ZMP
si:dkey-205o12.6
Ensembl ID:
ZFIN ID:
Description:
Brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2 [Source:UniProtKB/Swiss-
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31074 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29819 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13394 | Nonsense | Available for shipment | Available now |
sa24197 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31074
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 |
---|---|---|---|---|---|
ENSDART00000086356 | Nonsense | 26 | 436 | 2 | 16 |
ENSDART00000143811 | Nonsense | 27 | 498 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 31711738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29190816 |
GRCz11 | 22 | 29140011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACGCATGAATAAACACTATTTTTCTGTTTTTCTCCTCATCAAAGCGT[T/A]GGCTCTGACAAGCGAAGCCTACTTCAGCGCTCTTGCTAAGATGGGCGAAC
Long Flanking Sequence:
CATTTCTTTTGTTGTTGTTTTATGTATAGTAGGATTTTTTGTTTTATATGTGGTTTAGATTTTTATTTTGTCAGTTTATTTTTATTTTTTTTGTATGTGCGTGTGAAAAACGTCTTTAAATATTTTATGTTTACTTTTATTTTCTGTTGTATTTATATTTCTCCAAAATGTTGATTCGTTCTGTTATTATTTTTGTTATTGTTATTTTTCTAAGGTTTTCTAAGTGGTTGTGTAAGCATTTCACTGCATGTCTGACTGTTTTGAATTTGAATTTGATTGTTTTGAATTTTATAAAATGCCAAACCTACTGTAAAAAAAGACTCATCTCAGAACATTTTGTGGGGGTCTATTAAACTAGTAAACACTTCTATACACTAGTAAACACAATCTATACCACCAGGGGCTTATTTTAGCTATTAATAATATCATCATGATCATTAGGGAATGCTAAAAACGCATGAATAAACACTATTTTTCTGTTTTTCTCCTCATCAAAGCGT[T/A]GGCTCTGACAAGCGAAGCCTACTTCAGCGCTCTTGCTAAGATGGGCGAACAAGCTCTCAGCACACTATCATCTAGATCACTCGGTAAGAATCCTGTGCGTCTCTAAAGTAGTGCCAGCTGGGCAGATTGTGAAGCAAGATGTCCACTGAGTTTTTAACTCTACTTTCTGGCTGTACTAGCGCATGTTTGTCCTACAGACAATAGATGTTTCAGCGAACAGCATCCAGCGCCAGATGCTTCCTCTCCTCTGTCGAAAAACACAAGATTTGGCTGAGAGAAACCTTCAGGTTGATGCCAAAGTTATGAGTTTTAGTTTCAGTCACGAGATAAAGAAACGATGAATTACAGAATACTAGTTTAAGGGTTCCACTTTATATTAAGTGGCCTTAACTAATATGTACTTACATAGGAATTAATAGTTTGTTACAATGTACTTATTGTGCATATACATGTATTTACTGTGTACTTATGCTTGATTAAATACATGCATGTAATTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29819
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 |
---|---|---|---|---|---|
ENSDART00000086356 | Nonsense | 84 | 436 | 4 | 16 |
ENSDART00000143811 | Nonsense | 85 | 498 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 31722417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29201495 |
GRCz11 | 22 | 29150690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGGTCTTGATTACTGTTTCAGTTCCGCTGGTTCCATGTGGAGGTTCTG[C/T]AGGCCATGGACAAGAACGTGAAGCTGGACGAGGAATACATTGAGGTGAGT
Long Flanking Sequence:
ATGGTCTTTAGCCTCCTTGTTTGAGCAGCCGACTCCCATGCAAAGAATCGCCGGTTCGACCCCAGCTCAGTCCAGGTGCAATAGGACCAGTAGGTTACATAATTAATAATTTCTAGTATCTTTTACAGTAAAAATTATTTATATAGCACCTTTTACAGACAATAAGTAACAAAGTGCTTTACAGTAAAAAAAAAATCTATATTAAAACAGGTTAAAATCCAAGCTCAAATAACACCAAATGTAAAACCAGACCACCATACTGTTAATTAAAAGCTTGTCAAAAAAAAGTGTCTTAGGTACATATAAAGTACCTAAAGAATAATCATTAGTAGCTAATGAATTAGTTATAGTACTTGGAAAAGATACAAGTGTCTAAAAATAAGAGCTAGAGCAGGAAAACGGATACTAGTATGTTATATTGATTAAATGCTAAAGTGGCTTGCCTTACTCGTTGGTCTTGATTACTGTTTCAGTTCCGCTGGTTCCATGTGGAGGTTCTG[C/T]AGGCCATGGACAAGAACGTGAAGCTGGACGAGGAATACATTGAGGTGAGTCAAGAAGCTTGTGGTGTGTCTCTGTATATGTATATCCTGTGTGTGTATGAGCTAATATGTTCAATATATATATAAAGGGCAGTCGTAGAGTGTATGAACTGGAGGTGAGGAATCAGGCGGCATCGCTGGAGCGTCAGCTGAGACGTGGTGCCTTCAGAGACTCACTGGTAAGACCACGTTTTTGTTCATGTAAACATTTTTAAGGTGTCTAATGTTTGTTATGCAAACAAGTCTGTATTCTAAGAAACTAACTATCTGAATGTATCCTAAAAGATTGTAACTTGGCCTTATGATGTTGCTAAGTTAACATCAAAATACTAGAACAATCTCATTTCAGTTTTGTGGAGTTTGACGTGAGCATCAATTTTAAGATAATAACTCTTAAATAACCTCTGTCTCAGCTGAATCTATTGGTCTGTCATTGGTATGCTAATCTAAAAAACTAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13394
