WormBase Tree Display for Gene: WBGene00003778
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WBGene00003778 | SMap | S_parent | Sequence | C15H9 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | CGC_name | nnt-1 | |||||||
Sequence_name | C15H9.1 | ||||||||
Molecular_name | C15H9.1 | ||||||||
C15H9.1.1 | |||||||||
CE08176 | |||||||||
Other_name | CELE_C15H9.1 | Accession_evidence | NDB | BX284606 | |||||
Public_name | nnt-1 | ||||||||
DB_info | Database (13) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 07 Apr 2004 11:29:33 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | nnt | ||||||||
Allele (91) | |||||||||
Strain | WBStrain00001362 | ||||||||
WBStrain00031635 | |||||||||
WBStrain00035473 | |||||||||
WBStrain00035476 | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (12) | |||||||||
Ortholog (32) | |||||||||
Structured_description | Concise_description | nnt-1 encodes a proton-pumping nicotinamide nucleotide transhydrogenase predicted to be mitochondrial. | Paper_evidence | WBPaper00004424 | |||||
WBPaper00005552 | |||||||||
Curator_confirmed | WBPerson567 | ||||||||
Date_last_updated | 17 Jun 2004 00:00:00 | ||||||||
Automated_description | Predicted to enable NAD(P)+ transhydrogenase activity and NADP binding activity. Predicted to be involved in NADPH regeneration. Located in mitochondrion. Expressed in ganglia; intestine; pharyngeal-intestinal valve; and somatic nervous system. Human ortholog(s) of this gene implicated in familial glucocorticoid deficiency. Is an ortholog of human NNT (nicotinamide nucleotide transhydrogenase). | 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:0080620 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7863) | ||||
Molecular_info | Corresponding_CDS | C15H9.1 | |||||||
Corresponding_transcript | C15H9.1.1 | ||||||||
Other_sequence (79) | |||||||||
Associated_feature | WBsf662865 | ||||||||
WBsf662866 | |||||||||
WBsf1005484 | |||||||||
WBsf1005485 | |||||||||
WBsf1023060 | |||||||||
WBsf235801 | |||||||||
WBsf235802 | |||||||||
WBsf235803 | |||||||||
Experimental_info (9) | |||||||||
Map_info | Map | X | Position | -3.68202 | Error | 0.025708 | |||
Positive | Positive_clone | C15H9 | Inferred_automatically | From CDS info | |||||
From sequence, transcript, pseudogene data | |||||||||
Mapping_data | Multi_point | 4540 | |||||||
Pseudo_map_position | |||||||||
Reference (13) | |||||||||
Remark | Sequence connection from [Arkblad E]. krb 13/11/01 | ||||||||
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 |