Homo sapiens (human): 8799
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Entry
8799 CDS
T01001
Symbol
PEX11B, PEX11-BETA, PEX11beta, PEX14B
Name
(RefSeq) peroxisomal biogenesis factor 11 beta
KO
K13352
peroxin-11B
Organism
hsa
Homo sapiens (human)
Pathway
hsa04146
Peroxisome
Disease
H00177
Neonatal adrenoleukodystrophy
H00205
Peroxisome biogenesis disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04146 Peroxisome
8799 (PEX11B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
8799 (PEX11B)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
8799 (PEX11B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PEX11
TPR_2
Motif
Other DBs
NCBI-GeneID:
8799
NCBI-ProteinID:
NP_003837
OMIM:
603867
HGNC:
8853
Ensembl:
ENSG00000131779
UniProt:
O96011
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All DBs
Position
1:complement(145911348..145918717)
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AA seq
259 aa
AA seq
DB search
MDAWVRFSAQSQARERLCRAAQYACSLLGHALQRHGASPELQKQIRQLESHLSLGRKLLR
LGNSADALESAKRAVHLSDVVLRFCITVSHLNRALYFACDNVLWAGKSGLAPRVDQEKWA
QRSFRYYLFSLIMNLSRDAYEIRLLMEQESSACSRRLKGSGGGVPGGSETGGLGGPGTPG
GGLPQLALKLRLQVLLLARVLRGHPPLLLDVVRNACDLFIPLDKLGLWRCGPGIVGLCGL
VSSILSILTLIYPWLRLKP
NT seq
780 nt
NT seq
+upstream
nt +downstream
nt
atggacgcctgggtccgcttcagtgctcagagccaagcccgggagcggctgtgtagggcc
gcccagtatgcttgctctcttcttggccatgcgctgcagaggcatggagccagtcctgag
ttacagaaacagattcgacaactggagagccacctgagccttggaagaaagcttctacgc
ctgggtaactcagcagatgcccttgagtcagccaaaagagctgttcacctatcagatgtt
gtcctgagattctgcatcactgttagtcacctcaatcgagccttgtacttcgcctgtgac
aatgtcctgtgggctggaaagtctggactggctccccgtgtggatcaggagaagtgggcc
cagcgttcattcaggtactatttgttttccctcatcatgaatttgagccgtgatgcttat
gagattcgcctactgatggagcaagagtcttctgcttgtagccggcgactgaaaggttct
ggaggaggagtcccaggaggaagtgaaactgggggacttgggggaccagggactccagga
ggaggtctgccccaactggctctgaaacttcggctgcaagtcctgctcctggctcgagtc
cttagaggtcatcccccacttctgctagacgtggtcagaaatgcctgtgatctcttcatt
cctctggacaaactaggcctctggcgctgtggccctgggattgtggggctttgtggcctc
gtgtcctccatcctgtctattctcaccctaatctatccctggctacgactcaagccctga
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