Gene and Protein Information
Species	TM	AA	Chromosomal Location	Gene Symbol	Gene Name	Reference
Human	1	66	11q23.3	FXYD2	FXYD domain containing ion transport regulator 2
Mouse	1	70	9 A5.2	Fxyd2	FXYD domain-containing ion transport regulator 2
Rat	1	66	8q22	Fxyd2	FXYD domain-containing ion transport regulator 2

Previous and Unofficial Names

sodium pump gamma chain | Na(+)/K(+) ATPase subunit gamma

Database Links
Alphafold	P54710 (Hs), Q04646 (Mm), Q04679 (Rn)
ChEMBL Target	CHEMBL2095186 (Hs)
DrugBank Target	P54710 (Hs)
Ensembl Gene	ENSG00000137731 (Hs), ENSMUSG00000059412 (Mm), ENSRNOG00000016469 (Rn)
Entrez Gene	486 (Hs), 11936 (Mm), 29639 (Rn)
Human Protein Atlas	ENSG00000137731 (Hs)
KEGG Gene	hsa:486 (Hs), mmu:11936 (Mm), rno:29639 (Rn)
OMIM	601814 (Hs)
Orphanet	ORPHA121972 (Hs)
Pharos	P54710 (Hs)
RefSeq Nucleotide	NM_001680 (Hs), NM_007503 (Mm), NM_017349 (Rn)
RefSeq Protein	NP_001671 (Hs), NP_031529 (Mm), NP_059045 (Rn)
UniProtKB	P54710 (Hs), Q04646 (Mm), Q04679 (Rn)
Wikipedia	FXYD2 (Hs)

Clinically-Relevant Mutations and Pathophysiology
Disease:  Hypomagnesemia 2, renal; HOMG2 Synonyms: Autosomal dominant primary hypomagnesemia with hypocalciuria [Orphanet: ORPHA34528] OMIM: 154020 Orphanet: ORPHA34528 References:  1