MRS2 - magnesium transporter MRS2 Gene

Also Known as HPT; MRS2L

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57380

About MRS2

Cytogenetic location: 6p22.3 Genomic coordinates (GRCh38): 6:24,402,936-24,426,190 (from NCBI)

This gene has 6 transcripts (splice variants) and 200 orthologues. Ubiquitous expression in heart (RPKM 8.7), thyroid (RPKM 7.9) and 25 other tissues.

Summary

Enables magnesium ion transmembrane transporter activity. Involved in mitochondrial magnesium ion transmembrane transport. Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

MRS2 Products (4)

mRNA Protein Name
NM_001286264.2 NP_001273193.1 magnesium transporter MRS2 homolog, mitochondrial isoform a
NM_001286265.2 NP_001273194.1 magnesium transporter MRS2 homolog, mitochondrial isoform c
NM_001286266.2 NP_001273195.1 magnesium transporter MRS2 homolog, mitochondrial isoform d
NM_020662.4 NP_065713.1 magnesium transporter MRS2 homolog, mitochondrial isoform b precursor
Protein Preferred Names Protein Names

magnesium transporter MRS2 homolog, mitochondrial

  • MRS2, magnesium transporter

Related Diseases

Diseases Alias
Middle Cerebral Artery Infarction
  • Infarction, Middle Cerebral Artery

  • Infarction Middle Cerebral Artery

Basilar Artery Occlusion
Phlebotomus Fever
  • Pappataci Fever

  • Sandfly Fever

  • Sandfly-Borne Phleboviral Disease

  • Sandfly-Borne Arboviral Fever

  • Sandfly-Borne Bunyavirus Fever

  • Three Day Fever

  • Chitral Fever

  • Italy Summer Grippe

  • Italy Summer Grippe Influenza

Robinow Syndrome, Autosomal Dominant 2
  • Autosomal Dominant Robinow Syndrome 2

  • DRS2

  • Robinow, Autosomal Dominant Syndrome, Type 2

Vertebral Artery Occlusion
  • Occlusion And Stenosis Of Vertebral Artery

Ivic Syndrome
  • Oculootoradial Syndrome

  • Radial Ray Defects, Hearing Impairment, External Ophthalmoplegia, And Thrombocytopenia

  • IVIC

  • Instituto Venezolano De Investigaciones Cientificas Syndrome

  • Oculo-Oto-Radial Syndrome

  • Oors

Subdural Empyema
  • Empyema, Subdural

  • Subdural Abscess

Robinow Syndrome, Autosomal Dominant 1
  • Autosomal Dominant Robinow Syndrome 1

  • DRS1

  • Robinow Dwarfism

  • Fetal Face Syndrome

  • Acral Dysostosis With Facial And Genital Abnormalities

  • Robinow, Autosomal Dominant Syndrome, Type 1

Cerebral Arterial Disease
  • Cerebral Arterial Diseases

Intracranial Berry Aneurysm
  • Familial Aneurysmal Subarachnoid Hemorrhage

  • Familial Berry Aneurysm

  • Familial Intracranial Saccular Aneurysm

  • Saccular Cerebral Aneurysm

  • Aneurysm, Intracranial Berry

  • Aneurysmal Subarachnoid Hemorrhage

  • Aneurysm, Intracranial Berry, 1

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
Felis catus MRS2 VGNC VGNC:63627
Rattus norvegicus MRS2 RGD RGD:708529
Canis familiaris MRS2 VGNC VGNC:43429
Macaca mulatta MRS2 VGNC VGNC:74735
Bos taurus MRS2 VGNC VGNC:31679
Mus musculus MRS2 MGD MGI:2685748
Others MRS2 NCBI