WormBase Tree Display for Gene: WBGene00002247
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WBGene00002247 | SMap | S_parent | Sequence | W03F8 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | lam-1 | Person_evidence | WBPerson1052 | |||||
Sequence_name | W03F8.5 | ||||||||
Molecular_name | W03F8.5a | ||||||||
W03F8.5a.1 | |||||||||
CE47338 | |||||||||
W03F8.5b | |||||||||
CE49160 | |||||||||
W03F8.5b.1 | |||||||||
Other_name | LAMB/1 | ||||||||
CELE_W03F8.5 | Accession_evidence | NDB | BX284604 | ||||||
Public_name | lam-1 | ||||||||
DB_info | Database | AceView | gene | 4F943 | |||||
WormQTL | gene | WBGene00002247 | |||||||
WormFlux | gene | WBGene00002247 | |||||||
NDB | locus_tag | CELE_W03F8.5 | |||||||
Panther | gene | CAEEL|WormBase=WBGene00002247|UniProtKB=O44565 | |||||||
family | PTHR10574 | ||||||||
NCBI | gene | 177292 | |||||||
RefSeq | protein | NM_068333.6 | |||||||
NM_001380214.1 | |||||||||
TrEMBL | UniProtAcc | V6CIX7 | |||||||
O44565 | |||||||||
UniProt_GCRP | UniProtAcc | O44565 | |||||||
OMIM | gene | 150240 | |||||||
150310 | |||||||||
150325 | |||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 07 Apr 2004 11:29:27 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
2 | 30 Jan 2012 16:23:16 | WBPerson1867 | Event | Acquires_merge | WBGene00020998 | ||||
Acquires_merge | WBGene00020998 | ||||||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | lam | ||||||||
Allele (90) | |||||||||
Legacy_information | [C.elegansII] rh219 : resembles Epi-1, basal lamina missing or defective in epidermis, gonad, intestine;abnormal excretory canals, muscle cell positions, sheath cells, proximal gonad, basement membranes, ray morphology. rh219/Df is larval lethal. Cloned: rescued by cosmid C24D10, encodes lamininbeta chain. [NJ] | ||||||||
Strain | WBStrain00037319 | ||||||||
WBStrain00037470 | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00032878 | ||||||||
00032879 | |||||||||
00032880 | |||||||||
00032881 | |||||||||
00032882 | |||||||||
00032883 | |||||||||
00032884 | |||||||||
00032885 | |||||||||
00032886 | |||||||||
Contained_in_operon | CEOP4156 | ||||||||
Ortholog (53) | |||||||||
Paralog | WBGene00001328 | Caenorhabditis elegans | From_analysis | Panther | |||||
WormBase-Compara | |||||||||
WBGene00006787 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00002248 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00018304 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00006432 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00006746 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00016913 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00020581 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
Structured_description | Concise_description | lam-1 encodes a laminin beta that affects degenerin-induced cell death and is required redundantly with lam-2 for morphogenesis. | Paper_evidence | WBPaper00015206 | |||||
WBPaper00023289 | |||||||||
Curator_confirmed | WBPerson48 | ||||||||
Date_last_updated | 17 Jun 2004 00:00:00 | ||||||||
Automated_description | Involved in pharynx development and positive regulation of locomotion. Located in basement membrane. Expressed in intestine. Human ortholog(s) of this gene implicated in several diseases, including Pierson syndrome; amelogenesis imperfecta type 1A; and lung carcinoma (multiple). Is an ortholog of human LAMB1 (laminin subunit beta 1) and LAMB2 (laminin subunit beta 2). | Paper_evidence | WBPaper00065943 | ||||||
Curator_confirmed | WBPerson324 | ||||||||
WBPerson37462 | |||||||||
Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | ||||||||
Date_last_updated | 29 Nov 2023 00:00:00 | ||||||||
Disease_info | Potential_model | DOID:5409 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6490) | ||||
DOID:3908 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6490) | ||||||
DOID:0080380 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6487) | ||||||
DOID:1070 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6487) | ||||||
DOID:12849 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6486) | ||||||
DOID:3209 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6490) | ||||||
DOID:0110054 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6490) | ||||||
DOID:0112230 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6486) | ||||||
DOID:0060852 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6487) | ||||||
Molecular_info | Corresponding_CDS | W03F8.5a | |||||||
W03F8.5b | |||||||||
Corresponding_CDS_history | W03F8.5:wp101 | ||||||||
W03F8.5:wp230 | |||||||||
Corresponding_transcript | W03F8.5a.1 | ||||||||
W03F8.5b.1 | |||||||||
Other_sequence (45) | |||||||||
Associated_feature (11) | |||||||||
Experimental_info | RNAi_result (20) | ||||||||
Expr_pattern | Expr3984 | ||||||||
Expr10827 | |||||||||
Expr1019727 | |||||||||
Expr1031321 | |||||||||
Expr1158236 | |||||||||
Expr1158240 | |||||||||
Expr2013007 | |||||||||
Expr2031239 | |||||||||
Drives_construct | WBCnstr00005458 | ||||||||
WBCnstr00005751 | |||||||||
WBCnstr00006684 | |||||||||
WBCnstr00008702 | |||||||||
WBCnstr00008703 | |||||||||
WBCnstr00008704 | |||||||||
WBCnstr00008752 | |||||||||
WBCnstr00022483 | |||||||||
WBCnstr00024738 | |||||||||
Construct_product | WBCnstr00005458 | ||||||||
WBCnstr00005751 | |||||||||
WBCnstr00008752 | |||||||||
WBCnstr00017755 | |||||||||
WBCnstr00022483 | |||||||||
WBCnstr00022851 | |||||||||
WBCnstr00024738 | |||||||||
Microarray_results (37) | |||||||||
Expression_cluster (203) | |||||||||
Interaction (39) | |||||||||
Anatomy_function | WBbtf0735 | ||||||||
WBbtf0736 | |||||||||
Map_info | Map | IV | Position | 1.55302 | Error | 0.001128 | |||
Positive | Positive_clone (3) | ||||||||
Mapping_data | Multi_point | 4471 | |||||||
5450 | |||||||||
Pseudo_map_position | |||||||||
Reference (28) | |||||||||
Remark | 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 | |||||||
Method | Gene |