ZMP
DNAH5
Ensembl ID:
Description:
dynein, axonemal, heavy chain 5 [Source:HGNC Symbol;Acc:2950]
Human Orthologue:
DNAH5
Human Description:
dynein, axonemal, heavy chain 5 [Source:HGNC Symbol;Acc:2950]
Mouse Orthologue:
Dnahc5
Mouse Description:
dynein, axonemal, heavy chain 5 Gene [Source:MGI Symbol;Acc:MGI:107718]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17217 | Nonsense | Available for shipment | Available now |
sa16138 | Nonsense | Available for shipment | Available now |
sa22759 | Nonsense | Available for shipment | Available now |
sa12420 | Nonsense | Available for shipment | Available now |
sa36046 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39082 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11127 | Nonsense | Available for shipment | Available now |
sa12187 | Essential Splice Site | Available for shipment | Available now |
sa17649 | Splice Site, Nonsense | Available for shipment | Available now |
sa11262 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17217
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 151 | 1974 | 3 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10484460)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9267546 |
GRCz11 | 16 | 9156736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCYAACTTCCACWACATTTTTAACCTGCGTGACCTCTCCCGCATCTGG[C/T]AGGGAATGCTTGGTGTGACTGCAGAGGTCATCAGTACACCTCAAGTGAGT
Long Flanking Sequence:
TGCTTATGCAGAACCAATTCTGTAAATCCATATTGATTCTGATGATGAGCATCTGCTAGCGGTTCCCTCCTTGCCTGAAGGTCTGAGGCTTTTATATTGACAGTTTTTCTCTGTTGATAAGATTTTTCATGCTCTCGACATGTGTGTAAAATTGACATTTCTGACAAGCGGCGGTTCTTTTTTAGCTTCAGTATTTTATCATTCGGGAAGGTCACATTCTGTCCTTCACCTTTGAGAATTTTCCCGCCTGCTATCTCTCAGCTATTTTTCATTCACTTTTGTGTGTCATATATATATATATATCTTTCTTTTTCCCCATAGGCGTGATAGGCACAGGTCATTACTGTTCCCATCGAGGGTTTTCAGAGGAAGTACGCAATACAGTGGGCAGGCTGGTTCCACTGACCCGAAGACTGTGGCAAATGACAAAGGTTAAAATGCTGCCCACTCCTGCTAACTTCCACTACATTTTTAACCTGCGTGACCTCTCCCGCATCTGG[C/T]AGGGAATGCTTGGTGTGACTGCAGAGGTCATCAGTACACCTCAAGTGAGTAGAACTGTTTCTGTTACTTTTGAGGTTTTTTCCGGTCAGTCTTATTAGCCCTTCTGAATTATTAGCCCCCCCCCACCTATATATATTCTGTTTAATGGAAAGATCACATTTCTAAACATAATAGTTTAAATAACTCATTTCTAATAAAAGATTTCATTTATCTTTGCCATGATGACAATAAATAATATTTGACTAGGTATTTTTCAAGACACTATTATTAAGCTTAAAGTGACAAGGCTTTACTGGCTTAATTAGGTTAATTAGGCAATAGGTAGTTAGGCAAGTCATTGTATTACAATGGTTTGTTCTGTAGACAATTAAAAAAATTATTGCATTTTATTGACCTTACAATGGTTTTAAAGAAATAAAAATGGCTTTTATTCTAGCCTAAATAAAACAAATATGACTTTCTCCAGAAGAAAAAATATTGTAAGAAATGCTGTCAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16138
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 203 | 1974 | 4 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10486561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9269647 |
