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WormBase Tree Display for Gene: WBGene00019227

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Name Class

WBGene00019227SMapS_parentSequenceH22K11
IdentityVersion2
NameCGC_namesgca-1Person_evidenceWBPerson1263
WBPerson2876
Sequence_nameH22K11.4
Molecular_nameH22K11.4a
H22K11.4a.1
CE37119
H22K11.4b
CE40082
H22K11.4b.1
Other_nameCELE_H22K11.4Accession_evidenceNDBBX284606
Public_namesgca-1
DB_infoDatabaseWormQTLgeneWBGene00019227
WormFluxgeneWBGene00019227
NDBlocus_tagCELE_H22K11.4
PanthergeneCAEEL|WormBase=WBGene00019227|UniProtKB=H2L0C3
familyPTHR10132
NCBIgene180946
RefSeqproteinNM_001373339.3
NM_001373338.3
TREEFAMTREEFAM_IDTF314655
TrEMBLUniProtAccQ1XFY3
H2L0C3
UniProt_GCRPUniProtAccH2L0C3
OMIMgene600119
604149
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
229 Oct 2007 11:43:25WBPerson2970Name_changeCGC_namesgca-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsgca
Allele (40)
StrainWBStrain00032061
RNASeq_FPKM (74)
GO_annotation00022985
00022986
00022987
00124123
00124124
00124125
Ortholog (27)
Structured_descriptionConcise_descriptionsgca-1 encodes a protein orthologous to the human gene SARCOGLYCAN, ALPHA (50KD DYSTROPHIN-ASSOCIATED GLYCOPROTEIN) (SGCA; OMIM:600119), which when mutated leads to disease.Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated19 Dec 2009 00:00:00
Automated_descriptionPredicted to enable calcium ion binding activity. Located in striated muscle dense body. Expressed in anal depressor muscle; anal sphincter muscle; body wall musculature; and vulval muscle. Human ortholog(s) of this gene implicated in autosomal recessive limb-girdle muscular dystrophy type 2D; myoclonic dystonia 11; and stomach cancer. Is an ortholog of human SGCA (sarcoglycan alpha) and SGCE (sarcoglycan epsilon).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:0110278Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10805)
DOID:9884Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10805)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10808)
DOID:0090034Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10808)
Molecular_infoCorresponding_CDSH22K11.4a
H22K11.4b
Corresponding_CDS_historyH22K11.4:wp121
H22K11.4:wp128
H22K11.4:wp156
H22K11.4a:wp271
H22K11.4b:wp271
Corresponding_transcriptH22K11.4a.1
H22K11.4b.1
Other_sequenceOden_isotig26597
JI171235.1
DVC02223_1
CSC02338_1
Acan_isotig17435
Dviv_isotig28156
FD514430.1
EV852337.1
Associated_featureWBsf654088
WBsf654089
WBsf670663
Experimental_infoRNAi_resultWBRNAi00049458Inferred_automaticallyRNAi_primary
WBRNAi00016297Inferred_automaticallyRNAi_primary
Expr_patternExpr4924
Expr1015295
Expr1038304
Expr1153186
Expr2015800
Expr2034033
Drives_constructWBCnstr00006007
WBCnstr00012337
WBCnstr00025982
Construct_productWBCnstr00006007
WBCnstr00008298
WBCnstr00018329
WBCnstr00025982
AntibodyWBAntibody00002076
Microarray_results (24)
Expression_cluster (123)
InteractionWBInteraction000460218
Map_infoMapXPosition-2.43167Error0.004636
PositivePositive_cloneH22K11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005519
WBPaper00031003
WBPaper00035538
WBPaper00038491
WBPaper00039233
WBPaper00041089
WBPaper00055090
RemarkMap 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