SLC30A7 - solute carrier family 30 member 7 Gene

Homo sapiens

Also known as ZNT7; ZnT-7; ZnTL2

Gene ID: 148867 | Gene type: protein coding

About SLC30A7

Cytogenetic location: 1p21.2 Genomic coordinates (GRCh38): 1:100,896,090-100,996,078 (from NCBI)

This gene has 3 transcripts (splice variants), 197 orthologues and 8 paralogues. Ubiquitous expression in appendix (RPKM 3.9), thyroid (RPKM 3.9) and 25 other tissues.

Summary

Zinc functions as a cofactor for numerous enzymes, nuclear factors, and Hormones and as an intra- and intercellular signal ion. Members of the zinc transporter (ZNT)/SLC30 subfamily of the cation diffusion facilitator family, such as SLC30A7, permit cellular efflux of zinc (Seve et al., 2004 [PubMed 15154973]).[supplied by OMIM, Mar 2008]

SLC30A7 Products(2)

mRNA	Protein	Name
NM_001144884.2	NP_001138356.1	zinc transporter 7
NM_133496.5	NP_598003.2	zinc transporter 7

SLC30A7 Protein Structure

Cation_efflux

0
100
200
300
376 a.a.

Protein Preferred Names

Protein Names

zinc transporter 7

solute carrier family 30 (zinc transporter), member 7

Related Diseases

Diseases

Alias

Joubert Syndrome 1

Joubert Syndrome	Jbts
Cerebellooculorenal Syndrome 1	JBTS1
Joubert-Boltshauser Syndrome	Cerebelloparenchymal Disorder Iv
Cpd4	Cors1
Joubert Syndrome And Related Disorders	Jsrd
Familial Aplasia Of The Vermis	Joubert Syndrome Related Disorders
Js	Cerebellar Vermis Agenesis
Cerebelloparenchymal Disorder 4	Agenesis Of Cerebellar Vermis
Cerebello-Oculo-Renal Syndrome	Cors
Joubert-Bolthauser Syndrome	Cpd Iv
Classic Joubert Syndrome	Joubert Syndrome Type A
Pure Joubert Syndrome	Cerebello-Oculo-Renal Syndrome 1
Joubert Syndrome-1	Joubert Syndrome, Type 1
Joubert'S Syndrome

Acrodermatitis Enteropathica, Zinc-Deficiency Type

Acrodermatitis Enteropathica	AEZ
Enteropathica	Brandt Syndrome
Ae	Acrodermatitis Enteropathica Zinc Deficiency Type
Danbolt-Cross Syndrome	Acrodermatitis Enteropathica, Zinc Deficiency Type
Inherited Zinc Deficiency	Acrodermatitis Enteropathica, Zinc Deficiency
Danbolt-Closs Syndrome	Primary Zinc Malabsorption Syndrome

Mucinous Stomach Adenocarcinoma

Mucinous Adenocarcinoma Of The Stomach

Mucinous Gastric Adenocarcinoma

Diseases	Alias
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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13185	SLC30A7 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	SLC30A7	MGD	MGI:1913750
Felis catus	SLC30A7	VGNC	VGNC:65313
Canis familiaris	SLC30A7	VGNC	VGNC:46352
Macaca mulatta	SLC30A7	VGNC	VGNC:77514
Bos taurus	SLC30A7	VGNC	VGNC:34811
Rattus norvegicus	SLC30A7	RGD	RGD:1307873

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