Busch Lab

ZMP

tln1

Ensembl ID:
ENSDARG00000005333
ZFIN ID:
ZDB-GENE-031002-48
Description:
talin-1 [Source:RefSeq peptide;Acc:NP_001009560]
Human Orthologue:
TLN1
Human Description:
talin 1 [Source:HGNC Symbol;Acc:11845]
Mouse Orthologue:
Tln1
Mouse Description:
talin 1 Gene [Source:MGI Symbol;Acc:MGI:1099832]

Alleles

There are 15 alleles of this gene:

Allele Name Consequence Status Availability
sa6161 Nonsense Mutation detected in F1 DNA Not yet available
sa34845 Nonsense Mutation detected in F1 DNA Not yet available
sa11348 Nonsense Available for shipment Available now
sa34846 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa2572 Essential Splice Site F2 line generated Not yet available
sa21664 Essential Splice Site Available for shipment Available now
sa41593 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa5825 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38777 Nonsense Mutation detected in F1 DNA Not yet available
sa15487 Nonsense Available for shipment Available now
sa31764 Nonsense Available for shipment Available now
sa10075 Nonsense Available for shipment Available now
sa21665 Nonsense Available for shipment Available now
sa21666 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa6161
Status:
Mutation detected in F1 DNA
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
ENSDART00000013609 Nonsense 40 2538 2 56
ENSDART00000078135 Nonsense 40 2544 2 56
ENSDART00000098857 Nonsense 40 323 2 10
ENSDART00000098858 Nonsense 40 405 2 12
Genomic Location (Zv9):
Chromosome 10 (position 8155703)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6168865
GRCz11 10 6170074
KASP Assay ID:
554-5227.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTGGYGTACGACGCCTGTCGAATYATCAGGGAGAGAGTTCCAGAAGCA[C/T]AACTCGGCCAGCGTRAGTCCATCAGCAGTATACTCAGAACCCTGTCTTAT
Long Flanking Sequence:
TGGTTGTTACCTTGGGATAACATATCTTGCAACACAAAAAATTACTTTTGCTATTTGTTCAAACTACTTATTTAAAATAAGTTGAAACAACACATTTCTTAAGGTTTCATGTTCAATACAATTAAGTTAACTTAATAAAGTTTTGTTGTGACAACATGAAAAAATTGCGTTGAACTCAGCATTTTTTGCAGTGAATGTTGCAACTGACCAATCAGAATCTAGTTTTTAAACACTTGTGTCATACTAAACTTCACCACAAGTGGCTCCGCCTGTACTTTGTAACCAAACTTCAGTGATGCTTTTTAAAGTGAACATTGGAAATTTCTAACATCCTCATGTTTGTTTTGCAGGAGTAGCAGTGGCACAGTCCCGTATTGTCAGTCATGGTGGCGCTGTCGCTGAAGATCGGGGTGGGGAATGTGGTGAAGACGATGCAGTTTGAGCCCTCCACAGTGGTGTACGACGCCTGTCGAATCATCAGGGAGAGAGTTCCAGAAGCA[C/T]AACTCGGCCAGCGTGAGTCCATCAGCAGTATACTCAGAACCCTGTCTTATCTGATGCGTTCTGAAGTAAACAGACTGTTGACCAAACTGATGACAATGATCATTATGAACCAAGATATTGATATTGAAAAGTGGTCAAATTTAAAGTGCAGAACAAAACATTGCTTATTTTTTTTATTTTTATTTTTTTGTAATTACAATATAATTTTGCATCTATTTAGTTAAAATTCTTGCTTTTCAATTATTTGTGCAGTGTGTTTGTGTGCTGGCATACCTTTAGGCCTATCGTGGATTAATTAAAGGGATAGTTCACCCCTAAAAATAAAAGTTTACTCACTATCAAGGGGATTCAAAGAAGGGTCCCACAATACTGGGAAAATACGTCATTGCAATAATATTTTTTTTCGATATAATCTTTTCCTAAATAATGCTATTTAATTAGACATGTTTTTTCATTTGTCTTTGTAATGATGTTAAAATAAACAGGCAATAGATATTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34845
