ZMP
tln2
Ensembl ID:
ZFIN ID:
Description:
Putative uncharacterized proteinZgc:152648 [Source:UniProtKB/TrEMBL;Acc:Q0V975]
Human Orthologue:
TLN2
Human Description:
talin 2 [Source:HGNC Symbol;Acc:15447]
Mouse Orthologue:
Tln2
Mouse Description:
talin 2 Gene [Source:MGI Symbol;Acc:MGI:1917799]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40914 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45280 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34090 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3330 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa40914
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018142 | Nonsense | 13 | 289 | 3 | 10 |
ENSDART00000134068 | Nonsense | 13 | 115 | 4 | 5 |
ENSDART00000136555 | Nonsense | 13 | 2157 | 3 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 31226849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29619191 |
GRCz11 | 7 | 29890341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCCGTCAGGATGGTGGCGCTGTCTCTGAAGATCTGTGTGAGGCAGTG[T/A]AATGTGGTGAAGACCATGCAGTTTGAGCCCTCAACGGCTGTATATGACGC
Long Flanking Sequence:
GCTGCAATGATTATAAAAGTACATAATCATCATCAGACAATTAACTCTTGCATTAAAATATTACAAACTGTGTTGAAAAAAATGGAAACAAAAATTCTGGGAAAGTGAATTTATGGGTATTCACCATATACTGTACGTTAACGAAACTAACTAAAGGATTATTTTTTTAAATGGCCATTCAAATCATGACCATTTTTTTAATGGTGTAATAATATTTAGCATATTTTTTTACTTATGTTACATTTCTGTTTTACTATATTACTTTTTTTTTGCTGTTTTCTAAATTATTATATTGCATAGAGGAAACTAACTGCCGACAATCAAAAATGAATGTATTTGTAGTAGCTAACAATTAAAGTCTTCAACATCATTTTTGTGAATGTTGATTTAAATCCTAAAATCTCTAACACTCTGTCTGTTTCTCACAGGTGCAGAGTTGTTGGTGACCCTTAAGCCGTCAGGATGGTGGCGCTGTCTCTGAAGATCTGTGTGAGGCAGTG[T/A]AATGTGGTGAAGACCATGCAGTTTGAGCCCTCAACGGCTGTATATGACGCATGCCGGGTCATCAGAGAGAGGGTTCCAGAAGCCCAGACAGGACAAGGTTTGTCATCACGCCTTCTTGATTCTATACTATGTTCAGACTGAGAATAAATCTCAGTTTGTTTGACTAAGTTCTAATGGCGTGTGTTGTTTTTCCTCAGCTTCAGAATATGGGCTGTTTCTGTCAGACGAAGACCCTAGGAAAGGCATCTGGCTAGAAGGAGGCCGGACGCTGGATTATTACATGCTGAGAAATGGAGTAAGCGCTTTGATCATTTGTTTTACAAGCTCCTGTCAAATGTTCTGTGTCATGGCTTTGCACTGTTGTCTTTGTTTTGTGACATGTTTTTTAATTTTTTATGCTGAAGGGTGAGAAGTGGTCTAAACTGCTTTTGATTTTATTTTATAATCAGTGCGTGCGTGCACACGTTGTCACTTATCCGAGACAAACTACACTGATGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45280
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018142 | None | None | 289 | None | 10 |
ENSDART00000134068 | Nonsense | 90 | 115 | 5 | 5 |
