2. Gene
  3. SLC31A1 - solute carrier family 31 member 1 Gene

SLC31A1 - solute carrier family 31 member 1 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 1

种属: Homo sapiens

同用名: CTR1; COPT1

基因 ID: 1317 | 基因类型: protein coding

关于 SLC31A1

Cytogenetic location: 9q32 Genomic coordinates (GRCh38): 9:113,221,544-113,264,492 (from NCBI)

This gene has 2 transcripts (splice variants), 215 orthologues, 1 paralogue and is associated with 1 phenotype. Ubiquitous expression in liver (RPKM 33.0), duodenum (RPKM 22.8) and 25 other tissues.

功能概要

该基因编码的蛋白质是一种存在于细胞膜中的高亲和力铜转运蛋白。编码的蛋白质起到同源三聚体的作用，影响膳食铜的吸收。[RefSeq 提供，2011 年 8 月]

The protein encoded by this gene is a high-affinity copper transporter found in the cell membrane. The encoded protein functions as a homotrimer to effect the uptake of dietary copper. [provided by RefSeq, Aug 2011]

SLC31A1 基因产物(1)

mRNA Protein Name
NM_001859.4 NP_001850.1 high affinity copper uptake protein 1

SLC31A1 蛋白结构

Ctr

Ctr: Ctr copper transporter family (43 - 175)

  • 0
  • 100
  • 190 a.a.
蛋白主名 其他名称

high affinity copper uptake protein 1

copper transport 1 homolog

重组 SLC31A1 蛋白

目录号 产品名 蛋白编号 纯度
HY-P72011 SLC31A1 Protein, Human (Cell-Free, His-SUMO) O15431 (M1-H190) ≥95%

关联疾病

疾病名称 别名
Wilson Disease

Hepatolenticular Degeneration

WD

Wilson'S Disease

WND

Westphal-Strumpell Syndrome

Copper Storage Disease

Cerebral Pseudosclerosis

Westphal Pseudosclerosis

Hepatolenticular Degeneration Syndrome

Copper Retention

Hepatocerebral Degeneration

Kinnier-Wilson Disease

Neurohepatic Degeneration

Progressive Hepatolenticular Degeneration

Lenticular Degenerative Disease

Wilson'S Syndrome

Lenticular Syndrome
Combat Disorder

Combat Disorders

Combat Neurosis
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
Metal Metabolism Disorder

Metal Metabolism, Inborn Errors

Inborn Metal Metabolism Disorder
Deficiency Anemia

Anemia

Deficiency Anemias

Anaemia
Ovarian Cancer

Ovarian Carcinoma

Ovarian Neoplasm

Malignant Tumour Of Ovary

Cancer Of The Ovary

Epithelial Ovarian Cancer

Neoplasm Of Ovary

Ovarian Neoplasms

Ovarian Cancers

Malignant Neoplasm Of Ovary

Primary Malignant Neoplasm Of Ovary

Ovarian Cancer, Somatic

Malignant Ovarian Tumor

Ovary Neoplasm

Primary Ovarian Cancer

Tumor Of The Ovary

Malignant Neoplasm Of The Ovary

Malignant Tumor Of The Ovary

Ovarian Malignant Tumor

OC

Ovarian Carcinomas

Cancer, Ovarian

Cancer Of Ovary

Ovary Cancer

Ca Ovary
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-RS13188 SLC31A1 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 SLC31A1 VGNC VGNC:77455
Mus musculus SLC31A1 MGD MGI:1333843
Canis familiaris SLC31A1 VGNC VGNC:51761
Rattus norvegicus SLC31A1 RGD RGD:620059
Bos taurus SLC31A1 VGNC VGNC:34813
Felis catus SLC31A1 VGNC VGNC:102981
Others SLC31A1 NCBI
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