ZMP
si:dkey-14p11.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
C20orf117
Human Description:
chromosome 20 open reading frame 117 [Source:HGNC Symbol;Acc:16111]
Mouse Orthologue:
9830001H06Rik
Mouse Description:
RIKEN cDNA 9830001H06 gene Gene [Source:MGI Symbol;Acc:MGI:2444575]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15992 | Nonsense | Available for shipment | Available now |
sa8520 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37624 | Nonsense | Available for shipment | Available now |
sa5028 | Nonsense | F2 line generated | Not yet available |
sa11769 | Nonsense | Available for shipment | Available now |
sa11466 | Nonsense | Available for shipment | Available now |
sa8553 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37623 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15992
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 68 | 1793 | 1 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9598464)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9556605 |
GRCz11 | 23 | 9491575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTACAAGTTACCGAGAAAAAGAAAATACACCGGGCACCGTCTCCTGCA[C/T]GACCCAAAGATGTGGCCGGCTGGTCACTCACTAAAATCCGCGGCGGTATC
Long Flanking Sequence:
TCATTCGTCACGGTCAGAGCCGCTATTTTGGGCGGGGAAAAAGAAACCCAACTAACACTCCAGCAGCACTCAGCAGACGAGCAGCAGCAACTCTGCACGAGAAACGGGGACATATCTTGCAGACGAGGAGCACTGGAGAAAACAGAAACATCTTAATCCAAGCAATTGCATTGCCTTTAGGATTTCCCATGATTTGGATGTCGGCTGACCTGGTGTAAAGCGCTAACCAGCTCAACTTCAGTTTTTGGGGGGAGAAGGAGGTACATTTCGGCTTCATTTGTGTCTTGTAAACGGAATGAATGACCAAGACAAAGGTTGACACCGGTTCCCCGACGCATTTTGTCTCGTCGAAGGAGAAGAGGCAAAAGCAGAAAATGGAGAGCAGCACCGGCGAGCTAGAACAGCCGCAGCCGCAGCACCAACCGACACAACAGCCGCCGCCTGCGCCGCCGCTACAAGTTACCGAGAAAAAGAAAATACACCGGGCACCGTCTCCTGCA[C/T]GACCCAAAGATGTGGCCGGCTGGTCACTCACTAAAATCCGCGGCGGTATCGGCACGCCGACACTAAGCGTTAAACCGGGGGCCATTTATTTAGGTGGCCGCGTGTCCAGACGCAGCCCCGTTACCGGGAAAGACGCAAAAACAGAAAAGAATAAACCAACTGGCAAACCCGCGCTGTCAGCGACCGGTGCTCAGAAGAGCAGCGTAAAGTCTAATAAAAGCGGCCGGAGAAAAGTTTCAGATGCCAGCATCGGATCGGATGATTTAAGCAAGGACTCCGGATGCGCACCGGGGAAACTCTCACCCACCGACAGCAGTTCCGAGCTCTCCGACTGCGCCTCCGAGGAGAATAAAGTCTCCACAGACGCGCTTAGTAGCGACACGGAGACAAGCAGCCGCGGGGGGATCGACGGCGACAAAGCGGCAGCGGAACATGGATTACTGGACAAAAGTGGTCACACCAAGACCAGCGCAGAGAAAGAGCGACTCTCGCTGGGGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8520
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 534 | 1793 | 5 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9530034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9488175 |
GRCz11 | 23 | 9423145 |
KASP Assay ID:
2261-7355.1 (used for ordering genotyping assays)
KASP Sequence:
GAAACTAGTGGAGGAGGAAGCGAATCTTCTAAGTCGAYGGATTGTAGAGT[T/A]GGAGKTKGAAAACCGTGGCCTTCGTGCTGAAATGGACGACATGAAGATCC
Long Flanking Sequence:
ATTGTGTGAATGTAATCAGGAAAATGGCCTAATAGGACAATTTATACTTTGGAGAACTGGTGGATAGTTCTGTATAGAACTGAGTTCCTATAATTACAAATAATATACGAAAGCTCTTATTGTCCACTGGCCTTAGTCTTAGTCCTAGTACCATGGCGGTGGATGTGAGGTAACTAAAAGACAGCTTATTGTTGAATGTTTTAATTGCTAATAATCACTTTCTCTCCAGCCTCCAGAGGACAGTTCTGACCTCAAATGCCAGCTTCACTTCGCCAAGGAGGAATCAGCTCTCATGTGCAAAAAACTCACCAAGATGGTCAAAGACAACGAGTCTATGAGGGAGGAACTGGCAAAGTTTCGTTCCATGTATGGAGAAGTTGATGCCTCGCTGACCGTTGAAGAAGTGGCGGACTCTCCTCACACCAGAGAGGCAGAGGTCAAAGTTCACCTGAAACTAGTGGAGGAGGAAGCGAATCTTCTAAGTCGACGGATTGTAGAGT[T/A]GGAGGTGGAAAACCGTGGCCTTCGTGCTGAAATGGACGACATGAAGATCCAGGATTCTCCAGGTGGAATTGGTATCACGGGCGGAGTTGGAAGTCACCTGCTGTTTTCCACATCTGAGAATGTGATGGAGCTACAGCGACACCTACAGTTTGTGGAAGAAGAGGCAGATCTGCTTCGTAGGTCCTTGATCGAAATGGAGGAGCAGAACAAGCTCTTGATGAACGAGCTTAACCACTACAAGTCTGAGCTTCCCGCTGTCACTGAGATAGAGCCATCATCATCATCCACAACCATCACTTCGCCCACAATCCTTCCTGGTCCTTCTGAAGATGCACTAAATGAAGCCACCCATAAAGAACTTCTTGCTGCCAGACTTCAGATTGCAGAGCTGAACGGCAAAGTAAAGAAGCTCCAGTACGAGAACCGTGTGCTTTTGTCCAACCTTCAACGGTGTGACTTAGCTTCCAACCAAGGCTCCGCACGTCCATCACTGGAAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37624
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 596 | 1793 | 5 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9529848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9487989 |
GRCz11 | 23 | 9422959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGACACCTACAGTTTGTGGAAGAAGAGGCAGATCTGCTTCGTAGGTCCT[T/A]GATCGAAATGGAGGAGCAGAACAAGCTCTTGATGAACGAGCTTAACCACT
Long Flanking Sequence:
TATTGTTGAATGTTTTAATTGCTAATAATCACTTTCTCTCCAGCCTCCAGAGGACAGTTCTGACCTCAAATGCCAGCTTCACTTCGCCAAGGAGGAATCAGCTCTCATGTGCAAAAAACTCACCAAGATGGTCAAAGACAACGAGTCTATGAGGGAGGAACTGGCAAAGTTTCGTTCCATGTATGGAGAAGTTGATGCCTCGCTGACCGTTGAAGAAGTGGCGGACTCTCCTCACACCAGAGAGGCAGAGGTCAAAGTTCACCTGAAACTAGTGGAGGAGGAAGCGAATCTTCTAAGTCGACGGATTGTAGAGTTGGAGGTGGAAAACCGTGGCCTTCGTGCTGAAATGGACGACATGAAGATCCAGGATTCTCCAGGTGGAATTGGTATCACGGGCGGAGTTGGAAGTCACCTGCTGTTTTCCACATCTGAGAATGTGATGGAGCTACAGCGACACCTACAGTTTGTGGAAGAAGAGGCAGATCTGCTTCGTAGGTCCT[T/A]GATCGAAATGGAGGAGCAGAACAAGCTCTTGATGAACGAGCTTAACCACTACAAGTCTGAGCTTCCCGCTGTCACTGAGATAGAGCCATCATCATCATCCACAACCATCACTTCGCCCACAATCCTTCCTGGTCCTTCTGAAGATGCACTAAATGAAGCCACCCATAAAGAACTTCTTGCTGCCAGACTTCAGATTGCAGAGCTGAACGGCAAAGTAAAGAAGCTCCAGTACGAGAACCGTGTGCTTTTGTCCAACCTTCAACGGTGTGACTTAGCTTCCAACCAAGGCTCCGCACGTCCATCACTGGAAACAGATGCCGAAGCCGGAGACTCAGCTGAATGCATTCCTAGCCATACGCATCGCGAAGGTCCAGTGGGGGATGAGCAAACCGATATTCTGGAGGAGAAGAATCTAAAAGTTTCAAGAACAAGTCACACTCACACTTCTCAATGCCTCAGTGTAAAGGATCTCCTCGCTATCCGTGACCAGGCACAACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5028