ENSDART00000136555 | None | None | 2157 | None | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 31227180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29619522 |
GRCz11 | 7 | 29890672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTGAGAAATGGAGTAAGCGCTTTGATCATTTGTTTTACAAGCTCCTG[T/A]CAAATGTTCTGTGTCATGGCTTTGCACTGTTGTCTTTGTTTTGTGACATG
Long Flanking Sequence:
TGTATTTGTAGTAGCTAACAATTAAAGTCTTCAACATCATTTTTGTGAATGTTGATTTAAATCCTAAAATCTCTAACACTCTGTCTGTTTCTCACAGGTGCAGAGTTGTTGGTGACCCTTAAGCCGTCAGGATGGTGGCGCTGTCTCTGAAGATCTGTGTGAGGCAGTGTAATGTGGTGAAGACCATGCAGTTTGAGCCCTCAACGGCTGTATATGACGCATGCCGGGTCATCAGAGAGAGGGTTCCAGAAGCCCAGACAGGACAAGGTTTGTCATCACGCCTTCTTGATTCTATACTATGTTCAGACTGAGAATAAATCTCAGTTTGTTTGACTAAGTTCTAATGGCGTGTGTTGTTTTTCCTCAGCTTCAGAATATGGGCTGTTTCTGTCAGACGAAGACCCTAGGAAAGGCATCTGGCTAGAAGGAGGCCGGACGCTGGATTATTACATGCTGAGAAATGGAGTAAGCGCTTTGATCATTTGTTTTACAAGCTCCTG[T/A]CAAATGTTCTGTGTCATGGCTTTGCACTGTTGTCTTTGTTTTGTGACATGTTTTTTAATTTTTTATGCTGAAGGGTGAGAAGTGGTCTAAACTGCTTTTGATTTTATTTTATAATCAGTGCGTGCGTGCACACGTTGTCACTTATCCGAGACAAACTACACTGATGTTATTAAAGACATTTGTCATTGCCGCATGTGGTTTATGTTTGTGTTTGTTAAGTCCCTGTGCTCGCGTGTGCGTGTGCGAGTGCGTGTGCGTGTGTGTGTGTGTGTGTGCGTGTGTGTACGTGTGTGTGTGTGTGTGCGCGCGCGCGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGCGCGCGTATAAAAAGAAAAGCAGATGCTTGTTTTCAGGAAGGTATAAAAAAGTGTGTGGTATAAATTAAGAAGCGTTAAATGATGTTTTCATCAGGAGCTTTTTTTTTTTTGTTTATCAAAAAACCTCTTCTTCATTCATTCATATACTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34090
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 |
---|---|---|---|---|---|
ENSDART00000018142 | Nonsense | 246 | 289 | 8 | 10 |
ENSDART00000134068 | None | None | 115 | None | 5 |
ENSDART00000136555 | Nonsense | 246 | 2157 | 8 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 31236573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29628915 |
GRCz11 | 7 | 29900065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATCCGGTGTCGTTTGACAAGGCTTGTGAGTTTGGGGGAATTCAAACG[C/T]AGATCCAGTTCGGTCCTCATATTGAACATAAACACAAGACTGGATTTCTG
Long Flanking Sequence:
GGAAAGTGAAACATTACTTTTGAGACGAAAGTTCTTCTACTCCGATCAAAACGTGGACTCGCGAGATCCTGTGCAGCTCAATCTGCTCTACGTGCAGGTCAAACTTTCCTCATGCCACTTCATTTATCATAGCAAAAGCCATAATGCTCATCCAGCATTGGTTGACCTTAATGATCTGTTTCCATATAGGTCTTTACATATCAGTTCAATATAGAGGTTAAAATGCTGTAAATCTCTTATTGACACTTGCGCCTAAAAGCCTTTCTGAGTGCAGCACTAACATGCTGATGTACACATTGTATCGATCTGTTAAGTAGTGCAGTCCCTGTTTTCTTTATATCAGCTCTTCTTCTGTCAGTTGCTGATCTGGATTTAGTTGCATTTCTGTGGATTGGTAATAAAAGTCTGTTTGCATGTTTATCCAGGCACGTGATGACATTCTGAACGGTTCTCATCCGGTGTCGTTTGACAAGGCTTGTGAGTTTGGGGGAATTCAAACG[C/T]AGATCCAGTTCGGTCCTCATATTGAACATAAACACAAGACTGGATTTCTGGAGTAAGACATCATTCATTCAGAGCTTTCGGTTGTAGAGTGATGGAAAGAATCAAAGGACAGATTGAAAATTCTCAGATTTTCTGTATTTGCAATTTATGGTTATGTGATTTGAGTTAAATGTCATTTTTGTTTTATTCTATAAATGACAAGTGACTTTTATTTATAACAAAAAGTTGGCATGATTATATGAATTTTTAGACTACACACTTACAATGTTTTAACTCCAAAACTGTTACACAATCAATATTTGTTGGAATAAGCCAAATGTTTTTAACCACAACAACTGAAACATTAGTAATTCTGACCTATTGTCATTTTCTGGAAAATAAAAACCCATAAATGACAATATTTCTTTTCAAATTTGGAGGAAATGATATCAGACGTTTATACAGGGATCCCAAAACCTTGAGATTTAGAGGGTTGTTATCAGGTCTTGACAGAAAAGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3330
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018142 | None | None | 289 | None | 10 |
ENSDART00000134068 | None | None | 115 | None | 5 |
ENSDART00000136555 | Essential Splice Site | 668 | 2157 | 18 | 49 |
Genomic Location (Zv9):
Chromosome 7 (position 31249090)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29641432 |
GRCz11 | 7 | 29912582 |
KASP Assay ID:
554-2649.1 (used for ordering genotyping assays)
KASP Sequence:
AGATCTGCTCAGACAGATTGGAGAGAATGAAACCGATGAGCGCTTCCAGG[T/A]ACACAGGCGTCTAATAAAGTATACAATGCATGACGCGTGTTTATCACCCT
Long Flanking Sequence:
CATCCATTATTCCATTCATTCATTCATTCATGCAGTTTCTTTCATTCATGGTTTTATTTATTGTTTGCTTTTTCATTTATTCATTCGTTCGTTCGTTCATTCATTCATTGTTTCATTTATTGTTTGTTTTTTCATTCATTCATTCATTCATTGTTTCATGATTTTTTATTTCCCATGTTTAAATGCACAGTTTGTTAACTTGGTTTTACTTTTATAACTGATTTGCATGTTTTTCTATGTGACGTTTTCTTTCCAGATGTCAAATGTAACATTTTGAGTATTTTTTTATTCATTTCATTATTATCCCTGTATTAAATTTCATTAGAATTCCAGCAACACTGCACTACTATGAAGCTTGAGAGAGAAATCTATATTTACTAGTTTATGTTCTGTCACTCAGCCTCGACAGACTGTTCTGACTGCAGCTGGCAGCATCGGTCAGGCCAGTGGAGATCTGCTCAGACAGATTGGAGAGAATGAAACCGATGAGCGCTTCCAGG[T/A]ACACAGGCGTCTAATAAAGTATACAATGCATGACGCGTGTTTATCACCCTGAGCCTGTATATATGTGTCTGTTTTAGGATGTGCTGATGAACTTGGCAAAAGCTGTGGCCAATGCAGCAGCTATGATGGTTCTAAAGGCCAAGAACGTGGCGCAGGTTTCTGAAGACAGCGTGATGCAGAACAGGGTTATCGCTGCTGCCACCCAGTGTGCCCTTTCCACTTCACAACTAGTGGCCTGTGCCAAGGTGAAAACACACACACACACACAGTCATAATTGAGGTGGAAATCACAGATTAAAGGGATTATTCCCCCCAAAAATAGACTCATTAATTACTTAAAAAAAACTTTTGGTTTTCCAACTAGTGAAATCAGATTGTTTTTATTCATTGTCACTCCAAGACAACATACAAGTTTTTAATACTTGGAGAAGATCCTCCCTCCTGTTCGATTTGTAAAAGCACTTTAACTATGAAGCATGTTCTGTTGGATTGTGTTTCAG
Associated Phenotype:
Not determined