ZMP
si:ch211-175f11.2
Ensembl ID:
ZFIN ID:
Description:
intersectin-like [Source:RefSeq peptide;Acc:NP_001003547]
Human Orthologue:
ITSN2
Human Description:
intersectin 2 [Source:HGNC Symbol;Acc:6184]
Mouse Orthologue:
Itsn2
Mouse Description:
intersectin 2 Gene [Source:MGI Symbol;Acc:MGI:1338049]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36447 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25044 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23112 | Nonsense | Available for shipment | Available now |
sa42958 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32159 | Essential Splice Site | Available for shipment | Available now |
sa18555 | Nonsense | Available for shipment | Available now |
sa23111 | Nonsense | Available for shipment | Available now |
sa11862 | Nonsense | Available for shipment | Available now |
sa32158 | Nonsense | Available for shipment | Available now |
sa32157 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36447
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087111 | Essential Splice Site | 259 | 1741 | 8 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30562241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30486168 |
GRCz11 | 17 | 30503131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCAACAGTTTAACAGCCTGGACAAACTAATGAGCGGTTATCTAACAG[G/T]TACTTCAATGTAAATGATTTCCAAGTAAATAGTTTAAGAAATGTTTGAAA
Long Flanking Sequence:
CTGGGAATACTGTAATTTTGTTTACAAAATATGGCAGCATTTTATATTCTGGATGATATATTCTTTCTTTAATGGTCTGTACGTTCTGTTCTAGAAGCTTTTATAGAGCATCAGTGACTAGAGATTTTAATCCAGATGTGTGTTTGTTTATATTTTCTGCAGCTCTTCCACTGTCAAGTTCCTTTTCTGCTTCTCCGTTGGGTTTCTCCACCACTTCCATGAACAAAACATCGTCTTTGCTGGACCTAGGGTCGAGCAGGTCAGGATTTTTTACCTCCTTTATAGTAGATTATTAATTCATTGAAGCCGTATGCAATACTGTTTGCAAATAAAGTGATTAATGTAAAATGTGTGCAGCTCAAACTCCTCCCCCTCCACATCATTGGCCAGTAATTCACCTAAAGGCGGACCCTCTGATTGGGGCGTTCCACAGGCATCACGGCTCAAATACAGGCAACAGTTTAACAGCCTGGACAAACTAATGAGCGGTTATCTAACAG[G/T]TACTTCAATGTAAATGATTTCCAAGTAAATAGTTTAAGAAATGTTTGAAAAGAATTGCCAAATGTGTAGCTCAGCTAACACAAAGTTGATGCAGATTGTTTTTATGCCTGGGGACAAAACTTTTAAAATGCCCAGTGATTACTGTGATAATCTCATGATTTTATGTGATGTAAGGATTTTGGCTGAAAGCTAGTGTAGCAAAATGGCAATCCACACCCATGTGGCTCATCTGCATAGCTGTGGACTGTATCACTTGCATAACTCATGACAATAACGCATCTACTTGAGAATTTCAAGAATGTGGAAGTGGTTAAAGCACAACTTTGTGTTTGGTTTCACAGGTCTATGGTATTGTTTAAATAGAAGCCCACTGCCTAAACCTGCAAGCTGTTTTGTTACATGTAATTTGAGAAGGTTGTGCATTTTTCTGGCTGAGAACTGTTTTCTGATGTCGTAATGTGTTGCTGGTTTAAGCGAATTTTAACCCTGTTGCTTTAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25044
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 413 | 1741 | 12 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30559303)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30483230 |
