ZMP
slit3
Ensembl ID:
ZFIN ID:
Description:
slit homolog 3 protein [Source:RefSeq peptide;Acc:NP_571811]
Human Orthologue:
SLIT3
Human Description:
slit homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:11087]
Mouse Orthologue:
Slit3
Mouse Description:
slit homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1315202]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa202 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa1569 | Essential Splice Site | F2 line generated | Not yet available |
sa35691 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30677 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14755 | Nonsense | Available for shipment | Available now |
sa11742 | Nonsense | Available for shipment | Available now |
sa9875 | Nonsense | Available for shipment | Available now |
sa42392 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa202
Status:
Confirmed mutation in F2 line
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046112 | Nonsense | 163 | 1515 | 6 | 36 |
ENSDART00000126199 | Nonsense | 164 | 177 | 6 | 6 |
ENSDART00000146299 | Nonsense | 164 | 1516 | 6 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25601271)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24304362 |
GRCz11 | 14 | 24601607 |
KASP Assay ID:
554-0151.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGTCTCTCATCTGCAGGCAACTGGACAGCAACCACATCAGCTGCATC[G/T]AAGATGGAGCCTTCCGAGCCCTGCGCGATTTGGAGATACTGTGAGTCCCC
Long Flanking Sequence:
TGGATTGGCTGCTCTAATGTAATGAAATTACTCCCTTTCTGACTTAAAAAAAAAAAAAAAAGAAGAAGAGGGGGTGGACGATGTTGGGGGAGAAAATGCAATTAATATTTACAGAGAACTGACAGACGGGGTGGGCTGTGCACTATAGCCAGCCTCCTGTTCACCCTCTCTCTTTCTCTCTCTCTATCTCTCGCTGTCTTACCTCTCTTTGCCCCCACACTCAGCAGTGTGGCGAAAGAGAGAGAGAGGACGAGATAGGAGGAGGTTATAGCCAGACAGGCCACTTTTAGCCAGCTGGTCCTTTATCCCGACTGCGGTGAGGAGAGGAGAGTAGATATGAGATGCCCGCTTGTGTGTGTGTGTCTACCTCCCTCCCTCCTGCAGCCCCCACCTCTCCTCCTCCTCCCTCCCCTCAGCCCCCACCCGCTCGTCTGCAGACCTGCCGCTGACTTCTGTCTCTCATCTGCAGGCAACTGGACAGCAACCACATCAGCTGCATC[G/T]AAGATGGAGCCTTCCGAGCCCTGCGCGATTTGGAGATACTGTGAGTCCCCCTCCCGCCTCCTCTGCGGGGTTCTTTCCTCTCTTCTCACCTCTGCTGTCCCTTCCTCTAACTCTAACTCTGTGTGTCTGTGTGTTTCCTGATTGTTCCTGAAGGACAAACTGTGTTGCGTTGTGGACCTGTGGCACATAGTCTGGTGTCACCCTGTCCTGCGCTTAGCATGCGATCGTCCGTGCGACAGCTAAAGTTGCTCGTTTGTCATCCTGTGCTGCATTGTTGCCGCTCTAAAAAAAAAGAAAGTGTCTTGACTTTTCCGGGTGCACCTTACTGTTAAAAACACCAATGCACCATGCATGTTCTATCTGGAAGATCTGTAGAATTGGTTTTCAACCTTAAACCGGGTGTTAGACTCACTTAGATGTTCAGATCTTTCTTCTTTTGCCCGCTTCTTCGGTCGTCTTTAACCTCAGAACAGGTTTAATGCACAAGCTTTAATGACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1569
Status:
F2 line generated
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046112 | Essential Splice Site | 176 | 1515 | 7 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Essential Splice Site | 177 | 1516 | 7 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25591202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24294293 |
