KEGG   Homo sapiens (human): 23558
Entry
23558             CDS       T01001                                 
Symbol
WBP2, DFNB107, GRAMD6, WBP-2
Name
(RefSeq) WW domain binding protein 2
  KO
K22524  WW domain-binding protein 2
Organism
hsa  Homo sapiens (human)
Disease
H00605  Deafness, autosomal recessive
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]
    23558 (WBP2)
Domain-containing proteins not elsewhere classified [BR:hsa04990]
 Other domain-containing proteins
  WW domain-containing proteins
   23558 (WBP2)
SSDB
Motif
Pfam: GRAM Vps36_ESCRT-II
Other DBs
NCBI-GeneID: 23558
NCBI-ProteinID: NP_001335099
OMIM: 606962
HGNC: 12738
Ensembl: ENSG00000132471
UniProt: Q969T9
Position
17:complement(75845699..75856436)
AA seq 261 aa
MALNKNHSEGGGVIVNNTESILMSYDHVELTFNDMKNVPEAFKGTKKGTVYLTPYRVIFL
SKGKDAMQSFMMPFYLMKDCEIKQPVFGANYIKGTVKAEAGGGWEGSASYKLTFTAGGAI
EFGQRMLQVASQASRGEVPSGAYGYSYMPSGAYVYPPPVANGMYPCPPGYPYPPPPPEFY
PGPPMMDGAMGYVQPPPPPYPGPMEPPVSGPDVPSTPAAEAKAAEAAASAYYNPGNPHNV
YMPTSQPPPPPYYPPEDKKTQ
NT seq 786 nt   +upstreamnt  +downstreamnt
atggcgctcaacaagaatcactcggagggcggcggagtgatcgtcaataacaccgagagc
atcctaatgtcctatgatcacgtggaactcacattcaatgacatgaagaacgtgccagaa
gccttcaaagggaccaagaaaggcactgtctaccttaccccttaccgggtcatctttctg
tccaagggcaaggatgccatgcagtccttcatgatgccattttatctcatgaaagactgt
gagatcaagcagcccgtatttggtgcaaactacatcaagggaacagtgaaggcggaagcg
ggaggtggctgggaaggctctgcttcctacaagttgactttcacggcagggggcgccatt
gagttcggacagcggatgctccaggtggcatctcaagcctccagaggtgaagtccccagt
ggagcctatggctactcttacatgcccagcggggcctatgtctatcccccgccagtcgcc
aatggaatgtacccctgccctcctggctacccctatccaccgcccccacctgagttctat
ccaggaccccccatgatggacggggccatgggatacgtgcagcccccaccaccgccctac
cctgggcccatggaacctccggtcagcggccccgatgtcccctccactcctgcagccgaa
gccaaggccgcagaagcagccgccagcgcctattacaacccaggcaatcctcacaacgtc
tacatgcccacgagccagccgccgccacctccctactacccaccggaagataagaagacc
cagtag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (25)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (17)   
   OC (1)   
Protein sequence (7)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (33)   
   RefSeq(nuc) (5)   
   GenBank (14)   
   EMBL (14)   
Protein domain (2)   
   Pfam (2)   
All databases (73)   

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