GRCz11 | 17 | 30500193 |
KASP Assay ID:
554-7567.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAGCACAGAAGGCCAGAGAGGAGCAGGAGCGGAGAGAAAGAGAAGCA[C/T]GAGAGCTGGAGCTGAAGAGGAAGAGGGAAGAAGAGATCCGACTGGAGCGA
Long Flanking Sequence:
GTATGTACACCAGGGGCGTCACTAGACCCTATTTACTGGGGGTAAATGTCTCACACACTAACTATACTTTATATAACCATATAACTTTAAGCCAGAGTAAACTTTAACTTTTTCCCAACAGGGAAAAACACCAACAATTAAGAATGCATGATTATTTGTAGTCATGGCTTTTTAATCAATAAATGTCATAATAATGTAAGTCAATGGGGCAAAAACAACCACAAACATAACGAAAGTGTGCTCAATTTTAACAGTACCCAACGGGTAAAGTACCATTTATCTGGAAAATTACATAATGAACATTCTAGTTCATACTACTAATTTCCTGTATGTTTTTTGTGCATGCAGTGACTTTTGAGGATAAGTTCAAGAAAAACATGGAGCTTGGAAATGCAGAGCTGGAGAAGCGCCGACAGGTCCTGCAGGAGCAGCAGCGCAGGGAGGAGGAGAGGAGAGCACAGAAGGCCAGAGAGGAGCAGGAGCGGAGAGAAAGAGAAGCA[C/T]GAGAGCTGGAGCTGAAGAGGAAGAGGGAAGAAGAGATCCGACTGGAGCGACAGAGGGAGCTGGAGAGACAGAGAGAGGAGGAGAGACTCAAAGAGCTGGAGAGGAAGGAGGTAAGAGTTTGATCTTGCAAATGATCTTTTATGTTCTGACTGAAATTTGGCACATTCCTAATGTATAGGTCGTTCTTATTTTCTGTTGAAAAAGAATAAACATTTGACGATCTAGTTAACCTCATTAACATCATGAATCATTGTCGTCCTCATATTAAGTGAAATTTGTAAAACCGAAAGTAAAGCAAAATGTCTATATAGATATTCATGATTCATTTGGTCACACTATTGACCTTATTCTTGATGTATGAGCGGGTGCAGCCATTGGAATCTTTTTTGCTCGAGACTTCTGGTCTCATTTACTTTCATTAATTCTTAGATGTTAAAAACAGCTTGTAATGCTGCTTAATATTGCAAACTGTTGCAATTTTCGTATTATATTATTCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23112
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 647 | 1741 | 17 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30553182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30477109 |
GRCz11 | 17 | 30494072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAGAGTCTGCTTTGGAAAAACTGCGCACCATCAAGGAAGAAAAAATA[C/T]GAGAGCTTAAGAAGCGAAAGCAGGAAGAACTTGAAAAGAAAAGAAGAGAA
Long Flanking Sequence:
TTTTATATTAGTATTTTTTAATGTTTTTTCCATGTACATTTTAATTTTAAAGTTTTTGTTAATTTTACATTTATTTTAGTACATTAAAGTTAATCAAAATAAAACTTACCCCAATAAAAATGCTTACTTAGCTTGTTTTAAGGAAAAACTCACTTAGTTTTAACATATTTGTTCTTAAAACAAGACAATATTTTTTGCTTGTCTAGGAAATGATTCTTGATTTAATTATTATTAGATATTTTGACTAAAAACAAGACTAAAAGTCTAAGAAAAAAAAGCAGTGTACAAAAATGCTACTAAGGACAATTCTTAAAAACGGGTACAGTTTATTTTTTGTTTGTTTGTTTGTTTGTTTGTTTTTGTCTCAGTTGCATGAATTATGTCTGAATTGAATTCAATGTGTCAAAGTTCTGCAATTTGTTTATAAGGATCTCCGTGAGAGCCAGAGGATGCAAGAGTCTGCTTTGGAAAAACTGCGCACCATCAAGGAAGAAAAAATA[C/T]GAGAGCTTAAGAAGCGAAAGCAGGAAGAACTTGAAAAGAAAAGAAGAGAAGAGGAAGAACAGAAGTAAGTAATGATTTCCTAAACGTACACAACAATTTAAAATCAATCAGGATCTCACAAGCAAACGTTATTTGTCCCATCCAGACGCATCAAACTAGAAAAGGAGCGACAGTGGCAGGAGAAACTTCGTCGCGACGAAGAGGAGAAACAAAGGAAAATTCAGGAGGAACGAGATGCCAAACTTCGTGAGGAGGAAGAGAGAGAAAGACAAGCTCGCTTACAGGCTGCTAAAGAACAAGCAGAACGAGAGCGCAAGGCCCGTGAAGAAGAGGAGAGGAGGCGTAGGGAGGAGGAGGAAGAACGGAGAGAACAAGAGAGACGCAGACTGGAGGAGGAGGACCGCAGGCGGAGAGATGAAGAGAGGAGGAAGCTGGAGGAAGAAAGGAGGAAACTGGAGGAAGAAAGGAGAAAGCTGGAGGATGAGAGAAAAAGACAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42958