GRCz11 | 14 | 24591538 |
KASP Assay ID:
554-1512.1 (used for ordering genotyping assays)
KASP Sequence:
TACAAAGTGAAACATGCCTTTTTTMTAACGTGTTCTGTCTTCTTTTTTCT[A/G]GCACTCTCAACAACAACAATATCACCCTCATCCCACTGTCAAGCTTCAAC
Long Flanking Sequence:
TTAAACCTTTCATTAGAAGGAACACTCAGACCCCAAACCCAAGTTGTAAACTGAGTTGGCGTAATTGGCAGGATTTCTCCTCACCAAGCAGGAACCATTAAAATACTAAATTGAGAAATTCCAGACCGTTTTCCAAGAGGTTGGAGATGCAGGAGGCTGTGTGTTGTGCACGTCTGTGATAGGTCTGGGAGTTATGGGCTGGGATGGATCGATTACAAGATGAGGTCAGCTACTGTAGGTTGCACTAATCAGAACTGTAGCTGGCATGACAAGAAACAGAGAGGTCTGCCATGCGAAATTACAAGTACCCTGATTATAGATGATATCATTCTGTTGCAGATCTTTACATTGTTATGGAGTCCAAACACTACCCACTGATTGAATCTTTATTTTCTAATGTATCTAACAACTATTTCTGCTACAGTGTGTTGTCTACTACACTCTTATGTCTACAAAGTGAAACATGCCTTTTTTCTAACGTGTTCTGTCTTCTTTTTTCT[A/G]GCACTCTCAACAACAACAATATCACCCTCATCCCACTGTCAAGCTTCAACCACATGCCAAAGCTGCGGACACTGTAAGTACTGAGAAGCTTCTTGTCCACTACTAATGCTATACAATCAGACATTTATACAGTATATCTATATTTACTCACATTACTTTTGAATCTTCGCTCTTTTGCTTGGCTTAACTGGAGCCCCTTTCCAGGCTCTGTGGTGACGCCGTGTCAGTTATCAGAGCGGTGGTCTGTTTGTGCAGCAGACATTGTCCTAGCTGAAAATGTTGAGATAGTTCTCTTACACAGATGCTCTTGCGATTCCACTGTTGGACCAAACCACAATTGATATAAATAATTACACAGTCCCTGCGCTGTGCCAAAATGGTTCCCATCTGTGGCTGACCCAGAGATGCTTTTGTTATTATTCGAGTGTGGTCGTTCTTCTCAGAACTTTCAGTTTAATAAAGGGATAAAGGAATGAATATGTCAGGAGTAAACACTAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35691
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 |
---|---|---|---|---|---|
ENSDART00000046112 | Nonsense | 413 | 1515 | 13 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Nonsense | 414 | 1516 | 13 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25567330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24270421 |
GRCz11 | 14 | 24567666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACCTGCTGTCCCTCTATGACAACAAACTTCAGACCATCAGCAAAGGCT[T/A]GTTCGCTCCTCTGCGTGCCATCAAAACCCTGTGAGTTACACACACACACA
Long Flanking Sequence:
AATGTGTTAAAATGACTTAGAAAACACAGGTTGAATTTTTTTTAACGTGACTTTCAGATTCAGAGTGCAAAAACCTTTAGTTAATAGTTTGTTAATAGCATGAATTGTACCTTAAAATAAAGTATGACCCAAATTCATATGCAGAAGGCCAGCCACAAAAAAATATCATTCACTTTCTTTAAATCTCTAATATTTCACTGCATGTTTTTAGCAAGCGCCGACAATTAGTTTTTGCTGTGTATGAAAGAAGTAGGAAAGTGTTATGATTTAAATATAAATATTACTGCAGAGTCCTGCATAAGATTTTTTCCAGATTGCAGATTCAGACTTTGTGTATACTGATGAAAAAAGAAGTCATTCTAATGAAACGCTTGTTTACTCTTCCAGACTGCTGAACGCCAACAAGATCAACTGCCTTCGAGTGAACACTTTCAAAGATCTGCAGAACCTCAACCTGCTGTCCCTCTATGACAACAAACTTCAGACCATCAGCAAAGGCT[T/A]GTTCGCTCCTCTGCGTGCCATCAAAACCCTGTGAGTTACACACACACACACACACACACTTATAAACACCCCATCCTTCACTCCCACTTTCAGTCTAAATGACTTCAGTCTCTAAGCAACTGTTGAGCAGGACTGCCTTCACCCCGCAATTAATTAGCCACAAGTAGATGGCAAAACAACACCATTAACAGCAATGAGATAAATGTGAGCTAAACAAATGCAAAGCCTACATTAAATACAACATTTCATTTTTATGAATGCACAGCAATCTTATTGTTATCAGAGGATATTACTGTTTGATTATACAGACTCCCTTGGCTCTAATTAAGCGTTTTGAGCTATTGTTGTGTTGGCGCTCCACAGACACCTCGCTCAGAATCCGTTCATGTGTGACTGTCATCTGAAGTGGCTGGCCGACTACCTGTTTGACAATCCAATTGAGACCAGCGGGGCTCGATGCAGCCACCCGCGCCGCCTCGCCAACAAGCGCATCAGCCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30677
