ZMP
sb:cb1067
Ensembl ID:
ZFIN ID:
Human Orthologue:
BAIAP2L2
Human Description:
BAI1-associated protein 2-like 2 [Source:HGNC Symbol;Acc:26203]
Mouse Orthologue:
Baiap2l2
Mouse Description:
BAI1-associated protein 2-like 2 Gene [Source:MGI Symbol;Acc:MGI:2652819]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26057 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33164 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26056 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26055 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38386 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17195 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26057
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 |
---|---|---|---|---|---|
ENSDART00000024480 | Nonsense | 4 | 419 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 24747671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 24325882 |
GRCz11 | 3 | 24456430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTGTTTATTTGTTTGTTGTGCCACAGTGACAGATCAAGATGTCAGGA[C/T]AAAACAGTGATCAACTGCATCGCACCACTCTGGGCATTTATACGGTAAGC
Long Flanking Sequence:
ATATTTATAATTAATCTTTTAATTTATTACAAGTGTATGTGAAAAATGCATTAAAGCATATAACAAATTTGCATGAAAGTTCTGAGGTCTTGATTTAAATAAATAAATAAATAAAAAGTTATTTAGATAAAATATTTTTATACTTATAAACAAAATGCACTGTATAGATTAAAATGCCATTTTTGTATAAAAGCTACCAAATGCATAAAATGTAAAGAAAATGCCTAAAGGTTTCAAAAACAAGCACAAGTCTGGTCTCCTATCTGAAGTGTGCAGTGTTTACGGCAGGTGTCTAACCTCAGTCACACTTTTATTACTCTGCACTGTTCAATAATTCACAGGCCACACGGGTGACAATAGCTCACCATTTTCCTCTCTCACAAACAGGACGAGACGGGAAGGAGAGGGTCATCTGTCAGTCTGCTTGCTTGCTTGTTGTTTAGTCTGTGGATGTTGTTTATTTGTTTGTTGTGCCACAGTGACAGATCAAGATGTCAGGA[C/T]AAAACAGTGATCAACTGCATCGCACCACTCTGGGCATTTATACGGTAAGCAAGCCTCTCACCAGAGTTAGAAATTAATTACAATCACATGTTCAGTAGAGCAAAATTAATAAAATGGTCTAATGCTGGCTGGTTTACATTTATATAGGAATTTAGTTGTTCAAAATGTTTTGAAACGGTTATTTATAAATGAATAATAATAATAATAATAATTATTATTATTATTATTATATGAAATCTATAAAATATTCCGCACAAAACACAGGGTTGTCGACACATAATATGCTCATATTCAGTTACGGGGATAGTTTACCCAAAAGTAAAAATCCTACCATAATTGACATACTTTAACTTGTTCAAAAACTATTTGAGTTTCTTTTTTCCATTGAAGAAAAAAAAGTTGAAAAGAAGTTTTGCTGTTTTTACTAATACATTTTTACTACTAATTACTACAAAATTTTAGAAGTAATGTACTTAACAATTTACTCTACCTTTTGTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33164
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024480 | Essential Splice Site | 93 | 419 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 24742504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 24320715 |
