ZMP
baiap2a
Ensembl ID:
ZFIN ID:
Description:
BAI1-associated protein 2a [Source:RefSeq peptide;Acc:NP_001035335]
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 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33307 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11319 | Nonsense | Available for shipment | Available now |
| sa40162 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9258 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33308 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8395 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33307
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 |
|---|---|---|---|---|---|
| ENSDART00000091180 | Nonsense | 9 | 490 | 1 | 12 |
| ENSDART00000123659 | Nonsense | 33 | 514 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 52362153)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51487561 |
| GRCz11 | 3 | 51742224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCTCTCTCTCTTGCTTGCAGAACATCATGGAACAGTTCAATCCCTG[T/A]TTGCGGAATTTCATCGCAATGGGCAAGAACTACGAGAAGGCTCTCTCCAG
Long Flanking Sequence:
TCATCGCTATCTGTCTTTCTGTCTGCTTATGTTATTTTGTCTATCTGTCGTTCTGCCTGTCGTTTTGTCTCATTTTATCTGTTCTTCTATCTCTGCCGCTCTATCTATCTATCTTTGTCTGTATCTATCCATCTATCTGTCTTTCTGTCAGTCTATCTCTTGTTCTATCTATAATTATTCATTTATCCATCTGTCTGTTGTTCTGTCTATGCATCTGTCCTTTTATCTATTTGTCTATCCATCGTTCTGCCTTTCTCTATCATTCTGTTCTGTCTATCCTTATATCTTTCTGTCTGTCTGTCTGTCTGTCTGTCTTTCTTTCTGTTTTTCTGTCTATCTGTCGACCTAGAATTTCTCGCTGCATTATTGTACATGTTGGCAACCCTTAGTTTCAATCACAAGATCTACCAACAGCACATGTACAATTAACATAACTTGCTTCTAATCAAATCTCTCTCTCTCTCTTGCTTGCAGAACATCATGGAACAGTTCAATCCCTG[T/A]TTGCGGAATTTCATCGCAATGGGCAAGAACTACGAGAAGGCTCTCTCCAGTAAGTATCCACACATCACATCACCAAACATCGCCTGCGTTATCCACATTCAGGCAGCTGTCCAAACCCTCCACGCCTCCCCATCCACCTTTGATGCCACTTCATTTGAAGACGATGACAATATTTGTCATTCCGTCATTCAGATGGCCCCACGTTCTTATCAGCTCTCACACAGCTCCAGACACCTCCTGAGCTCAGATGGGCTCAAACACAAGCGTTCAGCTGATGAGGCCATTCACCCAGCAGATAATGTGCCCTGCCTTGCTGATGATTTGATATTTAGCCATTAGACAGAGGGAACAATCAGACGACTTTGAAGGCTTTGTGCAGTAGGTGACTGATGAAAGCCAGACAATTGGTCATTGACATCTGCGTTCACATTGGCGAATGTAATCTTGCACTGGCAGCCTTGGGTGGACAGTGGCTGTAAAACCTTGAGCATGGCATTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11319
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000091180 | Nonsense | 177 | 490 | 6 | 12 |
| ENSDART00000123659 | Nonsense | 201 | 514 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 52481705)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51607113 |
