ZMP
ZFHX3
Ensembl ID:
Description:
zinc finger homeobox 3 [Source:HGNC Symbol;Acc:777]
Human Orthologue:
ZFHX3
Human Description:
zinc finger homeobox 3 [Source:HGNC Symbol;Acc:777]
Mouse Orthologue:
Zfhx3
Mouse Description:
zinc finger homeobox 3 Gene [Source:MGI Symbol;Acc:MGI:99948]
Alleles
There are 12 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41077 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7104 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21139 | Nonsense | Available for shipment | Available now |
| sa18256 | Nonsense | Available for shipment | Available now |
| sa7105 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38655 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31615 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13265 | Nonsense | Available for shipment | Available now |
| sa13073 | Nonsense | Available for shipment | Available now |
| sa21140 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41077
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 361 | 3838 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70494962)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 68137680 |
| GRCz11 | 7 | 68372374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTCCATGACCATCGCATGACTCTATGTGAGGACGAGCGCAGACTTT[T/A]AGGCCACAAGCATGCATCGGCCATTATACAGGGCATTGGGAAAGACAAAG
Long Flanking Sequence:
CATTGTGGAGAGTCTCAGCCAGCTGATCCAAAGTGATGGGAGCATGGAACCAGGCCTGCTCTCCTCAAACTCTCTCACTAGTGGGGGAAAGCCAGGGGAACCTGTGGGAACTTCTTCAGTGTACCCTCAGATCATCAACACGTTTCATATAGCCTCGTCTTTCGGAAAATGGTTCGGCTCCTCAGACCAAGGTTTCCCCAATACCTCAACCCTGACAGGCCTCAGTCCTGTCCTGCACAGTTTCCGCGTCTTTGATGTGCGGCACAAAAGCAACAAGGATTACCTGAACAGCGACGGGTCTGCCAAGAAGTCCTGTGTATCCAAAGATGTTCCCAACAACGTGGATTTCTCCAAATTTGATGGCCTGGCCCTTTATGGCAAAGGCAAGCCCATCCTCATGTGTTTCCTTTGCAAGTTGTCTTTTGGCTACGCACGCTCCTTTGTCACTCATGCAGTCCATGACCATCGCATGACTCTATGTGAGGACGAGCGCAGACTTT[T/A]AGGCCACAAGCATGCATCGGCCATTATACAGGGCATTGGGAAAGACAAAGAGCCACTCATTAGCTTCCTAGAACCAAAAAATAAGAACTCTCCTTCACCACCTACCCTAGTGCCCATGAACTCAGGCCAGAGCTTCTATGGCACGTTCAGTGGGGTTCATTTAGAAGGGGGCAGCAGTAGTGAGGGAGGTGAGAGCCTCCTCAACAAAGACTCTGACTCGGGTCTCCAGCAACAAGCCCTTCTCACATTGGGGGGGCTAGGCAGCCCCAAAGCATCCTCCCTTACCTCAACCCCAGGCCCAGCCAAAGACTCCAGCACTCTGTCTAAGCCACAGGGTAGGAGAACAGACGGGTCTGTGGGGAAAGAGGGGACTCATAGAGGGGAGGATGGGAATGCAGAAATCTGTGAAAGAAAGACTCTGCTTCCTGGTGAGGAGATGCCCTCAGATGAAGAGGATGAGCTTCTTTTAGAAGAAGAGGATGAAGAGGTAGAGGATGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7104
