ZMP
si:dkey-221j11.2
Ensembl ID:
ZFIN ID:
Description:
Novel protien similar to H.sapiens FAM83H, family with sequence similarity 83, member H (FAM83H) [So
Human Orthologue:
FAM83H
Human Description:
family with sequence similarity 83, member H [Source:HGNC Symbol;Acc:24797]
Mouse Orthologue:
Fam83h
Mouse Description:
family with sequence similarity 83, member H Gene [Source:MGI Symbol;Acc:MGI:2145900]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35575 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28191 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35574 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42287 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30974 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35573 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22372 | Nonsense | Available for shipment | Available now |
sa10399 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35575
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099714 | Essential Splice Site | 203 | 2317 | 2 | 5 |
ENSDART00000135172 | Essential Splice Site | 203 | 302 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43225915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42446874 |
GRCz11 | 13 | 42572934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTTGCAATGGTGAACAACTGTAGGGTTAATCTGGAGGAGATAAAAG[T/C]AAGTGGCATATGCCTTTTTAAATATGAGGCTTGGCGCAAATTTAGTTGTC
Long Flanking Sequence:
CCCATTGGCGACTGAATCGGAAGTTCTAAAACAATCGCGAAAACAGACGCACTTCCGCATTTTAGATTAAGGTCAATAGTGGACATTTAAAAAAGGATGATATTTTGAAACACAAACAAGTTAACAGCTTTTCATTTTAGAATAAGGTCAATAGACAGGCCTGTAAAATGGCTCTACAAAAAAATGTCAGTGAAAAATATTTTATATTGTAATAAAACTACATACTAGTGGAAAAAAGTTCTAAAGCGATAAAAAAAAAACCTGAAACTCACTCTAACATCATTGCAACACAATTGTTTGTTTTTTTGTAATATATTTGTATTTTTTGTTCCAGGTTATTGCTGTGGTAATGGATATGTTTACAGATGTCGACATCTTTGCTGATATCCTTGGTGCAGCAGCACGTGGTGTGGCTGTCTATGTTCTTCTTGATGAACTAAATGCTCACCATTTTGTTGCAATGGTGAACAACTGTAGGGTTAATCTGGAGGAGATAAAAG[T/C]AAGTGGCATATGCCTTTTTAAATATGAGGCTTGGCGCAAATTTAGTTGTCGTAAAGAGGGTTTTGTTAGCATGTTAATTAAAGTGAAAGATCACCCAAAACTGAAAATTCTGTCATTATTTATGCACCTTTCATTTGTCACAAACCTGTTTGAGTTTTTTTGTTCTGTTGAACAATCAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTATTTTAAATATATATTATTTTTTCTAGAGCCATTTTTTCTAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATACTGTATATATATACTGTATATATACTCAAAGAGGTAAACATTGATTTATACTGTTAGTTTTTCCTACTGTGAAAGTCAATGGTTACAGGTTTCCAGCTTTCTAAAAAATATCTTATTTTAAGTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28191
