1. Gene
  2. MSGN1 - mesogenin 1 Gene

MSGN1 - mesogenin 1 Gene

Homo sapiens

Also known as MSOG; pMsgn1

Gene ID: 343930 | Gene type: protein coding

About MSGN1

Cytogenetic location: 2p24.2 Genomic coordinates (GRCh38): 2:17,816,460-17,817,798 (from NCBI)

This gene has 1 transcript (splice variant), 176 orthologues and 2 paralogues.

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in mesoderm formation and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within segment specification and somitogenesis. Predicted to be part of chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

MSGN1 Products(1)

mRNA Protein Name
NM_001105569.3 NP_001099039.1 mesogenin-1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 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

MSGN1 Protein Structure

HLH

HLH: Helix-loop-helix DNA-binding domain (125 - 178)

  • 0
  • 100
  • 193 a.a.
Protein Preferred Names Protein Names

mesogenin-1

pMesogenin1

MSGN1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MSGN1 A6NI15 ZWINT Homo sapiens O95229 32296183
Intra
MSGN1 A6NI15 ZWINT Homo sapiens O95229 32296183
Intra
MSGN1 A6NI15 ZWINT Homo sapiens O95229 32296183
Intra
MSGN1 A6NI15 NECAB2 Homo sapiens Q7Z6G3-2 32296183
Intra
MSGN1 A6NI15 NECAB2 Homo sapiens Q7Z6G3-2 32296183
Intra
MSGN1 A6NI15 NECAB2 Homo sapiens Q7Z6G3-2 32296183
Intra
MSGN1 A6NI15 MAGEA6 Homo sapiens P43360 32296183
Intra
MSGN1 A6NI15 MAGEA6 Homo sapiens P43360 32296183
Intra
MSGN1 A6NI15 MAGEA6 Homo sapiens P43360 32296183
Intra
MSGN1 A6NI15 BRAT1 Homo sapiens Q6PJG6 32296183
Intra
MSGN1 A6NI15 BRAT1 Homo sapiens Q6PJG6 32296183
Intra
MSGN1 A6NI15 BRAT1 Homo sapiens Q6PJG6 32296183
Intra
MSGN1 A6NI15 TEPSIN Homo sapiens Q96N21 32296183
Intra
MSGN1 A6NI15 TEPSIN Homo sapiens Q96N21 32296183
Intra
MSGN1 A6NI15 TEPSIN Homo sapiens Q96N21 32296183
Intra
MSGN1 A6NI15 CTAG1A Homo sapiens P78358 32296183
Intra
MSGN1 A6NI15 CTAG1A Homo sapiens P78358 32296183
Intra
MSGN1 A6NI15 CTAG1A Homo sapiens P78358 32296183
Intra
MSGN1 A6NI15 TCF12 Homo sapiens Q99081-3 32296183
Intra
MSGN1 A6NI15 TCF12 Homo sapiens Q99081-3 32296183
Intra
MSGN1 A6NI15 TCF12 Homo sapiens Q99081-3 32296183
Intra
MSGN1 A6NI15 AP1B1 Homo sapiens Q10567-3 32296183
Intra
MSGN1 A6NI15 AP1B1 Homo sapiens Q10567-3 32296183
Intra
MSGN1 A6NI15 AP1B1 Homo sapiens Q10567-3 32296183
Intra
MSGN1 A6NI15 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
MSGN1 A6NI15 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
MSGN1 A6NI15 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
MSGN1 A6NI15 TEX12 Homo sapiens Q9BXU0 32296183
Intra
MSGN1 A6NI15 TEX12 Homo sapiens Q9BXU0 32296183
Intra
MSGN1 A6NI15 TEX12 Homo sapiens Q9BXU0 32296183
Intra
MSGN1 A6NI15 ID1 Homo sapiens P41134 32296183
Intra
MSGN1 A6NI15 ID1 Homo sapiens P41134 32296183
Intra
MSGN1 A6NI15 ID1 Homo sapiens P41134 32296183
Intra
MSGN1 A6NI15 MYL9 Homo sapiens P24844-2 32296183
Intra
MSGN1 A6NI15 MYL9 Homo sapiens P24844-2 32296183
Intra
MSGN1 A6NI15 MYL9 Homo sapiens P24844-2 32296183
Intra
MSGN1 A6NI15 TCF4 Homo sapiens P15884-3 32296183
Intra
MSGN1 A6NI15 TCF4 Homo sapiens P15884-3 32296183
Intra
MSGN1 A6NI15 TCF4 Homo sapiens P15884-3 32296183
Intra
MSGN1 A6NI15 ID3 Homo sapiens Q02535 32296183
Intra
MSGN1 A6NI15 ID3 Homo sapiens Q02535 32296183
Intra
MSGN1 A6NI15 ID3 Homo sapiens Q02535 32296183
Intra
MSGN1 A6NI15 MYF5 Homo sapiens P13349 32296183
Intra
MSGN1 A6NI15 MYF5 Homo sapiens P13349 32296183
Intra
MSGN1 A6NI15 MYF5 Homo sapiens P13349 32296183
Intra
MSGN1 A6NI15 OST4 Homo sapiens P0C6T2 32296183
Intra
MSGN1 A6NI15 OST4 Homo sapiens P0C6T2 32296183
Intra
MSGN1 A6NI15 OST4 Homo sapiens P0C6T2 32296183
Intra
MSGN1 A6NI15 CCDC172 Homo sapiens P0C7W6 32296183
Intra
MSGN1 A6NI15 CCDC172 Homo sapiens P0C7W6 32296183
Intra
MSGN1 A6NI15 CCDC172 Homo sapiens P0C7W6 32296183
Intra
MSGN1 A6NI15 TRAF1 Homo sapiens Q13077 32296183
Intra
MSGN1 A6NI15 TRAF1 Homo sapiens Q13077 32296183
Intra
MSGN1 A6NI15 TRAF1 Homo sapiens Q13077 32296183
Intra
MSGN1 A6NI15 DNALI1 Homo sapiens O14645 32296183
Intra
MSGN1 A6NI15 DNALI1 Homo sapiens O14645 32296183
Intra
MSGN1 A6NI15 DNALI1 Homo sapiens O14645 32296183
Intra
MSGN1 A6NI15 EXOC7 Homo sapiens Q9UPT5-1 32296183
Intra
MSGN1 A6NI15 ITGB3BP Homo sapiens Q13352 32296183
Intra
MSGN1 A6NI15 ITGB3BP Homo sapiens Q13352 32296183
Intra
MSGN1 A6NI15 ITGB3BP Homo sapiens Q13352 32296183
Intra
MSGN1 A6NI15 HAP1 Homo sapiens P54257 32296183
Intra
MSGN1 A6NI15 HAP1 Homo sapiens P54257 32296183
Intra
MSGN1 A6NI15 HAP1 Homo sapiens P54257 32296183
Intra
MSGN1 A6NI15 ID2 Homo sapiens Q02363 32296183
Intra
MSGN1 A6NI15 ID2 Homo sapiens Q02363 32296183
Intra
MSGN1 A6NI15 ID2 Homo sapiens Q02363 32296183
Intra
MSGN1 A6NI15 LDOC1 Homo sapiens O95751 32296183
Intra
MSGN1 A6NI15 LDOC1 Homo sapiens O95751 32296183
Intra
MSGN1 A6NI15 LDOC1 Homo sapiens O95751 32296183
Intra
MSGN1 A6NI15 SERTAD3 Homo sapiens Q9UJW9 32296183
Intra
MSGN1 A6NI15 SERTAD3 Homo sapiens Q9UJW9 32296183
Intra
MSGN1 A6NI15 SERTAD3 Homo sapiens Q9UJW9 32296183
Intra
MSGN1 A6NI15 TTC23L Homo sapiens Q6PF05 32296183
Intra
MSGN1 A6NI15 TTC23L Homo sapiens Q6PF05 32296183
Intra
MSGN1 A6NI15 TTC23L Homo sapiens Q6PF05 32296183
Intra
MSGN1 A6NI15 IGFBP6 Homo sapiens P24592 32296183
Intra
MSGN1 A6NI15 IGFBP6 Homo sapiens P24592 32296183
Intra
MSGN1 A6NI15 IGFBP6 Homo sapiens P24592 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spondylocostal Dysostosis 4, Autosomal Recessive

