Free for academic non-profit institutions. Other users need a Commercial license
ZNF600 (Zinc Finger Protein 600) is a Protein Coding gene. Diseases associated with ZNF600 include Good Syndrome. Among its related pathways are Gene Expression and Herpes simplex virus 1 infection. Gene Ontology (GO) annotations related to this gene include nucleic acid binding and DNA-binding transcription factor activity. An important paralog of this gene is ZNF611.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0003676 | nucleic acid binding | IEA | -- |
GO:0003677 | DNA binding | IBA | -- |
GO:0003700 | DNA-binding transcription factor activity | IBA | -- |
GO:0046872 | metal ion binding | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IBA | -- |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | Gene Expression |
.48
|
|
2 | Herpes simplex virus 1 infection |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006355 | regulation of transcription, DNA-templated | IEA | -- |
ExUns: | 1a | · | 1b | · | 1c | ^ | 2a | · | 2b | ^ | 3a | · | 3b | ^ | 4 | ^ | 5 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | - | - | - | |||||||||||||
SP2: | - | ||||||||||||||||
SP3: | - | - | |||||||||||||||
SP4: |
This gene was present in the common ancestor of mammals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | ZNF600 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | -- 31 |
|
ManyToMany | |
Dog (Canis familiaris) |
Mammalia | -- 31 |
|
ManyToMany |
SNP ID | Clinical significance and condition | Chr 19 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
730384 | Benign: not provided | 52,767,564(-) | T/A | MISSENSE_VARIANT | |
731419 | Likely Benign: not provided | 52,765,820(-) | CTT/C | FRAMESHIFT_VARIANT | |
731531 | Likely Benign: not provided | 52,767,054(-) | T/C | SYNONYMOUS_VARIANT | |
734866 | Benign: not provided | 52,766,680(-) | T/C | MISSENSE_VARIANT | |
734867 | Benign: not provided | 52,767,004(-) | C/T | MISSENSE_VARIANT |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv3629n100 | CNV | loss | 25217958 |
dgv6527n54 | CNV | gain | 21841781 |
esv2664794 | CNV | deletion | 23128226 |
esv2671531 | CNV | deletion | 23128226 |
esv2718786 | CNV | deletion | 23290073 |
esv2718787 | CNV | deletion | 23290073 |
esv2718796 | CNV | deletion | 23290073 |
esv2718798 | CNV | deletion | 23290073 |
esv3644719 | CNV | gain | 21293372 |
esv3644720 | CNV | loss | 21293372 |
esv3644721 | CNV | loss | 21293372 |
esv3893231 | CNV | loss | 25118596 |
esv3893234 | CNV | gain | 25118596 |
nsv1055617 | CNV | loss | 25217958 |
nsv1057118 | CNV | gain | 25217958 |
nsv1062976 | CNV | gain | 25217958 |
nsv1066762 | CNV | gain | 25217958 |
nsv1067557 | CNV | gain | 25217958 |
nsv1078889 | OTHER | inversion | 25765185 |
nsv1140479 | CNV | deletion | 24896259 |
nsv1146332 | OTHER | inversion | 26484159 |
nsv458745 | CNV | gain | 19166990 |
nsv458746 | CNV | gain | 19166990 |
nsv509752 | CNV | insertion | 20534489 |
nsv527597 | CNV | loss | 19592680 |
nsv580030 | CNV | gain | 21841781 |
nsv580031 | CNV | gain | 21841781 |
nsv833875 | CNV | loss | 17160897 |
nsv961240 | CNV | duplication | 23825009 |
Disorder | Aliases | PubMed IDs |
---|---|---|
good syndrome |
|
|