MMD2 (-)

Download as csv Download as pdf
Log in to bookmark this gene

Bookmark This Gene

Gene Gene information from NCBI Gene database.
Download as csvDownload as pdf
Entrez ID 100505381
Gene name -
Gene symbol MMD2
Synonyms (NCBI Gene)
-
Chromosome 10
Chromosome location 10p
Summary This gene encodes a member of the PAQR (progestin and adipoQ receptor) family. Members of this family are evolutionarily conserved with significant sequence identity to bacterial hemolysin-like proteins and are defined by a set of seven transmembrane doma
miRNA miRNA information provided by mirtarbase database.
12 Show/Hide all (12)
Download as csvDownload as pdf
miRTarBase ID miRNA Experiments Reference
MIRT1152911 hsa-miR-2115 CLIP-seq
MIRT1152912 hsa-miR-3619-3p CLIP-seq
MIRT1152913 hsa-miR-4699-5p CLIP-seq
MIRT1152914 hsa-miR-4762-3p CLIP-seq
MIRT1152915 hsa-miR-4763-5p CLIP-seq
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Download as csvDownload as pdf
MIM HGNC e!Ensembl
613318 N/A N/A
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Download as csvDownload as pdf
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
ALZHEIMER DISEASE — GWAS catalog 39998322
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations

No strongly related genes found yet for MMD2.

No additional diseases found yet through genes similar to MMD2.