ZMP
bin2a
Ensembl ID:
ZFIN ID:
Description:
bridging integrator 2a [Source:RefSeq peptide;Acc:NP_001007422]
Human Orthologue:
BIN2
Human Description:
bridging integrator 2 [Source:HGNC Symbol;Acc:1053]
Mouse Orthologue:
Bin2
Mouse Description:
bridging integrator 2 Gene [Source:MGI Symbol;Acc:MGI:3611448]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24382 | Nonsense | Available for shipment | Available now |
sa15980 | Essential Splice Site | Available for shipment | Available now |
sa24381 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24382
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 |
---|---|---|---|---|---|
ENSDART00000025196 | Nonsense | 45 | 463 | 3 | 14 |
The following transcripts of ENSDARG00000003219 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 33961429)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 33821227 |
GRCz11 | 23 | 33747758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTTTGCAGGTCTTGCAGAGGCTTGGTAAATCTGAGGAGACCAAAGAT[G/T]AGCACTTTGAGCAGTGCGTGATGAACCTTCACATGCAACAGGTATCTTAG
Long Flanking Sequence:
GTGTGATTTATGCTAAGCTAAGCTAAAAGTGCTTTTGCCAGACACAGATATCGGTTGCTTGCGTTCAGACATAGTAAAACTCAACAATTCACTTCTTGGGGACTTGTAAAATGAGCCTATTTCTAAAAAAAAGTGGAGAGTTCCTTTAACAATCTCCTTTATTGCTGCTATTGATTTTCATTTGTCCGCCGAGGCTGACCAAGTCACTTTACTTTTCTGTTTTTGCCAGTTTACGCTGTTGTAACTTGCCACTGGCTTTTGGTGAAGTCAGGTGAAAAGTTCTTATAAGATCTGAATCCTTGTAAGGGGGCTTTATTCTTTGCCAGCGTGTGCTTATCAATATTTTAGGAGTCGGGTGTAACATCCATCCCAGCGCTGTCAGTATATTTCCAGAATCCCCTTGTCATGGCTGTCAGGTGTGTGTGTTTGTAGACACATTGTAATATGGGATTCTTTTGCAGGTCTTGCAGAGGCTTGGTAAATCTGAGGAGACCAAAGAT[G/T]AGCACTTTGAGCAGTGCGTGATGAACCTTCACATGCAACAGGTATCTTAGATCTACTATAGTAAATGAGGTAACGCCTTTAAAGATCTAATATGTCCTTGTGATCTCCTTTTGCAGAGCGATGGATACAGAATATACAAGGATCTTAAAGCGTACCTGAATGCTGTCACAGGTTTGATCTTTACTACAGGAGATCAGCTTCTTATAAACGAGAATACTGACGTGCTTTGCTGTGCTTGTGTGTTTAATAGTAATGAGGGATGCTTCCAGTCGGTTGTTTCAGTCCTTGTTTGACGCTTATGATGATAGATGGGATGGTGGACAAGATCTTGGAGAAGTTGTGGAGGTTAGTCTTACACCAAATACAGACCAATGCCAGATTATAACATGCCATTTAGATTGCAAACAATATAAGACCAATAAGTACTGAAGTTCAGTTGAAAACAAGCCCCGACAGAAGATAACAGATCAGGTAACGCTGATGTCTGTCTGCTTCTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15980
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025196 | Essential Splice Site | 176 | 463 | 7 | 14 |
The following transcripts of ENSDARG00000003219 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 33959419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 33819217 |
GRCz11 | 23 | 33745748 |
KASP Assay ID:
2261-8050.1 (used for ordering genotyping assays)
KASP Sequence:
TGACAGRGCTGCAGAATGCYAAGAAGAGGGACGATATCAAAATTGGAAAG[G/A]TAATATTATTCTTCCGGAAGTTACTGATAATTTTCWACCAATTTTACAAA
