ZNF280D - zinc finger protein 280D Gene

Also Known as SUHW4; ZNF634

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 54816

About ZNF280D

This gene has 13 transcripts (splice variants), 130 orthologues and 28 paralogues. Ubiquitous expression in ovary (RPKM 5.7), endometrium (RPKM 5.4) and 25 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. Predicted to be involved in regulation of transcription, DNA-templated. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZNF280D Products (5)

mRNA Protein Name
NM_001002843.3 NP_001002843.1 zinc finger protein 280D isoform 2
NM_001002844.3 NP_001002844.1 zinc finger protein 280D isoform 3
NM_001288588.2 NP_001275517.1 zinc finger protein 280D isoform 1
NM_001288589.2 NP_001275518.1 zinc finger protein 280D isoform 3
NM_017661.4 NP_060131.2 zinc finger protein 280D isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 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

ZNF280D Protein Structure

DUF4195

DUF4195: Domain of unknown function (DUF4195) (45 - 230)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 979 a.a.
Protein Preferred Names Protein Names

zinc finger protein 280D

  • suppressor of hairy wing homolog 4

Related Diseases

Diseases Alias
Borderline Glaucoma
  • Preglaucoma

Intellectual Developmental Disorder, X-Linked 109
  • Fraxe Syndrome

  • Fragile Xe Syndrome

  • Mental Retardation, X-Linked, Fraxe Type

  • XLID109

  • Mrx109

  • Mental Retardation, X-Linked, Associated With Fragile Site Fraxe

  • Fraxe Mental Retardation Syndrome

  • X-Linked Intellectual Developmental Disorder 109

  • Fraxe Intellectual Disability

  • Fraxe

  • Mental Retardation, X-Linked 109

  • Fragile Site On Chromosome Xq28

  • Fragile Site, Folic Acid Type

  • X-Linked Intellectual Disability Associated With Fragile Site Fraxe

  • Fraxe Intellectual Deficit

  • Intellectual Disability Associated With Fragile Site Fraxe

Dyslexia
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
Mus musculus ZNF280D MGD MGI:2384583
Macaca mulatta ZNF280D VGNC VGNC:99350
Felis catus ZNF280D VGNC VGNC:80787
Canis familiaris ZNF280D VGNC VGNC:49825
Bos taurus ZNF280D VGNC VGNC:52851
Rattus norvegicus ZNF280D RGD RGD:1560796
Others ZNF280D NCBI