WormBase Tree Display for Gene: WBGene00011437
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WBGene00011437 | SMap | S_parent | Sequence | T04F3 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | smoc-1 | |||||||
Sequence_name | T04F3.2 | ||||||||
Molecular_name | T04F3.2 | ||||||||
T04F3.2.1 | |||||||||
CE06357 | |||||||||
Other_name | susm-1 | ||||||||
CELE_T04F3.2 | Accession_evidence | NDB | BX284605 | ||||||
Public_name | smoc-1 | ||||||||
DB_info | Database | AceView | gene | 5M239 | |||||
WormQTL | gene | WBGene00011437 | |||||||
WormFlux | gene | WBGene00011437 | |||||||
NDB | locus_tag | CELE_T04F3.2 | |||||||
Panther | gene | CAEEL|WormBase=WBGene00011437|UniProtKB=Q22157 | |||||||
family | PTHR12352 | ||||||||
NCBI | gene | 179609 | |||||||
RefSeq | protein | NM_073563.4 | |||||||
TrEMBL | UniProtAcc | Q22157 | |||||||
UniProt_GCRP | UniProtAcc | Q22157 | |||||||
OMIM | gene | 608488 | |||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:52 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
2 | 11 Dec 2018 16:50:34 | WBPerson1983 | Name_change | CGC_name | smoc-1 | ||||
Other_name | susm-1 | ||||||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | smoc | ||||||||
Allele (30) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00118702 | ||||||||
Ortholog (39) | |||||||||
Structured_description | Automated_description | Predicted to enable calcium ion binding activity. Expressed in hypodermis; pharyngeal-intestinal valve cell; and pharynx. Human ortholog(s) of this gene implicated in microphthalmia with limb anomalies. Is an ortholog of human SMOC1 (SPARC related modular calcium binding 1) and SMOC2 (SPARC related modular calcium binding 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:0060861 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:20318) | ||||
Molecular_info | Corresponding_CDS | T04F3.2 | |||||||
Corresponding_transcript | T04F3.2.1 | ||||||||
Other_sequence | Dviv_isotig18039 | ||||||||
Acan_isotig12194 | |||||||||
Oden_isotig25710 | |||||||||
Dviv_isotig18040 | |||||||||
Associated_feature | WBsf718410 | ||||||||
WBsf1001435 | |||||||||
WBsf1001436 | |||||||||
WBsf1020499 | |||||||||
WBsf232540 | |||||||||
WBsf232541 | |||||||||
Experimental_info | RNAi_result | WBRNAi00052397 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00089144 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00018142 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00035142 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr14587 | ||||||||
Expr1026221 | |||||||||
Expr1035035 | |||||||||
Expr1156020 | |||||||||
Expr2005822 | |||||||||
Expr2024039 | |||||||||
Drives_construct | WBCnstr00030656 | ||||||||
WBCnstr00040362 | |||||||||
WBCnstr00040363 | |||||||||
Construct_product | WBCnstr00030656 | ||||||||
WBCnstr00040362 | |||||||||
WBCnstr00040365 | |||||||||
Microarray_results (20) | |||||||||
Expression_cluster (111) | |||||||||
Interaction | WBInteraction000571200 | ||||||||
WBInteraction000571203 | |||||||||
WBInteraction000586815 | |||||||||
WBInteraction000586816 | |||||||||
WBInteraction000586817 | |||||||||
WBInteraction000586818 | |||||||||
Map_info | Map | V | Position | 3.32874 | |||||
Positive | Positive_clone | T04F3 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Pseudo_map_position | |||||||||
Reference | WBPaper00030887 | ||||||||
WBPaper00038491 | |||||||||
WBPaper00055090 | |||||||||
WBPaper00062831 | |||||||||
WBPaper00066003 | |||||||||
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 |