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Nonsense 189 2538 6 56
ENSDART00000078135 Nonsense 189 2544 6 56
ENSDART00000098857 Nonsense 189 323 6 10
ENSDART00000098858 Nonsense 189 405 6 12
Genomic Location (Zv9):
Chromosome 10 (position 8163970)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6177132
GRCz11 10 6178341
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGTTGGATCATGGGCGGACGCTGCGGGAGCAGGGTGTCGAGGAGTCT[G/T]AGATGCTGCTTCTTAGGAGAAAGTTCTTCTACTCAGACCAGAATGTGGAT
Long Flanking Sequence:
GGCATCACAAATTATGATGAGTACTCACTGGTGCGTGACGTGGGAGAGGAAAAGAAGGAAGAGACCACAGGAACACTGAAGAGAGACAAGACCCTCCTGAGAGATGACAAAAAAATGGAGAAACTCAAACAGAAACTTCACACAGATGACGAGCGTATGTCTCAATACATATATAGTTTGCTATTTTAGCTGGTCTTCAATACAGTACATACTGTATATTCTTAATGTATTCACATACCTAGCAAATAATTGAGCACAAAACACTTCATCATTACACTTTTTGTCACATTATACTATAGAGAAAAACCTGTTAATTACATCAATAAAAATTTTAGTTTTGTAACCAAACTCCAATAGTATTATGTATATTAGAAAAATAAATAAAATCAAACCAGTTACAGTTATATCTAGTTGAATTCGCTGATTGGGATTTTAATGTGTATTCAGTGAATTGGTTGGATCATGGGCGGACGCTGCGGGAGCAGGGTGTCGAGGAGTCT[G/T]AGATGCTGCTTCTTAGGAGAAAGTTCTTCTACTCAGACCAGAATGTGGATTCCAGAGACCCTGTACAGCTCAACCTGCTGTATGTGCAGGTAAAAACCACAGGAAATTCTCTTCGCATCGCAATCATGGCCTTATGTCATCTGTAAAATGGTGTTTTTGTTTTGCCATCTGCACTAGTGCTTTCAAATGTTTTGCTCTCAGAAAACAATCAAATACTTTTGTCACAAATGTGTAAAGAGTAAAATGATGTGCCGGTCACTCTCAATCTAACATGAGCGTGAAACCTGGCATACGCAAACCTTTTGTGCGTACGCACTACGCAGTGTTGATACATGAGGCTCCTGATCATGTGGCGCAACACCTCATCACTCTACTTGGTCAAATAGCCCTTACATAGCCTGGAGGTGTGTTTTGGGTCATTTTCCTGTTCAAAAGTAAATTATGGTCCAACTAAATGCAAACCGGATGGAATAGCATGCCGCTGCAAGTTGCTGTGATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11348
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Nonsense 216 2538 6 56
ENSDART00000078135 Nonsense 216 2544 6 56
ENSDART00000098857 Nonsense 216 323 6 10
ENSDART00000098858 Nonsense 216 405 6 12
Genomic Location (Zv9):
Chromosome 10 (position 8164053)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6177215
GRCz11 10 6178424
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGACCAGAATGTGGATTCCAGAGAYCCTGTACAGCTCAACCTGYTGTA[T/A]GTGCAGGTAAWAACCACAGGAAATYCTCTTCGCATCGYAATCATGGCCTT
Long Flanking Sequence:
AGACAAGACCCTCCTGAGAGATGACAAAAAAATGGAGAAACTCAAACAGAAACTTCACACAGATGACGAGCGTATGTCTCAATACATATATAGTTTGCTATTTTAGCTGGTCTTCAATACAGTACATACTGTATATTCTTAATGTATTCACATACCTAGCAAATAATTGAGCACAAAACACTTCATCATTACACTTTTTGTCACATTATACTATAGAGAAAAACCTGTTAATTACATCAATAAAAATTTTAGTTTTGTAACCAAACTCCAATAGTATTATGTATATTAGAAAAATAAATAAAATCAAACCAGTTACAGTTATATCTAGTTGAATTCGCTGATTGGGATTTTAATGTGTATTCAGTGAATTGGTTGGATCATGGGCGGACGCTGCGGGAGCAGGGTGTCGAGGAGTCTGAGATGCTGCTTCTTAGGAGAAAGTTCTTCTACTCAGACCAGAATGTGGATTCCAGAGACCCTGTACAGCTCAACCTGCTGTA[T/A]GTGCAGGTAAAAACCACAGGAAATTCTCTTCGCATCGCAATCATGGCCTTATGTCATCTGTAAAATGGTGTTTTTGTTTTGCCATCTGCACTAGTGCTTTCAAATGTTTTGCTCTCAGAAAACAATCAAATACTTTTGTCACAAATGTGTAAAGAGTAAAATGATGTGCCGGTCACTCTCAATCTAACATGAGCGTGAAACCTGGCATACGCAAACCTTTTGTGCGTACGCACTACGCAGTGTTGATACATGAGGCTCCTGATCATGTGGCGCAACACCTCATCACTCTACTTGGTCAAATAGCCCTTACATAGCCTGGAGGTGTGTTTTGGGTCATTTTCCTGTTCAAAAGTAAATTATGGTCCAACTAAATGCAAACCGGATGGAATAGCATGCCGCTGCAAGTTGCTGTGATAGCCATGCTGGTTCAGTATGCCTTCAATTTTGAATAAATCCCCTACAGTGACCAGCAAAGCACCCCCATTTCGCAGCTCATTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34846