SCDO4

Spondylocostal Dysostosis 4

Autosomal Recessive Spondylocostal Dysostosis 4

Doid:0112364

Dysostosis, Spondylocostal, Autosomal Recessive, Type 4

Spondylocostal Dysostosis 1, Autosomal Recessive

Jarcho-Levin Syndrome

SCDO1

Vertebral Anomalies

Spondylothoracic Dysplasia

Costovertebral Dysplasia

Spondylothoracic Dysostosis

Spondylocostal Dysostosis 1

Autosomal Recessive Spondylocostal Dysostosis 1

Spondylocostal Dysostosis, Autosomal Recessive, 1

Doid:0112365

Dysostosis, Spondylocostal, Autosomal Recessive, Type 1

Spondylocostal Dysostosis

Jarcho-Levin Syndrome

Costovertebral Dysplasia

Spondylothoracic Dysostosis

Spondylothoracic Dysplasia

Scdo

Dysostosis, Spondylocostal

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

Orthologs Information

Species Symbol Source ID
Macaca mulatta MSGN1 VGNC VGNC:74771
Bos taurus MSGN1 VGNC VGNC:31692
Mus musculus MSGN1 MGD MGI:1860483
Rattus norvegicus MSGN1 RGD RGD:1587516
Canis familiaris MSGN1 VGNC VGNC:43437