GRCz11 | 3 | 24451263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATGTCAGACAGTCAGAGGAGACTCACCAACGAGCTGGAGGGAGTGG[T/A]CTGTTATTCATCCTTGACTATCGATCCATCGTTTGATATCTTCTGTTAGC
Long Flanking Sequence:
GGGAAGGAGTCTGTGTCCTTCACACACTATATTGTACTTTGCTCTTGTAAATGCACTCAGTTCCTCACTGAATCTCACACACACACAAGAGAGAAAGAGAGAGAGAGTGAGCGTGTGTGTGTGTGTGTGTGTGTGTTTATTTATGGCTGGCATCTCTCACCCTGTTGTGGTTTAATGGAAAAATTTCATTAAATTTCAATGGTGCTTTTGTTGCTATGAATCATATTTTATGACTGCAGAGAGGTGGCATGACTGTGTGTGTAGTCAATATCAGATAACCTCCTCTGTGATGTTAAATAATAAATGATGACACAACGTCAGCTTGGCAGTGCAACCTTTAGAGACTAATACCTTTACTTTAACACACAGACAGATACTATGGATGTTATAAGATCATAAATGAAAACTTCTCTTTTACTCGTGCGTTTGCTTCGCAGGTGATGTGTTGATACAGATGTCAGACAGTCAGAGGAGACTCACCAACGAGCTGGAGGGAGTGG[T/A]CTGTTATTCATCCTTGACTATCGATCCATCGTTTGATATCTTCTGTTAGCGTGTTGTTGACAATGCACGTTTGATTGGGTGTACAGTCAACCCCATGTTTAATGAGTCTGTGTGATTTGATTCAGTTTCGCTGGTTCCACTCGGAGGTCCTTCAAGAGATGGACAACAATGTCAGATTGGATAAAGATTACATATCGGTGAGTTTTATAGAGGCAACATCAGCCCTCCTGTGAATAAATATTTGTCAAACATTTCCTAGGTGATTTAACATGGCAAGGACAATTCACAGTATTTCCCTTTATATGTTTTGTGTACAGTGAAAGTAATTTTGTTCACTGGATAAGGTCAAAGTTATTAGTGCATTTAAGAAACCTTTTTGATTTGATTGGCTACAGAACAAACCACTCTTGTCCAATGAGTAGCCTAACTGATCTAATTAAGCACTTTAACATAAATATATTGAATAATGAATTGTAATTAAACATATAGACTGTAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26056
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024480 | Essential Splice Site | 117 | 419 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 24742305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 24320516 |
GRCz11 | 3 | 24451064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCAAGAGATGGACAACAATGTCAGATTGGATAAAGATTACATATCGG[T/A]GAGTTTTATAGAGGCAACATCAGCCCTCCTGTGAATAAATATTTGTCAAA
Long Flanking Sequence:
TGGTGCTTTTGTTGCTATGAATCATATTTTATGACTGCAGAGAGGTGGCATGACTGTGTGTGTAGTCAATATCAGATAACCTCCTCTGTGATGTTAAATAATAAATGATGACACAACGTCAGCTTGGCAGTGCAACCTTTAGAGACTAATACCTTTACTTTAACACACAGACAGATACTATGGATGTTATAAGATCATAAATGAAAACTTCTCTTTTACTCGTGCGTTTGCTTCGCAGGTGATGTGTTGATACAGATGTCAGACAGTCAGAGGAGACTCACCAACGAGCTGGAGGGAGTGGTCTGTTATTCATCCTTGACTATCGATCCATCGTTTGATATCTTCTGTTAGCGTGTTGTTGACAATGCACGTTTGATTGGGTGTACAGTCAACCCCATGTTTAATGAGTCTGTGTGATTTGATTCAGTTTCGCTGGTTCCACTCGGAGGTCCTTCAAGAGATGGACAACAATGTCAGATTGGATAAAGATTACATATCGG[T/A]GAGTTTTATAGAGGCAACATCAGCCCTCCTGTGAATAAATATTTGTCAAACATTTCCTAGGTGATTTAACATGGCAAGGACAATTCACAGTATTTCCCTTTATATGTTTTGTGTACAGTGAAAGTAATTTTGTTCACTGGATAAGGTCAAAGTTATTAGTGCATTTAAGAAACCTTTTTGATTTGATTGGCTACAGAACAAACCACTCTTGTCCAATGAGTAGCCTAACTGATCTAATTAAGCACTTTAACATAAATATATTGAATAATGAATTGTAATTAAACATATAGACTGTAAAAATGGCAACTAATAAAATGTTAGAATGCTAGCTCTCTGCAACTCTCACATGGTTGCCCGGTCATTACCTGGATGGGAGACCACATTGGAAAGCCAAGTTGTTACCGGAAGTGGTGTTGGTGAGACCAGTAGAGGCCGCTCAACCTGAGGTCTGTATGGGTCTTAATGCCCCAGTATATTGATGGGCACTCTATACTGCTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26055
