ZMP
BSN (1 of 2)
Ensembl ID:
Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Human Orthologue:
BSN
Human Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Mouse Orthologue:
Bsn
Mouse Description:
bassoon Gene [Source:MGI Symbol;Acc:MGI:1277955]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21962 | Nonsense | Available for shipment | Available now |
sa21961 | Nonsense | Available for shipment | Available now |
sa16951 | Nonsense | Available for shipment | Available now |
sa21960 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21962
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 |
---|---|---|---|---|---|
ENSDART00000109753 | Nonsense | 91 | 3142 | 1 | 13 |
ENSDART00000127184 | Nonsense | 91 | 3123 | 1 | 14 |
ENSDART00000127987 | Nonsense | 84 | 3144 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 38372723)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37184721 |
GRCz11 | 11 | 37451926 |
KASP Assay ID:
2260-4592.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCCAGTAAAACAAGGGGCACCACAATCCAAGGGCCCCTCTCAACAAT[T/A]ACCTGCAACTAAGACTGACACAAAAAAACAAGATCAAGGAAATAACAAGA
Long Flanking Sequence:
TTGGCCACAACCCAATTACACTTACTTGCTCAGCTTGACCAAATCCCTTTTGAATTACAATAGCAGTGTTACAAAGGCAGAGAGAGGAAGAGAGAATGTCAGTGAAGGATGAGTGATGTGATAAATTACATATAATCTGAGTATTGACACTTTCACCTTGTATTCAGTTGTTTTGCCCTTTTTATCTTGATTCTTTCAAGATATTCATCGCATGTTTGCTTTCTATTTTCAGAAGAAAGAATGGCTGTGTTTGACATGCCAAACCCAGAGAGCAATGTCAGGGAGCTTAGGGGATATTACTCCTCCTGTGCCACCATCCGTTGGATCTCCCCGACTACCAGGCCCAGCCAATCAACAGCAGCAGCAACGAGGGTCCAGTCAGCAAGCTTCACTGAGACCAACTGGCCCTCAGCAGCAAAAGCCAGCTGGAGCCCAAGTAAGTGTTCCTTTCTCTCCAGTAAAACAAGGGGCACCACAATCCAAGGGCCCCTCTCAACAAT[T/A]ACCTGCAACTAAGACTGACACAAAAAAACAAGATCAAGGAAATAACAAGAAACAAGTTATGTCCAAAACAGAAAAAGATGGGGACATCAAAGCATCATCTAAAAAGGGAACATCGGATAAAAAAGATGAGAAGAAAAGTAGTGGCATACAGAAATCTAAACAAGATGACGTGAGTGGTCCTCTGTGTCCTCATCACCACTGTCTGTGTCTTTCATAACAGATCACTTCAACATTCTTTGATGGGAATGTTATGTGTCAAATAAATTCACCAATTTCATCTGTATCCAAAACCAGTTTAAAATTTACTGTTGTTGGAACGTGTCACCATTTTTGCTGATACTGCCAGGTCACTAATCTAGCCCCATGCAATATATATAATTCTTCCAGAATTCTAATTTGAATTACAATTTATATAATAATATTTGCATGCCATTTATATGTGAATAAATAGTATTATTAATAGCATCAAGAGGATTTAAATTCACTTTTAACCTCATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21961
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109753 | Nonsense | 2181 | 3142 | 8 | 13 |
ENSDART00000127184 | Nonsense | 2173 | 3123 | 8 | 14 |
ENSDART00000127987 | Nonsense | 2169 | 3144 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 38364631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37176629 |
GRCz11 | 11 | 37443834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATTATGACACCAGCAATTCCCCATATATACAGTTCCCCTGGGGTATCC[C/T]AAAGGGTTTTGCCACGTACTGCACAGGGTGCAATGAAAGCAGGCTTGTTG
Long Flanking Sequence:
TGGTTGACGTCAAATCATTACAGTTAAATATTATTGTAGCCATTTTGTTCACACATAATGTATTGCTTGACTAATTATGGATCTTTTATAAAATACAGTGTCATGGTTATATATTTATAATTACTTTAATTAAAGCGTTTAGCATTTTGAGTGTGCTTGCAGTATATTGTCAGGTAATAGTTGGATTTTAATGTTGGTCTTTTTTCAATGTATGCCCTAAAGTCAGAGAAGATATAAAGTATAATAAAATAAAACAGAATGCAGTATGTTTATTATTAAGACAGATTTACCAACCTAATCTTAAAACATGCTTTGAAATATTTCTGGTTGCTTTTATTTTAATCTCTAAAATCTCTGCATTCCAGATGTCTGCCTTGCAACAGCAGAACGCAATGATGAGAAAGGTGAAGAGAACTCTCCCAAGTCCTCCTCCAGATGAGTCACCTTTACCGATTATGACACCAGCAATTCCCCATATATACAGTTCCCCTGGGGTATCC[C/T]AAAGGGTTTTGCCACGTACTGCACAGGGTGCAATGAAAGCAGGCTTGTTGAGTGAACTAAAAGCCGTAGAGCAAGAATCCACCAAATTACGTAAACAACAGGCTGAGCTAGAAGAAGAGGAGAAGGAGATTGATGCTAAGCTACGATGTTTGGAAATGGGCATCACTCAACGCAAGGAAACCAGAGTAAAAGAGAGAGAGAGGCGAGAGTTGGCATACTTGCGATGTATTGGGGATGCACGTGACTACATGTCAGACAGTGAACTGAATAATTTGAGATTAGCTGGGGTAGCGCCAGGCACCTATGAAGAAAATGGAATGCTGTCACGTCCAAGTACAGCTCCTCTCAGCCAGTTTACTTCCGATTTGAATGCATCTCAGTACCCTCCTACCTCTTCATATGTTCCATATCAATACCCACAGCCCCAACCCACACCCACGCAACCACCCACTGCCACCTATCAGATTGGGTTTCAGCCAGCACCATACCCAACCTCCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16951
