1. Gene
  2. ZMAT4 - zinc finger matrin-type 4 Gene

ZMAT4 - zinc finger matrin-type 4 Gene

Homo sapiens
Gene ID: 79698 | Gene type: protein coding

About ZMAT4

This gene has 9 transcripts (splice variants), 201 orthologues and 9 paralogues. Biased expression in thyroid (RPKM 4.9) and brain (RPKM 1.9).

Summary

Enables identical protein binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZMAT4 Products(2)

mRNA Protein Name
NM_001135731.2 NP_001129203.1 zinc finger matrin-type protein 4 isoform b
NM_024645.3 NP_078921.1 zinc finger matrin-type protein 4 isoform a
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ZMAT4 Protein Structure

zf-met

zf-met: Zinc-finger of C2H2 type (15 - 38)

zf-met

zf-met: Zinc-finger of C2H2 type (76 - 99)

zf-C2H2_jaz

zf-C2H2_jaz: Zinc-finger double-stranded RNA-binding (146 - 170)

zf-met

zf-met: Zinc-finger of C2H2 type (198 - 222)

  • 0
  • 100
  • 200
  • 229 a.a.
Protein Preferred Names Protein Names

zinc finger matrin-type protein 4

ZMAT4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
ZMAT4 Q9H898 CUL3 Homo sapiens Q13618 25416956
Intra
ZMAT4 Q9H898 CUL3 Homo sapiens Q13618 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spinocerebellar Ataxia, Autosomal Recessive 12

Autosomal Recessive Spinocerebellar Ataxia 12

SCAR12

Spinocerebellar Ataxia With Mental Retardation And Epilepsy

Autosomal Recessive Cerebellar Ataxia-Epilepsy-Intellectual Disability Syndrome Due To Wwox Deficiency

Autosomal Recessive Spinocerebellar Ataxia Type 12

Spinocerebellar Ataxia, Autosomal Recessive, 12

Ataxia, Spinocerebellar, Autosomal Recessive, Type 12

Myopia

Near-Sightedness

Short-Sightedness

Nearsightedness

Nearsighted

Near Vision

Close Sighted

Myopic

Short-Sighted

Near Sighted

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus ZMAT4 VGNC VGNC:37193
Macaca mulatta ZMAT4 VGNC VGNC:78424
Mus musculus ZMAT4 MGD MGI:2443497
Felis catus ZMAT4 VGNC VGNC:67254
Canis familiaris ZMAT4 VGNC VGNC:48641
Rattus norvegicus ZMAT4 RGD RGD:1584398