GRCz11 | 16 | 9158837 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGGACGTGGCCTGGTTTGACAGCACACTTGCCAAGCTRGTGGAAGAA[C/T]AGCTTGGGGAAGAAGAACGAGAGGTTGTGGATCTCGGGGTRGATTCTTAC
Long Flanking Sequence:
AAGATTCGCATCATGGATGTGCAGCCGACAAATTTGCAGCAACTGTGTGATGCTATTATGTCAATATGGAGCAAAATCTCTGAGGAATGTTTCTAGTACCTTGTTGAATCGAATGATTAAGGCAGTTCTAAAGGCAAAAGGGGGTCCAACCTGGTACTAGTAAAGTTTACCTTATAATGTGGCCGGTGAGTGTAACTGTCGTGTAACTTTCTTAGAGTTTTGTCTTGTTTGTAGTGCAGCTATCTAGTAATTCCTAGCATTTTCAATAATAAGACTGTAAGAGTTTTTTCAAGCTTAACCTGCCGATTGTGTAAGCAAAATATTCTTGTTTTTCACTTTGAATTGATATTTTCTTTAACAGAGAAATTGTTTCTGAATTGTTTGTGTAGTTATTACTACAGCTGTGGAAGCATGAATGCAAACGTGTTATTGCCGACCGGTTTACTGCCCCAGAGGACGTGGCCTGGTTTGACAGCACACTTGCCAAGCTGGTGGAAGAA[C/T]AGCTTGGGGAAGAAGAACGAGAGGTTGTGGATCTCGGGGTAGATTCTTACTTTGTGGACTTTCTTAGAGATGCACCCGAAGCAACAGGTAATGATGTTAATAGAACTCATCTAAAAAAAAATTACATTGAGTACATTTACATGAACAATCCGATTTTAATACAATTAAGACAATACACTGATTAAGATTAAATTGAAAGCATCATGTTCTGTGTTTCGTCATAAAAGTCCGTATAACTGGCATTAACAAATCAAAATGCAGGTTTTATTTAAACATCGTGTGTGAACTATTTAAATGGTCCATTAACTGTTATATTTCCTACTTCAAATTCACAAAACTGATATTTGGATTTGACGGAGACTTTGGGACATGATTTATAATCCATCCAAGACACGTTTTACCAATGCATGTTTTTTTATTTATTTAATTATTTTTTATTTCATGGGTTTTTATTTTTAGAATGCTGGCACCAGTACAAAATAATAAGTTGTAAAAACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22759
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 347 | 1974 | 7 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10494052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9277138 |
GRCz11 | 16 | 9166301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGTAGTTCCTACAACACCGCTAACCTGATGGAGGACCTGAAGGGCT[T/A]GTACAGGACTGCCGGACAACAGGGCAAAGGCATTAGCTTTATTTTCACTG
Long Flanking Sequence:
TTGACTCAACTTTTAAATACTATAGTTGACTCGATTTAAATTAAGTCAATTTAAAAAGCTGTGCAGCAAGTTGACTTACAATTTTAAGTTTAGGCTTAGGGTTCGTTTTCAGTTTGATTTGGTTTACACTGTATAAACAAAATCCCCATACTTTATTATTTTAGAAATACCATACATCAGCATAAAATACATAGCATTGTAATCTATCTTGGCCCACAGCCAGCCTAGTAAAAGGGTGGTCTTCTTTCTATTAATATTATATTAATTATATTATATATAATTATATTAATGATATTATATTATATATTGTTATATTAATATTCTATTGTATTATATTAATATTCTATCAAGAGTTATTTGCAGTTATATGCCTCATTTTCTATTTAATTATGAGATTTAAATGCTGCATTACTTGCTGAATTTCATGCCATAACTTCATTTTTTTTTCTTTTTCTGTAGTTCCTACAACACCGCTAACCTGATGGAGGACCTGAAGGGCT[T/A]GTACAGGACTGCCGGACAACAGGGCAAAGGCATTAGCTTTATTTTCACTGACAACGAGATCAAGGATGAATCCTTCCTGGAGTACATGAACAACGTCCTTTCATCAGGAGAGGTCAGAGAACATTATGACATCACTCTTATAGAAACACCTTTCCCCCCCTCAAGCCCCGCTGCATCCATTATGAGCTGATGTTTTTAGAACACACGCTAAAATAAGCCAAGCTACATGTGTTCCCAAGGTTACTACATATGTTCCCCTCTAATTCACTGCAAATAAGTCAGATCACCCGAGGTGCTGGTATAATGAAAATAAACAAAAGAACATGTTGTCCTGTGCTCAACAAATTACAAAGATCATTTTGTGTGGCAACCAAACAGGAATAAATGGGATCTGCGAGGCATGAGATGCATTGCTTCATATTAGAAAGACAGATGGGTTTGTCAAAAAGGGGAAAATGGTTGGTTTGCATGCTTTGCTCACTGCAAATAATGCTTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12420
