Gene
trpm7
- ID
- ZDB-GENE-021115-2
- Name
- transient receptor potential cation channel, subfamily M, member 7
- Symbol
- trpm7 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to enable calcium channel activity and protein kinase activity. Acts upstream of or within several processes, including exocrine pancreas development; swimming behavior; and thigmotaxis. Located in plasma membrane. Is expressed in several structures, including digestive system; immature eye; integument; nervous system; and renal system. Used to study sinoatrial node disease. Human ortholog(s) of this gene implicated in amyotrophic lateral sclerosis-parkinsonism/dementia complex 1. Orthologous to human TRPM7 (transient receptor potential cation channel subfamily M member 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 57 figures from 32 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb495 (20 images)
Wild Type Expression Summary
- All Phenotype Data
- 34 figures from 11 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Allele | Type | Localization | Consequence | Mutagen | Supplier |
---|---|---|---|---|---|
agu75 | Allele with one point mutation | Exon 18 | Unknown | ENU | |
b508 | Allele with one deletion | Unknown | Frameshift, Premature Stop | ENU | |
b722 | unknown | Unknown | Unknown | ENU | |
j124e1 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
j124e2 | unknown | Unknown | Unknown | ENU | |
la013193Tg | Transgenic insertion | Unknown | Unknown | DNA | |
mi174 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
os1 | unknown | Unknown | Unknown | not specified | |
os2 | unknown | Unknown | Unknown | not specified | |
sa36550 | Allele with one point mutation | Unknown | Splice Site | ENU |
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Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 | Alliance | {Amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to} | 105500 |
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Human Disease | Fish | Conditions | Citations |
---|---|---|---|
sinoatrial node disease | WT + MO3-trpm7 | standard conditions | Sah et al., 2013 |
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Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Domain | IPR004166 | Alpha-type protein kinase, alpha-kinase domain |
Domain | IPR005821 | Ion transport domain |
Domain | IPR029601 | Transient receptor potential cation channel subfamily M member 7, alpha-kinase domain |
Domain | IPR032415 | TRPM, tetramerisation domain |
Domain | IPR041491 | TRPM, SLOG domain |
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Domain Details Per Protein
Protein | Additional Resources | Length | Alpha-type protein kinase, alpha-kinase domain | Ion transport domain | Protein kinase-like domain superfamily | Transient receptor potential cation channel M | Transient receptor potential cation channel subfamily M member 7, alpha-kinase domain | TRPM, SLOG domain | TRPM, tetramerisation domain | TRPM, tetramerisation domain superfamily |
---|---|---|---|---|---|---|---|---|---|---|
UniProtKB:Q563W7 | InterPro | 1774 |
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Interactions and Pathways
No data available
Plasmids
No data available
Construct | Regulatory Region | Coding Sequence | Species | Tg Lines | Citations |
---|---|---|---|---|---|
Tg(isl1a-hsp70l:trpm7-EGFP) |
|
| Low et al., 2011 |
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Relationship | Marker Type | Marker | Accession Numbers | Citations |
---|---|---|---|---|
Contained in | Fosmid | CH1073-401P22 | ZFIN Curated Data | |
Encodes | EST | cb495 | Thisse et al., 2001 | |
Encodes | cDNA | MGC:194798 | ZFIN Curated Data |
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Type | Accession # | Sequence | Length (nt/aa) | Analysis |
---|---|---|---|---|
RNA | RefSeq:NM_001030061 (1) | 6259 nt | ||
Genomic | GenBank:CU633784 (1) | 34881 nt | ||
Polypeptide | UniProtKB:Q563W7 (1) | 1774 aa |
- He, X., Wang, Z., Cheng, L., Wang, H., Sun, Y. (2025) An antagonistic role of clock genes and lima1 in kidney regeneration. Communications biology. 8:2929
- Bowley, G., Irving, S., Hoefer, I., Wilkinson, R., Pasterkamp, G., Darwish, H.M.S., White, S., Francis, S.E., Chico, T., Noel, E., Serbanovic-Canic, J., Evans, P.C. (2024) Zebrafish model for functional screening of flow-responsive genes controlling endothelial cell proliferation. Scientific Reports. 14:3013030130
- Ercanbrack, W.S., Dungan, A., Gaul, E., Ramirez, M., J DelVecchio, A., Grass, C., Wingert, R.A. (2024) Frataxin is essential for zebrafish embryogenesis and pronephros formation. Frontiers in cell and developmental biology. 12:14962441496244
- Watai, K., Sadamitsu, K., Wada, S., Kashima, M., Hirata, H. (2024) Zebrafish trpm7 mutants show reduced motility in free movement. Development, growth & differentiation. 66(6):349-356
- Belcher, B., Vestal, J., Lane, S., Kell, M., Smith, L., Camarata, T. (2023) The zebrafish paralog six2b is required for early proximal pronephros morphogenesis. Scientific Reports. 13:1969919699
- Wesselman, H.M., Flores-Mireles, A.L., Bauer, A., Pei, L., Wingert, R.A. (2023) Esrrγa regulates nephron and ciliary development by controlling prostaglandin synthesis. Development (Cambridge, England). 150(10):
- Wesselman, H.M., Gatz, A.E., Pfaff, M.R., Arceri, L., Wingert, R.A. (2023) Estrogen Signaling Influences Nephron Segmentation of the Zebrafish Embryonic Kidney. Cells. 12(4):
- Weaver, N.E., Healy, A., Wingert, R.A. (2022) gldc Is Essential for Renal Progenitor Patterning during Kidney Development. Biomedicines. 10(12):
- Chambers, B.E., Clark, E.G., Gatz, A.E., Wingert, R.A. (2020) Kctd15 regulates nephron segment development by repressing Tfap2a activity. Development (Cambridge, England). 147(23):
- Chambers, J.M., Addiego, A., Flores-Mireles, A.L., Wingert, R.A. (2020) Ppargc1a Controls Ciliated Cell Development by Regulating Prostaglandin Biosynthesis. Cell Reports. 33:108370
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