WormBase Tree Display for Gene: WBGene00020382
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WBGene00020382 | SMap | S_parent | Sequence | T09B4 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | Sequence_name | T09B4.8 | |||||||
Molecular_name | T09B4.8 | ||||||||
T09B4.8.1 | |||||||||
CE33176 | |||||||||
Other_name | CELE_T09B4.8 | Accession_evidence | NDB | BX284601 | |||||
Public_name | T09B4.8 | ||||||||
DB_info | Database | AceView | gene | 1G742 | |||||
WormQTL | gene | WBGene00020382 | |||||||
WormFlux | gene | WBGene00020382 | |||||||
NDB | locus_tag | CELE_T09B4.8 | |||||||
Panther | gene | CAEEL|WormBase=WBGene00020382|UniProtKB=O02158 | |||||||
family | PTHR45688 | ||||||||
NCBI | gene | 172301 | |||||||
RefSeq | protein | NM_059376.11 | |||||||
TREEFAM | TREEFAM_ID | TF105945 | |||||||
TrEMBL | UniProtAcc | O02158 | |||||||
UniProt_GCRP | UniProtAcc | O02158 | |||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:31:03 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Allele (22) | |||||||||
Strain | WBStrain00001402 | ||||||||
WBStrain00002393 | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00026651 | ||||||||
00026652 | |||||||||
00026653 | |||||||||
00026654 | |||||||||
00026655 | |||||||||
00026656 | |||||||||
00125016 | |||||||||
00125017 | |||||||||
Ortholog (37) | |||||||||
Paralog | WBGene00001794 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||||
WBGene00015814 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
WBGene00020139 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
Structured_description | Automated_description | Predicted to enable alanine-glyoxylate transaminase activity. Predicted to be involved in L-alanine catabolic process, by transamination and glyoxylate catabolic process. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in several diseases, including artery disease (multiple); atrial fibrillation; and mild cognitive impairment. Is an ortholog of human AGXT2 (alanine--glyoxylate aminotransferase 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:6000 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||
DOID:3669 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||||
DOID:3526 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||||
DOID:0080832 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||||
DOID:0060224 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||||
DOID:3393 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||||
DOID:10763 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14412) | ||||||
Molecular_info | Corresponding_CDS | T09B4.8 | |||||||
Corresponding_CDS_history | T09B4.8:wp92 | ||||||||
Corresponding_transcript | T09B4.8.1 | ||||||||
Other_sequence (32) | |||||||||
Associated_feature | WBsf649221 | ||||||||
WBsf983849 | |||||||||
WBsf983850 | |||||||||
WBsf1009909 | |||||||||
WBsf219546 | |||||||||
WBsf219547 | |||||||||
WBsf219548 | |||||||||
Experimental_info | RNAi_result | WBRNAi00084404 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00024105 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00023307 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00004184 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00084382 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00023583 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00052937 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00117093 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00023817 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00033469 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Chronogram880 | ||||||||
Chronogram1492 | |||||||||
Expr6648 | |||||||||
Expr6649 | |||||||||
Expr1015137 | |||||||||
Expr1038883 | |||||||||
Expr1156538 | |||||||||
Expr2006034 | |||||||||
Expr2024249 | |||||||||
Drives_construct | WBCnstr00002292 | ||||||||
WBCnstr00004293 | |||||||||
WBCnstr00025177 | |||||||||
Construct_product | WBCnstr00025177 | ||||||||
Microarray_results (17) | |||||||||
Expression_cluster (199) | |||||||||
Interaction (116) | |||||||||
Map_info | Positive | Positive_clone | T09B4 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | I | 0.850703 | |||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00055090 | |||||||||
WBPaper00064339 | |||||||||
WBPaper00065140 | |||||||||
Method | Gene |