ZMP
zgc:153225
Ensembl ID:
ZFIN ID:
Description:
Protein TSSC4 [Source:UniProtKB/Swiss-Prot;Acc:Q0P4A6]
Human Orthologue:
TSSC4
Human Description:
tumor suppressing subtransferable candidate 4 [Source:HGNC Symbol;Acc:12386]
Mouse Orthologue:
Tssc4
Mouse Description:
tumor-suppressing subchromosomal transferable fragment 4 Gene [Source:MGI Symbol;Acc:MGI:1861712]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40935 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40935
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075263 | None | None | 306 | None | 4 |
ENSDART00000132020 | Essential Splice Site | None | 213 | 1 | 2 |
ENSDART00000133584 | None | None | 248 | None | 4 |
ENSDART00000135237 | None | None | 242 | None | 4 |
ENSDART00000137956 | None | None | 229 | None | 4 |
ENSDART00000140775 | None | None | 234 | None | 4 |
ENSDART00000140800 | None | None | 127 | None | 3 |
ENSDART00000142049 | None | None | 188 | None | 4 |
ENSDART00000145523 | None | None | 205 | None | 4 |
ENSDART00000146789 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 34232858)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32627198 |
GRCz11 | 7 | 32898348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTTTACTGAATGTGAAAGTATCTCCCCAATGTGTGAGTTAAGCAAG[G/A]TGAGTTATGATCAGTAGTTGTCTAACTACGGTTTCTATTTCAGGTTCCAA
Long Flanking Sequence:
ATCGCAACTTGTAACTTGTAATATCTTATGGTATTTTGAGTCATTTGATTAGTCTAGTTTATCATCGCAGATATACGTCATAGTTGCTTTAGCATGTAGCTTCATGCTAGCTGCGTTAAGTTTTCGGTTCATTAACGTTTCATTCTCGCAAATTATTTTAAAAATGCATTGCATGAACCCATGCGAACATTTTTAACTCCGTATGCAGATGTATAAATATTGTTTTTATCCTAACTTTGATAGGAAGAAGAGGACAGAATCGAGACTAAACGCTATGGCCACAACTTTCACCAATACTCCTTACTCAGAACTGACCAGCTCGCATTACCTGTGAGTCTTCAAGCCCAGTAAGATACAGTATGCACCGTAGCATTGTTCTTGATGCATTCTTCAGATTAGCACCATTGTAAACCATGTGACAAACGCAAAACGCATAAGATCTGTAAAAATATTATTTTACTGAATGTGAAAGTATCTCCCCAATGTGTGAGTTAAGCAAG[G/A]TGAGTTATGATCAGTAGTTGTCTAACTACGGTTTCTATTTCAGGTTCCAACAGGTGTCTCAAGAACATTTTGGTGAGTGTGATTACTCATTGCTTTTTTCTCTATGGTTCATGTTGGTTTCTCAAAAAATGGGTATATAATCAAGAACATGCATTTAATTGCACACTAACTTTATTTGGTAGCCTTTGAAGGAACTTTCAGGAAATTGCAGTTTAGTGCATTACTTATTCAAAGACTTCTTAATGTGTTTCTTCTTTAGATCCTTCATTCAGTATCTCAGTATAAATATCCAGCACAATGAGTGACCGAAAGCGCAAAGGCAACGACGCCCCCAACAGTCTGTCTAACAGAGACACTGTTGAACTTCCTGATGATCTCTCCTTGAGCGACTCTGACTCTGATGAGCCCTTAGAGAGTTTCGGTAGAAAAATTGAGGACTTATCCTCGTCCTCAGAGGAGGAAGGCGAGACTCGGCAGCCGGTCCAGTCAGTTCTTCAAGA
Associated Phenotype:
Not determined