2. Gene
  3. FEZF2 - FEZ family zinc finger 2 Gene

FEZF2 - FEZ family zinc finger 2 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as FEZ; TOF; FEZL; FKSG36; ZFP312; ZNF312

Gene ID: 55079 | Gene type: protein coding

About FEZF2

Cytogenetic location: 3p14.2 Genomic coordinates (GRCh38): 3:62,369,681-62,373,550 (from NCBI)

This gene has 3 transcripts (splice variants), 193 orthologues and 28 paralogues. Restricted expression toward brain (RPKM 4.1).

Summary

Predicted to enable transcription cis-regulatory region binding activity. Predicted to be involved in positive regulation of transcription, DNA-templated. Predicted to act upstream of or within several processes, including negative regulation of transcription by RNA polymerase II; nervous system development; and regulation of neuron differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

FEZF2 Products(1)

mRNA Protein Name
NM_018008.4 NP_060478.3 fez family zinc finger protein 2

FEZF2 Protein Structure

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (291 - 315)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (333 - 355)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (375 - 399)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (417 - 440)

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  • 400
  • 459 a.a.
Protein Preferred Names Protein Names

fez family zinc finger protein 2

forebrain embryonic zinc finger-like protein 2

Related Diseases

Diseases Alias
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MSMA

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Autosomal Dominant Hyaline Body Myopathy

Hyaline Body Myopathy Autosomal Dominant
Thymic Dysplasia
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Autoimmune Polyendocrine Syndrome Type 1

Whitaker Syndrome

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy

Autoimmune Polyglandular Syndrome I

Polyglandular Type I Autoimmune Syndrome
Autoimmune Polyendocrine Syndrome

Autoimmune Polyendocrinopathy

Autoimmune Polyglandular Failure

Autoimmune Polyglandular Syndrome

Polyendocrinopathies, Autoimmune

Lloyd'S Syndrome

Aps

Polyendocrinopathies Autoimmune

Polyendocrine Autoimmunity Syndrome

Lloyd Syndrome

Polyglandular Autoimmune Deficiency

Progressive Pluriglandular Insufficiency

Pluriglandular Autoimmune Atrophy

Pluriglandular Autoimmune Syndrome

Thyroid-Adrenocortical Insufficiency Syndrome
Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS04873 FEZF2 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus FEZF2 VGNC VGNC:28960
Mus musculus FEZF2 MGD MGI:1859823
Felis catus FEZF2 VGNC VGNC:62235
Canis familiaris FEZF2 VGNC VGNC:40829
Rattus norvegicus FEZF2 RGD RGD:1311068
Macaca mulatta FEZF2 VGNC VGNC:72485