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 800 | 1974 | 14 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10526028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9307737 |
GRCz11 | 16 | 9198639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACAGGCTGACCATAGCTAATKTGGACCTCCAGAAAGCCCAGGCAGAAT[T/A]GGATGCGAAACAAGCAGAGCTGGATGTGGTTCAAGMAGAGTATGAGAAGG
Long Flanking Sequence:
TTTAATGTTTCTAAACAGTTTGTAGCATTTATAAATCGAGAACAGAAAATATTAATGATAAACATCAGATTTTTTCCCCTTAACATCCAGTGATAATAAAAAAAATTAATAAATGTGAAGCTCAGTCAGTTTTGTATACATTAAAATAGAGTACATTTTAAAGTGTGGAAGTGTTTCAATTCATAAGCTCAGATTATATTTTAATGCAAAAGTCAAAATACAGTAAAGCCATTTATACTGCAATGCTAAGGTAAACAAAATCCAAACTAAATAATACTAACAGCAGTAAGTAGAAGTTGCAGATAGATTTAAAACAGTCTGTTTATACATTAAATAATGCTGTGACATAATAAATAATGGTGTTTTTACTGTGTTGCACTTTGGTTTCACACTAAGGCTGAAACGCTTTCTCTTTGTCTGTCACCCTCAGGCTAATCTGGCAGTGCAGGAGAACAGGCTGACCATAGCTAATTTGGACCTCCAGAAAGCCCAGGCAGAAT[T/A]GGATGCGAAACAAGCAGAGCTGGATGTGGTTCAAGCAGAGTATGAGAAGGCAATGATAGAAAAACAGGTAACCGCTGTGCTGGATATAATAGGGCAGGAGTGTAAAATCTAGCTCCTAAAGTGTGACTGTCCTGCACATTTTACCCTAAATAAAACACCTGGACAAGCTAATCAAGGTCTTCAGGATTACTAGAAACCAACATAAGGTTTTGTTGAGCCTGTACCATGATAGTGGCTGAACAAATTTGGGATTACAGGATTAGTTTTAAGTTGACAAATTCAAACCGGTGCAATCAAGCGTTGTTGGTACCATGTCTCTGATCATCGACTTTCTATGTGAACTCAGGCTTTGAGGGCATGACATCATTGGCAAAGAGACAATTAGGCCCTGTTTACACTGTCAGGTCTTGATGTCCAATTCCAATTTGTTACCTATATCAGATTTCTTTTTGTCTGTCCGTTTACACGTTCTTTTAATTGTGACCCATATCCAATTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36046
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 804 | 1974 | 14 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10526039)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9307748 |
GRCz11 | 16 | 9198650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATAGCTAATTTGGACCTCCAGAAAGCCCAGGCAGAATTGGATGCGAAA[C/T]AAGCAGAGCTGGATGTGGTTCAAGCAGAGTATGAGAAGGCAATGATAGAA
Long Flanking Sequence:
TAAACAGTTTGTAGCATTTATAAATCGAGAACAGAAAATATTAATGATAAACATCAGATTTTTTCCCCTTAACATCCAGTGATAATAAAAAAAATTAATAAATGTGAAGCTCAGTCAGTTTTGTATACATTAAAATAGAGTACATTTTAAAGTGTGGAAGTGTTTCAATTCATAAGCTCAGATTATATTTTAATGCAAAAGTCAAAATACAGTAAAGCCATTTATACTGCAATGCTAAGGTAAACAAAATCCAAACTAAATAATACTAACAGCAGTAAGTAGAAGTTGCAGATAGATTTAAAACAGTCTGTTTATACATTAAATAATGCTGTGACATAATAAATAATGGTGTTTTTACTGTGTTGCACTTTGGTTTCACACTAAGGCTGAAACGCTTTCTCTTTGTCTGTCACCCTCAGGCTAATCTGGCAGTGCAGGAGAACAGGCTGACCATAGCTAATTTGGACCTCCAGAAAGCCCAGGCAGAATTGGATGCGAAA[C/T]AAGCAGAGCTGGATGTGGTTCAAGCAGAGTATGAGAAGGCAATGATAGAAAAACAGGTAACCGCTGTGCTGGATATAATAGGGCAGGAGTGTAAAATCTAGCTCCTAAAGTGTGACTGTCCTGCACATTTTACCCTAAATAAAACACCTGGACAAGCTAATCAAGGTCTTCAGGATTACTAGAAACCAACATAAGGTTTTGTTGAGCCTGTACCATGATAGTGGCTGAACAAATTTGGGATTACAGGATTAGTTTTAAGTTGACAAATTCAAACCGGTGCAATCAAGCGTTGTTGGTACCATGTCTCTGATCATCGACTTTCTATGTGAACTCAGGCTTTGAGGGCATGACATCATTGGCAAAGAGACAATTAGGCCCTGTTTACACTGTCAGGTCTTGATGTCCAATTCCAATTTGTTACCTATATCAGATTTCTTTTTGTCTGTCCGTTTACACGTTCTTTTAATTGTGACCCATATCCAATTCATGTGTTTACTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39082
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 1025 | 1974 | 17 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10538971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9320680 |
GRCz11 | 16 | 9211582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTGGACAATGTCTTGGAGAAGAACTTCATCAAGACTGGCTTCACTTA[T/G]AAGGTATTGTTATAAAGAGCAATAAGCAAAAGAGGTCTGACATCACTGTG
Long Flanking Sequence:
CATACTTTTTTACATATGAAAGGAGAAAAAAAGTGAACAGACATTCACTTTGTCGTGCTAAACTGACAATGGTAAGAGAAAATATGCTTTAGGTGGTAAGTAAACATAAAGTACCCTAAAACAAAATACCTTTTCAGGTGTAAAAAGTTGAACACTTATATTCTTGCAAGCCATGCTGAAATCTAATTGGCCATGCACAGCTTGCACTGATGCATGGTTTCTTTTTGAGAGGTCAGACACCCTTTCCAAGGTTTGACCTCATAACAATTCACCTCCTCCTTAGGTAATAGCTTTCCCCAGGAACAGAACTTGAGTTGGGTCTGTAATAAGGTCTTGCTGTTTCCACAGATCACCTCGCTGAATCACAAGTATTTCAGAAACCATCTAGAGGACAGTTTATCTCTGGGGCGTCCGCTACTGATTGAGGATGTTGGGGAGGAATTGGATCCAGCCTTGGACAATGTCTTGGAGAAGAACTTCATCAAGACTGGCTTCACTTA[T/G]AAGGTATTGTTATAAAGAGCAATAAGCAAAAGAGGTCTGACATCACTGTGCTATATGTTTACAAATCTATGATAATGTCTATTTACAAATCTATGATAATGTTAAACCTTGCTGTTTGTATCTTATTAATTAATTTGAAGCATTAAAGAGGACATACTGTACAAAAATCACGTTTATAGGTGGTTTAAACACAGTTGTGTGTAGGGGTGTCACGATTTCGATTTTTGATCGAAATTTATGCTCAGTTTCGATTATCGAATCAAAAAATAGAATCGTCGAAGCTGCCACGCTCCCATGTCACGTCAGCTTGGCTTGCCAAGCGGGAAAAAAACAGGCTTGTTGAAGTGCTTGTTAAACTGCAGAAGCAGGAGACCCGTCGACAGAGCTCAAACCCTCTCCTCTTTCAATGAAGACGCTGGTGTTTAAGCATTTTGGATTTCCAGTGAGTTATGTTGACAACGTTCGTGTTGTCGACAAAAAAAACACAGTTTTGCAAGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11127
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 1386 | 1974 | 24 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10567535)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9349244 |
GRCz11 | 16 | 9240146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGGAGAAAGATATGCTGAGGGAGTTATTCTTGACYTGGAGAAGACCTG[G/A]GAAGAGTCTGAGCCTCGCACACCTCTCATCTGCTTCCTGTCTATGGGTTC
Long Flanking Sequence:
CTGGAAAACTTTTGCAGGGAAGAATGTCCCAAAATACTTTCAGCAAGAATTCAGTGACTTAGCCTTGACTATCTGAAGTGTCCACATGCTGTTATTTTAGCAAAAGGTGGCTGTACAAAAGATTGATGTCATTATTTTGTTGGGGTTCCCTAATTTATGCACCTTTCTGTTTTTGTTAAGACATAATTTACATTAAATCTGTTGACTAAACAAATGTTATGTCAGAACTAAAATGTTGCTTTTTCCCTAGGGTTTAAAACATATCCAAATGAATTGAAAGGCTTGCAGGCTATGGTTTGAAAAGTATCAGGGGTGGCCATACCTTTGCATAAGACTGTATATATATATTTTTTAATTGTTTATGAACTTATGCAATACCTAACTATCATTAGGCTAATGATTTATTTTCCAATTTGTAACTGACAGGCTCGAAAGTACATCACGCAATCAATGGGAGAAAGATATGCTGAGGGAGTTATTCTTGACCTGGAGAAGACCTG[G/A]GAAGAGTCTGAGCCTCGCACACCTCTCATCTGCTTCCTGTCTATGGGTTCAGACCCTACAGACTCCATCATTGCCCTGGGCAAACGGCAGAGAATTGAGACTCGCTACGTCTCAATGGGACAGGGGCAGGAAGTTCATGCACGCAAGCTTCTGCAGCACTCCATGGCTAATGTATGTTTATATTCATTTTTGATGTTCAAATGCATCTTGCTTGCCCCGTCTTGCTAAATTGACAATACCCTGGATTACAAAATCGAGTAGTCTCATCACTAATGGAGGGATGATCCAGCACCATCCATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATATTATAATATAATACTACAAAAAAATTCTTTGTTAATAACTCAATTCATTTTGTTAATAAAATTGTATAAAATGTATTTTAGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12187
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Essential Splice Site | 1516 | 1974 | 25 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10570870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9352579 |
GRCz11 | 16 | 9243481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACGAGCCTCCACAGGGACTGAAAGCYGGACTTAAGAGRACTTATGGAG[G/A]TGAGCYTGGTCTTTGGATATTTAGTTCTTGYYTGACTGACAGTTTNNCCCCT
Long Flanking Sequence:
ACGAGTTTGGTGACCCCTGTTTTAGACAATACCCAGATAAGATCAAAATAATTTTTCCTTCTTTTATGCCAAAAATCATTACAATAGTAAGTGAAGACTTTGTAAATATATAAAAATCTAATATTTGATAGTGTGCATCGCTAAAAATTTTAAAAGTGATTATGACTGGTTTTGTGGTCCTGGGTCACATGTTTTATTTTAAATGTATGTAGTTTTATTTATGCAAATAGTATAAAAATCACATTAATTTCTGTTTTTAATATATATTTCTTTCTACTAGGGAGGCTGGGCTTTACTTCAAAATTGCCATTTGGGTCTGGATTTTATGGATGAACTCATGGACACAATCACCGAGACAGACAGCGTTCATGATACCTTCAGACTGTGGATGACCACTGAGGTCCACAAACACTTTCCTATCACTCTTCTGCAGATGTCAATCAAATTCACCAACGAGCCTCCACAGGGACTGAAAGCTGGACTTAAGAGGACTTATGGAG[G/A]TGAGCCTGGTCTTTGGATATTTAGTTCTTGTCTGACTGACAGTTTCCCCTTTTCTATTTCTTGTACATGAATGTTTGATATATACTGATCTGGGCCCTGCAATTATTTGTAAAGGAGTCTCATTTTTCTGACTTATATAGATATATGGCAATATATGGAAATTATATATATATGACATACAACTTCATATTGGTTATTACAAATAAATGTCCTATATACAAAAATATTTTTTCAAATATTAATATATATATTAAATAATAGCTATATTTATCATTTAAATCTATATCTATAAATAATTTAATATATGGCCATATATGAACACACACATGAACTTGTCATTTAAGTAATGTCATAAGTAATGACACACATATATGTCAAATAAGCGATTTGCATACATTTTCATCAGGTCAGCTTTCTATATTGGGAGATAACTTGGTTAATATTTCATTTTGTGGTAATGTATGATAATATATTCAAGGTATCAGTCAGGATCTTCTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17649
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123150 | Splice Site, Nonsense | 1847 | 1974 | 30 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10584733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9366442 |
GRCz11 | 16 | 9257344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGGATGACAGGCKTCTTCRACYCACAGGGCTTTCTGACAGCTATGAGA[C/T]AGGTGAGTAACTATCACACAARCGCTTCTACTAAACTTACATTTGTACAT
