ZMP
ENSDARG00000091548
Ensembl ID:
Alleles
There are 20 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32167 | Essential Splice Site | Available for shipment | Available now |
sa11459 | Essential Splice Site | Available for shipment | Available now |
sa16123 | Nonsense | Available for shipment | Available now |
sa16149 | Nonsense | Available for shipment | Available now |
sa14840 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42980 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5903 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15359 | Nonsense | Available for shipment | Available now |
sa36482 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23141 | Nonsense | Available for shipment | Available now |
sa16538 | Nonsense | Available for shipment | Available now |
sa36483 | Nonsense | Available for shipment | Available now |
sa12181 | Nonsense | Available for shipment | Available now |
sa28904 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23142 | Nonsense | Available for shipment | Available now |
sa36484 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32167
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123298 | Essential Splice Site | 16 | 3594 | 1 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38644082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38528979 |
GRCz11 | 17 | 38476564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGGCCAACGTGAAAGTCGCGATTCGAGTCCGTCCACTGAACACCAGG[T/C]ACAGCAATCTGTTTTAAATAGCATGAATTAACTGTAAAGATGCATGAGAG
Long Flanking Sequence:
TTCCTACTATGGCGATGACATTGCTCATGAATATTAAAAAGAAAGATAATTTTATTCAGCTGCAGATCCGCGAAAACAACCAAATCGAATTAATATTAAAAATCATGTCCTTAATCAAAATAGAAGCAGGAATTCTGCGAACCATTGCGCACTATAGAACCAACGTCATGCTGCTCTCAGATATTCATGAGCCACGCCTTCACCGTAGTAGGATCCGTAAGCTCTCCTCCCATAGAGACGGCAGGAAGTTTCAGCGCAGTTCAAGCGCAGTCGCGGCTCCACGATGTGCTCAGCGATTGTCTAGACGATATCAATAACATGAGCCGAAAAACTTCTCATGGCTTTCATCACTCTGCTCGGAATTATTCGGAGCTCTTTATGGATTTAATAACTGGACTTTAAAGGACAGCAAGACTTCAGTTCACAGTTTCTCTCCTCCCGGTGTCAAACGAATGGCCAACGTGAAAGTCGCGATTCGAGTCCGTCCACTGAACACCAGG[T/C]ACAGCAATCTGTTTTAAATAGCATGAATTAACTGTAAAGATGCATGAGAGAGTGATGCGGAATGAAGCTGATAAACATCCTCGAGGTGTTGGTGCTGTTGCTATGTCAGGGAATAAACCTGCACTGACAGCCAACCGAAACTAGAACAAAACAAACAGTTAATTAAAACTTCTCCCTTATTATGCAAATCTAGGCTATATAGTGAAATAGATATATATTCGTAGATTTAACATAACGCATCAAGAATAAATTAAGCCTAAAAACTTTTCAAAACAATGCATAACCATGCTATAAAGGAATGCATGTATAATAATCAGTAAATCAGTTATATTGAGCTGCAATGTGCTTTTGTGCATGATAAAAATACTGTAATCTCCAAAACCTCTTTGAATCACGTTAAACCCTAAAAGTTATTCTTATCAAATGATTTTTAATATCTTGCAGCATCATCAGTAACATGCATGCTGTATTACACAAAAAGAAAGTTAAATGTGTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11459
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Essential Splice Site | 132 | 3594 | 5 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38678436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38563333 |
GRCz11 | 17 | 38510918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTTTGSCTTCTCAGGACTCCATTGGCCTGACACCAAGGATCTGTCAA[G/A]TAAGTCAAAACTGAAAATGGAATCARCATGTTCGCTCCTTCAYGTCATTT
Long Flanking Sequence:
GCAGCACATTCTCTATGCTCCACACACACATGCACAAACATTAGCAGATAACCTTCAAAGCCCAGTCTCTCTCTCTTTCTCTCTCTCTTACTCAAATAAGCACAGATCATGATCTCTCAATAAACATGATCAAAGAACACAGAAGGGGAATTTCACAACACCTTTACACCTTTGGGGTTTTTTAAATGTAAAATTGACATGTTAACAGAGATAAAGTGCAGTTTCTTCAAATTTTAAAAAGTGATTGATACAAGTGTCATCTCGTCTTCTAGGTGTTTCAGGACCTGGGTGTGTGTGTCCTGTCTGGGGCTTCAGAGGGGTATAATGTGTGTCTGTTTGCATATGGACAGACAGGCTCGGGGAAGACGCACACCATGATGGGTACTCCTGTAAGTAACAGTAGTAGCATGAGATGAAGATAAAGCATTTTTCAGCATAAATATAACACATCCTCTTTGCCTTCTCAGGACTCCATTGGCCTGACACCAAGGATCTGTCAA[G/A]TAAGTCAAAACTGAAAATGGAATCAACATGTTCGCTCCTTCATGTCATTTCAAGTTATTTTGTTGTATTTGAATTCATCTTTAAATAGCAAAGATTTTTTTAATGAATAAAGTCTTGATCTCACTGAAAGTCCGTGTTGCAAAAGTAAACATTAGGTTATTTAAAAAATGTATTTCAAGACATATAACCATATATGTATTTGTGACATATTCTATTGCATTAGTAACTTAATTTAGATACTTTGGAAGACTTAAGGTATGTAGCAAAAAGAGTCCTATATACTGTATACAGTTGAAACCAGAAGTTTACACACACTCTAAAAACGGAACATAACCATTTTTAAAAAAATGTCTGGTGTTAAATTATACTAAACGTTTACTATTTTATGTTCAATAGGATTACCTATATGATTTCATTCATTCATTTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGAGGAATGAACCGCCAACTTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16123
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 201 | 3594 | 8 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38682802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38567699 |
GRCz11 | 17 | 38515284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTGTGTTTATGTTAGGTCTTTCTCAGCATGTCGTGACTGACTACAAA[C/T]AAGCAGTGGATCTGTTGGAGGAGGGTATYGCTAACCGCATCACAGCCGCT
Long Flanking Sequence:
TTAGTTTAGATTACAATTCACGGGATTAACAAACCATCAACTAACACTTGTATCTTATAAAAACTACTAATTAGCTGTTTATTAATTAGTTAGTAAGGTAGAAGTTTTGTTTAGGATTACGGATGCAAAATAAGATCATACTGTATAACTACTAATGAACCGTTAGTAACTTAATAATAAGCAGGCAATAAGCCAGTAGTTAGCATAAATTGTGACAAACTAAAGGGTTACCTTTATTATTATAATTATTGTTTTTGAACATTACTTGCTATACATGCTCACAGCAACTGGGACAAAACTTTGATCTGTTTACATCTAAATTCTATTAGTATATGTTTTAGCACTGTAGTCCGTATTACGAACAGAGCGATGATTTTTGTTTACGCTAATATAAGTGTGGATCAGGAATAGAGTATCTGTGACTCATATTGTGGAAAGGATTATGATGCTATTGTGTGTTTATGTTAGGTCTTTCTCAGCATGTCGTGACTGACTACAAA[C/T]AAGCAGTGGATCTGTTGGAGGAGGGTATCGCTAACCGCATCACAGCCGCTACACACGTCCATGATGCTAGCAGTCGATCCCATGCCATCTTTACCATCCAGTACACACAGGTCTGAAGCTCAAATCATGTCCTTAAACACTCCAAGGTTCTCCATTAAACTTTTTGTGTATGTAAAGTAATATGACTGGATTAGTTGTATGAATTTTGGTGGCAAAAACGTTTTTGTATCACCTCGACACTACTGTTTGATAGGTGGGATTCAGTGTTGTTTTTAATGCTGCAATTAACAATATGTTCAAATATAAAATAGTAAAAATTATAATATTTAACAATATTTTGTGTTTTTGCATTTTTTAACCTTTTTTCCCAGTTTTAGTCATTAAGAAATCAGCTATAAGCAGTAGGCAGTGTGTTAGATTAAAAGGGATATTTTGCAGTAAATAACATAATTGTAAGATGTATATCCACATTCTGGGAAATAGAGAAAAAAATACATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16149
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 760 | 3594 | 21 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38703507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38588404 |
GRCz11 | 17 | 38535989 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATCGTGTGCGCCGCAAAAGGTTACATTACCAGCTGGAGAAGATTGCA[C/T]GAAAGCGCCATCTGTTGGAGGCAAAGCGTGAACTGCAGAGGCTGGAAAAT
Long Flanking Sequence:
CATATAGTAAGTACATGTAGTTTATTAACATTATCAAGTTGTTAAATGAATATTTAGACTGTAACTTGACACTTGAAGTTAACTGAAAATTTTTATGGAATTTGGAATAACGTGAGATATGTACATTTTGATTTTTATTTGAACTTTAAAACCAAATAAATCTTGGCTTTTTGTCCTAATAAATATAATAAATTCTAAACACTTTTCTAAAATTCTTTTTATTTTTGCCTAAAGTCCAGCAGTGGATCTTGCAAGAAAATCAGCGACTTGCAGCACACAGGGAAAAAACCACACTGGAATCCGGGGTCCAGACAGATCTTGTACTATCTGTTACTTCTGAAAGTCAGGAGGTCAGAGATGCTGAAACGGTCCCACCATCAATCTCAATGGGAGACAGGAAAAGAGTGGTGCAGGAGGAGCTGCTGAAGCACCATGCATTGCGCAGAGCTGAGAATCGTGTGCGCCGCAAAAGGTTACATTACCAGCTGGAGAAGATTGCA[C/T]GAAAGCGCCATCTGTTGGAGGCAAAGCGTGAACTGCAGAGGCTGGAAAATTTGCATCTAGAAGGTTGCAATGAAACCTCATCTCTAGAATTGGCATACTCTTTAAAGTTAAGGGGACGTCCGATGACTTTAAGAAGGCATTCCTTTTCTGCTGATCTACTGTCCCGGTTGTACCCCCAGCACACTCCTATTTTCAGGTAAGTGTAAACCATCTGATTACTAATTTTTGCCAAAAGGTGCTTTACTTTGGAAGATAACATCATGAGATTATCACAATCATTACACTGAGAACAGCATTTAAATAAATATTTTCTTTTCTTTAATCCAAACAGCCAGTTCCTTAAAAGGAACAAATCTTCTGACTTTACATACACTAAATGGGAATCTGATGAATGTCTCCAAGATCAAAAGATAAGAAGGCGTTCAAACACGATGCCCTCCAGATATGATCAAGGATCCTCAAGCTGGGCCAGTTTCTCAGACAACCTCGAAAGTCCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14840
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 796 | 3594 | 21 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38703616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38588513 |
GRCz11 | 17 | 38536098 |
KASP Assay ID:
1641-0504.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGGKTGCAATGAAACCTCATCTCTAGAATTGGCATACTCTTYAAAGT[T/A]AAGGGGACRTCCGATGACTTTAAGAAGGCATTCCTTTTCTGCTGATCTAC
Long Flanking Sequence:
ACGTGAGATATGTACATTTTGATTTTTATTTGAACTTTAAAACCAAATAAATCTTGGCTTTTTGTCCTAATAAATATAATAAATTCTAAACACTTTTCTAAAATTCTTTTTATTTTTGCCTAAAGTCCAGCAGTGGATCTTGCAAGAAAATCAGCGACTTGCAGCACACAGGGAAAAAACCACACTGGAATCCGGGGTCCAGACAGATCTTGTACTATCTGTTACTTCTGAAAGTCAGGAGGTCAGAGATGCTGAAACGGTCCCACCATCAATCTCAATGGGAGACAGGAAAAGAGTGGTGCAGGAGGAGCTGCTGAAGCACCATGCATTGCGCAGAGCTGAGAATCGTGTGCGCCGCAAAAGGTTACATTACCAGCTGGAGAAGATTGCACGAAAGCGCCATCTGTTGGAGGCAAAGCGTGAACTGCAGAGGCTGGAAAATTTGCATCTAGAAGGTTGCAATGAAACCTCATCTCTAGAATTGGCATACTCTTTAAAGT[T/A]AAGGGGACGTCCGATGACTTTAAGAAGGCATTCCTTTTCTGCTGATCTACTGTCCCGGTTGTACCCCCAGCACACTCCTATTTTCAGGTAAGTGTAAACCATCTGATTACTAATTTTTGCCAAAAGGTGCTTTACTTTGGAAGATAACATCATGAGATTATCACAATCATTACACTGAGAACAGCATTTAAATAAATATTTTCTTTTCTTTAATCCAAACAGCCAGTTCCTTAAAAGGAACAAATCTTCTGACTTTACATACACTAAATGGGAATCTGATGAATGTCTCCAAGATCAAAAGATAAGAAGGCGTTCAAACACGATGCCCTCCAGATATGATCAAGGATCCTCAAGCTGGGCCAGTTTCTCAGACAACCTCGAAAGTCCTTTAAAGGATTCAAGTTCAGCTGAAGCAACAAAAGCAAAAACTGCTTCCACAAGGTTGCTAGTCAAGAAAAGCACTAGTGATCAAGACAAACATTGTCTGGACTCAAATACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42980
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 1171 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38704877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38589774 |
GRCz11 | 17 | 38537359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAAATTGGAGACAAAAATATCCAAAGATGTGCCTGCAGAGGTTTACTG[G/A]AGCTTAAATGGTAGTCAGAAGCTAAAAACTGAGAATGGCCAAGGCATGGC
Long Flanking Sequence:
GACTTGGAGAAAATACACAAACAGTCCCCCATCAAATCAGCAATGTCATATGAAAGTTTAGGGCGGGTTGGCACACTAAAATATCAACACCAGAGGCACTGGCATAGTGCAGAAGCATTGACTAGTACTAAGCAATCGGTAGAAGTACAAAATAAAGCAGCCGGGTGGGTGGAACATGGCGATGTGGAGGACTCCAACAGATCTTCAGATTGTGAAAGTATTTTTTCATTAGACTCTCTCTCATCAGCTTACGCTAGAGCTCTGGCTGAGCAGCTTCAGCAAGAGGAATGTGATTCCAGTGAAGCTGAGAGTGAAGACAGTCAAATGTCCCAAGATTCTCTTGTTATGGAGAACAGTTGGAAGCATATGACTGCCAGACCTATGCTGAGGTTCAATAAGGTTCCAAGTCATCTAACTGTATCTACCTCATGTGGCTCTCCATCAATCAGTAATAAATTGGAGACAAAAATATCCAAAGATGTGCCTGCAGAGGTTTACTG[G/A]AGCTTAAATGGTAGTCAGAAGCTAAAAACTGAGAATGGCCAAGGCATGGCTAAAGGGCCTTCAAGCCTATCTTTTCTAGCATCTGAATCTAGGCCTTGCAGTGGTGCGAGTAACAGAGAGACAGAGAATCCACTTGCTCTTACTGATGCTTGGTCATCCACCGATGCAGCAGACAGTCCCCGTATCATCAGGGCATCAGGACACTTCAAGCAGGATCCACCGACACTGATAGAGAGCAGGAGTCTGGATCTGATCGGCAACAAAAATGACTTAGAAAGCCAGAGCTCACCTTGCTCTGACACCACTCAGGGTGAAAATGCAACACTTGAATCAAACGACACGTCATTTGAAAACACCCTGTTGCTTGATAACCATGAGAGTGTACCTACATTTATCCCAGGAATCCAGGATCTCACTGCTGAGAAAGATCCATGTACAATTCACACAGTCTATGATTTTACAGATGCCAGTCTAGATGGGGTAGCATGCACAAATAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5903
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 1269 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38705171)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38590068 |
GRCz11 | 17 | 38537653 |
KASP Assay ID:
554-3929.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGATCTGATCGGCAACAAAAATGACTTAGAAAGCCAGAGCTCACCTYG[C/A]TCTGACACCACTCAGGGTGAAAATGCAACACTTGAATCAAAYGACACGTC
Long Flanking Sequence:
TCCAGTGAAGCTGAGAGTGAAGACAGTCAAATGTCCCAAGATTCTCTTGTTATGGAGAACAGTTGGAAGCATATGACTGCCAGACCTATGCTGAGGTTCAATAAGGTTCCAAGTCATCTAACTGTATCTACCTCATGTGGCTCTCCATCAATCAGTAATAAATTGGAGACAAAAATATCCAAAGATGTGCCTGCAGAGGTTTACTGGAGCTTAAATGGTAGTCAGAAGCTAAAAACTGAGAATGGCCAAGGCATGGCTAAAGGGCCTTCAAGCCTATCTTTTCTAGCATCTGAATCTAGGCCTTGCAGTGGTGCGAGTAACAGAGAGACAGAGAATCCACTTGCTCTTACTGATGCTTGGTCATCCACCGATGCAGCAGACAGTCCCCGTATCATCAGGGCATCAGGACACTTCAAGCAGGATCCACCGACACTGATAGAGAGCAGGAGTCTGGATCTGATCGGCAACAAAAATGACTTAGAAAGCCAGAGCTCACCTTG[C/A]TCTGACACCACTCAGGGTGAAAATGCAACACTTGAATCAAACGACACGTCATTTGAAAACACCCTGTTGCTTGATAACCATGAGAGTGTACCTACATTTATCCCAGGAATCCAGGATCTCACTGCTGAGAAAGATCCATGTACAATTCACACAGTCTATGATTTTACAGATGCCAGTCTAGATGGGGTAGCATGCACAAATAAACCAACTGCTGAACCACTAAATACCATTGTGACTGAAGCACTGTTGATTGATTGTTCTTCCAAAGATGGGGACATCTCAACAAGTTCCAGTATTTCAAAGTGCTTCTTGGTCAACAGTACAAAGGAAGATTCAGATATTAGAGAGGACAATCCATCATCATCCCATGATCACCCATCTGTTTGTCAGGTTCCTCCATACAATAATGCAGGAAATTCAGAAATTAAGATCTCTGAAACCGCAAAAGTTCTTAATGAATTGCACAGCATTGCCAGCAATGGCCAAACCAATGCACAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15359
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 1685 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38706417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38591314 |
GRCz11 | 17 | 38538899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAAACTGGATGAATTCAAGTATGAGACGAAYCMCCATGAATATGATTAC[A/T]AAAGTATGCAGGATRGACAWTGTGAAAGTAGCTGTTCCCAGTTGTTCCCT
Long Flanking Sequence:
GTTCATCCATCAACAGTGAATCTGTAACCAGTGTATCTCTTTTGGAAAATTTGCCCACTAGGATGCAAAACTCTGATCAGGACAAGGAAATGAAAAGTGCCTCATCAGCCAGCGACGCCTACAGGGCTTTAATCAGCAAAGATCACATCAGTATTTTTAGAAATGACTGCACTGCATGCGATAATGGGTTGACGCAAACAAATTGCACTAGCCTGAAATCCTTTAGTAGTCCTGAGATTAAAAACATTACTGAAAACAGTAAAGAGCATAGAAAAGATGCTGTTCAGATTATAGACAGAAAAACGTTGAATAACAGATATTTTCAAATGAGTGACACAGCAATTAACGATAAGATATCAGAGGTGGTGAAAGAACACTTTAATTTGTCTTTGAGAGAAGACTGTGGTGAAGATTACAAGTTGGATAGCAAGAAGAAAATCTCTTCTTTGACTAAACTGGATGAATTCAAGTATGAGACGAACCACCATGAATATGATTAC[A/T]AAAGTATGCAGGATGGACATTGTGAAAGTAGCTGTTCCCAGTTGTTCCCTTTCTCTTGTATGGCAATTTCTACAGACAACACTATTGTGCTGAATGGCAATACAGAATCAAAGAATTTGCTGCCTACGAAGGATCAGGCATTCTTGAACTCCAGTGGCACAGAAGAGGCTACTGATAGAAAGACGGAGGGGAAAGTGGAACAATGTGGATATATTAATGAAGATGTGGAGTCAGTACTATATTGCACTATAGAATCACAGGGCACATTTGAATCAATGCTGCCATGTGTTAAAGAAACTGTTATTGGACTGAATACATCAAAAGAGAACATTATCGTCTGCACAGAACTAAGAAAAGACTATAGTGATGCTGCAAACCCTATTAAAAGGAATTGTTGCACCAAAAAACAGGTTATGGAGAATGGCAGTCCCACAGTATTAAAACCAGTGGTTTGCAAGCATGCACAAGCTACTCAGACTATTCAAATTACAAATGAGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36482
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 1887 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38707024)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38591921 |
GRCz11 | 17 | 38539506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGACTTGGCCAACTTCAAAAGAAATGCACAAATTTTATGAGCAACCAT[C/A]AATACATAAAACTTCAGGACTGTTAAATGAACTCAGATGTTCAGCAAGTG
Long Flanking Sequence:
ATCAAAGAATTTGCTGCCTACGAAGGATCAGGCATTCTTGAACTCCAGTGGCACAGAAGAGGCTACTGATAGAAAGACGGAGGGGAAAGTGGAACAATGTGGATATATTAATGAAGATGTGGAGTCAGTACTATATTGCACTATAGAATCACAGGGCACATTTGAATCAATGCTGCCATGTGTTAAAGAAACTGTTATTGGACTGAATACATCAAAAGAGAACATTATCGTCTGCACAGAACTAAGAAAAGACTATAGTGATGCTGCAAACCCTATTAAAAGGAATTGTTGCACCAAAAAACAGGTTATGGAGAATGGCAGTCCCACAGTATTAAAACCAGTGGTTTGCAAGCATGCACAAGCTACTCAGACTATTCAAATTACAAATGAGATGGATAAAGAACAAAAAGTAAATCAGTGTGCACAGATGAAAAATGAAACAAAACTAAATCAGACTTGGCCAACTTCAAAAGAAATGCACAAATTTTATGAGCAACCAT[C/A]AATACATAAAACTTCAGGACTGTTAAATGAACTCAGATGTTCAGCAAGTGAAAAATTTCTTATGGAGATGTCAACTCCAGTAGAGTCCAGTAAACGTGACAATCTTCAAGCATCGCTACCCACCAAAACAACAGTGAAACAGACAGTCTCTTTAGAGACCGAAAGAGATTTGGCTGATACATGGCAGAAAAGCATGGATGACAGCACTGGAATATTACCTAACTTAGAGGTACAAAATAAAAAGACATGTTCACATAACTCTTCTACATCAAGTATGGAACATTGGAACTCAAGTGAGGATGACAGTTACCCTGTTCCTGAAGTCCGACCTCTAAGCAAGTTAGCCTTTTATGAATTTGGTCCAAGAAACCATGAAAAACCTTGCGATGAACCTTGTGCTGAACATTCATTGAAGAACTACGCCACTATGATCAGTAGTTGTGATAATAAAGACAAAGTAAGATCTGCAGAGCACATACATATCAAAAAAGATGCTGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23141
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 1900 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38707064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38591961 |
GRCz11 | 17 | 38539546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAACCATCAATACATAAAACTTCAGGACTGTTAAATGAACTCAGATG[T/A]TCAGCAAGTGAAAAATTTCTTATGGAGATGTCAACTCCAGTAGAGTCCAG
Long Flanking Sequence:
AACTCCAGTGGCACAGAAGAGGCTACTGATAGAAAGACGGAGGGGAAAGTGGAACAATGTGGATATATTAATGAAGATGTGGAGTCAGTACTATATTGCACTATAGAATCACAGGGCACATTTGAATCAATGCTGCCATGTGTTAAAGAAACTGTTATTGGACTGAATACATCAAAAGAGAACATTATCGTCTGCACAGAACTAAGAAAAGACTATAGTGATGCTGCAAACCCTATTAAAAGGAATTGTTGCACCAAAAAACAGGTTATGGAGAATGGCAGTCCCACAGTATTAAAACCAGTGGTTTGCAAGCATGCACAAGCTACTCAGACTATTCAAATTACAAATGAGATGGATAAAGAACAAAAAGTAAATCAGTGTGCACAGATGAAAAATGAAACAAAACTAAATCAGACTTGGCCAACTTCAAAAGAAATGCACAAATTTTATGAGCAACCATCAATACATAAAACTTCAGGACTGTTAAATGAACTCAGATG[T/A]TCAGCAAGTGAAAAATTTCTTATGGAGATGTCAACTCCAGTAGAGTCCAGTAAACGTGACAATCTTCAAGCATCGCTACCCACCAAAACAACAGTGAAACAGACAGTCTCTTTAGAGACCGAAAGAGATTTGGCTGATACATGGCAGAAAAGCATGGATGACAGCACTGGAATATTACCTAACTTAGAGGTACAAAATAAAAAGACATGTTCACATAACTCTTCTACATCAAGTATGGAACATTGGAACTCAAGTGAGGATGACAGTTACCCTGTTCCTGAAGTCCGACCTCTAAGCAAGTTAGCCTTTTATGAATTTGGTCCAAGAAACCATGAAAAACCTTGCGATGAACCTTGTGCTGAACATTCATTGAAGAACTACGCCACTATGATCAGTAGTTGTGATAATAAAGACAAAGTAAGATCTGCAGAGCACATACATATCAAAAAAGATGCTGGCAATTCAGATTTAGGCCAGAGATCACAAAAACCACAAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16538