| GRCz11 | 3 | 51861776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGCAGAGGGCTACAAAACAGCGCTTTCAGAGGAACGTAGGAGATACTG[T/A]TTCCTGGTGGACCGCCAATGCGCTGTAGCCAAGAACAGCAGYGCCTACCA
Long Flanking Sequence:
ACTTTGCTCAAAAGGGACTTTGTTGAAATATTGCATACACAGATATAAGCTGACGCAATCATCAAACATGGACCGCATATAAATCAAAACTGCCTAACGTTACTGAATGAAATGTTGAGCTCAAAAAAGGAATATAACTGTGCAAGTTAGGATGATGGACTTCATATTCTCTGTCTATGCTTTGATCAGTTGTACACAAGTGTAACTTTTTTGTTAGTGGGGGTTTTCATTTTAAACCAGATACAAACTTTCTTTTGATATTTTGCATGTTCAAATATTCATACAACATAAGATTCAAGGGATCATGAAAATATAGTAACAGTCATCCAACATGTTAGTGCAGTTTTCAATTAATTTTATTAGTTCATTATTGAAACTAATCACTTTTCATTTTATCTTTGCCAGTATGTTGAGGCCATCAGCAGTAAACAGAGTGAGCTGGATACCTTCATTGCAGAGGGCTACAAAACAGCGCTTTCAGAGGAACGTAGGAGATACTG[T/A]TTCCTGGTGGACCGCCAATGCGCTGTAGCCAAGAACAGCAGCGCCTACCATGGCAAGGTGAGACCCAGATGCTTTTTTTTTTCCCTTCACCGTAAAAGATAGACAGCATCGCCAGCCATGTACTTTCACAGTCTCTCCTGTTATGTGGCCTGAAGACAGCAGCAGTTGCCATGGCAATCCCCAAAGATCACCCCTCACAACCGTCTCCATTGGGCACAGTTTGTTTGTGCTTATTGCGAAGATGAGATTTATTCTCTCCTGCAATTGTCTGTGTTCCAAAAGTGCTGTGAAGTAATGCACACCATTTCTGACATATCAATTATCCGTAATGGCGGAGCCACATCCTTACAGTAAAACCAAGTTATTGTAACTCCAGATTGTGGGAGGAGCAGTTATTAACATCTGCAGGTGGTCCCATCCCATATGCAGTATACTTAAATGCACCTTTTTACATCTGAAAACTTGTGTGCGTGTGCAGATTTATTTGGTTTGCTATATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40162
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 |
|---|---|---|---|---|---|
| ENSDART00000091180 | Nonsense | 258 | 490 | 7 | 12 |
| ENSDART00000123659 | Nonsense | 282 | 514 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 52491667)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51617075 |
| GRCz11 | 3 | 51871738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACTCATCCAAGGGGAACCTGGTCATCTCAGATCCCATTCCTGGAGCA[C/T]AACCGCTGCCCGTGCCCCCCGAACTAGCTGCCTTCATGGGAGGTGGCCTG
Long Flanking Sequence:
GCAACCACTAGAGTCATTCTTAACAACCTACTGATAACACCTTCGCAACAGAAATGAAACATCAAGGGAGCTAATCAGATTTTCTTCTGAAAGAGTACATCTAGTCACGATTTTGAAGTAGTAACAGTAACTGTAGTATCTGTGGTGTATTGGCCGAAACTGTGGTTACCATGGCAATATTTTTTTGTGAAGCGCAAGTATGTAGTGGTCTTAATGCAGCAGAGGCACCTCTATGTTTTTTTCAGTCATTCAAATGCATTTCAGCATTGTGGACAAGCTTTTCCAATTTCATCCTTAATTGTCTCTTTTTTTTGTAGGGTAAGGACTTGTTAACCCAGAAGATCCCGGTGTGGCAGCAGGCCTGTTCAGACCCCAACAAGCTGCCAGACAGGGCCATGATGCTCACCCAGCAGATGACCTCTGGAACGAGCACCCTCCTCTCCAGCCCTCTGCACTCATCCAAGGGGAACCTGGTCATCTCAGATCCCATTCCTGGAGCA[C/T]AACCGCTGCCCGTGCCCCCCGAACTAGCTGCCTTCATGGGAGGTGGCCTGGGCCAGGGGGTTAGTAAAGAACATTAGCCACCTGTTTAACAATACAAATGACTAACTGTTGTTCAAAGTGTACAAAATAGCAATTGAAGCTTCTTATGTCCTGATGTGAAAACCGCTCATTTGCATACTGCAGCGTTGGCTGAGCGTAGGATGATTCAACCTCTTTAAAACTCGATCCTTCAGGCAGTGCTTTGGTTGAGTGGCCCCTCGCTAGAACAGAACTCTAGTACAATTTTAATACTCACAACAACTGAGCCTCTGCACCTGTAATTTGCTATCACTTTATCGATGCTGCTGCTGCTGCTGGAGTGATACTCATACATCACAGAGCTTGTTTAGGAGTCTGTGGCCTCGTCTGCTAGTTTAAAACCCAGACTTTTGTGTGTCTGGTAGTGATAGACCAATATCAATCTTTTTGATTGCCAGTGTCAATGTCTTAGACAGCTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9258
