Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	487
Gene name Gene Name - the full gene name approved by the HGNC.	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	ATP2A1
Synonyms (NCBI Gene) Gene synonyms aliases	ATP2A, SERCA1
Chromosome Chromosome number	16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	16p11.2
Summary Summary of gene provided in NCBI Entrez Gene.	This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to

Show/Hide all(21)

SNP ID	Visualize variation	Clinical significance	Consequence
rs111266804	G>A,C	Likely-pathogenic	Splice donor variant
rs113803159	C>G	Conflicting-interpretations-of-pathogenicity, likely-benign	Synonymous variant, coding sequence variant
rs117350233	C>T	Conflicting-interpretations-of-pathogenicity	Coding sequence variant, missense variant
rs121918113	C>T	Pathogenic	Coding sequence variant, stop gained
rs121918114	C>A	Pathogenic	Coding sequence variant, stop gained
rs121918115	C>G,T	Uncertain-significance, pathogenic	Coding sequence variant, missense variant
rs398124554	C>-	Uncertain-significance, pathogenic	Frameshift variant, coding sequence variant
rs398124555	->T	Uncertain-significance, pathogenic	Frameshift variant, coding sequence variant
rs551660089	G>A	Likely-pathogenic, pathogenic	Splice donor variant
rs748241465	C>-	Pathogenic	Frameshift variant, coding sequence variant
rs751365374	C>-,CC,CCC	Pathogenic-likely-pathogenic, likely-pathogenic, pathogenic	Frameshift variant, coding sequence variant
rs755227074	G>A	Likely-pathogenic	Splice donor variant
rs895911431	C>T	Pathogenic	Stop gained, coding sequence variant
rs897301304	C>T	Pathogenic, likely-pathogenic	Stop gained, coding sequence variant
rs972494690	G>A,T	Pathogenic	Coding sequence variant, stop gained, missense variant
rs1409892710	T>G	Pathogenic	Stop gained, coding sequence variant
rs1421005631	CT>-	Pathogenic	Frameshift variant, coding sequence variant
rs1555515558	TGTGGCTGCCAT>ACGGCATA	Pathogenic	Frameshift variant, coding sequence variant
rs1555516994	C>T	Likely-pathogenic	Stop gained, coding sequence variant
rs1567479853	A>T	Likely-pathogenic	Splice acceptor variant
rs1596682330	GGT>TGG	Likely-pathogenic	Splice donor variant, coding sequence variant

Show/Hide all(3)

miRTarBase ID	miRNA	Experiments
MIRT807203	hsa-miR-4312	CLIP-seq
MIRT807204	hsa-miR-4660	CLIP-seq
MIRT807205	hsa-miR-646	CLIP-seq

