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  3. SLC31A2 - solute carrier family 31 member 2 Gene

SLC31A2 - solute carrier family 31 member 2 Gene

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

中文名称：溶质载体家族 31 成员 2

种属: Homo sapiens

同用名: CTR2; COPT2; hCTR2

基因 ID: 1318 | 基因类型: protein coding

关于 SLC31A2

Cytogenetic location: 9q32 Genomic coordinates (GRCh38): 9:113,151,007-113,164,140 (from NCBI)

This gene has 3 transcripts (splice variants), 223 orthologues and 1 paralogue. Broad expression in salivary gland (RPKM 28.8), spleen (RPKM 6.8) and 18 other tissues.

功能概要

预测可启用铜离子跨膜转运体活性。预计参与细胞铜离子稳态。预计在铜离子跨膜转运的调节上游或调节范围内起作用。预测位于膜中。预计在质膜上有活性。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable copper ion transmembrane transporter activity. Predicted to be involved in cellular copper ion homeostasis. Predicted to act upstream of or within regulation of copper ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC31A2 基因产物(1)

mRNA Protein Name
NM_001860.3 NP_001851.1 probable low affinity copper uptake protein 2

SLC31A2 蛋白结构

Ctr

Ctr: Ctr copper transporter family (1 - 135)

  • 0
  • 100
  • 143 a.a.
蛋白主名 其他名称

probable low affinity copper uptake protein 2

copper transporter 2

SLC31A2 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
SLC31A2 O15432 BNIP3 Homo sapiens Q12983
Validated Y2H
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Menkes Disease

Copper Transport Disease

Menkes Syndrome

MNK

Kinky Hair Disease

Steely Hair Disease

Menkes Kinky-Hair Syndrome

Mk

Steely Hair Syndrome

Menkea Syndrome

Md

Menkes Kinky Hair Syndrome

Hypocupremia, Congenital

Kinky Hair Syndrome

X-Linked Copper Deficiency

Menkes Kinky Hair Disease
Deficiency Anemia

Anemia

Deficiency Anemias

Anaemia
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-RS13189 SLC31A2 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta SLC31A2 VGNC VGNC:77456
Canis familiaris SLC31A2 VGNC VGNC:46355
Mus musculus SLC31A2 MGD MGI:1333844
Bos taurus SLC31A2 VGNC VGNC:34814
Rattus norvegicus SLC31A2 RGD RGD:1307963
Felis catus SLC31A2 VGNC VGNC:102982
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