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ZNF236 (Zinc Finger Protein 236) is a Protein Coding gene. Diseases associated with ZNF236 include Type 1 Diabetes Mellitus 6 and Chromosome 18Q Deletion Syndrome. Gene Ontology (GO) annotations related to this gene include nucleic acid binding.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0000978 | RNA polymerase II proximal promoter sequence-specific DNA binding | IBA | 21873635 |
GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific | IBA | 21873635 |
GO:0003677 | DNA binding | IEA | -- |
GO:0005515 | protein binding | IPI | 32296183 |
GO:0046872 | metal ion binding | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IBA | 21873635 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006357 | regulation of transcription by RNA polymerase II | IBA | 21873635 |
GO:0071333 | cellular response to glucose stimulus | IEP | 9299475 |
This gene was present in the common ancestor of animals and fungi.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | ZNF236 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | ZNF236 30 |
|
||
-- 31 |
|
ManyToMany | |||
Rat (Rattus norvegicus) |
Mammalia | Zfp236 30 |
|
||
Mouse (Mus musculus) |
Mammalia | Zfp236 30 17 31 |
|
OneToOne | |
Oppossum (Monodelphis domestica) |
Mammalia | ZNF236 31 |
|
OneToOne | |
Platypus (Ornithorhynchus anatinus) |
Mammalia | ZNF236 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | ZNF236 30 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | ZNF236 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | ZNF236 31 |
|
OneToOne | |
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | znf236 30 |
|
||
Str.17000 30 |
|
||||
African clawed frog (Xenopus laevis) |
Amphibia | Xl.5283 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | znf236 31 |
|
OneToOne | |
Baker's yeast (Saccharomyces cerevisiae) |
Saccharomycetes | FZF1 31 |
|
OneToMany |
SNP ID | Clinical significance and condition | Chr 18 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs111932063 | Benign: not provided | 76,928,075(+) |
G/T NM_007345.3(ZNF236):c.4557G>T (p.Gly1519=) |
SYNONYMOUS | |
rs113817245 | Benign: not provided | 76,956,014(+) |
G/A NM_007345.3(ZNF236):c.4938G>A (p.Pro1646=) |
SYNONYMOUS | |
rs139451924 | Likely Benign: not provided | 76,880,165(+) |
C/T NM_007345.3(ZNF236):c.1031C>T (p.Ser344Leu) |
MISSENSE | |
rs147362673 | Likely Benign: not provided | 76,927,412(+) |
A/C NM_007345.3(ZNF236):c.4303A>C (p.Ile1435Leu) |
MISSENSE | |
rs151294291 | Likely Benign: not provided | 76,899,136(+) |
G/A NM_007345.3(ZNF236):c.1802G>A (p.Arg601His) |
MISSENSE |
Disorder | Aliases | PubMed IDs |
---|---|---|
type 1 diabetes mellitus 6 |
|
|
chromosome 18q deletion syndrome |
|
|
cleft palate, isolated |
|
|