ZMP
si:ch211-278g15.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
PREX2
Human Description:
phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 [Source:HGNC Symbol;Acc:229
Mouse Orthologue:
Prex2
Mouse Description:
phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 Gene [Source:MGI Symbol;Acc
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18614 | Nonsense | Available for shipment | Available now |
sa12110 | Nonsense | Available for shipment | Available now |
sa13066 | Essential Splice Site | Available for shipment | Available now |
sa6763 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37864 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24475 | Nonsense | Available for shipment | Available now |
sa15890 | Nonsense | Available for shipment | Available now |
sa24476 | Essential Splice Site | Available for shipment | Available now |
sa24477 | Nonsense | Available for shipment | Available now |
sa39442 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37865 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18614
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 17 | 1600 | 1 | 40 |
ENSDART00000106186 | Nonsense | 17 | 1600 | 1 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19498296)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18804450 |
GRCz11 | 24 | 18948869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGACTGAGGAGAGCAAAGCCGAACACAGAGCCGAAAGTGGAAAAGATT[T/A]AGASAAGCAGCTTCGTTTGAGAGTTTGTGTTTTGAACGAACTTCTGAAGA
Long Flanking Sequence:
AAACATAACTCTCCTCTTTGGTTCCATTCAGCTTTTCAAAGCAATGTAACTAATATTGGAGTCTGGGAAAGTCTTGCATCGGTAATTACCCCCAATGTCATCAACATTTCCCCACTGTGCTGGCACGAATTCCCAGCCATTTATTTCCTGTCCTTTTCATGCTGGAGGGAGGCTGGATTTAGGATGAAGGTCTTGGGAGTCACATGGAGCAGCAAAGTTTTTGATTGATGTCCAAAAGCCATTACTACACTGTTCTCAGGCGTGTAGAGTAGACTAGTGCTGAACTTCTGAATGCAGCCGAGTAGTAGATTGTTTTTCAATTGCGTTCATTTGTTCTATTGACTTTGTCCGCTGCTTTTTTTTTTTTATCATGATTCAAACCTCCAGCCGGCGTCAGGTCGTTTAAACTTCTCCTGCGGCAACTTTGAAGACTTTAAGGAAGACGATCGACATGACTGAGGAGAGCAAAGCCGAACACAGAGCCGAAAGTGGAAAAGATT[T/A]AGAGAAGCAGCTTCGTTTGAGAGTTTGTGTTTTGAACGAACTTCTGAAGACCGAGCGGGATTATGTTGGGACGCTGGAGTTTCTTTCGGTAAGGGATTTTTTCTTTTCCTGTTTAGCATTTTTATATGTACGTTGTGCTTTATAGGATATATATTAGCTGGCTACAAGGTGTACACTCAAGTTATATTGAGATAAAACCTACCTCAAGCGCGTACATCTTCTTTGGCATCATGCGCGCGTTCACGAGAGACCAGAAGTCTGCGCGCGAACAGTGAACAAACTGGAGATTATAAAGTTATGCTTAACTTATTAATTTATTACAGTGGAAGCAAACGTCCAATTTCAATGGTGTTTTATAAGTGGAGTTGAGATCCAGTCTTTTGAAGTTGTCTCACATTAAAGGTTAACATTAATAGTTATTTTTTTGATATAGACTCAATAGTCTTCACTGTAAAACTGCACGGTTCCACACAATTCATTCATGTTGTTCCAACACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12110