Show/Hide all(67)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000166	Function	Nucleotide binding	IEA
GO:0005388	Function	P-type calcium transporter activity	IBA
GO:0005388	Function	P-type calcium transporter activity	IDA	1329967, 8729696
GO:0005388	Function	P-type calcium transporter activity	IEA
GO:0005388	Function	P-type calcium transporter activity	ISS
GO:0005388	Function	P-type calcium transporter activity	TAS
GO:0005509	Function	Calcium ion binding	IEA
GO:0005509	Function	Calcium ion binding	IMP	9405806
GO:0005509	Function	Calcium ion binding	ISS
GO:0005515	Function	Protein binding	IPI	9295312, 28890335
GO:0005524	Function	ATP binding	IEA
GO:0005524	Function	ATP binding	ISS
GO:0005739	Component	Mitochondrion	IEA
GO:0005783	Component	Endoplasmic reticulum	IEA
GO:0005789	Component	Endoplasmic reticulum membrane	IDA	11402072
GO:0005789	Component	Endoplasmic reticulum membrane	IEA
GO:0005789	Component	Endoplasmic reticulum membrane	TAS
GO:0005793	Component	Endoplasmic reticulum-Golgi intermediate compartment	ISS
GO:0006811	Process	Monoatomic ion transport	IEA
GO:0006816	Process	Calcium ion transport	IDA	11402072
GO:0006816	Process	Calcium ion transport	IEA
GO:0006816	Process	Calcium ion transport	IMP	9405806
GO:0006874	Process	Intracellular calcium ion homeostasis	IBA
GO:0006874	Process	Intracellular calcium ion homeostasis	IEA
GO:0006942	Process	Regulation of striated muscle contraction	IMP	9405806
GO:0008637	Process	Apoptotic mitochondrial changes	IMP	19061639
GO:0016020	Component	Membrane	IBA
GO:0016020	Component	Membrane	IEA
GO:0016020	Component	Membrane	ISS
GO:0016020	Component	Membrane	NAS	9405806
GO:0016529	Component	Sarcoplasmic reticulum	IEA
GO:0016529	Component	Sarcoplasmic reticulum	ISS
GO:0016529	Component	Sarcoplasmic reticulum	NAS	8841193
GO:0016887	Function	ATP hydrolysis activity	IEA
GO:0030899	Function	Calcium-dependent ATPase activity	ISS
GO:0031095	Component	Platelet dense tubular network membrane	IEA
GO:0031095	Component	Platelet dense tubular network membrane	TAS
GO:0031448	Process	Positive regulation of fast-twitch skeletal muscle fiber contraction	IDA	12479237
GO:0031673	Component	H zone	IDA	1329967
GO:0031674	Component	I band	IDA	1329967
GO:0032470	Process	Positive regulation of endoplasmic reticulum calcium ion concentration	IMP	11402072
GO:0032471	Process	Negative regulation of endoplasmic reticulum calcium ion concentration	IMP	11402072, 19061639
GO:0033017	Component	Sarcoplasmic reticulum membrane	IC	8040329
GO:0033017	Component	Sarcoplasmic reticulum membrane	IEA
GO:0033017	Component	Sarcoplasmic reticulum membrane	ISS
GO:0033017	Component	Sarcoplasmic reticulum membrane	TAS	11402072
GO:0034220	Process	Monoatomic ion transmembrane transport	TAS
GO:0034704	Component	Calcium channel complex	IC	11402072
GO:0034976	Process	Response to endoplasmic reticulum stress	IMP	19061639
GO:0042803	Function	Protein homodimerization activity	IPI	11402072
GO:0045988	Process	Negative regulation of striated muscle contraction	IMP	10914677
GO:0046872	Function	Metal ion binding	IEA
GO:0048471	Component	Perinuclear region of cytoplasm	ISS
GO:0051561	Process	Positive regulation of mitochondrial calcium ion concentration	IMP	19061639
GO:0051659	Process	Maintenance of mitochondrion location	IMP	19061639
GO:0070059	Process	Intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress	IEA
GO:0070059	Process	Intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress	IMP	19061639
GO:0070509	Process	Calcium ion import	IMP	8040329
GO:0070588	Process	Calcium ion transmembrane transport	IBA
GO:0070588	Process	Calcium ion transmembrane transport	IEA
GO:0090076	Process	Relaxation of skeletal muscle	IDA	8841193
GO:0106134	Process	Positive regulation of cardiac muscle cell contraction	ISS
GO:1901896	Process	Positive regulation of ATPase-coupled calcium transmembrane transporter activity	ISS
GO:1902082	Process	Positive regulation of calcium ion import into sarcoplasmic reticulum	ISS
GO:1903779	Process	Regulation of cardiac conduction	IEA
GO:1903779	Process	Regulation of cardiac conduction	TAS
GO:1990036	Process	Calcium ion import into sarcoplasmic reticulum	ISS

MIM	HGNC	e!Ensembl
108730	811	ENSG00000196296

Protein

UniProt ID

O14983

Protein name

Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 (SERCA1) (SR Ca(2+)-ATPase 1) (EC 7.2.2.10) (Calcium pump 1) (Calcium-transporting ATPase sarcoplasmic reticulum type, fast twitch skeletal muscle isoform) (Endoplasmic reticulum class 1/2 Ca(2+) ATPase)

Protein function

Key regulator of striated muscle performance by acting as the major Ca(2+) ATPase responsible for the reuptake of cytosolic Ca(2+) into the sarcoplasmic reticulum. Catalyzes the hydrolysis of ATP coupled with the translocation of calcium from th

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF00690	Cation_ATPase_N	4 → 72	Cation transporter/ATPase, N-terminus	Domain
PF00122	E1-E2_ATPase	121 → 329		Family
PF13246	Cation_ATPase	418 → 528		Family
PF00689	Cation_ATPase_C	784 → 987	Cation transporting ATPase, C-terminus	Family

Tissue specificity

TISSUE SPECIFICITY: Skeletal muscle, fast twitch muscle (type II) fibers. {ECO:0000269|PubMed:8825625}.