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 434 | 3838 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70495181)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 68137461 |
| GRCz11 | 7 | 68372155 |
KASP Assay ID:
554-5453.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCAGCAGTAGTGAGGGAGGTGAGAGCCTCCTCAACAAAGACTCTGACT[C/A]GGGTCTCCARCAACAAGCCCTTCTCACATTGGGGGGGCTAGGCAGCCCCA
Long Flanking Sequence:
CCTCAGTCCTGTCCTGCACAGTTTCCGCGTCTTTGATGTGCGGCACAAAAGCAACAAGGATTACCTGAACAGCGACGGGTCTGCCAAGAAGTCCTGTGTATCCAAAGATGTTCCCAACAACGTGGATTTCTCCAAATTTGATGGCCTGGCCCTTTATGGCAAAGGCAAGCCCATCCTCATGTGTTTCCTTTGCAAGTTGTCTTTTGGCTACGCACGCTCCTTTGTCACTCATGCAGTCCATGACCATCGCATGACTCTATGTGAGGACGAGCGCAGACTTTTAGGCCACAAGCATGCATCGGCCATTATACAGGGCATTGGGAAAGACAAAGAGCCACTCATTAGCTTCCTAGAACCAAAAAATAAGAACTCTCCTTCACCACCTACCCTAGTGCCCATGAACTCAGGCCAGAGCTTCTATGGCACGTTCAGTGGGGTTCATTTAGAAGGGGGCAGCAGTAGTGAGGGAGGTGAGAGCCTCCTCAACAAAGACTCTGACT[C/A]GGGTCTCCAGCAACAAGCCCTTCTCACATTGGGGGGGCTAGGCAGCCCCAAAGCATCCTCCCTTACCTCAACCCCAGGCCCAGCCAAAGACTCCAGCACTCTGTCTAAGCCACAGGGTAGGAGAACAGACGGGTCTGTGGGGAAAGAGGGGACTCATAGAGGGGAGGATGGGAATGCAGAAATCTGTGAAAGAAAGACTCTGCTTCCTGGTGAGGAGATGCCCTCAGATGAAGAGGATGAGCTTCTTTTAGAAGAAGAGGATGAAGAGGTAGAGGATGAAGGCACTGCGGTGGCCTGTAGTGGAAGTAGCAGCAGCAGTGGTAGATTTGTGGGGGAACCGGCTGTCTCAAACCAAAGCATCTCCAAATCTCCTTTATTAATGCCTAGTAGCGCTCTCCAGCCTTCTGCTTGTCTTTCTGCAGCCAGCCCCGCACTTAGCAGCAAATTCTCTGCTTCCATGTCCTCTTCTATCAGAGGAGCAGAGGACGGGATGGCTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34236
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 517 | 3838 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70495430)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 68137212 |
| GRCz11 | 7 | 68371906 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCTTCCTGGTGAGGAGATGCCCTCAGATGAAGAGGATGAGCTTCTTT[T/A]AGAAGAAGAGGATGAAGAGGTAGAGGATGAAGGCACTGCGGTGGCCTGTA
Long Flanking Sequence:
CATGACTCTATGTGAGGACGAGCGCAGACTTTTAGGCCACAAGCATGCATCGGCCATTATACAGGGCATTGGGAAAGACAAAGAGCCACTCATTAGCTTCCTAGAACCAAAAAATAAGAACTCTCCTTCACCACCTACCCTAGTGCCCATGAACTCAGGCCAGAGCTTCTATGGCACGTTCAGTGGGGTTCATTTAGAAGGGGGCAGCAGTAGTGAGGGAGGTGAGAGCCTCCTCAACAAAGACTCTGACTCGGGTCTCCAGCAACAAGCCCTTCTCACATTGGGGGGGCTAGGCAGCCCCAAAGCATCCTCCCTTACCTCAACCCCAGGCCCAGCCAAAGACTCCAGCACTCTGTCTAAGCCACAGGGTAGGAGAACAGACGGGTCTGTGGGGAAAGAGGGGACTCATAGAGGGGAGGATGGGAATGCAGAAATCTGTGAAAGAAAGACTCTGCTTCCTGGTGAGGAGATGCCCTCAGATGAAGAGGATGAGCTTCTTT[T/A]AGAAGAAGAGGATGAAGAGGTAGAGGATGAAGGCACTGCGGTGGCCTGTAGTGGAAGTAGCAGCAGCAGTGGTAGATTTGTGGGGGAACCGGCTGTCTCAAACCAAAGCATCTCCAAATCTCCTTTATTAATGCCTAGTAGCGCTCTCCAGCCTTCTGCTTGTCTTTCTGCAGCCAGCCCCGCACTTAGCAGCAAATTCTCTGCTTCCATGTCCTCTTCTATCAGAGGAGCAGAGGACGGGATGGCTGCAGACGGTGGAGGGAGGACTTCAGAACTCCCTCTGAGCTTTAACTGCCAGGGGTCTACAGTACCCATGGCAATGGCGGCAGTTGCTGGCAGAGGGGGTGAAGAGGATGGGGCCGCATGCTCTGCTGCGAGCACGTCCTCCCCTCTTGCCTCTAATGCTGCTGCTGAGGAAAGTGCCAATCGAGATAGTGCCACAGCTCCTGAACCAAATGAATGCCCAGCAGAGGGAGATGAGGACAACGGTGCCCTCCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21139
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 718 | 3838 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70496034)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 68136608 |
| GRCz11 | 7 | 68371302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACACCTCCATCACACAGCTGCTTGTGACTTGTCAGGAATAAGTGAATG[C/A]ACCCAGAACCATGGGGCTGGGGGCAGTGGAGGAAGTGGGGTAGAGTGCCC
Long Flanking Sequence:
CAAAGCATCTCCAAATCTCCTTTATTAATGCCTAGTAGCGCTCTCCAGCCTTCTGCTTGTCTTTCTGCAGCCAGCCCCGCACTTAGCAGCAAATTCTCTGCTTCCATGTCCTCTTCTATCAGAGGAGCAGAGGACGGGATGGCTGCAGACGGTGGAGGGAGGACTTCAGAACTCCCTCTGAGCTTTAACTGCCAGGGGTCTACAGTACCCATGGCAATGGCGGCAGTTGCTGGCAGAGGGGGTGAAGAGGATGGGGCCGCATGCTCTGCTGCGAGCACGTCCTCCCCTCTTGCCTCTAATGCTGCTGCTGAGGAAAGTGCCAATCGAGATAGTGCCACAGCTCCTGAACCAAATGAATGCCCAGCAGAGGGAGATGAGGACAACGGTGCCCTCCTCCACCACCACCTTCACCACCATCACCACCACCTACACCCTTCGCCCAATGCCCACACACACCTCCATCACACAGCTGCTTGTGACTTGTCAGGAATAAGTGAATG[C/A]ACCCAGAACCATGGGGCTGGGGGCAGTGGAGGAAGTGGGGTAGAGTGCCCAAAGTGTGATACTGTCTTAGGCTCTTCTCGCTCATTGGGTGGCCATATGACCATGATGCACTCACGAAATTCGTGCAAGACACTAAAGTGTCCTAAGTGCAACTGGCACTACAAATACCAGCAGACCTTGGAGGCCCACATGAAGGAGAAGCACCCCGACTCTGGAGGCTCTTGTGTGTACTGCAGCAGTGGGCAGAGTCATCCTCGCCTTGCCCGTGGGGAGAGCTACACTTGCGGCTATAAGCCCTTCCGCTGTGAGGTCTGCAACTATTCCACTACCACCAAAGGTAACCTAAGCATCCATATGCAGTCTGACAAGCATCTTAACAACATGCAGACGTTACAAAATGGAGGAACTATTCCAACTGGTGAGCAGGTGTTTGGACATGCGCCAGGTGGGGTGGTGCCTGTTTCTTCAGCTTCCCAGCCTGGCAGCCATCATCCAAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18256
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 760 | 3838 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70496160)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 68136482 |
| GRCz11 | 7 | 68371176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCGCTCATTGGGTGGCCATATGACCATGATGCACTCACGAAATTCGTG[C/A]AAGACACTAAAGTGTCCYAAGTGCAAYTGGCACTACAAATACCAGCAGAC
Long Flanking Sequence:
GCAGAGGACGGGATGGCTGCAGACGGTGGAGGGAGGACTTCAGAACTCCCTCTGAGCTTTAACTGCCAGGGGTCTACAGTACCCATGGCAATGGCGGCAGTTGCTGGCAGAGGGGGTGAAGAGGATGGGGCCGCATGCTCTGCTGCGAGCACGTCCTCCCCTCTTGCCTCTAATGCTGCTGCTGAGGAAAGTGCCAATCGAGATAGTGCCACAGCTCCTGAACCAAATGAATGCCCAGCAGAGGGAGATGAGGACAACGGTGCCCTCCTCCACCACCACCTTCACCACCATCACCACCACCTACACCCTTCGCCCAATGCCCACACACACCTCCATCACACAGCTGCTTGTGACTTGTCAGGAATAAGTGAATGCACCCAGAACCATGGGGCTGGGGGCAGTGGAGGAAGTGGGGTAGAGTGCCCAAAGTGTGATACTGTCTTAGGCTCTTCTCGCTCATTGGGTGGCCATATGACCATGATGCACTCACGAAATTCGTG[C/A]AAGACACTAAAGTGTCCTAAGTGCAACTGGCACTACAAATACCAGCAGACCTTGGAGGCCCACATGAAGGAGAAGCACCCCGACTCTGGAGGCTCTTGTGTGTACTGCAGCAGTGGGCAGAGTCATCCTCGCCTTGCCCGTGGGGAGAGCTACACTTGCGGCTATAAGCCCTTCCGCTGTGAGGTCTGCAACTATTCCACTACCACCAAAGGTAACCTAAGCATCCATATGCAGTCTGACAAGCATCTTAACAACATGCAGACGTTACAAAATGGAGGAACTATTCCAACTGGTGAGCAGGTGTTTGGACATGCGCCAGGTGGGGTGGTGCCTGTTTCTTCAGCTTCCCAGCCTGGCAGCCATCATCCAAGTCACCACCATCATCCAGCCCAGTCCTCTACTCACATGACAGGACCCTGTGGTGCCCCTTCACCCACCAAACCAAAAAGCAAACCCACTTGGCGATGTGAGGTGTGCGACTATGAGACCAATGTAGCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7105
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 1385 | 3838 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70635249)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67997393 |
| GRCz11 | 7 | 68232087 |
KASP Assay ID:
554-5425.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTTCGCTGCCCGYTGTGCCAGGAYATGCTCAACAACAAGGTCCACCTG[C/T]AGTTCCATCTCACCCACCTCCACAGCGTGGCACCAGACTGCGTGGACAAG
Long Flanking Sequence:
TCATTTTTGAGGTGCTGATGATCACAGAGAGCTGAACAGATCTTTTAATTCCAGTTGCTTTAAACACGCCCTGTCTTGTGGATATGATTATACACCTTACTACGGAGAAATGATAACATGGCTGTCAATCAATTTGGTGGGCGGGGAAACCACACTCCTACTTCACGTCGTGGTCGGCATCAAAATGGGAGGGATAAGGAACCTATTTTAACATCAGGAAATTTAAAAAAGAGACTTATTGTGTTTCTATCACTCCAATATGACTGTGGACACACAATAACAGCTTCCAAATAGGTTCCCTTTGAAGTAAACAGAACTTAACTACACTAATATTCGCTCTTTGCCTTCTTGTCATTGTGCAGATGTACCAGTGCCCCTACTGCAAGTTCAGCAACACAGATCTGAACCGGCTCAGAATGCACGTGATGACGCAGCACTCAGTGCAGCCCATGTTTCGCTGCCCGTTGTGCCAGGATATGCTCAACAACAAGGTCCACCTG[C/T]AGTTCCATCTCACCCACCTCCACAGCGTGGCACCAGACTGCGTGGACAAGCTTATTGCCACTGTAAGTTCCAGCGAAAACAACTATTTAACCTTCCGTTTCATGCGCAGAAATTAGTTTCTGCAGAACGTTTAAGACATTCAACTAAGTTTTACTCTACCTCAAAAGAGTCAAAAGAGCCGTGCTATTAATTTTCCATTCAGTCTCTCTCTCTGGTAGATGAATATTTACTGATTACAGTGAATTTCTCTCTGCGATCTTTTGTTTTTTGATGTTAGATTAGAGCAAAGGCCTCACTGCCCTGCTATTGTGTGGCATGAAGGCCATATGCATTCACTTTACTCCCCATGCTCAGCGCTGATTATGCCTCACACATGACTCACAGTTCCTTACTCACTCTCTCTTTGTGGGCTGAAAGTTGTTTCTTTTCATGTAATTAATGACATTTTAAAGCTTAATTAAATGCCATAGTAAACTGATCATTCTAATACGGCCCCTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38655
