WormBase Tree Display for Gene: WBGene00011938
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WBGene00011938 | SMap | S_parent | Sequence | T22H6 | ||
---|---|---|---|---|---|---|
Identity (6) | ||||||
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 | T22H6.2a | ||||
T22H6.2b | ||||||
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 | Map | X | Position | 8.39739 | ||
Positive | Positive_clone | T22H6 | Inferred_automatically | From sequence, transcript, pseudogene data | ||
Pseudo_map_position | ||||||
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 |