Homo sapiens (human): 55969
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Entry
55969 CDS
T01001
Symbol
RAB5IF, C20orf24, CFSMR2, OPTI, PNAS-11, RCAF1, RIP5
Name
(RefSeq) RAB5 interacting factor
KO
K26496
GEL complex subunit OPTI
Organism
hsa
Homo sapiens (human)
Disease
H02415
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
55969 (RAB5IF)
Membrane trafficking [BR:
hsa04131
]
Endosome - Lysosome transport
Rab GTPases and associated proteins
Rab associated proteins
55969 (RAB5IF)
Endoplasmic reticulum (ER) - Golgi transport
Others
Multi-pass translocon (MPT) complex
55969 (RAB5IF)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EMC6
Pox_polyA_pol_C
DUF2244
Motif
Other DBs
NCBI-GeneID:
55969
NCBI-ProteinID:
NP_001186463
OMIM:
619960
HGNC:
15870
Ensembl:
ENSG00000101084
UniProt:
Q9BUV8
LinkDB
All DBs
Position
20:36605779..36612557
Genome browser
AA seq
137 aa
AA seq
DB search
MSGGRRKEEPPQPQLANGALKVSVWSKVLRSDAAWEDKDEFLDVIYWFRQIIAVVLGVIW
GVLPLRGFLGIAGFCLINAGVLYLYFSNYLQIDEEEYGGTWELTKEGFMTSFALFMVCVA
DSFTTGHLDHLLHCHPL
NT seq
414 nt
NT seq
+upstream
nt +downstream
nt
atgagcggcgggcggcggaaggaggagccgcctcagccgcagctggccaacggggccctc
aaagtctccgtctggagtaaggtgctgcggagcgacgcggcctgggaggataaggatgaa
tttttagatgtgatctactggttccgacagatcattgctgtggtcctgggtgtcatttgg
ggagttttgccattacgagggttcttgggaatagcaggattctgcctgatcaatgcagga
gtcctgtacctctacttcagcaattacctacagattgatgaggaagaatatggtggcacg
tgggagctcacgaaggaagggtttatgacctcttttgccttgttcatggtatgtgtagct
gatagttttacaacaggtcatttggatcatcttttacactgccatccattatga
DBGET
integrated database retrieval system
