Homo sapiens (human): 5192
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Entry
5192 CDS
T01001
Symbol
PEX10, NALD, PBD6A, PBD6B, RNF69
Name
(RefSeq) peroxisomal biogenesis factor 10
KO
K13346
peroxin-10
Organism
hsa
Homo sapiens (human)
Pathway
hsa04146
Peroxisome
Disease
H00177
Neonatal adrenoleukodystrophy
H00205
Peroxisome biogenesis disorder
H01342
Zellweger syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04146 Peroxisome
5192 (PEX10)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
5192 (PEX10)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
Single Ring-finger type E3
Peripheral membrane proteins
5192 (PEX10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Pex2_Pex12
zf-RING_2
zf-C3HC4_3
zf-C3HC4
zf-RING_UBOX
zf-C3HC4_2
zf-RING_5
Prok-RING_4
zf-rbx1
zf-C3HC4_4
zf-ANAPC11
DUF3290
Zn-C2H2_12
zf-RING_4
Motif
Other DBs
NCBI-GeneID:
5192
NCBI-ProteinID:
NP_002608
OMIM:
602859
HGNC:
8851
Ensembl:
ENSG00000157911
Pharos:
O60683
(Tbio)
UniProt:
O60683
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All DBs
Position
1:complement(2403974..2413827)
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AA seq
326 aa
AA seq
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MAPAAASPPEVIRAAQKDEYYRGGLRSAAGGALHSLAGARKWLEWRKEVELLSDVAYFGL
TTLAGYQTLGEEYVSIIQVDPSRIHVPSSLRRGVLVTLHAVLPYLLDKALLPLEQELQAD
PDSGRPLQGSLGPGGRGCSGARRWMRHHTATLTEQQRRALLRAVFVLRQGLACLQRLHVA
WFYIHGVFYHLAKRLTGITYLRVRSLPGEDLRARVSYRLLGVISLLHLVLSMGLQLYGFR
QRQRARKEWRLHRGLSHRRASLEERAVSRNPLCTLCLEERRHPTATPCGHLFCWECITAW
CSSKAECPLCREKFPPQKLIYLRHYR
NT seq
981 nt
NT seq
+upstream
nt +downstream
nt
atggccccggccgccgccagccccccggaggtgatccgcgcggcgcagaaggacgagtac
taccgcggtgggctgcggagcgcggcgggcggcgccctgcacagcctggcgggtgcgagg
aagtggctggagtggaggaaggaggttgagctgctctcagatgtggcctactttggcctc
accacacttgcaggctaccagaccctgggggaggagtacgtcagcatcatccaggtggac
ccatcgcggatacatgtgccctcctcgctgcgccgtggcgtgctggtgacactgcatgcc
gtcctgccctacctgctggacaaggccctgctccccctggagcaggagctgcaggctgac
cccgacagtgggcgacccttgcaggggagcctggggccaggtgggcgtggctgctcaggg
gcgcggcgctggatgcgtcaccacacggccaccctgactgagcagcagaggagggcgctg
ctgcgggcggtcttcgtcctcagacagggcctcgcctgcctccagcggctacatgttgcc
tggttttacatccacggtgtcttctaccacctggccaagaggctcacggggatcacgtac
ctccgtgtccgcagcctgcccggagaggacctgagggcccgtgttagctacaggctgctg
ggggtcatctcactgctgcacctggtgctgtccatggggctgcagctgtacggtttcagg
cagcggcagcgagccaggaaggagtggaggctgcaccgcggcctgtctcaccgcagggcc
tccttggaggagagagccgtttccagaaaccccctgtgcaccctgtgcctggaggagcgc
aggcacccaacagccacgccctgcggccacctgttctgctgggagtgcatcaccgcgtgg
tgcagcagcaaggcggagtgtcccctctgccgggagaagttccctccccagaagctcatc
taccttcggcactaccgctga
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