Gene
smyhc1
- ID
- ZDB-GENE-030131-271
- Name
- slow myosin heavy chain 1
- Symbol
- smyhc1 Nomenclature History
- Previous Names
-
- smhc1 (1)
- fb18g10
- im:6897999
- wu:fb18g10
- Type
- protein_coding_gene
- Location
- Chr: 24 Mapping Details/Browsers
- Description
- Predicted to enable actin filament binding activity and microfilament motor activity. Acts upstream of or within several processes, including regulation of myofibril size; slow-twitch skeletal muscle fiber contraction; and striated muscle cell development. Predicted to be located in myofibril. Predicted to be part of myosin II complex. Predicted to be active in cytoplasm and myosin filament. Is expressed in cardiovascular system; musculature system; paraxial mesoderm; and somite. Used to study distal arthrogryposis and spondylocarpotarsal synostosis syndrome. Human ortholog(s) of this gene implicated in cardiomyopathy (multiple); congenital heart disease (multiple); distal myopathy 1; heart conduction disease (multiple); and hyaline body myopathy (multiple). Orthologous to human MYH6 (myosin heavy chain 6) and MYH7 (myosin heavy chain 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 110 figures from 52 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:6897999 (37 images)
Wild Type Expression Summary
- All Phenotype Data
- 27 figures from 6 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Allele | Type | Localization | Consequence | Mutagen | Supplier |
---|---|---|---|---|---|
kg179 | Allele with one delins | Unknown | Unknown | CRISPR | |
kg180 | Allele with one deletion | Unknown | Unknown | CRISPR | |
mb16 | Allele with one deletion | Unknown | Unknown | CRISPR | |
mb17 | Allele with one insertion | Unknown | Unknown | CRISPR | |
mb18 | Allele with one delins | Unknown | Unknown | CRISPR | |
sa12384 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
sa24569 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
sa30154 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
sa30155 | Allele with one point mutation | Unknown | Splice Site | ENU | |
sa30156 | Allele with one point mutation | Unknown | Premature Stop | ENU |
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Targeting Reagent | Created Alleles | Citations |
---|---|---|
CRISPR1-smyhc | Cai et al., 2018 | |
CRISPR1-smyhc1 | (2) | |
CRISPR1-smyhc1,smyhc2,smyhc3 | Li et al., 2020 | |
CRISPR2-smyhc | Cai et al., 2018 | |
CRISPR4-smyhc1 | (2) | |
CRISPR5-smyhc1 | Hall et al., 2020 | |
CRISPR6-smyhc1 | Hau et al., 2023 | |
CRISPR7-smyhc1 | Hau et al., 2023 | |
MO1-smyhc1 | N/A | (3) |
MO2-smyhc1 | N/A | (2) |
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Human Disease
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Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Domain | IPR001609 | Myosin head, motor domain-like |
Domain | IPR002928 | Myosin tail |
Domain | IPR004009 | Myosin, N-terminal, SH3-like |
Homologous_superfamily | IPR008989 | Myosin S1 fragment, N-terminal |
Homologous_superfamily | IPR014751 | DNA repair protein XRCC4-like, C-terminal |
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Domain Details Per Protein
Protein | Additional Resources | Length | DNA repair protein XRCC4-like, C-terminal | Kinesin motor domain superfamily | Myosin head, motor domain-like | Myosin, N-terminal, SH3-like | Myosin S1 fragment, N-terminal | Myosin tail | P-loop containing nucleoside triphosphate hydrolase |
---|---|---|---|---|---|---|---|---|---|
UniProtKB:Q508P8 | InterPro | 1938 | |||||||
UniProtKB:A0A0R4INI3 | InterPro | 1938 |
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Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