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000091180 | Nonsense | 343 | 490 | 8 | 12 |
| ENSDART00000123659 | Nonsense | 367 | 514 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 52493916)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51619324 |
| GRCz11 | 3 | 51873987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGCGACGTMTATTCCAACACCCTGCCTGTCCGCAGGCCTCAGYCCGCT[A/T]AAAACAAGACCACTGTGGGTAAGAAAACAAACTGTTTTGCTTAGCCATCC
Long Flanking Sequence:
GCACTCAGTCGTGTTATGGGGCTGTGTAGCCTCAGACCAATGAGAGTGCCTACGATCCGTCTTTCAGAGGACATGAAGCATAGAAACTGGACCTTAAAGTTATGGAAGAATGCCTCATCCTCAGGATGCACTAACTTGTTGTTATATTGCTGCCATTTACAAACAAATGTATTTTCTCTTTCAAAATGAAAACATTTCCAGCTAAGCCAAACAGGAACATGTAGAAAATAATATTTTAAAAATGTCAAATATTGTTTACATGCTAGTATCTGTAAATGCTATTTTGGTGATCTGTGTTTTTGCAGAGGCTAATGGGTCCTAATGGTATGTCTCTGGTTAATGGGACAACAGGGGTCCATGGAGATGATTACTGGACAGACGGAGTGTCTCAGGGAAGACCACCTTCCCCACAAAATCCATCTCAAACACAGAGCCAGCCCCAGAGACAGGTCAGCGACGTCTATTCCAACACCCTGCCTGTCCGCAGGCCTCAGCCCGCT[A/T]AAAACAAGACCACTGTGGGTAAGAAAACAAACTGTTTTGCTTAGCCATCCAACTTCAAGTACAAATGACTTTTTAAACAGTGATTTTAACAAATTGCACTCATATTACTATTTCAATTTCGAGGAGAGACACGAACTTTGCCCAGGTCAAGTTCTATGGCGGCTGGTCTGGAGAAGAACGGACGCTCTCGTGTACAGGCCATTTTCTCCCATGCCGCAGGCGACAACAGCACCCTCCTCAGCTTCACCGAGGGTGACATCATCACCCTTCTGGTGCCAGAGGCTCGGGACGGCTGGCACTATGGAGAGAATGAGAAAAACAAGATGTAAGCACTCAATGTCTACATTATCAACAGCCCTAAATGAAAACAGTATTACAATTTAGAATTTCAAAACTATTTCTTGAAAAAGAAAAAAGATTTCTTGCCGGTTTTGTACTTTTCGTCTCGGGTATATGTCCTGAGGAAAAGATGTTGAATATCTTGACTGTCAAGTCACCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33308
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 |
|---|---|---|---|---|---|
| ENSDART00000091180 | Nonsense | 477 | 490 | 11 | 12 |
| ENSDART00000123659 | Nonsense | 501 | 514 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 52499260)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51624668 |
| GRCz11 | 3 | 51879331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGCCTGACTATGGGTTGACTGCCCGACTGTTGGCACAGAGCCTTACA[C/T]AGAGCCGACAGCGTCCCTACAGCATGGCAGGCTTTGCACAGGTACACACA
Long Flanking Sequence:
ATAAATGTTTACCATAAGAGGCTGTCTATATTTACACACTTTTGCCACATAACTGTGCTTAAACCTCTGATAAAAGTGATTTTTGCATAATGAGACCCCTTTAGTAAGCAAAATTGCTAATGTTTGAACTATTACGCTAACCAGTTAAGCAGTTGGCACTGTTATCAACAAGGCTGCAAAAATAGTTTAAATTTTCAGTAAAGTGTTTATGATATCAATATTGTGCATGTTTATAATCATCCCAATATATGATCAATATGGTATTAAGTCTTATTGGTTGCATTAAAATAGATGTGTAAAAGCAATTGAGTGAAATGCTATGGGGATGTGAAGCACATGTTAATGGCAGGGTGTAAAAATGACTGACTGACTGACCTTCGTCCTGTAGTCTTCACCATGGGAAGAGCAGCAGCACAGGAAACCTGCTGGAGCGGGAGGACATGTCCTTGCCCATGCCTGACTATGGGTTGACTGCCCGACTGTTGGCACAGAGCCTTACA[C/T]AGAGCCGACAGCGTCCCTACAGCATGGCAGGCTTTGCACAGGTACACACACAAACTAGCACACACAAACTAGCATTAGACAGGTATCTCTCATTGATGTCTCCTTTCTTAGGACTTTTATTCTGTAATTCTCTTTTAACTCTGCTCAAAGCGTAATCTATATGTCAGCTCTTCTTTAATCTGTGCTGTAGCAGCTTACTGACTCAATCTGCTGGTGTGGCTCTTTCTAAAAACGCATGATTTTCTTATTTAACGGAGAGTTCGCTTTGAAATGAAAAGTTCTGTCATCATTCACTCACACTAATAATGTTTGAAATGATGGTTCTGCTGGGCATAAAAGCTGTTATGGGAATATCAGAGCTTTACTTTACAGTGTGGTGAAAGCAGGGTTAAATACTGTAGTGTATCATAAACAAACAAACAAAAACAAAACAAAAAAAACAGCATGGAAGTGATTTATATAATTTGTGGAGCTTTTTCACAGCCCGTCAAATCTCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8395
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 |
|---|---|---|---|---|---|
| ENSDART00000091180 | Nonsense | 480 | 490 | 11 | 12 |
| ENSDART00000123659 | Nonsense | 504 | 514 | 12 | 13 |
| ENSDART00000091180 | Nonsense | 480 | 490 | 11 | 12 |
| ENSDART00000123659 | Nonsense | 504 | 514 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 52499269)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51624677 |
| GRCz11 | 3 | 51879340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTATGGKTTGACTGCCCGACTGTTGGCACAGAGCCTTACACAGAGCCGA[C/T]AGCRTCCCTACAGCATGGCAGGCTTTGCACAGGTACACACACAAACTAGC
Long Flanking Sequence:
TACCATAAGAGGCTGTCTATATTTACACACTTTTGCCACATAACTGTGCTTAAACCTCTGATAAAAGTGATTTTTGCATAATGAGACCCCTTTAGTAAGCAAAATTGCTAATGTTTGAACTATTACGCTAACCAGTTAAGCAGTTGGCACTGTTATCAACAAGGCTGCAAAAATAGTTTAAATTTTCAGTAAAGTGTTTATGATATCAATATTGTGCATGTTTATAATCATCCCAATATATGATCAATATGGTATTAAGTCTTATTGGTTGCATTAAAATAGATGTGTAAAAGCAATTGAGTGAAATGCTATGGGGATGTGAAGCACATGTTAATGGCAGGGTGTAAAAATGACTGACTGACTGACCTTCGTCCTGTAGTCTTCACCATGGGAAGAGCAGCAGCACAGGAAACCTGCTGGAGCGGGAGGACATGTCCTTGCCCATGCCTGACTATGGGTTGACTGCCCGACTGTTGGCACAGAGCCTTACACAGAGCCGA[C/T]AGCGTCCCTACAGCATGGCAGGCTTTGCACAGGTACACACACAAACTAGCACACACAAACTAGCATTAGACAGGTATCTCTCATTGATGTCTCCTTTCTTAGGACTTTTATTCTGTAATTCTCTTTTAACTCTGCTCAAAGCGTAATCTATATGTCAGCTCTTCTTTAATCTGTGCTGTAGCAGCTTACTGACTCAATCTGCTGGTGTGGCTCTTTCTAAAAACGCATGATTTTCTTATTTAACGGAGAGTTCGCTTTGAAATGAAAAGTTCTGTCATCATTCACTCACACTAATAATGTTTGAAATGATGGTTCTGCTGGGCATAAAAGCTGTTATGGGAATATCAGAGCTTTACTTTACAGTGTGGTGAAAGCAGGGTTAAATACTGTAGTGTATCATAAACAAACAAACAAAAACAAAACAAAAAAAACAGCATGGAAGTGATTTATATAATTTGTGGAGCTTTTTCACAGCCCGTCAAATCTCAATTATGTCTGTG
Associated Phenotype:
Not determined