ZBTB16
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Homo sapiens |
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ZBTB16 is differentially expressed in 227 experiments: 117 organism parts: lung, skeletal muscle, ... (115 more);, 185 disease states: normal, lung adenocarcinoma, ... (183 more);, 77 cell types 145 cell lines 24 compound treatments and 65 other conditions. |
| Synonyms |
PLZF, ZNF145 |
| Orthologs |
ZBTB16
(Gallus gallus)
Q32PJ4_BOVIN
(Bos taurus)
Zbtb16
(Mus musculus)
Zbtb16
(Rattus norvegicus)
zbtb16
(Xenopus laevis)
XM_856200.1
(Canis familiaris)
ENSCAFG00000013538
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0009880, GO:0003677, GO:0009952, GO:0008285, GO:0008270, GO:0016607, GO:0016604, GO:0007417, GO:0042803, GO:0042802, GO:0005622, GO:0005515, GO:0006915, GO:0005634, GO:0048133, GO:0043065, GO:0046872, GO:0006355, GO:0045892, GO:0045893, GO:0030097, GO:0035110, GO:0017053, GO:0016605, GO:0051216, GO:0061036, GO:0045778, GO:0045600, GO:0045638, GO:0001823, GO:0001501, GO:0030099, GO:0030326, GO:0035116, GO:0035136, GO:0032332 |
| Gene Ontology Term |
transcriptional repressor complex, DNA binding, negative regulation of transcription, DNA-dependent, protein binding, nuclear speck, apoptosis, regulation of transcription, DNA-dependent, intracellular, negative regulation of cell proliferation, male germ-line stem cell division, metal ion binding, positive regulation of apoptosis, identical protein binding, hemopoiesis, leg morphogenesis, nucleus, nuclear body, protein homodimerization activity, positive regulation of transcription, DNA-dependent, central nervous system development, embryonic pattern specification, zinc ion binding, embryonic hindlimb morphogenesis, mesonephros development, positive regulation of chondrocyte differentiation, positive regulation of ossification, negative regulation of myeloid cell differentiation, forelimb morphogenesis, PML body, cartilage development, skeletal system development, positive regulation of cartilage development, embryonic limb morphogenesis, positive regulation of fat cell differentiation, myeloid cell differentiation, anterior/posterior pattern specification |
| InterPro Term |
Znf_C2H2-like, BTB_POZ, BTB/POZ-like, Znf_C2H2 |
| InterPro ID |
IPR000210, IPR007087, IPR013069, IPR015880 |
| Ensembl Family |
ENSFM00250000005403 |
| Gene-Disease Assocation |
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION |
| HGNC Symbol |
ZBTB16 |
| UniProt Accession |
Q05516, Q71UL6, Q71UL5, Q71UL7, F5H5Y7, F5H6C3 |
| Ensembl Protein ID |
ENSP00000376721, ENSP00000309507, ENSP00000338157, ENSP00000437716, ENSP00000443013, ENSP00000445047 |
| Ensembl Gene ID |
ENSG00000109906 |
| EMBL-Bank ID |
AF060568, S60093, BC026902, Z19002, BC029812, AF076615, AF076616, AF076613, AP000908, AP002755, AP002518 |
| RefSeq ID |
NP_005997, NM_001018011, NM_006006, NP_001018011 |
| Entrez Gene ID |
7704 |
| Description |
zinc finger and BTB domain containing 16 [Source:HGNC Symbol;Acc:12930] |
| UniGene ID |
Hs.591945 |
| Ensembl Family Description |
ZINC FINGER AND BTB DOMAIN CONTAINING 16 PROMYELOCYTIC LEUKEMIA ZINC FINGER ZINC FINGER PLZF |
| Ensembl Transcript ID |
ENST00000545851, ENST00000539918, ENST00000544220, ENST00000392996, ENST00000541602, ENST00000535379, ENST00000310883, ENST00000535700, ENST00000335953, ENST00000535509 |
| Design Element |
Z19002_at, g5174752_3p_at, ENST00000392996, ENST00000539918, ENST00000541602, ENST00000310883, ENST00000544220, ENST00000545851, ENST00000535509, ENST00000535700, 205883_at, ENST00000335953, ENST00000535379, 39681_at |
| Search EB-eye |
ENSG00000109906
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