SLC57A2

Protein name: NIPA2 Aliases: N/D Substrates: Mg2+ [PMID: 18667602] Transport type: N/D Tissue and cellular expression: N/D Subcellular expression: Early endosomes, as well as plasma membrane [PMID: 18667602] Disease: N/D Locus: 15q11.2 Sequence ID: NP_001008860.1, NM_001008860.2 NP_001008892.1, NM_001008892.2 NP_001008894.1, NM_001008894.2 NP_001171817.1, NM_001184888.1 NP_001171818.1, NM_001184889.1 NP_112184.4, NM_030922.6 XP_005272603.1, XM_005272546.3 XP_005272604.1, XM_005272547.4 XP_005272605.1, XM_005272548.3 XP_005272607.1, XM_005272550.3 XP_005272609.1, XM_005272552.3 XP_005272610.1, XM_005272553.4 XP_006720427.1, XM_006720364.2 XP_006720428.1, XM_006720365.2 XP_006720429.1, XM_006720366.3 XP_006720430.1, XM_006720367.1 XP_011542179.1, XM_011543877.2 XP_011542180.1, XM_011543878.2 XP_011542181.1, XM_011543879.2 XP_011542182.1, XM_011543880.2 XP_016878134.1, XM_017022645.1 XP_016878135.1, XM_017022646.1 XP_016878136.1, XM_017022647.1 XP_016878137.1, XM_017022648.1 XP_016878138.1, XM_017022649.1 XP_016878139.1, XM_017022650.1 XP_016878140.1, XM_017022651.1 XP_016878141.1, XM_017022652.1 XP_016878142.1, XM_017022653.1 XP_016878143.1, XM_017022654.1 XP_016878144.1, XM_017022655.1 XP_016878145.1, XM_017022656.1 XP_016878146.1, XM_017022657.1 XP_016878147.1, XM_017022658.1 XP_016878148.1, XM_017022659.1 XP_016878149.1, XM_017022660.1 XP_016878150.1, XM_017022661.1 XP_016878151.1, XM_017022662.1 XP_016878152.1, XM_017022663.1 Gene ID: 81614 Splice variants: N/D

NIPA2_HUMAN (UniProt)

Gene names: NIPA2
Protein names and data: NIPA2_HUMAN, Full=Magnesium transporter NIPA2, Full=Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 Length: 360 a.a., Mass: 39185 Da,
fasta formatted sequence

Database cross-references

UniProt: Q8N8Q9
OMIM: 608146
Ensembl: ENST00000398014
GeneCard: NIPA2
TCDB: 2.A.7.25.2
HGNC: HGNC:17044

Genetic variants

See also Ensembl:ENST00000398014