Homo sapiens (human): 84317
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Entry
84317 CDS
T01001
Symbol
VMA22, CCDC115, CDG2O, ccp1
Name
(RefSeq) vacuolar ATPase assembly factor VMA22
KO
K23543
coiled-coil domain-containing protein 115
Organism
hsa
Homo sapiens (human)
Disease
H00119
Congenital disorders of glycosylation type II
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
84317 (VMA22)
Membrane trafficking [BR:
hsa04131
]
Endosome - Golgi transport
Others
Others
84317 (VMA22)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Vma22_CCDC115
ATP-synt_D
Motif
Other DBs
NCBI-GeneID:
84317
NCBI-ProteinID:
NP_115733
OMIM:
613734
HGNC:
28178
Ensembl:
ENSG00000136710
UniProt:
Q96NT0
LinkDB
All DBs
Position
2:complement(130337933..130342681)
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AA seq
180 aa
AA seq
DB search
MAALDLRAELDSLVLQLLGDLEELEGKRTVLNARVEEGWLSLAKARYAMGAKSVGPLQYA
SHMEPQVCLHASEAQEGLQKFKVVRAGVHAPEEVGPREAGLRRRKGPTKTPEPESSEAPQ
DPLNWFGILVPHSLRQAQASFRDGLQLAADIASLQNRIDWGRSQLRGLQEKLKQLEPGAA
NT seq
543 nt
NT seq
+upstream
nt +downstream
nt
atggcggcgcttgacctgcgagcggagctggattcgctggtcctgcagctgcttggggac
ctggaggagctggaggggaaacgaacggtgttgaacgcccgggtggaggagggctggctc
tcgctcgccaaggctcgctacgcgatgggcgccaagtcggtagggcccctgcagtatgct
tcccacatggagccccaggtctgcctccacgccagcgaggcccaggagggactccagaag
ttcaaggtggtgagagctggtgtccacgccccagaggaggtggggcctcgcgaagcaggt
ctgcggaggcgcaagggccccactaagaccccagaaccggagtcctctgaggcccctcag
gaccccctgaactggtttggaatcctagttcctcacagtctacgtcaggctcaagcaagc
ttccgggatggcctgcagctggccgcagacatagccagcctccagaaccgcattgactgg
ggtcgaagccagctccggggactccaagagaaactcaagcagctggagcctggggctgcc
tga
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