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 17 | 1600 | 1 | 40 |
ENSDART00000106186 | Nonsense | 17 | 1600 | 1 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19498296)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18804450 |
GRCz11 | 24 | 18948869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGACTGAGGAGAGCAAAGCCGAACACAGAGCCGAAAGTGGAAAAGATT[T/A]AGASAAGCAGCTTCGTTTGAGAGTTTGTGTTTTGAACGAACTTCTGAAGA
Long Flanking Sequence:
AAACATAACTCTCCTCTTTGGTTCCATTCAGCTTTTCAAAGCAATGTAACTAATATTGGAGTCTGGGAAAGTCTTGCATCGGTAATTACCCCCAATGTCATCAACATTTCCCCACTGTGCTGGCACGAATTCCCAGCCATTTATTTCCTGTCCTTTTCATGCTGGAGGGAGGCTGGATTTAGGATGAAGGTCTTGGGAGTCACATGGAGCAGCAAAGTTTTTGATTGATGTCCAAAAGCCATTACTACACTGTTCTCAGGCGTGTAGAGTAGACTAGTGCTGAACTTCTGAATGCAGCCGAGTAGTAGATTGTTTTTCAATTGCGTTCATTTGTTCTATTGACTTTGTCCGCTGCTTTTTTTTTTTTATCATGATTCAAACCTCCAGCCGGCGTCAGGTCGTTTAAACTTCTCCTGCGGCAACTTTGAAGACTTTAAGGAAGACGATCGACATGACTGAGGAGAGCAAAGCCGAACACAGAGCCGAAAGTGGAAAAGATT[T/A]AGAGAAGCAGCTTCGTTTGAGAGTTTGTGTTTTGAACGAACTTCTGAAGACCGAGCGGGATTATGTTGGGACGCTGGAGTTTCTTTCGGTAAGGGATTTTTTCTTTTCCTGTTTAGCATTTTTATATGTACGTTGTGCTTTATAGGATATATATTAGCTGGCTACAAGGTGTACACTCAAGTTATATTGAGATAAAACCTACCTCAAGCGCGTACATCTTCTTTGGCATCATGCGCGCGTTCACGAGAGACCAGAAGTCTGCGCGCGAACAGTGAACAAACTGGAGATTATAAAGTTATGCTTAACTTATTAATTTATTACAGTGGAAGCAAACGTCCAATTTCAATGGTGTTTTATAAGTGGAGTTGAGATCCAGTCTTTTGAAGTTGTCTCACATTAAAGGTTAACATTAATAGTTATTTTTTTGATATAGACTCAATAGTCTTCACTGTAAAACTGCACGGTTCCACACAATTCATTCATGTTGTTCCAACACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13066
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Essential Splice Site | 46 | 1600 | 1 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19498385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18804539 |
GRCz11 | 24 | 18948958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTTCTGAAGACCGAGCGGGATTATGTTGGGACGCTGGAGTTTCTTTCG[G/A]TAAGGGATTTTTYCTTTTCCTGTTTAGCANTTTTAYATGTACGTTGTGCT
Long Flanking Sequence:
CCCCAATGTCATCAACATTTCCCCACTGTGCTGGCACGAATTCCCAGCCATTTATTTCCTGTCCTTTTCATGCTGGAGGGAGGCTGGATTTAGGATGAAGGTCTTGGGAGTCACATGGAGCAGCAAAGTTTTTGATTGATGTCCAAAAGCCATTACTACACTGTTCTCAGGCGTGTAGAGTAGACTAGTGCTGAACTTCTGAATGCAGCCGAGTAGTAGATTGTTTTTCAATTGCGTTCATTTGTTCTATTGACTTTGTCCGCTGCTTTTTTTTTTTTATCATGATTCAAACCTCCAGCCGGCGTCAGGTCGTTTAAACTTCTCCTGCGGCAACTTTGAAGACTTTAAGGAAGACGATCGACATGACTGAGGAGAGCAAAGCCGAACACAGAGCCGAAAGTGGAAAAGATTTAGAGAAGCAGCTTCGTTTGAGAGTTTGTGTTTTGAACGAACTTCTGAAGACCGAGCGGGATTATGTTGGGACGCTGGAGTTTCTTTCG[G/A]TAAGGGATTTTTTCTTTTCCTGTTTAGCATTTTTATATGTACGTTGTGCTTTATAGGATATATATTAGCTGGCTACAAGGTGTACACTCAAGTTATATTGAGATAAAACCTACCTCAAGCGCGTACATCTTCTTTGGCATCATGCGCGCGTTCACGAGAGACCAGAAGTCTGCGCGCGAACAGTGAACAAACTGGAGATTATAAAGTTATGCTTAACTTATTAATTTATTACAGTGGAAGCAAACGTCCAATTTCAATGGTGTTTTATAAGTGGAGTTGAGATCCAGTCTTTTGAAGTTGTCTCACATTAAAGGTTAACATTAATAGTTATTTTTTTGATATAGACTCAATAGTCTTCACTGTAAAACTGCACGGTTCCACACAATTCATTCATGTTGTTCCAACACAAATTCATTAAGTTAACCTAACAAATTTAAGTGGATTGAACATAATACAATTAAGTTTCCTGCAAAAAATCTCCACAGTTGTGTAGCTTCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6763
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106186 | Essential Splice Site | 111 | 1600 | 3 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19541427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18847581 |
GRCz11 | 24 | 18992000 |
KASP Assay ID:
554-4464.1 (used for ordering genotyping assays)
KASP Sequence:
GCCTGACCCAAACCCCTATCATGAAGTGGGCCACTGCTTCCTGCACTTTG[T/C]GAGTCACTGTCTGATACGCTCTCTCTTCACTTACTGTATTACACTCATCA
Long Flanking Sequence:
TAAACATGTTTAATGATTTATTATTACAGACATTGATTTTGATTTCCATATTTTTTCTTTTCTAACTATATAAACAATCACAGTTTTTGTATTTTTACTCCATTTTTACACACATGTTTGCAAAAAGACGATACCATATGAACCTCTGATATCCATTTATTTTTGCAAGTACAATGAAAATAGAAATTTCAATAACAGAATTAATTAATTAAAAGGCCATAAAAAATAAAACCTCACAGGTGCCACTTTAGACTCATGTTATCATCGATGAGGAAAGTGCAGTCACTTCCAGACATTTTTAGACTCCTCTGTTTTTCCAGATACAGACAATGTCTCTCAATCAGTAAGTCAATGTTTCCATGTGTTTGCTTCGCAGGTGCTGTTTTCAAACCTGGAGGAGATCCTGTCTGTGCACAGGGACTTCCTGAACATGGTGGAAGAGCTGCTGCAGCCTGACCCAAACCCCTATCATGAAGTGGGCCACTGCTTCCTGCACTTTG[T/C]GAGTCACTGTCTGATACGCTCTCTCTTCACTTACTGTATTACACTCATCACTGCTGAAAACAACAGCTGAAGATTGCTTCAAGCAGGTTTGAACTCCAGAGGCCTGTTGAGCAAAACAAGTTAAACAAACTCGCAGAGTGAGTTTTAGATTCAGATAAGAGATTTTGATGCAAATTATGGAAACAAGACAATAGTTTTGCTTTTCTGTAGAAGATATTTCTTTTTATTGAATAATTAAATATTTGAAGATTATTTCTGAAAATAAGACAATATTTTCTGCTTGTAAAGAAAACGTTTTTTTGATTGAAAATTTTTTTGATTGGACTTTTTTTCCGAAAACAAGAAAATATTTTTTGCTTGTCTAAAAAACGTTTATTTGAAGCTTTATTTTAGATGTTTAGACATTATTTCTAAAAACAAGATAATATTTTTGCTTGTCTAGAAAATGATTCTTGATTAAATATTGTTTTTAGATGTTTGGACATTATTTCTGAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37864
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106186 | Essential Splice Site | 412 | 1600 | 10 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19572569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18878723 |
GRCz11 | 24 | 19023142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGACCGCAAGCGAAAACTCACCACCTTCCCCAAGTGCTTCCTTGGAAG[G/A]TAGGTCAACAAAAGCTGGACCTCTGTGTGGATAATAGCTGTGGTAGACTT
Long Flanking Sequence:
ATACATACAAATAAGAAAATATTGATTTTTGTTAAAGCCATCTACAGGTAATTCTCAAAACAGCCACAGATTAGGTTTTACGCCAAAGAATGTGCTTATGAATTCTGTAAATTATTATTTATTTTGCGATTTATAATTTTATTTCAGTTAGTATTTCAGTGCTCATTATTAGTTTTATTTATTGTGATTTTTTTTTTTTTTTAAATATATATTTTTAAAAAATGTTGTTTGACCATTGGTATTGGTCTTTAGTTTTCATTTACTAATATAACCTTTATACATACTACTGTGTATTTCAGTATAATTCTGCCTTTCAGAAATTGAAATCTCTCTTTTATTTGTTTATTTTTTCCAGCATTGAGATTGGGCATGGAGCAGGACACCTGGGTGATGATCTCTGAGAAAGGCGAGAAGTTTTATAACCTCATGAGTAAACAGGGCCACCTCATTAAAGACCGCAAGCGAAAACTCACCACCTTCCCCAAGTGCTTCCTTGGAAG[G/A]TAGGTCAACAAAAGCTGGACCTCTGTGTGGATAATAGCTGTGGTAGACTTCAGGATGGAGGTTCACACTAGGGTTCATGAACTGTAGTTTATCTGGAGAGCCAGTGACATGCTGAGAATGAGAGTGTGTAGCTGTTGACTGACTGTAGTGATTGAGGACATAACATTTCATTTTGAACACCTTTACTCGCTCATAAATAACTAGGCAGTGGAGTTTAATGGAACTGTGGATGGACAGCATTTGGGGTGAACAGGTCTTAGTCTGCTGGACATGATAAATGGAGCTGAAATAGTAGTCAGGATCAGTTTTATTATCTGGGCTTTTTGTGCTTTTAAATCTGTCCTTTGTAGGGTCTTTCTGTCTTTTTTCCTCTTTTTCTTGAAGAAGTCACATTTAATTTTTTTCTTCTTTTTTTAAAAGTCAGTATGAAATTGGAATTTGTTCGATGGAAGCGTTCAATGATTGAGGTTTGCTACAGGTTGAGCTCGTATGAGTGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24475
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 662 | 1600 | 18 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19606202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18912356 |
GRCz11 | 24 | 19056775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGACCTTTCCAGGAAGTAGAAAACTTTCTAAAGCAGTGCTTCCACAGC[A/T]GAGGTCCCATCAGAGTCCTGGTCAGCACCAAACCCAGAGAGTAAGTGGAA
Long Flanking Sequence:
AAATACTGTGCATTGGCAAGTGGGCTTGTCAAGGTAAGTGTTTGGTGCATAAGAAGAGTAAATGACTGTCTCCTATAGGTGGTAGGAGACAAACTCTTTTTCTATCCATATGCACCAGACACTTTCAAGACACTCAATGTTTCTGGAAAACATTGTGCAATTCTGAGTGTGCTTCATGCAGGTGAGTGGACTTGACTAACCACCAGTAGGAAAACTCTCTCTGTGCGATTGTGTGTCTGTATGTATGTACAGTCAAGCCTTAATTTGTGGGGTTTGAAGAATTTATTATTTATAATATTTTATTTTGTGATTTTATTTTATCCTCATCTATATCACATTGGATAAAAGTGTTTGCTAAAAGAATAAATCCTAAAAAATATTATCTTTTGCAGATGGCAGGTCTGGAAGTGGGGAAGAAGATCTTTGCCATTAACGGGGACCTGGTTTTCTTGCGACCTTTCCAGGAAGTAGAAAACTTTCTAAAGCAGTGCTTCCACAGC[A/T]GAGGTCCCATCAGAGTCCTGGTCAGCACCAAACCCAGAGAGTAAGTGGAAAACCGCTCTGTCTCCATAACAGCTGATCTGCGCTATCTTACAGGCTGTCGATAAAGCAGTTAAATAAAGAACCCTCCCAGATAAACATCATTTTTATTGATTAAAATCAGCTTGATATTTAACTGCGGCTCAGAATACAAAAAACACTTGGAGCAGCAGCTGAAAATGCGGTGTGTTTGGCGACCAAACTGATGTCTCCGTGTCTTTATGCTCCACAGGACTGTGAAGATCCCAGACTCCGCAGACGGATTGGGCTTTCAGATCCGGGGGTTTGGGCCATCTGTGGTGCATGCGGTTGGCAGAGGTAAGAGGGAAACAGAGAGAAAGGAAAAGAGAAAAATTGAGTTTATCTGCAGGAGGATGCTGATACCCTTTATCCTTCTGAGTTTTTGAAGCTCAGCTGGATCACAGCTGGTGCTGGAGGTACATGACTGGACCTGAGTCAGACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15890
