ZMP
st5
Ensembl ID:
ZFIN ID:
Description:
suppression of tumorigenicity 5 protein [Source:RefSeq peptide;Acc:NP_001002327]
Human Orthologue:
ST5
Human Description:
suppression of tumorigenicity 5 [Source:HGNC Symbol;Acc:11350]
Mouse Orthologue:
St5
Mouse Description:
suppression of tumorigenicity 5 Gene [Source:MGI Symbol;Acc:MGI:108517]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20954 | Nonsense | Available for shipment | Available now |
| sa40902 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20954
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054368 | Nonsense | 127 | 1129 | 3 | 21 |
| ENSDART00000113313 | Nonsense | 127 | 1125 | 3 | 20 |
| ENSDART00000133050 | Nonsense | 127 | 1125 | 2 | 19 |
The following transcripts of ENSDARG00000037363 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 29853184)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 28245707 |
| GRCz11 | 7 | 28516900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAGCCACCAAGTGGTGATAGGCAGGATCAGAAGGAGAATCAGCCACAA[C/T]AGACCCCCCCTATTGGGGATGGATTGAATACTGGACTGCTCAGCTTAAGT
Long Flanking Sequence:
CTTTATATCTAAAAGCTTGTTGCATTACTAGTAGTATGTTGTTGCTTGTCATATTGACTTGTCCTTATTTGAACCCCTTTTGTAGTAATCTTTTTTGATTAGTGTCTTATTCACAGTAACATTATGAGACAAATGATATTTTGCTGTATCAAGCACAAGGGTTTCTTACACTTTGCTCGTTTACTTTGTTTTTTAGGTGTCAATCTGTGTCCCCACCACCAATTCTTACTACTGGAAAAGAGCCAGTTTCCTCTTACCTCAGTGGCAGCGAGGATACCAGTCAGCAAGGAAAGTACGGTAAAGCTGATGCTAAACTCTGGACTCAAAAGAACTGGAGCTGTAAGACTGCCAGCTTGAGAAGTGGCGCCTCGCTCTCCACTGACTTTGAATTTCAAAGCAGGCTGACAAAATCTAGGAGCATTAGCTGTCTGGACAAGAAGCTCACCATCCATAAGCCACCAAGTGGTGATAGGCAGGATCAGAAGGAGAATCAGCCACAA[C/T]AGACCCCCCCTATTGGGGATGGATTGAATACTGGACTGCTCAGCTTAAGTACTACTTCAGTAGGACCTTCTAAGCTTGGGCACAAGCGAACATTCTCACTCAGTCATACAGGGACGTGCACCTCATCAATCGCCATACGCAAAAAGATCTCGCAATGGGAGGGTCGGAAGGAGGCTTTGTCTAGGATGAGCCTTTGCCTTGAGAAGAGGCCTGGAGGTGGGAGCGAGGGTTGCCCAAGCCTGCTGTCCTCACCCTGCAGTGAGACGACCTTTGACTTTAAAGGGGTCAGGAGGATGAGCACGGCATTTTCTGAGTGCTCCTACCCCGAGACTGAGGAAGATGAGCACACATCAGATCGTGAAGCTCCTATAAGGTTCCAGAAGAGGCCTTCAAAGACAGAGTCCTCAGGGATTTTCCTCCGCACATTCTCGGCACGCAAGGAGACCTCAGCCGTGCTCAGCCGCATTCAAAAAATTGAACAAGCCTTGAAGGAAAGTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40902
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054368 | Essential Splice Site | 1086 | 1129 | None | 21 |
| ENSDART00000113313 | Essential Splice Site | 1086 | 1125 | None | 20 |
| ENSDART00000133050 | Essential Splice Site | 1086 | 1125 | None | 19 |
The following transcripts of ENSDARG00000037363 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 29803397)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 28195920 |
| GRCz11 | 7 | 28467113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCTGGATTCATCCAGGACCGGGAGATGAGGAAGTGCAGGGCCAAAGG[T/A]AAACCAATAAAAACAAGACCACTTCTCATCAGATGTGATGTCCTGTTAGC
Long Flanking Sequence:
AATGAAAAGACTTTACAGAGAAAGCAGATTTTATTCCTAACACTAAACATGTTTAGCACCTGTTTTTGCACACTATTAAAATGTGTTCTTCTTAAAGGTTGTGCATTGAACCAGGTTTGGATAAAAAATGTACACGTATATCTAAAAAAGTAAAGTATACTTTGTTGCTTCATTGCCAACGTCTTTACTTTTCAACCAAGATGAAAATGAATCAAATCTAATATTTAATTATGTATAATATTGTCCTTGATTTCAGAGTGCAGCACGTCGTTGAACAGTGTGGTATCGGAGGCCTTCATCCGCTTTTTCCTGGAGACCATTGGCCATTATTCACTGTTTCTCACCCAGGGTGAAAGAGGCGAACGGATCTTCCAGCGCGAACCCTTCCGCAAGTCTGTGGCTTCTAAGAGCATCCGCCGGTTTCTGGGCGTTTTCATGGAGTCTCAGATGTTTGCTGGATTCATCCAGGACCGGGAGATGAGGAAGTGCAGGGCCAAAGG[T/A]AAACCAATAAAAACAAGACCACTTCTCATCAGATGTGATGTCCTGTTAGCATCAGACCGCTGTAATCCACTTTCACATAGGGCTTTTTGAGGTGGGGTGGAGGGTAACGTTTTAAGCTGGCTGGGAGTCGGATCTTTACTGCCACCTTCTGGTTATCAAAAACAATGTTTTTACATTTAGTTTGTAGTGTATATAGTTGAAGTCAGAATTATTAGCCCCTCTTTGATTTTTTTTTTCTTTTGTAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCAAAGTGTGTCTGATAATATTTTTTCCTCTGGAGAAAGTCTTATTTGTTTTACTTAGGCTAGAATAAAAGCAGTTTTTTTTTGTTGTTTTTTTTACTTGCCTAATTACCCTAACCTGCTTAGTCAACCTAATTAACCTAGTTAAGCCTTTAAATGTCATGTTAAGCTGTATTGAAGTGTCTTGAAAAATATCTATTATAATATTATGTACTGTCAT
Associated Phenotype:
Not determined