Busch Lab

ZMP

BAI2 (1 of 3)

Ensembl ID:
ENSDARG00000088161
Description:
brain-specific angiogenesis inhibitor 2 [Source:HGNC Symbol;Acc:944]
Human Orthologue:
BAI2
Human Description:
brain-specific angiogenesis inhibitor 2 [Source:HGNC Symbol;Acc:944]
Mouse Orthologue:
Bai2
Mouse Description:
brain-specific angiogenesis inhibitor 2 Gene [Source:MGI Symbol;Acc:MGI:2451244]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa36892 Nonsense Mutation detected in F1 DNA Not yet available
sa18072 Essential Splice Site Available for shipment Available now
sa43330 Nonsense Mutation detected in F1 DNA Not yet available
sa36891 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36892
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
ENSDART00000130846 Nonsense 298 623 2 8
Genomic Location (Zv9):
Chromosome 19 (position 40546811)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 39410548
GRCz11 19 38997668
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGACGCAGAGGCCACGATCGGCTGACCAGCCAGGTGTGTTTCAGGCA[C/T]AGACTGGTGAGTCTCATTGTCTAGATGCATTTCGCTTAAATGCACTTCAG
Long Flanking Sequence:
GCCCAAGGATGAGGCCAGATATAGAAAACTCTCTGTTGGCTTATGTAGGTTTACTCAGTAGCTGCAGCACGAAGAGCACACTTAAAAAAGTTCCTCACACAATGGAGAGATTTACATTTCATTCAAGGACAAGAGGAAGCCTTGGCGGAGAGATGTATTACATCATTGTGTTAATGTAAAACACTACTAATAGTATGTGTGGGCTTTTTATCTTTTGTGTTCGTGCAACTTAATGCGTCAGTTCCATACTAATAAAGACGCATGTGCAACGTTTTCTAAATACGTTTTTACGGATGCTTCTGACTCTGAAATGCACTTTATTTAAAGTCAATACATTTATTGAAGCACATAATAGCAAAAATCAAACATGGCCTGTTTTGTTTATGTCTTCAATACCTTACTATGTTTGTGTATGTGTCTGTCTAGAACCTGACGATGATGAGCAGAAGGTGAAGACGCAGAGGCCACGATCGGCTGACCAGCCAGGTGTGTTTCAGGCA[C/T]AGACTGGTGAGTCTCATTGTCTAGATGCATTTCGCTTAAATGCACTTCAGAACCATGGACAGCGCTTACATTTAATCAAAAGAAGAGAGTCTGAAAAATAGCTGTAAAAAATGTTTGTCTGATTCTCATAAAGGTTTGTTGAGTAATGGAGGGTATAAACTATCTGAATTAGATGGGATTAAGCATCAGAACTCTAAACATTTTATTCCAAACATGTTTTTAAGTATTTGTCCATTGCCTTTTGTGATTTTAATTTGGTTTACATTTTATATGTCTAAATCAATTTATATTTATGAATCACAAAACTTCAAAATAAAGTTCAAAATGTTTTATTGTGTTTTCTGCTTCTAAGGGAATCTTCATAAAATATGTATCATTCATTCATTCATTCATCCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATCCATCCATTCATTCATTCATTCATTCATTCATTCATTTATTTATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18072
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130846 Essential Splice Site 300 623 2 8
Genomic Location (Zv9):
Chromosome 19 (position 40546803)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 39410540
GRCz11 19 38997660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CWGAGGCCACGATCGGCTGACCAGCCAGGTGTGTTTCAGGCACAGACTGG[T/G]GAGTCTCATTGTCTAGATGCATTTYGCTTAAATGCACTTCAGAACCATGG
Long Flanking Sequence:
ATGAGGCCAGATATAGAAAACTCTCTGTTGGCTTATGTAGGTTTACTCAGTAGCTGCAGCACGAAGAGCACACTTAAAAAAGTTCCTCACACAATGGAGAGATTTACATTTCATTCAAGGACAAGAGGAAGCCTTGGCGGAGAGATGTATTACATCATTGTGTTAATGTAAAACACTACTAATAGTATGTGTGGGCTTTTTATCTTTTGTGTTCGTGCAACTTAATGCGTCAGTTCCATACTAATAAAGACGCATGTGCAACGTTTTCTAAATACGTTTTTACGGATGCTTCTGACTCTGAAATGCACTTTATTTAAAGTCAATACATTTATTGAAGCACATAATAGCAAAAATCAAACATGGCCTGTTTTGTTTATGTCTTCAATACCTTACTATGTTTGTGTATGTGTCTGTCTAGAACCTGACGATGATGAGCAGAAGGTGAAGACGCAGAGGCCACGATCGGCTGACCAGCCAGGTGTGTTTCAGGCACAGACTGG[T/G]GAGTCTCATTGTCTAGATGCATTTCGCTTAAATGCACTTCAGAACCATGGACAGCGCTTACATTTAATCAAAAGAAGAGAGTCTGAAAAATAGCTGTAAAAAATGTTTGTCTGATTCTCATAAAGGTTTGTTGAGTAATGGAGGGTATAAACTATCTGAATTAGATGGGATTAAGCATCAGAACTCTAAACATTTTATTCCAAACATGTTTTTAAGTATTTGTCCATTGCCTTTTGTGATTTTAATTTGGTTTACATTTTATATGTCTAAATCAATTTATATTTATGAATCACAAAACTTCAAAATAAAGTTCAAAATGTTTTATTGTGTTTTCTGCTTCTAAGGGAATCTTCATAAAATATGTATCATTCATTCATTCATTCATCCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATCCATCCATTCATTCATTCATTCATTCATTCATTCATTTATTTATTTATTTATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43330
