KEGG   Homo sapiens (human): 6663
Entry
6663              CDS       T01001                                 
Symbol
SOX10, DOM, PCWH, SOX-10, WS2E, WS4, WS4C
Name
(RefSeq) SRY-box transcription factor 10
  KO
K09270  transcription factor SOX7/8/10/18 (SOX group E/F)
Organism
hsa  Homo sapiens (human)
Disease
H00759  Waardenburg syndrome
H02356  PCWH syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    6663 (SOX10)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  beta-Scaffold factors with minor groove contacts
   HMG SOX
    6663 (SOX10)
SSDB
Motif
Pfam: Sox_N HMG_box HMG_box_2
Other DBs
NCBI-GeneID: 6663
NCBI-ProteinID: NP_008872
OMIM: 602229
HGNC: 11190
Ensembl: ENSG00000100146
UniProt: P56693
Position
22:complement(37972312..37984555)
AA seq 466 aa
MAEEQDLSEVELSPVGSEEPRCLSPGSAPSLGPDGGGGGSGLRASPGPGELGKVKKEQQD
GEADDDKFPVCIREAVSQVLSGYDWTLVPMPVRVNGASKSKPHVKRPMNAFMVWAQAARR
KLADQYPHLHNAELSKTLGKLWRLLNESDKRPFIEEAERLRMQHKKDHPDYKYQPRRRKN
GKAAQGEAECPGGEAEQGGTAAIQAHYKSAHLDHRHPGEGSPMSDGNPEHPSGQSHGPPT
PPTTPKTELQSGKADPKRDGRSMGEGGKPHIDFGNVDIGEISHEVMSNMETFDVAELDQY
LPPNGHPGHVSSYSAAGYGLGSALAVASGHSAWISKPPGVALPTVSPPGVDAKAQVKTET
AGPQGPPHYTDQPSTSQIAYTSLSLPHYGSAFPSISRPQFDYSDHQPSGPYYGHSGQASG
LYSAFSYMGPSQRPLYTAISDPSPSGPQSHSPTHWEQPVYTTLSRP
NT seq 1401 nt   +upstreamnt  +downstreamnt
atggcggaggagcaggacctatcggaggtggagctgagccccgtgggctcggaggagccc
cgctgcctgtccccggggagcgcgccctcgctagggcccgacggcggcggcggcggatcg
ggcctgcgagccagcccggggccaggcgagctgggcaaggtcaagaaggagcagcaggac
ggcgaggcggacgatgacaagttccccgtgtgcatccgcgaggccgtcagccaggtgctc
agcggctacgactggacgctggtgcccatgcccgtgcgcgtcaacggcgccagcaaaagc
aagccgcacgtcaagcggcccatgaacgccttcatggtgtgggctcaggcagcgcgcagg
aagctcgcggaccagtacccgcacctgcacaacgctgagctcagcaagacgctgggcaag
ctctggaggctgctgaacgaaagtgacaagcgccccttcatcgaggaggctgagcggctc
cgtatgcagcacaagaaagaccacccggactacaagtaccagcccaggcggcggaagaac
gggaaggccgcccagggcgaggcggagtgccccggtggggaggccgagcaaggtgggacc
gccgccatccaggcccactacaagagcgcccacttggaccaccggcacccaggagagggc
tcccccatgtcagatgggaaccccgagcacccctcaggccagagccatggcccacccacc
cctccaaccaccccgaagacagagctgcagtcgggcaaggcagacccgaagcgggacggg
cgctccatgggggagggcgggaagcctcacatcgacttcggcaacgtggacattggtgag
atcagccacgaggtaatgtccaacatggagacctttgatgtggctgagttggaccagtac
ctgccgcccaatgggcacccaggccatgtgagcagctactcagcagccggctatgggctg
ggcagtgccctggccgtggccagtggacactccgcctggatctccaagccaccaggcgtg
gctctgcccacggtctcaccacctggtgtggatgccaaagcccaggtgaagacagagacc
gcggggccccaggggcccccacactacaccgaccagccatccacctcacagatcgcctac
acctccctcagcctgccccactatggctcagccttcccctccatctcccgcccccagttt
gactactctgaccatcagccctcaggaccctattatggccactcgggccaggcctctggc
ctctactcggccttctcctatatggggccctcgcagcggcccctctacacggccatctct
gaccccagcccctcagggccccagtcccacagccccacacactgggagcagccagtatat
acgacactgtcccggccctaa

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Ontology (2)   
   KEGG BRITE (2)   
Disease (6)   
   KEGG DISEASE (2)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (19)   
   RefSeq(nuc) (1)   
   GenBank (9)   
   EMBL (9)   
Protein domain (3)   
   Pfam (3)   
All databases (51)   

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