Homo sapiens (human): 10981
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Entry
10981 CDS
T01001
Symbol
RAB32, PARK26
Name
(RefSeq) RAB32, member RAS oncogene family
KO
K07918
Ras-related protein Rab-32
Organism
hsa
Homo sapiens (human)
Disease
H00057
Parkinson disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
10981 (RAB32)
09183 Protein families: signaling and cellular processes
04031 GTP-binding proteins [BR:
hsa04031
]
10981 (RAB32)
Membrane trafficking [BR:
hsa04131
]
Others
Specific organelles associated proteins
Melanosome
10981 (RAB32)
Mitochondrion
10981 (RAB32)
GTP-binding proteins [BR:
hsa04031
]
Small (monomeric) G-proteins
Rab Family
Rab29/32/38 [OT]
10981 (RAB32)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ras
Roc
Arf
Gtr1_RagA
GTP_EFTU
PduV-EutP
ATP_bind_1
MMR_HSR1
AAA_22
AAA_7
AAA_16
nSTAND3
TsaE
Sigma54_activat
Motif
Other DBs
NCBI-GeneID:
10981
NCBI-ProteinID:
NP_006825
OMIM:
612906
HGNC:
9772
Ensembl:
ENSG00000118508
UniProt:
Q13637
Structure
PDB
PDBj
LinkDB
All DBs
Position
6:146543833..146554953
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AA seq
225 aa
AA seq
DB search
MAGGGAGDPGLGAAAAPAPETREHLFKVLVIGELGVGKTSIIKRYVHQLFSQHYRATIGV
DFALKVLNWDSRTLVRLQLWDIAGQERFGNMTRVYYKEAVGAFVVFDISRSSTFEAVLKW
KSDLDSKVHLPNGSPIPAVLLANKCDQNKDSSQSPSQVDQFCKEHGFAGWFETSAKDNIN
IEEAARFLVEKILVNHQSFPNEENDVDKIKLDQETLRAENKSQCC
NT seq
678 nt
NT seq
+upstream
nt +downstream
nt
atggcgggcggaggagccggggaccccggcctgggggcggccgccgccccagcgcccgag
acccgcgagcacctcttcaaggtgctggtgatcggcgagcttggcgtgggcaagaccagc
atcatcaagcgctacgtccaccagctcttctcccagcactaccgggccaccatcggggtg
gacttcgccctcaaggtcctcaactgggacagcaggactctggtgcgcctgcagctgtgg
gacatcgcggggcaggagcgatttggcaacatgacccgagtatactacaaggaagctgtt
ggtgcttttgtagtctttgatatatcaagaagttccacatttgaggcagtcttaaaatgg
aaaagtgatctggatagtaaagttcatcttccaaatggcagccctatccctgctgtcctc
ttggctaacaaatgtgaccagaacaaggacagtagccagagtccttcccaggtggaccaa
ttctgcaaagaacatggctttgccggatggtttgaaacctctgcaaaggataacataaac
atagaggaagctgcccggttcctagtggagaagattcttgtaaaccaccaaagctttcct
aatgaagaaaacgatgtggacaaaattaagctagatcaagagaccttgagagcagagaac
aaatcccagtgttgctga
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