2. Gene
  3. SLC37A3 - solute carrier family 37 member 3 Gene

SLC37A3 - solute carrier family 37 member 3 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 37 成员 3

种属: Homo sapiens

同用名: SPX3

基因 ID: 84255 | 基因类型: protein coding

关于 SLC37A3

Cytogenetic location: 7q34 Genomic coordinates (GRCh38): 7:140,333,752-140,398,530 (from NCBI)

This gene has 28 transcripts (splice variants), 295 orthologues and 12 paralogues. Ubiquitous expression in endometrium (RPKM 19.0), thyroid (RPKM 9.8) and 25 other tissues.

功能概要

预测启用跨膜转运蛋白活动。预计参与糖类转运和跨膜转运。是内质网膜的组成部分。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable transmembrane transporter activity. Predicted to be involved in carbohydrate transport and transmembrane transport. Is integral component of endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC37A3 基因产物(9)

mRNA Protein Name
NM_001287498.2 NP_001274427.1 sugar phosphate exchanger 3 isoform 3
NM_001363373.1 NP_001350302.1 sugar phosphate exchanger 3 isoform 4
NM_001363374.1 NP_001350303.1 sugar phosphate exchanger 3 isoform 5
NM_001363375.1 NP_001350304.1 sugar phosphate exchanger 3 isoform 6
NM_001363376.1 NP_001350305.1 sugar phosphate exchanger 3 isoform 7
NM_001363377.1 NP_001350306.1 sugar phosphate exchanger 3 isoform 8
NM_001363378.1 NP_001350307.1 sugar phosphate exchanger 3 isoform 9
NM_032295.4 NP_115671.1 sugar phosphate exchanger 3 isoform 2
NM_207113.3 NP_996996.1 sugar phosphate exchanger 3 isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
NOT enables glucose 6-phosphate:phosphate antiporter activity IDA
IDA: 通过直接分析推断
21949678 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
29745899 GOA
enables xenobiotic transmembrane transporter activity IDA
IDA: 通过直接分析推断
29745899 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
NOT involved in glucose-6-phosphate transport IDA
IDA: 通过直接分析推断
21949678 GOA
NOT involved in phosphate ion transmembrane transport IDA
IDA: 通过直接分析推断
21949678 GOA
involved in xenobiotic transmembrane transport IDA
IDA: 通过直接分析推断
29745899 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in endoplasmic reticulum membrane IDA
IDA: 通过直接分析推断
21949678 GOA
located in lysosomal membrane IDA
IDA: 通过直接分析推断
29745899 GOA
EXP：通过实验结果推断 IDA：通过直接分析推断 IPI：通过物理相互作用推断 IMP：通过突变表型推断 IGI：通过遗传相互作用推断 IEP：通过表达模式推断

SLC37A3 蛋白结构

MFS_1

MFS_1: Major Facilitator Superfamily (82 - 410)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 494 a.a.
蛋白主名 其他名称

sugar phosphate exchanger 3

solute carrier family 37 (glycerol-3-phosphate transporter), member 3

关联疾病

疾病名称 别名
Deafness, Autosomal Recessive 8

Neurosensory Nonsyndromic Recessive Deafness 8

DFNB8

Dfnb10

Deafness, Autosomal Recessive 10

Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8

Nsrd8

Autosomal Recessive Nonsyndromic Deafness 8

Deafness, Autosomal Recessive 8/10

Autosomal Recessive Deafness 10

Autosomal Recessive Deafness 8

Childhood-Onset Neurosensory Autosomal Recessive Deafness 8

Nrsd8

Deafness, Autosomal Recessive, 8

Childhood-Onset Neurosensory Deafness Autosomal Recessive 8

Deafness Autosomal Recessive 10

Deafness Autosomal Recessive 8/10

Deafness Neurosensory Autosomal Recessive 8

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 8

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 8

Deafness, Autosomal Recessive, Type 8/10
Caffey Disease

Infantile Cortical Hyperostosis

CAFYD

Cortical Congenital Hyperostosis

Caffey-Silverman Syndrome

De Toni-Caffey Disease

Hyperostosis Cortical Infantile

Hyperostosis, Cortical, Congenital
Glycerol Kinase Deficiency

Hyperglycerolemia

GKD

Gk Deficiency

Gk1 Deficiency

Deficiency Of Glycerol Kinase

Isolated Glycerol Kinase Deficiency

Glycerol Kinase Deficiency, Adult Form

Glycerol Kinase Deficiency, Juvenile Form

Deficiency, Glycerol Kinase
Glycogen Storage Disease Ia

Von Gierke Disease

Glycogen Storage Disease Type I

Glycogen Storage Disease I

Hepatorenal Form Of Glycogen Storage Disease

Hepatorenal Glycogenosis

Glucose-6-Phosphatase Deficiency

Glycogen Storage Disease, Type I

Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency Type Ia

GSD1A

Gsd1

Von Gierke'S Disease

Glycogen Storage Disease Type 1a

Glycogen Storage Disease 1a

Glucose-6-Phosphate Transport Defect

Gsd Ia

Deficiency Of Glucose-6-Phosphatase

Glycogenosis Type I

Glucose-6-Phosphatase Deficiency Glycogen Storage Disease

Glycogenosis Type 1

Glucose-6-Phosphate Deficiency

Gsd I

Gsd Type I

G6p Deficiency Type 1a

Gsd Due To G6p Deficiency Type 1a

Gsd Due To G6p Deficiency Type Ia

Gsd Type 1a

Gsdia

Glycogen Storage Disease Due To G6p Deficiency Type Ia

Glycogenosis Due To Glucose-6-Phosphatase Deficiency Type 1a

Glycogenosis Due To Glucose-6-Phosphatase Deficiency Type Ia

Glycogenosis Type Ia

Gsd-Ia

Storage Disease, Glycogen, Type 1a

Glycogen Storage Disease Type Ia
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-RS13215 SLC37A3 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus SLC37A3 RGD RGD:1310346
Canis familiaris SLC37A3 VGNC VGNC:46388
Mus musculus SLC37A3 MGD MGI:1919394
Felis catus SLC37A3 VGNC VGNC:80719
Bos taurus SLC37A3 VGNC VGNC:34844
Macaca mulatta SLC37A3 VGNC VGNC:81574
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