggccaaggactctgccgcc
ttcttcagcaccaagtttgatgacgcggactatgactga
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integrated database retrieval system