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Essential Splice Site 261 2538 7 56
ENSDART00000078135 Essential Splice Site 261 2544 7 56
ENSDART00000098857 Essential Splice Site 261 323 7 10
ENSDART00000098858 Essential Splice Site 261 405 7 12
Genomic Location (Zv9):
Chromosome 10 (position 8165130)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6178292
GRCz11 10 6179501
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAGTTTGGAGACCACAATGAGTCCAAACACAAACCTGGATTCCTAGA[G/A]TAAGCACTCACGTTTCTATAATTCGAAAATCCTGCTTTTGTGTGGTGTCG
Long Flanking Sequence:
AACTAACAAAAGCATAGATGGCTTTCTCAAGATCAGCCTTGCTCAGGAAGGGCCTGACTTCAGAGAGAAGGCGAAGCTGAAAAAAGCTGGCTTTAATCAGCGAATCAATCTGCTTATCAAATTTTAGACTACTAAAGTTCAGATCTGTTGATGACACAAACATCTGTGCTAATCTACAATCAAATGGCATGTTGAACATCAAATGTGATCTGAATGTCTGTAAATGTGCCACGTTATGCATGATTTTCTTAAAGGTATAAACAGACAGACAAGATTACTTCTTGTTGAAAATGTGCCTGGTTCATTAAATTACGATGTTGCTAATTCTGTTCAATTTCAGGTACATTTAAGGTATCGTGTTTTGTATTCCAGGCCCGTGATGACATTTTGAACGGCTCTCACCCTGTCTCCTTCGATAAGGCCTGTGAGTTTGCTGGATACCAGTGCCAGATTCAGTTTGGAGACCACAATGAGTCCAAACACAAACCTGGATTCCTAGA[G/A]TAAGCACTCACGTTTCTATAATTCGAAAATCCTGCTTTTGTGTGGTGTCGTTGAAAAGAAACCTCTGTGTTTGGGTTGATAATGTATAAACATTTGATCATAATTTAATTATTTCATAGTTAAGACATTTTTAAAAAAAACTCAAGAAATGATCCCAAACTGCATGAAAAATGAAAACATCTACAGTCAATATTACAATTATTGATAAGTTTTTTAAGCAGATTATCAGAGAAATATGACTCTGAATATGATTTTATAGGAAAGTTTTTAGATAAAAGTGCACTATAAGAATAAGTCAGTAAAATATACGGTTAAAAATTAGCATTTTACTTTATTTCATCATTTGTTTTTGACATACAGCAATGATTCAATGTTTTTATGTCTACACAACATATCACAGACAGCAAAAGGAACACAACCATAAACATACAGTTGAAGTCAGAATATTTAGCCCCCGTGTTTATTTTTTTCCCAATTTCTGTTTAAAAAAAAAGAGATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2572
Status:
F2 line generated
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
ENSDART00000013609 Essential Splice Site 398 2538 11 56
ENSDART00000078135 Essential Splice Site 402 2544 11 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 Essential Splice Site 402 405 11 12
ENSDART00000013609 Essential Splice Site 398 2538 11 56
ENSDART00000078135 Essential Splice Site 402 2544 11 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 Essential Splice Site 402 405 11 12
Genomic Location (Zv9):
Chromosome 10 (position 8174609)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6187771
GRCz11 10 6188980
KASP Assay ID:
554-3431.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGATTGCACAACTCATTGCTGGATACATTGACATCATTCTCAAAAAGG[T/C]AACACGCTATGACTTCTCAGGGGTGTGCAGCATTGACCAGAATGTTTTCT
Long Flanking Sequence:
