ZMP
si:ch211-148j1.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate tensin 1 (TNS1) [Source:UniProtKB/TrEMBL;Acc:B0R0Y9]
Human Orthologue:
TNS1
Human Description:
tensin 1 [Source:HGNC Symbol;Acc:11973]
Mouse Orthologue:
Tns1
Mouse Description:
tensin 1 Gene [Source:MGI Symbol;Acc:MGI:104552]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17234 | Nonsense | Available for shipment | Available now |
sa10585 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17234
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 |
---|---|---|---|---|---|
ENSDART00000015159 | Nonsense | 771 | 1769 | 17 | 31 |
ENSDART00000134480 | None | None | 722 | None | 13 |
The following transcripts of ENSDARG00000020845 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 48583144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 47804803 |
GRCz11 | 9 | 47502198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTACTACAATCCCACAGCCTTCCAGAGTTCCCTCAGATGGCATCTCAA[C/T]AAGAGATTGAGCAGTCCATTGAAGCCCTCAAMATGCTGATGCTGGACCTT
Long Flanking Sequence:
ATGGACACAGCAACATAGACAGAGAGACAGATATCCTTGATGATGACTTGCCCATCAGCCAGGAAGGGAACAGTGTGGACAGTCTTGGAACTCTCTCATCTTTTGAGGGCAGAGCCACTCCTGCGGATCTATACTACCAGTCAGAGACAGTCATTAATGGACAAGATATGCCCTACTTAGAGAAGAGTGTCCATGAGAAAATGCTAGAGCCCAGAGTTCACAGCTCATCATCTGTCCAAGAGCACTTGGGAGCCCCTAGTGGGTATGCTAACCAGAATGGCAACATCTATCGATCTCAGTCATTAGGAGCAACCCCGAACACAGACCAGAAGTACATGCCCAAAGCTCCAGCACGCACAACCAGCAGTAGGGATGCCGTGCAGAGACTGAATGTTTGGCAACAATTTGGTGTACCAGAAGTCCCAGTCACAGATGGGGTCACCTTCAACCCTGTACTACAATCCCACAGCCTTCCAGAGTTCCCTCAGATGGCATCTCAA[C/T]AAGAGATTGAGCAGTCCATTGAAGCCCTCAACATGCTGATGCTGGACCTTGATCCAGCACTTACTCAAGTCCCCAAATCCCACAGCGCTCCATCTGGAGAAAGTGGTGTGGTCACCACCCAACCATCTTTCTCTCAAACCCAAGCACGCCCATCCTACCAGGCTGACACTGCTATTCATGACCGCGGTGCGGCCTCTTCAATGGGATTTCCTTTGACCTTTCAACAAGTAACTGGAGAGCCTTCACAACCCACCATGAAACAGCAGAAACCCACAACTACATCCCAGCATGTCGAATTCGCTTCTGAAGCAGGAGGTCAGGCCCCCATGTCCCAGTCCACAGTGCCTTCCTCCACCTTTGGAGTTCTCCAGTTGAAACCCCTCAACATTTATCCCTCAAGTACCACATCCCAGTCCCCCGAGCCTCAGGAGACTCAGCGTAGCTACTCTTCTTCCTCATCCCCTCTTCCCAAAGAGTCTGAACCAGAAGATAGCAGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10585
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015159 | Essential Splice Site | 949 | 1769 | 17 | 31 |
ENSDART00000134480 | None | None | 722 | None | 13 |
The following transcripts of ENSDARG00000020845 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 48582608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 47804267 |
GRCz11 | 9 | 47501662 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGRTAGCAGCTACAAATTGGAGGGTCTTGTAGCTCACCGTGTAGCTGG[T/C]AAGATCAACCTCGAAATACYTTTTTAACAGTCAGTTTWYTTGCTCAYATG
Long Flanking Sequence:
CTGATGCTGGACCTTGATCCAGCACTTACTCAAGTCCCCAAATCCCACAGCGCTCCATCTGGAGAAAGTGGTGTGGTCACCACCCAACCATCTTTCTCTCAAACCCAAGCACGCCCATCCTACCAGGCTGACACTGCTATTCATGACCGCGGTGCGGCCTCTTCAATGGGATTTCCTTTGACCTTTCAACAAGTAACTGGAGAGCCTTCACAACCCACCATGAAACAGCAGAAACCCACAACTACATCCCAGCATGTCGAATTCGCTTCTGAAGCAGGAGGTCAGGCCCCCATGTCCCAGTCCACAGTGCCTTCCTCCACCTTTGGAGTTCTCCAGTTGAAACCCCTCAACATTTATCCCTCAAGTACCACATCCCAGTCCCCCGAGCCTCAGGAGACTCAGCGTAGCTACTCTTCTTCCTCATCCCCTCTTCCCAAAGAGTCTGAACCAGAAGATAGCAGCTACAAATTGGAGGGTCTTGTAGCTCACCGTGTAGCTGG[T/C]AAGATCAACCTCGAAATACCTTTTTAACAGTCAGTTTTCTTGCTCATATGTGCATTTCTGATGGTTTGTTGATCAATAAAAACATGTGCTAACTAGTTAAGACTTTTAACTATTAGGCTGCAATGCTTTATCAGATTTTTTAAATGTAGAAAATGCTAATTGCGTAATTATGTCATTGGAACTATAGTACAGGAATTCATCTCTATGTTTGAGTGCTTAAGCTAAGGTTGTCTTAAAAGCTGCCTTTTACATTGAAGGCGGTGCCTTTTTTGGTGGAGTTTCTTTGTAGTCAATGACAGAAGCACTGTGAGATCACAAAGAAAGCTTTGTCCAAAGTGCTTCTGGCCTAAGCCTCAGTATCAGACCACATTTCTTTTTTTGTGCCAAACCAAAACTGAACATTTGTACATCACATCTGGAAAGATGCCCAAAGAACTGAGGGCTGTTATAGAGCAGTGTACTTTTTTTCTGTTTAAATTATCTGTTCAGCTTAAAAGTTT
Associated Phenotype:
Not determined