ZMP
dnah9l
Ensembl ID:
ZFIN ID:
Description:
Dynein heavy chain 9-related protein [Source:UniProtKB/TrEMBL;Acc:Q56HA9]
Human Orthologue:
DNAH11
Human Description:
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Mouse Orthologue:
Dnahc11
Mouse Description:
dynein, axonemal, heavy chain 11 Gene [Source:MGI Symbol;Acc:MGI:1100864]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11038 | Essential Splice Site | Available for shipment | Available now |
sa20655 | Nonsense | Available for shipment | Available now |
sa33819 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33818 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20654 | Nonsense | Available for shipment | Available now |
sa38541 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20653 | Nonsense | Available for shipment | Available now |
sa9392 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33817 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20652 | Essential Splice Site | Available for shipment | Available now |
sa20651 | Essential Splice Site | Available for shipment | Available now |
sa20650 | Nonsense | Available for shipment | Available now |
sa40642 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33816 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11038
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Essential Splice Site | 565 | 4461 | 11 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10593979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10447605 |
GRCz11 | 6 | 10683032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATGCTCTTGAACATGTTCAAGTACTTCTGTGTTGTTTTAYGTGGTACA[G/A]CTRAGGACCGGCAGTCCCATCCTTGGTAAAAACATGCCAGCTGTTGCTGG
Long Flanking Sequence:
AATTTTTTTGTTATATTTCATTAGGTAATTATAAAATATTAGCAATTTGTTTGTAAAATTTGTCATGTTTGGACTGTATCCTCGTTGTCCAGCAGGTGTCGCCAGATTGCAATGTTTTTAAAGCTTCGTTTCACTCGTGACAGATTATACTCTTTTTAAATTTTTTTTTTTTTTTACCATAAAACAACTGATTCTGACATTTTAAGAAATGAAATTTTATTTGGATGTGATATTTATTTAAGTATTTGTAAGCTTTTCTTCTGTCAGTATCATTGTACCGTACCGTGCTGGGCAAACACTGTATTGTTCAGGTACTTGCGTTAATTCGGTTAATTCTGCATTTGAAATGGTTTCAGTTGTGGATAAACTTGCGTTGCATTATAGACTCAGTTATTTAATATTAATTCATAACATTTAAATGTAAATATTTGTCATTAAATGTGAAAATGAATATGCTCTTGAACATGTTCAAGTACTTCTGTGTTGTTTTACGTGGTACA[G/A]CTGAGGACCGGCAGTCCCATCCTTGGTAAAAACATGCCAGCTGTTGCTGGGAACCTGAAATGGTCTCAAGAACTTCGAGAACGGATCCTGTCAAACCGCAGTAAACTCAGCCAGCTCACACACATGTATATAAAAGACCTCACACATCTTTTTATGACACTCAAATACATGTACATTTGTTTCTGGAGCCATGAATTACAACGTGTGTGTGCGTGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTTTAGGCCATTGGAGAGTTCTGAGGCCAAGCAGGTGCTGCAGATGTGTGAGTGTGTATTGGAGGTTCTGGATGTGATGGATGAAGAAGTCTACAATAACTGGAGTGTTGGCATGGATGAGTTGTGTCAAACACATCTCAACAAACCACTTCTGATACTGGATGAGGAGAGCAGCCTGTACAGTCTGAACTTTAATCCTGCTGTAAGACACACACACAAACAAACTAAACCCATGTACCAAGCTAACTAAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20655