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 1911 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38707096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38591993 |
GRCz11 | 17 | 38539578 |
KASP Assay ID:
2261-1396.1 (used for ordering genotyping assays)
KASP Sequence:
GTTAAATGAACTCAGATGTTCAGCAAGTGAAAMATTTCTTATGGAGATST[C/A]AACTCCAGTAGAGTCCAGTRAAYRTGACAATCTTCAAGCATCGCTACCCA
Long Flanking Sequence:
AAAGACGGAGGGGAAAGTGGAACAATGTGGATATATTAATGAAGATGTGGAGTCAGTACTATATTGCACTATAGAATCACAGGGCACATTTGAATCAATGCTGCCATGTGTTAAAGAAACTGTTATTGGACTGAATACATCAAAAGAGAACATTATCGTCTGCACAGAACTAAGAAAAGACTATAGTGATGCTGCAAACCCTATTAAAAGGAATTGTTGCACCAAAAAACAGGTTATGGAGAATGGCAGTCCCACAGTATTAAAACCAGTGGTTTGCAAGCATGCACAAGCTACTCAGACTATTCAAATTACAAATGAGATGGATAAAGAACAAAAAGTAAATCAGTGTGCACAGATGAAAAATGAAACAAAACTAAATCAGACTTGGCCAACTTCAAAAGAAATGCACAAATTTTATGAGCAACCATCAATACATAAAACTTCAGGACTGTTAAATGAACTCAGATGTTCAGCAAGTGAAAAATTTCTTATGGAGATGT[C/A]AACTCCAGTAGAGTCCAGTAAACGTGACAATCTTCAAGCATCGCTACCCACCAAAACAACAGTGAAACAGACAGTCTCTTTAGAGACCGAAAGAGATTTGGCTGATACATGGCAGAAAAGCATGGATGACAGCACTGGAATATTACCTAACTTAGAGGTACAAAATAAAAAGACATGTTCACATAACTCTTCTACATCAAGTATGGAACATTGGAACTCAAGTGAGGATGACAGTTACCCTGTTCCTGAAGTCCGACCTCTAAGCAAGTTAGCCTTTTATGAATTTGGTCCAAGAAACCATGAAAAACCTTGCGATGAACCTTGTGCTGAACATTCATTGAAGAACTACGCCACTATGATCAGTAGTTGTGATAATAAAGACAAAGTAAGATCTGCAGAGCACATACATATCAAAAAAGATGCTGGCAATTCAGATTTAGGCCAGAGATCACAAAAACCACAAATTCACAATAAGCTTATTGAGAAAACTGACAAGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36483
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 2457 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38708733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38593630 |
GRCz11 | 17 | 38541215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATAAAGGGCTCTCCAGCACACTGAGTAGTAATGGATATTCTAGAGAT[C/T]AAATTTCTTCTGAACCTTTGCTGAAGGCCACTTCTTTGTCCTCAAGTGGT
Long Flanking Sequence:
CTGTGGTTGGAGCTCTCATACACAGGGAGGCTGGAATTAAGACAACTGCATGTCAACAAAAGAATGGTTCAACTGTTAAAATCCAACCAACCAAGATAATTGAAACAAAGCATAATAAAAATGTTACTTTAGGGAAGAATGGGTCTTCTGATGATGTTTTAGTTGATTGTGTGGAAGTACATGGTAATCTAGTTGATACCGTTTCAGACAGAAAAGATTCTGCAATGCATTTTGCCTCGAGTGATATTAACCCATATATTCACACAAGAACTGCTATAGGCACAAACCCAGCAGTCCACAAAAAGCAGGCATTTGGAAGTGTAGCCAATATATCCTGCCATCACTCTCCGCCCAGTAGTTCTAACAAAAATATGACCAGGTGCTGTAGTGTAGACAATGGGCTGAATATTCAGGACTGCCCTTTCAGTTCCCATTTGAGCGCATATGTAAATAATAAAGGGCTCTCCAGCACACTGAGTAGTAATGGATATTCTAGAGAT[C/T]AAATTTCTTCTGAACCTTTGCTGAAGGCCACTTCTTTGTCCTCAAGTGGTTTTGATAAGCAGACTCCAAATGATTTGAAATGTGAGTCTTGCAATGACGCTTCCGAGGAGTTATGCAACTGTTCAGGTCAAGTTGATGAAATAGTACTGGTCTACTCTTCTGAATATGAATCTCCGGAACAACCAAATCCAAGCACTTGTGATCAAGGCACACAGACCATTAAAGCCAATAAAGACCTTAAAACCAAGAGCCGTCATAGAAGAAGCAGCACTCAGACACCATTGTCCAAACCAGGAAACAGTGCCCAAACCACATGGGCAAGTCTACAGAACATGTCTGAACATCTTTCTGACCTGATACACAACACCTCTGATCTTCTAGGGAACATACAATGTATGCGGACAGGAGAAAAGCCTTCAAAACATGACCTTCCTAAACCCTGTTTTCAGGTTTCTACTGCACATTCTGGCAGTAACTACAAGAGGGACTGTTGTACACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12181
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 2675 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38709387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38594284 |
GRCz11 | 17 | 38541869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAGTGTATCCCAGCTAGATGGTGAGGCCAAGATCTTGAAGAACAATTAT[G/T]AAAGTGAACAGGCCTAYGAMAGGATAAAAAGCATGCCTGATTTACGTCCC
Long Flanking Sequence:
ACTCTTCTGAATATGAATCTCCGGAACAACCAAATCCAAGCACTTGTGATCAAGGCACACAGACCATTAAAGCCAATAAAGACCTTAAAACCAAGAGCCGTCATAGAAGAAGCAGCACTCAGACACCATTGTCCAAACCAGGAAACAGTGCCCAAACCACATGGGCAAGTCTACAGAACATGTCTGAACATCTTTCTGACCTGATACACAACACCTCTGATCTTCTAGGGAACATACAATGTATGCGGACAGGAGAAAAGCCTTCAAAACATGACCTTCCTAAACCCTGTTTTCAGGTTTCTACTGCACATTCTGGCAGTAACTACAAGAGGGACTGTTGTACACAAACTTCATTGGACATTGGTGTCCAGACAGAGATTGCTTCAGCTTCAAAGAATGCTACAGCTCATGAAGTAAATGTTATTGTTAAATTGATTGGCTCAGATATTTGTAGTGTATCCCAGCTAGATGGTGAGGCCAAGATCTTGAAGAACAATTAT[G/T]AAAGTGAACAGGCCTACGAAAGGATAAAAAGCATGCCTGATTTACGTCCCAGAGGCTCAAAGGTAACTGGCAGTCAAAATGGTCTGACTCCTTCACAAAGGGTTATTTCATTAGACACTGTTGTGCCAAATCAGGAGTCCTCAACTTTGGAAGCATTTGAAAGTAGTAAAGTAGACCCTTCCTTTAAGAGGTCTTTACCCAGCTACCTTGAAGCAAAACACTCAAATATGAAGCTAGAGAAGAATCAGACTTGTACCAGAAATGTAGACCTAAAGAATGGCTTTAGTAAACAAGTTATGCTTATGGATCGCGCATGCTCCCCTATCCTAACTCTGAAGGCTGCAAGATACTCTCAGCAGAAACTCTTACAAACAAACCTTAAGACAACCAAAGGACAAAAAGAATGCTCCAATTTATACAGCATGCCATTAAAATGTCATAAAATATCTAACTATGAACAAATGGCTCTAGATCAGCAGAAGGCTTGTAGAAATGCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28904
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 2772 | 3594 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38709678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38594575 |
GRCz11 | 17 | 38542160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATCAGACTTGTACCAGAAATGTAGACCTAAAGAATGGCTTTAGTAAA[C/T]AAGTTATGCTTATGGATCGCGCATGCTCCCCTATCCTAACTCTGAAGGCT
Long Flanking Sequence:
TTCAGGTTTCTACTGCACATTCTGGCAGTAACTACAAGAGGGACTGTTGTACACAAACTTCATTGGACATTGGTGTCCAGACAGAGATTGCTTCAGCTTCAAAGAATGCTACAGCTCATGAAGTAAATGTTATTGTTAAATTGATTGGCTCAGATATTTGTAGTGTATCCCAGCTAGATGGTGAGGCCAAGATCTTGAAGAACAATTATGAAAGTGAACAGGCCTACGAAAGGATAAAAAGCATGCCTGATTTACGTCCCAGAGGCTCAAAGGTAACTGGCAGTCAAAATGGTCTGACTCCTTCACAAAGGGTTATTTCATTAGACACTGTTGTGCCAAATCAGGAGTCCTCAACTTTGGAAGCATTTGAAAGTAGTAAAGTAGACCCTTCCTTTAAGAGGTCTTTACCCAGCTACCTTGAAGCAAAACACTCAAATATGAAGCTAGAGAAGAATCAGACTTGTACCAGAAATGTAGACCTAAAGAATGGCTTTAGTAAA[C/T]AAGTTATGCTTATGGATCGCGCATGCTCCCCTATCCTAACTCTGAAGGCTGCAAGATACTCTCAGCAGAAACTCTTACAAACAAACCTTAAGACAACCAAAGGACAAAAAGAATGCTCCAATTTATACAGCATGCCATTAAAATGTCATAAAATATCTAACTATGAACAAATGGCTCTAGATCAGCAGAAGGCTTGTAGAAATGCCAAAACAATATCTAAATCGCTATCATCCATGAACTTTGAAAGCCTGAGCAACCTTGCTTGTCCAAATCTGGATGGATCTGAGGACTTCTCAAATGCCGTCTGTCCCCGCATGTACAATGAGGGAAACAAATACTATCATGAAGTTGAGGACAGGGTAACAAGCAAACAAAAAACTTGTTCTCCGACTCATCTCCAAAGAACATCCTATTCCACTTCAAGTGGTACCATTGATGTCCAACTTGCATCATCCTCAGTTAAAGTCAGGCAATCTAAAATGGAATCCTCAGACAAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23142
