ZMP
si:ch211-113e8.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens testis-specific kinase [Source:UniProtKB/TrEMBL;Acc:B7ZDC6]
Human Orthologue:
TESK1
Human Description:
testis-specific kinase 1 [Source:HGNC Symbol;Acc:11731]
Mouse Orthologue:
Tesk1
Mouse Description:
testis specific protein kinase 1 Gene [Source:MGI Symbol;Acc:MGI:1201675]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1979 | Essential Splice Site | F2 line generated | Not yet available |
| sa11795 | Nonsense | Available for shipment | Available now |
| sa32723 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1979
Status:
F2 line generated
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112133 | Essential Splice Site | 251 | 657 | 7 | 10 |
| ENSDART00000140619 | None | None | 75 | None | 2 |
| ENSDART00000146680 | Essential Splice Site | 231 | 259 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 1 (position 40609509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 39498918 |
| GRCz11 | 1 | 40216991 |
KASP Assay ID:
554-2741.1 (used for ordering genotyping assays)
KASP Sequence:
GATTATTGCTCGAATTGAGGCTGACCCAGATATCCTCCCACGGACAGAGG[T/C]ACATACAACTGTACAGCAGAACATGAAGCACAGAATCAGGCTTAGAATCA
Long Flanking Sequence:
TAGCCATTGACATCCATCATAGGAAAAAATAATACAGAACTCAATTCCTACAGATTTCCAGAACTCTTTAAAATGTCTTCTTTTGTTTTTCATCGAAGAAAAAAGTAAGAAATGGAGGGCAATTAAAATATGTCAGAATTATCATCACTATCAATTTTCTAAGACTGTATTCACAATACCTTTCCAAATATAGCCCAAAAATGTATTAAACAGAGGTGTATAACATGTCTAACTTGTCTACAGTGATGGGGTTGAAAAACAACCTTTAGCCGTTGTGGGCTCCCCCTACTGGATGGCTCCAGAAATGTTAAGAGGAGAGCTGTACAATGAGAAGGTATTCTGCCTTTAAAAACTCAGCATTACACTCTTGCTTGTGTGCTTGTGTCACTTTATTTACGCTGTTTTCATATCATAGGTGGATGTCTTTGCATATGGAATAATCCTTTGTGAGATTATTGCTCGAATTGAGGCTGACCCAGATATCCTCCCACGGACAGAGG[T/C]ACATACAACTGTACAGCAGAACATGAAGCACAGAATCAGGCTTAGAATCAAGCAGTGCTTTACCAAATATACAAGCTTTGAGTCAGGCAAATAAGATTTTCTTTGAAATATTATTTTAAAGCTAAATTTAATCAAGGGCAAGTCTTAGACCAGGGGAATCAAACACATGGCTTGCAGGCTGTAAATGCATAGGATAACATGTGAAGCTCCTGAGTACAGATTTTGCAGTATGTGACATTGTGATGTGTAATTAAATTTTGAGAGGTTTATGTCAGTGTACAGTACCATAGGTTATACAGCTGCATAACTAATGTGTTTACTTGATGCAGAAAGTCTGTTGTTTATAGTCTAAAATTGCATTAAATGAAACAAAACTAGTCATAAGTATACTTACAATATACACCCACCAGCCACTTTATTAAGTACACTTTACTAGTAGAGGGTTGGACCTCCTTTTGCCTTCAGAACTGCCCTAATCCTTTGTGGCATGGATTTAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11795
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112133 | Nonsense | 419 | 657 | 10 | 10 |
| ENSDART00000140619 | None | None | 75 | None | 2 |
| ENSDART00000146680 | None | None | 259 | None | 8 |
Genomic Location (Zv9):
Chromosome 1 (position 40604658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 39494067 |
| GRCz11 | 1 | 40212140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGAGCCCAGGGCTTCGAGGACCCCCTCGAAGGTGTCGGTCYCTGCCCTG[C/A]ACCCCTGAACTAGGACGAMAGTTACCCTTCAGAGATCAAGAGGTAGAAGA
