protein-coding

Gene 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]

MANE transcript

NM_133478.3

Inheritance

—

ClinVar variants

U:178B:22

Top phenotype

SLC4A5-related disorder

Max pathogenic AF

—

External References & Databases

Transcript & Mutation Effects

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GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to variants in ClinVar

3 Conditions Cataloged
not specifiedTotal: 167
SLC4A5-related disorderTotal: 15
not providedTotal: 12

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_133478.3. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
4
12
1
17
missense
167
9
176
nonsense
1
1
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
6
6
Total00178211200
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Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 19 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_133478.3RefSeqNP_597812.125MANE Select
ENST00000394019.7EnsemblENSP00000377587.225MANE Select
NM_001386136.1RefSeqNP_001373065.123Standard
NM_021196.3RefSeqNP_067019.326Standard
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