KEGG   Homo sapiens (human): 100128927
Entry
100128927         CDS       T01001                                 
Symbol
ZBTB42, LCCS6, ZNF925
Name
(RefSeq) zinc finger and BTB domain containing 42
  KO
K23196  zinc finger and BTB domain-containing protein 18/42
Organism
hsa  Homo sapiens (human)
Disease
H00865  Lethal congenital contractural syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    100128927 (ZBTB42)
   03036 Chromosome and associated proteins [BR:hsa03036]
    100128927 (ZBTB42)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Zinc finger
   Cys2His2 BTB-ZF factors
    100128927 (ZBTB42)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Chromatin remodeling factors
   Other chromatin remodeling factors
    100128927 (ZBTB42)
SSDB
Motif
Pfam: BTB zf-C2H2_4 zf-C2H2 zf-H2C2_2 zf-C2H2_jaz zf-C2H2_6 zf-C2H2_11 zf-met zf-LYAR Zn-C2H2_12
Other DBs
NCBI-GeneID: 100128927
NCBI-ProteinID: NP_001131073
OMIM: 613915
HGNC: 32550
Ensembl: ENSG00000179627
UniProt: B2RXF5
Position
14:104800554..104804712
AA seq 422 aa
MEFPEHGGRLLGRLRQQRELGFLCDCTVLVGDARFPAHRAVLAACSVYFHLFYRDRPAGS
RDTVRLNGDIVTAPAFGRLLDFMYEGRLDLRSLPVEDVLAAASYLHMYDIVKVCKGRLQE
KDRSLDPGNPAPGAEPAQPPCPWPVWTADLCPAARKAKLPPFGVKAALPPRASGPPPCQV
PEESDQALDLSLKSGPRQERVHPPCVLQTPLCSQRQPGAQPLVKDERDSLSEQEESSSSR
SPHSPPKPPPVPAAKGLVVGLQPLPLSGEGSRELELGAGRLASEDELGPGGPLCICPLCS
KLFPSSHVLQLHLSAHFRERDSTRARLSPDGVAPTCPLCGKTFSCTYTLKRHERTHSGEK
PYTCVQCGKSFQYSHNLSRHTVVHTREKPHACRWCERRFTQSGDLYRHVRKFHCGLVKSL
LV
NT seq 1269 nt   +upstreamnt  +downstreamnt
atggagttccctgagcacggcggacggctgctgggccgcctgagacagcagcgcgagctg
ggcttcctatgcgactgcaccgtgctggtgggcgacgcgcgcttcccggcccaccgtgcc
gtgctggccgcgtgcagcgtctacttccatctcttctacagggaccggcccgcgggcagt
cgcgacacggtgcggctcaacggcgacatcgtcacggcgcccgccttcggccgcctactg
gacttcatgtacgagggccgcctggacctgcgcagcctgcctgtggaggacgtcctggca
gccgccagctacctgcacatgtatgacatcgtcaaggtctgcaagggcaggctccaggag
aaggatcgaagtctggacccggggaaccctgcccctggggcagaacctgctcagccaccg
tgcccctggcctgtctggaccgcggacctctgcccagctgcccgaaaggccaagctcccc
ccgtttggggtcaaggctgccctccctcctcgagcatctgggcctcctccctgccaggtc
ccagaagagtcagaccaggccctggacctgtcgttgaagtctggcccaaggcaggagcgg
gtccacccaccgtgcgtcctccagacacccctctgcagccagaggcagccaggggcccag
ccactggtgaaggacgaacgggactcactgtccgaacaggaggagagcagcagctctagg
agcccccacagtcccccgaagccacctcctgttcctgcagccaagggcctggtggtgggc
ttgcagccgctgcccctcagcggagagggcagccgggagctggagcttggtgcagggcga
ctggcgagtgaggacgagctggggcctggtgggcccctctgcatctgcccgttgtgcagc
aagctgtttcccagctcccacgtgctgcagctgcacctcagtgcccacttccgtgagcga
gacagcacccgggcccggctctcacccgacggcgtggcacccacctgcccgctctgtggg
aagaccttctcgtgcacatacacactgaagaggcacgagcggacacactcgggtgagaag
ccctatacgtgtgtgcagtgtggcaaaagttttcagtactcccacaacctgagccggcac
accgtagtgcacactcgagagaagccgcatgcctgccggtggtgtgagcgccgtttcacg
cagtccggggacctctaccgccacgtccgcaagtttcactgtggcctcgtcaagtccctt
ctggtgtga

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Ontology (3)   
   KEGG BRITE (3)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (33)   
   KEGG ORTHOLOGY (1)   
   RefGene (27)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (12)   
   RefSeq(nuc) (2)   
   GenBank (5)   
   EMBL (5)   
Protein domain (10)   
   Pfam (10)   
All databases (66)   

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