ZMP
tlk2
Ensembl ID:
ZFIN ID:
Description:
Serine/threonine-protein kinase tousled-like 2 [Source:UniProtKB/Swiss-Prot;Acc:Q1ECX4]
Human Orthologue:
TLK2
Human Description:
tousled-like kinase 2 [Source:HGNC Symbol;Acc:11842]
Mouse Orthologue:
Tlk2
Mouse Description:
tousled-like kinase 2 (Arabidopsis) Gene [Source:MGI Symbol;Acc:MGI:1346023]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14440 | Nonsense | Available for shipment | Available now |
sa45138 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26040 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10364 | Nonsense | Available for shipment | Available now |
sa18506 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14440
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 |
---|---|---|---|---|---|
ENSDART00000006490 | Nonsense | 124 | 697 | 7 | 21 |
ENSDART00000141937 | Nonsense | 124 | 697 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 19584931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19547966 |
GRCz11 | 3 | 19697706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRTTGATGGTAAATAGAAATGTTTGTTTTGGTTTTGATTGACAGGWGCAG[C/T]AAGGAAGCCCCTCCTCCATCAGTTCAGTAAACACAGAYCACTCCCACACC
Long Flanking Sequence:
AACCAGTTCTGTTAAGTAAATCGATCAGCTCTCTTAGTAACACTTTGTTTGTTGTTCCTTTGTACCAAAAGTGTTACAGTTTTAAAAGTAAACATTCCAAGTGGAACCAAACATTGCACTTGCTAAGAGTAATTCGTTTATGGTGATGAGAGTTGGTAAGAAAAAAACAGTACATCGGGACACATGTAGATTGTATTAGATTATATATTGAAGTTGATGCCTTTAAACAGAGGCCAATAACCTCTTCTTACTCTAGTTTAAGTAGTTTAGTACTGACAATATAATCGTAGATTTATATTTTGTACTCACATAATGACAATAGCTACTTTAATATATTAATAATAATAATAATAAGAAGAAGAAGAACAAACATAAGAAGCAGACTGATTTGAAGTACAGAAAACTGACAGAAGTGCACAATGAGGCTCTTATCAGTGACACTTACTGTTTTGTTGATGGTAAATAGAAATGTTTGTTTTGGTTTTGATTGACAGGTGCAG[C/T]AAGGAAGCCCCTCCTCCATCAGTTCAGTAAACACAGACCACTCCCACACCTCCACCTCCCACAAGCCAGCCTCAATACACACTCAGCACCGAGCTTCACAGGTAACACACACTACCAAAAGCACTCGCAACACACAGATGCTTTCACTTTCTCACACTTAACACTCACCTTCGGTTACTGTTTCCTCAGTCTGAGCTGACTATGGAGAAATTAGCAGCGCTGGAGAGCAGTAAGAGTTCAGATCTGGAGAAGAAAGAAGGACGTATCGATGACCTGCTCAGGGTATGACTTCAATTTAGCCTATTGTCTGAAAGTTTATGTTGATTGTTTCTCATTGCTTCATGTTCAAACAGCAAATCATTTTAGGATGTTTAACTCGTATTAAGAGTAATGCTGCTGATTATTCAGCTTTGTGTGACAGGATAAAATTGTATCATATATGAGTAATTCAATGCAAATGTCAACCTTTCCATTTAAAAAAAAAAAAGGTTAATATAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45138
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006490 | Essential Splice Site | 225 | 697 | 9 | 21 |
ENSDART00000141937 | Essential Splice Site | 225 | 697 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 19589510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19552545 |
GRCz11 | 3 | 19702285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCCTCAATAAATGTGTGACCATGAGTAAGAAACTGCTTATCGAAAAGG[T/C]AAACAGATTTTGCTTAGTATTGTTCTTTATGTATGCCGCATTCTTTAATT
Long Flanking Sequence:
GTAAACACAAGACACCTCCTCCATGGGACTCCACACTTGTAAACACTCGCATCAACAGGCTCTTCACACCACCCACGTGTGTCAACACTACCAAACCGACTAATCACAGAGCTAGCACCACGCGTCTTCGCAACTTGCAGTTAAATTTTTTAAGAGGTGCGTGGGTATGCGACCGCCCGAAGACTTTGCTAGACCTTCCTTAACAAAGCGGGGTCACGTGACCCCACACACAGTAGGCAAAATAATCGATAAAATCAACCTGGGAAAATTTGATCGATTATAGTTTCTGAATTTTGATTATTTTTCCATTAATAATGCTTTGCTGAATTCATTAATTTCCATTTCGTGCTTTGCTGAAGAATACAATGTTTGGGTTTGTGCACTTCAGGTGAACTGTGACCTGCGCAGACAGATCGATGAGCAGCAGAAGATGCTGGAGTGGTGTAAAGAACGCCTCAATAAATGTGTGACCATGAGTAAGAAACTGCTTATCGAAAAGG[T/C]AAACAGATTTTGCTTAGTATTGTTCTTTATGTATGCCGCATTCTTTAATTCGATATTTTTTAAAAAAATGCACAGCTATATTATTTGAAGCACTGCATTTAGTGTCTATGGGGTATGTCTTCAGTAATGTGCTAGTGTGTGTGTCTCAGTCCAAACAGGAGAAAATTGCTTGCAGAGAAAAGAGCATGCAGGACCGACTACGACTTGGTCATTTCACCACTGTACGACACGGAGCCTCATTTACAGAGCAGTGGACGGATGGATATGCGTTTCAGAATCTAGTCAAGTACGTGAGTTGCACATGCTCATGCTTTAGAGGCTAGTTAAATGCTGCATGCATGCACACTGGACAAACATTAGCCATGAAAGCCTTATTCAGGACTGTGTTCTGGTATGATGGTGAATCAATGCAGTGCATTCAGAATGTAACAGGGCGCTAACATGCACACTGACTTTCCATGGACTTTTTTTTTTTTTTTCTTTTTTTATGAAGTCAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26040
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 |
---|---|---|---|---|---|
ENSDART00000006490 | Nonsense | 243 | 697 | 10 | 21 |
ENSDART00000141937 | Nonsense | 243 | 697 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 19589711)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19552746 |
GRCz11 | 3 | 19702486 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAACAGGAGAAAATTGCTTGCAGAGAAAAGAGCATGCAGGACCGACTA[C/T]GACTTGGTCATTTCACCACTGTACGACACGGAGCCTCATTTACAGAGCAG
Long Flanking Sequence:
AACAAAGCGGGGTCACGTGACCCCACACACAGTAGGCAAAATAATCGATAAAATCAACCTGGGAAAATTTGATCGATTATAGTTTCTGAATTTTGATTATTTTTCCATTAATAATGCTTTGCTGAATTCATTAATTTCCATTTCGTGCTTTGCTGAAGAATACAATGTTTGGGTTTGTGCACTTCAGGTGAACTGTGACCTGCGCAGACAGATCGATGAGCAGCAGAAGATGCTGGAGTGGTGTAAAGAACGCCTCAATAAATGTGTGACCATGAGTAAGAAACTGCTTATCGAAAAGGTAAACAGATTTTGCTTAGTATTGTTCTTTATGTATGCCGCATTCTTTAATTCGATATTTTTTAAAAAAATGCACAGCTATATTATTTGAAGCACTGCATTTAGTGTCTATGGGGTATGTCTTCAGTAATGTGCTAGTGTGTGTGTCTCAGTCCAAACAGGAGAAAATTGCTTGCAGAGAAAAGAGCATGCAGGACCGACTA[C/T]GACTTGGTCATTTCACCACTGTACGACACGGAGCCTCATTTACAGAGCAGTGGACGGATGGATATGCGTTTCAGAATCTAGTCAAGTACGTGAGTTGCACATGCTCATGCTTTAGAGGCTAGTTAAATGCTGCATGCATGCACACTGGACAAACATTAGCCATGAAAGCCTTATTCAGGACTGTGTTCTGGTATGATGGTGAATCAATGCAGTGCATTCAGAATGTAACAGGGCGCTAACATGCACACTGACTTTCCATGGACTTTTTTTTTTTTTTTCTTTTTTTATGAAGTCAGTTTTGAAATGTTATCAAAAATAGATTCTAATGATGAGTTCACACCAAAGTGCACTTTTGCTTTACATTATTTGTGGGATGTTTTTTAGTCTTTAAAGTATTTATGCTCAAGTTTATTATTTTTACTTGTGTGAAAGAAACATAACACCATAACAAATAACACCAGTTTGTTCACGGGGTAATGCATATTAATGTCTTAAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10364
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006490 | Nonsense | 441 | 697 | 16 | 21 |
ENSDART00000141937 | Nonsense | 441 | 697 | 15 | 20 |
ENSDART00000006490 | Nonsense | 441 | 697 | 16 | 21 |
ENSDART00000141937 | Nonsense | 441 | 697 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 19597290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19560325 |
GRCz11 | 3 | 19710065 |
KASP Assay ID:
2259-3305.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTACTAAAATGTTTCTTGACATGTTTTTAGGCATGCCTGTCGAGAATA[T/A]AGAATCCATAAAGAGCTGGACCATCCCAGAATAGTCAAAYTGTATGACTA
Long Flanking Sequence:
TTTAAACTTTAAAGTGAAGTACAACAGTTTTAGAAATGTTCCAATGAGCTGTTTTTACAACAGCCATAAATGCACTTGATAAAGCCGTGAAACAATGTCTTGAATTACATAATACGATTAATGCATACTTGGATTGTCTGTTTCTCTTTAAATGAAAATGAAATTTTTATGTATTGTGCACTTTCTCTTTTATTGGTGTTTTATTTATTATTTATTGTATACATTCTGATTTGTTCCTCACTTTTAATATAGGATATATTTTGGATTTAGGGTCAAATCTGACTGTACTTGCATTTAATATAAAAAGGTCACTGATCTGGTTTTTCTGTAAATGAATAAGATAAGGGTTTCAAAGATTTTTTTGTGACCTGCTATGTTTTCCCATAGCATTTCCTTACTTCACATATGATCTTTTTATTTTATTCAAGCCTTCTTGAGGTCTTTTGTTAATGTTACTAAAATGTTTCTTGACATGTTTTTAGGCATGCCTGTCGAGAATA[T/A]AGAATCCATAAAGAGCTGGACCATCCCAGAATAGTCAAACTGTATGACTACTTTTCCCTGGATACTGACTCGTGAGTGAACTTGCCCTCATGTTATTGAAAAGTGTACAATTTATACTTTTTCCCATTTCAAGACCCTCGTTTTGACCAATTTTTAGGATTTTAACTGAAATATTTTATGAACTTTTATGCATTGATGCATTTCTGTTATGTCACTGTGTAACGTGGACTGCTGAGAAAGTTGTTCTAATGCTTTGTAGATTCTGCACTGTTCTGGAGTACTGCGAGGGAAACGATCTGGATTTCTACCTGAAGCAGCACAAGTTAATGTCAGAAAAAGAGGCCCGGTCCATCATAATGCAGGTCGTCAATGCCCTCAAGTACCTAAATGAAATCCGCCCGCCGATCATCCATTACGACCTCAAACCAGGTCAGACACCAGTTGATCCACGTCCCAATGAACTCTTCTGTACAATGCTGAGCATGACAGCTAGCACCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18506
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006490 | Nonsense | 441 | 697 | 16 | 21 |
ENSDART00000141937 | Nonsense | 441 | 697 | 15 | 20 |
ENSDART00000006490 | Nonsense | 441 | 697 | 16 | 21 |
ENSDART00000141937 | Nonsense | 441 | 697 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 19597290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19560325 |
GRCz11 | 3 | 19710065 |
KASP Assay ID:
2259-3305.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTACTAAAATGTTTCTTGACATGTTTTTAGGCATGCCTGTCGAGAATA[T/A]AGAATCCAKAAAGAGCTGGACCATCCCAGAATAGTCAAAYTGTATGACTA
Long Flanking Sequence:
TTTAAACTTTAAAGTGAAGTACAACAGTTTTAGAAATGTTCCAATGAGCTGTTTTTACAACAGCCATAAATGCACTTGATAAAGCCGTGAAACAATGTCTTGAATTACATAATACGATTAATGCATACTTGGATTGTCTGTTTCTCTTTAAATGAAAATGAAATTTTTATGTATTGTGCACTTTCTCTTTTATTGGTGTTTTATTTATTATTTATTGTATACATTCTGATTTGTTCCTCACTTTTAATATAGGATATATTTTGGATTTAGGGTCAAATCTGACTGTACTTGCATTTAATATAAAAAGGTCACTGATCTGGTTTTTCTGTAAATGAATAAGATAAGGGTTTCAAAGATTTTTTTGTGACCTGCTATGTTTTCCCATAGCATTTCCTTACTTCACATATGATCTTTTTATTTTATTCAAGCCTTCTTGAGGTCTTTTGTTAATGTTACTAAAATGTTTCTTGACATGTTTTTAGGCATGCCTGTCGAGAATA[T/A]AGAATCCATAAAGAGCTGGACCATCCCAGAATAGTCAAACTGTATGACTACTTTTCCCTGGATACTGACTCGTGAGTGAACTTGCCCTCATGTTATTGAAAAGTGTACAATTTATACTTTTTCCCATTTCAAGACCCTCGTTTTGACCAATTTTTAGGATTTTAACTGAAATATTTTATGAACTTTTATGCATTGATGCATTTCTGTTATGTCACTGTGTAACGTGGACTGCTGAGAAAGTTGTTCTAATGCTTTGTAGATTCTGCACTGTTCTGGAGTACTGCGAGGGAAACGATCTGGATTTCTACCTGAAGCAGCACAAGTTAATGTCAGAAAAAGAGGCCCGGTCCATCATAATGCAGGTCGTCAATGCCCTCAAGTACCTAAATGAAATCCGCCCGCCGATCATCCATTACGACCTCAAACCAGGTCAGACACCAGTTGATCCACGTCCCAATGAACTCTTCTGTACAATGCTGAGCATGACAGCTAGCACCATT
Associated Phenotype:
Not determined