ZMP
BAI1 (2 of 3)
Ensembl ID:
Description:
brain-specific angiogenesis inhibitor 1 [Source:HGNC Symbol;Acc:943]
Human Orthologue:
BAI1
Human Description:
brain-specific angiogenesis inhibitor 1 [Source:HGNC Symbol;Acc:943]
Mouse Orthologue:
Bai1
Mouse Description:
brain-specific angiogenesis inhibitor 1 Gene [Source:MGI Symbol;Acc:MGI:1933736]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14551 | Nonsense | Available for shipment | Available now |
| sa15683 | Nonsense | Available for shipment | Available now |
| sa22905 | Essential Splice Site | Available for shipment | Available now |
| sa36209 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa28704 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25026 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42780 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42781 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa12101 | Nonsense | Available for shipment | Available now |
| sa44857 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14551
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 |
|---|---|---|---|---|---|
| ENSDART00000112003 | Nonsense | 74 | 767 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38935212)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37570975 |
| GRCz11 | 16 | 37521007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCAGCATGCCCTGCACCTGGACCCTACAGAACCCTGATCCACGGCGCTA[C/A]ACCATCTTCATCAAAGTCACAAAACCAACTAGAGACTGCATTGCCCGGCA
Long Flanking Sequence:
CTGGTCAATGGATAATTGCTGTTGTTTTCCCATCTGGCTCATAGTCTTTTTTTCTGTCTTCTCTAATCTTGCAGATCTCTCTGAGGGCGTTTGGCATCATGGACAGCAAACTGGATCAATGAGCCAAGGTTCCGTCTCATCCTGAGCTGACGGTTCTGCAAACATAAGAGAATATCGGCGAGTCAACAAAACGAGGCTGTCGATCCTAAATTTACAAGAAACCTCGCAAAAATAAGGCTTTGCTATCTTCAGCCTCACTCTTTTCTGCTGTTAACAGCCATGATATCAAAATTTTTAGGTAACTGTTCATCGCTGATCCTGCTGTTCCCTCTTCTTCAACTGCTGCGGATGGACATGCTCAACGCTGCCCCCTCTGGTCCGGAGACTGACAGCTGCTCCACATTAGTCCAGAGCCGCTTCTTTGGATTCTTCCTCTCGTCTTCTGCATTTCCCAGCATGCCCTGCACCTGGACCCTACAGAACCCTGATCCACGGCGCTA[C/A]ACCATCTTCATCAAAGTCACAAAACCAACTAGAGACTGCATTGCCCGGCAGCACCGGACCTTCCAGTTTGACTCCTTCTTAGAGACGACTCGGACCTTTCTCGGAATGGAGAGCTTTGATGAAGTGGTGAAGCTGTGCGATGCCTCTACCCATGTTGCCTTCTTGGAAGCTGGGAAACAATTCCTGCAGATCCGGAAAGGGCTGCCTAGAGCAGGCGCTGGGTCTAGAAATGGGGATGGGGAATTTAAAGTGGAGTATCTTGTGGTTGGGAAGCGTAACCCCAGCATGGCTGCGTGTCAAATGCTTTGCCAGTGGTTGGAGGACTGCCTGACCTACAGTTCTTCCACCCGACCCTGTGGCATCATGCAGACCCCATGCCAATGCTGGGACCAGCCTCCACTAGACAAAGAATCCAATGGATGCTATCGAGATGGGGTCTTTCTGGAAAACTGCATCCCTGTTGTGAAAGAAGGAGCGTCTGAAACTGACAATAGCGGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15683
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 |
|---|---|---|---|---|---|
