SLC26A7 - solute carrier family 26 member 7 Gene

Homo sapiens

Also known as SUT2

Gene ID: 115111 | Gene type: protein coding

About SLC26A7

Cytogenetic location: 8q21.3 Genomic coordinates (GRCh38): 8:91,209,496-91,398,155 (from NCBI)

This gene has 10 transcripts (splice variants), 139 orthologues and 9 paralogues. Restricted expression toward thyroid (RPKM 194.6).

Summary

This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Aug 2013]

SLC26A7 Products(4)

mRNA	Protein	Name
NM_001282356.2	NP_001269285.1	anion exchange transporter isoform a
NM_001282357.2	NP_001269286.1	anion exchange transporter isoform c
NM_052832.4	NP_439897.1	anion exchange transporter isoform a
NM_134266.2	NP_599028.1	anion exchange transporter isoform b

SLC26A7 Protein Structure

Sulfate_transp

STAS

0
200
400
600
656 a.a.

Protein Preferred Names

Protein Names

anion exchange transporter

solute carrier family 26 (anion exchanger), member 7

Related Diseases

Diseases

Alias

Congenital Hypothyroidism

Cretinism	Neonatal Hypothyroidism
Ch	Cht
Congenital Myxedema	Myxedema, Congenital
Endemic Cretinism	Congenital Iodine-Deficiency Syndrome
Fetal Iodine Deficiency Syndrome	Congenital Iodine-Deficiency Hypothyroidism Nos

Dyshormonogenic Goiter

Dyshormonogenic Goitre

Pendred Syndrome

Goiter-Deafness Syndrome	Deafness With Goiter
PDS	Thyroid Dyshormonogenesis 2b
Tdh2b	Autosomal Recessive Sensorineural Hearing Impairment And Goiter
Pendred'S Syndrome	Thyroid Hormonogenesis, Genetic Defect In, 2b
Hypothyroidism, Congenital, Due To Dyshormonogenesis, 2b	Congenital Hypothyroidism Due To Dyshormonogenesis 2b
Genetic Defect In Thyroid Hormonogenesis 2b	Autosomal Recessive Sensorineural Hearing Impairment, Enlarged Vestibular Aqueduct, And Goiter
Goiter-Hearing Loss Syndrome	Goitre-Deafness Syndrome
Goitre Deafness

Diastrophic Dysplasia

Diastrophic Dwarfism	DTD
Dd	Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant
Dysplasia, Diastrophic	Diastrophic Dysplasia Variant

Renal Tubular Acidosis

Acidosis Renal Tubular	Acidosis, Renal Tubular
Lightwood-Albright Syndrome	Lightwood Syndrome
Idiopathic Infantile Hypercalcemia - Mild Form	Kidney Tubular Acidosis
Renal Tubule Acidosis	Kidney Acidosis
Renal Acidosis	Renal Hyperchloremic Acidosis
Rta - [Renal Tubular Acidosis]

Hypothyroidism

Thyroid Diseases	Thyroid Disease
Thyroid Deficiency	Thyroid Insufficiency
Dysfunction Thyroid	Thyroid Dysfunction

Brown-Vialetto-Van Laere Syndrome 2

BVVLS2	Rfvt3-Related Riboflavin Transporter Deficiency
Rtd3	Riboflavin Transporter Deficiency 3
Brown-Vialetto-Van Laere Syndrome, Type 2

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-RS13141	SLC26A7 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	SLC26A7	MGD	MGI:2384791
Canis familiaris	SLC26A7	VGNC	VGNC:46326
Rattus norvegicus	SLC26A7	RGD	RGD:1310846
Bos taurus	SLC26A7	VGNC	VGNC:34782
Felis catus	SLC26A7	VGNC	VGNC:65285
Macaca mulatta	SLC26A7	VGNC	VGNC:77478

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