2. Gene
  3. MAZ - MYC associated zinc finger protein Gene

MAZ - MYC associated zinc finger protein Gene

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

Also known as PUR1; ZF87; Pur-1; SAF-1; SAF-2; SAF-3; Zif87; ZNF801

Gene ID: 4150 | Gene type: protein coding

About MAZ

Cytogenetic location: 16p11.2 Genomic coordinates (GRCh38): 16:29,806,124-29,811,164 (from NCBI)

This gene has 15 transcripts (splice variants), 248 orthologues and 36 paralogues. Ubiquitous expression in bone marrow (RPKM 38.3), colon (RPKM 34.1) and 25 other tissues.

Summary

Enables DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in several processes, including regulation of gene expression; regulation of signal transduction; and transcription by RNA polymerase II. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]

MAZ Products(4)

mRNA Protein Name
NM_001042539.3 NP_001036004.1 myc-associated zinc finger protein isoform 2
NM_001276275.2 NP_001263204.1 myc-associated zinc finger protein isoform 3
NM_001276276.2 NP_001263205.1 myc-associated zinc finger protein isoform 4
NM_002383.4 NP_002374.2 myc-associated zinc finger protein isoform 1

MAZ Protein Structure

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (190 - 212)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (293 - 318)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (337 - 360)

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (366 - 385)

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  • 477 a.a.
Protein Preferred Names Protein Names

myc-associated zinc finger protein

MAZI

Related Diseases

Diseases Alias
Amyloidosis

Amyloid Disease

Amyloid

Amyloid Degeneration

Amyloidosis Nos

Amyloid Deposition

Amyloid Infiltration

Idiopathic Amyloidosis

Hyaloid Degeneration

Lardaceous Degeneration
Von Hippel-Lindau Syndrome

Von Hippel-Lindau Disease

Vhl

Vhl Syndrome

VHLS

Von Hippel-Lindau Syndrome, Modifier Of

Hippel Lindau Syndrome

Angiomatosis Retinae

Cerebelloretinal Angiomatosis, Familial

Hippel-Lindau Disease

Familial Cerebelloretinal Angiomatosis

Lindau Disease

VHLD
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 (2)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-116624 MAZ51 99.96% Unkown
HY-RS08178 MAZ Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris MAZ VGNC VGNC:54041
Rattus norvegicus MAZ RGD RGD:1594632
Felis catus MAZ VGNC VGNC:107761
Bos taurus MAZ VGNC VGNC:106813
Mus musculus MAZ MGD MGI:1338823