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WormBase Tree Display for Gene: WBGene00000996

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Name Class

WBGene00000996SMapS_parentSequenceF49E8
IdentityVersion2
NameCGC_namedif-1Person_evidenceWBPerson8
Sequence_nameF49E8.5
Molecular_nameF49E8.5
F49E8.5.1
CE28408
F49E8.5.2
Other_nameslc-25A20Person_evidenceWBPerson555
CELE_F49E8.5Accession_evidenceNDBBX284604
Public_namedif-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
226 Apr 2016 15:37:44WBPerson2970Name_changeOther_nameslc-25A20
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdif
Allele (32)
Legacy_information[Ahringer J] maternal-effect embryonic lethal (mn); embryos arrest at the completion of gastrulation with little or no tissue differentiation; e2562 and e2577 are apparantly null alleles; e2591 is cold-sensitive, with 100% dead eggs at 15C but is variably viable, and sometimes dumpy at 25C. NA5.
[C.elegansII] e2562 : maternal-effect embryonic lethal (mn); embryos arrest at the completion of gastrulation with little or no tissue differentiation; probable null. OA4: e2577 (similar), e2591cs (100% dead eggs at 15C, variably viable and sometimes dumpy at 25C; TSP hrs 5-8embryo), etc. Cloned: 1.2 kb transcript, present at all stages;encodes predicted 312 aa protein with similarity to mitochondrial carrier proteins. [Ahringer 1995]
StrainWBStrain00004627
RNASeq_FPKM (74)
GO_annotation (16)
Contained_in_operonCEOP4228
Ortholog (46)
Paralog (35)
Structured_descriptionConcise_descriptiondif-1 encodes a putative mitochondrial solute carrier, orthologous to human SLC25A20 (OMIM:212138, mutated in carnitine-acylcarnitine translocase deficiency) that is required for the maintenance of embryonic tissue differentiation and viability; expressed throughout development and in the intestinal cells and hypodermis of the embryo.Paper_evidenceWBPaper00002188
Curator_confirmedWBPerson48
WBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable acyl carnitine transmembrane transporter activity. Involved in mitochondrial transport. Located in mitochondrial envelope. Expressed in intestine. Human ortholog(s) of this gene implicated in carnitine-acylcarnitine translocase deficiency. Is an ortholog of human SLC25A20 (solute carrier family 25 member 20).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:0111585Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1421)
Molecular_infoCorresponding_CDSF49E8.5
Corresponding_transcriptF49E8.5.1
F49E8.5.2
Other_sequence (52)
Associated_featureWBsf651923
WBsf230293
WBsf230294
Experimental_infoRNAi_resultWBRNAi00015334Inferred_automaticallyRNAi_primary
WBRNAi00047872Inferred_automaticallyRNAi_primary
WBRNAi00090632Inferred_automaticallyRNAi_primary
WBRNAi00077274Inferred_automaticallyRNAi_primary
WBRNAi00030258Inferred_automaticallyRNAi_primary
WBRNAi00077288Inferred_automaticallyRNAi_primary
WBRNAi00047873Inferred_automaticallyRNAi_primary
Expr_patternExpr628
Expr629
Expr1017246
Expr1030621
Expr1151702
Expr2010927
Expr2029166
Drives_constructWBCnstr00037149
Construct_productWBCnstr00037149
Microarray_results (21)
Expression_cluster (116)
Interaction (19)
Map_infoMapIVPosition3.35417Error0.001455
Well_ordered
PositiveInside_rearrstDf7
Positive_cloneF49E8Inferred_automaticallyFrom sequence, transcript, pseudogene data
T08G12
Mapping_dataMulti_point2022
2023
2024
2025
2026
4190
4439
Pos_neg_data5935
Reference (11)
MethodGene