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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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zgc:153018
- Ensembl ID:
- ENSDARG00000060977
- ZFIN ID:
- ZDB-GENE-060929-752
- Description:
- hypothetical protein LOC767701 [Source:RefSeq peptide;Acc:NP_001070107]
- Human Orthologue:
- TMEM179
- Human Description:
- transmembrane protein 179 [Source:HGNC Symbol;Acc:20137]
- Mouse Orthologue:
- Tmem179
- Mouse Description:
- transmembrane protein 179 Gene [Source:MGI Symbol;Acc:MGI:2144891]
Alleles
There is 1 allele of this gene:
Allele name | Consequence | Status | Availability Estimate |
---|---|---|---|
sa39014 | Essential Splice Site | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa39014
- Current Status:
-
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs. - Availability:
- We currently estimate that this allele will be available during 2018.
- Mutation:
- A > T
- Consequence:
- Essential Splice Site
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090844 | Essential Splice Site | 108 | 248 | 2 | 4 |
- Genomic Location (Zv9):
- Chromosome 14 (position 48284791)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 14 46357371 GRCz11 14 45344663 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- TATAAAAGGAATAAAATTATTATTTTTTTAATGTTGCCTTCTGTTTATCC[A/T]GCACTCTGTTCTCTGCATTCCTGACACTGCTGCTGAGCTTGTGTGTGCTT
- Associated Phenotype:
- Not determined
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