Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55892
Gene name Gene Name - the full gene name approved by the HGNC.
Myoneurin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MYNN
Synonyms (NCBI Gene) Gene synonyms aliases
OSZF, SBBIZ1, ZBTB31, ZNF902
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q26.2
Summary Summary of gene provided in NCBI Entrez Gene.
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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT442893 hsa-miR-1179 PAR-CLIP 22100165
MIRT442892 hsa-miR-1253 PAR-CLIP 22100165
MIRT442893 hsa-miR-1179 PAR-CLIP 22100165
MIRT442892 hsa-miR-1253 PAR-CLIP 22100165
MIRT1169045 hsa-miR-1254 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606042 14955 ENSG00000085274
Protein
UniProt ID Q9NPC7
Protein name Myoneurin (Zinc finger and BTB domain-containing protein 31)
PDB 2VPK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 14 118 BTB/POZ domain Domain
PF00096 zf-C2H2 303 324 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 330 352 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 387 409 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 415 437 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 443 465 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 471 493 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 499 524 Domain
Tissue specificity TISSUE SPECIFICITY: Mainly expressed in the neuromuscular system. Located in and around synaptic myonuclei in adult muscle. Expression is dysregulated after nerve injury. Also found in the testis, ovary and placenta. {ECO:0000269|PubMed:10873615, ECO:0000
Sequence
MQYSHHCEHLLERLNKQREAGFLCDCTIVIGEFQFKAHRNVLASFSEYFGAIYRSTSENN
VFLDQSQVKADGFQKLLEFIYTGTLNLDSWNVKEIHQAADYLKVEEVVTKCKIKMEDF
AF
IANPSSTEISSITGNIELNQQTCLLTLRDYNNREKSEVSTDLIQANPKQGALAKKSSQTK
KKKKAFNSPKTGQNKTVQYPSDILENASVELFLDANKLPTPVVEQVAQINDNSELELTSV
VENTFPAQDIVHTVTVKRKRGKSQPNCALKEHSMSNIASVKSPYEAENSGEELDQRYSKA
KPMCNTCGKVFSEASSLRRHMRIHKGVKPYVCHLCGKAFTQCNQLKTHVRTHTGEKPYKC
ELCDKGFAQKCQLVFHSRMHHGEEKPYKCDVCNLQFATSSNLKIHARKHSGEKPYVCDRC
GQRFAQASTLTYHVRRH
TGEKPYVCDTCGKAFAVSSSLITHSRKHTGEKPYICGICGKSF
ISSGELNKHFRSH
TGERPFICELCGNSYTDIKNLKKHKTKVHSGADKTLDSSAEDHTLSE
QDSIQKSPLSETMDVKPSDMTLPLALPLGTEDHHMLLPVTDTQSPTSDTLLRSTVNGYSE
PQLIFLQQLY
Sequence length 610
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Celiac disease Celiac disease N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Glioma Glioma N/A N/A GWAS
Lung adenocarcinoma Lung adenocarcinoma (conditioned on cigarettes per day), Lung adenocarcinoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Associate 21708826, 22999960, 24875374
Alzheimer Disease Associate 32309439
Atherosclerosis Associate 32486379
Carcinogenesis Associate 24163127
Carcinoma Pancreatic Ductal Associate 32312758
Cerebral Infarction Associate 28057933
Cerebral Small Vessel Diseases Associate 30769869
Colorectal Neoplasms Associate 20972440, 21708826, 22999960, 24875374, 24978480, 30518759
Coronary Disease Associate 24904205
Death Associate 33763035