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 |
---|---|---|---|---|---|
ENSDART00000024480 | Nonsense | 137 | 419 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 24740010)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 24318221 |
GRCz11 | 3 | 24448769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGAGATATGAGATGGAGGTGAGAAACCAGGCAACAGCACTGGAGAGA[C/T]AGATGAGGCGAGGAGTACCGCAGGTCAGAGCACGTTTATCAATGTACATG
Long Flanking Sequence:
TATCCTATATATATTTTTAATATTTTGATAATTTTTCATATGTAAAGATATTTGCAAATTGCTCTACATCTTGTTTGTATTAAGTAGTGTTTAAGCGAGGCGCATAACTAACGTGCTCTGCCCTGGACTTTAGACTGGCTTTGTTCCCGTCTAAAGAACAGACTATTATAGTTTCTCAAAATAGCAACGCGTCAGCAATGCGCCTCAAAATGCCTCCTTTTTTAGACTAGAACGTCTATGGGCGCACATGAGCACAAATGCATTTGCTATTTAAACAGCATGGCGCAAAACGTCAAAACGACTCTTGCGCCAAGCTGAAACTAGCAAACAACTATTGCGTCGCGCCTTGTGCCACATTGCACGGAGTGTATGATAGGGCTCTAAATATGATTGGACTGAAATCAATCTGCATGTTGAAACTAAAGGTTGACTTTCTCCTCCAGACCAGCAGGAGGAGATATGAGATGGAGGTGAGAAACCAGGCAACAGCACTGGAGAGA[C/T]AGATGAGGCGAGGAGTACCGCAGGTCAGAGCACGTTTATCAATGTACATGAGGACATGTGCAGATTTTAAAAGGCATTTTTTTGAAAATCTTATAATCATTTAACAATGTACAAGCTGACAAAACGTTTGTCACATACCATACTTTATAAAAAAAAAAAAAAAAAGATTTGAAAGCAAAAAGAGTGGTAACACCATCATAAGAGTGATGTTATTGATTTTACATAATAGTTAAGCAAATAAGAAGTGAATACTGAAGGTTACATTTTAGACACAATATCGTCAGTTTTTGTTCTGCAAATAAAAAGTTTTAAACATAGCCAGGGCAGAATGTTTGTTCTTTTCTGAGAATGAATCTATTTTTGAATGAATCAGTTGAATCGTTGATTCTTGATCCAGTTTCAGTGCTTGTTTATTTGCCTCTTACAATACCTCCAACAAAAGAAGCTTTTTAGTGCTAGCCTGAAGCCAAGCATCATTATCTTTCATGATGGCGGTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38386
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 |
---|---|---|---|---|---|
ENSDART00000024480 | Nonsense | 168 | 419 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 24739392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 24317603 |
GRCz11 | 3 | 24448151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCAAGGAGTGTCAGAAGGAGGCGTTAAAGGAGGAGGAAAGGCGATA[T/A]CGATTCCTGGCGGAAAAACACTGTGGGCTGACTCAGTCTATTGCTCATCT
Long Flanking Sequence:
GACAAAACGTTTGTCACATACCATACTTTATAAAAAAAAAAAAAAAAAGATTTGAAAGCAAAAAGAGTGGTAACACCATCATAAGAGTGATGTTATTGATTTTACATAATAGTTAAGCAAATAAGAAGTGAATACTGAAGGTTACATTTTAGACACAATATCGTCAGTTTTTGTTCTGCAAATAAAAAGTTTTAAACATAGCCAGGGCAGAATGTTTGTTCTTTTCTGAGAATGAATCTATTTTTGAATGAATCAGTTGAATCGTTGATTCTTGATCCAGTTTCAGTGCTTGTTTATTTGCCTCTTACAATACCTCCAACAAAAGAAGCTTTTTAGTGCTAGCCTGAAGCCAAGCATCATTATCTTTCATGATGGCGGTGGTAATGGCTAATCAACATGAGTTATGTTGATGGTTTTGTTTGTGTTTAGGATGGCAGTGAATATGTGCACTTTCTCAAGGAGTGTCAGAAGGAGGCGTTAAAGGAGGAGGAAAGGCGATA[T/A]CGATTCCTGGCGGAAAAACACTGTGGGCTGACTCAGTCTATTGCTCATCTCATGAACAAGGTTAATATCATTCATTTTCATTAGTGTCCAAACTGTTTAATGTGTATTGGAGAGCTCTGGGCTGTAATCAAGGTGATGCTATACTAGGGAAAATCTATGATTAAAATGACTTCTCGCGATTGAACTTAATGTGTTAGTGTAAAAGCATTCCATCTCAATTTTGCCAAGTTATGTGCAATTCTTTAAAGAGAAAGTTTACCCAAGAATGTAAATTTACTCACCCTTAAGTGGTTCCAAAACTGTATGAGTTTCTTTATTCTGTTTAACACAAAAGCAGTTATTTTGAAGAAAGGTGAAAAACTCTAACCACTGACTTCCAAAAATACTATGGATGTCAACGGTTATAGGTTTCCAACATTCTTCAAAATGTCTTCTTTTGTCTTCAATAGAAAAAAAGAAAGTCAAACAGATTTGGAACAAGGGTGAGTAAATGATGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17195
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 |
---|---|---|---|---|---|
ENSDART00000024480 | Essential Splice Site | 222 | 419 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 3 (position 24738651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 24316862 |
GRCz11 | 3 | 24447410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACAAGAGAATCMCGTTCACGCACTCCTTCAMGGCTGGAGGACAACATTG[T/A]GMGAAATAGTAMCATTTAACCCNAAAAACCCTTTTGCCCTAAATAATGATA
Long Flanking Sequence:
CTTTAAAGAGAAAGTTTACCCAAGAATGTAAATTTACTCACCCTTAAGTGGTTCCAAAACTGTATGAGTTTCTTTATTCTGTTTAACACAAAAGCAGTTATTTTGAAGAAAGGTGAAAAACTCTAACCACTGACTTCCAAAAATACTATGGATGTCAACGGTTATAGGTTTCCAACATTCTTCAAAATGTCTTCTTTTGTCTTCAATAGAAAAAAAGAAAGTCAAACAGATTTGGAACAAGGGTGAGTAAATGATGACATTTCTTTAAATTTTAAGTTTTATGCTTTAGAAAACTGGCTATAATCATTTTTGTTTGCCTAATATCAAATTGCTTAGAGCTAAATTTTGTCCATATTTTTTTTTGTCTGATGTGATTGTGTTTAAATGACTCCCACAGACAGGGGGCAGCCTGCAAAACAGAGCAGAGGGGTGGAAAGATCTGGTGGATCACACAAGAGAATCCCGTTCACGCACTCCTTCACGGCTGGAGGACAACATTG[T/A]GAGAAATAGTAACATTTAACCCAAAAACCCTTTTGCCCTAAATAATGATACAGTCAATAGATGAGTTTGTTGAAACTCACATTTCCATTTCTTTCTGTTAGCCTGATGTTAACCGCTGGGCAGAGCAGCCGCTGGGCACAGTGCCCTCTAGAGGTGTGAAGACTTTATTCTGACATGCAAACAAACATCTGATGAACATTAAACTCCTTGTTTAAGTTCAGTATAACAAACTTTCACCTCTTTTTCTCAGGCCCTTCCCCTCAGCCCAGTCGTTCCAACTCAACTTCAGGACAGGCTGGAGCCAGAGTGATGCGTGCACTGGTGCCACACCCACCTTCTGCAAACTCCACCCTCCTGCCATTCGCCAAAGGAGAAAGCATTACACTTCTCGTCAAAGAGCCAAGGAACGGCTGGCTGTTTGGACGCGCTGACAGCTCTGGACGGTGAGAACACTTTCACACCATAATCCATGTTTGCACAACACAGTTTTCAACAAAAAC
Associated Phenotype:
Not determined