KEGG   Homo sapiens (human): 55670
Entry
55670             CDS       T01001                                 
Symbol
PEX26, PBD7A, PBD7B, PEX26M1T, Pex26pM1T
Name
(RefSeq) peroxisomal biogenesis factor 26
  KO
K13340  peroxin-26
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
    55670 (PEX26)
SSDB
Motif
Pfam: Pex26
Other DBs
NCBI-GeneID: 55670
NCBI-ProteinID: NP_001121121
OMIM: 608666
HGNC: 22965
Ensembl: ENSG00000215193
UniProt: Q7Z412 A0A024R100
Position
22:18077990..18105396
AA seq 305 aa
MKSDSSTSAAPLRGLGGPLRSSEPVRAVPARAPAVDLLEEAADLLVVHLDFRAALETCER
AWQSLANHAVAEEPAGTSLEVKCSLCVVGIQALAEMDRWQEVLSWVLQYYQVPEKLPPKV
LELCILLYSKMQEPGAVLDVVGAWLQDPANQNLPEYGALAEFHVQRVLLPLGCLSEAEEL
VVGSAAFGEERRLDVLQAIHTARQQQKQEHSGSEEAQKPNLEGSVSHKFLSLPMLVRQLW
DSAVSHFFSLPFKKSLLAALILCLLVVRFDPASPSSLHFLYKLAQLFRWIRKAAFSRLYQ
LRIRD
NT seq 918 nt   +upstreamnt  +downstreamnt
atgaagagcgattcttcgacctctgcagcccccctcagggggctcgggggacccctgcgc
agcagcgagccggtgcgcgcggtcccggcccgggcgccggccgtggaccttctggaggag
gcggccgacctcctggtggtgcacctggacttccgggcggcgctggagacctgcgagcgg
gcctggcagagtctggccaaccacgccgtggcagaggaacccgcgggcacctcattggag
gtgaagtgctccctgtgtgttgtggggatccaggccctggcagaaatggatcggtggcaa
gaagtcctctcctgggtccttcagtattaccaggtccctgaaaagctaccccccaaagtc
ctggagctgtgcattcttttatacagcaaaatgcaagagcctggagctgtgctggatgtg
gtgggtgcctggctccaagacccagccaatcaaaaccttccagaatatggagccttggca
gaatttcacgtgcagcgggtgctgctgcctctgggctgcttatcggaggctgaggagcta
gtggtgggctctgcagcctttggtgaggagcggcgactggatgtacttcaggccattcac
acagcgaggcagcagcagaaacaggaacactcaggctctgaggaggcccagaagccaaac
ctggaaggctctgtctcccacaagttcctgtcactaccgatgttggttcgccagctttgg
gactctgcggtgagccacttcttttctctgcccttcaaaaagagtctcctggctgccttg
atcctctgtctcctggtggtgagatttgatccagcttccccttcctccctgcacttcctc
tacaagctggcccagctcttccgctggatccggaaggctgcattttctcgcctctaccag
ctccgcatccgtgactga

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