Gene and Protein Information
Species	TM	AA	Chromosomal Location	Gene Symbol	Gene Name	Reference
Human	10	622	14q32.12	SLC24A4	solute carrier family 24 member 4
Mouse	10	622	12 E	Slc24a4	solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
Rat	-	-	6 q32	Slc24a4	solute carrier family 24 member 4

Previous and Unofficial Names

NCKX4 | solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 | solute carrier family 24 (sodium/potassium/calcium exchanger)

Database Links
Specialist databases
Bioparadigms SLC Tables	SLC24A4 (Hs)
RESOLUTE	SLC24A4 (Hs)
Other databases
Alphafold	Q8NFF2 (Hs), Q8CGQ8 (Mm)
Ensembl Gene	ENSG00000140090 (Hs), ENSMUSG00000041771 (Mm), ENSRNOG00000006729 (Rn)
Entrez Gene	123041 (Hs), 238384 (Mm), 314396 (Rn)
Human Protein Atlas	ENSG00000140090 (Hs)
KEGG Gene	hsa:123041 (Hs), mmu:238384 (Mm), rno:314396 (Rn)
OMIM	609840 (Hs)
Pharos	Q8NFF2 (Hs)
UniProtKB	Q8NFF2 (Hs), Q8CGQ8 (Mm)
Wikipedia	SLC24A4 (Hs)

Clinically-Relevant Mutations and Pathophysiology
Disease:  Amelogenesis imperfecta, hypomaturation type, IIA5; AI2A5 Synonyms: Amelogenesis imperfecta [Disease Ontology: DOID:2187] Hypomaturation amelogenesis imperfecta [Orphanet: ORPHA100033] Disease Ontology: DOID:2187 OMIM: 615887 Orphanet: ORPHA100033