ZMP
TLN2 (1 of 2)
Ensembl ID:
Description:
talin 2 [Source:HGNC Symbol;Acc:15447]
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 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17241 | Essential Splice Site | Available for shipment | Available now |
sa13127 | Essential Splice Site | Available for shipment | Available now |
sa19370 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9473 | Nonsense | Available for shipment | Available now |
sa44343 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11842 | Essential Splice Site | Available for shipment | Available now |
sa32542 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17241
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023584 | Essential Splice Site | 192 | 2010 | 4 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 34091397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32565577 |
GRCz11 | 25 | 33051004 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGCCAYKCAGTGYGCACTKTCCACATCACAGCTGGTGGCCTGTACTAAG[G/A]TACTWCTGACAGATGAAGAGAAATGATGCYGMTAACATTATACACAACTG
Long Flanking Sequence:
CTAAGGAACTGAACTGTCATGCTTTGATATTTGCTTTATCCTGCTCTTCTGACTGGTTAATTCAAAATCCCTCAGCCAATTGCACGCTCCCAGTCTCATTATGTCCCGTCAAGGCAGTTTTCTCATGTAGTAAACACTTTAGCGCCCATCTTCGACACGTAAAATTTGATTTCGTGTGGTTCAGCTGATGCTGTCACAGTCGGTTAGCCTCGGCGAGCCTCTGATTGCCCTCTATTTGATTGTGTTACACTCTATCCTTGTGCTGATTTCATTCATTAGCCTGGGCCAGGTTGCTTCACAGTGTGTTTCTTTGGATGACGAATGTGTTTCAGGACATTATGATGAACCTGGCTAAAGCCGTAGCGAACGCCGCCGCTATGCTTGTGCTGAAGGCCAAGAACGTGGCGCAGGTGGCCGAGGACACGGCGCTCCAGAACCGGGTCATTACCGCCGCCACGCAGTGTGCACTTTCCACATCACAGCTGGTGGCCTGTACTAAG[G/A]TACTTCTGACAGATGAAGAGAAATGATGCCGATAACATTATACACAACTGCTTTTTAGGATGAATCAAATTATATTTAGCTAAGATATTAACTAATCATTCTAAAGGAAATTATTCAACCTTTCCAAAGTTGAAAAATGTTTTTGATTATAAGCGTCTTCTGTCAATATAGAGTAGAAACTGTACAATTATTATTATTACTCTTTAATAGAACTGTTTTTAATTTTAATTAATTTTAAATTGTCATTTATTTCTGCAATGCAAAGCTGAATTTTAAGTGTCTTTAATGCCTCACGATCCTACCACAATCCTTCTAATTTGCTGATTTGCAGCTGAATTATTCAGTTTTTGTTTGTTTTGGGATTTTTATAAACTGTACCTTGCGAAGGAACCTCCTTTATGGAATAGTGTGGTGGGACGGGGGAGATGGTGGGGTGTTATAGTGAGGGATGGATTGCGGATGAAAGTGAAGAGCGGGGTGCGGGTAGAGGATGAAAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13127
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023584 | Essential Splice Site | 389 | 2010 | 7 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 34080934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32576040 |
GRCz11 | 25 | 33061467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCAGCTGCCCAAAACGCCATCAAAAARAAGCTCATTCACAGACTGGAG[G/A]TGAGCAGATGCATTACAGGACATGTTACAGATANNCCTGTTGAAAGTGTTCA
Long Flanking Sequence:
GTATTTATGTCATAACATGCGTTATAGGTGAATCAAATAAGCTAAATTGGCCGTAGTGTATGTGAATGTTAGTGTATGGGTGTTTCCCACTACGGGGTTGCGGCTGGAAGGGCATCCACTGCGTAACACATATGTTGAATAAGTTGGCGGTTCATTTCGCTGTGGCAACCCCTGATTAATAAAGGGACTAAGCCAGAGGAAAATTAATAAACGACCCTTCATAGGAAATTGTGCTAAATGATCCCGGACGAGCCCCCACAGCTTGGTATTCAGTATATTAGAAACGTTGACTACAATTAAAAACACCTGACCCAAAGTTGATGAACTATATAAACTAATTTAGTAATCGTATCTGAACTGTTTTTGTGCAGGGAGCTGCGGCTTATCCGGAAAATGAAGACCAGCAGCAGCGGCTGAGAGAGGCGGCTGAAGGACTACGGGTCGCCACCAACGCAGCTGCCCAAAACGCCATCAAAAAGAAGCTCATTCACAGACTGGAG[G/A]TGAGCAGATGCATTACAGGACATGTTACAGATACCTGTTGAAAGTGTTCATATGTCATACTGAGTGATTCATTTGTGAATGATTCGATTCATATGGCCTTGAATCATGGAATCACTGATTCAAATTAATCAATCAGAAGACGTCTACAGTTGTGATATACAATTTTTATTTATTTGGTCACAGTAAGGCTTTAGTTACCAATTTACTGAATCACATTGATTCAGTCAGATAGAATATGTGGTTAAAGACTCACTGATTCAATGTTCCTGTCAGAGCAAGTCTCCATTAAATGATTTACTGATTTAAAATAATCCTATCAGAGAGAGTGTGTAGTTAAAGACTCACAGATTCATATGTTCCCATCAGAGAGTCTCCGGTGAGCGATTCACTGATTCAAATGTTCCAGTTAGAGCAACTCTCTAGGTAATGATTTACTGATTCAAATGATCAAATAAGAGAGTATGCTGTATGCTTACTGATTCAAATGTCCAGTTAGAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19370
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023584 | Nonsense | 703 | 2010 | 15 | 43 |
ENSDART00000023584 | Nonsense | 703 | 2010 | 15 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 34062492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32594347 |
GRCz11 | 25 | 33079774 |
KASP Assay ID:
554-5506.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTATCATATCTCCCTTTCTGTAATATTTCCAGCTTCCTCCATGCTCT[A/T]AATCCTTCCAAGAGGCGCAGACGGACTTGAACCACACAGCAGCCGAGCTC
Long Flanking Sequence:
TCCCGTTCGCTTCATTCGCCTGAGCAAATTTTCTCAGGAGACCTATAGTTTTACCGAGTCATGCGACTTCGGTAATATCGAAAAAAATTAATATTGCGGTATGACGGTATTTACAATACCGTTACATCCCTAATAATCACACTTGATAAAAAGTCAGCAGAAACAGGGGAATGGGGGAAGCCCCGTCCATTAGGGACCATCTTTTCCTCATCAGCATAGAATGTTAATCTTGTTTTTGAATCTGCCACTATGCTGACACGTAGGCATTTGCAGCTCCGCCCTCTTTCGAAAAGCTCACAATCTCATTTGAATTAAAAGCGACAGTCACTAAAATGGCACAATTAGGACCAAAGCCTAAAAGGGGCAGTTTTAAAGAGTTATAAAATATTATTTGTTGGGTATTTTGAGCTGAAACTTCACACTCTAGGGACATGAGAAACTCAACCAAAACTCTTATCATATCTCCCTTTCTGTAATATTTCCAGCTTCCTCCATGCTCT[A/T]AATCCTTCCAAGAGGCGCAGACGGACTTGAACCACACAGCAGCCGAGCTCAACCATTCGGCCGGGGATGTTGTGCAGTCTTCGCGCGGGAGCAGCAGCCAGCTGGCCGTGGCTTCTGGGAAATTCAGCCAAGACTTTGACGAGTTTTTAGACGCTGGCATCGAGATGGCAGGACACACTCAGGTACAGCTTCAGTGCCCTCTTAGAGAAGGGAGACCATTTGTGTTTCTCCACCTTACATACAGTTGAAGTCAGAATTATCAGCCCTCCTAAATATTTTTTGCCCAATTTTTGTTTAAAGAAAAGAAGATTTTTTTTCAACATAAAAAAACAAACAAAAAAAACGAACCATCATTGTATTAATAACTAATTTCTAAAAACTGATTACCTTTTTTTCCCCATGATGAAAGTAAGTAGTATTTGACTATATATTTTTCAAGATACAAGTTCAAGTTCAAGTTGCTTTATTGGCATGACATTTAATACAGTATTGCCAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9473
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023584 | Nonsense | 703 | 2010 | 15 | 43 |
ENSDART00000023584 | Nonsense | 703 | 2010 | 15 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 34062492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32594347 |
GRCz11 | 25 | 33079774 |
KASP Assay ID:
554-5506.1 (used for ordering genotyping assays)
KASP Sequence:
CTCTTATCATRTCTCCCTTTCTGTAATATTTCCAGCTTCCTCCATGCTCT[A/T]AATCCTTCCAAGAGGCGCAGACGGACTTGAACMACACAGCAGCCGAGCTC
Long Flanking Sequence:
TCCCGTTCGCTTCATTCGCCTGAGCAAATTTTCTCAGGAGACCTATAGTTTTACCGAGTCATGCGACTTCGGTAATATCGAAAAAAATTAATATTGCGGTATGACGGTATTTACAATACCGTTACATCCCTAATAATCACACTTGATAAAAAGTCAGCAGAAACAGGGGAATGGGGGAAGCCCCGTCCATTAGGGACCATCTTTTCCTCATCAGCATAGAATGTTAATCTTGTTTTTGAATCTGCCACTATGCTGACACGTAGGCATTTGCAGCTCCGCCCTCTTTCGAAAAGCTCACAATCTCATTTGAATTAAAAGCGACAGTCACTAAAATGGCACAATTAGGACCAAAGCCTAAAAGGGGCAGTTTTAAAGAGTTATAAAATATTATTTGTTGGGTATTTTGAGCTGAAACTTCACACTCTAGGGACATGAGAAACTCAACCAAAACTCTTATCATATCTCCCTTTCTGTAATATTTCCAGCTTCCTCCATGCTCT[A/T]AATCCTTCCAAGAGGCGCAGACGGACTTGAACCACACAGCAGCCGAGCTCAACCATTCGGCCGGGGATGTTGTGCAGTCTTCGCGCGGGAGCAGCAGCCAGCTGGCCGTGGCTTCTGGGAAATTCAGCCAAGACTTTGACGAGTTTTTAGACGCTGGCATCGAGATGGCAGGACACACTCAGGTACAGCTTCAGTGCCCTCTTAGAGAAGGGAGACCATTTGTGTTTCTCCACCTTACATACAGTTGAAGTCAGAATTATCAGCCCTCCTAAATATTTTTTGCCCAATTTTTGTTTAAAGAAAAGAAGATTTTTTTTCAACATAAAAAAACAAACAAAAAAAACGAACCATCATTGTATTAATAACTAATTTCTAAAAACTGATTACCTTTTTTTCCCCATGATGAAAGTAAGTAGTATTTGACTATATATTTTTCAAGATACAAGTTCAAGTTCAAGTTGCTTTATTGGCATGACATTTAATACAGTATTGCCAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44343
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 |
---|---|---|---|---|---|
ENSDART00000023584 | Essential Splice Site | 1166 | 2010 | 24 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 34036817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32619114 |
GRCz11 | 25 | 33104541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGCCGTGGGTCAGAGTTTGCCACGCAGAGATGACATTTCCCTGGAGG[T/C]AACCAATAAAATCATGTCTGTGTCAGTACCTGCCCTCTTTTCGTTACAGG
Long Flanking Sequence:
TGGTAATCTGATACCTTGTGATAATTTCCAGAATTATCTGACAAACCATATTTACCACTCACTGTTATTAATGTTCATAACACCATTAGGAACTGCTGTGGAAGAGCTGAAATTAGGATATAGTAATAGCCATTTGGTTTCTAACAGACTGTAAGTGATCAACCATTCACAATAGCAAATTAACTGACCAATCAGAGTAGAGTTGCCTTTGGGGTTTAGCGATGTGGGTTTTTTTAAGATGTTGGATGAAAAGAGCTGATGCAGCAGTGTACATTATGACGAAATAAATATTTTTTAACCTTGAGTGGATGTAAATCTAATGTAGGAGAACAAAACCTAGTAACCCATTCTGTGCTGTTGTGACAGGGACAAGGCTCCTGGGCAGCGGGAGTGTGACCAGTCCATCGACAGCATCAATAAGAGCATCAGGGACATCGAGCAAGTCTCTCTTGCTGCCGTGGGTCAGAGTTTGCCACGCAGAGATGACATTTCCCTGGAGG[T/C]AACCAATAAAATCATGTCTGTGTCAGTACCTGCCCTCTTTTCGTTACAGGTGCTCTGGAACAGGGTTGCTTTTATGTCTGCAACAGCTCGTCGTGATGGCAAGGATGATAAATCTATTAATAAATCTATTAAGGACTTGGAATGCTGCTTAACAAATAAAAACAATATAAATAAAAAGGAATGTACTGATTAAATTAATACAAATTAATAAAGTTATCAGTCTATTTATTAAAAAACGTGAAACTTTTCATCGTAACAAACATTTTTAAGGAAACTATTTAATTTGTTGAAGATTTTATTTAAATATTTAAACAACAGTTTGTCACGTCACACGTGAGAGCATCTAAATAATATTTGTTTAAAACATGCTAGATTAAATTTATATTATTTATAATATTCATTAGATTTATAGAAGCAATATCACACAAGTAGCAGTGCAATATGGCTGTATATTGGCACTGCTGGGTGGTTTACGATCAACCCAAGCTCATTCTCAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11842
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 |
---|---|---|---|---|---|
