KEGG   Homo sapiens (human): 51398
Entry
51398             CDS       T01001                                 
Symbol
WDR83OS, ASTERIX, C19orf56, NEDFHCA, PAT-10, PAT10, PTD008
Name
(RefSeq) WD repeat domain 83 opposite strand
  KO
K24963  PAT complex subunit Asterix
Organism
hsa  Homo sapiens (human)
Disease
H02838  Neurodevelopmental disorder with variable familial hypercholanemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03110 Chaperones and folding catalysts [BR:hsa03110]
    51398 (WDR83OS)
   04131 Membrane trafficking [BR:hsa04131]
    51398 (WDR83OS)
Chaperones and folding catalysts [BR:hsa03110]
 Other chaperones and cochaperones
  Others
   51398 (WDR83OS)
Membrane trafficking [BR:hsa04131]
 Endoplasmic reticulum (ER) - Golgi transport
  Others
   Multi-pass translocon (MPT) complex
    51398 (WDR83OS)
SSDB
Motif
Pfam: ASTER Dcst2
Other DBs
NCBI-GeneID: 51398
NCBI-ProteinID: NP_057229
OMIM: 618474
HGNC: 30203
Ensembl: ENSG00000105583
UniProt: Q9Y284
LinkDB
Position
19:complement(12668073..12669415)
AA seq 106 aa
MSTNNMSDPRRPNKVLRYKPPPSECNPALDDPTPDYMNLLGMIFSMCGLMLKLKWCAWVA
VYCSFISFANSRSSEDTKQMMSSFMLSISAVVMSYLQNPQPMTPPW
NT seq 321 nt   +upstreamnt  +downstreamnt
atgtccactaacaatatgtcggacccacggaggccgaacaaagtgctgaggtacaagccc
ccgccgagcgaatgtaacccggccttggacgacccgacgccggactacatgaacctgctg
ggcatgatcttcagcatgtgcggcctcatgcttaagctgaagtggtgtgcttgggtcgct
gtctactgctccttcatcagctttgccaactctcggagctcggaggacacgaagcaaatg
atgagtagcttcatgctgtccatctctgccgtggtgatgtcctatctgcagaatcctcag
cccatgacgcccccatggtga

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