KEGG   Homo sapiens (human): 10472
Entry
10472             CDS       T01001                                 
Symbol
ZBTB18, C1DELq42q44, C1DELq43q44, C2H2-171, DEL1Q42Q44, DEL1Q43Q44, MRD22, RP58, TAZ-1, ZNF238
Name
(RefSeq) zinc finger and BTB domain containing 18
  KO
K23196  zinc finger and BTB domain-containing protein 18/42
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
   03000 Transcription factors [BR:hsa03000]
    10472 (ZBTB18)
   03036 Chromosome and associated proteins [BR:hsa03036]
    10472 (ZBTB18)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Zinc finger
   Cys2His2 BTB-ZF factors
    10472 (ZBTB18)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Chromatin remodeling factors
   Other chromatin remodeling factors
    10472 (ZBTB18)
SSDB
Motif
Pfam: BTB zf-C2H2 zf-C2H2_4 zf-H2C2_2 zf-C2H2_jaz zf-C2H2_6 zf-C2H2_11 zf-met CpXC zf_C2H2_10 zf-LYAR
Other DBs
NCBI-GeneID: 10472
NCBI-ProteinID: NP_001265125
OMIM: 608433
HGNC: 13030
Ensembl: ENSG00000179456
UniProt: Q99592
Position
1:244048491..244057476
AA seq 522 aa
MEFPDHSRHLLQCLSEQRHQGFLCDCTVLVGDAQFRAHRAVLASCSMYFHLFYKDQLDKR
DIVHLNSDIVTAPAFALLLEFMYEGKLQFKDLPIEDVLAAASYLHMYDIVKVCKKKLKEK
ATTEADSTKKEEDASSCSDKVESLSDGSSHIAGDLPSDEDEGEDEKLNILPSKRDLAAEP
GNMWMRLPSDSAGIPQAGGEAEPHATAAGKTVASPCSSTESLSQRSVTSVRDSADVDCVL
DLSVKSSLSGVENLNSSYFSSQDVLRSNLVQVKVEKEASCDESDVGTNDYDMEHSTVKES
VSTNNRVQYEPAHLAPLREDSVLRELDREDKASDDEMMTPESERVQVEGGMESSLLPYVS
NILSPAGQIFMCPLCNKVFPSPHILQIHLSTHFREQDGIRSKPAADVNVPTCSLCGKTFS
CMYTLKRHERTHSGEKPYTCTQCGKSFQYSHNLSRHAVVHTREKPHACKWCERRFTQSGD
LYRHIRKFHCELVNSLSVKSEALSLPTVRDWTLEDSSQELWK
NT seq 1569 nt   +upstreamnt  +downstreamnt
atggagtttccagaccatagtagacatttgctacagtgtctgagcgagcagagacaccag
ggttttctttgtgactgcactgttctggtgggagatgcccagttccgagcgcaccgagct
gtactggcttcatgcagcatgtatttccacctcttttacaaggaccagctggacaaaaga
gacattgttcatctgaacagcgacattgttacagcccccgctttcgctctcctgcttgaa
ttcatgtatgaagggaaactccagttcaaagacttgcccattgaagacgtgctagcagct
gccagttatctccacatgtatgacattgtcaaagtctgcaaaaagaagctgaaagagaaa
gccaccacggaggcagacagcaccaaaaaggaagaagatgcttcaagttgttcggacaaa
gtcgagagtctctccgatggcagcagccacatagcaggcgatttgcccagtgatgaagat
gaaggagaagatgaaaaattgaacatcctgcccagcaaaagggacttggcggccgagcct
gggaacatgtggatgcgattgccctcagactcagcaggcatcccccaggctggcggagag
gcagagccacacgccacagcagctggaaaaacagtagccagcccctgcagctcaacagag
tctttgtcccagaggtctgtcacctccgtgagggattcggcagatgttgactgtgtgctg
gacctgtctgtcaagtccagcctttcaggagttgaaaatctgaacagctcttatttctct
tcacaggacgtgctgagaagcaacctggtgcaggtgaaggtggagaaagaggcttcctgt
gatgagagtgatgttggcactaatgactatgacatggaacatagcactgtgaaagaaagt
gtgagcactaataacagggtacagtatgagccggcccatctggctcccctgagggaggac
tcggtcttgagggagctggaccgggaggacaaagccagtgatgatgagatgatgacccca
gagagcgagcgtgtccaggtggagggaggcatggagagcagtctgctcccctacgtctcc
aacatcctgagccccgcgggccagatcttcatgtgccccctgtgcaacaaggtcttcccc
agcccccacatcctgcagatccacctgagcacgcacttccgcgagcaggacggcatccgc
agcaagcccgccgccgatgtcaacgtgcccacgtgctcgctgtgtgggaagactttctct
tgcatgtacaccctcaagcgccacgagaggactcactcgggggagaagccctacacatgc
acccagtgcggcaagagcttccagtactcgcacaacctgagccgccatgccgtggtgcac
acccgcgagaagccgcacgcctgcaagtggtgcgagcgcaggttcacgcagtccggggac
ctgtacagacacattcgcaagttccactgtgagttggtgaactccttgtcggtcaaaagc
gaagcactgagcttgcctactgtcagagactggaccttagaagatagctctcaagaactt
tggaaataa

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Ontology (3)   
   KEGG BRITE (3)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (15)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (13)   
DNA sequence (35)   
   RefSeq(nuc) (13)   
   GenBank (11)   
   EMBL (11)   
Protein domain (11)   
   Pfam (11)   
All databases (82)   

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