Busch Lab

ZMP

BAIAP2 (2 of 2)

Ensembl ID:
ENSDARG00000060587
Description:
BAI1-associated protein 2 [Source:HGNC Symbol;Acc:947]
Human Orthologue:
BAIAP2
Human Description:
BAI1-associated protein 2 [Source:HGNC Symbol;Acc:947]
Mouse Orthologue:
Baiap2
Mouse Description:
brain-specific angiogenesis inhibitor 1-associated protein 2 Gene [Source:MGI Symbol;Acc:MGI:2137336

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa12233 Nonsense Available for shipment Available now
sa38901 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12233
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
ENSDART00000085523 Nonsense 17 559 1 15
Genomic Location (Zv9):
Chromosome 12 (position 38143503)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 35935165
GRCz11 12 35629420
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTAGTATAACTGCTGCTGTGGTGTTGACAAAATCTGTGTTGTTTCTGT[T/A]GCAGTCCATCATGGAGCAGTTCAAYCCTTGCTTRAGGAACTTTGTTGCCA
Long Flanking Sequence:
TTTAAAGGGCAACTCTTAATGTTGGATTAGGTGAGTCAGGCTGTGGGTAGATCTCCACATTCTCCCGCAATCCTGTGCTCACCAGCAACAAAAGAATGGCAAATCCCAGCTGGCACAATGCCCTCCCAGTCCTGCTAATAAGTGTTCTGAAGGGAGGGGGCATTAGAGCTCTGGCTCACTTTTTCTCCCTCTATTCATCTCTCTTGTTATCTCCACATGCACTGCATCATCCTGTCCATAATCATTAACAATAGACAGATCCTTTATTGTAATATGGAGTTGACACTTACAAGCAGCTATCTGCTTTCTTAAACATGATTTATCATTAAACTTCATTACATTTCTCATTTTTGGTGGTGATCAACATTTGGTTAAAAGGAATATATAACAATTTTAACAGTACTTACTTTTAAAAAGTGACTTTATATTGTAATAATTTACCTTTTCCCCAATTAGTATAACTGCTGCTGTGGTGTTGACAAAATCTGTGTTGTTTCTGT[T/A]GCAGTCCATCATGGAGCAGTTCAACCCTTGCTTAAGGAACTTTGTTGCCATGGGGAAGACTTATGAGAAGGCCCTTTCCAGTGAGTACATCAGCGGCTTGTTCATTACCACTCTTGCAGGCAATGAGCCAGCTATTCAAGCTTTTTTTTCATTGGTCTGCTTTTATTTTTGAGAATAAGTTGCTTGAAATTCATGCTTCAATGGGGCTCTGCTCCTTGACATTCCTTGGTTGCATACACCTTCACGACCAGCATCTGGGATTTTTTTTTCTGATATACAAACTCAAGTTCTTGCATAGAAATAGCAGATTGTTGTTTAAATGTTTGTTGAATGTTTGTTAAGAATTTATGTTTTTATGTTTGTGGGGCAGGATACTTCCTGCTTCTTTGTAGTCATAGAATGTTTAACGTCTAAATCCATCTGCACCCTGAAACCCTTGAGCATCCATCCGGTTCATGCATGTTGCATCTCCAGAGCTGTCACATCCATGTAACCAATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38901
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085523 Nonsense 130 559 5 15
Genomic Location (Zv9):
Chromosome 12 (position 38118138)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 35960530
GRCz11 12 35654785
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCGTCTGGCAGGCAGCTCTGAAGAAATATCAGATGGAACACAAAAGT[A/T]AAGGAGAAAGTCTGGAGAAATGCCAGGCCGAGCTGAAGAAACTGCGCAGG
Long Flanking Sequence:
AAAAAAACTCAGTCAAATGTACCAGAAGGCTTTGGCAGGGAAGACTGGTGGAAACAAAGAGGCATGGTCTGAAACACAATGAATCCCAGGAGCAGGAAGATGCATTGAGGACAATGAAAGAGCTGATTGGACCAACTTAGCCAAGTTCCCATTAGTAATGAACACGTGAAACCTTCAGGTCTTTTAAATTCTGGGTTAAGCATTGCTAAGAAACAGTCGATTCAAGATGAGCATTTATTATTAACTTTTAAACCTCAGGATGTCCTGAGAATAACAGTATAATGCATGCTACAATAAAGAGGCCCATCTCATCCCATACTAGTTGGCATTCATCCACTTGAGGTCTTTTTGGGATGGAAGCTTGATAAATTTATTTAAAATGCAACCATTAAATTCCTCGTCTTGTCCATTTGGATATTGTTAGCCGCTGATTGAGATGAGAGCTGTGTTGTGTCGTCTGGCAGGCAGCTCTGAAGAAATATCAGATGGAACACAAAAGT[A/T]AAGGAGAAAGTCTGGAGAAATGCCAGGCCGAGCTGAAGAAACTGCGCAGGAAGAGTCAGGGCAGCAAGAACCCCTCCAAATATGGAGACAAGGAGATGCAGGTGAGTCAGCGCTCTTCTTCTTTTTCGTTGGATTAGTTATGGATTAATTCTGTCATTCATTTTCAATGTGTCAATCCAAACCTGCACAACCTACCTTTCTGTTTTCAACAACAGAATTGTTCACTTTTCTTGCTGAAGACCTACAGTTTTTCATAAAAATCTCTATTATATGGCTTCAGAAGATTTAAAATCTACCAAATGAGCTTGTCCTGTTAATTATGTCTGCATGGAAAGTCCTCTTCACTCCATGGATTATGGTCATAAAGATTTGCAATGACATGAGGTTGAGTAAAAGATTTATTTTTGGATGAAATATTCCTTTAAAAATCGCTCTGTCAATCTACTCTTAATAAATATCATACTAAAATAAATGTCCAAATAAGTTCGGCAGTGCTTTGG
Associated Phenotype:
Not determined