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 608 | 4461 | 12 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10593721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10447347 |
GRCz11 | 6 | 10682774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCGTGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTTTAGGCCAT[T/A]GGAGAGTTCTGAGGCCAAGCAGGTGCTGCAGATGTGTGAGTGTGTATTGG
Long Flanking Sequence:
TTCTGTCAGTATCATTGTACCGTACCGTGCTGGGCAAACACTGTATTGTTCAGGTACTTGCGTTAATTCGGTTAATTCTGCATTTGAAATGGTTTCAGTTGTGGATAAACTTGCGTTGCATTATAGACTCAGTTATTTAATATTAATTCATAACATTTAAATGTAAATATTTGTCATTAAATGTGAAAATGAATATGCTCTTGAACATGTTCAAGTACTTCTGTGTTGTTTTACGTGGTACAGCTGAGGACCGGCAGTCCCATCCTTGGTAAAAACATGCCAGCTGTTGCTGGGAACCTGAAATGGTCTCAAGAACTTCGAGAACGGATCCTGTCAAACCGCAGTAAACTCAGCCAGCTCACACACATGTATATAAAAGACCTCACACATCTTTTTATGACACTCAAATACATGTACATTTGTTTCTGGAGCCATGAATTACAACGTGTGTGTGCGTGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTTTAGGCCAT[T/A]GGAGAGTTCTGAGGCCAAGCAGGTGCTGCAGATGTGTGAGTGTGTATTGGAGGTTCTGGATGTGATGGATGAAGAAGTCTACAATAACTGGAGTGTTGGCATGGATGAGTTGTGTCAAACACATCTCAACAAACCACTTCTGATACTGGATGAGGAGAGCAGCCTGTACAGTCTGAACTTTAATCCTGCTGTAAGACACACACACAAACAAACTAAACCCATGTACCAAGCTAACTAAGCAGAGCTTTCCCTTTCCCCTTTTAAATTAAGATTGTCCTTTTTTTCCCTCTTTTGTGACCTAAGTCCACTTGCTAACAAAATAAAAGAAGATTTGATAGAAGATGTCAATTTATAAGTAGGATATGTTCCTGTTATACATCTGACATAGATATTGATCCAGGAACAACATTTCAATGAGTCAGTCGGTCGGTCGGTCGGTCGGTCGGTCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33819
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 798 | 4461 | 15 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10590994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10444620 |
GRCz11 | 6 | 10680047 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTGGAGAAACTGCAGGGGCTGATGGGAGTTTTCAGTCACTCGGCCTG[T/A]ATTACACGTAAGACTAGCCATCGGGGGAATCTGCTGAACCTCACCGATGT
Long Flanking Sequence:
TTCCCAAAGCTGCTGTGAGTCTGTACTCCAAACGGGAAATGCTTCACATGGTAAGACCGGGCCTTTATTTTTTGAGAAACAGATTGCACAGTGCCAAGAAAAGGCCCACTTATTCCATTCTTTTCTTTCGCTCTCCTCTGTGTGAGTTTAGTACACCAGCACTCTGCTCCAGATCACTCAGTGGTATAATAAACTGCACAGCACTATTCTAGCTGTCGAGCTGCGTTTGGTTGAGTCTGAGCTGGAGGAAGTGAGGAACACTTTAAAGCCAGCATTACAGGAACTACAATGGATCGACGAGGATCTTGCTGATTACATCAAGAGGTAACACCTGTACTTTCACTTGTTAGAAAGCTCCACAATGCGAAGGCGCTCATGGTAAAGTGTGTGTATTGTAGCACGTGTGACCTGGTGCGCGGTGTGTCGGAGCGAGTGCAGAAGAGCAAGGCTAACCTGGAGAAACTGCAGGGGCTGATGGGAGTTTTCAGTCACTCGGCCTG[T/A]ATTACACGTAAGACTAGCCATCGGGGGAATCTGCTGAACCTCACCGATGTTGAGGAGAACTTCAAGCGACAGTACGGTCTCATCGCTCGCACAGGAGAGAAGATACATGAGCTTGTGCAGGTGCTGGCTTCAGTCTTTTATTTGACACAGTGAACGTGCTTTAGGTTTCTGCTAGAGTAGGCAAAATCAGGTAAAGAAATAGAATTAGTAAACATGTACACTTACCGGCCTCTTTATTAGGTACACCTTACTAGTACCTGGTTGAACCCCCTTTTGCCTTCAGAACTGCCTTAATCCTTCGCAGTATAGATTCAACAAGGTACTGGAAATATTCCTCAAAGATTTAGCCCCATATTAAAATGATAGCATCATGCAGTGGCTGCAGATTTGTTGGCTGCACATCCATGATGTGAATCTCCCATTCCACCACATCTTAAAGGTGCTCTATTAGATTGAGTGCTGGTGACTGTGGAGGCCATTTCAGAACAGTGAACTCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33818