Sequence

MEAAHAKTTEECLAYFGVSETTGLTPDQVKRNLEKYGLNELPAEEGKTLWELVIEQFEDL
LVRILLLAACISFVLAWFEEGEETITAFVEPFVILLILIANAIVGVWQERNAENAIEALK
EYEPEMGKVYRADRKSVQRIKARDIVPGDIVEVAVGDKVPADIRILAIKSTTLRVDQSIL
TGESVSVIKHTEPVPDPRAVNQDKKNMLFSGTNIAAGKALGIVATTGVGTEIGKIRDQMA
ATEQDKTPLQQKLDEFGEQLSKVISLICVAVWLINIGHFNDPVHGGSWFRGAIYYFKIAV
ALAVAAIPEGLPAVITTCLALGTRRMAKKNAIVRSLPSVETLGCTSVICSDKTGTLTTNQ
MSVCKMFIIDKVDGDICLLNEFSITGSTYAPEGEVLKNDKPVRPGQYDGLVELATICALC
NDSSLDFNEAKGVYEKVGEATETALTTLVEKMNVFNTDVRSLSKVERANACNSVIRQLMK
KEFTLEFSRDRKSMSVYCSPAKSSRAAVGNKMFVKGAPEGVIDRCNYVRVGTTRVPLTGP
VKEKIMAVIKEWGTGRDTLRCLALATRDTPPKREEMVLDDSARFLEYETDLTFVGVVGML
DPPRKEVTGSIQLCRDAGIRVIMITGDNKGTAIAICRRIGIFGENEEVADRAYTGREFDD
LPLAEQREACRRACCFARVEPSHKSKIVEYLQSYDEITAMTGDGVNDAPALKKAEIGIAM
GSGTAVAKTASEMVLADDNFSTIVAAVEEGRAIYNNMKQFIRYLISSNVGEVVCIFLTAA
LGLPEALIPVQLLWVNLVTDGLPATALGFNPPDLDIMDRPPRSPKEPLISGWLFFRYMAI
GGYVGAATVGAAAWWFLYAEDGPHVNYSQLTHFMQCTEDNTHFEGIDCEVFEAPEPMTMA
LSVLVTIEMCNALNSLSENQSLLRMPPWVNIWLLGSICLSMSLHFLILYVDPLPMIFKLR
ALDLTQWLMVLKISLPVIGLDEILKFVARNYLEDPEDERRK

Sequence length

1001

Interactions

View interactions

	KEGG		Reactome
	Calcium signaling pathway cGMP-PKG signaling pathway cAMP signaling pathway Efferocytosis Cardiac muscle contraction Adrenergic signaling in cardiomyocytes Osteoclast differentiation Thyroid hormone signaling pathway Pancreatic secretion Alzheimer disease Spinocerebellar ataxia Pathways of neurodegeneration - multiple diseases Hypertrophic cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy Dilated cardiomyopathy Diabetic cardiomyopathy		Reduction of cytosolic Ca++ levels Ion homeostasis Ion transport by P-type ATPases

Show/Hide Causal Diseases (1)

Disease merge term	Disease name	dbSNP ID	References
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Brody Myopathy	brody myopathy	rs551660089, rs972494690, rs897301304, rs895911431, rs141559558, rs1596682330, rs1421005631, rs111266804, rs1555516994, rs1024976181, rs751365374, rs1963456518, rs121918113, rs1555515558, rs121918114 View all (7 more)	N/A

Show/Hide Unknown Diseases (2)

Disease merge term	Disease name	Evidence	References	Source
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Diabetes	Type 2 diabetes, Youth-onset type 2 diabetes	N/A	N/A	GWAS
Hypogonadism	Hypogonadism	N/A	N/A	GWAS

Show/Hide Text Mining Associations (20)

Disease Name	Relationship Type	References
Associations from Text Mining Disease associations identified through Pubtator
Adenocarcinoma	Associate	37510286
Breast Neoplasms	Associate	34684111
Brody myopathy	Associate	32040565, 40323132, 8825625
Carcinoma Squamous Cell	Associate	37510286
Diabetes Mellitus	Associate	28694205
Dyslipidemias	Associate	28694205
Glycogen Storage Disease Type V	Associate	22347505, 35563042
Malignant Hyperthermia	Associate	32040565
Microcystic adnexal carcinoma	Stimulate	35509066
Multiple Myeloma	Associate	37227248
Muscle Neoplasms	Associate	32040565
Muscular Atrophy	Associate	35563042
Muscular Diseases	Associate	8825625
Myotonic Dystrophy	Associate	20071745, 22758909, 29947794, 36631509
Neoplasms	Associate	35133336
Oropharyngeal Neoplasms	Associate	32415241
Pneumonia Ventilator Associated	Associate	22916119
Prostatic Neoplasms	Associate	35133336
Pulmonary Disease Chronic Obstructive	Associate	15718407
Stomach Ulcer	Associate	35133336

ATP2A1 (ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1)