ZMP
si:ch73-289a15.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
DNAH12
Human Description:
dynein, axonemal, heavy chain 12 [Source:HGNC Symbol;Acc:2943]
Mouse Orthologue:
Dnahc12
Mouse Description:
dynein, axonemal, heavy chain 12 Gene [Source:MGI Symbol;Acc:MGI:107720]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43947 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9091 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29902 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24295 | Essential Splice Site, Missense | Available for shipment | Available now |
sa17291 | Essential Splice Site | Available for shipment | Available now |
sa17673 | Nonsense | Available for shipment | Available now |
sa13034 | Essential Splice Site | Available for shipment | Available now |
sa37669 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43947
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084477 | Nonsense | 128 | 3515 | 4 | 68 |
ENSDART00000134012 | Nonsense | 408 | 3841 | 8 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19839190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19624297 |
GRCz11 | 23 | 19550640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCAGAGACAGAGCTTTGAAAGTCCCTGAAACGACAGAGGAAATGATG[G/T]AAATGATTACTTACATTAATCAGGTGAAAACCAAAGGAATAGAGGAGCTC
Long Flanking Sequence:
GTAACAGATGACTATCTTTGTATAAAATGTCTTATTTCAGTTAAAGTTGGTCAGTCATAAATCATTCTGTAAATAGATTCAAGATTTGTATCCACTGGGCCATTGTTGGAGGTTGTGGTTTCATCCAATCAACTATTATTACTCTGGCTTTTATTACATGTATTACATGTAAAAAAGGGAATAAAATCCAAGTCTGTATGGCGAATTTTCATAATCTCAGCTTTTACCCCTTGCCAAAATCTAAATATTTCTGGACACTTACCTTCCTACATTCTCACACTTCCTCAAAATTAATTATCTGCCATCGTCTATTTACCTTTAAATCTTCCAAAACAATTGTGACATTTTCAGGTGAAGTATAATTTCCTGTTAAATCTGTGGTGTAAATACTTTATGTGCAGCTTAGCGATGGCGTGTTTTTGTTTTTTAGGATTTGTGAAGAGTTTGAGGCCATCAGAGACAGAGCTTTGAAAGTCCCTGAAACGACAGAGGAAATGATG[G/T]AAATGATTACTTACATTAATCAGGTGAAAACCAAAGGAATAGAGGAGCTCAACAATAGGATAATGGTAAGCATTTCACAGCTGGCTACTTTTTACATTGCGAATAACAGTTCAGATTTGTAACTTTCAAACCGACTTTTTCTAGGAAGCACAACAAAGGATGAATTATTTGATGGATGTCCATATTTTTAATGAGGAGCACCTTGATCTGAACACCACAGTACTGCTCTGGCCACAAAACATAAACCCGATCTTCGATCAAAGTGATGAGGTGATGTTTTTTTTTACAAAGATATGTAGCGTTGAATTTTCAATAAGACCTAATTTAAGAGCACTTACACACTCTGTTGCAATAGGTGATGGATGAAGCCAAGCTAAAGGGTCAAAATGATCTTTCTGGTCGAAGAGAAAAGCTGCTGCTGGAACTCGACAAAGTAGGCCGCAGGATGGAGGAATTTGCTGAGTGCTCTGAACTCGATATGATTCAACAGGTACATTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9091
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084477 | Nonsense | 321 | 3515 | 10 | 68 |
ENSDART00000134012 | Nonsense | 624 | 3841 | 12 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19836999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19622106 |