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 795 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43222334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42443293 |
GRCz11 | 13 | 42569353 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAGAGGGTGCTCAGGAAGAAAAAGACCTGCCTCAAACCACAGTGCCT[G/T]AAGGAAATAGCAAAAGGATGGAATCTCCATCAAATGCATTGCAAAAATCA
Long Flanking Sequence:
ATTTCAAATCAACACCAACATCGACCTCAGAGTCTTCTTGCACCACTGAGGGTGACAAAGCAGAGGAGATGCAGAATAGAGAACCCAAAGAGACTAACCGGATTAGTGAAGAGTTCCTCAAGAGAAAACCCAGCAGACCTGTTCAGAGGAGTTCCAGACTGAGACACTCGTTGATATTCAGTTCAAATTTAGAGTTGAATACACAAGAAGAGATGAAAGATACAGCAGGAGAAATAGATGGGGATGAAGCTTCAAAACTGTCAGCTCGTGTGTCACATATTTTGGATAAGAGGAGGACTGGTTCTCCATTTCAGCCATTTCAGTGGAGCAATTTTACTAAGTCAGCCACATTTGATAACTCTGCCACAGAGTCTGCAGAACCTGAGGATGAACTAAGCAAAACAAGTGAAAAATCGGATTTGGAAAACCCACAAAATCTTCAAAAGAAACCAATAGAGGGTGCTCAGGAAGAAAAAGACCTGCCTCAAACCACAGTGCCT[G/T]AAGGAAATAGCAAAAGGATGGAATCTCCATCAAATGCATTGCAAAAATCATCATCTCTCATAGATATGAATGACCCGGACTGTAGACTGAGATATTTCAAAGAGTTGGCAGCCAAACGCAAACTTTCAGCAGCAAAGTCTTCTCAGAACAATCCAGTGAAAGCCACCCAAAAATTTGCTCTACCAGAGAAACCTGCAAGTAATGACACAGATAAAAAAGCTGTTTTCAAAACTCCAGACACTTCACTTAAATCAAAAACGACAGCTGTTGCAGCAGAAATCAAAGAGACATATAAAGATCCCAAATGTGAAGAATCAGGTAAAGACATTCTTCAAAGAGCTACAGATGCTGAAAAAATTAGATTTAAGAAAAAACTTGCAGAAGAGTCTGGTTCAACTTGCTCTGGCTCAAAAAATTTTTTCCAAGAAATCAGAGATTCAGCTCTAAAACCTGTTGAGGAGGCCAAAACGGTGTCTACAGTTAAAAATCAAACCACTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35574
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 1472 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43220301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42441260 |
GRCz11 | 13 | 42567320 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCTGCTGAAACAGAAGTAGACAATACCCTGAAATTTACAACACCATA[C/A]ACAGTTTCTTCCCAGAAGCCCAGTGCAACACAGAATGTTTCTTCAGTTCT
Long Flanking Sequence:
AATCCATCTGCTTCAGCCTCTTCACAACATCTGAATGCAACTAAGACAGACTCGTCTCAAAACCCCACTGCATCAATCACAGACTCTTCCCAGCAACCCACTGCAACAGCCACAGACTCTTTTCAGCACTCCACTGCCAGTTCCAGCCAGTCCACTGCAAAAGTCACAGAATCTTCTCAGAACTCTACTGTAACAGGCACAGATTCCTCCCAGCAACCATCTTCAACTGAGGCAGATTCTGCACAGCTGCCTATTGTAGCAGAGGTAGACTCTTCCCAACAGATTCTGCATGCTACAACAGAAACAGACCAATCCCAGCAGTATACTGCACCAATCACAGACTCCTCTAAGCAGCTCACCGCCGAGGTCACAAAGTCTTTCCAGCAGCCTCCTCCAAAAGACGCACATGCTTTACAGGAGGCTGCTTCAAAAGTGGTAGACTCTTCCCAGAAGCCTGCTGAAACAGAAGTAGACAATACCCTGAAATTTACAACACCATA[C/A]ACAGTTTCTTCCCAGAAGCCCAGTGCAACACAGAATGTTTCTTCAGTTCTGTCCGTTGCAACTGAGATTGACTCATTCCATCAGCCTGCTGCAAGAGAGACAGACTGCTTCCAGCATCCCAGTCTAACAGAGGCCCACTTTCCCCAGCAACCCTCTATGACTGAAACAGACTCTCTCCAGAAACCCCCTGAAACAGTCACAGATTCTTGCCAGCACCCTGCTCCACCAGGGACAAACACTTCTCCGCAACCTGCGTCATCTGAGAGAGACTCTTCAGAGCAACTGTCTGTCACTGCTGGAGTGGTAAAACAAACCACTCCAACATTCACAGACACGTCCCAGCAGACACCTAAATCAGAGACATACTTTTCCCAGAAAACACTTCCAATAGACAGAGACAACTCCCAGCACCCCACTGCAAAGCAGATGCAGTCCACACAGCAACACACTGCACAAGACAGCGACTCCTCCCATCAGTCCACTCCTGTAGAAGCAGATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42287
