Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
50804
Gene name Gene Name - the full gene name approved by the HGNC.
Myelin expression factor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MYEF2
Synonyms (NCBI Gene) Gene synonyms aliases
HsT18564, MEF-2, MST156, MSTP156, myEF-2
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q21.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029056 hsa-miR-26b-5p Microarray 19088304
MIRT030757 hsa-miR-21-5p Microarray 18591254
MIRT049561 hsa-miR-92a-3p CLASH 23622248
MIRT047609 hsa-miR-10a-5p CLASH 23622248
MIRT045916 hsa-miR-125b-5p CLASH 23622248
Transcription factors
Transcription factor Regulation Reference
HDAC9 Repression 10487760
MYOG Activation 1656214
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003697 Function Single-stranded DNA binding IEA
GO:0003723 Function RNA binding HDA 22681889
GO:0003729 Function MRNA binding IBA 21873635
GO:0005634 Component Nucleus IBA 21873635
GO:0005634 Component Nucleus IDA 8455629
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619395 17940 ENSG00000104177
Protein
UniProt ID Q9P2K5
Protein name Myelin expression factor 2 (MEF-2) (MyEF-2) (MST156)
Protein function Transcriptional repressor of the myelin basic protein gene (MBP). Binds to the proximal MB1 element 5'-TTGTCC-3' of the MBP promoter. Its binding to MB1 and function are inhibited by PURA (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00076 RRM_1 102 172 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
PF00076 RRM_1 235 304 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
PF00076 RRM_1 525 593 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
Sequence
MADANKAEVPGATGGDSPHLQPAEPPGEPRREPHPAEAEKQQPQHSSSSNGVKMENDESA
KEEKSDLKEKSTGSKKANRFHPYSKDKNSGAGEKKGPNRNRVFISNIPYDMKWQAIKDLM
REKVGEVTYVELFKDAEGKSRGCGVVEFKDEEFVKKALETMNKYDLSGRPLN
IKEDPDGE
NARRALQRTGGSFPGGHVPDMGSGLMNLPPSILNNPNIPPEVISNLQAGRLGSTIFVANL
DFKVGWKKLKEVFSIAGTVKRADIKEDKDGKSRGMGTVTFEQAIEAVQAISMFNGQFLFD
RPMH
VKMDDKSVPHEEYRSHDGKTPQLPRGLGGIGMGLGPGGQPISASQLNIGGVMGNLG
PGGMGMDGPGFGGMNRIGGGIGFGGLEAMNSMGGFGGVGRMGELYRGAMTSSMERDFGRG
DIGINQGFGDSFGRLGSAMIGGFAGRIGSSNMGPVGSGISGGMGSMNSVTGGMGMGLDRM
SSSFDRMGPGIGAILERSIDMDRGFLSGPMGSGMRERIGSKGNQIFVRNLPFDLTWQKLK
EKFSQCGHVMFAEIKMENGKSKGCGTVRFDSPESAEKACRIMNGIKISGREID
VRLDRNA
Sequence length 600
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Oculocutaneous albinism Oculocutaneous albinism type 6, ALBINISM, OCULOCUTANEOUS, TYPE VI rs387906240, rs121918167, rs121918169, rs121918170, rs28940876, rs104894314, rs61754388, rs61753185, rs104894313, rs61754393, rs28940879, rs61753178, rs61753180, rs61754375, rs61754387
View all (55 more)
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 36658471
Disease Resistance Associate 37908128
Glioblastoma Associate 37556355
Leukemia Lymphoma Adult T Cell Associate 35449091
Neoplasms Associate 36658471, 37556355