CATAAATGCGTGTTTTTTTGTTTAGAGAATGTAAGAAATCTGGTGCAAATGAGCAAAACTGGTGTGAGTGTCAGTTAAAGTGTCAGAGATGAAAGAGTGTGTTTTCTGCAGGTGGTTTGTCAAGCCCACTCACATTTAGAAATGCGTAATGTTTTGGGGTTGTCTCATCTAAAGTTTCAAAATTGGCTCTTTCGTTGGTGGGAAAGTAACACTTTTACATTTGCAAACTACATAATAGACTAAATAACAGGTGGAATTTTAAAATCATAGAGACATTTTAATACGGAAAAGCATGCACTTCTGAGAGAAATGATCTGTAGTTTGCTGTATTATTTGTGCTGTAATTTTTACCTACCATTCGAAGTTACATGTCATGTGTGTACTCTTTCCTCTTCAGGACTTTGGAGACTATCAGGATGGTTACTACTCAGTTCAGACCACTGAAGGAGAACAGATTGCACAACTCATTGCTGGATACATTGACATCATTCTCAAAAAGG[T/C]AACACGCTATGACTTCTCAGGGGTGTGCAGCATTGACCAGAATGTTTTCTGTATATAAATAGGGCCTCTCCTATCATGTTTAAATAGATATAAGACTAAAACCACCAAGAGGAGGTAAAATTACGCTTATAATGTGTGATTCATTCATTCAAATGATTCAATCTAAATGAAATTTACTCTATTGAACAATTAAAAGGATCATTAAATCAGTGATTTGTTCAAAAACAGATTAATTTAATAACAAAACACCACATTGCTGCCCAGTATTGCACAAATGTTCTGCTAAAGCTTTATTTGGAAACGTTTTATTGGCGTAAGTCTAAGAAAAAGAAAAGAACAAATATTTTGACTAAAACATAACTTGCCTACTATTGACTACACTTTTACTTGTGTGATATTACATTACTATATCATGTTTTACAAATAGAATCTAGAATACATTTTACATTTTACATTTTTATTTACAAAACATGTGCTTGTTTGTTGTAAAAATTCATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21664
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Essential Splice Site 424 2538 12 56
ENSDART00000078135 Essential Splice Site 428 2544 12 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8176680)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6189842
GRCz11 10 6191051
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGAGATGAAGAGTCAACCATGTTGGAGGACTCCGTCTCTCCGAAAAAG[T/C]GAGCCCCTTTAATAGTTCATTGCATTCTGGATACACAGAAACAGATATTT
Long Flanking Sequence:
GTGACGCGGCAGAAATATGAAGTTTCCTGAATTGTAGCTGGGCACCGCGGACAGCAGCCGACTTGCAGCGCCAGTGTGTGTACACTGATAGAAACCCATGTTTCCAATTCTGAAAAGCATGGCGCATCTGGTGACCCCCTTTACACTTTTGTAGGCACTGTTCATAATTTCCTATGCATTTGTGCAGTACTGTCACTAAGCAGCTCTTTTTCATATCAGTCTTATTTTGAATGGTTGTGTATCGTGTCCATGTGAAATTGCTGCTGCTGGTTCTCTACATTATGAGGAATTCCTCAACAAACCTCCATGTTTGAGCAACTGAGAATGAAACAATCTGCTCTGGCAACTAAATGCCTCTTTCAGGTTCTTTTCATAAGCATCTTTCCTCAAGTCACTGTGTCTGAAAACCTCTTCCTCTGCAGAAAAAGAGCAAAGATCACTTCGGCCTGGAGGGAGATGAAGAGTCAACCATGTTGGAGGACTCCGTCTCTCCGAAAAAG[T/C]GAGCCCCTTTAATAGTTCATTGCATTCTGGATACACAGAAACAGATATTTCCCAGTATTTCTCTGTTGCAATCGTGATATCCCAATAATTAACCCTGAAAAAATCGAAGCAGCGCAGTCACAACCAGGTTACTGTTGTGTTTGCGATAAGGAAAAACACTGAACACATGCGGGCATTTCTTCTTTCTTTCTGTTTACTGAACTAGTCCGCAGTAACGAAAACAGGCAACAAATTAGAAACAGATGACCAACCAAAAAGTAACTCAGGGTTATACAAACACAAAATACACTTTTGGCCAACACAAAATACATACATTCCTGATATGCGAGTCCCATCTCGCACTCAATACACTACAATTACTATAGCATAAATACAGAACTGCAACATACAAAAGAGAGAGATCGACTTAGAAAGTCACTTACCAGTTTTATATTGATTTGATCCGCTGTAGTTAGGAATAACACTAACACAATGCTTTTCTCTTCTAAGGGCTTATTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41593
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Essential Splice Site 558 2538 15 56
ENSDART00000078135 Essential Splice Site 562 2544 15 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8182461)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6195623
GRCz11 10 6196832
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGATGCCATCACTGCGGGAACTGCTTCCATGGTCAATCTGACTGCAG[G/A]TGAGACGCTCGCAACATCTCACCGTTCACATCTTTGCGGCGGGTGGTTTA
Long Flanking Sequence:
GGTTTAATAGTTTTTTGTTGTTAAAATTGAAAAATTGAAGTTCCTGTTTCGAAACTTACAGATAGATGGCTAATTTGTATGTCATTGATATGTTCAGTGCTAAGATAAATAAACACTTTTGGCACTTTTTTCGAGTCTTTTCATTAGTTTAGTTTTTCCTGTAAATTATTCAATAAATACCGTACCGTGCCATTCATACCGAGGTATTATCGTACAGTGAAATTCTAATATCCCTAATAATCACCCTTGTAATCAGGATTGACATTGTTGGAAAATGGTTTCTCCTTCAATGTGTTTTTGACCCTGAAAGTTCGAAAACAGAAGAAAAAAACTGCAAAAAAACTATTTATTTTGTTAAATAAACTAAAATCCTGTGTCTCTTCTTGTTCAGGCATCTCAAGCCTGGAGGAAGAACAAAATGGATGAGTCCAAACACGAGATTCACTCTCAGGTGGATGCCATCACTGCGGGAACTGCTTCCATGGTCAATCTGACTGCAG[G/A]TGAGACGCTCGCAACATCTCACCGTTCACATCTTTGCGGCGGGTGGTTTATACTGCGAGACCTTTTTTCTGCTGAATATACAATTCATGGTGTAACTTTACACTGTGATTCGTGCGTAATTGAGTGTTTTGCAGGCAAAATATGTGCAGCTTCAGTGAGAGTAAAGGATTTTCTGTCCATCTACTGTGTCTGTCTATGATTTTCGTCTGAAACATGCCAGATGTTGTGTTGGACGCTGTAGAGCCTGGGCAGGAATTTGATTTTGTGCCTGCTGAGACTTTTTTGTTCTTCATTTAAGGAGGAAAACAAACGCAGGCATCATTATACTGTTAGTAAACTGCTGACGCTGCGTGCATGTGCTGTTTAGAGACATATGTAAACCTGTTGTTCATTTTAGCTCCATTTTACTAAAACTATTTTCTAAAATTGATCACATGACCAAATGATGTGGCCATCCTCTGGTTGATATTTTAACTGTAATGACCAATTTTTACTTTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5825
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Essential Splice Site 1438 2538 33 56
ENSDART00000078135 Essential Splice Site 1441 2544 33 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8240105)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6253267
GRCz11 10 6254476
KASP Assay ID:
554-3889.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGTTCAGCGTCTAAAGCGCTGTGTGGTCTCACTGAAGCAGCTGCTCAG[G/A]TAAAAACRCTTATGTGTGTGTGTGTCNNNNTGTGTGAAGCTCATCTCTCCTAAA
Long Flanking Sequence:
TTTGTGTGTGTTTGTGTGTGTTTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTGTGTGTTTGTGTGTGTTTTTGTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTCTGTCTGCAGACGGTTGGAGGAATGCTGGAGAACCCAACAGAAGCAGTCAATGATTTGGGCTACTTTGACTGCATTGACAGTGTGATGGAGAACTCAAAGGTGCCACAGTGATCACAATAAAACGAAAACTAAATCACCCAATCTCAGTGTTGAGCTAATGCTTTATTAATGTTGATGTTGTTTGCAGGTTTTGGGTGAGGCCATGGCTGGCATTTCCCATAATGCCAAAAACAGTAACTTGCCAGAGTTTGGAGATTCGGTCAGTTCAGCGTCTAAAGCGCTGTGTGGTCTCACTGAAGCAGCTGCTCAG[G/A]TAAAAACACTTATGTGTGTGTGTGTCTGTGTGAAGCTCATCTCTCCTAAATTAGAGAGCTGAAGAGGTGGTGCGTGATGAAATGTACCAGTGCTATGATGCGTCAAACATCTGGACTTACAGGAGCGCATTAAATGAACAAACACATCCGCTGTTCTTCATCGCTGTCTTCTGTGCCTTTGCTCACACCTCCGTGCTTTTGTTATTTATGGGCACAAGAATACACTCTCACACACTTGTGCAAAAAGATTTCCTAATGGCTTTGATGGGCAGTGAGTCATTTAACTGCTTTCTGAGCTTAGCCCTAAAAAATTGTTCACTCAGAGCTGCCATTTCTGTAGTGATTCATTTTATTTGTCTGGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTGTGGATGGGGGGAGGAGTGTGATGTACCAATAATGTGAACTTGATTGTGTTTGTTTGGTTGTGTCTTGTGTTTCTCACAGGGGGCGTATCTGGTTGGTGTGTCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38777
Status:
Mutation detected in F1 DNA
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
ENSDART00000013609 Nonsense 1520 2538 35 56
ENSDART00000078135 Nonsense 1523 2544 35 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8243369)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6256531
GRCz11 10 6257740
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCTGCCGGCTCGCCTCCTCCAAGACATCCAACCCAGTTGCTAAGAGA[C/T]AGTTCGTCCAGAGTGCCAAAGAGGTGGCCAACAGCACAGCCAACCTCGTC