GRCz11 | 23 | 19548449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTTAGAGAGATGTACAAGATGCTGAAGTTCTTCCAGCAGAAACWGAAG[A/T]AGGCAGAGCTARAGAAGGARAAAACAGCAGGACTAAAGAAGAAGACCAAG
Long Flanking Sequence:
CCAGATTATTGGATTTCACAAAGACACTTTGTGATGATTTATAATGTGATTATTTTCTTTTTTATAATGTGGTTCTCTCTTTTTTTTTCTTTTTTTTTATCTAGTATGCCGCTGATGTGAGAACAGTTCTGAAAAGACTTCAGGATATTGAAGAATCAATAGACTTTATCAACAAAGAAGAAGCCCTGTACCAATGGGAGAAAACCTCATACCCAGAGGTGGAGGTGATCAAGGAAAGCATTGAGCCTTATCAGAAGCTCTTCACCTTGGTTCTGAAATGGCAACGTACAAGAAAGAAGTTTGTAGAGACCTTATATCTTTATTATTTATTTTTATTTTTCTCAAAAATCTTGATTTATTTGACAAAGAATGATATCTTGCTCCATAGATGGATGGACGGCTCTTTCTTGGATTTGAACGGTGAGAGTATAGAGCTGGAGGTTGAGGAGTATGTTAGAGAGATGTACAAGATGCTGAAGTTCTTCCAGCAGAAACAGAAG[A/T]AGGCAGAGCTAAAGAAGGAGAAAACAGCAGGACTAAAGAAGAAGACCAAGGAGGATCAGGAAGATGACAAAAAGGAGAGTGCCACCATTCTCATTTGTTCCAGTGTTGTGAAGCAGGTTAAAGAATTCAAGGTAGTTTTTTTAATTCACAAAATTCAACAACATTTACTCCCCCTCAGGGAATTACATGAAAACAAATCATAAACATTTCAGTTTTAGGATGAATCGTCCCATTAAAATAATGATTTATATTCTCAGGAGTACATTCCACTGGTGTCCATATTGTGTAATCCTGGCATTAGACCACGGCACTGGGAGCAAATGTCAGAAATTGCAGGTCAGGACTTGACGCCTGATTCTGGCAGCACTCTGCGCAAAATCCTCAAACAGAATCTCACTCCGTACCTGGAACTTTTCGAGGGCATCAGTGCAGGAGCCAGCAAAGTAATAATGCTGTCAATCCACTGCAGTTAAGCTATTAAATGCAATTAAAGGAAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29902
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 |
---|---|---|---|---|---|
ENSDART00000084477 | Essential Splice Site | 1214 | 3515 | 27 | 68 |
ENSDART00000134012 | Essential Splice Site | 1540 | 3841 | 28 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19824399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19609506 |
GRCz11 | 23 | 19535849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTTTTAAATCGGTTTGTGTATTCATTAATTCTTTTATTTCATTTTA[G/A]CTATGCCTCATGAGCGGGGAGATTATTCAGATGTCCAGTCAGATGAGTCT
Long Flanking Sequence:
AATATCTTTAAAAATAGGTTCATGCTTGTCGGAGAACCATTTGCTGGAAAAACCAAAGTACTTCATGTTCTTGCTGATACTTTGACCCTGATGAATGAGTCGGGCTACAACGAAGAAGAAAAAGTAATTTACCAAACTGTCAATCCTAAATCCATCACGATGGGTCAGCTTTTTGGCCAATTTGATCCTGTGTCACATGAGGTGAGAGTTTGATTTCTGCATCAAACAGATTTTAAAAGCTATAGTATATTTGTATATGCATATGTCCCTTTTATCAGTGGACTGATGGGATTGTGGCAAACACCTTTCGAGAATTTGCCTCAAGCGAGACCCCAGAGAGGAAATGGGTGGTGTTTGATGGCCCCATAGACACTCTGTGGATTGAGAGTATGAACACTGTGCTGGATGACAACAAAAAGGCAAATCAACATTATTTGATGTGTTCCTTCTCAGCTTTTTAAATCGGTTTGTGTATTCATTAATTCTTTTATTTCATTTTA[G/A]CTATGCCTCATGAGCGGGGAGATTATTCAGATGTCCAGTCAGATGAGTCTGATTTTTGAGGCCATGGATCTGTCACAAGCCTCTGTGAGTCAACCACAGTATTTGATATTAAGCACTGTTCACATATGCACCACTTCAGATTAAGCGTACTAGCAGTTTGTGATTTCTGCTATAGCCTGCCACAGTAAGCCGCTGTGGAATGATCTACATGGAGCCGTCTCAGCTAGGATGGACTCCTCTGGTGCTGTCATGGATGAAAACACTTCCTGACCCACTTCAGGCACAAGACAATTCCACTTTACTGCAGCAACTCTTCGAGTGGCTGCTTCCTCCCACACTTGTTTTGTTGCGCAAGCAATGCCGGGTAATTGTTTTATGTATAGTACTTTAACCACATCTCCAGTATTTTCTGATCTTAGATGGTATTAATACATACAGTACTTCATAGTATATTGCTTTACATGTTCCAGGAGGTAATTCCCAGCAGCAATAGCAATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24295
