MSANTD1 (Myb/SANT DNA binding domain containing 1)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
345222
Gene name Gene Name - the full gene name approved by the HGNC.
Myb/SANT DNA binding domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MSANTD1
Synonyms (NCBI Gene) Gene synonyms aliases
C4orf44
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.3
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(13)
miRTarBase ID miRNA Experiments Reference
MIRT047517 hsa-miR-10a-5p CLASH 23622248
MIRT045317 hsa-miR-185-5p CLASH 23622248
MIRT680664 hsa-miR-6746-3p HITS-CLIP 23706177
MIRT682730 hsa-miR-1226-3p HITS-CLIP 23706177
MIRT606901 hsa-miR-4632-3p HITS-CLIP 23706177
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(2)
GO ID Ontology Definition Evidence Reference
GO:0016604 Component Nuclear body IBA
GO:0045893 Process Positive regulation of DNA-templated transcription IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q6ZTZ1
Protein name Myb/SANT-like DNA-binding domain-containing protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13837 Myb_DNA-bind_4 43 → 131 Domain
Sequence 
MVRGAGPGPSLSALSHPTGASGMAAAEGPGYLVSPQAEKHRRARNWTDAEMRGLMLVWEE
FFDELKQTKRNAKVYEKMASKLFEMTGERRLGEEIKIKITNMTFQYRKLKCMTDSESAPP
DWPYYLAIDGILAKVPESCDGKLPDSQPPGPSTSQTEASLSPPAKSTPLYFPYNQCSYEG
RFEDDRSDSSSSLLSLKFRSEERPVKKRKVQSCHLQKKQLRLLEAMVEEQRRLSRAVEET
CREVRRVLDQQHILQVQSLQLQERMMSLLERIITKSSV
Sequence length 278
Interactions View interactions
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
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
Myocardial Infarction Myocardial infarction N/A N/A GWAS