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 918 | 4461 | 16 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10589059)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10442685 |
GRCz11 | 6 | 10678112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACATGATCTTTCACCCCTCGCTCAACCTCTCCAGGAAAGGCAACTTCTA[T/A]GACATCATTGACCAGATGGTGTCAGACATTTTTAAAATGGCTTCCTTCAT
Long Flanking Sequence:
AATCAGGACTGATGGTTTGATCCATCTGTGTCAGTGAAAGTGTTAAAAATTTTAAAATATGATATATTTATGATTTATTTATGAACTTATGATGTATTTTTTACAGACATTTGCATCTTTATGTAACTTTTTTCTAAATAAAAGCTTTTCTTCAACTTAATTTTTCTGTAATGTAAAAAAAAACAATTCTACAGTTGTATTTTGTCTAGTTTATTTGTATTAATAGCATTTTTTTATAAGATTGAATTCTTTCTTGTTTAGGAGAATGCTGAGCTTCTTGGTGCTGATTTGGACTCAGAGGCTTGGCAGTCTTACACAGAATACGTGGACAGACACATTCTCACTGGCTTCTGCAGCGCTGTGCGATGCTCCCTGCAGTATTTAGTTGAGAACACGGATGCGGCGCTCAGTATCGCTCCCCTGTTTGAAGTACAGCTCACCCTGACCACAGACATGATCTTTCACCCCTCGCTCAACCTCTCCAGGAAAGGCAACTTCTA[T/A]GACATCATTGACCAGATGGTGTCAGACATTTTTAAAATGGCTTCCTTCATCAAAAGAGTAGCCAAGAGCAAACAGTCAGAGACTTACAAGGTGTGTAAAGTTGGACTATTATTTGTAATAGCCAGGGTACAACTAAGAGTAACTGTTATGACTAAACATTAGTAAAGAAGAAGTCAGCAAGTGGAGTTGCTAAATGAATGAATTTAACTGTAAATAAAATGAATAAGTTGTGGATAATTTTGGAGGACACTTTGCTTTTAATACAGATGTTGAAGTAGGGTGTCAGCGGGGTCTTAAAAAGGTCTTTAAATGTCTTAAATCTCAAATACAAAATTTTAGGCCTTAAAAAGTCTTAAATTGACTGAAATATTTTGTTGTAGGTCTTAAATCTTTTTAAACTTAATTTTCCTTTATTCAATTATTCTCCAACAATCCATCTCAATAAAACTTTTAACTTTTTTATTTAAGAATGTAATCTGTGACTCTATTTACATTAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20654
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 1031 | 4461 | 17 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10586302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10439928 |
GRCz11 | 6 | 10675355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATGCAGATTATGAGCTACCTAAGAATCCACCCAAACTGCAGAACTTC[A/T]GAGAGCAGGTATCTGTCAGTCATGGAGTGAATAATAAAAGTGATTTTTTG
Long Flanking Sequence:
AAAAATGTTAGTAAAAGTAACTTTGTTAAACTTTTGAACATCAGATGTTCACAGAGCAGATAATGCACTTTAAAAATCCTATTAAACAGAAAACAGTCACGAAACAAAATATTGTAAGGAAACATATTTTTACAGGGCATCTTTTCATGTTTACACTATAAAGACCATCATAATTAAAGTTTTATGGTTATTTTGGAAAAACATTCTCCGCAACATGATTTATGTCTGATTTTGTCCTGTCATTTTTTTTTTAGGAGGATGTAGATCAGATACCTGAGCTAGTGGAGTTGGCTCAGCTGGTGCGATATCGTGCTCGCGGAGCCATTGCTAAGGTCAAAGAATTCCAGCATTCCTTCGATTCCTACCGTTACCTTTGGACTGGAGACAGGGCGGAGTTTATGAGGCAGTTTCTGCTCTATGGACACGCCCTCTCTGCTGAAGAGGCGGAGCTTTATGCAGATTATGAGCTACCTAAGAATCCACCCAAACTGCAGAACTTC[A/T]GAGAGCAGGTATCTGTCAGTCATGGAGTGAATAATAAAAGTGATTTTTTGTGTGATTTTGAAATACATGATATAATTATTAAAGCCTATATATTTCACAATTACATTTCTTTTTATAAAAAGAAGACTATATATTGTTAATGTAACAACTAACATTTGATACCCTAGATTCATTCATTCATCCATTTTCTTTCGGCTTAGTCCCTTATTTATCAAGGGTGTGCAACAAGGGAATGAACCACCAACTATTCCAGCTACACCGCAACCCAGTACTGGGTAACACTCATACACTCTTGCATTCACAAAGGCACACAAACTACGACAATTTTTGTTTGCCCAATTCACTAATACCGCATGGCTTTGTACTTTCGGGGAAACTGAAGCACCCGGAGGAAAACTGCTGACCACTGAAACACCATGCCACCTGATAACCTACAGTTTGCTTTAAAAATAACAGCGGACATTATAAAGTATCTAATTTTCTTGTCATAACAAATATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38541