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 |
---|---|---|---|---|---|
ENSDART00000046112 | Nonsense | 768 | 1515 | 21 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Nonsense | 769 | 1516 | 21 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25537865)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24240956 |
GRCz11 | 14 | 24538201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGGAAACCTCCTCACATCCGTTCCCAAAGAGCTTCCTAATCTGAAA[C/T]AACTGACACTCCTGTATGTATTTTTGCTCTTTTGATTGAATTTATTTATT
Long Flanking Sequence:
CTCTTGCTCACTGACAGACCCATTACCAGCTCACTTTGAAAGCAGACCCTGAAGTCCCTATCAAAGCCCCATCTATCTGCGTCCTGTCATCTAGCAGTGACCGGGTCTGCTGATGTTCTGCTGGGTTCAGCTGAGAATGGCCTTTTAGCACGTCACATAGTGGCAAAATTAGGATGAAACTATCCCAAGAGAGCTACAGTACACTTCATGGACAATTTTACTGTAGCTCTGAAATCTTCAAACTTAAAAATGTAGACAGCAAAGCAGCTCGCTGTAACGTCTCTCTGTAAATCTCGAGTCACTTTGTGGTGATAACTCTATATATTCCGTTTACAAATTGATTTTTAAGCATGAAATGAAATTTCAAATGAAATCTGGTTTTGCTTTGTAGCTTGTCTGAGGTTTGCAAGCTTGTCTGTTAACAGGATTTTTCTTACCATTTCAGATACTTGGAAGGAAACCTCCTCACATCCGTTCCCAAAGAGCTTCCTAATCTGAAA[C/T]AACTGACACTCCTGTATGTATTTTTGCTCTTTTGATTGAATTTATTTATTTGGGATGCTCTTTTATCCAAAAGGGTTTTAAGCAGACCAGTTTTTATATCCTCTACAGAAATTTTTTAGATTTCAGGAAATAAGAGGCACCTGTTTGCACTCAAGTCTCACCATATAAATAGAAATGCTACAGTGTATGTTAATTGATTAATAATGATAAACACACACATACAGTTGAAGTCAGAAATATTAGCCCTCATTTGAATTTTTATTTTTGTATAAATATAAATTTTTCAAATGATGTTTAACACAGCAAGAGAATTTTCCTAGTATGTCTGATAATATTTTTCTTCTAGAGAAAGTCTTATCTGTTTTATTTCGGCTAGAATAAAAGCTGTTTTTATTTTTTATGAACCATTTTAAGTATTAGCCCCTTTTAAGCATTTTGAAAGCAGTATACTCATTTACAGTATGCTGGGCACTGTATATATGCAAGATTCCAGCGACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14755
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 |
---|---|---|---|---|---|
ENSDART00000046112 | Nonsense | 1054 | 1515 | 30 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Nonsense | 1055 | 1516 | 30 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25515239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24218330 |
GRCz11 | 14 | 24515575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTTCAAGCCTCTACACTGTGCTTTTGTTGTTTTCTTCAGATRTGAGTG[T/A]TTGCCTGGTTATGTTGGCCAGCAGTGTGAGCAGGATTAMAATGACTGTCT
Long Flanking Sequence:
TTGTTAATAGGGGTTGTAAAATAATTAAGGAAAACACTACCACTTGACAGATTAAAGTCATTTGAAACTGATCACTGTCCTTTTTTTAAAAATCTCATTTGTTTTTATACTTCGTTTGCAGTATATGTCTTTCACAAAATACGCTTTAAAAAAATACTATTTTATATCTCTTAATATAATTTTAAAAAGGACTAAACCGTGACCTCGAATTTTATGAAACTGCACAATTTAAATACATATATGTACTTTACATAAGTCATGGCAACATATGTTTTTGTTAACAATTTATTAACATAAGTAAACAATGTTTATTATTTATTTATTTTTTTTCATTTTAATGTAATGCAAGGTTAATTTGATCCAACTTAAAAATGTAAGGAAATTCCTAAGGCATACTGTAAAACTGTGTTTTTAACTCAGCTCTTCCCCAAAACATCCCTCTTTGCTAGCGATTTCAAGCCTCTACACTGTGCTTTTGTTGTTTTCTTCAGATGTGAGTG[T/A]TTGCCTGGTTATGTTGGCCAGCAGTGTGAGCAGGATTACAATGACTGTCTGGAGAACAAATGTCAGCATGGGGCAGAGTGTGTTGACGCCATCAATGGATACACATGTGTGTGCAAGGAGGGCTTCAGGTATGTGGGTTGTTAAAGATCACACACATGCATGTTCTATTGCAAATAAGGGTACACTAATTAATTCAGTTGTTGTCATGTTATGTTAAATACTGTAATACAGACAAAACACAACGTGAACCCTACTTCTACTTTTCTAAGAAAATATTCAGAATTATTATTTTTCTGCATTCAAATGTAATACAGTAGGTTTCAGTAACTATTGAAGAAATTTGCATTGAGCTAGAAATAATCAAATAATCTGCAATTTTATGGTTGTTGATATTATTAGTATTACTAGTAAAAGTAATAGTAAATATTGTGTGAATTTATTCCTTATAATACAATAATTAGATTCCAAAACTGCTAAAGAAGCAACTTTTTTTTATTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11742
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 |
---|---|---|---|---|---|
ENSDART00000046112 | Nonsense | 1067 | 1515 | 30 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Nonsense | 1068 | 1516 | 30 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25515200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24218291 |
GRCz11 | 14 | 24515536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGTGAGTGWTTGCCTGGTTATGTTGGCCAGCAGTGTGAGCAGGATTA[C/A]AATGACTGTCTGGAGAACAAATGTCAGCATGGGGCAGAGTGTGTTGACGC
Long Flanking Sequence:
CCACTTGACAGATTAAAGTCATTTGAAACTGATCACTGTCCTTTTTTTAAAAATCTCATTTGTTTTTATACTTCGTTTGCAGTATATGTCTTTCACAAAATACGCTTTAAAAAAATACTATTTTATATCTCTTAATATAATTTTAAAAAGGACTAAACCGTGACCTCGAATTTTATGAAACTGCACAATTTAAATACATATATGTACTTTACATAAGTCATGGCAACATATGTTTTTGTTAACAATTTATTAACATAAGTAAACAATGTTTATTATTTATTTATTTTTTTTCATTTTAATGTAATGCAAGGTTAATTTGATCCAACTTAAAAATGTAAGGAAATTCCTAAGGCATACTGTAAAACTGTGTTTTTAACTCAGCTCTTCCCCAAAACATCCCTCTTTGCTAGCGATTTCAAGCCTCTACACTGTGCTTTTGTTGTTTTCTTCAGATGTGAGTGTTTGCCTGGTTATGTTGGCCAGCAGTGTGAGCAGGATTA[C/A]AATGACTGTCTGGAGAACAAATGTCAGCATGGGGCAGAGTGTGTTGACGCCATCAATGGATACACATGTGTGTGCAAGGAGGGCTTCAGGTATGTGGGTTGTTAAAGATCACACACATGCATGTTCTATTGCAAATAAGGGTACACTAATTAATTCAGTTGTTGTCATGTTATGTTAAATACTGTAATACAGACAAAACACAACGTGAACCCTACTTCTACTTTTCTAAGAAAATATTCAGAATTATTATTTTTCTGCATTCAAATGTAATACAGTAGGTTTCAGTAACTATTGAAGAAATTTGCATTGAGCTAGAAATAATCAAATAATCTGCAATTTTATGGTTGTTGATATTATTAGTATTACTAGTAAAAGTAATAGTAAATATTGTGTGAATTTATTCCTTATAATACAATAATTAGATTCCAAAACTGCTAAAGAAGCAACTTTTTTTTATTTACACAAATGTTTCAATGGGTCAAAGACAAAAAGTGGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9875
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 |
---|---|---|---|---|---|
ENSDART00000046112 | Nonsense | 1102 | 1515 | 31 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Nonsense | 1103 | 1516 | 31 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25512675)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24215766 |
GRCz11 | 14 | 24513011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAATGTTTAAAAATGTGTCCCTCTCACTTTTYTTAGTGGGCTATTCTGT[G/T]AGAATCATCCACCAATGGTAYTGCTCCAGAACACAAGTCCATGCGATCAG
