2. Gene
  3. MESD - mesoderm development LRP chaperone Gene

MESD - mesoderm development LRP chaperone Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as BOCA; OI20; MESDC2

Gene ID: 23184 | Gene type: protein coding

About MESD

Cytogenetic location: 15q25.1 Genomic coordinates (GRCh38): 15:80,946,289-80,989,819 (from NCBI)

This gene has 7 transcripts (splice variants), 207 orthologues and is associated with 3 phenotypes. Ubiquitous expression in thyroid (RPKM 16.9), placenta (RPKM 10.6) and 25 other tissues.

Summary

Predicted to enable low-density lipoprotein particle receptor binding activity. Involved in ossification and protein folding. Located in endoplasmic reticulum. Implicated in osteogenesis imperfecta type 20. [provided by Alliance of Genome Resources, Apr 2022]

MESD Products(1)

mRNA Protein Name
NM_015154.3 NP_055969.1 LRP chaperone MESD precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence Reference Source
involved in ossification IMP
IMP: Inferred from mutant phenotype
31564437 GOA
involved in protein folding IMP
IMP: Inferred from mutant phenotype
31564437 GOA
Cellular Component GO Annotation Evidence Reference Source
located in endoplasmic reticulum IMP
IMP: Inferred from mutant phenotype
31564437 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

MESD Protein Structure

Mesd

Mesd: Chaperone for wingless signalling and trafficking of LDL receptor (51 - 222)