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 824 | 1600 | 22 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19616660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18922814 |
GRCz11 | 24 | 19067233 |
KASP Assay ID:
2261-8622.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCTAACGGTGGATAACGWATATCTGGAGTACGGCGTCATGTATGAATA[C/A]GACAGCACAGCTGGCAYGAAGTGTYACRTCTTGGAGAAAATGGTRGAACC
Long Flanking Sequence:
AAAATCCTGTAATTTTCTAAGCAATTTAGTAGTTTTGATCAGGACTGAGTTTGATTAACAGACTAATGCAAAACAAAAATCCTTTGAAAATTATTTATCTGATGCATTTTTACAGCAGTTTAATTCAGTAGATGTTTTCATTCCTAATATAACAAAAGGGTAGTAAATTTGAGCAGTGCACTTGAGTAATGTGCCTAGTAAACATACCTAATTTTTGATTGTTGCATGTTTTTTTTTTGTATATGAAGCTGCTTTGACATAATTAATAAGAAATAAAAATGGCTATTTGATTATAAAATAATAAAATTTACTTCTATATAGTTGTATGTTGATGTTTGTATCTTTTGATCTGCTAACACTAAATCAAGCTGACGTATCTGCATTTGCTCAACAGAAGTCATGGACAAATTCAACACCATCGCCATAATAGATGGAAAAAAGGACCACGTTAGCCTAACGGTGGATAACGTATATCTGGAGTACGGCGTCATGTATGAATA[C/A]GACAGCACAGCTGGCATGAAGTGTCACGTCTTGGAGAAAATGGTGGAACCGAAAGGCTTCTTCAGCCTCACAGCGAAGGTAAATCCCATGAGTATTGACTATTATCTCTGCTGTAGAGAAGTGTATGAATTTATCCAGAAGCTGACAAGACCACAGCGATTATCTTGTACATTTGCAAGGGCCTCTTCACAGTTCACAGTAACACACAGGTGCTGATAGAAGCTGACAGCCGAGTATATTAAACCAAGTGTGTGTGACAAATGAAAGTGGTCTTTACGACCCCCTGCTGTGGAATAAGAGGATAAACACTTTAAATCACCGGTGGTGTGGAGGCTTAAGTGACTCGCATGGAACCATTGTTGTTACAAGAGGATTTTTTTTTTCATTTCACTTTTCAGACTTGATCATTTTTTGTTGGCGCTACCACAAACGCAATTCATTTTTTAGAAAGCTTTATTTTTTTATTCAAATATATCATAAGAAGTACTGAGAAACATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24476
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Essential Splice Site | 1107 | 1600 | 26 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19640569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18946723 |
GRCz11 | 24 | 19091142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGGAGGACTCAGGTCATGACACCATCAGCAACCGGGACTCCTACAG[G/A]TAAATGTGCATACAGTGACCATACGTTTACTGTTAAATGGGGTGTCTGTC
Long Flanking Sequence:
TCCCAGTTGGTGCTTAACAGAGCAAGACATTTTGTACATAATTTTTTTCTAAGCGCTAATCATTTTCTAGTGCTAATAATTCTTCAACAGTATATATTTTTGTTTGTTTTGTTGTGTTTTCAACAGCTAATATTTATAGAGTTGTCCATTATGGTGACCCGTGCTTCACATTAACAGAGTAACATAGTGATGTTTCATTCTGTGAGTCCTGAACATTGTTTCTGGAGGTGTGGAGTCTGACTGTTTTATTGCACATTGATTGCGGTGCGATTAATCTTTCTCTGCTTCTCCCTCTGTCTCTCTGTGTGTGTTTTCCCCAGTTTGCTCTCTTCCATCACACATCCCACTGGCTCTGAAGGGAAGCCCACAGAGAGCTACATTTCAGCGGAGAGTGAGAGCGACAGAAGTGAACGCAATGGGAAGAAAGTGTGTTTTAATGTGGCGGGAGATGAGCAGGAGGACTCAGGTCATGACACCATCAGCAACCGGGACTCCTACAG[G/A]TAAATGTGCATACAGTGACCATACGTTTACTGTTAAATGGGGTGTCTGTCTTCTGTAAAATAACTTCTCTGATAGGTTTCTCAATTTCTGTTTTATTGTACACATCTTTCTGATGTGAAATAGGTCAGAAAGCAATTCATCAGCCCGAAAAAAATTGTTGATGGCAAAATTCAAAGTTAAAATAACAAATGTGTCATTTGTTGAATTTTCCCTTCAGAATATTGATATCTGAACTCTCTCGATAATAATATTACTTTAAACTACACTTATTTTAAGCTAACTGAAGCATAATGTCACAGCAAAAATGTAATTTTCCCAAGTTCCATAATTCCATTTCGTTTTTAAACATTTTTTAAAATATTATATTATATTATATTATATTATATTATTTTATATTTTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATGCGTTTCATGCCTTTTTATGCCTTATTAAACTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24477
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 1185 | 1600 | 29 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19649678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18955832 |
GRCz11 | 24 | 19100251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCCATCACTAGTTTGCTAAAAGGGGCAACCGTGACACGAGCTTTTGAA[C/T]AAACTAAATGCTTCACTCCAGGACGAGGACTTCAAGGTACTAAACCTACT
Long Flanking Sequence:
TGTTTATATGCAACATCTATGTATATTGCGTAAAGATTTATGCTTTAACATGGTCAAACTGTGTGTATCTGCAACCCTAAAGAAATCAGTTAAAAATGGCTAATGCCATAACAAACTATGTCTCGAAAATTACATTTTAACACATTTGGTTTCAATTGTATACTTTTGGCCCCAGTAGCCCTCCATAATTACAGAAATTAAATGTTTTATGGCTAGATTGTTGGATTTCAAGTCATTAGTAGAAGATTTCATATCATATGCTACTTAGTTATGCTGATTTTTGAATATTATTGAATATTATTACTGATTCTTTTTAGTTGTTCATTACGCAACTACATATTATTGGGAAATGTAATTTTACTGTACAGTAATGCACATAATTTGTCAATGTTTGGTAATTTCAAAAGAAGCTTTTTCTGATGGTTTGGTACTGGTCTTATTTTCAGGTGGAGTCCATCACTAGTTTGCTAAAAGGGGCAACCGTGACACGAGCTTTTGAA[C/T]AAACTAAATGCTTCACTCCAGGACGAGGACTTCAAGGTACTAAACCTACTGACACACATGCACACAAACTAGTTCTTCAGCGCTTCATTAAGGGCTCATATATGTAGCTAAGGTGATATATATAGTACCTCTACTTTATGAAAGACCTGTTAAGCCAAGTATGCTTTTTCAGCAGCTCTTTGAGGTGGCTAATGTGCTTTATATTCTCTATTCCATTCTAAGAATTTGCTCTCTAATCCTTTCTTAGGCATTGTTTACTCTAGCATTTTCATTTTTTGTTTATTTATAAGTTTGGCATGTTTACATCTGGTATCCATTGTACTTCAGCATCTTCAATCTGTAAAAAGTGTTTTGAAGAAAAAAAAAAAAAAACTTTTAAAAAAGAAGCACGGCTATCCACAATTGCTCTCTGATTGGTCTTCTATACTATTGCATATCGTTCCCAGATTTGTCAAGCCCTTCTCATATGATCATTACACAACCGCCATGGTGCAAGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39442
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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 1193 | 1600 | 29 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19649702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18955856 |
GRCz11 | 24 | 19100275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCAACCGTGACACGAGCTTTTGAACAAACTAAATGCTTCACTCCAGGA[C/T]GAGGACTTCAAGGTACTAAACCTACTGACACACATGCACACAAACTAGTT
Long Flanking Sequence:
