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WormBase Tree Display for Gene: WBGene00004063

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Name Class

WBGene00004063SMapS_parentSequenceCHROMOSOME_I
IdentityVersion1
NameCGC_namepmr-1
Sequence_nameZK256.1
Molecular_name (11)
Other_namepmr1Accession_evidenceEMBLAJ303081
AJ303082
CELE_ZK256.1Accession_evidenceNDBBX284601
Public_namepmr-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpmr
Allele (285)
RNASeq_FPKM (74)
GO_annotation00010846
00010847
00010848
00010849
00010850
00010851
00010852
00010853
00010854
00010855
00010856
00010857
00010858
00010859
00010860
00010861
00010862
00010863
00010864
00010865
00010866
00010867
00010868
00010869
00010870
00010871
00010872
00010873
00112336
00112337
00112338
00112339
00112340
00112341
00112342
Contained_in_operonCEOP1682
Ortholog (42)
Paralog (14)
Structured_descriptionConcise_descriptionThe pmr-1 gene encodes a Golgi P-type ATPase Ca^2+/Mn^2+-pump; mutations in its human ortholog, ATP2C1, cause Hailey-Hailey disease (OMIM:169600).Paper_evidenceWBPaper00004659
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables P-type calcium transporter activity and P-type manganese transporter activity. Involved in several processes, including metal ion transport; response to metal ion; and response to oxidative stress. Located in Golgi apparatus and membrane. Expressed in male gonad; seam cell; and spermatheca. Human ortholog(s) of this gene implicated in Hailey-Hailey disease. Is an ortholog of human ATP2C1 (ATPase secretory pathway Ca2+ transporting 1) and ATP2C2 (ATPase secretory pathway Ca2+ transporting 2).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0050429Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13211)
Disease_relevanceC. elegans is an effective model system to study heat-related pathologies like heat stroke; in elegans, a small heat shock protein (sHSP), HSP-16.1 has a protective effect against heat-induced necrosis; HSP-16.1 localizes to the golgi and functions together with the PMR-1/PMR1 Ca2+ and Mn2+ transporting ATPase, and NUCB-1/Nucleobindin1, a golgi-located calcium-buffering protein, to maintain calcium homeostasis, under heat stroke; overexpression of pmr-1/PMR1 is sufficient to promote survival after heat stroke, bypassing both HSF-1 and HSP-16.1, indicating that PMR-1/PMR1 functions downstream of both these genes.Homo sapiensPaper_evidenceWBPaper00041564
Curator_confirmedWBPerson324
Date_last_updated29 May 2013 00:00:00
Molecular_infoCorresponding_CDSZK256.1a
ZK256.1b
ZK256.1c
Corresponding_CDS_historyZK256.1:wp114
ZK256.1a:wp49
ZK256.1b:wp77
Corresponding_transcript (5)
Other_sequence (75)
Associated_feature (13)
Experimental_infoRNAi_resultWBRNAi00059919Inferred_automaticallyRNAi_primary
WBRNAi00038238Inferred_automaticallyRNAi_primary
WBRNAi00116858Inferred_automaticallyRNAi_primary
WBRNAi00059917Inferred_automaticallyRNAi_primary
WBRNAi00059303Inferred_automaticallyRNAi_primary
WBRNAi00059920Inferred_automaticallyRNAi_primary
WBRNAi00086175Inferred_automaticallyRNAi_primary
WBRNAi00059921Inferred_automaticallyRNAi_primary
Expr_patternChronogram1105
Expr3187
Expr7200
Expr1017781
Expr1031961
Expr1162731
Expr2014977
Expr2033212
Drives_constructWBCnstr00003233
WBCnstr00011207
Construct_productWBCnstr00011207
AntibodyWBAntibody00000363
Microarray_results (31)
Expression_cluster (114)
Interaction (69)
Map_infoMapIPosition17.0977Error0.064933
PositivePositive_cloneZK256Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point5071
Pseudo_map_position
Reference (22)
RemarkSequence connection from [Van Baelenk, Wuytack, F]
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene