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  2. MTX3 - metaxin 3 Gene

MTX3 - metaxin 3 Gene

中文名称:metaxin 3

种属: Homo sapiens

基因 ID: 345778 | 基因类型: protein coding

关于 MTX3

Cytogenetic location: 5q14.1 Genomic coordinates (GRCh38): 5:79,976,716-79,991,262 (from NCBI)

This gene has 4 transcripts (splice variants), 201 orthologues and 3 paralogues. Ubiquitous expression in brain (RPKM 5.4), thyroid (RPKM 5.2) and 25 other tissues.

功能概要

预测参与线粒体组织。 MIB 复合体和 SAM 复合体的一部分。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to be involved in mitochondrion organization. Part of MIB complex and SAM complex. [provided by Alliance of Genome Resources, Apr 2022]

MTX3 基因产物(3)

mRNA Protein Name
NM_001010891.5 NP_001010891.4 metaxin-3 isoform 2
NM_001167741.2 NP_001161213.1 metaxin-3 isoform 1
NM_001363818.2 NP_001350747.1 metaxin-3 isoform 3

MTX3 蛋白结构

Tom37

Tom37: Outer mitochondrial membrane transport complex protein (8 - 74)

Tom37_C

Tom37_C: Tom37 C-terminal domain (94 - 153)

GST_C_3

GST_C_3: Glutathione S-transferase, C-terminal domain (163 - 236)

  • 0
  • 100
  • 200
  • 312 a.a.
蛋白主名 其他名称

metaxin-3

MTX3 抗体

目录号 产品名 应用 反应物种
HY-P83516 MTX3 Antibody (YA3261) WB Mouse, Rat

关联疾病

疾病名称 别名
Loeys-Dietz Syndrome 1

Furlong Syndrome

Loeys-Dietz Aortic Aneurysm Syndrome

LDS1

Aat5

Loeys-Dietz Syndrome Type 1

Aortic Aneurysm, Familial Thoracic 5

Familial Throacic Aortic Aneurysm 5

Loeys-Dietz Syndrome

Aortic Aneurysm Syndrome, Loeys-Dietz Type

Familial Thoracic Aortic Aneurysm 5

Ldas

Marfanoid Disorder-Craniosynostosis Syndrome

Aneurysm, Aortic, Thoracic, Familial, Type 5

Loeys-Dietz Syndrome, Type 1

Loeys-Dietz Syndrome, Type 2a

Transient Arthritis
Childhood Lymphoma

Pediatric Lymphoma

Robinow Syndrome, Autosomal Recessive 1

Robinow Syndrome, Autosomal Recessive

Autosomal Recessive Robinow Syndrome

Covesdem Syndrome

RRS1

Costovertebral Segmentation Defect-Mesomelia Syndrome

Rrs

Costovertebral Segmentation Defect With Mesomelia, Formerly

Covesdem Syndrome, Formerly

Costovertebral Segmentation Defect With Mesomelia

Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly

Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly

Robinow, Autosomal Recessive Syndrome, Type 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
Macaca mulatta MTX3 VGNC VGNC:84449
Canis familiaris MTX3 VGNC VGNC:53189
Mus musculus MTX3 MGD MGI:2686040
Rattus norvegicus MTX3 RGD RGD:1583002
Felis catus MTX3 VGNC VGNC:63663
Bos taurus MTX3 VGNC VGNC:55125