KEGG   Homo sapiens (human): 5195Help
Entry
5195              CDS       T01001                                 

Gene name
PEX14, NAPP2, PBD13A, Pex14p, dJ734G22.2
Definition
(RefSeq) peroxisomal biogenesis factor 14
  KO
K13343  peroxin-14
Organism
hsa  Homo sapiens (human)
Pathway
hsa04146  Peroxisome
Disease
H00205  Peroxisome biogenesis disorder
H01342  Zellweger syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04146 Peroxisome
    5195 (PEX14)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    5195 (PEX14)
Membrane trafficking [BR:hsa04131]
 Autophagy
  Pexophagy
   Selective cargos
    5195 (PEX14)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: Pex14_N HemX DUF948 Spc7 Bacillus_HBL TolA_bind_tri DUF1664 Fib_alpha DUF3573
Motif
Other DBs
NCBI-GeneID: 5195
NCBI-ProteinID: NP_004556
OMIM: 601791
HGNC: 8856
Ensembl: ENSG00000142655
Vega: OTTHUMG00000001908
Pharos: O75381(Tbio)
UniProt: O75381
Structure
PDB: 

Position
1p36.22
AA seq 377 aa AA seqDB search
MASSEQAEQPSQPSSTPGSENVLPREPLIATAVKFLQNSRVRQSPLATRRAFLKKKGLTD
EEIDMAFQQSGTAADEPSSLGPATQVVPVQPPHLISQPYSPAGSRWRDYGALAIIMAGIA
FGFHQLYKKYLLPLILGGREDRKQLERMEAGLSELSGSVAQTVTQLQTTLASVQELLIQQ
QQKIQELAHELAAAKATTSTNWILESQNINELKSEINSLKGLLLNRRQFPPSPSAPKIPS
WQIPVKSPSPSSPAAVNHHSSSDISPVSNESTSSSPGKEGHSPEGSTVTYHLLGPQEEGE
GVVDVKGQVRMEVQGEEEKREDKEDEEDEEDDDVSHVDEEDCLGVQREDRRGGDGQINEQ
VEKLRRPEGASNESERD
NT seq 1134 nt NT seq  +upstreamnt  +downstreamnt
atggcgtcctcggagcaggcagagcagccgagccagccaagctctactccaggaagtgaa
aatgtgctgcctcgagagccgctgattgccacggcagtgaagtttctacagaattcccgg
gtccgccagagcccacttgcaaccaggagagcattcctaaagaagaaagggctgacagat
gaagagattgatatggccttccagcagtcgggcactgctgccgatgagccttcgtccttg
ggcccagccacacaggtggttcctgtccagccccctcacctcatatctcagccatacagt
cccgcaggctcccgatggcgagattacggcgccctggccatcatcatggcaggcattgca
tttggctttcaccagctctacaagaaatacctgctccccctcatcctgggcggccgagag
gacagaaagcagctggagaggatggaggccggtctctctgagctgagtggcagcgtggcc
cagacagtgactcagttacagacgaccctcgcctccgtccaggagctgctgattcagcag
cagcagaagatccaggagcttgcccacgagctggccgctgccaaggccaccacatccacc
aactggatcctggagtcccagaatatcaacgaactcaagtccgaaattaactccttgaaa
gggcttcttttaaatcggaggcagttccctccatccccatcagccccgaagatcccctcc
tggcagatcccagtcaagtcaccgtcaccctccagccctgcggccgtgaaccaccacagc
agcagcgacatctcacctgtcagcaacgagtccacgtcgtcctcgcctgggaaggagggc
cacagccccgagggctccacggtcacctaccacttgctgggcccccaggaggaaggcgag
ggggtggtggacgtcaagggccaggtgcggatggaggtgcaaggcgaggaggagaagagg
gaggacaaggaggacgaggaggatgaggaggatgatgatgtgagccatgtggacgaggag
gactgcctgggggtgcagagggaggaccgccggggcggggatgggcagatcaacgagcag
gtggagaagctgcggcggcccgagggcgccagcaacgagagtgagcgggactag

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (4)   
   KEGG DISEASE (2)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   UniGene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
   PHAROS (1)   
   VEGA (1)   
Protein sequence (9)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (37)   
   RefSeq(nuc) (7)   
   GenBank (15)   
   EMBL (15)   
Protein domain (9)   
   Pfam (9)   
All databases (80)   

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