Long Flanking Sequence:
CTGACCCAGTCGTGGCTCAAACCAGCAACCTTCTTGCTGTGAGGCGATTATGCTACCCACTGCATTATTAATAATACTACTAACTGTATTTTGATAAAAAAAAAATTACTTTGGTGAGACATTTTTAGAATTAGTAGTTATTCCAGATTTTGGAACACATGAGGCATCTGAATTGTTCATTTTAATCACATGATCTTTTTTTATCATGAAAACATTACAAAGACACATGTTTTATTCGTTTTTATTGTGTTCTGCATGTGTTTCATATGTTACTTTACCATGTAAAGCTCATGTGGCATAAAATAAAATAACAATGATATTATTAATAATCTGTATTCTGCATTTGAATTTGACAGACTTCAGCAAGTATTCAATAAAATATATTCACGTAGCTAACTAACTGATTAAATTACACTCAAATGTTTGAATAAAATATTAAAGAACTGATAATAAATGTTTAAAAATGTGTCCCTCTCACTTTTTTTAGTGGGCTATTCTGT[G/T]AGAATCATCCACCAATGGTATTGCTCCAGAACACAAGTCCATGCGATCAGTCGGATTGTCAAAATGGATCCGAATGTCTGGTCATGGAAGGAGAGCCAGTGTGCCGTTGTCTGCCTGGTTACTTCGGCACTAAGTGTCAAAAAATGGTCACACTGCACTTTCTCGGCAAGGAAGCTTACGTGGAGCTCTCCGGCACCAGGATCCGACCACCCATGCACATTTCCTTCCAGGTACACCTATAACCTGTAACCTTCCTGTAATGCTTTATAATAGATCCCAGATCACCTTCTCTAATATAGACTTCACATTTCAGCCTCAGATAAGTGTGCATATCCTTCACGAGAAGCAATCTAGCTCTGTCATATGTCTTTTTTTTCTCGCATTGCGTGGTCTAAGCCAGCTTTGGCCTCTTTGACATTATGAGAATGTCATCTCTTGTCCACCTGCGTGAATAATTCCTCTCCTGAGGATATATATTATGGTAATGGAGGTTGAGCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42392
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 |
---|---|---|---|---|---|
ENSDART00000046112 | Essential Splice Site | 1367 | 1515 | 34 | 36 |
ENSDART00000126199 | None | None | 177 | None | 6 |
ENSDART00000146299 | Essential Splice Site | 1368 | 1516 | 34 | 36 |
Genomic Location (Zv9):
Chromosome 14 (position 25497295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 24200386 |
GRCz11 | 14 | 24497631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCCACTATGTGAACAGATGAGCTCCCAAGACCCCTGTGAAAGCAGCAG[G/T]TACACAAACACATACGCACTGGATACTAATGCCTGTCCTGATTTTGCAGA
Long Flanking Sequence:
ATATTGTGCAGCCCTAGTTCGTTTCATAATTTATGTTAATTTAGACTAGACTTAGAAGTTCTCTGATTATACAATTTAACTATGAAAATGTCAGGGTAAAAATCCAGATACATTTAACTAAATAAATTGAAATGGTAAAATAAAAAAAAAAACTAAATAAATATCAGTTATGTGTGTGTAGTTATAGTACAAAACTAATGTTTGCTTGTTGATATTTCAGGTGTGCCATCTCTGATTGGCACATCAGGCCTTCGGCCGGGCCCATTCCAGTCCTTCAACGGCTGCCTTCATGACGTACGCCTGAATGGAGAGCTCCAGGACCTCGGTGCTGGACTGGCGGGGATAGAAGGCGTCCTGTTTGGGTGTCACTCCTGCAGCGTCTGTGACCAGGGAGCCTGCAGACAAAGAGGAGACGAAGGGGTGACCTGTGACTGCCCCACAGGACACAGCGGCCCACTATGTGAACAGATGAGCTCCCAAGACCCCTGTGAAAGCAGCAG[G/T]TACACAAACACATACGCACTGGATACTAATGCCTGTCCTGATTTTGCAGAGTGGCGCAAATTCCATTGACAACATATTTTGTTTTTGGAACAATCATTACTGTCTAAAAATCTTTAAATGTGTGGATTTGTTTGATCTGTGAAGTAATTTCAACTGAAACATTAAGGCAGAGCGGGACCTATTGAGTAGCTTTTTGTCTTTTTTTAAAAATAGCCAATAGTGTTTTGTTTATATCACAGATCTGCTCTTCAGAACTACAGAGCAAATGAAAAGATCTACTGTAATCACTTAGCCACTAAACATTCTAACTTGCAGATTTAGGAGAAAAATCTGCATTTAACACTGAAAAAAAGCACAATCATTACCTTAGGTGATTGTTGTCATAGAAGTTTATGCTTTTCTTCAGCAGGCTTGTCAAAAGGTGTTTTGAACTTGAACTGCAACACCTAGTTCAACCACTGCTTTTCAATCTTATATAGACTTGCTGCACCTTTGTGCTC
Associated Phenotype:
Not determined