MYNN - myoneurin Gene

Homo sapiens

Also known as OSZF; SBBIZ1; ZBTB31; ZNF902

Gene ID: 55892 | Gene type: protein coding

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	Reference	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

zf-H2C2_2

0
100
200
300
400
500
610 a.a.

Protein Preferred Names

Protein Names

myoneurin

zinc finger and BTB domain-containing protein 31

MYNN Protein-protein interaction Information

Type Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08929	MYNN Human Pre-designed siRNA Set A	Pre-designed Sets	/	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

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