KEGG   Homo sapiens (human): 5459
Entry
5459              CDS       T01001                                 
Symbol
POU4F3, BRN3C, DFNA15, DFNA42, DFNA52
Name
(RefSeq) POU class 4 homeobox 3
  KO
K09366  POU domain transcription factor, class 4
Organism
hsa  Homo sapiens (human)
Disease
H00604  Deafness, autosomal dominant
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    5459 (POU4F3)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain POU
    5459 (POU4F3)
SSDB
Motif
Pfam: Pou Homeodomain HTH_31 Homeobox_KN DUF4770
Other DBs
NCBI-GeneID: 5459
NCBI-ProteinID: NP_002691
OMIM: 602460
HGNC: 9220
Ensembl: ENSG00000091010
UniProt: Q15319
Position
5:146338839..146341728
AA seq 338 aa
MMAMNSKQPFGMHPVLQEPKFSSLHSGSEAMRRVCLPAPQLQGNIFGSFDESLLARAEAL
AAVDIVSHGKNHPFKPDATYHTMSSVPCTSTSSTVPISHPAALTSHPHHAVHQGLEGDLL
EHISPTLSVSGLGAPEHSVMPAQIHPHHLGAMGHLHQAMGMSHPHTVAPHSAMPACLSDV
ESDPRELEAFAERFKQRRIKLGVTQADVGAALANLKIPGVGSLSQSTICRFESLTLSHNN
MIALKPVLQAWLEEAEAAYREKNSKPELFNGSERKRKRTSIAAPEKRSLEAYFAIQPRPS
SEKIAAIAEKLDLKKNVVRVWFCNQRQKQKRMKYSAVH
NT seq 1017 nt   +upstreamnt  +downstreamnt
atgatggccatgaactccaagcagcctttcggcatgcacccggtgctgcaagaacccaaa
ttctccagtctgcactctggctccgaggccatgcgccgagtctgtctcccagccccgcag
ctgcagggtaatatatttggaagctttgatgagagcctgctggcacgcgccgaagctctg
gcggcggtggatatcgtctcccacggcaagaaccatccgttcaagcccgacgccacctac
cataccatgagcagcgtgccctgcacgtccacttcgtccaccgtgcccatctcccaccca
gctgcgctcacctcacaccctcaccacgccgtgcaccagggcctcgaaggcgacctgctg
gagcacatctcgcccacgctgagtgtgagcggcctgggcgctccggaacactcggtgatg
cccgcacagatccatccacaccacctgggcgccatgggccacctgcaccaggccatgggc
atgagtcacccgcacaccgtggcccctcatagcgccatgcctgcatgcctcagcgacgtg
gagtcagacccgcgcgagctggaagccttcgccgagcgcttcaagcagcggcgcatcaag
ctgggggtgacccaggcggacgtgggcgcggctctggctaatctcaagatccccggcgtg
ggctcgctgagccaaagcaccatctgcaggttcgagtctctcactctctcgcacaacaac
atgatcgctctcaagccggtgctccaggcctggttggaggaggccgaggccgcctaccga
gagaagaacagcaagccagagctcttcaacggcagcgaacggaagcgcaaacgcacgtcc
atcgcggcgccggagaagcgttcactcgaggcctatttcgctatccagccacgtccttca
tctgagaagatcgcggccatcgctgagaaactggaccttaaaaagaacgtggtgagagtc
tggttctgcaaccagagacagaaacagaaacgaatgaagtattcggctgtccactga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (6)   
   KEGG ORTHOLOGY (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (5)   
   RefSeq(nuc) (1)   
   GenBank (2)   
   EMBL (2)   
Protein domain (5)   
   Pfam (5)   
All databases (25)   

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