KEGG   Homo sapiens (human): 6664
Entry
6664              CDS       T01001                                 
Symbol
SOX11, CSS9, IDDMOH, MRD27
Name
(RefSeq) SRY-box transcription factor 11
  KO
K09268  transcription factor SOX11/12 (SOX group C)
Organism
hsa  Homo sapiens (human)
Disease
H00773  Autosomal dominant intellectual developmental disorder
H01403  Coffin-Siris syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    6664 (SOX11)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  beta-Scaffold factors with minor groove contacts
   HMG SOX
    6664 (SOX11)
SSDB
Motif
Pfam: HMG_box HMG_box_2 HMG_WDHD1
Other DBs
NCBI-GeneID: 6664
NCBI-ProteinID: NP_003099
OMIM: 600898
HGNC: 11191
Ensembl: ENSG00000176887
UniProt: P35716
Structure
Position
2:5692384..5701385
AA seq 441 aa
MVQQAESLEAESNLPREALDTEEGEFMACSPVALDESDPDWCKTASGHIKRPMNAFMVWS
KIERRKIMEQSPDMHNAEISKRLGKRWKMLKDSEKIPFIREAERLRLKHMADYPDYKYRP
RKKPKMDPSAKPSASQSPEKSAAGGGGGSAGGGAGGAKTSKGSSKKCGKLKAPAAAGAKA
GAGKAAQSGDYGGAGDDYVLGSLRVSGSGGGGAGKTVKCVFLDEDDDDDDDDDELQLQIK
QEPDEEDEEPPHQQLLQPPGQQPSQLLRRYNVAKVPASPTLSSSAESPEGASLYDEVRAG
ATSGAGGGSRLYYSFKNITKQHPPPLAQPALSPASSRSVSTSSSSSSGSSSGSSGEDADD
LMFDLSLNFSQSAHSASEQQLGGGAAAGNLSLSLVDKDLDSFSEGSLGSHFEFPDYCTPE
LSEMIAGDWLEANFSDLVFTY
NT seq 1326 nt   +upstreamnt  +downstreamnt
atggtgcagcaggcggagagcttggaagcggagagcaacctgccccgggaggcgctggac
acggaggagggcgaattcatggcttgcagcccggtggccctggacgagagcgacccagac
tggtgcaagacggcgtcgggccacatcaagcggccgatgaacgcgttcatggtatggtcc
aagatcgaacgcaggaagatcatggagcagtctccggacatgcacaacgccgagatctcc
aagaggctgggcaagcgctggaaaatgctgaaggacagcgagaagatcccgttcatccgg
gaggcggagcggctgcggctcaagcacatggccgactaccccgactacaagtaccggccc
cggaaaaagcccaaaatggacccctcggccaagcccagcgccagccagagcccagagaag
agcgcggccggcggcggcggcgggagcgcgggcggaggcgcgggcggtgccaagacctcc
aagggctccagcaagaaatgcggcaagctcaaggcccccgcggccgcgggcgccaaggcg
ggcgcgggcaaggcggcccagtccggggactacgggggcgcgggcgacgactacgtgctg
ggcagcctgcgcgtgagcggctcgggcggcggcggcgcgggcaagacggtcaagtgcgtg
tttctggatgaggacgacgacgacgacgacgacgacgacgagctgcagctgcagatcaaa
caggagccggacgaggaggacgaggaaccaccgcaccagcagctcctgcagccgccgggg
cagcagccgtcgcagctgctgagacgctacaacgtcgccaaagtgcccgccagccctacg
ctgagcagctcggcggagtcccccgagggagcgagcctctacgacgaggtgcgggccggc
gcgacctcgggcgccgggggcggcagccgcctctactacagcttcaagaacatcaccaag
cagcacccgccgccgctcgcgcagcccgcgctgtcgcccgcgtcctcgcgctcggtgtcc
acctcctcgtccagcagcagcggcagcagcagcggcagcagcggcgaggacgccgacgac
ctgatgttcgacctgagcttgaatttctctcaaagcgcgcacagcgccagcgagcagcag
ctggggggcggcgcggcggccgggaacctgtccctgtcgctggtggataaggatttggat
tcgttcagcgagggcagcctgggctcccacttcgagttccccgactactgcacgccggag
ctgagcgagatgatcgcgggggactggctggaggcgaacttctccgacctggtgttcaca
tattga

  All links  
Disease (2)   
   OMIM (2)   
Gene (11)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (7)   
   RefSeq(nuc) (1)   
   GenBank (3)   
   EMBL (3)   
3D Structure (4)   
   PDB (4)   
Protein domain (3)   
   Pfam (3)   
All databases (30)   

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