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 1877 | 3838 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70641674)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67990968 |
| GRCz11 | 7 | 68225662 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCAGCAGTTGGCCCAGGCTCAAGCACAGGCACAGGCTCAGCTCCAG[C/T]AGGAGCTCCAGCAGGCCGCACTCCTTCAGTCCCAGCTTTTTAACCCTCTT
Long Flanking Sequence:
CGGAGCCTACCAGCAGCCCTGATAACAAACCCTTCAAGTGCAGCACTTGCAATGTAGCATATAGCCAGAGCTCTACACTGGAGATTCACATGCGCTCTGTTCTTCATCAAACCAAGGCCAGGGCAGCAAAGCTTGAAGCAGCTGGTGGCAGTTCTACTGCTGTTAGCAGTAGTGGCCCAAGCGGAAGCACTTCCAATAGCACTTCAACCCCGAGCCCTATTCCAGCCACTAACTCAACTACCAGCTCTAGCAACAGCAGCAGCTCTCCTGCAGGAGCACAGACAGCACAGAGCATAATAGGAGGCAATCATCTGTCAAGCCATTCACACAGTGTTGAGAATTTGGGTAATTCAGCTAGTCATACTTCCTCCTCTGAGAATCATGAAGTGAAAAAGAAGAAATTTTCTGACATGCTCTCCTCAAGAAGTCATCAACAGCAGCTCCAACAACAGCAGCAGCAGTTGGCCCAGGCTCAAGCACAGGCACAGGCTCAGCTCCAG[C/T]AGGAGCTCCAGCAGGCCGCACTCCTTCAGTCCCAGCTTTTTAACCCTCTTCTCCAGCACTTCCCAATGACAACAGATGCTCTTCTCCCTCTTCAGCAACAGCAGCTGCTTTTCCCCTTTTACATTCCCGGGGCAGAATTTCAACTTAATCCAGAAATGAACCTAAATAGCTCTTCGTTGAACTTGAGTGGATCTACTGCATCATTGTTGGAGGAACAGAAAAACTCTGTCCAGCAGGCCCAACAAAGTTGCTTACAACAACAACTTATGCACCACCACCTTCAGCAACAGCACCAAGCTCATTCCCACTCGCAAGGTTCAAGCCAAATGGCTTTACTTCAACAGAGTGCCCTCTCTCACCCTGTAGACAAAAAGACAAAGCCATCTCCCCACACTGAGAAAGAAAGAGATCTGCCAAAGGACAAAGAAATTAGTGATAAATCAGAGGATCACGTTCCAAAAGATTTGTCAGACAAGTCCAAAGAAAAGATAGATGCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31615
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 1880 | 3838 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70641683)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67990959 |
| GRCz11 | 7 | 68225653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGGCCCAGGCTCAAGCACAGGCACAGGCTCAGCTCCAGCAGGAGCTC[C/T]AGCAGGCCGCACTCCTTCAGTCCCAGCTTTTTAACCCTCTTCTCCAGCAC
Long Flanking Sequence:
CCAGCAGCCCTGATAACAAACCCTTCAAGTGCAGCACTTGCAATGTAGCATATAGCCAGAGCTCTACACTGGAGATTCACATGCGCTCTGTTCTTCATCAAACCAAGGCCAGGGCAGCAAAGCTTGAAGCAGCTGGTGGCAGTTCTACTGCTGTTAGCAGTAGTGGCCCAAGCGGAAGCACTTCCAATAGCACTTCAACCCCGAGCCCTATTCCAGCCACTAACTCAACTACCAGCTCTAGCAACAGCAGCAGCTCTCCTGCAGGAGCACAGACAGCACAGAGCATAATAGGAGGCAATCATCTGTCAAGCCATTCACACAGTGTTGAGAATTTGGGTAATTCAGCTAGTCATACTTCCTCCTCTGAGAATCATGAAGTGAAAAAGAAGAAATTTTCTGACATGCTCTCCTCAAGAAGTCATCAACAGCAGCTCCAACAACAGCAGCAGCAGTTGGCCCAGGCTCAAGCACAGGCACAGGCTCAGCTCCAGCAGGAGCTC[C/T]AGCAGGCCGCACTCCTTCAGTCCCAGCTTTTTAACCCTCTTCTCCAGCACTTCCCAATGACAACAGATGCTCTTCTCCCTCTTCAGCAACAGCAGCTGCTTTTCCCCTTTTACATTCCCGGGGCAGAATTTCAACTTAATCCAGAAATGAACCTAAATAGCTCTTCGTTGAACTTGAGTGGATCTACTGCATCATTGTTGGAGGAACAGAAAAACTCTGTCCAGCAGGCCCAACAAAGTTGCTTACAACAACAACTTATGCACCACCACCTTCAGCAACAGCACCAAGCTCATTCCCACTCGCAAGGTTCAAGCCAAATGGCTTTACTTCAACAGAGTGCCCTCTCTCACCCTGTAGACAAAAAGACAAAGCCATCTCCCCACACTGAGAAAGAAAGAGATCTGCCAAAGGACAAAGAAATTAGTGATAAATCAGAGGATCACGTTCCAAAAGATTTGTCAGACAAGTCCAAAGAAAAGATAGATGCTACTCAAGCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13265
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 2377 | 3838 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70643176)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67989466 |
| GRCz11 | 7 | 68224160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAATTGATTCAAAACCCCCCTCCCCTGAACCTCTAAAACAGGAAGCATA[T/A]GGAAATAAGCGGTCTTCAAGAACACGGTTCACAGACTACCAACTGAGAGT
Long Flanking Sequence:
CCAACTGCTCCAACCCCTCAGCCTCCAGTTCCACTTTCCCAAATTCCAATGGCAATGGATCTCCCTCTATTCTCTCCACTAATGATGCAGCCCATGTCACTCCAATCATTGCCTTCACAAATTCCTGCCCAGCTGCCAACTGTGGAGCCCAGTTTGGCCACTGATCTTGCCCAGCTCTATCAACAGCAGCTTACCCCTGCCATGTTGCAGCAACAGAATAAGAGACCTCGCACCCGAATCACAGACGACCAGCTAAGGGTGCTCCGACAGTATTTCGATATCAACAACTCTCCCAATGAAGAGCAAATTAAAGAAATGGCAGATAAATCGGGACTCCCCCAGAAAGTCATTAAGCACTGGTTTCGAAACACACTCTTCAAGGAGCGGCAGCGCAACAAAGACTCACCTTATAACTTTAACAACCCTCCAATTACAACTCTTGAAGAAACAAAAATTGATTCAAAACCCCCCTCCCCTGAACCTCTAAAACAGGAAGCATA[T/A]GGAAATAAGCGGTCTTCAAGAACACGGTTCACAGACTACCAACTGAGAGTCCTGCAAGATTTCTTTGACGCTAATGCTTATCCTAAAGATGATGAATTTGAGCAGTTATCTAATCTCCTGAACCTTCCAACTCGAGTAATTGTTGTGTGGTTTCAAAATGCCAGACAAAAAGCCCGTAAAAATTATGAGAACCAGGGAGATGGAGTAAAAGAAGGTGACCGACGTGAGTTATCCAATGACAGATACATTCGCACTACCAACTTAAACTATCAGTGCAAGAAGTGCAGCCTGGTTTTCCAGCGCATATTTGACCTTATTAAACACCAAAAGAAGCTCTGTTACAAAGACGAAGAGGATGACGGCCAGTATGACAGCCTAAATGAGGACTCTCTGGATCTCTCCCATGAATACTATACTCCATCTGGGTCATCGGGTCAAACACCAATGCCCTCATCCTCAAGCCTCTGCCCTCTTCCTCCATCCTCTGCATTCTCTCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13073
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 |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 2422 | 3838 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70643309)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67989333 |
| GRCz11 | 7 | 68224027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAAAGATGATGAATTTGAGCAGTTATCTAATCTCCTGAACCTTCCAACT[C/T]GAGTAATTGTTRTGTGGTTTCAAAATGCCAGACAAAAAGCCCGTAAAAAT
Long Flanking Sequence:
TGCCAACTGTGGAGCCCAGTTTGGCCACTGATCTTGCCCAGCTCTATCAACAGCAGCTTACCCCTGCCATGTTGCAGCAACAGAATAAGAGACCTCGCACCCGAATCACAGACGACCAGCTAAGGGTGCTCCGACAGTATTTCGATATCAACAACTCTCCCAATGAAGAGCAAATTAAAGAAATGGCAGATAAATCGGGACTCCCCCAGAAAGTCATTAAGCACTGGTTTCGAAACACACTCTTCAAGGAGCGGCAGCGCAACAAAGACTCACCTTATAACTTTAACAACCCTCCAATTACAACTCTTGAAGAAACAAAAATTGATTCAAAACCCCCCTCCCCTGAACCTCTAAAACAGGAAGCATATGGAAATAAGCGGTCTTCAAGAACACGGTTCACAGACTACCAACTGAGAGTCCTGCAAGATTTCTTTGACGCTAATGCTTATCCTAAAGATGATGAATTTGAGCAGTTATCTAATCTCCTGAACCTTCCAACT[C/T]GAGTAATTGTTGTGTGGTTTCAAAATGCCAGACAAAAAGCCCGTAAAAATTATGAGAACCAGGGAGATGGAGTAAAAGAAGGTGACCGACGTGAGTTATCCAATGACAGATACATTCGCACTACCAACTTAAACTATCAGTGCAAGAAGTGCAGCCTGGTTTTCCAGCGCATATTTGACCTTATTAAACACCAAAAGAAGCTCTGTTACAAAGACGAAGAGGATGACGGCCAGTATGACAGCCTAAATGAGGACTCTCTGGATCTCTCCCATGAATACTATACTCCATCTGGGTCATCGGGTCAAACACCAATGCCCTCATCCTCAAGCCTCTGCCCTCTTCCTCCATCCTCTGCATTCTCTCACATCGCATCATCTGAAAAGGAGGAGCCTACACCAGCTAACACATCCAACTCCTTTGATGAAAAATCAAGACACTCTGCAGAAACAACATTGGGTCAAAGAGAGCAGACATCTTTGAAACAGGAAACCAGTCATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21140
Status:
Available for shipment
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114582 | Nonsense | 3518 | 3838 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 70646706)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 67985936 |
| GRCz11 | 7 | 68220630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACAGCGGCAGCTTCAGCAGATCCAGCAGCCCAAAGCAAGCCAAACTT[C/A]ACAAAACTCGGTGGACCGCAAGGACTCTGCCAAAGATTCAGTAAAAACAG
Long Flanking Sequence:
GGCAAGGGAGAAAGAGAAACCCAAGGAGAAAGCTGAGAAATCCTCTACACCATCCTCAGCAGGGGGAACTCCTGCTCCCTCCACTTCTGCTGCCAGTGCCAAGAAAGAAAAAACAGACACTGCTGTTCCGGCCACCTCAATGCCAACACCTGGCATGGAGTATGTGGTCGATACTGCCCAACTCCAAGCTCTACAAGCAGCTTTAGCTTCAGATCCAACCGCTCTGCTAACAAGTCAGTTCCTGCCCTACTTTATGCCTGGCTTCTCTCCATACTATGCCCCTCAGATCCCAGGTGCTCTTCAAGGTGGATATCTTCAGCCCATGTATGGCATGGAAAGTCTTTTTCCCTACAACCCAGCTTTATCGCAGGCTCTGATGGGACTGTCACCTGGATCTTTGCTTCAGCATTACCAGCAATATCAGCAGAGCCTGCAGGAGGCACTTCAGCAGCAACAGCGGCAGCTTCAGCAGATCCAGCAGCCCAAAGCAAGCCAAACTT[C/A]ACAAAACTCGGTGGACCGCAAGGACTCTGCCAAAGATTCAGTAAAAACAGAGCAAAAAAGCACCCCCTCAGCTGAAACCTCTTCCACTCACAACAACGTAGCCGCTGAGCAGCACGAAGTGGATGGCAAAGGTGCAGACCCCCATCTTGACCAATATATTGTCCCTAAAGTTCAGTACCGGCTGGCGTGCCGCAAGTGTCAAGCTGTCTTCAGCAAGGAGGAAGCGGCTATCAGCCACCTTAAGTCAATTTGTTTTTTTGGTCAGTCTGTGGCAAACCTGCAAGAGATGTTGCTTCGGGTCCCCAACAGTGGGAATGCAGCAGAAGGCGGCCTCTACGACTGCCTTGCCTGTGACACCACGCTAGAAGGGGACAAAGCGCTCAGTCAACACCTGGATTCAGCCTTGCACAAACACAGAACAATCAAGAGATCCAGAAATGCCAAAGAGCACGCTACTAATTTATTACCTCACTCTTCAGCCTGCTTCCCCAGTCCTAACA
Associated Phenotype:
Not determined