KEGG   Homo sapiens (human): 5195
Entry
5195              CDS       T01001                                 
Symbol
PEX14, NAPP2, PBD13A, Pex14p, dJ734G22.2
Name
(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)
SSDB
Motif
Pfam: Pex14_N DUF948 INTS1_R4 Bacillus_HBL DUF1664
Other DBs
NCBI-GeneID: 5195
NCBI-ProteinID: NP_004556
OMIM: 601791
HGNC: 8856
Ensembl: ENSG00000142655
UniProt: O75381
Structure
Position
1:10474950..10630758
AA seq 377 aa
MASSEQAEQPSQPSSTPGSENVLPREPLIATAVKFLQNSRVRQSPLATRRAFLKKKGLTD
EEIDMAFQQSGTAADEPSSLGPATQVVPVQPPHLISQPYSPAGSRWRDYGALAIIMAGIA
FGFHQLYKKYLLPLILGGREDRKQLERMEAGLSELSGSVAQTVTQLQTTLASVQELLIQQ
QQKIQELAHELAAAKATTSTNWILESQNINELKSEINSLKGLLLNRRQFPPSPSAPKIPS
WQIPVKSPSPSSPAAVNHHSSSDISPVSNESTSSSPGKEGHSPEGSTVTYHLLGPQEEGE
GVVDVKGQVRMEVQGEEEKREDKEDEEDEEDDDVSHVDEEDCLGVQREDRRGGDGQINEQ
VEKLRRPEGASNESERD
NT seq 1134 nt   +upstreamnt  +downstreamnt
atggcgtcctcggagcaggcagagcagccgagccagccaagctctactccaggaagtgaa
aatgtgctgcctcgagagccgctgattgccacggcagtgaagtttctacagaattcccgg
gtccgccagagcccacttgcaaccaggagagcattcctaaagaagaaagggctgacagat
gaagagattgatatggccttccagcagtcgggcactgctgccgatgagccttcgtccttg
ggcccagccacacaggtggttcctgtccagccccctcacctcatatctcagccatacagt
cccgcaggctcccgatggcgagattacggcgccctggccatcatcatggcaggcattgca
tttggctttcaccagctctacaagaaatacctgctccccctcatcctgggcggccgagag
gacagaaagcagctggagaggatggaggccggtctctctgagctgagtggcagcgtggcc
cagacagtgactcagttacagacgaccctcgcctccgtccaggagctgctgattcagcag
cagcagaagatccaggagcttgcccacgagctggccgctgccaaggccaccacatccacc
aactggatcctggagtcccagaatatcaacgaactcaagtccgaaattaactccttgaaa
gggcttcttttaaatcggaggcagttccctccatccccatcagccccgaagatcccctcc
tggcagatcccagtcaagtcaccgtcaccctccagccctgcggccgtgaaccaccacagc
agcagcgacatctcacctgtcagcaacgagtccacgtcgtcctcgcctgggaaggagggc
cacagccccgagggctccacggtcacctaccacttgctgggcccccaggaggaaggcgag
ggggtggtggacgtcaagggccaggtgcggatggaggtgcaaggcgaggaggagaagagg
gaggacaaggaggacgaggaggatgaggaggatgatgatgtgagccatgtggacgaggag
gactgcctgggggtgcagagggaggaccgccggggcggggatgggcagatcaacgagcag
gtggagaagctgcggcggcccgagggcgccagcaacgagagtgagcgggactag

  All links  
Disease (2)   
   OMIM (2)   
Gene (13)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (21)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (19)   
DNA sequence (49)   
   RefSeq(nuc) (19)   
   GenBank (15)   
   EMBL (15)   
3D Structure (4)   
   PDB (4)   
Protein domain (5)   
   Pfam (5)   
All databases (94)   

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