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 |
---|---|---|---|---|---|
ENSDART00000086356 | None | None | 436 | None | 16 |
ENSDART00000143811 | Nonsense | 126 | 498 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 31722623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29201701 |
GRCz11 | 22 | 29150896 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGAATCAGGCGGCATCGCTGGAGCGTCAGCTGAGACGTGGTGCSTTC[A/T]GAGACTCACTGGTAAGACCACGTTTTTGTTCATGTAAACATTTTTAWGGT
Long Flanking Sequence:
ACAGGTTAAAATCCAAGCTCAAATAACACCAAATGTAAAACCAGACCACCATACTGTTAATTAAAAGCTTGTCAAAAAAAAGTGTCTTAGGTACATATAAAGTACCTAAAGAATAATCATTAGTAGCTAATGAATTAGTTATAGTACTTGGAAAAGATACAAGTGTCTAAAAATAAGAGCTAGAGCAGGAAAACGGATACTAGTATGTTATATTGATTAAATGCTAAAGTGGCTTGCCTTACTCGTTGGTCTTGATTACTGTTTCAGTTCCGCTGGTTCCATGTGGAGGTTCTGCAGGCCATGGACAAGAACGTGAAGCTGGACGAGGAATACATTGAGGTGAGTCAAGAAGCTTGTGGTGTGTCTCTGTATATGTATATCCTGTGTGTGTATGAGCTAATATGTTCAATATATATATAAAGGGCAGTCGTAGAGTGTATGAACTGGAGGTGAGGAATCAGGCGGCATCGCTGGAGCGTCAGCTGAGACGTGGTGCCTTC[A/T]GAGACTCACTGGTAAGACCACGTTTTTGTTCATGTAAACATTTTTAAGGTGTCTAATGTTTGTTATGCAAACAAGTCTGTATTCTAAGAAACTAACTATCTGAATGTATCCTAAAAGATTGTAACTTGGCCTTATGATGTTGCTAAGTTAACATCAAAATACTAGAACAATCTCATTTCAGTTTTGTGGAGTTTGACGTGAGCATCAATTTTAAGATAATAACTCTTAAATAACCTCTGTCTCAGCTGAATCTATTGGTCTGTCATTGGTATGCTAATCTAAAAAACTAATGATCTTATTTGAGTCTTGTAGCATTTGCAATTAGCATGTTAGTAAGTTGGTAAGAAACTCAGTATTCTCATTTGTTGTTAACTCTGTCATTAGCATGTTGTTAGCAAACAAAGTCTAACAATTTAAATGTTCCAGCAAACTTTACCAGTTTTTACCTGTTTAGCATTTGCTAAGACAAATCAAAATTCTAATAAGTCTGACTGTTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24197
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 |
---|---|---|---|---|---|
ENSDART00000086356 | None | None | 436 | None | 16 |
ENSDART00000143811 | Nonsense | 411 | 498 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 31732907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29211985 |
GRCz11 | 22 | 29161180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTCCTGCTCCAGCCACACAGCTGCGCCGTGGCTCGGCCGATGTTCGCT[C/A]GATATCTCCTCTCCCTGACAGGAGGGCGGAGTCTCATTTTGAGAGCAAAG
Long Flanking Sequence:
AGTGGCCGGTGAGTGTATGTTTTTTTTTATCTTTTTACAAAAAACTTTCAAGGATTTAAGATGCTAATGACTGTTAAACATGCCATTACAGTCTTGTGAAAACATTACACAATCAAGGCTTCATATCTTGTTTCTAATGTATCAACACTAGCCGTTAAAAAAAACAAAAGCAAAATCAGTCGACTACTAGTTATACCTACATCTAAATTAATACATTTTTATGTTAATGTGTTGATTTGTCTGTAGTATGTCACACCGAAGCCACAGCATGAACAACCTCCTGGAGCCGACCAGCCAATCAGAATCCGACACCCAGACCTACAGTGAAGTTTCTTCTCCAGTGGTCTCCATGCGCCGTGCGTCGGCAGACGTTCGCTCAGTATCTCCCCTCCCCGAAAAGAAGACAGAGTCCAACAACGAGCTCAAGAGCGGCCAGAAAGTCTTCCACGAGATTCCTGCTCCAGCCACACAGCTGCGCCGTGGCTCGGCCGATGTTCGCT[C/A]GATATCTCCTCTCCCTGACAGGAGGGCGGAGTCTCATTTTGAGAGCAAAGTGGAGCTCAAACATTACAACGAACTTCCACCTCCAGCTCCACCCCTTCCAAACTCTCCTCTGCCTGAGCGAAAGACTGACTCAACCTCAGAGGTGAGCATTTGTGTTTTTAATTTTACTTTTAGTCTAGACCAGGGGTGTCCAAACTCTGGAGAGTTTAGCTCCAACCCTAATCAAACACACCTGAACCAGCTAATCAAGCTCTTACTAGATATACTAAGTATAAACTTCCAAGCAGGTGTGTTAAAGCAAGTTAGAGCTAAATTCAGCAGGACACCAGCCCTCCAGAACCGAGTTTGGACACCCTGTCTAGTCTTTATCTTAAGCTGACATTTTAAAAAATTTGTTTTAGTCATGTTCAGACTCTTTTTAGTCTAGTCGTGTTTTAATCAACTAAAGTCTGAGCATTTTTGTCTTATTTTGCTCAGAATCATCCATGACTATTTTCGTC
Associated Phenotype:
Not determined