Homo sapiens (human): 55670
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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)
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Pex26
Motif
Other DBs
NCBI-GeneID:
55670
NCBI-ProteinID:
NP_001121121
OMIM:
608666
HGNC:
22965
Ensembl:
ENSG00000215193
Pharos:
Q7Z412
(Tbio)
UniProt:
Q7Z412
A0A024R100
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All DBs
Position
22:18077990..18105396
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AA seq
305 aa
AA seq
DB search
MKSDSSTSAAPLRGLGGPLRSSEPVRAVPARAPAVDLLEEAADLLVVHLDFRAALETCER
AWQSLANHAVAEEPAGTSLEVKCSLCVVGIQALAEMDRWQEVLSWVLQYYQVPEKLPPKV
LELCILLYSKMQEPGAVLDVVGAWLQDPANQNLPEYGALAEFHVQRVLLPLGCLSEAEEL
VVGSAAFGEERRLDVLQAIHTARQQQKQEHSGSEEAQKPNLEGSVSHKFLSLPMLVRQLW
DSAVSHFFSLPFKKSLLAALILCLLVVRFDPASPSSLHFLYKLAQLFRWIRKAAFSRLYQ
LRIRD
NT seq
918 nt
NT seq
+upstream
nt +downstream
nt
atgaagagcgattcttcgacctctgcagcccccctcagggggctcgggggacccctgcgc
agcagcgagccggtgcgcgcggtcccggcccgggcgccggccgtggaccttctggaggag
gcggccgacctcctggtggtgcacctggacttccgggcggcgctggagacctgcgagcgg
gcctggcagagtctggccaaccacgccgtggcagaggaacccgcgggcacctcattggag
gtgaagtgctccctgtgtgttgtggggatccaggccctggcagaaatggatcggtggcaa
gaagtcctctcctgggtccttcagtattaccaggtccctgaaaagctaccccccaaagtc
ctggagctgtgcattcttttatacagcaaaatgcaagagcctggagctgtgctggatgtg
gtgggtgcctggctccaagacccagccaatcaaaaccttccagaatatggagccttggca
gaatttcacgtgcagcgggtgctgctgcctctgggctgcttatcggaggctgaggagcta
gtggtgggctctgcagcctttggtgaggagcggcgactggatgtacttcaggccattcac
acagcgaggcagcagcagaaacaggaacactcaggctctgaggaggcccagaagccaaac
ctggaaggctctgtctcccacaagttcctgtcactaccgatgttggttcgccagctttgg
gactctgcggtgagccacttcttttctctgcccttcaaaaagagtctcctggctgccttg
atcctctgtctcctggtggtgagatttgatccagcttccccttcctccctgcacttcctc
tacaagctggcccagctcttccgctggatccggaaggctgcattttctcgcctctaccag
ctccgcatccgtgactga
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