  • 0
  • 100
  • 200
  • 234 a.a.
Protein Preferred Names Protein Names

LRP chaperone MESD

LDLR chaperone MESD

MESD Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MESD Q14696 CENPH Homo sapiens Q9H3R5
Validated Y2H
32296183
Intra
MESD Q14696 NRDE2 Homo sapiens Q9H7Z3
Validated Y2H
32296183
Intra
MESD Q14696 TEKTL1 Homo sapiens Q8IYK2
Validated Y2H
32296183
Intra
MESD Q14696 CENATAC Homo sapiens Q86UT8
Validated Y2H
32296183
Intra
MESD Q14696 CDR2L Homo sapiens Q86X02
Validated Y2H
32296183
Intra
MESD Q14696 LCE1A Homo sapiens Q5T7P2
Validated Y2H
32296183
Intra
MESD Q14696 TEX12 Homo sapiens Q9BXU0
Validated Y2H
32296183
Intra
MESD Q14696 ZNF493 Homo sapiens Q6ZR52-3
Validated Y2H
32296183
Intra
MESD Q14696 CNOT9 Homo sapiens Q92600-3
Validated Y2H
32296183
Intra
MESD Q14696 C17orf75 Homo sapiens Q9HAS0
Validated Y2H
32296183
Intra
MESD Q14696 MKNK2 Homo sapiens Q9HBH9-2
Validated Y2H
32296183
Intra
MESD Q14696 RCOR3 Homo sapiens Q9P2K3-2
Validated Y2H
32296183
Intra
MESD Q14696 LY96 Homo sapiens Q9Y6Y9
Validated Y2H
32296183
Intra
MESD Q14696 ACBD7 Homo sapiens Q8N6N7
Validated Y2H
32296183
Intra
MESD Q14696 AKNAD1 Homo sapiens Q5T1N1-2
Validated Y2H
32296183
Intra
MESD Q14696 MCM9 Homo sapiens Q9NXL9-3
Validated Y2H
32296183
Intra
MESD Q14696 ADAL Homo sapiens Q6DHV7-2
Validated Y2H
32296183
Intra
MESD Q14696 TREX2 Homo sapiens Q9BQ50
Validated Y2H
32296183
Intra
MESD Q14696 TRMT2A Homo sapiens Q8IZ69
Validated Y2H
32296183
Intra
MESD Q14696 ARB2A Homo sapiens Q8WUF8
Validated Y2H
32296183
Intra
MESD Q14696 CLP1 Homo sapiens Q92989
Validated Y2H
32296183
Intra
MESD Q14696 MAP1LC3B Homo sapiens Q9GZQ8
Validated Y2H
32296183
Intra
MESD Q14696 ABCG8 Homo sapiens Q9H221
Validated Y2H
32296183
Intra
MESD Q14696 CYP4F11 Homo sapiens Q9HBI6
Validated Y2H
32296183
Intra
MESD Q14696 GOLGA7 Homo sapiens Q7Z5G4
Validated Y2H
32296183
Intra
MESD Q14696 ASH2L Homo sapiens Q9UBL3
Validated Y2H
32296183
Intra
MESD Q14696 MRM1 Homo sapiens Q6IN84
Validated Y2H
32296183
Intra
MESD Q14696 CHCHD1 Homo sapiens Q96BP2
Validated Y2H
32296183
Intra
MESD Q14696 ZNF827 Homo sapiens Q17R98
Validated Y2H
32296183
Intra
MESD Q14696 COX14 Homo sapiens Q96I36
Validated Y2H
32296183
Intra
MESD Q14696 PMF1 Homo sapiens Q6P1K2
Validated Y2H
32296183
Intra
MESD Q14696 CUTC Homo sapiens Q9NTM9
Validated Y2H
32296183
Intra
MESD Q14696 GTPBP3 Homo sapiens Q969Y2
Validated Y2H
32296183
Intra
MESD Q14696 UBQLN1 Homo sapiens Q9UMX0
Validated Y2H
32296183
Intra
MESD Q14696 AKIRIN2 Homo sapiens Q53H80
Validated Y2H
32296183
Intra
MESD Q14696 BORCS8 Homo sapiens Q96FH0
Validated Y2H
32296183
Intra
MESD Q14696 ENKD1 Homo sapiens Q9H0I2
Validated Y2H
32296183
Intra
MESD Q14696 GPKOW Homo sapiens Q92917
Validated Y2H
32296183
Intra
MESD Q14696 FAM13C Homo sapiens Q8NE31
Validated Y2H
32296183
Intra
MESD Q14696 ATP6V1E2 Homo sapiens Q96A05
Validated Y2H
32296183
Intra
MESD Q14696 TTC23 Homo sapiens Q5W5X9-3
Validated Y2H
32296183
Intra
MESD Q14696 ABITRAM Homo sapiens Q9NX38
Validated Y2H
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant MESD Proteins

Cat. No. Product Name Accession Purity
HY-P76492 MESDC2 Protein, Human (HEK293, His) Q14696-1 (A34-K230) ≥95%

Related Diseases

Diseases Alias
Osteogenesis Imperfecta, Type Xx

OI20

Osteogenesis Imperfecta Type 20

Osteogenesis Imperfecta, Type 20

Osteogenesis Imperfecta Type Xx

Osteogenesis Imperfecta 20
Osteogenesis Imperfecta, Type Ii

Vrolik Type Of Osteogenesis Imperfecta

Osteogenesis Imperfecta Type 2

OI2

Oi, Type Ii

Osteogenesis Imperfecta Congenita

Oic

Osteogenesis Imperfecta Type Ii

Lethal Osteogenesis Imperfecta

Oi Type 2

Osteogenesis Imperfecta Congenita Perinatal Lethal Form

Osteogenesis Imperfecta Congenita, Perinatal Lethal Form

Perinatal Lethal Osteogenesis Imperfecta Congenita

Perinatally Lethal Oi

Osteogenesis Imperfecta 2

Oi-Ii

Oi-Iia

Oi Type Iia

Osteogenesis Imperfecta Type Iia

Osteogenesis Imperfecta Type Ii Autosomal Dominant

Oi Type Ii

Osteogenesis Imperfecta, Dominant Perinatal Lethal
Epilepsy, Nocturnal Frontal Lobe, 2

