2. Gene
  3. SFXN2 - sideroflexin 2 Gene

SFXN2 - sideroflexin 2 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：sideroflexin 2

种属: Homo sapiens

同用名: SLC56A2

基因 ID: 118980 | 基因类型: protein coding

关于 SFXN2

Cytogenetic location: 10q24.32 Genomic coordinates (GRCh38): 10:102,714,636-102,743,492 (from NCBI)

This gene has 13 transcripts (splice variants), 205 orthologues and 4 paralogues. Broad expression in kidney (RPKM 25.3), thyroid (RPKM 4.8) and 16 other tissues.

功能概要

预测可启用丝氨酸跨膜转运蛋白活性。参与线粒体跨膜转运。位于线粒体中。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable serine transmembrane transporter activity. Involved in mitochondrial transmembrane transport. Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

SFXN2 基因产物(2)

mRNA Protein Name
NM_001350989.2 NP_001337918.1 sideroflexin-2
NM_178858.6 NP_849189.1 sideroflexin-2

SFXN2 蛋白结构

Mtc

Mtc: Tricarboxylate carrier (15 - 322)

  • 0
  • 100
  • 200
  • 300
  • 322 a.a.
蛋白主名 其他名称

sideroflexin-2

关联疾病

疾病名称 别名
Combined Oxidative Phosphorylation Deficiency 18

Growth And Developmental Delay-Hypotonia-Vision Impairment-Lactic Acidosis Syndrome

COXPD18

Combined Oxidative Phosphorylation Deficiency, Type 18
Combined Oxidative Phosphorylation Deficiency 7

COXPD7

Combined Oxidative Phosphorylation Defect Type 7

Severe C12orf65-Related Combined Oxidative Phosphorylation Defect

Severe C12orf65-Related Coxpd

Combined Oxidative Phosphorylation Deficiency, Type 7
Sengers Syndrome

Mitochondrial Dna Depletion Syndrome 10

Cardiomyopathy And Cataract

Cataract And Cardiomyopathy

MTDPS10

Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome

Cardiomyopathic Mitochondrial Dna Depletion Syndrome 10

Senger Syndrome
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS12786 SFXN2 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus SFXN2 MGD MGI:2137678
Bos taurus SFXN2 VGNC VGNC:34531
Rattus norvegicus SFXN2 RGD RGD:1306131
Felis catus SFXN2 VGNC VGNC:65070
Canis familiaris SFXN2 VGNC VGNC:46088
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