smyhc1-201
(1)
|
Ensembl | 6,575 nt | ||
mRNA |
smyhc1-202
(1)
|
Ensembl | 6,147 nt | ||
ncRNA |
cu633479.5-201
(1)
|
Ensembl | 762 nt |
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Interactions and Pathways
No data available
Plasmids
Construct | Regulatory Region | Coding Sequence | Species | Tg Lines | Citations |
---|---|---|---|---|---|
Tg(smyhc1:mCherry-CAAX) |
|
| 1 | (3) | |
Tg2(smyhc1:EGFP) |
|
| 1 | (2) | |
TgBAC(smyhc1:EGFP) |
|
| 1 | (8) | |
Tg(smyhc1:EGFP) |
|
| 5 | (26) | |
Tg(smyhc1:GAL4-VP16) |
|
| 1 | Yin et al., 2018 | |
Tg(smyhc1:GCaMP3) |
|
| 1 | (3) | |
Tg(smyhc1:LOX2272-LOXP-Tomato-LOX2272-Cerulean-LOXP-EYFP) |
|
| 1 | Abe et al., 2019 | |
Tg(smyhc1:LY-Tomato) |
|
| 2 | (7) | |
Tg(smyhc1:musk-002-MYC) |
|
| 1 | (3) | |
Tg(smyhc1:musk-003-MYC) |
|
| 1 | (4) |
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Relationship | Marker Type | Marker | Accession Numbers | Citations |
---|---|---|---|---|
Contained in | BAC | CH211-24N20 | ZFIN Curated Data | |
Encodes | EST | fb18g10 | ||
Encodes | EST | IMAGE:6897999 | Thisse et al., 2004 | |
Encodes | cDNA | MGC:194801 | ZFIN Curated Data |
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Type | Accession # | Sequence | Length (nt/aa) | Analysis |
---|---|---|---|---|
RNA | RefSeq:NM_001020507 (1) | 5905 nt | ||
Genomic | GenBank:CU929259 (1) | 140786 nt | ||
Polypeptide | UniProtKB:A0A0R4INI3 (1) | 1938 aa |
No data available
- Donaka, R., Zheng, H., Ackert-Bicknell, C.L., Karasik, D. (2024) Early life lipid overload in Native American Myopathy is phenocopied by stac3 knockout in zebrafish. Gene. 936:149123
- Nemoz-Billet, L., Balland, M., Gilquin, L., Gillet, B., Stévant, I., Guillon, E., Hughes, S., Carpentier, G., Vaganay, E., Sohm, F., Misiak, V., Gonzalez-Melo, M.J., Koch, M., Ghavi-Helm, Y., Bretaud, S., Ruggiero, F. (2024) Dual topologies of myotomal collagen XV and Tenascin C act in concert to guide and shape developing motor axons. Proceedings of the National Academy of Sciences of the United States of America. 121:e2314588121e2314588121
- Hau, H.A., Kelu, J.J., Ochala, J., Hughes, S.M. (2023) Slow myosin heavy chain 1 is required for slow myofibril and muscle fibre growth but not for myofibril initiation. Developmental Biology. 499:47-58
- Luckner, B., Essfeld, F., Ayobahan, S.U., Richling, E., Eilebrecht, E., Eilebrecht, S. (2023) Transcriptomic profiling of TLR-7-mediated immune-challenge in zebrafish embryos in the presence and absence of glucocorticoid-induced immunosuppression. Ecotoxicology and environmental safety. 266:115570115570
- 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):
- Lukowicz-Bedford, R.M., Farnsworth, D.R., Miller, A.C. (2022) Connexinplexity: The spatial and temporal expression of connexin genes during vertebrate organogenesis. G3 (Bethesda). 12(5):
- Zhou, C., Zhao, W., Zhang, S., Ma, J., Sultan, Y., Li, X. (2022) High-throughput transcriptome sequencing reveals the key stages of cardiovascular development in zebrafish embryos. BMC Genomics. 23:587
- Ghilardi, A., Diana, A., Bacchetta, R., Santo, N., Ascagni, M., Prosperi, L., Del Giacco, L. (2021) Inner Ear and Muscle Developmental Defects in Smpx-Deficient Zebrafish Embryos. International Journal of Molecular Sciences. 22(12):
- Hall, T.E., Martel, N., Ariotti, N., Xiong, Z., Lo, H.P., Ferguson, C., Rae, J., Lim, Y.W., Parton, R.G. (2020) In vivo cell biological screening identifies an endocytic capture mechanism for T-tubule formation. Nature communications. 11:3711
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