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Gene Gene information from NCBI Gene database.
Entrez ID 56917
Gene name Meis homeobox 3
Gene symbol MEIS3
Synonyms (NCBI Gene)
MRG2
Chromosome 19
Chromosome location 19q13.32
Summary This gene encodes a homeobox protein and probable transcriptional regulator. The orthologous protein in mouse controls expression of 3-phosphoinositide dependent protein kinase 1, which promotes survival of pancreatic beta-cells. [provided by RefSeq, Sep
miRNA miRNA information provided by mirtarbase database.
15 Show/Hide all (15)
miRTarBase ID miRNA Experiments Reference
MIRT016926 hsa-miR-335-5p Microarray 18185580
MIRT038310 hsa-miR-130b-5p CLASH 23622248
MIRT2040662 hsa-miR-127-3p CLIP-seq
MIRT2040663 hsa-miR-193a-5p CLIP-seq
MIRT2040664 hsa-miR-3144-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17 Show/Hide all (17)
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0001228 Function DNA-binding transcription activator activity, RNA polymerase II-specific IBA
GO:0001525 Process Angiogenesis IBA
GO:0001654 Process Eye development IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619443 29537 ENSG00000105419
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99687
Protein name Homeobox protein Meis3 (Meis1-related protein 2)
Protein function Transcriptional regulator which directly modulates PDPK1 expression, thus promoting survival of pancreatic beta-cells. Also regulates expression of NDFIP1, BNIP3, and CCNG1.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05920 Homeobox_KN 280 → 319 Homeobox KN domain Family
PF16493 Meis_PKNOX_N 96 → 180 N-terminal of Homeobox Meis and PKNOX1 Family
Sequence
MARRYDELPHYPGIVDGPAALASFPETVPAVPGPYGPHRPPQPLPPGLDSDGLKREKDEI
YGHPLFPLLALVFEKCELATCSPRDGAGAGLGTPPGGDVCSSDSFNEDIAAFAKQVRSER
PLFSSNPELDNLMIQAIQVLRFHLLELEKVHDLCDNFCHRYITCLKGKMPIDLVIEDRDG

GCREDFEDYPASCPSLPDQNNMWIRDHEDSGSVHLGTPGPSSGGLASQSGDNSSDQGDGL
DTSVASPSSGGEDEDLDQERRRNKKRGIFPKVATNIMRAWLFQHLSHPYPSEEQKKQLAQ
DTGLTILQVNNWFINARRR
IVQPMIDQSNRTGQGAAFSPEGQPIGGYTETQPHVAVRPPG
SVGMSLNLEGEWHYL
Sequence length 375
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
Abnormality of neuronal migration Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Glioblastoma Glioblastoma Pubtator 38563293 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 35180817 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Hodgkin Disease Hodgkin disease Pubtator 33539429 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only
Hypoxia Hypoxia Pubtator 38563293 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only