Long Flanking Sequence:
TGGGCGACTATATTGTATCTGTAATCCACTGACCTCATTAGTTGTCCATGTCTCACCTGGTTGCCCATTTGTTTGCCTAACAACATTGCTCAGAAAGTTGCCCTGTTTATCATCAGCATTAAATAATTGTTTTCAGTACAGTCAGTTCACAGACAACCAATGCTTGTTGTGATTTCTTCAGAACCCATTGCCATTGACGTCAGCCCATATCGAAGGAGAAGCTCGCCATGCCATCCCTGTGACCAGCGCCTGTCCCGCAGCCAGTCAGATATGCTTCCTCCTGCCACTTCCCCATGTTTAGGCACACCTGCAAGGGTCAACCCATTCTCTCTTCGGCAAGACCTCAACGGTGGCCGCATCAAGCTGTTTGACACCCCTAGCAAATCCGTCATTTCCCTTACCTTTACCCTTCCACCACCTCCAGACCCCTCTGCGTCTCCACCGCTGAGCGGGAGCCCAGGGCTTCGAGGACCCCCTCGAAGGTGTCGGTCCCTGCCCTG[C/A]ACCCCTGAACTAGGACGACAGTTACCCTTCAGAGATCAAGAGGTAGAAGAAGATCGGAGTGAAGAACTGGGCCAGGAAACGAAAGACAAAGAGTTGGAAGGACAACAAGATGCGGTGGAGGACTCAGGCCTGGTTCTGGACTTAGATATGGTGTCTTTAGAACGGGTTGAGGAGGAAGAGGAGGATGAAGAGGTGGAGAAAGAAGGACAAAGTCTCACCGAGCCCATGGACTGCAGTAGCTCACCTGACACGACTGAAGGAAATGTTTCAGGGAAGCGTTTAATCAGCGGATCATCTTATTCCTCGTCCTTGCAGTCCAATGGTTGGGCTACACCCATCTCTAATGGACCACCATTATTACCTCCTCTTCCTCGTTTGGACAATAATAATGGAGTTCTGAGGCCTGGACGTCCATTTGCATGGGTGAGACTGAACGGGTACCGAGGCCCTGCTCCAGAACCTTTACCGCCTACCGAACAAGACGATGTGATTTCGTGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32723
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112133 | Nonsense | 455 | 657 | 10 | 10 |
| ENSDART00000140619 | None | None | 75 | None | 2 |
| ENSDART00000146680 | None | None | 259 | None | 8 |
Genomic Location (Zv9):
Chromosome 1 (position 40604552)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 39493961 |
| GRCz11 | 1 | 40212034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGTGAAGAACTGGGCCAGGAAACGAAAGACAAAGAGTTGGAAGGACAA[C/T]AAGATGCGGTGGAGGACTCAGGCCTGGTTCTGGACTTAGATATGGTGTCT
Long Flanking Sequence:
TTATCATCAGCATTAAATAATTGTTTTCAGTACAGTCAGTTCACAGACAACCAATGCTTGTTGTGATTTCTTCAGAACCCATTGCCATTGACGTCAGCCCATATCGAAGGAGAAGCTCGCCATGCCATCCCTGTGACCAGCGCCTGTCCCGCAGCCAGTCAGATATGCTTCCTCCTGCCACTTCCCCATGTTTAGGCACACCTGCAAGGGTCAACCCATTCTCTCTTCGGCAAGACCTCAACGGTGGCCGCATCAAGCTGTTTGACACCCCTAGCAAATCCGTCATTTCCCTTACCTTTACCCTTCCACCACCTCCAGACCCCTCTGCGTCTCCACCGCTGAGCGGGAGCCCAGGGCTTCGAGGACCCCCTCGAAGGTGTCGGTCCCTGCCCTGCACCCCTGAACTAGGACGACAGTTACCCTTCAGAGATCAAGAGGTAGAAGAAGATCGGAGTGAAGAACTGGGCCAGGAAACGAAAGACAAAGAGTTGGAAGGACAA[C/T]AAGATGCGGTGGAGGACTCAGGCCTGGTTCTGGACTTAGATATGGTGTCTTTAGAACGGGTTGAGGAGGAAGAGGAGGATGAAGAGGTGGAGAAAGAAGGACAAAGTCTCACCGAGCCCATGGACTGCAGTAGCTCACCTGACACGACTGAAGGAAATGTTTCAGGGAAGCGTTTAATCAGCGGATCATCTTATTCCTCGTCCTTGCAGTCCAATGGTTGGGCTACACCCATCTCTAATGGACCACCATTATTACCTCCTCTTCCTCGTTTGGACAATAATAATGGAGTTCTGAGGCCTGGACGTCCATTTGCATGGGTGAGACTGAACGGGTACCGAGGCCCTGCTCCAGAACCTTTACCGCCTACCGAACAAGACGATGTGATTTCGTGTCCAGCCTGCTGTCTGGCCGGCTTCAGCTTCCCTTCCTTGTGCCTGCGTGGAGCTCCTCCATCACGCCGTGGGCCTCCACGAAGACCCTACAGGACCTTTAACGGAGGG
Associated Phenotype:
Not determined