Long Flanking Sequence:
ACTTGATTTAACCGGCGTCTGCTACAGTATGTGTCTAGGCTCTTTTTCTTTGCTACTGTTTGTGGGCGGGGCTGCAGTTTTCAATTTTCCCGTATTTGCACGCGCAACAACTGGGTGGGACTAACGTTTTGTATCAACATCATGCTGAAACGACTAAAGACTCGTTATCAAGATGATTCATTTGAAGCATTATGAGTCGACTCTTTTATAAATGAATCAAAAGTTTTAAACACTGTGCACTTTCAGATTTAAGCCTTAGCTGGATATTTCACTTCACTCAGTTCTCAGTTCATTCTCAAAAACCCATTACAGGGGCTCTTTAAATCCAATCTATATTAGTCACTTCAAATAACTTCATAGTGAGTCATAGTCATGTTTCATTCACCTGCATATTTTCCTAGGTTCTCTCTGCTGCCACCATCGTTGCCAAACACACTTCGGCCTTGTGCAATGCCTGCCGGCTCGCCTCCTCCAAGACATCCAACCCAGTTGCTAAGAGA[C/T]AGTTCGTCCAGAGTGCCAAAGAGGTGGCCAACAGCACAGCCAACCTCGTCAAGTCCATCAAGGCAAGTTTGGAGAATATCAGTCAGTGTTTATGTGCTAGTGTTATTGCGGTGATCATAACTCTGTGTTTGTGTGATCATGTCAGGCTCTCGACGGGGCCTTTAACCAGGAAAACAGACAGAAGTGTAAGGAAGCCACTGGGCCACTCATTGAGGCTGTGGATAACCTGACTGCCTTCGCTTCAAACCCAGAGTTCGCAAGTGTACCCGCTCAGATCAGCCCAGAGGTGTGTTAAATCACTGTTATATCACAGTAATCTTATTTATTTTATTGCTTGTCCAAAAGTTTAGGGACAGTAAGCGTTATGTAATTCCTTCTTTTATTCAGAAAGGATGTATTTAATTCATATAAGAGTGATTTCAGAAGGATCACACAACAAAGCTTATTTATTCAGTCTTCATGTGCTATTTACAGGGCTGGACTTAACTAATAAGCAAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15487
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Nonsense 2108 2538 46 56
ENSDART00000078135 Nonsense 2114 2544 46 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8263823)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6276985
GRCz11 10 6278194
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCCACCAAAGCAGCGGCCGGCAAACCTCACGATGACCCCGCCATGCTG[C/T]AGCTCAARAACTCTGCTAAGGTACAAAACATTCTCCAACACACAGCCCTT
Long Flanking Sequence:
TGAAGACATCCAGTAGTCTGCATGTTTGATTCATTTATTAAGCGCAAAGATTTGTTTTAAAGCTATTTCTTAGCTTTAAACGAATAAATGAACAATAATAACGAAGTGTGGTCAAAAACCACATATCCAAGTTATATCCAAACACACATCCTATTCTTATGCCCCATATGGTCCAAAACCAGACAAATGAACAAATCTAAACTAGTTTTTATTTAAACAAATATAAATATGCTTATAATAAATACTTCTAATAATAATAACATTATACAAATGCAAATTGTCATGAATAAATAAAAAAGTATTACTCTGATAAACATCATTTAGGAAATATCTGAAAAAGAAAAAAAATCACAGTAGGGCTTATAATTTTATCAACTGTATTTGTTGTTTGTCAGGTGGTTCTGATCAACGCTGTGAAGGACGTGGCTAAAGCTCTGGGTGACCTGATCAGCGCCACCAAAGCAGCGGCCGGCAAACCTCACGATGACCCCGCCATGCTG[C/T]AGCTCAAAAACTCTGCTAAGGTACAAAACATTCTCCAACACACAGCCCTTAGACTGTCTCTGCTCGGGGCTTTCAGTGGTTGAGCTCAATCAAAATGACTGTCCTGATTATTATGGGCTGCCAGACAACATTAGCTGACCTGAAATCATGATTCTGTGACCTACAAACCAAACTGGAAGAACTGATGACGATGATTTACGCTTGGATAAGTGGTTGTTATTGGTAGCTAAAACTAATAAAATAAATATTAGATAAACATTTTTAAAACACATTAATATTGCTTTAACAAATTTAAACACAAAATAAAACAATTCAACACAAATGTAAAAACAAATATTATATATTAATATGGCATGACTAATAACTAATGAAACCACAAGTGCACATAATAAAATTATTTAAATAAAAAATAAGAAAAAAGAAAATCTGAAAAGAAAAGATCATTTAAAATGTGAATAAATACTATGATAGTATATACGTATTGCTAACGCAACTGACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31764
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Nonsense 2136 2538 47 56
ENSDART00000078135 Nonsense 2142 2544 47 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8266596)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6279758
GRCz11 10 6280967
