MAS1L - MAS1 proto-oncogene like, G protein-coupled receptor Gene

Also Known as MRG; MAS-L; dJ994E9.2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 116511

About MAS1L

Cytogenetic location: 6p22.1 Genomic coordinates (GRCh38): 6:29,486,697-29,487,956 (from NCBI)

This gene has 1 transcript (splice variant), 1 gene allele, 205 orthologues and 10 paralogues.

Summary

Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Located in cytosol; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

MAS1L Products (1)

mRNA Protein Name
NM_052967.2 NP_443199.1 mas-related G-protein coupled receptor MRG

MAS1L Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (93 - 314)

  • 0
  • 100
  • 200
  • 300
  • 378 a.a.
Protein Preferred Names Protein Names

mas-related G-protein coupled receptor MRG

  • MAS-R

MAS1L Antibodies

Cat. No. Product Name Application Reactivity
HY-P83453 MAS1L Antibody (YA3198) WB, IP Human, Mouse, Rat
HY-P83453A MAS1L Antibody (YA3198)(PBS only) WB, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Hypotrichosis 1

  • HYPT1

  • Hhs

  • Hts

  • Hypotrichosis Simplex

  • Hypotrichosis Simplex, Generalized, Hereditary

  • Hereditary Generalized Hypotrichosis Simplex

  • Generalized Hypothricosis Simplex

  • Hypotrichosis Simplex Hereditary

  • Hypotrichosis, Type 1
Vitreoretinal Degeneration, Snowflake Type

  • Snowflake Vitreoretinal Degeneration

  • SVD

  • Snowflake Degeneration In Hereditary Vitreoretinal Degeneration
Meningeal Melanocytoma

  • Leptomeningeal Melanocytoma

  • Melanocytoma Of Meninges
Tumoral Calcinosis, Hyperphosphatemic, Familial, 1

  • Hyperphosphatemic Familial Tumoral Calcinosis

  • Hftc

  • Hyperostosis-Hyperphosphatemia Syndrome

  • Familial Hyperphosphatemic Tumoral Calcinosis/Hyperphosphatemic Hyperostosis Syndrome

  • Tumoral Calcinosis, Hyperphosphatemic, Familial

  • Phptc

  • Lipocalcinogranulomatosis

  • Morbus Teutschlaender

  • Hhs

  • Hyperostosis With Hyperphosphatemia

  • Cortical Hyperostosis With Hyperphosphatemia

  • Primary Hyperphosphatemic Tumoral Calcinosis

  • Familial Tumoral Calcinosis

  • HFTC1

  • Hypercalcemic Tumoral Calcinosis

  • Hyperphosphatemia Hyperostosis

  • Hyperphosphatemia Hyperostosis Syndrome

  • Hyperphosphatemia Tumoral Calcinosis

  • Tumoral Calcinosis

  • Calcinosis, Tumoral, With Hyperphosphatemia

  • Tumoral Calcinosis, Primary Hyperphosphatemic

  • Teutschlaender Disease, Familial

  • Familial Teutschlaender Disease

  • Tumoral Calcinosis With Hyperphosphatemia

  • Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome

  • Ftc/Hhs

  • Familial Tumoral Calcinosis With Hyperphosphatemia

  • Teutschlaender Disease

  • Tumoral Calcinosis Primary Hyperphosphatemic

  • Calcinosis, Tumoral, Hyperphosphatemic, Familial
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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08158 MAS1L Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus MAS1L RGD RGD:738049