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 > G
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084477 | Essential Splice Site | 2174 | 3515 | None | 68 |
ENSDART00000134012 | Missense | 2500 | 3841 | 44 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19817377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19602484 |
GRCz11 | 23 | 19528827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCATCCCGGCTCTCGAGGCTGCGCTGTCTGCCCTGGACACACTCAAGG[T/G]CAGTTATGCATTTCACATACTGCTTTTCACATGCTAAAAAAGCAAGCAGA
Long Flanking Sequence:
GTTGGGGATAATGAGGAAAATAGCAGATAAACATATCATAATACTAAATAATATTTTTTCATAACTTTGTAATCATGGATGAAGTGGCTGAGAAGCCATTTTAACACATTTGTTATGCTGGTTAGGTGAGTGAAATGAAAAAGGAGTTGGTGGACCTGCAGCCTAAGCTAGAGCAGGCTAAGATTGACAACACCAAAATAATGGAAGTAAGTGACAGTAACATCTAGCATTGTTTGTCATTTGTATCAGCCTTTATACAATCAATGATTAGATTTACAGTGTTTTAGTCTTATTTTTGATCAAATTTTGTTTGCTTGTGCAGGTGATAGAAGTTGAGTCAGTGGAGGTTGAGGCAAAGAGCAAACTTGTTCGTGTGGATGAAGAAGCAGCTACTTTAAAAGCCAATGAAGCCCAGGCCTTGAAGAATGAGTGTGAGAGTGACTTGGCTGAGGCCATCCCGGCTCTCGAGGCTGCGCTGTCTGCCCTGGACACACTCAAGG[T/G]CAGTTATGCATTTCACATACTGCTTTTCACATGCTAAAAAAGCAAGCAGACATATTCAAACACAGAGAAAGGACATGTACTGTGTGAAAGTTTTAGGCAAAGTACATGCAAATAAGATATATATATACATATTCAGTCCCAATTCTGTATGCAATGCAAATAAGACTAATATTAATATTAAACAGTATTATCTGTTGTCAGTTACTCTTTAAATGATGAATTCCCCCAATATCAGGTTTTCAAATGTTTATTTTATAATTATTGATAGTCCATACTTATTACAATCTCTTGTTTAATTATTATTTTAGTGATTTTTGTAACACCAGCTGGATAGGACTCCATTTTTCAAACTTTTAAGTGTGAAACAGTTGCAGAAGTGCAGTGAAGAGTCCCAAAAAAGAGACAAAGAGACCAAAAAAAAGTAAAAAGGGAGAAAATGACAACCCTGCAGCTCTTTTTACAATTGTGAATCTCATAATTACTGTACATTTATTCACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17291
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084477 | Essential Splice Site | 2248 | 3515 | 45 | 68 |
ENSDART00000134012 | Essential Splice Site | 2574 | 3841 | 46 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19814234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19599341 |
GRCz11 | 23 | 19525684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGAATTTCCTCAGAGACTTGAAGGAAWATGACAAAGATAACATCCCTG[T/A]AAGTCTTTTTTGCAGTGTGTGTGYTTCATAACACTGRCTRAGGTATTTTA
Long Flanking Sequence:
AATATTTGAAGGGGAAACTGCTGGTATTTTCACATGCAACCAGAAACCTACAGAGATTCTTTTAATAGAAAATATAACTAATGAGCAGTTACAGTATGTGGGTGAAAAAACCTCAGTGTTGATTCAGGTCAGAGGAGACAAGCCAGATAGATTTGTACTGTTAGAAAAGCAACAGCAACTTGTGTTGATGTGTGATTTCAGCCTGCTGACGTGACCATAGTGAAGGCAATGAAGAATCCTCCAGCAGGAGTCAAGCTGGTGATGGCAGCGGTGTGTGTCATGAAGGACATCAAACCAGAGAGGATCAATGATCCTTCAGGAACTGGACAGAAGGTCAAAAGCAAGTCTGGACATGACTAGAGATTGTTTTGATAATGTTTTAGTGACAGTATGGTGTCTGTTCTAATAGATTCTTGACTACTGGGGTCCAAGCAAAAAGCTGCTAGGGGACATGAATTTCCTCAGAGACTTGAAGGAATATGACAAAGATAACATCCCTG[T/A]AAGTCTTTTTTGCAGTGTGTGTGTTTCATAACACTGGCTGAGGTATTTTAATGATGTTGTATTGTGACAGGCTCAAGTGATGCATAAAATTCGTAGTGAGTACATGACCAACCCTGACTTTGACCCTACCAAAGTGGTCAAAGCCTCATCTGCAGCTGAGGGGCTTTGCAGATGGATAACTGCTATGGAGGTTTATGACAGAGTGGCAAAGGTAGGCAGATCTTACCTTAATTTAACCCTTTTTCTATATCACTCTGTCTGTGTATCTAAACATCAATAAATAATTTATTATATTTTTAATTATATGTATTTTTGTAATAAATTAATCAACACATATATAATACATATATATGTACACAGTTAAAGGCAAAATTCTCCAATAGGATCTTAATGCAGACATGGATTTGCGTGCTGAGACTGTATATCTTGAGCTAGTGACGTCGCTGTGGGGGAAGGGGTGGGGTTAGGTGTGCACATTAAAAGGTGTGCATGCAGCTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17673
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 |
---|---|---|---|---|---|
ENSDART00000084477 | Nonsense | 3154 | 3515 | 61 | 68 |
ENSDART00000134012 | Nonsense | 3480 | 3841 | 62 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19801417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19586524 |
GRCz11 | 23 | 19512867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACTGGGACCGTCGCCTCCTCATGACGATCCTCGCTGACTTCTACAAC[A/T]AAGAYGTTATTGACCACCCACGCTACTCCTTCTCYCCTAGTGGCAAATAT
Long Flanking Sequence:
ATGGGCCAGCCTTCGGTTTGAGTGGGCCTGTGCCACCCTGGCCCTTGTGTTCCCCCTCCACTGCTTTACAGTACATCAAGCACACAGACCTAATAACAATAGGGTCAGAAAAATGTCACTGACAGTTGATACAAGTATGTGAATGGATGATAGTGTAAAATGTTTAAATAATAAATGCTGTTATTTTTTTTTCAGCTTATTTAACTTTTTTTATTTAAAAAAATGAAGAATAAAATCTTGTGATGAAAGTTTTAAAATATCTGGAAAATGTTTTGACGCTCAATCCAAATTAAAGCATGGAACAAAAGGAAATCTTTTAAACGAACAGCAAAGAAGGTAATTTTTTTGCTGTCTTTGTTCCTCAGCTCTTTGTGAATGAGTACCAGGAAGTTCCCTTTGAGGCCATCACATATCTCACAGGAGAGTGTAACTATGGAGGACGTGTAACAGATGACTGGGACCGTCGCCTCCTCATGACGATCCTCGCTGACTTCTACAAC[A/T]AAGACGTTATTGACCACCCACGCTACTCCTTCTCCCCTAGTGGCAAATATCACGCACCTCCAAAGTCCATCTACGAAGACTATGTAGAGTTTATCAAGGTGCAACTTTCATGTTATTCAATTACCAAGTACTCAAGTTTATTTGTATAGCACTTTTTATGATACATATCATTTCAAAGCAGCTTTACAGATTGCAAACATGATTTCACTTCACAATTAAAAGTAATCTTTTTGTCAGAGTTTACTTTGTCTAAGTAATGTCCATATTGCAGAACTGGAAACGCGGGGTCATGCGTCAAGTTTTGCAGTTTGCTGCTATGCAAAGTTCAAGCTTGGTGAACTCTGACCTGCGAAGTGGCATCACTTGACTGCGTGAGACCAATCAAGGATCAAAACATGACCTCTCTGGACAGAAATTTAAAACATGGAGCAATCGCTCGCTTTTTTAATGTCTAATCATCTTGTTTAATCCCACCCCTTTTCGCTGCGCCATACAACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13034
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 |
---|---|---|---|---|---|
ENSDART00000084477 | Essential Splice Site | 3249 | 3515 | 62 | 68 |
ENSDART00000134012 | Essential Splice Site | 3575 | 3841 | 63 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19799122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19584229 |
GRCz11 | 23 | 19510572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCGGAGACAGCACCCTTCTGGAYAKTGCTAATGACATCCTTTCTAAAG[T/C]AACTCGTCCTTTATTAAATTATACATTGTTATTRGCATAYAAATGCAGTT
