ZMP
si:ch1073-436c4.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens BAI1, brain-specific angiogenesis inhibitor 1 (BAI1) [Source:UniP
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 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23396 | Essential Splice Site | Available for shipment | Available now |
| sa23397 | Nonsense | Available for shipment | Available now |
| sa11442 | Nonsense | Available for shipment | Available now |
| sa9373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7457 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa43190 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23396
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 |
|---|---|---|---|---|---|
| ENSDART00000109554 | Essential Splice Site | 294 | 1493 | 3 | 30 |
| ENSDART00000133757 | None | None | 283 | None | 6 |
| ENSDART00000141359 | None | None | 254 | None | 7 |
| ENSDART00000143118 | None | None | 269 | None | 5 |
| ENSDART00000144323 | None | None | 331 | None | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 19983)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 102868 |
| GRCz11 | 19 | 102958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCGTGACTCTGACGGCACCCTCATGGCTAACCAGGCCCCTCAGAAAG[G/A]TGTGTTTCTATGGCAACACTAAATCTGCTCCAGCCGGCAGCAGAGCAAGT
Long Flanking Sequence:
GGCATTACCCACACACTGAGTGCTCTTCAGCTCAGCTCATCTGGGTTCCTCCACTGCTTCTACACTGTAGATTGTGACAGAAGTTCTAGTAGATAGTGTCAGTCCAGTTCTCAGGGTCAGTGTGCACTCTTAACAGAAGTGTGTGTGTGTGTGTGTGTGTGTGCAGAAGGCTGGAGCGGGTGGGGCCGCTGGTCTGAGTGCAGTAGCGAGTGTGGTGGTGGAGTGCAGGTGCGCAGCCGCGCATGCCAACCTGAAGATGGCATCTGTGAGGGCGTGGTGGAGGAGGGACGAGCCTGCAACCCTCAGCCCTGCATCGGTCAGTTGCACATCCATACCAGTACACCACAGTGAGTGTGTGCGCATGCTGTCACATCTTACATGTGTGTTTGTGTTCATTTACACAGGTCAAGTCCGGCAGAAAAGCCAAGGTCTGCGCTCCATCATCGGCCAGCGGCGTGACTCTGACGGCACCCTCATGGCTAACCAGGCCCCTCAGAAAG[G/A]TGTGTTTCTATGGCAACACTAAATCTGCTCCAGCCGGCAGCAGAGCAAGTGCTGAACTAAACCAAACCCTCTCTTCCCCATGCAGAAGAGGCGCAGCAGGACACGTGGTCCTCCTGGAGTGTGTGTTCTGTGAGCTGCGGTGAGGGCTGGCAGTCTCGCACCCGCTCCTGCATGAACTCCGCTCAGTGTATCGGCCCTTTAAGAGAGAACCGACCCTGCAACAACACCGCCGTCTGCCCAGGTACTTCACGTCACACACACACTCGGTTATGTTCAGTTATGTGGCATGGGGCGGGGACTGATGAACTGTGCTGTGTGCAGTAAACGGAGCCTGGGATGAATGGGCACCCTGGAGCCTGTGCTCCTCCACGTGTGGCCGTGGGTACCGGGATCGAGTCCGCACCTGCAAACAACCTAAGAACGGTGGAGAACCCTGCCGAGGACCCTTCAAACAGACCAAGTTCTGCAACATTGCCGTGTGCCCAGGTGAGCAAACTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23397
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 |
|---|---|---|---|---|---|
| ENSDART00000109554 | Nonsense | 328 | 1493 | 4 | 30 |
| ENSDART00000133757 | None | None | 283 | None | 6 |
| ENSDART00000141359 | None | None | 254 | None | 7 |
| ENSDART00000143118 | None | None | 269 | None | 5 |
| ENSDART00000144323 | Nonsense | 78 | 331 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 20167)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 102684 |
| GRCz11 | 19 | 102774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCGGTGAGGGCTGGCAGTCTCGCACCCGCTCCTGCATGAACTCCGCT[C/T]AGTGTATCGGCCCTTTAAGAGAGAACCGACCCTGCAACAACACCGCCGTC
Long Flanking Sequence:
GCCGCTGGTCTGAGTGCAGTAGCGAGTGTGGTGGTGGAGTGCAGGTGCGCAGCCGCGCATGCCAACCTGAAGATGGCATCTGTGAGGGCGTGGTGGAGGAGGGACGAGCCTGCAACCCTCAGCCCTGCATCGGTCAGTTGCACATCCATACCAGTACACCACAGTGAGTGTGTGCGCATGCTGTCACATCTTACATGTGTGTTTGTGTTCATTTACACAGGTCAAGTCCGGCAGAAAAGCCAAGGTCTGCGCTCCATCATCGGCCAGCGGCGTGACTCTGACGGCACCCTCATGGCTAACCAGGCCCCTCAGAAAGGTGTGTTTCTATGGCAACACTAAATCTGCTCCAGCCGGCAGCAGAGCAAGTGCTGAACTAAACCAAACCCTCTCTTCCCCATGCAGAAGAGGCGCAGCAGGACACGTGGTCCTCCTGGAGTGTGTGTTCTGTGAGCTGCGGTGAGGGCTGGCAGTCTCGCACCCGCTCCTGCATGAACTCCGCT[C/T]AGTGTATCGGCCCTTTAAGAGAGAACCGACCCTGCAACAACACCGCCGTCTGCCCAGGTACTTCACGTCACACACACACTCGGTTATGTTCAGTTATGTGGCATGGGGCGGGGACTGATGAACTGTGCTGTGTGCAGTAAACGGAGCCTGGGATGAATGGGCACCCTGGAGCCTGTGCTCCTCCACGTGTGGCCGTGGGTACCGGGATCGAGTCCGCACCTGCAAACAACCTAAGAACGGTGGAGAACCCTGCCGAGGACCCTTCAAACAGACCAAGTTCTGCAACATTGCCGTGTGCCCAGGTGAGCAAACTCTTCGCTAGTCCACATCTCGCCAGCAGAGGGCGCTGTAGACCTCATTCCCTCACAGCTCCAGCATTTCTCACTGTACTCTGTGTTTGTCTGCTCTATAGTTGATGGATTCTGGAACGACTGGTCTGCGTGGACCCCTTGCTCATCCTCCTGTTCCAATGGGACGACTCAGAGAACCCGCGAGTGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11442
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 |
|---|---|---|---|---|---|
| ENSDART00000109554 | Nonsense | 576 | 1493 | 9 | 30 |
| ENSDART00000133757 | None | None | 283 | None | 6 |
| ENSDART00000141359 | None | None | 254 | None | 7 |
| ENSDART00000143118 | None | None | 269 | None | 5 |
| ENSDART00000144323 | Nonsense | 323 | 331 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 21525)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 101326 |
| GRCz11 | 19 | 101416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGGGTCTGGCCTTCTGGGAAAACCCCACTCACATCAAATGCGTCTCT[A/T]AAGACTTCCAGGAGATCCAGAGCTTGGTAAGAGAGASAGACASACACACA
Long Flanking Sequence:
TGACGGAGATGAGTGTTCATCAGAGCAGCGTCTGTAAGTGTCTCTACTGCTGTCTGCAGAACCACACGAGATCTGCGGAGAGGAGAACTACGGCAGCATGGTGTGGAAGAAAACTCCGGCTGGAGACACGGCTGCACTGCCCTGCCCTGCTGACGCCACAGGTACTGATCCGAGACCTGCTCCTTCAGTCTGAAACTAGGTCACAGGAACTCCTGGCCTGATCTGAGTTCTAGAGATGCAGTCTTCAGATCAGCCCCAGTGTATCCGTCTATGTTCTGTATATTAATGTGTAAAGCAGCTCTACAGCAGGTGTTCATCACTGCAGCACACTGAGCTCAGATCAGGGAAGGACTTTAGTGGCCAGAACTTGACTATAGCAGCTGTTGTAGAGTCACACTAACCCTGCTGCGCCCCCTGCAGGCCTGATCCTCCGCAGATGCACACTGGACGCTGTGGGTCTGGCCTTCTGGGAAAACCCCACTCACATCAAATGCGTCTCT[A/T]AAGACTTCCAGGAGATCCAGAGCTTGGTAAGAGAGAGAGACACACACACACACACACACTCTTTCTCACACACACACACACACACACACACACTGACTCAGAGCTGACGTGTGGTGTTTGCAGATGCGTAATGATGTGGATCAGTCTCAGCTGGTGGAGGGTGTGTCGGCGGTTCTGTCCCGCCTCAGGGTGGCGTCGGCGGGCAGCACACGCTACAGCGGAGACCTGCTGACGGTGATGGAGATCCTGAAGAACAGCACCGGGATCTTCAGAGGATCCAAGATGAGCCTGAGCAACGCTGATGTGGAGGTACACACTGATCCACACACACACACACTCATCAATGTATGCCAATATATGCTCATCTAACAGCATCTGTGTGTGTGTGTGTGTGTGTGTGTGACCCGCAGAACTACGCACACACCATCAGCAACCTCCTGCAGGACACACACCGAGAGAAATGGGACGAAGCTCAGCTGGTGAGTTTGAGGAGATTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9373
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109554 | Nonsense | 907 | 1493 | 21 | 30 |
| ENSDART00000133757 | Nonsense | 40 | 283 | 2 | 6 |
| ENSDART00000141359 | Nonsense | 39 | 254 | 3 | 7 |
| ENSDART00000143118 | None | None | 269 | None | 5 |
| ENSDART00000144323 | None | None | 331 | None | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 26208)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 96643 |
| GRCz11 | 19 | 96733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAGCTGAAGCTAATGTGGAGTGTTTCCCTCCTCAGGTACAWCCGCTCT[G/T]AGCGATCCRTKATCCTGWTCAACTTCTGCCTGWCCATCATCTKCTCCAAC
Long Flanking Sequence:
TGTGAGCTTGTGTGTGTGTGTGTGTGCGCTTGTGTGTGTGTGTGAGACACTGACGTTTCCGTGTTTCTCCACAGAACATGGACAGGTCTCTGTTGCCGTCGGTTACGATGATCGTGGGATGCGGGGTGTCGTCGCTCACCCTCCTCCTCCTCATCATCATCTACGTCTCGGTCTGGAAGTAAGACAATCTGCTTTTCTTTTATTGATCGTCTGCTGATATTACTGTGTCATGGCTGATTACTGATATCCGCTATAGATGAGTAATGAATTAAAGGGCCGGTAACCTCATCACTCAGTATTTAGAAAGCAAAATAAAGCCGTCACAATCATCATATTTATTTATAAAATCATTTATTTCTTGCACTTTTCAATAATTATGTTTATCTAAAAGCATAGCTTTGCACAGCAGTGGAGGCCCTCAGAGTCCCCGGGGCCGAACGCTGCATTGTGTTGAGCTGAAGCTAATGTGGAGTGTTTCCCTCCTCAGGTACATCCGCTCT[G/T]AGCGATCCGTTATCCTGATCAACTTCTGCCTGTCCATCATCTGCTCCAACGCGCTCATTCTGATTGGCCAGACTCAAGCGCGCAACAAGGTGAGCCCGAGACCTCTGACCAATCAAAGCTTAGATGCCCAGCTCTGGGGGCGGGTCTCACCTGTGTGTGTGTGTGTGTCTCACAGGTGATGTGCACTCTGGTGGCGGCGCTCCTGCACTTCTTCTTCTTGTCCTCCTTCTGCTGGGTGCTGACTGAGGCCTGGCAGTCCTACATGGCCGTCACGGGGCGCCTGCGCAACCGCATCATCCGCAAGCGCTTCCTCTGCCTGGGCTGGGGGCTGCCGGCACTGGTGGTGGCCATCTCTGTGGGGTTCACTAAAGCTAAAGGCTATGGAACCGTCAACTAGTGAGTAACTGTCCCACTGCCGGTCCGACTCTCTGCTTCACTGTGGAGATGAGTTTAAGGCTGTGTCCTCGTAATGCTGTGTCCTCGTAGTGCTGTGTCCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7457
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109554 | Missense | 1307 | 1493 | 27 | 30 |
| ENSDART00000133757 | None | None | 283 | None | 6 |
| ENSDART00000141359 | None | None | 254 | None | 7 |
| ENSDART00000143118 | Missense | 67 | 269 | 1 | 5 |
| ENSDART00000144323 | None | None | 331 | None | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 27950)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 94901 |
| GRCz11 | 19 | 94991 |
KASP Assay ID:
554-4041.1 (used for ordering genotyping assays)
KASP Sequence:
GCAAGTACAACATCAGCACCGACCTTCCGCAGGCACGCCTCATGCACATT[A/T]GCGGWACCTACGCCGAGCCGCAAGCTGCCTACGCCACGCAGACGCTGCCC
Long Flanking Sequence:
TCAAACCGACCAGGTGAGTCTCACATGATCGACAGCTTAATGCATTCATCTCACCAAACAGCATGTGTTCTTAAGATGCTAATCGATTGGCATTGCTCTTCTCTTCAGGTGGAATGAAGAGCTCCTCTGAGGAGAAGATGCCCCCTCCACAGATGCCCCTGCCCCTCGGCCCAAACTTCCACACGCTGCCCAACCCCAGTGGGAAGAGCCACATTCCCCCAGTGCCGGAATACTCCAGCCACACACTGACCCTGCGCAGAGAGAAGGGCCGCGACCCATCCTGTGGGAAACCAGTGTATGTGTGTGACAGCGAGCTCTTCAAGCAGCTGGATGCGGATCTGGCTCGTGCTCAGGCAGAGAGTGTGTGTGCGGACGGCAGCGGGTACGTGCTCCTGCCCAACACCACCTCCACGCTCCGCGCCAAGCCCAAAGACGACTCCAGTGGCTCCAGCAAGTACAACATCAGCACCGACCTTCCGCAGGCACGCCTCATGCACATT[A/T]GCGGAACCTACGCCGAGCCGCAAGCTGCCTACGCCACGCAGACGCTGCCCGCTGACCGCGTCAGTGTGTCCTACTCAGAGCGGGACTCACCCATCCAGAACATCCACAACATCTCCAGCGAGAGCCACATGACCAGCAGCCTGGGTGACACCTTCGACTCCATGAACTCCATGATGTCCAAGAGTGAGACCATCTCCACACTGTCCATGAGCTCCCTGGAGGTCAGCGAAGGGGTACGAGACTGCTCCACTGCTCAACCATCATTCTGTTCAGTATCAATGTGATGTTAATGTTGTCCTGTTTCACTCTCACAGAGGCAGAAATCTCGCTATGCAGAACTGGACTTTGAGGTAAACACTCGTGACAAGGCGCGTCTTCTTGGTTGAGTGTGTGATTCTGCAAGGTTTAACCGTTCCTTCATCTCTCTTGCAGAAAATCATGCACACACGAAAGCGTCACCAGAACATGTTTCAGGATCTGAACAGGAAAGTCCACCATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43190
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109554 | Essential Splice Site | 1380 | 1493 | 27 | 30 |
| ENSDART00000133757 | None | None | 283 | None | 6 |
| ENSDART00000141359 | None | None | 254 | None | 7 |
| ENSDART00000143118 | Essential Splice Site | 140 | 269 | 1 | 5 |
| ENSDART00000144323 | None | None | 331 | None | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 28172)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 94679 |
| GRCz11 | 19 | 94769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGTCCAAGAGTGAGACCATCTCCACACTGTCCATGAGCTCCCTGGAG[G/T]TCAGCGAAGGGGTACGAGACTGCTCCACTGCTCAACCATCATTCTGTTCA
Long Flanking Sequence:
TGCCGGAATACTCCAGCCACACACTGACCCTGCGCAGAGAGAAGGGCCGCGACCCATCCTGTGGGAAACCAGTGTATGTGTGTGACAGCGAGCTCTTCAAGCAGCTGGATGCGGATCTGGCTCGTGCTCAGGCAGAGAGTGTGTGTGCGGACGGCAGCGGGTACGTGCTCCTGCCCAACACCACCTCCACGCTCCGCGCCAAGCCCAAAGACGACTCCAGTGGCTCCAGCAAGTACAACATCAGCACCGACCTTCCGCAGGCACGCCTCATGCACATTAGCGGAACCTACGCCGAGCCGCAAGCTGCCTACGCCACGCAGACGCTGCCCGCTGACCGCGTCAGTGTGTCCTACTCAGAGCGGGACTCACCCATCCAGAACATCCACAACATCTCCAGCGAGAGCCACATGACCAGCAGCCTGGGTGACACCTTCGACTCCATGAACTCCATGATGTCCAAGAGTGAGACCATCTCCACACTGTCCATGAGCTCCCTGGAG[G/T]TCAGCGAAGGGGTACGAGACTGCTCCACTGCTCAACCATCATTCTGTTCAGTATCAATGTGATGTTAATGTTGTCCTGTTTCACTCTCACAGAGGCAGAAATCTCGCTATGCAGAACTGGACTTTGAGGTAAACACTCGTGACAAGGCGCGTCTTCTTGGTTGAGTGTGTGATTCTGCAAGGTTTAACCGTTCCTTCATCTCTCTTGCAGAAAATCATGCACACACGAAAGCGTCACCAGAACATGTTTCAGGATCTGAACAGGAAAGTCCACCATGCTGAAAAGGACAGGGAGTCTCCAGCCTCTGACAGCAAGGTGAGCCACTGAACACACGCACACACACACACACACACACACACACACACACACACACCTGAAGATCTGTCCTGTGTGTTTACCCTGCAGTCATAACTCTGTGTTCTCTCCGCAGTCCGTCAGGTGGAGCGTTTCCTCCGCTGGCAGCGACAAGACCAACCACAGCGTAAGTGTGGCCATCCTTT
Associated Phenotype:
Not determined