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 1805 | 4461 | 34 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10570106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10423732 |
GRCz11 | 6 | 10659159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATGGGCCGAGCAGCAGAAGCACTGTTATATCAACATCTGTGATGCA[C/T]AGTTTCAGTTCTCATACGAGTATCTAGGGAATACTAACAGATTGGTTATC
Long Flanking Sequence:
TCTTAAGGTGGCGTTGACTGGAAGCCAAATATGGTGGGCGACAGATGTGGGCATTGCTTTTGAGAGGGTGGAGGAAGGTTTTGAGACTGCCCTGAAAGACTACAACCGAAAACAGGTACGCAAACATTTCAAAACAATAACTTGTCTCACTTCTGTTGATATCTGACAAAATGACTGTAGTTTGTGAATGAGTGCAGATCAGTCAGCTGAACTCTCTGATAAACATGTTACTGGGTGAACTCACTCCTGGAGACAGACAAAAGATCATGACCATCTCCACTATCGATGTCCACGCTCGAGATGTAGTTGCTAAACTCATATCTCAGAAGGTAATGAACCCCAAGTGGCCTTACATTTGAGTCTTGAATGATGAAATATAATGATGATAAAATGACCTGTTTTTTAAGGTGACCAGTGGACAGGCGTTTGCGTGGCTGTCGCAGTTACGGCACAGATGGGCCGAGCAGCAGAAGCACTGTTATATCAACATCTGTGATGCA[C/T]AGTTTCAGTTCTCATACGAGTATCTAGGGAATACTAACAGATTGGTTATCACACCACTCACTGACCGGTCAGTGTCACACACTCTTACTGATCTGAAATTTGATGGTTGATTTATGTTTTTTACTATTCGAGTTAGTTTCAATTTACTTGAACGGGCTGTTCATAATAATCTTTATAATCATGCTATGACACATGTTATTAATATGAAGAAGATTTTATGCATTCTTATGAAAACGGTCATTATGGTGCAGTAGTTGATCTTCCTAAATGCTAACCAGTAAGAATCATGTTTGAAACACATTCTCTGCCCTGCAGTCCAATGCCAAGCCTTCTGAAATCACGATCGCGCTTATTTTTTAACTATTTAAAAAAAAAAAATTTTAGGGGTTTTCACCTTTATTGGGATAGGACAGTGGAGATTTTTACAGACAGGAAATGTGCGGAGCAGAGATAGGGGAAGGATCGGCAAAGGACCTCGAGCCGGGAATCGAACTCAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20653
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 1984 | 4461 | 38 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10565084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10418710 |
GRCz11 | 6 | 10654137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCATGTGCAATGGTGATTCCAGATTATGAGTTAATCTGTGAAATCTTGT[T/A]GGTGGCGGAAGGTTTTCTCGATGCACGGCTGCTTGCACGCAAGTTCATCA
Long Flanking Sequence:
CTCAAGTGCTTCTAAAATTCTATTGAAGAATGAAAGTGAATGTTTTTTACCAACATTCTTTAGTATATGTTCTTTTATGTTCAACAGAAAAAAAATGCTCATACAGGTTTGGAACAAGTCGAGGATGAGTAAACGATGACAGAACTTTCATTTTTGGGCAAACTATACTTTTCAGTCCTCATGTATCCATGCAGTTCCAAACAAATTTCCCCTTTAAATTCCATTTCATTGTCTATCATTTATCAGGTTCCACTTTCTGGGGGAAGATATTGAGTTGAGGTCAACAGTTGGTATCTTCATCACTTTGAACCCTGGATATGCAGGAAGGACTGAACTCCCAGAGAACCTCAAAGCACTTTTCAGGTGTTTTGTTATGCTTTGAAGTGAATTAGAATCAACAATAGTCATATTTGGTGTCTGCTAACCATGAATTTTGTCTTGTTGTGTCAGGCCATGTGCAATGGTGATTCCAGATTATGAGTTAATCTGTGAAATCTTGT[T/A]GGTGGCGGAAGGTTTTCTCGATGCACGGCTGCTTGCACGCAAGTTCATCAGCCTGTATACACTATGCAAAGAGCTGCTGTCCAAACAGGTACATTGACTCACATACGCATTCATACATAAACACGCTTCGTGATCTGTTGAAAAACCTTGTGGTTTCTTGTAGGATCATTATGACTGGGGCTTGAGGGCCATAAAGTCAGTCTTGGTTGTAGCTGGGTCACTGAAGAGGGAAGACAGGAGCTGTCCGGAAGAGCAGGTCTTCATGGGAATTTAGTGTAGAAATTTAGTATTTCTCTATCACTTTATTTTCAAAATTGACTTATTTTACAACTACCTTAGAGATAAACAGTCGAGTTATACACTTTTTTGAATCCATTCAGCTGATCTTTTAGCACTTTTAGCTTAGTGTAGCGAATTAGCTCAAAGGGAACCGAAGATTCATTTAAACGGGGCTTCAAAAGAATCAACTCTTTAAATCCAAACAAACGAATCATCCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9392
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125876 | Essential Splice Site | 2180 | 4461 | 42 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10562499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10416125 |
GRCz11 | 6 | 10651552 |
KASP Assay ID:
2259-7217.1 (used for ordering genotyping assays)
KASP Sequence:
GATGAGCTGTTTGGCTTTCTCCACCCAGCCACACGGGAGTGGAAAGATGG[T/A]GTGTGTGTATGTGGGTGTTTATGTGCAGTCTCTTAGTTTAAGGATCATCT
Long Flanking Sequence:
TCGAATATTTTGACATTTGATAGTTTTAAATATAAGGGTGCAGTTCATTTCAAATCTTCTAAATGTGTTTGTTTCTTCTTCCTCTTTTAGGTGACTCAACTGGAGGAGTTGCTGGCAGTGAGACACTCCGTTTTCGTAGTAGGTGGTCCTGGATCGGGAAAAAGTCAGGTGAGTCTAGTAAATAGTTGAAGTAAGGCTCAGATATAAATGTTTTGTATTGTGATAACCATTTGAGTTTCTTAGTCAGTGTGTTTGCTATTAGTTGCGTTTCTAACACAATACAAATGTCAGTGTTTCACAGCTCAAATGTTAAAATATTAAATTGACATCACTTAAGGTTGAATTATGTGTTTGTTTGTGGGTCAGATTTTGAAGACGCTTCATAAGACCTACTCTAACATGAAACTGAAACCTATCTGGACTGACATCAACCCTAAAGCTGTCACCACTGATGAGCTGTTTGGCTTTCTCCACCCAGCCACACGGGAGTGGAAAGATGG[T/A]GTGTGTGTATGTGGGTGTTTATGTGCAGTCTCTTAGTTTAAGGATCATCTCTGTAGACAGCTGTCTGCTGGGCTGTGATTGTGTTTATATGTGATTGTTTTACTTCACTTTTAAAGGTGCCATTGACACAATATGTTAAGTTGTTCTCTGGTATCTACATAGCATGTGGCTTAGGAATGCTCAAAAATTTTCCAGAAATGGTTTTATATGCTAATTCATATCCAATAGAATTATTCCTAGAATGAAAAGCTCAGTTTTGACCATATTTGGAATGGTCATGAATATTAATTAGCTCTGCTTTGATGTTCTGCAGTTCATATCAGTTCCTAAAGCAATCTCTTTCACATACACACACACAAACACACACATAAACACAAACACAGATTGATGTACTGTGAAATAACCATGCAAAATAACCATACATCAGTTTTCCAAACTATTTTAACAAATTAAGTAGATTCCTTTTTTGAAAATCTTTTCAACGGAAGTGTAGAAAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33817
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 3003 | 4461 | 58 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10536183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10389809 |
GRCz11 | 6 | 10625236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTTATCTCATTCGCTCACACTTGTGTGAATGAAGTCAGTGTAAAGTA[T/A]CAGCAGAATGAAAAGCGCTTCAATTACACCACACCCAAGAGCTTCTTGGA
Long Flanking Sequence:
TTGGCCCCAGCATGCATTGCAGTCCGTCAGCAGCACTTTCATACAAAATATCCCCGACTTGGAGGTAACAGAATCTACATTGCAATATTCCGCACAGCACTGCATTGCGTCTTAATCAGGGACAAATTTGGGGGTCAATAGGATTTTTAAAAATACATAGTATTTTTTTTATTTAGCATATAATAACATAAAAATTGGAGGAAAATTAACACAAATATTTAGCGTCTGATTTATTAAAGTACTGCGCATCAAAATGTCCTTACAGAAAATGATCATATATTATATTAATAAAGAAATTATGTATAAATATTTCTAAATAAATAATAAATGAATAATAATATATTAATTATATATTTAGAGTTTTTAACAGAACTGTAGATTTATTAAACAAGATGTTTTCATTTTTCTTTTTTCTTTTTTTTTTAGCCGGATGTGAGAGTGTCTATTAGTGAGTTTATCTCATTCGCTCACACTTGTGTGAATGAAGTCAGTGTAAAGTA[T/A]CAGCAGAATGAAAAGCGCTTCAATTACACCACACCCAAGAGCTTCTTGGAGTTCATGAAACTTTACGGCAACCTGCTGGGCTCAAAGAGAACAGAACTGAGACAAAAGACAGAACGCCTGGAGAATGGCCTGCAGAAGCTGCTGACCACGGCATCACAGGTCAACTTTACTTTAAAAAAGTACCAAACAATTTATAAATGTAAACTGATTAGTCTGTATTTTGGCACAACCAATGAATGCATCTCATTATAGAAGCAGAAGGAGTTGCACAAATTAAATTAAACCAGAAATGAAAATTGATAATAACTATATTTGAGTTTAATTGTTACACCACCTTCTTAATCATAAATCTTACAGACACATTATGTTTAGTTGTTGCATTTCATTATGTATCTCTATTTTAGGTGGAGGATCTGAAGGCTAAACTGGCCATACAGGAAGTGGAGCTGCATCTAAGAAACACTGATACTGAAGCTCTCATTGCTAAAATTGGCCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20652
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Essential Splice Site | 3191 | 4461 | 61 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10533227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10386853 |
GRCz11 | 6 | 10622280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATCCCTAAAGACCGCAGCTGGAAAGCATCTAAAGTTGTCATGAGTAAA[G/A]TGAGTGAGTGTAGGGCTGACATTTGTAAATGTTCCTATTTTACTTTTGCT
Long Flanking Sequence:
TATTTATTCATTATAGATACGCATCAAACTAAAACAGCATTACTAAACATTTTGCAATACTTAAATCCTTATCCTTATATCAGGTGGAAGCGATCCAAGCAGAAGTGACCAAACAGCAGCAGGAGACGGAAGCTGACCTGGAGAAAGCCGAGCCAGCTCTACAGGCAGCAAATGCAGCCCTCAACACACTCAACAGGGTCTGTTTTTTCGTCTATATCCAGTGTGTTTGACTTAACTTTGGGCACTAATGTGTGTTTTCTCTCTACTGAATCATCCTCTCACATATAATCTAAATGCCCGGTTTTGATGAGCATTTTGTTTAAAGTAGTTTGTGCATTTTTTTTGTGTGTGAATAGCTGAATCTGACAGAGCTGCGGACGTTTCCGAATCCTCCTGCCATCGTATCGAATGTGACTGCAGCTGTTTTGGTGCTCTTGTCTCCTAATGGCCGTATCCCTAAAGACCGCAGCTGGAAAGCATCTAAAGTTGTCATGAGTAAA[G/A]TGAGTGAGTGTAGGGCTGACATTTGTAAATGTTCCTATTTTACTTTTGCTGATGTTTAACTTCAGTCATATTATTGAAATTTGGATTTTACATCTATAAACAATAGCTTGAAATTTACTCAAATTGGCACCATTTAAGCATAAAAGATTTTAGTTTGAATGCCTGGATGCATGAACAATCAGTCAGTGAAATTGTAATGTAAATTAACAGGTTATTTAAAAAGTTTTACTTAATTCTATTCACTATTAACTAGGGATGTAACGGTATCAGAATTTCACGGTACGGTAATACCTCGGTATGAATGTCACGGTACGGTATTTATTGAATCATTTACAGGAAAAAACAAAACTTATGAAAATACTCCAAAAAAGTGCCAAAAGTGTCAATGACATACAAATTAGTCATCTATCTGTAAGCTTTGAAACAGGAACTTCAATTTTAATAACAAAAAAATATTAAACCATGTAAAAAAATTAAGTTTCAATTTAGTAGTGTTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20651
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Essential Splice Site | 3286 | 4461 | 63 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10527006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10380632 |
GRCz11 | 6 | 10616059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGGTTGAGGCTGCAGAAAAGTTAGAGATCATCAGAAAGAAGCTGGCC[G/A]TAAGTATCTCTTATTTGCTCTCTCGATATCTCATCATTGTTTTACAAAAA
Long Flanking Sequence:
TGTTAATATGGTGTATTATTTTTTTCAGTTTGTGCTATTCAACAAGCTTTTTTAATTCAATACTTTTGGCATTGATTTTGTTCCATATTATTTTTACATCCCAATGTTGAAATATATAAGAGAGGTATTGCAAAAAAATGTAACAAATTTTAGCAATGCCGAAAGAATCATGCTTTTAATGTTTCTCTGTTTTGAATTTGTTTGTGTATAAATTCACACGTGATGATTTTTACATTTTAAAATGACTTGTTTAAATGCCTGCCAGAGTTTTGTATTGATGAAGAATGATCAATCTCCACACACTCCTGTGCTCTATAAAGCACTCTACAATCTGTCATTGCAGAAGCTGAAGCTCTGCTGTTGTGTCTGTGTGTTTAAACATGTTTGGGTTTAATCAGGTGTTCTGTGAGGTGGAGGTGAAGAGGTTGTGTCTGGCTCAAGCAAACGCTGATCTGGTTGAGGCTGCAGAAAAGTTAGAGATCATCAGAAAGAAGCTGGCC[G/A]TAAGTATCTCTTATTTGCTCTCTCGATATCTCATCATTGTTTTACAAAAAAAGTCAAATGTGTTTATGAAATATGCAGGAGTTGGACGGTAGTTTGGAGACACTGACAGCTGCATTTGAAAAAGCAACCTCGGAGAAATTGCGCTGTCAGGATGAGGTGAACCAGACCAACACAACCATCCTGCTGGCCAACCGCCTGGTCAAGGGTTTAGAGGTTAGAATATTGATTTGTGTTTGTGTGTGTTTGTGTGTGTGTGTGTGTGTTTTAGACCTTGTATGCATGTTTATGTTGTCATGCTAATCTTACATGTAAAATACTAATATATAGGCATCTATAAATGCTTTAGAAATTAATATTGTCCATTAAAACTATTATATAAAAACTATTAGACCTCATGTTGTTAATTGTTATCCATCTTTTTTGTTCTGTTTGTTCCTTTTTTCTTTTATTTTACTGTCAATGTATTTGTGTCTGCTGCAGAAATCTCTGTAATGCTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20650
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 3374 | 4461 | 65 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10525358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10378984 |
GRCz11 | 6 | 10614411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCGGCCTTCATCTCTTATGCTGGATCTTTCTCAAAGAGATACAGATA[T/G]GAGTTGCTCCATAACCTCTGGATGCCCTATCTCCGTGCACAAAAGGTAAC
Long Flanking Sequence:
TTTCCCTGAAACAAGCAAAATAATCTTATTCCAAACCAAAAACAAGATTATTTTGCCTACTTCATTGGCAGCTTATTTAGCTTGTTTAAAAAAAACACTTAATTTTGACATATTTTTTTCTGAAAACAAAACCGTATTTTCACTTGTCTGTAAAATGCTTCTTGATGATTAAATTGTTTAAATATTTAGACAGGAAACAAGACCAAAACTCAAAGTAAGGAAAACATTTTTGCCATTAAGAAGACAAAGTATAAATAATACTATTATAAACCATTAATATTTCAGCTTCATTATAGCAAATATGCATTGCTGTTAGAGAATATACATTTATTAAAATCTTCTAAAATAAAAAATAATGCCTGTGTATTCCAGTCAGAAAACATACGCTGGGCTCATTCTGTGGCTCAGTACCGTGAACAGGAATCAACTCTTTGTGGAGACGTTCTCCTCACTGCGGCCTTCATCTCTTATGCTGGATCTTTCTCAAAGAGATACAGATA[T/G]GAGTTGCTCCATAACCTCTGGATGCCCTATCTCCGTGCACAAAAGGTAACTGTGTGTCACTGTCATTCCGTTTATCTTGGGATCCCATTTGGAATTGCATGTTTTAAACAATTCTTATACTTAACCTGATCTTATATTGACAAACTAAGAATAGTTGGTAAAAGCTCTAAGTGTGTACTTTTCATATTTGACCATTTTTATGCAGGAAATATTGTTTTGACAATAATTTATTAATGTGTAAGAGAAGGTAGCAGGAAAAAGCCAATAAACACTTACAATCACTTAAACTTCAGTTTTACTGTATGTTAATAGTCTAAACAAAATATATTTTCTTGTATTTCTATCAAAATATTTAAGATTTAATTGAAATTTAATATGAAGTGATGGTTACCAAGTGTCCTTTAGGAATCATCAATTAGTCATAAATGTGGTATTTGTTGGTATAGGAGCTCACAAAAACCTGAAAAAATATTAGTGATGTCAGTTACAGATTTGGAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40642
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 4015 | 4461 | 77 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10505150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10358776 |