ENSDART00000023584 | Essential Splice Site | 1627 | 2010 | 34 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 34018354)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32637633 |
GRCz11 | 25 | 33123060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACGAGGGCTCTGGAAGCCACTATTGAGTGCATCAAACAAGAACTCACTG[T/C]ACGKAACATTATGTGTGAATATTRAWCCCTCATACTGATGTCATTTCATA
Long Flanking Sequence:
CAGGGCTTTGTTTTAGGCCTGCTTTGTTTTCTTGGGTTTCCTCCTTTGTTCGTTCTGCATTTATAAATTTGCCTGAAGCAAAAGCTTGGAAATCTGTTACTAACCTCAGCTGCTGTCCATTAAAAGGTTCGGTTTTATCTCTTGAACTTTTCATAATGATTTAGATTGTACTTTCTTGTGTTGCAAAGAACAGAATCCTGTCGGTTTTACTGTGCTGTTTGATTCAGTTGTTCCTGTCGTAACATTGCCTCTGATCTCTTTCAGTGCGTGAGGTGAAAAACTGGCCACAAAGCTGTTGACATTCTCGCTCACTTGAGACATTGTACTCAGAGTAAGAAATGCAGCTTCAACTTTGACCTTACTGTGTTTTCTGATATTACAGGTCATGGTGACGAACGTGACCTCTCTGCTGAAAACTGTGAAAGCTGTGGAAGACGAGGCCACTCGCGGGACGAGGGCTCTGGAAGCCACTATTGAGTGCATCAAACAAGAACTCACTG[T/C]ACGGAACATTATGTGTGAATATTGAACCCTCATACTGATGTCATTTCATATATTGTACCTTTCTGCCATTATTCTTTACCTTCATATGGTTTCACACCTGCATGACAGATTCTCTCATGTGAAAAGCAAAAGATCAATTTGGAGCAAACGACACTGGACCCATTACTTTTATTTGTCTGGAATAGTTCCACAAGAGAATTCAAGGTTCAGAACCCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTTGACCAGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAATCGTTTCGGTTAACATAATTTAAGCACATTTTGAGACTATATGCTAATTTGTAAAACAATATGGCCGTGAATTGGTATAGATTAGGCTCAGCCTAATTCGTTTTTAACCCAGGTAATACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32542
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023584 | Nonsense | 1914 | 2010 | 41 | 43 |
Genomic Location (Zv9):
Chromosome 25 (position 33996869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32659118 |
GRCz11 | 25 | 33144545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAACAGGTGGCGGCGTCCACTGCACAGCTGCTGGTGGCCTGCAAAGTC[A/T]AAGCAGACCAGGACTCTGAGGCCATGAGGAGATTACAGGTCAACTTTTCC
Long Flanking Sequence:
ATGAACACATTCTTGCTGCTTAGTTTTTGATTGTTCATTTTAGCGTTTCGTCTTTGACAATGTGAAAGATATACCTGTAGAAAACGATAAAAATGTTCTGAAGCTTCTGAAATTACTACTGTAAATACATATAAAAGTAACACCAAATTACCCACTGCTCTTCAGTGGTTTAAACATGACTAAAATAACACTTTGTGATATGTGACGCAGGTGGGCTCCATCCCTGCCAATGCAGTAGATGACGGCCAGTGGTCTCAAGGTCTCATATCAGCTGTAAGTTGAGCTTTTTCTCACATTTCTTAGTCACTTTGACCTGTATTATAAGCAGGATGACGGTGATGAATTGTGTGTTTCAGGCACGGATGGTTGCGGCCGCCACTAGTAACCTGTGTGAGGCGGCGAACGCTTCGGTTCAGGGTCACGCCAGTGAGGAGAAGCTCATCTCTTCTGCTAAACAGGTGGCGGCGTCCACTGCACAGCTGCTGGTGGCCTGCAAAGTC[A/T]AAGCAGACCAGGACTCTGAGGCCATGAGGAGATTACAGGTCAACTTTTCCCATGTCCCATGATGCTTTACCTGAATTACGAAAGTACAGTCGCTTCCATTAACGCACTTTATCAGGACACTTTTTCAAAATATCACTTTTTTTGTAATGAAATTGTAATCTAATCATGACAAAGTGTATACAGTTTAAAAAATGCAAAATGTTTATATTTATTAATTTGTTTATTTAATCATAATTATCACCTTTCTGTGGATTTACTCAAAAACTAAACCCAACTTTAACCCTACTATTAATAAGCCACTAATTAGTAGTTTATTGAGGTAAGAGTCTTAGTGAAAAAAAAAACTTGAGATTGGTCAACAGGTGGCGCTATACACCTTAAAAATGTCAAAAATGCTGTATTTCTATTGGAAATGAACACATGTAATGCCTTTGTTTGTTTGTTTTTCTAATCATTGTCTTTGTGTTCACACAGGCTGCTGGTAACGCGGTCAAGCGAGC
Associated Phenotype:
Not determined