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 1586 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43219961)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42440920 |
GRCz11 | 13 | 42566980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGCTGGAGTGGTAAAACAAACCACTCCAACATTCACAGACACGTCC[C/T]AGCAGACACCTAAATCAGAGACATACTTTTCCCAGAAAACACTTCCAATA
Long Flanking Sequence:
ACTCCTCTAAGCAGCTCACCGCCGAGGTCACAAAGTCTTTCCAGCAGCCTCCTCCAAAAGACGCACATGCTTTACAGGAGGCTGCTTCAAAAGTGGTAGACTCTTCCCAGAAGCCTGCTGAAACAGAAGTAGACAATACCCTGAAATTTACAACACCATACACAGTTTCTTCCCAGAAGCCCAGTGCAACACAGAATGTTTCTTCAGTTCTGTCCGTTGCAACTGAGATTGACTCATTCCATCAGCCTGCTGCAAGAGAGACAGACTGCTTCCAGCATCCCAGTCTAACAGAGGCCCACTTTCCCCAGCAACCCTCTATGACTGAAACAGACTCTCTCCAGAAACCCCCTGAAACAGTCACAGATTCTTGCCAGCACCCTGCTCCACCAGGGACAAACACTTCTCCGCAACCTGCGTCATCTGAGAGAGACTCTTCAGAGCAACTGTCTGTCACTGCTGGAGTGGTAAAACAAACCACTCCAACATTCACAGACACGTCC[C/T]AGCAGACACCTAAATCAGAGACATACTTTTCCCAGAAAACACTTCCAATAGACAGAGACAACTCCCAGCACCCCACTGCAAAGCAGATGCAGTCCACACAGCAACACACTGCACAAGACAGCGACTCCTCCCATCAGTCCACTCCTGTAGAAGCAGATTCTTCCCAGCAGCCCACTATAATAGAAGCAAGCTCTACACAGCAGACTACTTTATATGAAGCAAACTCTTCCCCGCAGACCATTGCAACTGAAACAGACTCTTCCCAACAGACCACTATCATAAAAGCAAACTCTTCGCAGCAGACCACTGCAACTGAAACAGATTCTTCCCAACAGACCACTATCATAAAAGCAAACTCTTCGCAGCAGACCACTGCAACTGAAACAGATTCTTCCCAACAGACCACTGTAATAGAAGCAGACTCTTCCCAGCAGACCACTCTAATAGATGCAAGCTCTACACAGCAGACCACTTTAATTGAAGCAAACTCTTCCCCGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30974
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 1614 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43219877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42440836 |
GRCz11 | 13 | 42566896 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAACACTTCCAATAGACAGAGACAACTCCCAGCACCCCACTGCAAAG[C/T]AGATGCAGTCCACACAGCAACACACTGCACAAGACAGCGACTCCTCCCAT
Long Flanking Sequence:
CTTCAAAAGTGGTAGACTCTTCCCAGAAGCCTGCTGAAACAGAAGTAGACAATACCCTGAAATTTACAACACCATACACAGTTTCTTCCCAGAAGCCCAGTGCAACACAGAATGTTTCTTCAGTTCTGTCCGTTGCAACTGAGATTGACTCATTCCATCAGCCTGCTGCAAGAGAGACAGACTGCTTCCAGCATCCCAGTCTAACAGAGGCCCACTTTCCCCAGCAACCCTCTATGACTGAAACAGACTCTCTCCAGAAACCCCCTGAAACAGTCACAGATTCTTGCCAGCACCCTGCTCCACCAGGGACAAACACTTCTCCGCAACCTGCGTCATCTGAGAGAGACTCTTCAGAGCAACTGTCTGTCACTGCTGGAGTGGTAAAACAAACCACTCCAACATTCACAGACACGTCCCAGCAGACACCTAAATCAGAGACATACTTTTCCCAGAAAACACTTCCAATAGACAGAGACAACTCCCAGCACCCCACTGCAAAG[C/T]AGATGCAGTCCACACAGCAACACACTGCACAAGACAGCGACTCCTCCCATCAGTCCACTCCTGTAGAAGCAGATTCTTCCCAGCAGCCCACTATAATAGAAGCAAGCTCTACACAGCAGACTACTTTATATGAAGCAAACTCTTCCCCGCAGACCATTGCAACTGAAACAGACTCTTCCCAACAGACCACTATCATAAAAGCAAACTCTTCGCAGCAGACCACTGCAACTGAAACAGATTCTTCCCAACAGACCACTATCATAAAAGCAAACTCTTCGCAGCAGACCACTGCAACTGAAACAGATTCTTCCCAACAGACCACTGTAATAGAAGCAGACTCTTCCCAGCAGACCACTCTAATAGATGCAAGCTCTACACAGCAGACCACTTTAATTGAAGCAAACTCTTCCCCGCAGACCATTGCAACTGAAACAGACTCTTCCCAACAGACCACTGTAATGGAAGAAAACCTTTTCCAGCAGACCACTGCAACTGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35573
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 1762 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43219433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42440392 |
GRCz11 | 13 | 42566452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAGCAAACTCTTCCCCGCAGACCATTGCAACTGAAACAGACTCTTCC[C/T]AACAGACCACTGTAATGGAAGAAAACCTTTTCCAGCAGACCACTGCAACT
Long Flanking Sequence:
TTTCCCAGAAAACACTTCCAATAGACAGAGACAACTCCCAGCACCCCACTGCAAAGCAGATGCAGTCCACACAGCAACACACTGCACAAGACAGCGACTCCTCCCATCAGTCCACTCCTGTAGAAGCAGATTCTTCCCAGCAGCCCACTATAATAGAAGCAAGCTCTACACAGCAGACTACTTTATATGAAGCAAACTCTTCCCCGCAGACCATTGCAACTGAAACAGACTCTTCCCAACAGACCACTATCATAAAAGCAAACTCTTCGCAGCAGACCACTGCAACTGAAACAGATTCTTCCCAACAGACCACTATCATAAAAGCAAACTCTTCGCAGCAGACCACTGCAACTGAAACAGATTCTTCCCAACAGACCACTGTAATAGAAGCAGACTCTTCCCAGCAGACCACTCTAATAGATGCAAGCTCTACACAGCAGACCACTTTAATTGAAGCAAACTCTTCCCCGCAGACCATTGCAACTGAAACAGACTCTTCC[C/T]AACAGACCACTGTAATGGAAGAAAACCTTTTCCAGCAGACCACTGCAACTGAAACAGACTCTTCCCAACAGACCACTGTAATAGAAGCAGACTCGTCCCAGCAGTCTACTTTAATAGAAGCAGACTCCAAGCAACCCACTGCAACTGAAACAAAGTCTTCCCATCAGTCCACTCCAGTAGAAGTAGAGTCTCCCCAATACCCCAGTGCAACAGATACATACTCTTCCCAGCAGACCACTGCAACTGAAACAAAGTCTTCCCATCAGTCTGCTCCAGTAGAACCAGACTCTTCCCAGCCGACCACTGCAACTGAAACAATGTCTTCTCAGCAGATTACTCTAGTAGAATCAGACGCTTCCCAGCAGACCACTGCAATGGAGACAATCTCTTCCCAGCAGACCACTCTAGTAGAAGCAGATTCTTCCCAGCAGTTCACTGCAACAGAGACAGTTTTTTCCCAGCAGACCACTCCAATAGAAGCAGACTCTATTTCAGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22372
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 2087 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43218458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42439417 |
GRCz11 | 13 | 42565477 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTTCACTTGTCAGTACTGGTGACGTAGATGTGAGCTCTACCCAGCCT[C/T]AAGTTTTACCAGAGCCTTGCCTTTCCTCAACTAAAATTACATCAAATCAA
Long Flanking Sequence:
TAGAAGCAGACTCTATTTCAGAAGAAATAGGCTTGTCTGAAAGATCCACTGCAACAGAAACCGACTCTACCCAGCAGACCAATCTAATACAAACAAACCCTTCCCAGCAGACTACTGCAACAGAAACAGATTCTTCCCAACAGACCTCTCTAACCGATATAGACTCTTTACAGCAGACCATTTTAACAGAAGCAAACTCTTCCCTGAAGCCGACTGCCACTACCACAGACTCCTTCCAGCAGCCTGTAGCAGTAGAGGTTGACCAAACCATGCAGCTCAATGTAACAGAACAAGTATCTTTTCTAAATATTTCTAAAATTGGAGAAGATACTTCCAAACATCCTATTGAAACAGAAAACAATTCCCATCAAATCATCACTGCAACAAGTTCTGACTGTGCAGATGAGAAAAAAGACATTATTGTATCTAAAGACTTGAGCAAAGCATTACCCATTTCACTTGTCAGTACTGGTGACGTAGATGTGAGCTCTACCCAGCCT[C/T]AAGTTTTACCAGAGCCTTGCCTTTCCTCAACTAAAATTACATCAAATCAAGATAGCACAGAAATCCAAGCTAACATATCATCAAATTCTATGGAATCTAGCTGTCCAAATGACCCAAAACCTGAGAAAACTGATGAATGCCAGAAGAATGAATCCATTACAGTACAACCACAGAAGAATGACACCTCGGCTATAGTTCCAGAGAATGAGATACCTCACACAGAGGTTTCTACAGTCATAGGCCCTAATAAGGTTGATGAAATCAAACAAACATCTTTAGAAAAAGAAAACTCTGTCTCTGACATTTCAGAAGTGTCAGAAAAGTCCAATTTGACTGTAACCCATGATTCAGAAAATAAGTCTACTGTTGCAGACAGTCCAAAATTGATTTTGTCTGCCCATCAGTCATCTACAGCGAATGTTATCTCATGCAGCAACCTTAGAGATGACACTAAAGTTCTTTTAGAGCAAATTTCAGCAAAGAACCAAAGCAGATCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10399
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 |
---|---|---|---|---|---|
ENSDART00000099714 | Nonsense | 2215 | 2317 | 4 | 5 |
ENSDART00000135172 | None | None | 302 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 43218073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42439032 |
GRCz11 | 13 | 42565092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAACCCATGATTYAGAAAATAAGTCTACTGTTGCAGACAGTCCAAAAT[T/A]GATTTTGTCTGCCCATCAGTCATCTACAGCGAATGTTATCTCATGCAGCA
Long Flanking Sequence:
AAGTTCTGACTGTGCAGATGAGAAAAAAGACATTATTGTATCTAAAGACTTGAGCAAAGCATTACCCATTTCACTTGTCAGTACTGGTGACGTAGATGTGAGCTCTACCCAGCCTCAAGTTTTACCAGAGCCTTGCCTTTCCTCAACTAAAATTACATCAAATCAAGATAGCACAGAAATCCAAGCTAACATATCATCAAATTCTATGGAATCTAGCTGTCCAAATGACCCAAAACCTGAGAAAACTGATGAATGCCAGAAGAATGAATCCATTACAGTACAACCACAGAAGAATGACACCTCGGCTATAGTTCCAGAGAATGAGATACCTCACACAGAGGTTTCTACAGTCATAGGCCCTAATAAGGTTGATGAAATCAAACAAACATCTTTAGAAAAAGAAAACTCTGTCTCTGACATTTCAGAAGTGTCAGAAAAGTCCAATTTGACTGTAACCCATGATTCAGAAAATAAGTCTACTGTTGCAGACAGTCCAAAAT[T/A]GATTTTGTCTGCCCATCAGTCATCTACAGCGAATGTTATCTCATGCAGCAACCTTAGAGATGACACTAAAGTTCTTTTAGAGCAAATTTCAGCAAAGAACCAAAGCAGATCCACCCAGTCCAAACAGACTCTTTCTTCACCCAATGAAGCTAAAGAGGGTGAGGTTAAATCTGCATATAAATCACTCTCAAAATATTCGGGAAGGCCCTGGTCCGAAAAGGCTACAGCAGAAGAACGGGAGATGTTGCTACAGAGGATGGATCAAATGCGGAAAGAGAGGAAGGTCTACAGCCGTTTTGAGGTATGTTATGGGATTTATGTAAATTGAAAATTTCTAGTTTTATTTTACCAGATTGTGTAAGGGTGCATGTACTTTGTTTCAAGTAGGTTAATTGTTTGAATTTGATGTTTTCACAGGCTTCATGAATTTAACTTTTTGGAAAAGTGACTGCAGGAGTAGACTGTAAAAAGGAAACAATATTTCCTAATTTTGCTCTTTC
Associated Phenotype:
Not determined