| ENSDART00000112003 | Nonsense | 217 | 767 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38935639)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37571402 |
| GRCz11 | 16 | 37521434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAATGCTGGGACCAGCCTCCACTAGACAAAGAMTCCAATGGATGCTAT[C/T]GAGATGGGGTCTTTCTGGAAAACTGCAYCCCTGTTGTGAAAGAAGGAGCG
Long Flanking Sequence:
TCTTCCTCTCGTCTTCTGCATTTCCCAGCATGCCCTGCACCTGGACCCTACAGAACCCTGATCCACGGCGCTACACCATCTTCATCAAAGTCACAAAACCAACTAGAGACTGCATTGCCCGGCAGCACCGGACCTTCCAGTTTGACTCCTTCTTAGAGACGACTCGGACCTTTCTCGGAATGGAGAGCTTTGATGAAGTGGTGAAGCTGTGCGATGCCTCTACCCATGTTGCCTTCTTGGAAGCTGGGAAACAATTCCTGCAGATCCGGAAAGGGCTGCCTAGAGCAGGCGCTGGGTCTAGAAATGGGGATGGGGAATTTAAAGTGGAGTATCTTGTGGTTGGGAAGCGTAACCCCAGCATGGCTGCGTGTCAAATGCTTTGCCAGTGGTTGGAGGACTGCCTGACCTACAGTTCTTCCACCCGACCCTGTGGCATCATGCAGACCCCATGCCAATGCTGGGACCAGCCTCCACTAGACAAAGAATCCAATGGATGCTAT[C/T]GAGATGGGGTCTTTCTGGAAAACTGCATCCCTGTTGTGAAAGAAGGAGCGTCTGAAACTGACAATAGCGGTAAGACAGTTTTGTCTAGTTATAATTCAGCATGGTTTGATTGTTATTCAATTGTTATTCCACCACTGTAAGGTTGGTAGCTTGTCATATTTGTTAGCAAATAAACAAAAGAATCAAAGCTGAAGATACACAACAAGAGTTCAGAGAGAACTGATGCAGGTTAAAAAAAAAGAGAAGGGAGGTAAAAGGAGTTTTAGGTTTCAGCTGATGTGTCCTAGCTGGGTGACCTTGGCTTCTTGGCGCCATGTGTGATCCTGTGAGGGTTCAGATAGGGATATTGGATCGGCCCGTGGGAGAGTTGATGCGGCAGACATGCTCTGGGAGTGTCACAGGATAGTGGTGGTGCTGCTCTTGGCGATTGATTATTAGGAAAAAAATGGGGCCAGTTACTGAGTTCAGTGCTATGATGTGATCTCTTTTCCAAGACTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22905
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112003 | Essential Splice Site | 240 | 767 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38935710)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37571473 |
| GRCz11 | 16 | 37521505 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGCATCCCTGTTGTGAAAGAAGGAGCGTCTGAAACTGACAATAGCGG[T/A]AAGACAGTTTTGTCTAGTTATAATTCAGCATGGTTTGATTGTTATTCAAT
Long Flanking Sequence:
TACACCATCTTCATCAAAGTCACAAAACCAACTAGAGACTGCATTGCCCGGCAGCACCGGACCTTCCAGTTTGACTCCTTCTTAGAGACGACTCGGACCTTTCTCGGAATGGAGAGCTTTGATGAAGTGGTGAAGCTGTGCGATGCCTCTACCCATGTTGCCTTCTTGGAAGCTGGGAAACAATTCCTGCAGATCCGGAAAGGGCTGCCTAGAGCAGGCGCTGGGTCTAGAAATGGGGATGGGGAATTTAAAGTGGAGTATCTTGTGGTTGGGAAGCGTAACCCCAGCATGGCTGCGTGTCAAATGCTTTGCCAGTGGTTGGAGGACTGCCTGACCTACAGTTCTTCCACCCGACCCTGTGGCATCATGCAGACCCCATGCCAATGCTGGGACCAGCCTCCACTAGACAAAGAATCCAATGGATGCTATCGAGATGGGGTCTTTCTGGAAAACTGCATCCCTGTTGTGAAAGAAGGAGCGTCTGAAACTGACAATAGCGG[T/A]AAGACAGTTTTGTCTAGTTATAATTCAGCATGGTTTGATTGTTATTCAATTGTTATTCCACCACTGTAAGGTTGGTAGCTTGTCATATTTGTTAGCAAATAAACAAAAGAATCAAAGCTGAAGATACACAACAAGAGTTCAGAGAGAACTGATGCAGGTTAAAAAAAAAGAGAAGGGAGGTAAAAGGAGTTTTAGGTTTCAGCTGATGTGTCCTAGCTGGGTGACCTTGGCTTCTTGGCGCCATGTGTGATCCTGTGAGGGTTCAGATAGGGATATTGGATCGGCCCGTGGGAGAGTTGATGCGGCAGACATGCTCTGGGAGTGTCACAGGATAGTGGTGGTGCTGCTCTTGGCGATTGATTATTAGGAAAAAAATGGGGCCAGTTACTGAGTTCAGTGCTATGATGTGATCTCTTTTCCAAGACTGAATGTGGCACAGAAACTCAAGCCCTGGGAGAGGCTGTAGCCACTGAGCTGGAAGATCACTCAGCCACTGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36209
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112003 | Essential Splice Site | 293 | 767 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38957112)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37593202 |
| GRCz11 | 16 | 37543234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGTGTTCTGGAAGAAGGTCGTCCATGCAATGCTCAGCCCTGCATCGG[T/G]AAGTGTCAGACTAAATATATGCACGCATGTGACCGTTTACATATTCACTT
Long Flanking Sequence:
GATTTGTGAGTAATTAAAAATGTCTGCAGCTGGACATGGTCCAGCTTCATGTTCTATTCATGCAGATTAATACATATTTGTCGGGGCCTCCGGGATCAGACAGGCAGCAATGTCTCCTATTAAACATTCATGAGGGAGCAGAACGCAGGGACTCATATCCTACTAGTATTTATGGGACCATTTCTACATCTTAGTGCCATCATAATGGATTACGAAATCAGAACATTATTGCTTAGCTGGGATGGAAATTTAATTTGTGTCACAGAAATTTATTAATAAATGGATTTTTTTTCTTGGTAATTACGCTCACATGGATTGTCCGCATGTCTGTTTAATGCAGGTGGCTGGAGTGGGTGGGGCAACTGGGCGGAGTGTAGCAGTGAATGCGGGGGTGGAGTCCAGAAGCGAACGCGCAACTGTCAATCACCTCCTGATGAAGCCTACCTGTGCGAAGGTGTTCTGGAAGAAGGTCGTCCATGCAATGCTCAGCCCTGCATCGG[T/G]AAGTGTCAGACTAAATATATGCACGCATGTGACCGTTTACATATTCACTTCTTCCCCTGCTTTCACTTTCTGACACCTCATTTATTTTCATTCTTCACATTTCACTTTAAAAAATTATATATGTTCTGTTTCTTGTGTGACATAATGATAGAGCAGTAATGATAATATTGCTATGTAAGCTTTTTCTATGATTAACAGCCTTATGATTTCTGAGTTAAAGCTGTTTGAGGTTTAACTATTATAGATGTGGATGTCTTTTACGGTTTTGTCTTGTAATAAAATGTATTACAAACCCCATACAACTGATCTGAGAGTAATTAAAAATGCCTGCATGATATTCAAGATCTTAACTTCCTCAATAAGCCCTCCAGTGAAATTTTTATTCTTTTCTCAAATATTTCCTAAGTGATGTTTAACAGGACAAGGGCCTTTATAAGTATTTTCTATTATACATATTTATATGAGCAATATCACATGAGTAGCAGTGCGATATGGCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28704
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 |
|---|---|---|---|---|---|
| ENSDART00000112003 | Nonsense | 304 | 767 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38960184)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37596274 |
| GRCz11 | 16 | 37546306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCATTGGACCCATAGGCTACAGGCAGTATTCCTCAAAAGGCCAGGGTT[T/A]AAGTCCAGTGAAATACAAAGGAATGCAAGAGGCCATGCTTGGTAAGAGCG
Long Flanking Sequence:
GGCCATCCCAGAATAATAAAGGGACTAAGCTGAAAAGAAAATGAATGAATGAATGAATGAATGAAGGAATTAATTAATGTGTTAAAACATCTTCTCAATTAAACAGCACTTGGGAACATTTGGAAAGGAATTTTAATTTCACAGGAGGGCTAACAATTTTGCCTTGAACTTTGTATATTTTACCTTCTCATACCTAATAATGAAATAAGCAAAACTATATACATATCCCTATTGTGAATATCCTGGCATTTATTAATTTTATACAAACGTTCATACATATATCATAATTTTTTTTTTACCTCTTCAAAATTGAATGTATTTTCTTTTCTTTAGACAAAGTCATTTAACTATTCTACCATTATTACATCAGAACTGGCATTTGCTTTTTTTTAAATTATATAAATTCATCAAATTGATAGAGCAATGACAGAATAAGCATTTGTGTGTGCTTTTCATTGGACCCATAGGCTACAGGCAGTATTCCTCAAAAGGCCAGGGTT[T/A]AAGTCCAGTGAAATACAAAGGAATGCAAGAGGCCATGCTTGGTAAGAGCGTCATTGACCGAGTCCGCGTGAATGTGACCGTAGTGAGTAGATCTTCACTCAGTTTGGATGGGGGCCATGAGTAAATAACCCACTCCATGGTCAAGGCCATCAGCTGCAGATGTCTTCACCTCGATTGTCTGTGTCTCCGTTCCGCATGGTCTGCTTATTTTTCTGTCATCCACCATCCACTGCTCACTTCATCATGCACACTTTTTCGGTGTTCTATGCACAAGAGGTCACGCCAACTCAGAGTTTCGCATGGAGAGTATATCGAACTAAACACAGGTTGACCGCTATGTAACCTTAAACTTCACACAAAATCCCAAGCATGGCTGATGCTGGTCTAAATGTTCAGGTGGCACAGCACTGACCCTATCAGAAGTCGAGTGTAGTTGCTAACCCCACCCCATCCTGCAGGCAAAGGCCGGCTTGGCTCTCGTAGCCAATCCCTGCGCTCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25026
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112003 | Nonsense | 375 | 767 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38963289)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37599379 |
| GRCz11 | 16 | 37549411 |
KASP Assay ID:
554-7737.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGAGTGGTCTGCGTGGAGCGTGTGTTCGGCCACGTGTGGTGAGGGCT[G/A]GCAGAGCCGCACACGCTTCTGCGTCTCCGTGTCGTACAGCACGCAGTGCA
Long Flanking Sequence:
AACTGCTAAAATGCTAACTCGCCTCCAGGTTTTTGCATGCAAATTGATGTCATAGTTCCTCCACTCTATTGGACAACCCATATTACCCATTGAACTGTTAGAACTAAAATGCTTTCTATTGGACATTTAATATGCTACTCTTGCTTTGGAATTGCAACATGATTCCTTGGCTTTCCAAGTTGCTCAGATAATAAAGTCTGATCAATTGGACAGCCTTGTGAATTCCTCCTGTAGTAACTGACTTGCATATCCCAGAACTGAAAGCATGAACGTCTACCACGATGAAATGCTGAGGATATGGAACCAGCGAAGAAATGATTTAAGCCTCCCCTGATCGATGAGGCGGCTAATCCTGCATGCTAATTAGTTTTGGCCCTTTTCCTACCCTTTCCTCCACACCCTACCCCATCCCACTTCCCCTACACCCCTCTCAGTGGATTCTCCGTCGGGTGAGGAGTGGTCTGCGTGGAGCGTGTGTTCGGCCACGTGTGGTGAGGGCT[G/A]GCAGAGCCGCACACGCTTCTGCGTCTCCGTGTCGTACAGCACGCAGTGCAGCGGGCCACTGCGCGAACAGAGACCCTGCAATAACACTGCTGTGTGTCCAGGTAAGCACAGCCCACCTCAGGCCTCTCCTCACCCCCACCATCTTCCTTATCCACCTTTTGTTACCCGCCCCACCTCCACTAAGGCCCGATAGCTTTGCCCACTCACTCTCCAGTTGCTGCCCACCTGAGGCTAACTCTCCCTGCGCTTCCATGTACGGCTGCTCCCCTTCTCAACCCTGGATGCTGGAGAGCCGTGGTAAGATGTTAATGGGTTTAAGTGCAGCATTGTCAGCTAAGTCCCTATAGTTCCCACTGCATGTAGGATGGACTCTCAGTCTCTATTCATTCCATTATTTCAGCTTCCCAGGGGGCCCAGACAAACATGTTTTTCAGATTAAAAAATGTGTCTAGCAAAGCACAATGATGTATTAAGTGCTAATCATATTATGCAGAACTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42780
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 |
|---|---|---|---|---|---|
| ENSDART00000112003 | Nonsense | 543 | 767 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38966848)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37602938 |
| GRCz11 | 16 | 37552970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGCACTTGGTCTGGTTGCACCAAAACCTGTGGTGGAGGAAGTCAGCAG[A/T]GACAGAGGCTGTGTTATGGTCCCTTTTTTGGGGGAGAGGCATGCCCGGGG
Long Flanking Sequence:
GAGGCACTGTAGGAGCAGGAGATTGAAAGAAACCATTGTGAAGTTCCCAGCAAATGATGGTGATTAATTGAGGCTTTAAATCACTATGGATTGGACTAAAGTTTAGCAACCCAAAGCTCGTCTTCCATTCCCCCCGCAATATATCTTTCAGTAATGTGCCCTTATCACGCAAGCCTCACTTTTGTCTTCCTAATGGCACTTTGTATTTTCTATCCTCATTCAGAATATTTTTCAGTCTCTTATTCTGAGTCTTTTTCTCTGTAGTGGATGGCGTGTGGAACGAGTGGTCTGGTTGGAGTTCCTGTTCTTCAACTTGTTCGAATGGAACAATGCAGCGAATTCGGGAGTGTAACGGGCCCTCGTATGGGGGCTTAGAGTGTCAAGGCGAGTGGCACGAGACACGGGATTGCTTCCTTAGAGAATGTCCTGTGGATGGCCAATGGCAACTTTGGAGCACTTGGTCTGGTTGCACCAAAACCTGTGGTGGAGGAAGTCAGCAG[A/T]GACAGAGGCTGTGTTATGGTCCCTTTTTTGGGGGAGAGGCATGCCCGGGGGACCGAGAAGAAGTTAGACGTTGCAATGAGAAGCGATGCCCAGGTAAGACAACCATGTTGCTGTAGTCTAAACTTATGGTAACACTTTATTTTGATGGTTCATTTGAGTATTAGTTGACTTGCTTAAAATCTGTTGATACTGCTCCTTCAACAGACATTTAACTGACTAAGAAACTTTGCAAGTACATGTCAACTTAACCCTAACCCTAACCCCAACCTAACAATCTACTTATAATGTAATGAGAATCAGTTGGCATGTAGATGCAATTTAACTTAAATTCAACAAATGAACAATTAAAATAAAGTGTGACCAAACGTATTCTTACTATGGCTGAGTTTTTTGTATGTTTGTGCTTTCTGAAATCTTTGGTTTTATGCAGAGCCACATGAAATCTGTGATGAGGAGAATTTCTCTAATGTAGTGTGGAAGAAAACACCTGCAGGGGACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42781
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112003 | Essential Splice Site | 608 | 767 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38968382)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37604470 |
| GRCz11 | 16 | 37554502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACCAATCCTCATAATAGATTTGGTAATCATGTCTTACATCTGTGATGC[A/T]GGATTAATTCTACGGCGATGTTCATTAGACAATGAGGGTATAGCATACTG
Long Flanking Sequence:
TTTTCCATTCAAAATATGCCCTATACTTATATATTTTTTTGTTTACATACCTGATGGACATACGTGACCATTACACTCCCATCTCACTTTTTTTTTTTGCAGCTCCTCGCAAATAAGCGTCATGTTTTTAAGATGTCAAGTGATTCAAGCATTTTTTTAAACTACTCCTGAGCACTCACTTCTAAGTTTGGTGTGAATAGCCTTGTTTTAGCCAAGACGTCTATTTTTATATGTGTTTTAACATAATAATGCTTGCTGTAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATTATTACAGTGTTTGACCAATCCTCATAATAGATTTGGTAATCATGTCTTACATCTGTGATGC[A/T]GGATTAATTCTACGGCGATGTTCATTAGACAATGAGGGTATAGCATACTGGGAGAACCCAACATATATGAAGTGCGTCTCAAATGATTACAGAAGTATCCAAACACTGGTAGGTGACCTCTAAACGAGCCCCCAACTAGGTATTAACTAAAATTGTGTCTGCAAATCTGATTTTTTTTTAATTATTATTATTCCAGACCAGAGATCACCTGTCCAAGGCGCAGCGAGGGCTTGTGGGGGATGGTGTTTCTGAAGTGATGACAAAGCTGAGGGTGACGTCAAGTGATGGAACGAGCTACAGCGGAGATCTTTTGGCTATCATAGATGTGCTAAAAAACATGACAGAGATATTTAGGAGATCCTACTACAGCCCCAGTAATGCAGACATGAGGGTTAGTGTGGTATTATGTGCTTATGGAAAGGTGCTATAGAATGAATAGCTGGATTTAGTTTGGCATAATAAAAGTTTAGTACATGTAACTGGCATACTGTGAGCCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12101
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112003 | Nonsense | 624 | 767 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38968433)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37604521 |
| GRCz11 | 16 | 37554553 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATTAATTCTACGGCGATGTTCATTAGACAATGAGGGTAKAGCATACTG[G/A]GAGARCCCAACATAWATGAAGTGCGTCTCAAATGATTACAGAAGTATCCA
Long Flanking Sequence:
TGATGGACATACGTGACCATTACACTCCCATCTCACTTTTTTTTTTTGCAGCTCCTCGCAAATAAGCGTCATGTTTTTAAGATGTCAAGTGATTCAAGCATTTTTTTAAACTACTCCTGAGCACTCACTTCTAAGTTTGGTGTGAATAGCCTTGTTTTAGCCAAGACGTCTATTTTTATATGTGTTTTAACATAATAATGCTTGCTGTAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATTATTACAGTGTTTGACCAATCCTCATAATAGATTTGGTAATCATGTCTTACATCTGTGATGCAGGATTAATTCTACGGCGATGTTCATTAGACAATGAGGGTATAGCATACTG[G/A]GAGAACCCAACATATATGAAGTGCGTCTCAAATGATTACAGAAGTATCCAAACACTGGTAGGTGACCTCTAAACGAGCCCCCAACTAGGTATTAACTAAAATTGTGTCTGCAAATCTGATTTTTTTTTAATTATTATTATTCCAGACCAGAGATCACCTGTCCAAGGCGCAGCGAGGGCTTGTGGGGGATGGTGTTTCTGAAGTGATGACAAAGCTGAGGGTGACGTCAAGTGATGGAACGAGCTACAGCGGAGATCTTTTGGCTATCATAGATGTGCTAAAAAACATGACAGAGATATTTAGGAGATCCTACTACAGCCCCAGTAATGCAGACATGAGGGTTAGTGTGGTATTATGTGCTTATGGAAAGGTGCTATAGAATGAATAGCTGGATTTAGTTTGGCATAATAAAAGTTTAGTACATGTAACTGGCATACTGTGAGCCTCAAACTTAATTTCCTTGTTATCATGTATTTTTCTGAGTGCAAAATCTTGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44857
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112003 | Essential Splice Site | 708 | 767 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 38968774)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37604862 |
| GRCz11 | 16 | 37554894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGATATTTAGGAGATCCTACTACAGCCCCAGTAATGCAGACATGAGG[G/A]TTAGTGTGGTATTATGTGCTTATGGAAAGGTGCTATAGAATGAATAGCTG
Long Flanking Sequence:
ATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATTATTACAGTGTTTGACCAATCCTCATAATAGATTTGGTAATCATGTCTTACATCTGTGATGCAGGATTAATTCTACGGCGATGTTCATTAGACAATGAGGGTATAGCATACTGGGAGAACCCAACATATATGAAGTGCGTCTCAAATGATTACAGAAGTATCCAAACACTGGTAGGTGACCTCTAAACGAGCCCCCAACTAGGTATTAACTAAAATTGTGTCTGCAAATCTGATTTTTTTTTAATTATTATTATTCCAGACCAGAGATCACCTGTCCAAGGCGCAGCGAGGGCTTGTGGGGGATGGTGTTTCTGAAGTGATGACAAAGCTGAGGGTGACGTCAAGTGATGGAACGAGCTACAGCGGAGATCTTTTGGCTATCATAGATGTGCTAAAAAACATGACAGAGATATTTAGGAGATCCTACTACAGCCCCAGTAATGCAGACATGAGG[G/A]TTAGTGTGGTATTATGTGCTTATGGAAAGGTGCTATAGAATGAATAGCTGGATTTAGTTTGGCATAATAAAAGTTTAGTACATGTAACTGGCATACTGTGAGCCTCAAACTTAATTTCCTTGTTATCATGTATTTTTCTGAGTGCAAAATCTTGTTAAAAACAGGCCAATTGGAACTCACACTGACACTGATCCACACACACACACACACACACACACACACATATATACATATAAAATCTCATCACGGCTTACCAGAAAACCACTTTTGGGAAAGATGATTGATACATTTTTTTATATTCTAAATATGTACATTTATCCTGGATAATAAGTTTACAATCTTATGCCAGAAGGGCTATAATGTCAGAAAAGCTATGATGTCTCTTTAACTGTGTCATTTGTTAGTTTAACATGTTTATTGTACAATGTGTACAATTGTACTATGTGTGTATTGAGGCAGCAAACACATGTAGACTGCTGAAAAGAAGTGTTTAACGCATG
Associated Phenotype:
Not determined