Gene Gene information from NCBI Gene database.
Entrez ID 23184
Gene name Mesoderm development LRP chaperone
Gene symbol MESD
Synonyms (NCBI Gene)
BOCAMESDC2OI20
Chromosome 15
Chromosome location 15q25.1
SNPs SNP information provided by dbSNP.
3
SNP ID Visualize variation Clinical significance Consequence
rs745891632 TT>-,T,TTT Pathogenic Non coding transcript variant, frameshift variant, coding sequence variant, intron variant
rs780491808 GTTTT>- Pathogenic Intron variant, frameshift variant, coding sequence variant, non coding transcript variant
rs1021282486 G>A,C Pathogenic Stop gained, non coding transcript variant, coding sequence variant, intron variant, missense variant
miRNA miRNA information provided by mirtarbase database.
60
miRTarBase ID miRNA Experiments Reference
MIRT664770 hsa-miR-6890-3p HITS-CLIP 23824327
MIRT664769 hsa-miR-1247-3p HITS-CLIP 23824327
MIRT664768 hsa-miR-4532 HITS-CLIP 23824327
MIRT664767 hsa-miR-4485-5p HITS-CLIP 23824327
MIRT664766 hsa-miR-1281 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0001503 Process Ossification IMP 31564437
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005783 Component Endoplasmic reticulum IMP 31564437
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607783 13520 ENSG00000117899
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q14696
Protein name LRP chaperone MESD (LDLR chaperone MESD) (Mesoderm development LRP chaperone MESD) (Mesoderm development candidate 2) (Mesoderm development protein) (Renal carcinoma antigen NY-REN-61)
Protein function Chaperone specifically assisting the folding of beta-propeller/EGF modules within the family of low-density lipoprotein receptors (LDLRs) (PubMed:15014448). Acts as a modulator of the Wnt pathway through chaperoning the coreceptors of the canoni
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10185 Mesd 52 212 Chaperone for wingless signalling and trafficking of LDL receptor Family
Sequence
Sequence length 234
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Osteogenesis imperfecta, type 20 Pathogenic; Likely pathogenic rs759048290, rs745891632, rs1021282486, rs780491808 RCV003152498
RCV000853610
RCV000853611
RCV000853612
RCV000853613
★★★★☆
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 Evidence Score
BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cholangiocarcinoma Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DESBUQUOIS SYNDROME CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MESD-related disorder Likely benign; Benign; Uncertain significance 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
Bone Diseases Bone disease Pubtator 33596325 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Carcinoma Colorectal Cancer BEFREE 30876480
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 30876480 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 30876480
★☆☆☆☆
Found in Text Mining only
Osteogenesis Imperfecta Osteogenesis Imperfecta BEFREE 31564437
★☆☆☆☆
Found in Text Mining only
Osteogenesis Imperfecta Osteogenesis Imperfecta GENOMICS_ENGLAND_DG 31564437
★☆☆☆☆
Found in Text Mining only
Osteogenesis Imperfecta Osteogenesis imperfecta Pubtator 33596325, 36526215 Associate
★☆☆☆☆
Found in Text Mining only
Teratoma Teratoma BEFREE 15917269
★☆☆☆☆
Found in Text Mining only
Triple Negative Breast Neoplasms Triple Negative Breast Neoplasms BEFREE 28247948
★☆☆☆☆
Found in Text Mining only
Triple Negative Breast Neoplasms Triple negative breast cancer Pubtator 28247948 Associate
★☆☆☆☆
Found in Text Mining only