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 3395 | 3594 | 28 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38716103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38601000 |
GRCz11 | 17 | 38548585 |
KASP Assay ID:
2261-1399.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGAATGTGAAATACTTCATTGGTATGCTTGTCTGTTTTAGGTATATT[T/A]GGCCTCTGGAGGTGATGTGAGGAATCTGCTGGCTGGGAAGGCAGCAGCTG
Long Flanking Sequence:
TCATTTTTTTTCATTCAAAATGCTTTTTTTCTTAGTATTCATTCTCCTTCTCCTTAGGTGAATGGAGTCTCAGACTTCAAAATAAGGACTCGACCTCCTTTGATTCCGTTGCAGACTTCAAAAGCCCAGCGTAAATGGCTATCAGTCCAAGGTGAGCATTAATTGGATAACAATTGCAAACCTTAGTGTTATTAGTATTATGCTTTGAATCCACCTAATTAACCAGATTACGTATTCATACTAGATGTCAGCCTGGAGACTTCTGTCATTGGATATGAGCCTGAGTCATCCTCCACTCCATCATCTCCTCCCTGTGCTCGACAGCGCACTCTTTCTTTCGGCTCTCCCTCGTCCATGTTGACTTCATATCAGGATATTGCAGACTGCACACTTGCCAGTGCAATTTCAGAAGTATGCAATTGTTCATCTAGGTTCAAAATATACAAGGACACATGAATGTGAAATACTTCATTGGTATGCTTGTCTGTTTTAGGTATATT[T/A]GGCCTCTGGAGGTGATGTGAGGAATCTGCTGGCTGGGAAGGCAGCAGCTGGCTGGAGGTACACTAATGCATATTGTTTTTGTATAAGTATTTTACATGTTTTCCATCCTCATATTTAATTTCTAACTAGGCACCAAGGTGTGGAAAGAGGAATTCAGGTGTTTTACAAGGCCACTTCAAGAACTTCAGCTCATGGGTTTCTTGGAGCAGTCGAGCTGGATAGACCTTTGTCCAGTCTGTGGTCTATAGTTCGAGATCACTCAAAGATTCACCTTTACAACGAGTCTGTTAAATCTGCCTGGACACGACCACTGGATGAAAGCACACAACTTGGTAAAACCCAAGATTTTTGATATCATAAAGGGTTTCTGTTGTCTAATGGTAAATTTTAAGTCACTAGCTATGTTTCCATCTACCTATTTTTATGTTTATTTTGGAATATCGCATAAAACCTGCTTAGTGGAAATGCCAAGATGCACAAATATTTTGAAAATGCACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36484
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 |
---|---|---|---|---|---|
ENSDART00000123298 | Nonsense | 3480 | 3594 | 29 | 32 |
Genomic Location (Zv9):
Chromosome 17 (position 38716429)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38601326 |
GRCz11 | 17 | 38548911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACGAGTCTGTTAAATCTGCCTGGACACGACCACTGGATGAAAGCACA[C/T]AACTTGGTAAAACCCAAGATTTTTGATATCATAAAGGGTTTCTGTTGTCT
Long Flanking Sequence:
CACTCTTTCTTTCGGCTCTCCCTCGTCCATGTTGACTTCATATCAGGATATTGCAGACTGCACACTTGCCAGTGCAATTTCAGAAGTATGCAATTGTTCATCTAGGTTCAAAATATACAAGGACACATGAATGTGAAATACTTCATTGGTATGCTTGTCTGTTTTAGGTATATTTGGCCTCTGGAGGTGATGTGAGGAATCTGCTGGCTGGGAAGGCAGCAGCTGGCTGGAGGTACACTAATGCATATTGTTTTTGTATAAGTATTTTACATGTTTTCCATCCTCATATTTAATTTCTAACTAGGCACCAAGGTGTGGAAAGAGGAATTCAGGTGTTTTACAAGGCCACTTCAAGAACTTCAGCTCATGGGTTTCTTGGAGCAGTCGAGCTGGATAGACCTTTGTCCAGTCTGTGGTCTATAGTTCGAGATCACTCAAAGATTCACCTTTACAACGAGTCTGTTAAATCTGCCTGGACACGACCACTGGATGAAAGCACA[C/T]AACTTGGTAAAACCCAAGATTTTTGATATCATAAAGGGTTTCTGTTGTCTAATGGTAAATTTTAAGTCACTAGCTATGTTTCCATCTACCTATTTTTATGTTTATTTTGGAATATCGCATAAAACCTGCTTAGTGGAAATGCCAAGATGCACAAATATTTTGAAAATGCACATTAAAAATGTATAATAAACTTTTTGTCCAATACCCTATGGAAATGCACTTACTGAATATATTCCAGTATGCGCATGTGATTTTATTTGAACTGATCACATGATAACAAAAATGGGCTAGATGGGACAAACCAGTGGACCTGCAACACTGTAAAACATCTTAAATGTTGTTTTGGTCATTCAAAAATCCCTTGGTCAAAGTTTGTAATCAAAATTTGGTTTGATTTTATTAACTCCAGAAGTTTCTTAAGTAAAATCGCTCCCAAAGAGTATGTGGACGTAAACTGCATTATTTTCAAATCTTTTATGCAATAAAACTTGCATTTTTGT
Associated Phenotype:
Not determined