Gene Gene information from NCBI Gene database.
Entrez ID 54531
Gene name MIER family member 2
Gene symbol MIER2
Synonyms (NCBI Gene)
KIAA1193Mi-er2
Chromosome 19
Chromosome location 19p13.3
miRNA miRNA information provided by mirtarbase database.
127
miRTarBase ID miRNA Experiments Reference
MIRT051939 hsa-let-7b-5p CLASH 23622248
MIRT044345 hsa-miR-106b-5p CLASH 23622248
MIRT038143 hsa-miR-423-5p CLASH 23622248
MIRT1148919 hsa-miR-1193 CLIP-seq
MIRT1148920 hsa-miR-1200 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IBA
GO:0003714 Function Transcription corepressor activity IBA
GO:0004407 Function Histone deacetylase activity IDA 28046085
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IDA 28046085
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620092 29210 ENSG00000105556
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N344
Protein name Mesoderm induction early response protein 2 (Mi-er2)
Protein function Transcriptional repressor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01448 ELM2 197 247 ELM2 domain Family
PF00249 Myb_DNA-binding 300 345 Myb-like DNA-binding domain Domain
Sequence
MAEASSLGRQSPRVVSCLEHSLCPGEPGLQTTAVVSMGSGDHQFNLAEILSQNYSVRGEC
EEASRCPDKPKEELEKDFISQSNDMPFDELLALYGYEASDPISDRESEGGDVAPNLPDMT
LDKEQIAKDLLSGEEEEETQSSADDLTPSVTSHEASDLFPNRSGSRFLADEDREPGSSAS
SDTEEDSLPANKCKKEIMVGPQFQADLSNLHLNRHCEKIYENEDQLLWDPSVLPEREVEE
FLYRAVK
RRWHEMAGPQLPEGEAVKDSEQALYELVKCNFNVEEALRRLRFNVKVIRDGLC
AWSEEECRNFEHGFRVHGKNFHLIQANKVRTRSVGECVEYYYLWK
KSERYDYFAQQTRLG
RRKYVPSGTTDADQDLDGSDPDGPGRPRPEQDTLTGMRTDPLSVDGTAGGLDEPGVASDG
LPSSEPGPCSFQQLDESPAVPLSHRPPALADPASYQPAVTAPEPDASPRLAVDFALPKEL
PLISSHVDLSGDPEETVAPAQVALSVTEFGLIGIGDVNPFLAAHPTCPAPGLHSEPLSHC
NVMTC
Sequence length 545
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Malignant tumor of esophagus Uncertain significance rs762665176 RCV005932669