ZNF44 - zinc finger protein 44 Gene

Homo sapiens

Also known as ZNF; KOX7; ZNF55; ZNF58; GIOT-2; ZNF504

Gene ID: 51710 | Gene type: protein coding

About ZNF44

Cytogenetic location: 19p13.2 Genomic coordinates (GRCh38): 19:12,224,686-12,294,883 (from NCBI)

This gene has 9 transcripts (splice variants), 45 orthologues and 15 paralogues. Ubiquitous expression in thyroid (RPKM 2.6), kidney (RPKM 2.3) and 25 other tissues.

Summary

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZNF44 Products(7)

mRNA	Protein	Name
NM_001164276.2	NP_001157748.1	zinc finger protein 44 isoform 1
NM_001353549.2	NP_001340478.1	zinc finger protein 44 isoform 3
NM_001353550.2	NP_001340479.1	zinc finger protein 44 isoform 3
NM_001353551.1	NP_001340480.1	zinc finger protein 44 isoform 3
NM_001353552.2	NP_001340481.1	zinc finger protein 44 isoform 4
NM_001353553.2	NP_001340482.1	zinc finger protein 44 isoform 4
NM_016264.4	NP_057348.3	zinc finger protein 44 isoform 2

ZNF44 Protein Structure

KRAB

zf-C2H2

zf-H2C2_2

0
200
400
600
663 a.a.

Protein Preferred Names

Protein Names

zinc finger protein 44

gonadotropin inducible transcription repressor-2

Related Diseases

Diseases

Alias

Immunodeficiency 55

Combined Immunodeficiency Due To Gins1 Deficiency	IMD55
Cid Due To Gins1 Deficiency	Combined Immunodeficiency With Intrauterine Growth Retardation-Nk Cell Deficiency-Neutropenia
Combined Immunodeficiency With Intrauterine Growth Retardation-Natural Killer Cell Deficiency-Neutropenia

Myopathy, Tubular Aggregate, 1

Tubular Aggregate Myopathy	Tam
Myopathy With Tubular Aggregates	TAM1
Myopathy, Tubular Aggregate	Tubular Aggregate Myopathy 1

Autosomal Dominant Intellectual Developmental Disorder 40

Autosomal Dominant Non-Syndromic Intellectual Disability 40	Autosomal Dominant Mental Retardation 40
Mrd40	Mental Retardation, Autosomal Dominant 40

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-RS16141	ZNF44 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

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