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  2. MRS2 - magnesium transporter MRS2 Gene

MRS2 - magnesium transporter MRS2 Gene

中文名称:镁转运体 MRS2

种属: Homo sapiens

同用名: HPT; MRS2L

基因 ID: 57380 | 基因类型: protein coding

关于 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.

功能概要

启用镁离子跨膜转运蛋白活性。参与线粒体镁离子跨膜转运。位于线粒体中。 [由基因组资源联盟提供,2022 年 4 月]

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 基因产物(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
蛋白主名 其他名称

magnesium transporter MRS2 homolog, mitochondrial

MRS2, magnesium transporter

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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