METTL24 (methyltransferase like 24)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 728464
Gene name Methyltransferase like 24
Gene symbol METTL24
Synonyms (NCBI Gene)
C6orf186
Chromosome 6
Chromosome location 6q21
miRNA miRNA information provided by mirtarbase database.
24
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (24)
miRTarBase ID miRNA Experiments Reference
MIRT723145 hsa-miR-1237-3p HITS-CLIP 19536157
MIRT723144 hsa-miR-1248 HITS-CLIP 19536157
MIRT723143 hsa-miR-4778-3p HITS-CLIP 19536157
MIRT723142 hsa-miR-5007-3p HITS-CLIP 19536157
MIRT723141 hsa-miR-6868-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (4)
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0008168 Function Methyltransferase activity IEA
GO:0016740 Function Transferase activity IEA
GO:0032259 Process Methylation IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5JXM2
Protein name Probable methyltransferase-like protein 24 (EC 2.1.1.-)
Protein function Probable methyltransferase.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13383 Methyltransf_22 118 → 342 Methyltransferase domain Family
Sequence
Sequence length 366
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (3)
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 Evidence Score
COLOR VISION DISORDER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORONARY THROMBOSIS — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (1)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Renal Cell Renal cell carcinoma Pubtator 36311770 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only