Long Flanking Sequence:
GGAAATCACCAGGCGACCCCCCTTCATTGTTACGCGACCCCCACTTTGAGAACCATTGTTATAGTATATAATTTCAGTATGGGCACAATAATTAGCTACTAAATCAAAATGTATATCATTTTGATAACATTGTGTCTATTCCAACATATATAAGTGTCTATTCCAACACATATATTAATGCAAATGTGTTTTCAAAAGGGAGAAGATCTGCTGTGGAAGGATTATGAAAGCAAGCTGCACGATCAGGCATTAATCACTATGGAGTCTTACATGAGCCAGTTTCCGGATGTCAGGGTAACAGTGGCCGACTCACATACACCTCGCACAATCCTCTCAATGATTTTTTTTACAAACGACACTGTAACTGTAAACAATTTGTCTTCATGATTTAGGACAGAGTGGCCAAGCGAAACAGGAAACTCGTAGACTATGACTCCGCTCGCCATCAGCTGACAGGGCTGCAGAATGCCAAGAAGAGGGACGATATCAAAATTGGAAAG[G/A]TAATATTATTCTTCCGGAAGTTACTGATAATTTTCAACCAATTTTACAAATTTTCATTCAATAATTTGTTTACTACTGATACAAGACATATAGCAACAAACCTATGGTTCACAAGTATGAGGGCCAAATTTATAAGACTTTAATTTTTGCTGTCGTTATTCTTCCAGGCAGAGGATGAGATGAATGCGGCCAAAGTGATATTTGAGGACATAAACAGGGAACTGAAAATGGAACTGCCTATTCTGTTTGACAGGTTTGACAGTTGTTTTTGTAACGACTCCTGCTTAAAGTCGCCATGAAATCAAAATCGACTCTTCATATATACACAATATGTATATTGTAGTATATATAATAGTTATATATAATATAACTATTATTTATAATAGTTTGTGTTTATGGATATTTTTTACAGTGTGGTTATGAGATATTGAGGGAGTAACTAAAGTGACGCATATTATATTATATCTATGAACTTTTTCAAAAATGAAATTGATCATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24381
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 |
---|---|---|---|---|---|
ENSDART00000025196 | Nonsense | 275 | 463 | 11 | 14 |
The following transcripts of ENSDARG00000003219 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 33958470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 33818268 |
GRCz11 | 23 | 33744799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGGGCTCCTTGAAGAGAAGGTCATTCAGAGACACTTTGTCCCCCAGAT[C/A]ACTTAAAAGCTTTTATGATTTCCACATGACTATGAACCCCAGAGGCTCTC
Long Flanking Sequence:
CGCATATTATATTATATCTATGAACTTTTTCAAAAATGAAATTGATCATAAAAACATTTTATTTCTGCATTTCTTAGTCGCATTGGCTGCTATGTCACAGTCTTCCAAGCCGTTTGCAGCCTCAGAGAAACCTTTTACAAGGAAATTACCAAGGTAAACCAAATGTGAAAAAATACAGCTGTGTATTAAAACACTGGAGTCATAATGAGCAGTGATTCCTCATGGTTGTTTTTTTTATTGGCTCCAGAACAATGATGTTCTCCAGACTGTGATGAAAGAGTTGAGCGCCCAGCATCCTGACCAGAGCTTTGTCGTGAAGAACTTCAATCGGTAAAAGATTTCATAGTCTGTTCTTTGATCAATTTTTTTATTTTTAGTTAAATGTCTGTAATAAAATGGCTTCAGCTGCTGCATGTAGTAACAAATGAATCTCTTTGTTGTCCTTTTAAGCTCGGGCTCCTTGAAGAGAAGGTCATTCAGAGACACTTTGTCCCCCAGAT[C/A]ACTTAAAAGCTTTTATGATTTCCACATGACTATGAACCCCAGAGGCTCTCTCAGGTAAAACCCTCTTTTCAGCTCTCCTCTTTGCCTTCACATTTAAGTTGGGGAATTACTCCATCTGCTGGTGAATCTGCATGTTGTACAATACTTCTTGTATATTATTATATATTTATTTATTACAGTGCAGGGTTCAATGCTAAGGATTTTTTCTGCTGGCCCAATCGGACTAATGGTTCAGATTTTTACTTGCCCTGCCCATATTTTCACTGGCCCCTCTAAAAAAAGTTAATAGCTATTTCTTAGCCACAAATATAACAAAAAGTGTCAAAATGTTTGTAAATATAAAATGTAAATATTTTTTAAAAATTATAAATGTGTAACGAGCAAAATTCATAGTGTTTTGAAACAAAAGATGGCTAAAGACCAGCCAAACTGACAGCAAACTGTACAAAAGATCACTTAATTTTTTTTAGTCGTGGTGTACCCTGGTATATGTCTGCTTC
Associated Phenotype:
Not determined