KEGG   Homo sapiens (human): 10771
Entry
10771             CDS       T01001                                 
Symbol
ZMYND11, BRAM1, BS69, MRD30
Name
(RefSeq) zinc finger MYND-type containing 11
  KO
K23218  zinc finger MYND domain-containing protein 11
Organism
hsa  Homo sapiens (human)
Disease
H00773  Autosomal dominant intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    10771 (ZMYND11)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   Other histone modification proteins
    10771 (ZMYND11)
SSDB
Motif
Pfam: PWWP Bromodomain SAMD1_WH zf-MYND PHD vRNAP_dom DUF1002
Other DBs
NCBI-GeneID: 10771
NCBI-ProteinID: NP_006615
OMIM: 608668
HGNC: 16966
Ensembl: ENSG00000015171
UniProt: Q15326 Q5UGI2 Q5BJG6
Structure
Position
10:130088..254637
AA seq 602 aa
MARLTKRRQADTKAIQHLWAAIEIIRNQKQIANIDRITKYMSRVHGMHPKETTRQLSLAV
KDGLIVETLTVGCKGSKAGIEQEGYWLPGDEIDWETENHDWYCFECHLPGEVLICDLCFR
VYHSKCLSDEFRLRDSSSPWQCPVCRSIKKKNTNKQEMGTYLRFIVSRMKERAIDLNKKG
KDNKHPMYRRLVHSAVDVPTIQEKVNEGKYRSYEEFKADAQLLLHNTVIFYGADSEQADI
ARMLYKDTCHELDELQLCKNCFYLSNARPDNWFCYPCIPNHELVWAKMKGFGFWPAKVMQ
KEDNQVDVRFFGHHHQRAWIPSENIQDITVNIHRLHVKRSMGWKKACDELELHQRFLREG
RFWKSKNEDRGEEEAESSISSTSNEQLKVTQEPRAKKGRRNQSVEPKKEEPEPETEAVSS
SQEIPTMPQPIEKVSVSTQTKKLSASSPRMLHRSTQTTNDGVCQSMCHDKYTKIFNDFKD
RMKSDHKRETERVVREALEKLRSEMEEEKRQAVNKAVANMQGEMDRKCKQVKEKCKEEFV
EEIKKLATQHKQLISQTKKKQWCYNCEEEAMYHCCWNTSYCSIKCQQEHWHAEHKRTCRR
KR
NT seq 1809 nt   +upstreamnt  +downstreamnt
atggcacgtttaacaaaaagacgacaggcggatacaaaagctatccagcatctttgggca
gccattgagattatacggaaccagaagcagattgccaacattgaccgtattacaaagtat
atgtctcgagtccacggtatgcaccctaaagagaccacccgtcagctgagcttagctgtg
aaagatggtcttattgtcgaaactctaacagtgggctgcaaaggttcaaaagctggtatt
gaacaagaaggatattggttgccaggagatgagattgactgggaaacagaaaatcatgac
tggtattgttttgaatgccatttgcctggagaggtgttgatatgtgacctgtgttttcgt
gtgtatcattccaagtgtttgtctgatgagttcaggcttagagacagcagtagtccctgg
cagtgcccagtttgcaggagcattaagaagaagaatacaaacaaacaggagatgggcaca
tacctcagattcattgtctcccgcatgaaggagagggctatagatcttaataaaaagggg
aaggacaataaacacccgatgtacaggaggctggtgcactcagctgtggacgttcccacc
attcaagagaaagtgaatgaagggaaataccgaagttatgaagagttcaaagctgatgcc
caattgcttctccacaataccgtgattttctatggagcagacagtgagcaagctgacatt
gcgaggatgctatataaagacacatgtcatgagctggatgaactgcagctttgcaagaat
tgcttttacttgtcaaatgctcgtcctgacaactggttctgttatccttgtatacctaat
catgagctggtttgggctaaaatgaaaggttttgggttttggccagccaaagtcatgcag
aaagaagacaatcaagtcgacgttcgcttctttggccaccaccaccagagggcctggatt
ccttctgaaaacattcaagatatcacagtcaacattcatcggctgcacgtgaagcgcagt
atgggttggaaaaaggcctgtgatgagctggagctgcatcagcgtttcctacgagaaggg
agattttggaaatctaagaatgaggaccgaggtgaggaagaggcagaatccagtatctcc
tccaccagtaatgagcagctaaaggtcactcaagaaccaagagcaaagaaaggacgacgt
aatcaaagtgtggagcccaaaaaggaagaaccagagcctgaaacagaagcagtaagttct
agccaggaaatacccacgatgcctcagcccatcgaaaaagtctccgtgtcaactcagaca
aagaagttaagtgcctcttcaccaagaatgctgcatcggagcacccagaccacaaacgac
ggcgtgtgtcagagcatgtgccatgacaaatacaccaagatcttcaatgacttcaaagac
cggatgaagtcggaccacaagcgggagacagagcgtgttgtccgagaagctctggagaag
ctgcgttctgaaatggaagaagaaaagagacaagctgtaaataaagctgtagccaacatg
cagggtgagatggacagaaaatgtaagcaagtaaaggaaaagtgtaaggaagaatttgta
gaagaaatcaagaagctggcaacacagcacaagcaactgatttctcagaccaagaagaag
cagtggtgctacaactgtgaggaggaggccatgtaccactgctgctggaacacatcctac
tgctccatcaagtgccagcaggagcactggcacgcggagcacaagcgcacctgccgccgg
aaaagatga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (29)   
   KEGG ORTHOLOGY (1)   
   RefGene (19)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (42)   
   UniProt (3)   
   SWISS-PROT (1)   
   RefSeq(pep) (38)   
DNA sequence (89)   
   RefSeq(nuc) (39)   
   GenBank (25)   
   EMBL (25)   
3D Structure (2)   
   PDB (2)   
Protein domain (7)   
   Pfam (7)   
All databases (175)   

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