Homo sapiens (human): 9094
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Entry
9094 CDS
T01001
Symbol
UNC119, CORD24, HRG4, IMD13, POC7, POC7A
Name
(RefSeq) unc-119 lipid binding chaperone
KO
K23539
protein unc-119
Organism
hsa
Homo sapiens (human)
Disease
H00481
Cone-rod dystrophy and cone dystrophy
H02526
Disorders of adaptive immunity
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
9094 (UNC119)
Membrane trafficking [BR:
hsa04131
]
Protein recycling
Rab GTPases and associated proteins
Rab11 associated proteins
9094 (UNC119)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
GMP_PDE_delta
IIGP
Motif
Other DBs
NCBI-GeneID:
9094
NCBI-ProteinID:
NP_005139
OMIM:
604011
HGNC:
12565
Ensembl:
ENSG00000109103
UniProt:
Q13432
Structure
PDB
PDBj
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All DBs
Position
17:complement(28546707..28552628)
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AA seq
240 aa
AA seq
DB search
MKVKKGGGGAGTATESAPGPSGQSVAPIPQPPAESESGSESEPDAGPGPRPGPLQRKQPI
GPEDVLGLQRITGDYLCSPEENIYKIDFVRFKIRDMDSGTVLFEIKKPPVSERLPINRRD
LDPNAGRFVRYQFTPAFLRLRQVGATVEFTVGDKPVNNFRMIERHYFRNQLLKSFDFHFG
FCIPSSKNTCEHIYDFPPLSEELISEMIRHPYETQSDSFYFVDDRLVMHNKADYSYSGTP
NT seq
723 nt
NT seq
+upstream
nt +downstream
nt
atgaaggtgaagaagggcggcggtggggccgggacggcgacggagtccgctccggggccc
tcgggccagagcgtggcccccataccacagccgcctgcggaatccgaatctgggtccgag
tcggagccggacgcaggcccagggcccaggccggggccgctgcagaggaagcagccgatc
gggccggaggacgtgctggggctgcagcggatcaccggtgactacctctgctcccctgag
gagaatatctacaagatcgactttgtcaggtttaagattcgggacatggactcaggcact
gtcctctttgaaatcaagaagcccccagtctcagaacggttgcccatcaaccggcgggac
ctggaccccaatgctgggcgctttgtccgctaccagttcacgcctgccttcctccgcctg
aggcaggtgggagccacggtggagttcacagtgggagacaagcctgtcaacaacttccgc
atgatcgagaggcactacttccgcaaccagctactcaaaagcttcgacttccactttggc
ttctgcatccccagcagcaagaacacctgcgagcacatttacgacttcccccctctctcc
gaggagctgatcagcgagatgatccgccacccgtatgagacccagtctgacagcttctac
ttcgtggatgaccggctggtgatgcacaataaagcagactattcctacagcgggacaccc
tga
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integrated database retrieval system