ATTGCGTAAAGATTTATGCTTTAACATGGTCAAACTGTGTGTATCTGCAACCCTAAAGAAATCAGTTAAAAATGGCTAATGCCATAACAAACTATGTCTCGAAAATTACATTTTAACACATTTGGTTTCAATTGTATACTTTTGGCCCCAGTAGCCCTCCATAATTACAGAAATTAAATGTTTTATGGCTAGATTGTTGGATTTCAAGTCATTAGTAGAAGATTTCATATCATATGCTACTTAGTTATGCTGATTTTTGAATATTATTGAATATTATTACTGATTCTTTTTAGTTGTTCATTACGCAACTACATATTATTGGGAAATGTAATTTTACTGTACAGTAATGCACATAATTTGTCAATGTTTGGTAATTTCAAAAGAAGCTTTTTCTGATGGTTTGGTACTGGTCTTATTTTCAGGTGGAGTCCATCACTAGTTTGCTAAAAGGGGCAACCGTGACACGAGCTTTTGAACAAACTAAATGCTTCACTCCAGGA[C/T]GAGGACTTCAAGGTACTAAACCTACTGACACACATGCACACAAACTAGTTCTTCAGCGCTTCATTAAGGGCTCATATATGTAGCTAAGGTGATATATATAGTACCTCTACTTTATGAAAGACCTGTTAAGCCAAGTATGCTTTTTCAGCAGCTCTTTGAGGTGGCTAATGTGCTTTATATTCTCTATTCCATTCTAAGAATTTGCTCTCTAATCCTTTCTTAGGCATTGTTTACTCTAGCATTTTCATTTTTTGTTTATTTATAAGTTTGGCATGTTTACATCTGGTATCCATTGTACTTCAGCATCTTCAATCTGTAAAAAGTGTTTTGAAGAAAAAAAAAAAAAAACTTTTAAAAAAGAAGCACGGCTATCCACAATTGCTCTCTGATTGGTCTTCTATACTATTGCATATCGTTCCCAGATTTGTCAAGCCCTTCTCATATGATCATTACACAACCGCCATGGTGCAAGTACAAATGCAGACAAACATTTAAATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37865
Status:
Available for shipment
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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 |
---|---|---|---|---|---|
ENSDART00000106186 | Nonsense | 1437 | 1600 | 35 | 40 |
Genomic Location (Zv9):
Chromosome 24 (position 19681149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18987303 |
GRCz11 | 24 | 19131722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGAGTATCAGGCTCAGATCAATGCGGGCTCTCTGGAGAAGGTCAAG[C/T]AGTACTACAAGAGACTCCGGTAAGCCTGATTCAGCTGTCAGTCAAACCTC
Long Flanking Sequence:
TTCCTAGAGGCGTTTTACTTCCAGCAGTTGCCCCAGAGACTGAGGCATGGCGGCAGCTTCAAAATATACCCCGTCCTGTTCACTCAGGGTATGGACACACTTAGCCTAAAGCACAACAAAAAAAAAATTGTGCTTTTCAATGTGAAGCCAGTGATCATTGCAACTATAAAAAATAACAATAATGTAAACATATTATTTTGATTATTGCAACGTATTATATATTATACCCACTTTATATACTGACATTTCTAAAAATATATTTCCAAATCAGATGTTTCAGCCTAATTTATAACAGATATAGATAGATAGATGGATGGATGGATGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATTTTGAAAATCCAAAGTTTTACATCATCTTTCTTCCACAGCCTTGGAGAGCATGGAGGGATATTATTACAGAGAAAACGTGTCAGTGGAGGAGTATCAGGCTCAGATCAATGCGGGCTCTCTGGAGAAGGTCAAG[C/T]AGTACTACAAGAGACTCCGGTAAGCCTGATTCAGCTGTCAGTCAAACCTCAACTCTTCTCTACACCTTCAGGCCTGATGAGCTGGGAATTTTGAAAGATTTGGATAGTAATGGTCATAGTGGCTCAGTTGGATTTTTGACAGATGGGCAGTAAAAGTAAAAAAAAAAAAAGAAAGTGGTCAAGTTCTAGTTTATAGATCAGTTTGGAAGATACATAACGCTATACCGTAGCAGGCTCGTAGCCAGCCTGGTAAATGGGGTGTTTTTTTTCTCTCAAAAAGTGGACATTTTTGCAGTTATTCACTTTATTTTTTTAACTATTTGGTTTAAACACTGCATGTACAGTATGTGTCATTTTAAGCACTATTTTTGCTGGATTAGCTAGTCAGGTGGTCATCATAACCGCACTTTTTGATGTACCAAAATCATTTCCTAAAGATTTAGAATAAAGAAATATTAAAAAAAAGAAATAAACTTATTTTTATGGTTTATTTTTAAAAT
Associated Phenotype:
Not determined