KEGG   Homo sapiens (human): 5192
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)
SSDB
Motif
Pfam: Pex2_Pex12 zf-RING_2 zf-C3HC4_3 zf-C3HC4 zf-RING_UBOX zf-C3HC4_2 RING_XB3-XBAT31 zf-RING_5 Prok-RING_4 zf-rbx1 zf-C3HC4_4 zf-ANAPC11 DUF3290 Zn-C2H2_12 zf-RING_4
Other DBs
NCBI-GeneID: 5192
NCBI-ProteinID: NP_002608
OMIM: 602859
HGNC: 8851
Ensembl: ENSG00000157911
UniProt: O60683
Position
1:complement(2403974..2413827)
AA seq 326 aa
MAPAAASPPEVIRAAQKDEYYRGGLRSAAGGALHSLAGARKWLEWRKEVELLSDVAYFGL
TTLAGYQTLGEEYVSIIQVDPSRIHVPSSLRRGVLVTLHAVLPYLLDKALLPLEQELQAD
PDSGRPLQGSLGPGGRGCSGARRWMRHHTATLTEQQRRALLRAVFVLRQGLACLQRLHVA
WFYIHGVFYHLAKRLTGITYLRVRSLPGEDLRARVSYRLLGVISLLHLVLSMGLQLYGFR
QRQRARKEWRLHRGLSHRRASLEERAVSRNPLCTLCLEERRHPTATPCGHLFCWECITAW
CSSKAECPLCREKFPPQKLIYLRHYR
NT seq 981 nt   +upstreamnt  +downstreamnt
atggccccggccgccgccagccccccggaggtgatccgcgcggcgcagaaggacgagtac
taccgcggtgggctgcggagcgcggcgggcggcgccctgcacagcctggcgggtgcgagg
aagtggctggagtggaggaaggaggttgagctgctctcagatgtggcctactttggcctc
accacacttgcaggctaccagaccctgggggaggagtacgtcagcatcatccaggtggac
ccatcgcggatacatgtgccctcctcgctgcgccgtggcgtgctggtgacactgcatgcc
gtcctgccctacctgctggacaaggccctgctccccctggagcaggagctgcaggctgac
cccgacagtgggcgacccttgcaggggagcctggggccaggtgggcgtggctgctcaggg
gcgcggcgctggatgcgtcaccacacggccaccctgactgagcagcagaggagggcgctg
ctgcgggcggtcttcgtcctcagacagggcctcgcctgcctccagcggctacatgttgcc
tggttttacatccacggtgtcttctaccacctggccaagaggctcacggggatcacgtac
ctccgtgtccgcagcctgcccggagaggacctgagggcccgtgttagctacaggctgctg
ggggtcatctcactgctgcacctggtgctgtccatggggctgcagctgtacggtttcagg
cagcggcagcgagccaggaaggagtggaggctgcaccgcggcctgtctcaccgcagggcc
tccttggaggagagagccgtttccagaaaccccctgtgcaccctgtgcctggaggagcgc
aggcacccaacagccacgccctgcggccacctgttctgctgggagtgcatcaccgcgtgg
tgcagcagcaaggcggagtgtcccctctgccgggagaagttccctccccagaagctcatc
taccttcggcactaccgctga

  All links  
Disease (3)   
   OMIM (3)   
Gene (36)   
   RefGene (27)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (11)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (9)   
DNA sequence (24)   
   RefSeq(nuc) (10)   
   GenBank (7)   
   EMBL (7)   
Protein domain (15)   
   Pfam (15)   
All databases (89)   

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