Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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492 |
Gene nameGene Name - the full gene name approved by the HGNC.
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ATPase plasma membrane Ca2+ transporting 3 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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ATP2B3 |
SynonymsGene synonyms aliases
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CFAP39, CLA2, OPCA, PMCA3, PMCA3a, SCAX1 |
ChromosomeChromosome number
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X |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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Xq28 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs150989590 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, coding sequence variant |
rs368215361 |
C>G,T |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
rs397514619 |
G>A |
Likely-pathogenic, pathogenic |
Non coding transcript variant, missense variant, coding sequence variant |
rs724160009 |
GCTGGT>- |
Pathogenic |
Non coding transcript variant, inframe deletion, coding sequence variant |
rs724160011 |
CTGGTC>- |
Pathogenic |
Non coding transcript variant, inframe deletion, coding sequence variant |
rs724160012 |
TCGTGG>- |
Pathogenic |
Non coding transcript variant, inframe deletion, coding sequence variant |
rs782596945 |
G>A,T |
Pathogenic |
Synonymous variant, genic downstream transcript variant, missense variant, 3 prime UTR variant, coding sequence variant, non coding transcript variant |
rs1603040061 |
C>T |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, missense variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
Q16720 |
Protein name |
Plasma membrane calcium-transporting ATPase 3 (PMCA3) (EC 7.2.2.10) (Plasma membrane calcium ATPase isoform 3) (Plasma membrane calcium pump isoform 3) |
Protein function |
ATP-driven Ca(2+) ion pump involved in the maintenance of basal intracellular Ca(2+) levels at the presynaptic terminals (PubMed:18029012, PubMed:22912398, PubMed:25953895, PubMed:27035656). Uses ATP as an energy source to transport cytosolic Ca |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00690 |
Cation_ATPase_N |
51 → 121 |
Cation transporter/ATPase, N-terminus |
Domain |
PF00122 |
E1-E2_ATPase |
190 → 306 |
|
Family |
PF00122 |
E1-E2_ATPase |
341 → 451 |
|
Family |
PF13246 |
Cation_ATPase |
516 → 612 |
|
Family |
PF00689 |
Cation_ATPase_C |
876 → 1058 |
Cation transporting ATPase, C-terminus |
Family |
PF12424 |
ATP_Ca_trans_C |
1100 → 1146 |
Plasma membrane calcium transporter ATPase C terminal |
Family |
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Sequence |
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Sequence length |
1220 |
Interactions |
View interactions |