MYNN - myoneurin Gene

Also Known as OSZF; SBBIZ1; ZBTB31; ZNF902

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 55892

About MYNN

Cytogenetic location: 3q26.2 Genomic coordinates (GRCh38): 3:169,773,396-169,789,716 (from NCBI)

This gene has 5 transcripts (splice variants), 149 orthologues and 51 paralogues. Ubiquitous expression in bone marrow (RPKM 4.7), testis (RPKM 4.6) and 25 other tissues.

Summary

This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14. [provided by RefSeq, Jun 2010]

MYNN Products (3)

mRNA Protein Name
NM_001185118.2 NP_001172047.1 myoneurin isoform A
NM_001185119.1 NP_001172048.1 myoneurin isoform B
NM_018657.5 NP_061127.1 myoneurin isoform A

Gene Ontology

  • Molecular Function
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

MYNN Protein Structure

BTB

BTB: BTB/POZ domain (14 - 115)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (316 - 340)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (345 - 368)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (373 - 398)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (401 - 425)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (430 - 453)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (458 - 480)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (486 - 509)

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  • 500
  • 610 a.a.
Protein Preferred Names Protein Names

myoneurin

  • zinc finger and BTB domain-containing protein 31

MYNN Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MYNN Q9NPC7 JPH3 Homo sapiens Q8WXH2
Validated Y2H
32814053
Intra
MYNN Q9NPC7 JPH3 Homo sapiens Q8WXH2
Y2H Array
32814053
Intra
MYNN Q9NPC7 JPH3 Homo sapiens Q8WXH2
Y2H Pooling
32814053
Intra
MYNN Q9NPC7 NEK7 Homo sapiens Q8TDX7
Y2H Array
32814053
Intra
MYNN Q9NPC7 NEK7 Homo sapiens Q8TDX7
Y2H Pooling
32814053
Intra
MYNN Q9NPC7 NEK7 Homo sapiens Q8TDX7
Validated Y2H
32814053
Intra
MYNN Q9NPC7 TGFBR2 Homo sapiens P37173
Validated Y2H
32814053
Intra
MYNN Q9NPC7 TGFBR2 Homo sapiens P37173
Y2H Array
32814053
Intra
MYNN Q9NPC7 TGFBR2 Homo sapiens P37173
Y2H Pooling
32814053
Intra
MYNN Q9NPC7 CDH1 Homo sapiens P12830
Y2H Pooling
32814053
Intra
MYNN Q9NPC7 CDH1 Homo sapiens P12830
Validated Y2H
32814053
Intra
MYNN Q9NPC7 CDH1 Homo sapiens P12830
Y2H Array
32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Cogan-Reese Syndrome
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

Pre-clinical Phase

Bioactive Molecules (2)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08929 MYNN Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS15971 ZBTB32 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus MYNN RGD RGD:1307889
Felis catus MYNN VGNC VGNC:63684
Canis familiaris MYNN VGNC VGNC:57342
Mus musculus MYNN MGD MGI:1931415
Macaca mulatta MYNN VGNC VGNC:74958
Bos taurus MYNN VGNC VGNC:53589
Others MYNN NCBI