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 |
---|---|---|---|---|---|
ENSDART00000109753 | Nonsense | 2642 | 3142 | 9 | 13 |
ENSDART00000127184 | Nonsense | 2638 | 3123 | 9 | 14 |
ENSDART00000127987 | Nonsense | 2630 | 3144 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 38363144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37175142 |
GRCz11 | 11 | 37442347 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTGTCCAGGACTGGTGTGAAAAAAGGCTATGACCAGCAGAAGTACTA[T/A]GGATCAAGGGAGGCATTGGAAGAGGAYGATCGCCTCTATGGCTCTGGACG
Long Flanking Sequence:
ATCCCCAGAAATTATGTCATGATTGATGATATCAGCGAACTCACAAAAGAGAATATGGGGTCCTCTGATATGGCACGGTTAGGTTATGGAAGTGAGAATGGCCCACGTGGACCGACTTATGGTGATGGTTCTGAGAATTTATATGGAAGAACTTCAAACACCTATCAAGGTGGAGTCGACAGCCATGGACACCCAATCACCTCTGGAAGTGGTGGTTCTGGTTATTATTATGATGACTATAAGCACTCTTCACGCAGCAGTGGGGGAATGGGCAGCCAGAAGCACTCATCCAAAAATCTGGCACCTGCTGTTTCGTCCAAACGTAGCAAACATAGAAAGCAAGGCATGGAGCAAAAAATTTCCAAGTTCTCTCCAATTGAAGAAGCTCGAGATGTAGAGTCCGATCTCGCTTCGTACACTATGACCACATCGACTGGTGGTAGTTGCACTGTGGTGTCCAGGACTGGTGTGAAAAAAGGCTATGACCAGCAGAAGTACTA[T/A]GGATCAAGGGAGGCATTGGAAGAGGATGATCGCCTCTATGGCTCTGGACGATCAAGGTCCACAGGTTATGGTATGGATAAAATTTCCTCCAGAGACTCAAGTGGCTACCGAAGTAAGTCTTATGAGAGGGATGCTATGGAGCGATCACAAAGGGGCACCCATGGTCGTAGTGGCCGTCCTTCTATGCGTACACAAAACTCGGAGGAAGAGAGCCCTCTGAGTCCTGTTGGAAAGCCCATGGGAATCGGTCGTGGCTCTGTGCCAGATGATGTACGAAATCAGTATGGCTCCAGCCATTCGTTACCAGATGTACAGGACCACCATATGAGGGATATTCCTAAGAGTCATGTATATAAGCCAGATGACCCTTACCTTGCAGATGACATGCACTGTGCTGTTTCAGACAGTGAAGGTAACTGGTGCTGAATTTAAAAACTGCATGTTTAAATGCACCCAGCAATTAAAAAAACTTGCATGCCAATGATCTTGCCTTGAGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21960
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109753 | Nonsense | 3008 | 3142 | 10 | 13 |
ENSDART00000127184 | Nonsense | 2994 | 3123 | 11 | 14 |
ENSDART00000127987 | Nonsense | 2996 | 3144 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 38361669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37173667 |
GRCz11 | 11 | 37440872 |
KASP Assay ID:
2260-4587.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAATTGGGACAGACAACCCGTACACAACAGCAGCCACTACAGCATCCT[G/T]GACAACAGCCAGCGACCACAATGGGAGCAAGTCAGCCCACAACCACAGCT
Long Flanking Sequence:
GGCATTCCTCTTCCACCTCATCTCGAGAACACCGTCACCATGGCAGCAGTTCAGGAAGACACACCTCTTCCCGTCATACCACAGATGATCCCAGGTCATCTCGTTCTTCACGATCACATCCAAAAGATCCTTCCATCCGGTCAGATGGGCGAACCACCTCATCCTCAACACAGAAAAGATCCTCAGATCCACGATCTGGCAGCCACCGAGACTCCGGAGAATATTCTCGTGATCCATCAGGCCACCACCATGGTTCAAGTGGACAAAGAGGCCAGAGACAACCAGGTTCATCCAGGAGGCAGGAGCCCTCTTCAGGTTCGAGGCCACAGCAGGGTCTTGGAGAGCAGCAACCGCAATCCCAGCAAGGACAGCAGCGATCAAGTGCTGGCCAGCAAGTGTCTGCCAAGCAGACAGGTTCTTTGCCACCTGAGACAGGGCAGCAAGGACAACAACAATTGGGACAGACAACCCGTACACAACAGCAGCCACTACAGCATCCT[G/T]GACAACAGCCAGCGACCACAATGGGAGCAAGTCAGCCCACAACCACAGCTGCTGGTATGGGAACAGGAACAACTCAACAGCAGCAATCTAAGCCGGGTCAGGCTCCAGCACAGGCAAGACAACAACCAGGAGGACCACCCACTGCCCAGCCAGCTGCTGCTATGGTGAGTTTTTATGAGTCCCTCTGTGGCTTGGCATACAAGCTTTCCTTTGTCTCTTATTAAGTTTTGCATATGTGATTGACTTTTAATGTGATGCAAAAGAAATTTATAAATATATATATAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTAACATTGACTTTTCATTGGCTTTACAGGCCAAGTCTGACATAGCTGCACCTGCTCCTGCTCCTGCTCCTGCACCAACTCCTGCAGTTGCAATTGGATCAAAAGCTGCAC
Associated Phenotype:
Not determined