Long Flanking Sequence:
AAAACTATGGAGATTAGTGTCATGATGAACTGCTGTTCAGTTACGTTTTGTTTAATAAGTTGCATATAAAAGTCATTTTAAAACCACCCAAATTTTTTCAACCCGCCTATGCCATTTTTTACCTGCACAATTTAACCGCCCAACTGGGTGGGAAACCGCCCAATCTGGCAACACTAAAGACTTTCTCCAGAAGAAAAAATATATAGTAGGAAATACTGTGAAAATGTCCTAGTTCCTTTAAAAACTTGGGAAATATTTGAAAAATAATTCAAATTTCACAGGAGGGCTTAAAACTGTGTATGCTCCACAGAAACTCCCATTTACCCAGCATCCCGAGGTGTTTGGCATGCATGAGAACGTGGACATCTCCAAAGACCTTCAACAGACAAAACTCCTGTTCGATTCCCTCCTTCTGACGCAAGGTGGAGGCTCAAAGGGCGGAGGAGGCTCTGGCGGAGACAGCACCCTTCTGGACATTGCTAATGACATCCTTTCTAAAG[T/C]AACTCGTCCTTTATTAAATTATACATTGTTATTGGCATACAAATGCAGTTTGCATATGTGCCGGTGATTTATTGACATTCCCATTTGACCCATGCAGCTTCCAGGTAACTTTGACATCGAGTCTGCCCTCGTCAAGTTTCCTGTGTGTTATGAGGAGAGCATGAATACGGTGCTCGTGCAGGAGATGCAGCGCTACAACAAGTGAGTCCTTTTAGATCCACAATTACCAATTCAGGGAAGATGTGTGTTGGATTGTAACTTCTCTGTGTGTTTTTATCTCTCAGTTTGAGCAGTACCATACGTGTGAGTCTACAGAATCTAATAAAGGCCATTAAGGGGCTGGTGGTGATGGATGCAGAGCTGGAGGCTGTAGCCGGCAGTCTGTTGGTGGGGAAAGTGCCAGAAAAGTGGGCCAAATGCTCCTATCCCAGTCTCAAGCCATTGGGTAGCTATGTCAATGACTTCCTGGCCAGACTCAAGTTTTTGCAGGTCAGTGACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37669
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 |
---|---|---|---|---|---|
ENSDART00000084477 | Nonsense | 3340 | 3515 | 64 | 68 |
ENSDART00000134012 | Nonsense | 3666 | 3841 | 65 | 69 |
Genomic Location (Zv9):
Chromosome 23 (position 19798669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19583776 |
GRCz11 | 23 | 19510119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGTGGGCCAAATGCTCCTATCCCAGTCTCAAGCCATTGGGTAGCTA[T/A]GTCAATGACTTCCTGGCCAGACTCAAGTTTTTGCAGGTCAGTGACCACAC
Long Flanking Sequence:
CGGAGACAGCACCCTTCTGGACATTGCTAATGACATCCTTTCTAAAGTAACTCGTCCTTTATTAAATTATACATTGTTATTGGCATACAAATGCAGTTTGCATATGTGCCGGTGATTTATTGACATTCCCATTTGACCCATGCAGCTTCCAGGTAACTTTGACATCGAGTCTGCCCTCGTCAAGTTTCCTGTGTGTTATGAGGAGAGCATGAATACGGTGCTCGTGCAGGAGATGCAGCGCTACAACAAGTGAGTCCTTTTAGATCCACAATTACCAATTCAGGGAAGATGTGTGTTGGATTGTAACTTCTCTGTGTGTTTTTATCTCTCAGTTTGAGCAGTACCATACGTGTGAGTCTACAGAATCTAATAAAGGCCATTAAGGGGCTGGTGGTGATGGATGCAGAGCTGGAGGCTGTAGCCGGCAGTCTGTTGGTGGGGAAAGTGCCAGAAAAGTGGGCCAAATGCTCCTATCCCAGTCTCAAGCCATTGGGTAGCTA[T/A]GTCAATGACTTCCTGGCCAGACTCAAGTTTTTGCAGGTCAGTGACCACACAGACAGAGAACTGCGTGAAAAAAAATTTTTTGCAAAAATTGGTTTAGTGAGAGAAGTTGTGCAGAATTCTGTCAACTTTGTTATGTGTTCTTAGTATTTTAGACTTCAATATAGTTATATTATGTAGCATATAAATATTCTTCGTATTCCTTTATTCATTTTCCTTCAACTTAGTCCCTTATTTATCAGGGGTCGTCACAGCAGAATGAACTGCCACTTATTCCAGTATGTTTTACGCAGCGGTTACATGCAACGGGGAAAACATGCAAACTCCACATAAAAAAGGCACCTGGGCCAGCCGGGACTCAAACCAGCAACCTTCTTGCTGTGAAGCGGCAGTGCTAACCACTGAGCCACCATGCTGCCATTCTTCTTGTTAATGTATATATTTTTATATTATATTGCAGGAACTATTCATAGTTAATAGAACCAAAAAATGATTTGTTAGCG
Associated Phenotype:
Not determined