WormBase Tree Display for Gene: WBGene00011938
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WBGene00011938 | SMap | S_parent | Sequence | T22H6 | |||
---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||
Name | CGC_name | alh-13 | Person_evidence | WBPerson651 | |||
Sequence_name | T22H6.2 | ||||||
Molecular_name | T22H6.2a | ||||||
T22H6.2a.1 | |||||||
CE47944 | |||||||
T22H6.2b | |||||||
CE47964 | |||||||
T22H6.2b.1 | |||||||
Other_name | CELE_T22H6.2 | Accession_evidence | NDB | BX284606 | |||
Public_name | alh-13 | ||||||
DB_info | Database (13) | ||||||
Species | Caenorhabditis elegans | ||||||
History | Version_change (2) | ||||||
Status | Live | ||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | alh | ||||||
Allele (61) | |||||||
Strain | WBStrain00001713 | ||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (27) | |||||||
Ortholog (35) | |||||||
Structured_description | Automated_description | Predicted to enable glutamate-5-semialdehyde dehydrogenase activity. Predicted to be involved in L-proline biosynthetic process and phosphorylation. Located in mitochondrion. Human ortholog(s) of this gene implicated in several diseases, including cutis laxa (multiple); enterocele; and hereditary spastic paraplegia (multiple). Is an ortholog of human ALDH18A1 (aldehyde dehydrogenase 18 family member A1). | 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:0110825 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||
DOID:0110824 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
DOID:0070143 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
DOID:0070131 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
DOID:1283 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
DOID:2476 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
DOID:0070132 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
DOID:83 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9722) | ||||
Molecular_info | Corresponding_CDS (2) | ||||||
Corresponding_CDS_history | T22H6.2:wp42 | ||||||
Corresponding_transcript | T22H6.2a.1 | ||||||
T22H6.2b.1 | |||||||
Other_sequence (56) | |||||||
Associated_feature | WBsf648627 | ||||||
WBsf663444 | |||||||
WBsf663445 | |||||||
WBsf663446 | |||||||
WBsf663447 | |||||||
WBsf1007420 | |||||||
WBsf236510 | |||||||
Experimental_info | RNAi_result | WBRNAi00096926 | Inferred_automatically | RNAi_primary | |||
WBRNAi00090699 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00096927 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00053869 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00035830 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00096986 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00009210 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00026362 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00071636 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr6745 | ||||||
Expr1024987 | |||||||
Expr1035269 | |||||||
Expr1157418 | |||||||
Expr2009302 | |||||||
Expr2027539 | |||||||
Drives_construct | WBCnstr00002537 | ||||||
WBCnstr00030267 | |||||||
Construct_product | WBCnstr00030267 | ||||||
Microarray_results (25) | |||||||
Expression_cluster (248) | |||||||
Interaction (78) | |||||||
Map_info (3) | |||||||
Reference | WBPaper00038341 | ||||||
WBPaper00038491 | |||||||
WBPaper00040958 | |||||||
WBPaper00042257 | |||||||
WBPaper00049828 | |||||||
WBPaper00055090 | |||||||
WBPaper00061842 | |||||||
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 |