KEGG   Homo sapiens (human): 10785
Entry
10785             CDS       T01001                                 
Symbol
WDR4, GAMOS6, MIGSB, TRM82, TRMT82, Wuho, hWH
Name
(RefSeq) WD repeat domain 4
  KO
K15443  tRNA (guanine-N(7)-)-methyltransferase subunit TRM82
Organism
hsa  Homo sapiens (human)
Disease
H01722  Galloway-Mowat syndrome
H02132  Microcephaly syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03016 Transfer RNA biogenesis [BR:hsa03016]
    10785 (WDR4)
Transfer RNA biogenesis [BR:hsa03016]
 Eukaryotic type
  tRNA modification factors
   Methyltransferases
    10785 (WDR4)
SSDB
Motif
Pfam: WD40
Other DBs
NCBI-GeneID: 10785
NCBI-ProteinID: NP_061139
OMIM: 605924
HGNC: 12756
Ensembl: ENSG00000160193
UniProt: P57081
Structure
Position
21:complement(42843094..42892998)
AA seq 412 aa
MAGSVGLALCGQTLVVRGGSRFLATSIASSDDDSLFIYDCSAAEKKSQENKGEDAPLDQG
SGAILASTFSKSGSYFALTDDSKRLILFRTKPWQCLSVRTVARRCTALTFIASEEKVLVA
DKSGDVYSFSVLEPHGCGRLELGHLSMLLDVAVSPDDRFILTADRDEKIRVSWAAAPHSI
ESFCLGHTEFVSRISVVPTQPGLLLSSSGDGTLRLWEYRSGRQLHCCHLASLQELVDPQA
PQKFAASRIAFWCQENCVALLCDGTPVVYIFQLDARRQQLVYRQQLAFQHQVWDVAFEET
QGLWVLQDCQEAPLVLYRPVGDQWQSVPESTVLKKVSGVLRGNWAMLEGSAGADASFSSL
YKATFDNVTSYLKKKEERLQQQLEKKQRRRSPPPGPDGHAKKMRPGEATLSC
NT seq 1239 nt   +upstreamnt  +downstreamnt
atggcgggctctgtgggactggcgttgtgcgggcagacgttggtggtgcggggcggcagc
cgattcctggccacctccatagcaagcagtgatgatgacagcctcttcatctatgactgc
agtgctgcagaaaagaagtcacaagaaaataaaggggaggacgcgcccttggaccagggg
agcggtgcgattctggcgtccaccttctccaagtctggcagctattttgctttaaccgat
gacagtaagcgtctgattcttttccgtacaaaaccatggcaatgtctgagtgtcaggacc
gtggcaaggaggtgtacagccctgactttcatagcctcggaggagaaggtcttggtggcc
gacaagtctggagacgtctactccttttcggtgctggagccacacgggtgtggccgtcta
gagctggggcacctgtctatgctgttagatgtggctgtgagtcctgatgaccgcttcatc
ctcactgccgaccgggacgagaagatccgagtcagctgggccgcggcgccccatagcatc
gagtccttctgcttggggcacacagagtttgtgagccgtatctccgtggtgccaactcag
cccgggctgcttctgtcctcctctggggacggcaccctgaggctctgggagtacaggagc
ggccgccagctgcactgctgtcacctggccagtctgcaggagctggtggacccccaggcc
ccccagaagtttgccgcgtccaggattgcattctggtgccaggagaactgcgtggcgctc
ctgtgcgacggcactcctgtggtctacatcttccagctggacgcccgcagacagcagttg
gtgtacaggcagcagctggcgttccagcaccaagtgtgggacgtggctttcgaggagacc
caggggctgtgggtgctccaggactgccaggaagcccccctggtgctctacaggcctgtg
ggcgaccagtggcagtctgttcctgagagcaccgtgttaaagaaagtctctggtgttctt
cgtgggaactgggccatgctggaaggctctgccggcgcagacgccagcttcagcagtctc
tacaaggccacgttcgacaacgtgacctcctacctgaagaagaaagaggagagactgcag
cagcagctagagaagaagcagcggcgccggagtcccccgcctgggcccgacgggcatgcc
aagaagatgagaccgggggaggcgacgctaagttgctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (19)   
   KEGG ORTHOLOGY (1)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (18)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (16)   
DNA sequence (49)   
   RefSeq(nuc) (17)   
   GenBank (16)   
   EMBL (16)   
3D Structure (8)   
   PDB (8)   
Protein domain (1)   
   Pfam (1)   
All databases (103)   

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