AAMDC (adipogenesis associated Mth938 domain containing)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
28971
Gene name Gene Name - the full gene name approved by the HGNC.
Adipogenesis associated Mth938 domain containing
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AAMDC
Synonyms (NCBI Gene) Gene synonyms aliases
C11orf67, CK067, PTD015
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q14.1
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(2)
miRTarBase ID miRNA Experiments Reference
MIRT022818 hsa-miR-124-3p Microarray 18668037
MIRT029807 hsa-miR-26b-5p Microarray 19088304
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(9)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183, 32814053
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
GO:0005737 Component Cytoplasm ISS
GO:0006366 Process Transcription by RNA polymerase II IEA
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
620474 30205 ENSG00000087884
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q9H7C9
Protein name Mth938 domain-containing protein (Adipogenesis associated Mth938 domain-containing protein)
Protein function May play a role in preadipocyte differentiation and adipogenesis.
PDB 2AB1 , 2Q4Q
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04430 DUF498 6 → 119 Protein of unknown function (DUF498/DUF598) Domain
Sequence
Sequence length 122
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)
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
Glioblastoma Glioblastoma N/A N/A GWAS