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
ENSDART00000130846 Nonsense 358 623 4 8
Genomic Location (Zv9):
Chromosome 19 (position 40510617)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 39374354
GRCz11 19 38961474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTTTTTCTTTTTGCGTGCCTCTGTGGTTGTGTTTGCAGTGGAAGGT[C/T]AATGGTTGGACTGGGCCACCTGGTCTCAGTGCTCTGTCTCCTGCGGCACC
Long Flanking Sequence:
TGGAAGCTATTACATCATAGATATGTACGTTCCAGGAACTTCCATGTCAATAAAAACAGTTATTTCACTAAAAAGAATGTTTTCGGCCTTGACACTTATATGGTAACCTCTAAGTTCAATTACCTTCTATATATCAAATGCTTAAGTAAGACATGAGATCTCCGTTCATGACTCTTTAAAGTTTCATTCTGATGGTTTCATTTGTAATTGCGAAATAAATGCATTGCATATCTCCTAACGGTATCAGATTGAGGTTTGTATGAGGGTAAGTGAGGATAATTTTGAGTTTCAGACTAACACAGAGCCCTGCTGTATACCCCGTCTCTCTGTCTGCACCTCCGACCGTCCGCTTCCTATGTTTGTTTCTGTCCTTTACTTCTATGTCCTTCTCTTTCCTGTCCTTCTCCACATCTGCACTGTCATATTTTGTTCTCACCTTTGCATCTCTCTCTCTCTTTTTCTTTTTGCGTGCCTCTGTGGTTGTGTTTGCAGTGGAAGGT[C/T]AATGGTTGGACTGGGCCACCTGGTCTCAGTGCTCTGTCTCCTGCGGCACCGGGACTCAACAGCGGCAGCGGCGGTGCAGCGTTTCGGTTCATGGCTGGGCTGAGTGTAAAGGGCCGCATGCGGAAACTCGTGAGTGCACCAACCCATCTTGCGGGGGTGAGTGTCTCTCTGGTGGGCTTCCAGTCTTAAATTGACAGGTAGTTTATGTGCACAGCTGCAATTTGTTTGCTGTCATGGTCTAATTAATTGCAGAGAACGCTCTGAATTGTCTGCGGTACCAAACCACAGAGACGTAGCGGCCTGCATTGCTCATCTTGCTCCACAAATGCGTTGCTGTGTCAGCATATGCCAGTTCGCACCCCTGATAATAATTAATAAGCGCAAATTAGCCTCGTGCAGGTGCTTTATGACCATGCTCACATTGCAGCTAAATATGGCTGTCACTTCACTTCTGAATTTTTTTTTTCTTCACTTTTTTGGAACAAACTGGATGAATCTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36891
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130846 Nonsense 573 623 8 8
Genomic Location (Zv9):
Chromosome 19 (position 40494604)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 39358341
GRCz11 19 38945461
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCTCCTGGAGTTAATGTCCCGTAAGAATTATTACAGTGGAGACCTCT[T/A]ATTCTCCGTGGAGATTCTCCGAAATGTGACAGACACCTTCAAGCGAGCAA
Long Flanking Sequence:
ACCATAAATACATTGGTTATTATACACAAGCAAAACTCATTGGTTACTGTAGAAACCCAAACCTCATTGGTTTTTGTAGAAACCCTGATCTCATTGGTTACCATAGAAACTCAAACCTCATCGGTTATTGTAGAAACCCAAATCTCATTGGTTATCATAGAAACTCAAACCTCATTGGCTATTGTGGAATCTCAAACCTCATTGGTTACTATAGAATCTCAAACCTCATTGGTTCTTGCAGAAGGTCAGACGTGTTCAAGCAAAATGCAAGAATGACTCAATGGTTCTCGTGTGTCAAGCAAAAGCAGGCTATAACTTCATGCTCCTGGTTTTTATCTCTAGGTTTATTTACTGATGTATAAACCATTTTTTTCTTCCTCTGCAGTTGCGAGAACATCTTGCGAAGGGTCAGAGGACCCTGGCAGGGGAGGGCATGTCTCAGATCGTGAGGAGTCTCCTGGAGTTAATGTCCCGTAAGAATTATTACAGTGGAGACCTCT[T/A]ATTCTCCGTGGAGATTCTCCGAAATGTGACAGACACCTTCAAGCGAGCAACCTACATCCCAGCTCCTGACGACGTGCAGGTGGGTGTTCGTCTGTGGGGGTGTGGAAAGAAAGTAGTTATAAATGGGGAAGTGATAAAAAGTGTCACCGAGCAAAAATTATTTTCACATTTTCATCTTTTTGAAAGATTTATTGACTTTTGTGCTTTTTAAAATTGATTTTAAAAAAATACATATACAAATGATCACAATAAAACTCCTTTTTAAAAGTTTTTCATTAGAGTGTGAGATTTATTTATTTATTTTATTTTATTTTTTATTTTTTGTTAATCATTGACTGTCCTGTTTGTTTTTATGGCTTATAGAAGACACTATAAAAAAGTGATTAAAAATAAAAAGCATTAGATGCAGCAAGTTGACATTACTTTAAGTGAGTAAACCCATTGCAACTTGGAGTTGTTAAAATGATAGAACTTATTTTTTTATTTTTGTACACAGTTTA
Associated Phenotype:
Not determined