SLC34A2 Q486* [plasma membrane]

Stable Identifier
R-HSA-5687587
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
Sodium-dependent phosphate transport protein 2B, NPT2B_HUMAN
Icon
SLC34A2 Q486* [plasma membrane] icon
SLC34A2 Q486* [plasma membrane] icon
Locations in the PathwayBrowser
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External Reference Information
External Reference
UniProt:O95436 SLC34A2
Gene Names
SLC34A2
Chain
chain:1-690
Reference Genes
BioGPS Gene:10568 SLC34A2
COSMIC (genes):SLC34A2 SLC34A2
CTD Gene:10568 SLC34A2
dbSNP Gene:10568 SLC34A2
ENSEMBL:ENSG00000157765 SLC34A2
HGNC:11020 SLC34A2
KEGG:hsa:10568 SLC34A2
Monarch:10568 SLC34A2
NCBI Gene:10568 SLC34A2
OMIM:604217 SLC34A2
UCSC:O95436 SLC34A2
Reference Transcript
Participates
as a member of
Other forms of this molecule
SLC34A2 N38Tfs*8 [plasma membrane]
SLC34A2 K304* [plasma membrane]
SLC34A2 V448* [plasma membrane]
SLC34A2 Q76* [plasma membrane]
SLC34A2 G106R [plasma membrane]
SLC34A2 [plasma membrane]
Modified Residues
Name
Nonsense mutation at L-glutamine 486
Coordinate
486
PsiMod
L-glutamine removal [MOD:01637]
A protein modification that effectively removes or replaces an L-glutamine.
Disease
Name Identifier Synonyms
pulmonary alveolar microlithiasis DOID:12117 pulmonary alveolar microlithiasis (disorder)
Cross References
Guide to Pharmacology - Targets
ENSEMBL
OpenTargets
GeneCards
HPA
PRO
Pharos - Targets
GlyGen
Orphanet
HMDB Protein
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