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 784 | 1793 | 5 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9529283)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9487424 |
GRCz11 | 23 | 9422394 |
KASP Assay ID:
554-3573.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCTTCTGACTTCACCCGACACCTCCTGTATCTCACCGGACTCTGTCTA[T/G]CGCAAGATCACCGCCAATGATTCTGCTGAACCGGTTCTACTAGAGAAGAG
Long Flanking Sequence:
CCCGCTGTCACTGAGATAGAGCCATCATCATCATCCACAACCATCACTTCGCCCACAATCCTTCCTGGTCCTTCTGAAGATGCACTAAATGAAGCCACCCATAAAGAACTTCTTGCTGCCAGACTTCAGATTGCAGAGCTGAACGGCAAAGTAAAGAAGCTCCAGTACGAGAACCGTGTGCTTTTGTCCAACCTTCAACGGTGTGACTTAGCTTCCAACCAAGGCTCCGCACGTCCATCACTGGAAACAGATGCCGAAGCCGGAGACTCAGCTGAATGCATTCCTAGCCATACGCATCGCGAAGGTCCAGTGGGGGATGAGCAAACCGATATTCTGGAGGAGAAGAATCTAAAAGTTTCAAGAACAAGTCACACTCACACTTCTCAATGCCTCAGTGTAAAGGATCTCCTCGCTATCCGTGACCAGGCACAACTTGTTACCTCAGCCATTCAGCTTCTGACTTCACCCGACACCTCCTGTATCTCACCGGACTCTGTCTA[T/G]CGCAAGATCACCGCCAATGATTCTGCTGAACCGGTTCTACTAGAGAAGAGTCAGACCCCGAGCTCCACACTGCCTGTGGTAGAGGTCCTGCATGGCAGACTGCAGTTCCTTCAGGCTCAGCTCCAGGCCCTCAGTGAGAGGGTGGATGCCCTGGATGAGCCCGCAGTGAGAGATTGTTTTGACGGGATGTCCCAGATGCCCCTGCTGTCTGAGGCAGAAGACCCTACAGCAAATTGCTTATGCCCTGCAGATGCTCAGTTTAACCTGAACACAGCCCAACAGAAGGTATGCACCCAATTGCTTAGTCAGATATTCTCTTGCATCGTACTCTTTCCTTTTTGCTTTGTTTTGTGCCTTTTTATCAGCAATATTGCTTTTTGTTGCTTTGCTTGATTAGTATTTACACATAAAGGTTTGCCGACCATTATAACAATGCATGTTTGTAGTGCATTATAAGACCTCATAGTGGATAACATTTAGGCCTCTAATGGAGTAGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11769
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 935 | 1793 | 7 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 9522633)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9480774 |
GRCz11 | 23 | 9415744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTCTCTCCAGCTGACAGAGCAGGTTCATGAGCTGCACGCTCTGCTGT[C/A]GGAGGYGAGAGAGAAGGCTCATGGAGCACAAGAAGCTCTGTCACAGGAGA
Long Flanking Sequence:
TGGCTGAGGTGATTCCCTTGAGCAAAGCACCGAACTGCATAAATAATAATAATAATAATTCCTTACATTTATATAGCGCTTTTCTGGACACTCAAAGCACTTAAAACATTGTAGGAAATCTCCTCATCCACCATCAGTGTGCAACATCCACATGGATGACACGGCGGCAGCCATACTTCACCAGACCACACACCCATAAATGTAAATGTAGTATAGAACTAGGTTTTTGTGCACTCTTTTCTTGCAATACGACAAAGCAGATTGTGTTCTGTCAGCACACTTGATGCCAAGAACAGACAGATTGTCATTAATATGATGTGCTTTAAAGACAGCTATTGACATTGTAGCACCGAAACATTTTGACATGGCAGCAGATTTGCAGTTGTTCCAGTTTGTTTGTATTACAAATACTGAACAGATCGATTAATTACCTGTTATTCTCTCTCTTCCTGTTTCTCTCCAGCTGACAGAGCAGGTTCATGAGCTGCACGCTCTGCTGT[C/A]GGAGGCGAGAGAGAAGGCTCATGGAGCACAAGAAGCTCTGTCACAGGAGAGACTCGAGCGCCACAGCGACATTCACAAACTGTCTCAGGTACAAACATGTTAAAACGTGCTAATTTAGGTCTTTCACAAACACCGAACACAAAATTTAGCATAACTGTAATATCTGGTTGCAAACCTGCAAACAGGCATGTTTTCCTCATATCTTTTTCTTTCTGTAGCTTCAGGAAGAGCATCAGAAGGCCCTCCTCCGCCGAGACTTCCAGCTGCAGAGTCTGAGCCTACAGACACGTCTGCAGCAGAAGCTGTGGAGTCAGGAGAGGAACCTGCTGGTGCAGGAGTCACAGCAGCTGAAAGAGAGCCTGCTCCTCATCAGCCTCAAGCTGCGCTGGCTCCTCAAACAGTGGAGACTCGGCAAGAAACTAGACACAGAGAGCAAGGACATCCTAGAGGTATGGAGACGTTTTTTTTTTAAAGCAGCTGAGGGGGAACTCATTAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11466
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 1204 | 1793 | 11 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9512532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9470673 |
GRCz11 | 23 | 9405643 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTKATGGACCTTACCAAACAACTGCAGATCAGTGAGAAAAACTGGAGC[C/T]GAGAGCGGCKAGAGCTTCTGGAGCACTTCAACCAGGAAAGAAGTCAATGG
Long Flanking Sequence:
GAGAGGAGTAGCCCGGCTTCCTAATTACCATCGCTACTTACCAATTTTATTGAATGAGCCTTGTTTGAAGCTGTTGTAAAACTGTCGATACAATACATAGAGCTGATGTTGTTTAGTGTAAACAGACAGTCCTTAAAGAACTGTCAATGTTGGGCACATTTAATTGCACTTTGATCTCTTTGTGTAATAGTAAAATGAAATCTATAAACCTGCCTTGATGTCTGGATACTACTCAGACTGCATATAAATATGGTCACTTCTGCTTGTAAGATTTCAAACATTCTTTTTTTTGTCTCAGTCTCTAATTTGCACTTCATCTTTGTCATCAGCTGGAGGGTAAGCTGGGGAAGGCGTCTGTGGCTGTGGGTGAAAAGGATTTTTCAGACCTTAAGGAGGCACTAAAAAAGGAGCGAGAGGAGCATCAACATCTCTTGGCGGACTCTTATGCTGCTGTTATGGACCTTACCAAACAACTGCAGATCAGTGAGAAAAACTGGAGC[C/T]GAGAGCGGCGAGAGCTTCTGGAGCACTTCAACCAGGAAAGAAGTCAATGGGATCAGCGGGTACGCGATGCGCAGAGCAAAGGCGCACAGGTAGAATGTCATATTGTGGTGTTAGGATTTGTTTGCTTAAATGAAAATTCTGTCATTGCTTATTTATTTTCATGATGCTAAAATCTAGTTTGATGTTAAGTCAAGTCTTCTTAATTTCTAAAAAAAATATCTTTCTTCTATAGAACACAAATAATAGTAAGTGGTCAAGTCTTCTTAATTTCTAAAATAAATATCTTTTTACAATAGAACACAAATAATAAGTGTTCAAATAATAATAATAATAAAATACACTCACCGGCCATTTATTAGGTACCTATCTAGTTCTGAGTTGGACCCTCTTTTGCCTTTATAATTGGCTTAATCCTTTGTGGCAAAGATTCAATCAGGTACTGGAAATGTTCCTCAGAGATTTTGGTCCATATTGACGAGATAGCATCACGCAGTTGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8553
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091852 | Essential Splice Site | 1257 | 1793 | 13 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9510255)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9468396 |
GRCz11 | 23 | 9403366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MCATTTAATCAGGCATTATTATTTTRTAATCTTTTCCAATCTCTTACWAC[A/T]GGACCAAATCAATATCCMCCCTCACTGAGTTGAAGAGTCTGCTAGACACC
Long Flanking Sequence:
ACAAGTAATAAGACTGGAAAAACTAATAGGACTATAGTTTTCTTTACATCTTCCTCCTACTCTGTCTCTTGTCACAAGTCTGGCTCGGGGCTCTAATATCTTTGTTTCATTTAACATCCTGAATGGAAAACTCTAATACCATGCCTCACTGAGAGAAATTGGGTCATTTACTTAGACGTGATGAACCATACCACAATCATTAGTCCCACAGAAGAAACTAGCTGTTTTGAATGACCTAATTTCCTGAGGAGAATATTGGCTGACTCAGTAATGCCACATAAATGAATGGGTGTATTGTGACAGGATGTGGCCATGACATACTAAAATAGATCATTTCTCTTTCAGTCTCTCCATGACAAAACTTCAGAGAAGGAAGCCTTAGCTGATGTAGTCGCGGGTAGTTCAGCAATGCAAAGGTAAAATTACTTTCATACAAAATAATCTGCATTCCCATTTAATCAGGCATTATTATTTTGTAATCTTTTCCAATCTCTTACTAC[A/T]GGACCAAATCAATATCCACCCTCACTGAGTTGAAGAGTCTGCTAGACACCAGTCTACTCCTTCATAGTCACAAGGTCATTGGGGAACCAGAGTACGCCATGGCACAGCACCAATCTGCTGCTCCTGCTTCTATTCTGGCTCGCACTGACTTAAGTGATCTCAACAATAAAAACTGGAAGTACCTGACCAGTGATTCAGCCATACTGGAGAAGGGTGACCAGTTTAAGACATGGGACTGCCCAAGCACCAACTCTAACAGCAGCTTTCCAGGGCTGGAGCTGAACAAGGAGTACATTCAGAGAAGCTACACCGCTCCAGATAAGACGGGCATCCGCATCTACTACAGTCCTCCGACAGTGAGGAGAATGGAGAGGAGGCCAGTCAAAGAAAACACACAGCAGGATTACCAACAAGGACTATCATCTAGGGATGCAGCAATGATAGATCCATCTGGTCAGATTGCTGCATCTGCACCATTATTGACAACTTCCCCATCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37623
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 |
---|---|---|---|---|---|
ENSDART00000091852 | Nonsense | 1470 | 1793 | 13 | 14 |
ENSDART00000139688 | None | None | 339 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 9509616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9467757 |
GRCz11 | 23 | 9402727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTTCAGGCAACCTTAGCGATGACATGAAGGAGATGACCAATTGTGTA[C/T]GACAGGCCATTCGTTCCAGTTCCCTGGAAAGGAAATGCAGCAAAGATACA
Long Flanking Sequence:
CTCGCACTGACTTAAGTGATCTCAACAATAAAAACTGGAAGTACCTGACCAGTGATTCAGCCATACTGGAGAAGGGTGACCAGTTTAAGACATGGGACTGCCCAAGCACCAACTCTAACAGCAGCTTTCCAGGGCTGGAGCTGAACAAGGAGTACATTCAGAGAAGCTACACCGCTCCAGATAAGACGGGCATCCGCATCTACTACAGTCCTCCGACAGTGAGGAGAATGGAGAGGAGGCCAGTCAAAGAAAACACACAGCAGGATTACCAACAAGGACTATCATCTAGGGATGCAGCAATGATAGATCCATCTGGTCAGATTGCTGCATCTGCACCATTATTGACAACTTCCCCATCTGCATACGAGCAGTGGTTGAGTTCACTTTCACAGCAGCACAGAGATCTGCTTGAAGGGCGGACAGGAGGTTCTGCACCTTTCCATGGATTAGAGATTTCAGGCAACCTTAGCGATGACATGAAGGAGATGACCAATTGTGTA[C/T]GACAGGCCATTCGTTCCAGTTCCCTGGAAAGGAAATGCAGCAAAGATACAGGGAGCCAGACAGTTGGTGTTTGTAGTACAGGAACGCAGACTGCACAGTTTGTCAGCATTGGTATGCAAACTGATGTACCCATCTCAACAGCAAGAGGCCTTCAAGGGAAAGCATGGTCTCCTCGTCCATCCACCTCACTTGCATCTGCACGTTCTCGACAGATCTCTTCATCTTTGGACAAAGTCCACAGTCGCATAGATAGACCTTGTTGCTCTCCCAAATATGGCTCACCTAAGCTCACACGCAGGGTTTCCACCTCCTCCTCCAAACTCGAGACCTCATCAACATCTTCAAGGGATCGCAGTGTCTGGAATCTGCATAACCGAACTGGATCTCAAAATGGTTCTGCCTGGGCTCGTTCCACCACCACCCGTGATAGCCCAGTGCTTAGTGGACTCAATGATGGCTTGACCAGTCTCTTCAGTGTGGTGGAACACTCTGGAAGTGTT
Associated Phenotype:
Not determined