ZMP
tlk1a
Ensembl ID:
ZFIN ID:
Description:
Tousled-like kinase 1 [Source:UniProtKB/TrEMBL;Acc:B8A5H2]
Human Orthologue:
TLK1
Human Description:
tousled-like kinase 1 [Source:HGNC Symbol;Acc:11841]
Mouse Orthologue:
Tlk1
Mouse Description:
tousled-like kinase 1 Gene [Source:MGI Symbol;Acc:MGI:2441683]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16145 | Nonsense | Available for shipment | Available now |
sa41339 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16145
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 |
---|---|---|---|---|---|
ENSDART00000062265 | Nonsense | 232 | 730 | 10 | 22 |
ENSDART00000102892 | Nonsense | 219 | 332 | 10 | 12 |
ENSDART00000123074 | Nonsense | 232 | 730 | 11 | 23 |
ENSDART00000130861 | Nonsense | 219 | 333 | 10 | 12 |
ENSDART00000147650 | None | None | 131 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 3586449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 3618470 |
GRCz11 | 9 | 3589999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCTGTTCTCCRCAGGCAAACTGTGATCTTAGGAGACAAATTGACGAA[C/T]AACARAAGCTTCTAGAAAAATACAAGGAACGTTTAAACAAGTGCATCACT
Long Flanking Sequence:
ATAACTGATTTATTTAATCTTTGCCATGTTGACAGTATATAATATTTTACTATATATTTTTTGAGATACTAGTATTCAGCTTAATGTGACGTTTAAAGGCCTAACTAGGTTAATTAAGGTGAAGGAAGGGTAATTAGGCAAGTTATTGTATAACAGTGGTTTGTTTTGTAGACAATCAAAAAAAATATTGCTTAAGGGGACTAATAATATTGACCTTAAAATTATTATTATTTTTTTTATTAAAACTGCTTTTATTCTAGTCGAACTAAAACAAATTAGACTTTCTCCAGAAGAAAAAAATGTTATAGGAAATACTAGTAAAAAATTCCTCGCTCTGTTAAACATCATTCGGGAAATATTTGAAAAAGAAAGAAATTTACAGGACGGCGAATCATTTTGACTTCAACTGTATGTGTATATTTTTTCCAAGTGTTTTAATAAATATAAACCCTCTCTGTTCTCCGCAGGCAAACTGTGATCTTAGGAGACAAATTGACGAA[C/T]AACAGAAGCTTCTAGAAAAATACAAGGAACGTTTAAACAAGTGCATCACTATGAGCAAGAAGCTTCTGATTGAGAAGGTAATTGCGAGGTTTGAATGTGAGATGTAATGTGTGTTTAAAAGTGCTTTGACTCCTCTAAAGCATAAAAATACCATAATATGTTTGCAGATATTTAAGAAACATGCTAAGTGAAAATGCTTGTTTATCTGAAAAACTGCTGAAGTCAGATATTCTGCCTTGAAAATGTGCTTTACGTGCTGGAACGTATTTTTTTTTTGTTTTGGTCATTTAACCCACCCAATGCCAGTTTAGCCAATTGTATTTCAGCACTCCGGGTTGCCTTGGTGCAAAACCGCTTATTTCATTCATTTAGTCATAAAGGCTCTCACAGTAGGCATCCGTGACCGAAATGCGACCTCTGGTAGACAGTAGCAGCCTCCGAAATGAGATTCAGAGTTCCACATGAGGTGGTTATTAATTAGCAAATAATAAAAATATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41339
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 |
---|---|---|---|---|---|
ENSDART00000062265 | Nonsense | 404 | 730 | 14 | 22 |
ENSDART00000102892 | None | None | 332 | None | 12 |
ENSDART00000123074 | Nonsense | 404 | 730 | 15 | 23 |
ENSDART00000130861 | None | None | 333 | None | 12 |
ENSDART00000147650 | None | None | 131 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 3593606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 3625627 |
GRCz11 | 9 | 3597156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGAGGAGGCAGAGATTCAGGCCGAGCTGGAGAGGTTGGAGAGGGTG[C/T]GAAATCTCCACATCCGGGAGTTGAAAAGAATAAACAATGAAGACAGCTCA
Long Flanking Sequence:
TGATTAGTAAAAATACTTTAAATATATTTTGACCCCTTTACAATATGTATTTCAATATTTCATTGATTAGAAAAATCAATAAATTATAGATATTTTGGAAGTTTACTATTGTATATATTTCAATATTTAATTTTTAATTTGTAATATTCATTGCTAAGCACTTCAACAGCTTTAAAAGGTGGTTTGATAAATATTTAATTTTATTTCTTGTGACTTTAGATTTTAAATATTTAAATAATTGCGTCCCAGCCTAATATTCTCTTACCCTAATAACCACACACAGATGGAACGCTGAATTATTTTACATTTCATATGATGTAAAAATAGTCATTTCAAAAGATTTACCTTTGATTGGTTTTGTGGTTCAGTGTCTCCAAATACATGTTTTCTGCTCAAGAAAGATTTGACAACTATATAAGTACAGTCAAACGAATACAATTTCTGTATGTTTGAAGGAGGAGGCAGAGATTCAGGCCGAGCTGGAGAGGTTGGAGAGGGTG[C/T]GAAATCTCCACATCCGGGAGTTGAAAAGAATAAACAATGAAGACAGCTCACAGTATGTACTCAGACTCTGACCACATCTGCCTCTGATCTTTATTTATCTCTTCTTTTATCATGCATCACATGTACTGGACATTGAGTACTTTTACATGGACCACCTCAATGTCATTATAATGGGGTTTTGGCAATATGATGATTCAACTTTACCTCATGTAAATGCAATAATTTGATATAAATAATGCGAGTAAGCTCATAATTGTATTAACGTAGGTGTCTTATGCTGATTTAAATGGAATTATTGATTTTGGCAATATAGTGATTTAAAATTGACCTAATGTAAACACAATTTACTATAAATAATGCGAGTAAGCTTATAATCATATTGACATAAGTGCCGTTCGTTGATTTTAATCTAAATATTCATTTTGGCAATATAGCAATTTAAACTACCTCATGAAAACGCAACAGTTTGATATAAATAGTGCGAGTAAGCGCATTATCGC
Associated Phenotype:
Not determined