Module
- Number
- 106
- Regulatory Genes
- 4
- Module Genes
- 16
Regulatory Genes
Public Gene Name | Sequence Name | WB ID | Weight | Description | Actions |
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K10B3.5 | K10B3.5 | WBGene00019611 | 881 | View | |
C04F5.9 | C04F5.9 | WBGene00015451 | 239 | View | |
B0261.1 | B0261.1 | WBGene00015091 | 108 | View | |
gpa-17 | Y71H2B.7 | WBGene00022196 | 105 |
gpa-17 encodes a divergent Gq alpha subunit paralogous to EGL-30; gpa-17 is reported to be expressed in intestine, but has no known function in vivo.
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CLR Predictions
13 are found.Module Genes
Public Gene Name | Sequence Name | WB ID | Description | Actions |
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asm-1 | B0252.2 | WBGene00000211 |
asm-1 encodes a protein similar to human acid sphingomyelinase (ASM) or sphingomyelin phosphodiesterase; the ASM-1 protein has a putative secretory signal peptide at the N-terminus, saposin-like and proline-rich domains and putative N-linked glycosylation sites; asm-1 shows phosphodiesterase activity when expressed in COS-7 cells; while mammalian ASM is detected as both intracellular and secreted forms, asm-1 was detected exclusively in the secreted form; northern blot analysis indicates that asm-1 is expressed at higher levels in the embryo compared with other stages.
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C01G10.9 | C01G10.9 | WBGene00007236 | View | |
C29F7.2 | C29F7.2 | WBGene00007811 | View | |
cyn-6 | F42G9.2 | WBGene00000882 |
cyn-6 encodes a cyclophilin most similar to human secreted cyclophilin type B isoforms that is functional when expressed in E. coli; it is expressed in the intestine.
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cyp-29A2 | T19B10.1 | WBGene00011830 | View | |
F01G10.7 | F01G10.7 | WBGene00008510 | View | |
F07A11.5 | F07A11.5 | WBGene00008548 | View | |
F37C4.6 | F37C4.6 | WBGene00018146 | View | |
F53H8.3 | F53H8.3 | WBGene00018779 | View | |
fmo-5 | H24K24.5 | WBGene00001480 |
fmo-5 encodes a flavin-containing monoxygenase homologous to human FMO1, FMO2, and FMO3 (OMIM:602079, mutated in trimethylaminuria).
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gana-1 | R07B7.11 | WBGene00011095 |
gana-1 encodes a protein with homology to both human alpha-galactosidase (alpha-GAL) and alpha-N-acetylgalactosaminidase (alpha-NAGA) enzymes; these dual enzymatic activities were detected in mixed culture homogenates; immunofluorescence studies show cytoplasmic expression of GANA-1 in body wall muscle and intestinal cells and in coelomocytes; the human gene alpha-galactosidase B (GALB; OMIM:104170), when mutated leads to Schindler disease, Kanzaki disease, or NAGA deficiency.
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T01H8.2 | T01H8.2 | WBGene00011353 | View | |
T09B4.8 | T09B4.8 | WBGene00020382 | View | |
T22H6.2 | T22H6.2 | WBGene00011938 | View | |
Y105C5B.9 | Y105C5B.9 | WBGene00013650 | View | |
ZC373.1 | ZC373.1 | WBGene00013866 |
The ZC373.1 gene encodes an ortholog of the human gene CYSTATHIONINE-BETA-SYNTHASE (CBS), which when mutated leads to homocystinuria (OMIM:236200).
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