Long Flanking Sequence:
ATCAGGCTGTAACTTACTCTGTGCGTGCATGTTGATGTGAATTTAAAGGGTTGCTTTGATTTGTTATGACCTGCTATATACACAGTCTCCTCAAACCATACAGCGACATCCTGTAATAAACAGACATAAATTATATTTAGTTATTACATAAAAACATATTATATACTTATACTTATTGCATTTAATTATCTTTAAGCTTAATTGTTTGTAATTATATTTAAGTTGTTTAAAAAGTTTGTGTTTTGGTTGATTCGTGTGCAGCGTGTGCCTCAAAATCTCTTTGAGATCTGGATTCGCTAAGTATTACTAAGTTTCTATCTGCCTGTGCGTGTGTGTCTGTCTGTATACAGGCCTCTTGGGCTTCCACTACACTGGGGTTTTGGTTCACGGAGTTGCTGGAGCGGAACAGACAGTTCCACTCTTGGATTTTTGAGGGGCGACCTAACTGCTTTTGGATGACAGGCTTCTTCAACCCACAGGGCTTTCTGACAGCTATGAGA[C/T]AGGTGAGTAACTATCACACAAGCGCTTCTACTAAACTTACATTTGTACATTTCCCTCCTAATTTGTGTTCCTCACTAAAAAAAATGAAACGTTGTCTTTTATGCAATTTTGAACTATAAAGGGGCTAGATTTAGCACAAGCTGTCTTTCTGGCATTAAAACAATATCGTCGGTATTTACTAAAGATGTGCAGCAAAGCATAGTGCAGAAAAGGCCTGAACACAGCTAGTTCTGGGTCTGATGTTATTGAATATGCATTTGATGCAGATATTATAGGAGAGAAGTATTTAAATGAAGCACACAACCCAAAGTGCTCCTCAAATTATGGGTGTTTGCGTCATTTAATGCATAAAAAAGCATGTCTTAAATGTTGCCTGGAAATGGCTGAAGTTATTGATCTCAGGAGGAAGCACTGGAGAGAATAGAGAATGCATAGAATGAGAAAGAAGATTTTTTTTAAGTATTTATTTGTAATGCCAGAGAAACATATCATTCGAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11262
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 |
---|---|---|---|---|---|
ENSDART00000123150 | Nonsense | 1891 | 1974 | 31 | 32 |
Genomic Location (Zv9):
Chromosome 16 (position 10593358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 9375067 |
GRCz11 | 16 | 9265969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCACGCAGCCTCCTGCAGAAGGGGTRTAYGTCTATGGCCTMTACCTT[G/T]AAGGGGCTGGCTGGGACCGCAGGAACTGCAAACTYATTGATTCCAAACCA
Long Flanking Sequence:
CGTATTACCACAGCAAATGATTGAATTGGTTATTTGTGAGCTTTGGTCATTTTTAATTGTGATGCTAATGGTCCAATCCAATTCAATAATCTATGCTAAGCTAAGCTTAAAGAGCTCCGGAGATGAGCTGATTAGATTTTAAAAGGGTAAAATTCATTGTTTAACACTAGGGGAGTTAAAAGATGAACTATTTTGAAGAAAAAAATGGAGTGTTTCTTGAATAACAACATGAGTTTTTGTGTGTACTTCATGAATGACTAATATTACCTTATTTAAACAGGATGGCTTCAGAAATTTCATTTATATTGAGTGTTGATGTAAAAATGAGTGACAAGCACATCTGCACATTAATCATATCACTAACTTGACAGGAGATCACTCGTGCTAACAAGGGGTGGGCACTGGACCGTATGGTTCTGTGTAATGAAGTTACAAGATGGATGAAGGATGACATCACGCAGCCTCCTGCAGAAGGGGTATACGTCTATGGCCTATACCTT[G/T]AAGGGGCTGGCTGGGACCGCAGGAACTGCAAACTCATTGATTCCAAACCAAAAGTGCTCTTTGAGATGATGCCTGTGATCAGGATGTACGCTGAGAACAATGGTGAGTTTTTTATTTTATTTTATTTTTTACACTTGAAATTAATCAGCTCTAATTGCAACAAATATTTAATAAAGCAGGAAATTAAACTGTCATATAAATACATTAGAGAAATTCCATTTTTTATTATAAGAGACAGTAGCTTAAATTAAAGATTTTAAGTCAAACTGTATGAAAATGTATGAATAAATGCATATTACATGTAGGAGTGGGACAGAATATTGATATGTTGATTTATTATGATATTTCCACTACGATACATTATTGGTACTCAATGCTTTATACACCAAACCTAGATATTTTTTAAATATGGAAGTCGTCTGTGTCTTTCAACATCCCAAATCTCCCAGAAGCTTCCATGAGTTTCTCCCTCACAGACTCACATTCACTTTGCTAGTTAC
Associated Phenotype:
Not determined