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 744 | 1741 | 18 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30552810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30476737 |
GRCz11 | 17 | 30493700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAGAAGAGGAGAGGAGGCGTAGGGAGGAGGAGGAAGAACGGAGAGAA[C/T]AAGAGAGACGCAGACTGGAGGAGGAGGACCGCAGGCGGAGAGATGAAGAG
Long Flanking Sequence:
ATGAATTATGTCTGAATTGAATTCAATGTGTCAAAGTTCTGCAATTTGTTTATAAGGATCTCCGTGAGAGCCAGAGGATGCAAGAGTCTGCTTTGGAAAAACTGCGCACCATCAAGGAAGAAAAAATACGAGAGCTTAAGAAGCGAAAGCAGGAAGAACTTGAAAAGAAAAGAAGAGAAGAGGAAGAACAGAAGTAAGTAATGATTTCCTAAACGTACACAACAATTTAAAATCAATCAGGATCTCACAAGCAAACGTTATTTGTCCCATCCAGACGCATCAAACTAGAAAAGGAGCGACAGTGGCAGGAGAAACTTCGTCGCGACGAAGAGGAGAAACAAAGGAAAATTCAGGAGGAACGAGATGCCAAACTTCGTGAGGAGGAAGAGAGAGAAAGACAAGCTCGCTTACAGGCTGCTAAAGAACAAGCAGAACGAGAGCGCAAGGCCCGTGAAGAAGAGGAGAGGAGGCGTAGGGAGGAGGAGGAAGAACGGAGAGAA[C/T]AAGAGAGACGCAGACTGGAGGAGGAGGACCGCAGGCGGAGAGATGAAGAGAGGAGGAAGCTGGAGGAAGAAAGGAGGAAACTGGAGGAAGAAAGGAGAAAGCTGGAGGATGAGAGAAAAAGACAGGAGGAGATAAGATTGAAGGAAGAGAGGGAGAGGGAGGAGCGCAGGAGAGCAGAGGAGGAGAGGAGGAGGAAAGAGGAAGAGAGACGAGAAGAGGAGAGGAAGAGAGAGCGTGAGGAGGAGGAAAGGAGACGTCATCGAGCACAGGAAGCGGCTATGAGGGATGCGGAGGAGAGGAAGAGGATCGAGGAGGAGAGGAAGAGAAAAGAGGAAGAGCGGAGAAAGCAGGAAGAGGAGGACAGGAGGCGGAGGGAGGAGGAGCAAAGGAAACAGGATGAGGAGAGGAAAAGGAAACAGCAGCAGGAAGAGGCAGCAGCCGCCAGATTGAGGGATGATGAACAGAATAAGAAGAACACTGTTAAATCAGACCTCGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32159
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Essential Splice Site | 1015 | 1741 | 20 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30551138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30475065 |
GRCz11 | 17 | 30492028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGTCGTGGCTAAACAAGCCCTAAAACCCCAGGTCTCCATCTCTGTCAG[G/A]TGTGGTCCCCATTCTAAATTTATCATCCTCTCGAAATGCATCATTTACAC
Long Flanking Sequence:
TTCATTTATTGAATCAAATATAATTCAACTATAATCAATTATATAACATTTTAATTATTGTTATGAATTCTGTTACAGTAATTACAGTTTTGCAGGGAATACTGTTTTATGGAGAGAAAGTTCTGAAGGCTGTTACCTAAAAGCAATTAATAATTTTTGTGTGTGTATGTAAGTGTATTGGATCAAGGGTGTTGCTTTCAGCTGCTTCCTGAAAGATGTGTTGGTGTCAGCAGTTCAGATGGAGCCTTCAAATGAGAAGGTTCAGAGCATGTGGTGAAAGAGCATGTCCACTGCATGGAGTTCAAATCTAGAGTTTGCTCAGCTGGATTTTTGTTTGTTTAGGTGGATGAGAGCGTAGAGCGTGAGCAGGGCTGGCTATATGGCAGTTGGCAAGGGAAGATGGGCTGGTTCCCTGAGAGCTATGTGGAGAAGCAGACCAAGTCTGAGGCTCCGGTCGTGGCTAAACAAGCCCTAAAACCCCAGGTCTCCATCTCTGTCAG[G/A]TGTGGTCCCCATTCTAAATTTATCATCCTCTCGAAATGCATCATTTACACCCTTGTTTTACATTTGTACACACTTTCTCATGCACACTCACAGACAAAGTGCATGTTGCTGTAGATCCATTACAGAAAAAAAAAACATTCACAGCTACAGACTGCATGTCTTCATTTTGATATTTTCACACAAAGTCCAAAAGTATTAGCAAAGAATTTTTCACATCAGGTCTGATACCTTGTCTTACTCTGATATAAAATTGATGTCCAAAAAATAAATAAAAGAAGGATTGTTTTATGTAAGGACTTTGTGTGAATCTGTTCTTGGAGGTGCACTCTTTCTTTTTAAAATATTGCTGGGCAATATTAGGAATATTCTAAACCCCTTCTTCATTAGCAAACTGAGTGACGGACCGGGTGGATCACGACTGAACTCTGCCTTCACCCCTACACATGCCACAGGCTCCACCTCTTCCAACCACGGACAGGTATGCAGGACTCCTTGACGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18555
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 1037 | 1741 | 22 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30546189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30470116 |
GRCz11 | 17 | 30487079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATGTTATAYATTTATCWCATCCTCAGAATAYGTSGCTCTTTACACTTA[T/A]GAGAGTCCTGAGCCTGGAGACCTGACCTTCAATGAGGGYGAMACTATCCT
Long Flanking Sequence:
TCATCATAGAAACAAAAAATCTATGTTAGTCAATGTTCTATGACTAACTTAAGTATATCTTCCTTTTGGAACAGTTGAGGATGAGTAAATGAGGATGGACTTTTTATTTTTTGGGTGGACTATTCTTTTAAGTTCCTGAAAACAACATGTTCTTAAAATATTTAAGAGTTTTTAAGTATTTGATGTCTTTTTGATGTCAGTTTAATGCACCCTTGTTACAAAGCAAACTATTAATTTACCTTTAATAAATGATCCCAAACCTTTAAATTTCAGTATTTTGTGTAATTTGTTTTTTTTAATGTAACACAAATGTGTCTTTAATATAAACTTAAACAATCATTTCCAATATTTGTGCATGTGTATGTTCATTTACATAATGTTTTGTGTCTGGTATGCCTGTGAACTCATGTATGTACATAAGCATTGTCCTTTCCTGAGATTCCGTAAACCCTATGTTATACATTTATCTCATCCTCAGAATACGTCGCTCTTTACACTTA[T/A]GAGAGTCCTGAGCCTGGAGACCTGACCTTCAATGAGGGCGACACTATCCTGGTCTCAGAGAGAGAGGGAGAATGGTGGAGGGGAAGCATCGGAGACCGAGCAGGACTCTTCCCGTCCAATTACGTCAAGCCAAAGGAGACCGATGTAAATTTGAATTTTAGATGTAGCTATGCTGCTACTTGTACAAGTTGTTGTGATTTTTAAAGCTTTTTTTTTTTTTTCCTTTTTATTCATTAGACATCAAGTCTCTCTGGCAAATCTGGAACGCCTGGCAAGAAACCTGGTAAATAAAAGAGCCAAGTTAAATAACAAAATAAAAATCATTGTTTATTTATTGTAATTTGTAATATATGTTTTTTTTTTATTTATTAATTTTTTTTGGTAGAAGTGGCTCAGGTTACTACTGCATGCACAGCTGCAGGTGCAGAACAGCTAAATCTCTCCCCTGGTCAACTCATTCTTATCCTCAACAAAAACCCCTCCGGCTGGTGGCTCGGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23111
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 1194 | 1741 | 26 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30543387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30467314 |
GRCz11 | 17 | 30484277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGCTATTTACGACTACACCGCAGCGAACGAGGACGAGCTGAGCTTCT[C/A]GAAGAGTCAAGTCATCAACGTTCTGGACAAAAGCAATCCTGACTGGTGGA
Long Flanking Sequence:
TTTTTTTGCATGATTTCAATATGTTCAAATTTAATATACATTTTTTTTTTTTTTTGGTGAAGACCAATACAAACAAATGTATTTTTAGAATACAAGCAAAATTAATTATTGGATAAATAGAAGAATATATGGATGAATGCGTAGATAATAAACAGATGAAGTGATGTATAAATTGATGGAATAAATTATTAACTAACAACCAAGTAGATGAAAAACAGATTAATATACCTGTCATGTTTTTTATTCCTTGTGTCATCAGGCCAGGGGGAAGAAACGTCAGAAGGGCTGGTTCCCTGCTTCACATGTCAAGCTCCTGGGATCAAACAGCGGCAAATCCACACCTGCAACGCCATCAGGTTAAAAACACAGTCATAATCCAAGGTTGGTTATTTTGCTGTAGTCATTTCACCAATCATTTATCTTCCTCTCCTTTTTTTCAGTTGGCCAAGTCATCGCTATTTACGACTACACCGCAGCGAACGAGGACGAGCTGAGCTTCT[C/A]GAAGAGTCAAGTCATCAACGTTCTGGACAAAAGCAATCCTGACTGGTGGAAAGGAGAGCTCAATGGGGTCACAGGCTTGATTCCTACCAACTATGTGAAATTGACCACAGATTCTGACCCCAGTCAGCAGTGTAAGTAGAGACCCATAAACAGACCAGTTTATTTTGGCTCTGTGTTTCAGATTATCACGCAAGCACTTGGTTGACAGTTTCAGATTATTTTCAAAAAAAGCGTGTTGCTGATTATGCTTTTTAAATGTGGGTGTTTATTATCTGATAGGGTTTGTATTTATGACAGAATGTATTTAATCACTTCATCACAATGACATTTTACCCAGAATGAAATATTTTAATCATCAGTATCAATTGTTAATTCATGGTGCCTTCTTTTGTGCTCTGTATATAAGGGGTGTTTTCCAGTTATTTCAAGTTGTACAGGTAGTGTCTAATATAATGTCAGACATTTGTTCACCTCATCCATATTTAGGCACACATTCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11862
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 1311 | 1741 | 28 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30538708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30462635 |
GRCz11 | 17 | 30479598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ARATGAACATGATAYTTGCCAACTGGAGAGAGCTTATTCAGTGCAGCTCC[A/T]AGATGCTYAAGTATGTGTGGTTCATTTGAAAATGTATATACTGTACWTGG
Long Flanking Sequence:
AAAGTATGCTTATAAAAATATTGTTAACTCTAACAAAATAGTGGTCATAAAAACAATTTATTTTTATGTAACTATTTTATGGGCTTGTGCTTGGTTTAAAGGGAAAAATAATTGGACTATTGATCATTTTTGTTAGCACCAGTCTACATAAACAAGTGTGAAGTAGTATTTGTAGTTTTTTTTCCTCATTAAACCTGCCAAGCCAAGTTCAGTTGTACATTTTATGGATTTCTGCGCTTCAAAGAAAGTTTCTTCTCATAGCCATGTTGCTTTTTTTAAACTGCATCTTGGAAAATTTTAAATATAAAACTATTTCTGGAAAGCACAGATTTATTTATTTTATTTTTTTAAATTGCATTTATAAAGAACGTGATGATAATAAAATATATATTTTCTTTCTTAAGGTCTTCTACAAGCCCATGTCTGAATCAAATCGTCTCTCTGAGGCTGAAATGAACATGATATTTGCCAACTGGAGAGAGCTTATTCAGTGCAGCTCC[A/T]AGATGCTTAAGTATGTGTGGTTCATTTGAAAATGTATATACTGTACATGGATACATCATTTTCTTTGGTGTGCAGTGTATTAATAAGTGTATATTGTTAGGGCCCTGAAGGCAAGGAAAAAGAGCGGAGGAGACAACATGCCAGTTCACATGATTGGCGATATCCTGACATCCGAGCTGTCAAACATGCAGGCCTACATCCGCTTCTGCAGCTGCCAGTTGGAGGGTGCTGCGCTGCTACAACAGAGAACTGATCAGGAGCCAGACTTCAAAACCTTCCTCAAGGTACAGAAGACTACTGTAGTTCACTTGCCGCTCTTAAAAAAAAAAAAAAGACAAAAGCCATATCTAAAAACAAATTGTAATCAACACTTTATTCGAGTTTTGGGTTTAGTAACAATGTTGCTCTCATTACTTCATATTTTTCAGAAAATTGCTACAGACTACCGTTGTAAAGGAATGCCTTTGTCCAGCTTTTTACTCAAACCTATGCAAAGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32158
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Nonsense | 1344 | 1741 | 29 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30538519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30462446 |
GRCz11 | 17 | 30479409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAGTTCACATGATTGGCGATATCCTGACATCCGAGCTGTCAAACATG[C/T]AGGCCTACATCCGCTTCTGCAGCTGCCAGTTGGAGGGTGCTGCGCTGCTA
