ZMP
BAIAP3
Ensembl ID:
Description:
BAI1-associated protein 3 [Source:HGNC Symbol;Acc:948]
Human Orthologue:
BAIAP3
Human Description:
BAI1-associated protein 3 [Source:HGNC Symbol;Acc:948]
Mouse Orthologue:
Baiap3
Mouse Description:
BAI1-associated protein 3 Gene [Source:MGI Symbol;Acc:MGI:2685783]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45155 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20116 | Splice Site, Nonsense | Available for shipment | Available now |
sa11970 | Essential Splice Site | Available for shipment | Available now |
sa18764 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40147 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45155
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 |
---|---|---|---|---|---|
ENSDART00000111363 | Essential Splice Site | 442 | 1070 | 14 | 32 |
Genomic Location (Zv9):
Chromosome 3 (position 45545902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47555455 |
GRCz11 | 3 | 45507789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTCAAACCGCAGTGAACTGCATTTGGAAATAGCCACAGTTATAAAGG[T/A]AATAAGGTCGTCCAGACCAACTGTGAGAAGTACCATGGTCCTGAAAGGTA
Long Flanking Sequence:
TTTTTCTCACAGGAACCCAAGTAATGTTCTCAAAAGATCAAAAATGACCGCCATTGCTACACTTGTCAGGAGAATTGCACATATGTGTACAGAAACCTGCATTCATCCGGTCGATTTCCTGGCTGAAGGACCAAAATAAGTCCATTTGAATTCAGATATTTCCACCATCAATTGCAGCTGGGCTCATGGTGATCTGCCCTTTCTGACTCCCTCTGGCTAGATCAGTATTGGGAAGCGGGACACAGAAAAATTGATATCCTGTGGGGTTTTCTAGTGTTGTAGTACAGTACACTGGGCTCAGAGACACAGCAATAGTATATTCAGGTTTCAGATAGTGTGACCGAAACTGTTCTTTGGGTATTGATCCACTGCTGTGTATGTGTACGTCTGTGTATGTGTGTGCTTCAGGAGCGTCGGTCACATGCAGTCGATGGCAGCCTTTAGAGCGGTGTGTTCAAACCGCAGTGAACTGCATTTGGAAATAGCCACAGTTATAAAGG[T/A]AATAAGGTCGTCCAGACCAACTGTGAGAAGTACCATGGTCCTGAAAGGTATTTGGACACTGAAACTTCATTGGCTAAGATGTACACAAGTATTCAGAAGCATTAGTTTGGAGACGGTGAAAATTCTCTGACGTCCACCTCTAATGTTATTAAGATTTTTATATTAAAAACATTCCCATTTAGAATTAATAGATTATTTTTGTCCTGCTTTGAACTCACTTCGTTAGAACATAGTATGATAGGTACTGAGAAGTAAATAGTAAAAAAATGACCATAATCTTGCTGACGCAGTCTGGGACTTGTATGTAAAAAAGTCAATAAGTGAAGTTTATTTATAAAATAATTTCGAGAGTAGCATGCACTTATGATTGATGGCAGCTAACACTGATTCACCAAGCAGATGACTCCTTAACCATTAGAAATAACCAGAGTATCTTACCATAGCCATCTTCGTCTTGAAGAATCCCCCCTTCCACCCCTACTCCTCCCATTACCTTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20116
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111363 | Splice Site, Nonsense | 522 | 1070 | 18 | 32 |
Genomic Location (Zv9):
Chromosome 3 (position 45550305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47559858 |
GRCz11 | 3 | 45512192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTGTGCTGTTTCTCCAGGTGGCGGATGATGTGAATGTAGCGATGGAG[C/T]GAGTATGTGGGAATCTGGAGCAGGAGAGTTCACGGCTCACCCAAACTATG
Long Flanking Sequence:
TACTTTTTTATGCTCATTTTATGTGCATAAAAATAGATTGATGGAGAATAGCTAGTGTTGCAGGGTTGTTTAAACAAATATAGCGGATATTATTTGCCTTCAAAAAAAGGCAGGTTTCTCTGCAAGGCTTTGAATAGCTTATATATAACCATCTCTGCGAATTAAACTGGGATAAAAAAGACAAATGAGAAGGACTTGGGAAAAAAGCACACTTCAGTGAATGAGATGGGTTGGTGCACACTAAAAAAGGGAGCAATAAAAGCAAAAGAAAACACAGGAAGGACATTTTTGTCTTGTCTTTCAGCTCTGTGAAGGTTGACTTCTTCAGCATCTCCTACCGGCAGTTAGAGAAGCTTGTAAGTTTGAGCTCTCTTGGGAACGCTTATAGATCTTTGTTAAAAATAAGCCTTGCCTTGATAAACGCGAATCGGCGATAGAGATGGAGCTTTAATGTTGTGCTGTTTCTCCAGGTGGCGGATGATGTGAATGTAGCGATGGAG[C/T]GAGTATGTGGGAATCTGGAGCAGGAGAGTTCACGGCTCACCCAAACTATGGGAGAGACCCTGTTTGAGCTCTACATGTCACTCAAATCCCTCAAACGCTTCAGGGAGTACCTGCCTCTCAAGTTAGTCATTAAAGCTTCTCTTCATCCATGTGCATGAGAGCTAATACATTGGCTAAGCTATTATGCAAACAATGAATGTTCATGAGGGTTTATATATACACTCTTGATTGAATGAGCGTGAGCATGGCTAATTCATGACCGGCTTGTATAAATGTGGTAATTTCTTTCCAGGGACACTAAGATGTTGGCTCTTACTGGATTCCATAACTGGTTTAAGACTTCTATTCACAAATGGCTGCAGATTGTACATGAACGATCCACTGAGAGGATCCGTAAAGCAGTGGAAATGGATCCGGTGAGCTTCTGACCAAAACCAAAAGCCAAGATTATACTCTCTAAAAATGTTGCGTTAAACCAATTCTGGGTCAGATATGAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11970
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111363 | Essential Splice Site | 596 | 1070 | 20 | 32 |
Genomic Location (Zv9):
Chromosome 3 (position 45550723)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47560276 |
GRCz11 | 3 | 45512610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGAACGWTCCACTGAGAGGATCCGTAAAGCAGTGGAAATGGATCCGG[T/C]GAGCTTCTGAMCAAAACCAAAARCCAAGATTATACTCTCTAAAAATGTTG
Long Flanking Sequence:
AAACGCGAATCGGCGATAGAGATGGAGCTTTAATGTTGTGCTGTTTCTCCAGGTGGCGGATGATGTGAATGTAGCGATGGAGCGAGTATGTGGGAATCTGGAGCAGGAGAGTTCACGGCTCACCCAAACTATGGGAGAGACCCTGTTTGAGCTCTACATGTCACTCAAATCCCTCAAACGCTTCAGGGAGTACCTGCCTCTCAAGTTAGTCATTAAAGCTTCTCTTCATCCATGTGCATGAGAGCTAATACATTGGCTAAGCTATTATGCAAACAATGAATGTTCATGAGGGTTTATATATACACTCTTGATTGAATGAGCGTGAGCATGGCTAATTCATGACCGGCTTGTATAAATGTGGTAATTTCTTTCCAGGGACACTAAGATGTTGGCTCTTACTGGATTCCATAACTGGTTTAAGACTTCTATTCACAAATGGCTGCAGATTGTACATGAACGATCCACTGAGAGGATCCGTAAAGCAGTGGAAATGGATCCGG[T/C]GAGCTTCTGACCAAAACCAAAAGCCAAGATTATACTCTCTAAAAATGTTGCGTTAAACCAATTCTGGGTCAGATATGAACAATCCCAATTAAATTGAATTAACCACTTAAACTCTGCGGACCCAGGTCTGTGACGTCATCGACTTTCGCTTTCAGATTTAAAGGGCTAGCGTTGCACCAGACCCCCGTAAGTGGTGTCGTTTGAAAGTGTAGAATCTATATTTTATGCACATATGCATCACTTTGGTTTTTATTCTACTGTATAAAAGTTATTTACACTTAAATACACAGTATTTTGGATACCTGAGCTAGGTATTTTACATTGGTTCTTTTTCATATTATTTCATATGACACATGTACAAGTTATAGCTCAAATGAAAACTCTTGCTGGTGCTCATACAGTTTTAGCATTGTTTTTACTGAATTATATTCATATGCCAAACAGTTGTTGAATGAATTGTGGTGTTTCCATGGCGCAGAAATGTAAACAATACATTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18764
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111363 | Essential Splice Site | 858 | 1070 | 27 | 32 |
Genomic Location (Zv9):
Chromosome 3 (position 45561794)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47571347 |
GRCz11 | 3 | 45523681 |
KASP Assay ID:
2259-3997.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGGAGAAGGGTTGCTCTTGGAAGACCTTAAGAGTGGAGACTATAAGG[T/G]ATTCTCAACTACGACCAATATATCTGACCAAACGAATGAGCATAGCTTCA
Long Flanking Sequence:
ATTTTTCAGGCCTTGAAAAGTTTTGTAAAAACAGAAAAACCCACAAAGTTTTGGAAATGTCTCGGAAAACATTTGGATACTTGAATATAGGTTATTTACTTCTGTCCTTGGTCAATCACATACTCTTACATTATTAGTGAGGTGTAAGCATTATCTAAATCAATGTTACATAGTTATAAACATAAATTGAAACTAAATAGTTTGTTGCGTGTTTTACGATATGCTGTGATAAATTTGAACAAAAATTTACTAGAAAGTCTTGGAAAAATCAGGGAAAAGTCATGGAATTTTTGTTGTTATAATGTGTATGAACCCTGTGTTTACATTCAATAGAATATGTCCTGTTCAGTTTTGTTTTTTCCAGAAAAATAACATACTACCATACATTTTTTTCCTATGTATAATTCAACCAGTATTTTACTTGCAGACACTGGTGCGGTTCTTCCACGCTGATGGAGAAGGGTTGCTCTTGGAAGACCTTAAGAGTGGAGACTATAAGG[T/G]ATTCTCAACTACGACCAATATATCTGACCAAACGAATGAGCATAGCTTCATCTGCCTTCCTTCTCTCCTTCCTTTTCTTCAGGGCCTGGATGAGGAGCTGCGTCTGAACAAATGCTCCTCCTTTGAGCTGATCGAACAGTATTTCCTGGAGAAAATCTCCCAGCAGGTGGGTAGGAGCCCTGCTGGGCCGCCACAGCTTTTAGCTCAAGCCCTGCGGAGAGAGGAGGTGTTGATTAGGAGCTAAGACATCACAAATACTATTCCTTCCTCTGATGATTAAAAGTTTACATCAGTCATTTCCTCTTTGACTAAGCGTTCTTTGCACTGCGCAGGATTTCACAGTTTCTGACTGTCTAAAATCCTGCTAAGCTCCCTTGCAGCCTGCTGCCTACGGGGCAGATGTCTGCATAACCAGCATGTTGCGAAGCTGAAATGAAACCTCATAAATTTCTTATCTAAACTGCTCTTTAAAGACAGCAACTTTATTAACGTCATTGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40147
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111363 | Essential Splice Site | 1037 | 1070 | 31 | 32 |
Genomic Location (Zv9):
Chromosome 3 (position 45568674)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 47578227 |
GRCz11 | 3 | 45530561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCCTTCAACCCGTCATCCTGCACTTATCCCGTCAAAAACCAAGCGG[T/G]ATGCTAATCTGCCCTTTTTATTATATTCCTCCTTTCAAGAGTCCACACTT
Long Flanking Sequence:
AATCCAGTTTGAGACCACTGCACTATAGTCTTTTGCTGTTTTTCGTTATTAAATTTGTCTTCAAACGTCTGCTTTCCCAGGCCTCAGCGACCCATTTGTCATCGTGGAGCTGTGTCCTCACCATCTGTTCCCCACTGCTCGCAGTCAGCGCACCCAAGTAAAGCTCAAAACCCTGCACCCTGTTTTTGATGAGCTTTTTTACTTGTGAGTACCAGATCGTCTGCCTTCCTGAAAACTTGCTATTTAGTCCCAGCACCCCAAACAGCCCTTTGACCCCGTTTGCTTCTTCACAGTCACGTCAGCCCAGAGCAGTACAGGCACAGGTGTGCTTGTCTGACCTTCACTGTGATGGACTATGATTGGTTATCCACTAATGATTTCGCTGGCGAGGCGGTGGCTCCACTGAGTGACTTTTGCTGGCCGGGCAGACCGAGTGCCACACCTGCCGGAAAGACCCTTCAACCCGTCATCCTGCACTTATCCCGTCAAAAACCAAGCGG[T/G]ATGCTAATCTGCCCTTTTTATTATATTCCTCCTTTCAAGAGTCCACACTTAGCTGATGATTGATTATAAAGCTTGTTTGGCATGCTGTCCCACGAGAGAGCCCTGAGCTCTCTCCAGTTTGCAAGGCGAGAGGGGAGTTTGAGCTCGAGAACACCCCTGCTGTAGGTGCTAATGAACAAATAGCGATTACTCTTAAGAGATAACTACTAGGAGCATGTCTATGGTGCTGATTTGGATTAGCAAATTAACTTAAGATGCTTGTTTTTGAATGGTGGGAGGAAACCGGGGAACCCGGAGGAAACCCACGTGAGCACGGGGAAAACGTGTAAATGTCGGCTGGCTTGGTAAGGATTAGAACCAGTGATGTTCTTGCTGAGAGGCAACAGTGCTAACCACTGGACTACCATGCCACCCATCTAGGAAAGGAGGAGGAGTAGGGGTAGAAGGGGAGATTCTTCCAAATAAAGATGGCTGTCATATGGAACTTAGGGTATTTATAG
Associated Phenotype:
Not determined