ZFHX2 - zinc finger homeobox 2 Gene
Also Known as ZFH5; ZFH-5; MARSIS; ZNF409
Species: Homo sapiens
About ZFHX2
This gene has 4 transcripts (splice variants), 169 orthologues, 20 paralogues and is associated with 1 phenotype. Biased expression in testis (RPKM 3.0), brain (RPKM 0.7) and 5 other tissues.
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in regulation of sensory perception of pain. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]
ZFHX2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_033400.3 | NP_207646.2 | zinc finger homeobox protein 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32814053 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in regulation of sensory perception of pain |
IMP
IMP: Inferred from mutant phenotype
|
29253101 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in nucleus |
IDA
IDA: Inferred from direct assay
|
29253101 | GOA |
ZFHX2 Protein Structure
zf-C2H2_2: C2H2 type zinc-finger (2 copies) (566 - 595)
zf-C2H2_2: C2H2 type zinc-finger (2 copies) (1247 - 1280)
Homeobox: Homeobox domain (1598 - 1652)
Homeobox: Homeobox domain (1858 - 1914)
Homeobox: Homeobox domain (2066 - 2122)
- 0
- 400
- 800
- 1200
- 1600
- 2000
- 2400
- 2572 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
zinc finger homeobox protein 2 |
|
ZFHX2 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
ZFHX2 | Q9C0A1 | MAPT | Homo sapiens | P10636 | 32814053 | |
|
Intra
|
ZFHX2 | Q9C0A1 | MAPT | Homo sapiens | P10636 | 32814053 | |
|
Intra
|
ZFHX2 | Q9C0A1 | MAPT | Homo sapiens | P10636 | 32814053 | |
|
Intra
|
ZFHX2 | Q9C0A1 | PMP22 | Homo sapiens | A0A6Q8PF08 | 32814053 | |
|
Intra
|
ZFHX2 | Q9C0A1 | PMP22 | Homo sapiens | A0A6Q8PF08 | 32814053 | |
|
Intra
|
ZFHX2 | Q9C0A1 | PMP22 | Homo sapiens | A0A6Q8PF08 | 32814053 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Marsili Syndrome |
|
|
| Chromosome 8q21.11 Deletion Syndrome |
|
|
| Congenital Ptosis |
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | ZFHX2 | MGD | MGI:2686934 |
| Macaca mulatta | ZFHX2 | VGNC | VGNC:99346 |
| Bos taurus | ZFHX2 | VGNC | VGNC:37156 |
| Canis familiaris | ZFHX2 | VGNC | VGNC:48606 |
| Felis catus | ZFHX2 | VGNC | VGNC:80786 |
| Rattus norvegicus | ZFHX2 | RGD | RGD:735143 |
| Others | ZFHX2 | NCBI |