Long Flanking Sequence:
TAAACCTGCCAAGCCAAGTTCAGTTGTACATTTTATGGATTTCTGCGCTTCAAAGAAAGTTTCTTCTCATAGCCATGTTGCTTTTTTTAAACTGCATCTTGGAAAATTTTAAATATAAAACTATTTCTGGAAAGCACAGATTTATTTATTTTATTTTTTTAAATTGCATTTATAAAGAACGTGATGATAATAAAATATATATTTTCTTTCTTAAGGTCTTCTACAAGCCCATGTCTGAATCAAATCGTCTCTCTGAGGCTGAAATGAACATGATATTTGCCAACTGGAGAGAGCTTATTCAGTGCAGCTCCAAGATGCTTAAGTATGTGTGGTTCATTTGAAAATGTATATACTGTACATGGATACATCATTTTCTTTGGTGTGCAGTGTATTAATAAGTGTATATTGTTAGGGCCCTGAAGGCAAGGAAAAAGAGCGGAGGAGACAACATGCCAGTTCACATGATTGGCGATATCCTGACATCCGAGCTGTCAAACATG[C/T]AGGCCTACATCCGCTTCTGCAGCTGCCAGTTGGAGGGTGCTGCGCTGCTACAACAGAGAACTGATCAGGAGCCAGACTTCAAAACCTTCCTCAAGGTACAGAAGACTACTGTAGTTCACTTGCCGCTCTTAAAAAAAAAAAAAAGACAAAAGCCATATCTAAAAACAAATTGTAATCAACACTTTATTCGAGTTTTGGGTTTAGTAACAATGTTGCTCTCATTACTTCATATTTTTCAGAAAATTGCTACAGACTACCGTTGTAAAGGAATGCCTTTGTCCAGCTTTTTACTCAAACCTATGCAAAGGATCACCCGCTACCCTCTTCATATTAAACATGTAATGTTATATTTTCAATTTTTCTCCCTATATCTTTTGTTAAATATTACTAGTTAATGCATAAAATTAAGTGCATTCTTAACCAATACTTGTATGTCCAGATTTTAGAAAACACTCCAGAGAGCCATGTTGACTACATTCAGCTGACTGAGGCTTTGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32157
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 |
---|---|---|---|---|---|
ENSDART00000087111 | Essential Splice Site | 1689 | 1741 | 36 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 30534418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30458345 |
GRCz11 | 17 | 30475308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGTCCTCTGCATTACGATTAACGAGAAAGAGCTGTTTTCACCAGATG[G/A]TTAGTATGAAATAACATGTATGATACTATTTCTAAACCAGACCGAAACAA
Long Flanking Sequence:
TACTGAGCCACATTTTAAGGAGTGTGTTTTATGCTCTAAGATGTCAGTATTAATAATACAGCAGGTTAGAAAATTTTTATGTATTTATTATCTTTTTAATTTTATTTACATATTTTACAGCTCGATCAATGAAGGGAAGTGGCATTGGTCGCCTGCTTGTCACCATCTTAGAAGCAACTGAGCTAAAATCCTCCAAACCAAATGGTGAGTGGTTTCATTTGAAAACATGATTAATACTTTTTTAATAATCTGTTTTCAATCTACATTTACTATTCATAAATTACATCACTGCTTTTGCACTTTTTTTCTATAATTATTTTATTTAGGAAAGAGTAATCCATACTGTGAAGTGACCATGGGCTCTCAGTGTTACACTTCCCGAACCATCAATGACACCGTCAACCCCAAGTGGAACTTCAACTGTCAGTTTCACATTAAAGACCTGTATCAAGATGTCCTCTGCATTACGATTAACGAGAAAGAGCTGTTTTCACCAGATG[G/A]TTAGTATGAAATAACATGTATGATACTATTTCTAAACCAGACCGAAACAAATTGTGCTGAATTGTATATTTTTATCCTTTAAAAGGGTGGTCCACTACGATATCATGCCTTAAACTTTAGTTGATGTGTAATGTAGCTGTGTGAACATAAACAACATCTCTAAATCTCTAATGTTAGTTTGCCAATGGGGAATGAAAAAGCCCCACTACTCAATATTTTCTTTTAGTCTGAAGTTCATCCACATACTGAAATAAAATTCTCAGAATCTTCTGGTTATTGCTGACTTAAAAATGGATGAGATTTAGGTCATTTGCATTACAACAGCCAGTTGGGTGGAGTGTGGATTGGGGAAGGGCATGTACATGCAAACAAAATCGGTTTCAAAATGCAATTTTTTTAACGCTATGCTGTTAGTATCTTCATGTAAACTACAAAAGCATTTATTAAAAGCTGACTTTTTTTTTATTGTGAATTGATATGCATTGACATTTATATTCACT
Associated Phenotype:
Not determined