Gene: C49A1.4
C49A1.4 | Evidence | Person_evidence | WBPerson634 | |||
---|---|---|---|---|---|---|
SMap | S_parent | Sequence | C49A1 | |||
Chromosome | I | |||||
Identity (5) | ||||||
Gene_info | Gene_class | eya | ||||
Allele (7) | ||||||
Strain | VC528 | |||||
Structured_description | Provisional_description | eya-1 encodes a protein orthologous to Drosophila EYES ABSENT (EYA), human EYA1, and human EYA4; the human genes EYA1 and EYA4, when mutated, lead to branchiootorenal dysplasia syndrome (BOR; OMIM:113650) and autosomal dominant nonsyndromic sensorineural (late-onset) deafness (DFNA10; OMIM:601316). | Paper_evidence | WBPaper00004103 | ||
Person_evidence | WBPerson567 | |||||
Curator_confirmed | WBPerson567 | |||||
Date_last_updated | 17 Jun 2004 00:00:00 | |||||
Concise_description | eya-1 encodes a protein orthologous to Drosophila EYES ABSENT (EYA), human EYA1, and human EYA4; the human genes EYA1 and EYA4, when mutated, lead to branchiootorenal dysplasia syndrome (BOR; OMIM:113650) and autosomal dominant nonsyndromic sensorineural (late-onset) deafness (DFNA10; OMIM:601316). | |||||
Molecular_info | Corresponding_CDS | C49A1.4a | ||||
C49A1.4b | ||||||
Corresponding_CDS_history | C49A1.4:wp114 | |||||
Corresponding_protein | WP:CE15722 | |||||
WP:CE36113 | ||||||
KOG | KOG3107 | |||||
Corresponding_PCR_product | smd_C49A1.4 | |||||
sjj_C49A1.4 | ||||||
Corresponding_RNAi_reagent | Cenix:83-c7 | |||||
mv_C49A1.4 | ||||||
Experimental_info (5) | ||||||
Reference | WBPaper00010115 | |||||
WBPaper00025897 | ||||||
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 |