7 results for nlp-23

nlp-23

(Caenorhabditis elegans)
Gene
Name: Neuropeptide-Like Protein 23
Synonyms: CELE_T24D8.4, T24D8.4
Source: WB:WBGene00003761
Biotype: protein coding gene
Symbol: nlp-23 (Cel)
Symbol: nlp-23
Gene Synopsis: nlp-23 encodes three predicted neuropeptide-like proteins; in C. elegans, nlp-23 is part of the FRPamide...neuropeptide family that also contains nlp-2 and nlp-22; nlp-23 is expressed in the tail and in dorsal...and ventral hypodermis; as loss of nlp-23 activity via large-scale RNAi screens does not result in any
Cross References: nlp-23...WB:nlp-23...nlp-23

Source: GO:0007218
Synonyms:
  • neuropeptide signalling pathway
Branch: biological process
Genes: nlp-23 (Cel)

(WBcel235)X:2342473A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.2342473A>T
Genes: nlp-23 (Cel), T01B6.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:2342473A>T

(WBcel235)X:2342447C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.2342447C>T
Genes: nlp-23 (Cel), T01B6.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:2342447C>T

(WBcel235)X:2342669T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.2342669T>C
Genes: nlp-23 (Cel), T01B6.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:2342669T>C

(WBcel235)X:2342926G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.2342926G>A
Genes: nlp-23 (Cel), T01B6.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:2342926G>A

(WBcel235)X:2342692G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003284.9:g.2342692G>A
Genes: nlp-23 (Cel), T01B6.1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)X:2342692G>A