1. Gene
  2. SLC4A5 - solute carrier family 4 member 5 Gene

SLC4A5 - solute carrier family 4 member 5 Gene

Homo sapiens

Also known as NBC4; NBCe2

Gene ID: 57835 | Gene type: protein coding

About SLC4A5

Cytogenetic location: 2p13.1 Genomic coordinates (GRCh38): 2:74,216,242-74,343,416 (from NCBI)

This gene has 14 transcripts (splice variants), 279 orthologues and 9 paralogues. Broad expression in thyroid (RPKM 9.5), testis (RPKM 8.1) and 14 other tissues.

Summary

This gene encodes a member of the sodium bicarbonate cotransporter (NBC) family, part of the bicarbonate transporter superfamily. Sodium bicarbonate cotransporters are involved in intracellular pH regulation and electroneural or electrogenic sodium bicarbonate transport. This protein is thought to be an integral membrane protein. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]

SLC4A5 Products(3)

mRNA Protein Name
NM_001386136.1 NP_001373065.1 electrogenic sodium bicarbonate cotransporter 4 isoform e
NM_021196.3 NP_067019.3 electrogenic sodium bicarbonate cotransporter 4 isoform a
NM_133478.3 NP_597812.1 electrogenic sodium bicarbonate cotransporter 4 isoform c

SLC4A5 Protein Structure

Band_3_cyto

Band_3_cyto: Band 3 cytoplasmic domain (141 - 408)

HCO3_cotransp

HCO3_cotransp: HCO3- transporter family (487 - 953)

  • 0
  • 200
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  • 600
  • 800
  • 1040 a.a.
Protein Preferred Names Protein Names

electrogenic sodium bicarbonate cotransporter 4

solute carrier family 4 (sodium bicarbonate cotransporter), member 5

Related Diseases

Diseases Alias
Alstrom Syndrome

ALMS

Alström Syndrome

Alss

Alstrom-Hallgren Syndrome

Alstroem Syndrome

Intestinal Impaction
Corneal Dystrophy, Band-Shaped

Band Keratopathy

Band-Shaped Keratopathy

Complex Partial Epilepsy

Epilepsy, Complex Partial

Complex Partial Epileptic Seizure

Epilepsy, Psychomotor

Psychomotor Epilepsy

Corneal Dystrophy And Perceptive Deafness

Corneal Dystrophy-Perceptive Deafness Syndrome

CDPD

Harboyan Syndrome

Cdpd1

Corneal Dystrophy And Sensorineural Deafness

Corneal Endothelial Dystrophy And Perceptive Deafness

Corneal Dystrophy With Progressive Deafness

Congenital Corneal Dystrophy, Progressive Sensorineural Deafness

Corneal Dystrophy With Progressive Hearing Loss

Corneal Dystrophy-Perceptive Hearing Loss Syndrome

Dystrophy, Corneal, Endothelial, And Perceptive Deafness

Corneal Degeneration

Degenerative Corneal Opacity

Hypertension, Essential

Essential Hypertension

Hypertension

High Blood Pressure

Hypertension, Essential, Susceptibility To

Hypertensive Disease

Primary Hypertension

EHT

Hypertension, Salt-Sensitive Essential, Susceptibility To

Hyperpiesia

Idiopathic Hypertension

Hypertensive Disorder

Hypertension, Essential, Susceptibility To, 3

Hypertension, Essential 3

Hypertension, Essential, Salt-Sensitive

Hypertension, Essential, Susceptibility To, 6

Hypertension, Essential 6

Hypertension, Salt-Sensitive Essential

Hypertension, Susceptibility To

Hypertension, Essential, Susceptibility To, 4

Hypertension, Essential 4

Hypertension, Essential, Susceptibility To, 2

Hypertension, Essential 2

Hypertension, Essential, Susceptibility To, 1

Hypertension, Essential 1

Hypertension, Essential, Susceptibility To, 5

Hypertension, Essential 5

Htn

Vascular Hypertensive Disorder

Systemic Primary Arterial Hypertension

Hbp - [High Blood Pressure]

Systemic Arterial Hypertensive Disorder

Elevated Blood Pressure

Arterial Hypertension Nos

Hypertension Nos

Benign Hypertension

Systemic Arterial Hypertension

Systemic Hypertension

Artery Htn

Benign Htn

Vascular Htn

Vascular Hypertension

Cholesterol Hypertension

Cholesterol Htn

Idiopathic Htn

Malignant Hypertension

Malignant Htn

Raised Blood Pressure

Cardiovascular Hypertension

Primary Htn - [Hypertension]

High Arterial Tension

High Blood Pressure Disorder

Ht - [Hypertension]

Htn - [Hypertension]

Hypertensive Vascular Disease

Hypertensive Vascular Degeneration

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

Orthologs Information

Species Symbol Source ID
Mus musculus SLC4A5 MGD MGI:2443220
Felis catus SLC4A5 VGNC VGNC:65390
Bos taurus SLC4A5 VGNC VGNC:34895
Rattus norvegicus SLC4A5 RGD RGD:1303009
Canis familiaris SLC4A5 VGNC VGNC:46435
Macaca mulatta SLC4A5 VGNC VGNC:106220