Epilepsy, Nocturnal Frontal Lobe, Type 2

Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2

ENFL2

Nocturnal Frontal Lobe Epilepsy 2
Dentinogenesis Imperfecta

Hereditary Opalescent Dentin

Dentinogenesis Imperfecta Without Osteogenesis Imperfecta

Dgi

Capdepont Teeth

Dgi Without Oi

Di

Non-Syndromic Dgi

Non-Syndromic Dentinogenesis Imperfecta

Opalescent Teeth Without Oi

Opalescent Teeth Without Osteogenesis Imperfecta

Opalescent Dentin
Osteoporosis-Pseudoglioma Syndrome

OPPG

Ops

Osteoporosis With Pseudoglioma

Osteogenesis Imperfecta, Ocular Form

Ocular Form Of Osteogenesis Imperfecta

Osteogenesis Imperfecta Ocular Form

Osteoporosis Pseudoglioma Syndrome

Pseudoglioma With Bone Fragility
Brittle Cornea Syndrome 1

Brittle Cornea Syndrome

Fragilitas Oculi With Joint Hyperextensibility

Dysgenesis Mesodermalis Corneae Et Sclerae

BCS1

Corneal Fragility, Keratoglobus, Blue Sclerae, Joint Hyperextensibility

Ehlers-Danlos Syndrome, Type Vib, Formerly

Eds6b, Formerly

Type Vib Ehlers-Danlos Syndrome

Eds Vib

Ehlers-Danlos Syndrome Type 6b

Corneal Fragility Keratoglobus Blue Sclerae Joint Hyperextensibility

Eds6b Formerly

Ehlers-Danlos Syndrome Type Vib Formerly

Ehlers-Danlos Syndrome Type 6

Cornea, Brittle, Syndrome

Cornea, Brittle, Syndrome, Type 1

Ehlers-Danlos Syndrome 6b
Brittle Bone Disorder

Osteogenesis Imperfecta

Brittle Bone Disease

Fragilitas Ossium

Osteopsathyrosis

Lobstein Disease

Oi

Vrolik Disease

Lobstein'S Disease

Lobstein'S Syndrome

Vrolik'S Disease

Porak And Durante Disease

Glass Bone Disease

Osteogenesis Imperfecta, Dominant Perinatal Lethal

Osteogenesis Imperfecta, Recessive Perinatal Lethal

Brittle Bone Syndrome

Oi - [Osteogenesis Imperfecta]

Ossium Fragility

Osteitis Fragilitans

Bony Fragility

Blue Sclera With Fragility Of Bone And Deafness

White Blue Sclera - Fragility Of Bone - Deafness
Respiratory Failure

Acute Respiratory Failure

Chronic Respiratory Failure

Respiratory Insufficiency

Acute-On-Chronic Respiratory Failure

Respiratory Disease

Acute And Chronic Respiratory Failure

Respiratory Insufficiency/Failure

Chronic Respiratory Disease

Pulmonary Valve Insufficiency

Chronic Disease Of Respiratory System

Respiration Disorders

Respiratory Tract Diseases

Lung Failure Nos

Pulmonary Failure

Arf - [Acute Respiratory Failure]

Acute Respiratory Insufficiency

Acute Pulmonary Insufficiency

Acute Respiration Failure

Chronic Respiration Failure
Tooth Agenesis

Oligodontia

Hypodontia

Selective Tooth Agenesis

Tooth Agenesis, Selective

Familial Tooth Agenesis

Anodontia

Congenital Absence Of One Tooth
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (2)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-D0858S MES-d13 98.78% Unkown
HY-RS08341 MESD Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus MESD VGNC VGNC:63452
Mus musculus MESD MGD MGI:1891421
Rattus norvegicus MESD RGD RGD:1310344
Macaca mulatta MESD VGNC VGNC:74507
Bos taurus MESD VGNC VGNC:31392
Others MESD NCBI