GRCz11 | 6 | 10594203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTAATCAACTGCAAACATGTCTGTTCATGCGTAGGACATTCTGGAC[C/T]AGTGTTCCCGTGAGCAGGAGTTTAAGACCATCCTGTTCTCGCTGTGTTAT
Long Flanking Sequence:
TCGCATTTAAGAGCAATGGGCGGCCCCTGGTAGTTTGGCTGTATGGATTGCGTATGGGAGGCTCGACTCTTTAATGTTTATTTGCCACCCTTCAGAGAAAGACTGAAAATACAGGAAAAATACGGGAAAATACCTTTACGGGATCATATCGGGATAGAACTGTAAAACACGGGAGAATCCCGGGAAAAACGGGAGGGTTGACAGGTATGCAGATTGAGCTCAGCCACTGTCAATAAAGTTTAATCCTTTAAAATGAAAAGACAATAAAAAAAATGTAATAAATAAAACGAAAAACAGAATTTGGGGTGAAAAAATTATGATATCATAAGACCCTTCATTTTTTTCTAATAGCCTGTGATTGAAATTCTAACACAATTCGACAAGCCTTCTGATGATGATTTGCGTCAGCGCTTCTTTAGTTAGAATGAGAAGGAAATTAACTACAGAAACTCTTTTAATCAACTGCAAACATGTCTGTTCATGCGTAGGACATTCTGGAC[C/T]AGTGTTCCCGTGAGCAGGAGTTTAAGACCATCCTGTTCTCGCTGTGTTATTTCCACGCCTGTGTGGCTGAGAGACGCAAATTTGGACCGCAGGGCTGGAACAGGAAGTACCCATTCAACACCGGAGATCTCACCATATCAGTCAACGTGCTCTACAACTACCTAGAAGCAAACTCACAGGTGTGCAATTAACCACAGGACAAACACTGAGCTTCCTCTGAGGGATAAAGACAGCTCTTAAAACCAAACTTCATTCCAATCTCAAGAGGCGTTTTTTTAGCCTCGCTAGGAACATTGTGATCTGTCTGTATTTAATGCAGAGCAGTGTAAACAGACTTCTTTTACCCAGGTGCCGTGGGAAGACCTTCGCTACTTGTTTGGTGAGATCATGTATGGAGGCCACATTACCGATGACTGGGACAGGAGACTGTGCAGAACTTACCTGGAAGAGTACATGCAGCCTAACCAGGTGCACGCGTCGCACGCACAATGCAATTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33816
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 |
---|---|---|---|---|---|
ENSDART00000125876 | Nonsense | 4180 | 4461 | 79 | 84 |
Genomic Location (Zv9):
Chromosome 6 (position 10504382)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10358008 |
GRCz11 | 6 | 10593435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAGTGATGTCCGACAGCCTCTTCCACACTCTTCTAGAGCTTCAGTCC[A/T]GAGACTCCAGCATGGGGGAAGGAGCTTCGCAGACCACTGAAGAGAAGGTC
Long Flanking Sequence:
GCGTTTTTTTAGCCTCGCTAGGAACATTGTGATCTGTCTGTATTTAATGCAGAGCAGTGTAAACAGACTTCTTTTACCCAGGTGCCGTGGGAAGACCTTCGCTACTTGTTTGGTGAGATCATGTATGGAGGCCACATTACCGATGACTGGGACAGGAGACTGTGCAGAACTTACCTGGAAGAGTACATGCAGCCTAACCAGGTGCACGCGTCGCACGCACAATGCAATTTACAACCGTAAATAAACAGCTATTTTGTACAGTGTAGCTTGAACAGGCCATAACACTTTTCCCTTTGCATTTACAGTTTGACAGGAAGATGTCATTGGCCCCGGGATTTATTGTACCTTCTAACCTGGATTACCAGGGTTACCACGCATACATAGATGAGATGCTGCCCCACGAAAGCCCAGTGCATTACGGTCTGCATCCAAACGCAGAGATCGAGTTTCTCACAGTGATGTCCGACAGCCTCTTCCACACTCTTCTAGAGCTTCAGTCC[A/T]GAGACTCCAGCATGGGGGAAGGAGCTTCGCAGACCACTGAAGAGAAGGTCTGTTTCTCACTGCACATCTTGGTTTGGTGAGAGACTTTCATAGAGGTTTAAAGTAGGGCTGCGAAATTACCATTATCCCTCTAATAGTGTATATGCAATATAAAGTTGAAGTCAAAATGATGAGCCCTGCTGTGAATTTTTGTTTTATTTTTCAAATATCTCCCAAATTATGTTTAACAGAGCAAGGAAATTTTCACAGTATTTCTTATAATATGTTTGATTTGTTTTATTTCAGCTACAATAAAAGCAGATTTAAGGTCAATATGATTAGCTCCCTTAAGCTATATATTTTTTTAATTGTCTACAGAACAAACCACTGTTATACAATAACTTGCCTAATTAACCTAGTTAAGCCTTTAATTGTCACTTTAAGCCAGGGGTCTCAAACTCGCAGCCCGCGGGCCATTTGCGGCCCTCAGTGCAATATTTTGTGGCCCGCGCCGACCGCTG
Associated Phenotype:
Not determined