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WormBase Tree Display for Gene: WBGene00002056

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Name Class

WBGene00002056SMapS_parentSequenceCHROMOSOME_X
IdentityVersion4
NameCGC_nameifc-2Person_evidenceWBPerson105
WBPerson293
WBPerson260
Sequence_nameM6.1
Molecular_name (19)
Other_nameCel IF C2Accession_evidenceX70832
CelIF c2
ecp-1Paper_evidenceWBPaper00057164
exc-2Person_evidenceWBPerson260
Curator_confirmedWBPerson51134
Date_last_updated07 Aug 2023 16:20:23
CELE_M6.1Accession_evidenceNDBBX284606
Public_nameifc-2
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
209 Mar 2021 13:49:30WBPerson1983Name_changeOther_nameecp-1
307 Aug 2023 16:03:35WBPerson51134EventAcquires_mergeWBGene00001363
413 Oct 2023 01:37:05WBPerson51134Name_changeCGC_nameifc-2
Other_nameexc-2
Acquires_mergeWBGene00001363
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classifc
Allele (153)
Legacy_information[Buechner M] exc for excretory canal defect. Canals are very short and consist of a series of vacuoles. 100% penetrant. Usually visible by low-power microscopy.
[C.elegansII] rh90 : excretory canal defect. Canals are very short and consist of a series of vacuoles. Luminal coat partly detached, floats in canal.100% penetrant.Usually visible by low-power microscopy. Affects tail spike ??? OA1: rh105. [NJ]
StrainWBStrain00002850
WBStrain00028840
WBStrain00047374
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (61)
Paralog (12)
Structured_descriptionConcise_descriptionifc-2 encodes three isoforms of an intermediate filament protein dispensable for viability but required for normal movement, growth rate, body size, body shape, and cuticle strength; IFC-2 is present in the cytoplasm of intestinal cells, and at the desmosomes of intestinal and pharyngeal cells.Paper_evidenceWBPaper00001981
WBPaper00004761
WBPaper00005492
WBPaper00006137
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to be a structural constituent of cytoskeleton. Involved in post-embryonic digestive tract morphogenesis. Located in cytoplasm and desmosome. Expressed in several structures, including excretory canal; pharyngeal-intestinal valve; pharynx; rectal valve cell; and uterus. Human ortholog(s) of this gene implicated in several diseases, including Dowling-Degos disease; ichthyosis (multiple); and palmoplantar keratosis (multiple). Is an ortholog of several human genes including KRT1 (keratin 1); KRT2 (keratin 2); and KRT3 (keratin 3).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_model (14)
Molecular_infoCorresponding_CDS (6)
Corresponding_CDS_historyM6.1a:wp272
M6.1b:wp272
M6.1c:wp272
Corresponding_transcriptM6.1a.1
M6.1a.2
M6.1b.1
M6.1c.1
M6.1d.1
M6.1e.1
M6.1f.1
Other_sequenceCR07924
FD516689.1
CBC09732_1
CJC02211_1
CBC03886_1
CSC00034_1
CRC05750_1
Associated_feature (13)
Experimental_infoRNAi_result (27)
Expr_pattern (17)
Drives_constructWBCnstr00003372
WBCnstr00036488
WBCnstr00042147
WBCnstr00042148
WBCnstr00042149
Construct_productWBCnstr00036488
WBCnstr00042019
WBCnstr00042020
WBCnstr00042147
AntibodyWBAntibody00000563
WBAntibody00002893
WBAntibody00002913
Microarray_results (39)
Expression_cluster (285)
Interaction (77)
Map_infoMapXPosition-19.5186Error0.005743
PositivePositive_cloneM6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4971
Pseudo_map_position
ReferenceWBPaper00001981
WBPaper00003721
WBPaper00004761
WBPaper00005485
WBPaper00010375
WBPaper00012337
WBPaper00014610
WBPaper00014967
WBPaper00015113
WBPaper00015411
WBPaper00018665
WBPaper00019618
WBPaper00021085
WBPaper00026926
WBPaper00027245
WBPaper00028004
WBPaper00030603
WBPaper00030667
WBPaper00031650
WBPaper00031849
WBPaper00036800
WBPaper00036842
WBPaper00038491
WBPaper00038564
WBPaper00040999
WBPaper00041022
WBPaper00042728
WBPaper00047346
WBPaper00048264
WBPaper00052179
WBPaper00054672
WBPaper00055090
WBPaper00056033
WBPaper00056896
WBPaper00057164
WBPaper00057758
WBPaper00057939
WBPaper00059330
WBPaper00061547
WBPaper00061750
WBPaper00065558
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