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGACGTCTCTACTTAAGACGGTGAAGGCGGTGGAGGATGAAGCCACT[A/T]AAGGCACACGAGCACTAGAGGCCACCATAGAGCACATCAAACAAGAGCTG
Long Flanking Sequence:
TTTAGTTATTGATATTATTTATGTTACCACTAAACCGCATGTCTTTGGGCTTGTGGGGGAAACCGGAGCACCTGGAGAAAACCCACGCCAACACGAGGAGAACATGCAAATTCCACACAGGAACGCCAACTTACCCAGCCGGGGCTTGAACCAGCGACCTTCTTGCTGCGAGGCAATTGTGCTACCCACTGCGCCACCATGCTGCCTCGATTATTCCATTTAATTTTTTTTTTATTCTTATTTCCAATCAATTTTTCTGATTTGCTTGATTTCTGAACGTCTCTTTCAATATTTCTTTCTGTGCCAGGCTTCAGCAAAGCAAACCTTTCTGTATTGCCTCTATTAATAAAACTGATTTCTCCTTTGATTTCCCATTCATGTTAAGTGGCATTGCTAATGTGTTTTTGGATTCGTGTCGTTTCTGTGGTGTTCATTAGGTGATGGTGACCAATGTGACGTCTCTACTTAAGACGGTGAAGGCGGTGGAGGATGAAGCCACT[A/T]AAGGCACACGAGCACTAGAGGCCACCATAGAGCACATCAAACAAGAGCTGGCTGTAAGAAACACACACTCTCTAAATCAGTGCATTCATGGCTACAGTTCAATCAAGTATATTAACAAATATTTCAATAATAATTATTATGAATGGTTAAGGATGTCAATATATGGATTTTGACATTTATTTTAATATTTTATATGCTCTTTTGGGGGTTCAAAAATTGTTTGTACACAATTTTCATTCACTCATTTTGTTGTCGGCTTAGTCCCTTTATTATATCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCATCACTGGGAAACATCCACACACACATTCACACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCATCTGTACCACATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCAAAGGCAGGGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10075
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Nonsense 2205 2538 48 56
ENSDART00000078135 Nonsense 2211 2544 48 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8267645)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6280807
GRCz11 10 6282016
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAACTCCTGCCRTCAGGAGGAYGTGATCGCCACWGCTAACCTAAGCAGA[C/T]GAGCTGTCGCAGACATGCTGCGCTCCTGCAAGGTGAGGCCACTTTCAMAG
Long Flanking Sequence:
CGACCTTCTTGCTGTGAGGCAACAGCACTACCTACTGCGCCACTGCCTCGCCCACACAATTGTCAAACTTTTTCAAATATTACAAAGTAATTTTTAAGACAGCAAGGACATTTTTCACAGTATTTCCTATTATATTTTTTATACTAATTAAGTTAGATTTTCTCCAGAAGTCTAACTTTCTAAATAATTTAAAATTTGTGATAAGGTCAATAAAATCAGCGCCTTTTATACATTTGCTTTAGACGGAAAAAACTTAATTCAGAAATTGAAACAAAATAAACCTTAACTTACTTAAGTCTTTGAGATCATCTTATGATTTAAACACAATCTGTGTGTCTTTCCCTCAGGTTTTCAGCAGTGCAGATCCTCCTCCAAAGACGGCCACTCCAGAGGAGTTCATCCGCATGACCAAAGGCATCACATTGGCCACAGCTAAAGCAGTGGCTGCTGGGAACTCCTGCCGTCAGGAGGACGTGATCGCCACTGCTAACCTAAGCAGA[C/T]GAGCTGTCGCAGACATGCTGCGCTCCTGCAAGGTGAGGCCACTTTCACAGTGTCAACATCACGTCTGACAATGACTCCATATGAACAGATGAACAGTCAGGACCGCTTCAAAATGATATATATGTTTGGCCCCTTAAGAGTTTATACACTAATGAGCAATGGTCTCAAACTCAATTCCTGGACAGCTCTGCACAGTTTAGCTCCAACTCAAACCTGCTTAATAGTTTCTAGTAGTCTTGAACAACTTGATTGGTTTGATCAGGTGTGATTAATTAGGGTTTGAAGCGGAGTCGGATACTTCCTTACTATATAGTACGCTAAAAATAGTATTTGAGCCGAGAAGTATGCCCCAATTCATAGAATTTAAAAACAACAGTATCCAAGAAGTACCTGGATGACCTCCTACTTCCAGCGAGTATCTAAAGTGAGCATCCAACGGATGCTACGCCATCCCATGATCCACCGCGAGAGAATTCATGAATGGGAGTGAAGCGATGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21665
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Nonsense 2306 2538 51 56
ENSDART00000078135 Nonsense 2312 2544 51 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8284155)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6297317
GRCz11 10 6298526
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGGTGGATCCCGAAGACCCCACCGTCATTGCAGAAAACGAGCTGCTG[G/T]GAGCCGCAGCTGCCATTGAAGCTGCCGCGAAGAAACTAGAGCAGCTCAAA
Long Flanking Sequence:
TAACTACTAATCCACCCAAACACTGCAGAAATTGCATATCTCATCAATGGTGAAGAAAGACTTTAGATGTATTAAACTTAACTTTAGTCAACACCAAACATAATGTTGATTTCTTTTTTGTTTCGCTTTCACACTGCCCTTTTTGCAGTTAAACAGTGATTGTAAACAAAACCAAATGTGTTATGTCAGCTGTTTGTTGGACAGAAGTTGCTATATTCACACCTGCACCAAAGGGGAAAACAAACTTATGTTTGATTCAAACAAACAAAACAAGACCGATGTAATTCCCTCCTTAATGAAATAAACAGTCCAGCATCAGGTATTGGTGTAATTGTCATCATAACACTATGAGGTTTTGATGCAGCAGTAGTTCTCAGTAGTGTAGTATAACAGACACACAGCACAATCTTACAGAGGAGTTTGATTGGCTGTGATCCTGTCTAGGTACGGAGTGGGTGGATCCCGAAGACCCCACCGTCATTGCAGAAAACGAGCTGCTG[G/T]GAGCCGCAGCTGCCATTGAAGCTGCCGCGAAGAAACTAGAGCAGCTCAAACCCCGAGCCAAACCCAAGGTGAGGAAATGTTTAGACACATCCTTCAGGCTAAACTGACACTGCCTACAGCTTGACATTTCTATATTTAGCTCTGGAAATCCCACTCTGTGTTCATATATTCTTAAGCCAATACATTATCTGACCATTGTACAACTTCTCCTGTTTGTGCTTACCAGTATGGATTTGGATTTAAGGTAACTTCAATCAGCCATGACTACAGTCACTGAGCATGAATTAAAGGGATAGTTCACTCCAAAAAAATGACAAGTCTATCACCTATGCCACTTGATCCAAACTTGTCTGAGGTGCTTTAATCTGCTAAACACAAAAGAGGATCAACTGAAGAGTGTTGGAAACAAAAGCAACCCTTGACTTTCATAGTATTTTATATTCCTACTAGTATATCCCTATGAATTTGGTCACCTACTGTAGCACTTTTAGGAATAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21666
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013609 Essential Splice Site 2328 2538 51 56
ENSDART00000078135 Essential Splice Site 2334 2544 51 56
ENSDART00000098857 None None 323 None 10
ENSDART00000098858 None None 405 None 12
Genomic Location (Zv9):
Chromosome 10 (position 8284225)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 6297387
GRCz11 10 6298596
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGCCGCGAAGAAACTAGAGCAGCTCAAACCCCGAGCCAAACCCAAGG[T/C]GAGGAAATGTTTAGACACATCCTTCAGGCTAAACTGACACTGCCTACAGC
Long Flanking Sequence:
ATTAAACTTAACTTTAGTCAACACCAAACATAATGTTGATTTCTTTTTTGTTTCGCTTTCACACTGCCCTTTTTGCAGTTAAACAGTGATTGTAAACAAAACCAAATGTGTTATGTCAGCTGTTTGTTGGACAGAAGTTGCTATATTCACACCTGCACCAAAGGGGAAAACAAACTTATGTTTGATTCAAACAAACAAAACAAGACCGATGTAATTCCCTCCTTAATGAAATAAACAGTCCAGCATCAGGTATTGGTGTAATTGTCATCATAACACTATGAGGTTTTGATGCAGCAGTAGTTCTCAGTAGTGTAGTATAACAGACACACAGCACAATCTTACAGAGGAGTTTGATTGGCTGTGATCCTGTCTAGGTACGGAGTGGGTGGATCCCGAAGACCCCACCGTCATTGCAGAAAACGAGCTGCTGGGAGCCGCAGCTGCCATTGAAGCTGCCGCGAAGAAACTAGAGCAGCTCAAACCCCGAGCCAAACCCAAGG[T/C]GAGGAAATGTTTAGACACATCCTTCAGGCTAAACTGACACTGCCTACAGCTTGACATTTCTATATTTAGCTCTGGAAATCCCACTCTGTGTTCATATATTCTTAAGCCAATACATTATCTGACCATTGTACAACTTCTCCTGTTTGTGCTTACCAGTATGGATTTGGATTTAAGGTAACTTCAATCAGCCATGACTACAGTCACTGAGCATGAATTAAAGGGATAGTTCACTCCAAAAAAATGACAAGTCTATCACCTATGCCACTTGATCCAAACTTGTCTGAGGTGCTTTAATCTGCTAAACACAAAAGAGGATCAACTGAAGAGTGTTGGAAACAAAAGCAACCCTTGACTTTCATAGTATTTTATATTCCTACTAGTATATCCCTATGAATTTGGTCACCTACTGTAGCACTTTTAGGAATAAAAAGTTTATTCATTTAAATTTAAATGATTTATTGCTAAAACATTTTATATTTTTTTTGTTTCTCTTTTTTTTT
Associated Phenotype:
Not determined