ZMP
si:ch211-199g17.1
Ensembl ID:
ZFIN ID:
Description:
Protein FAM83H [Source:UniProtKB/Swiss-Prot;Acc:Q1LVV0]
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 |
|---|---|---|---|
| sa36912 | Nonsense | Available for shipment | Available now |
| sa43341 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23591 | Nonsense | Available for shipment | Available now |
| sa32261 | Nonsense | Available for shipment | Available now |
| sa23592 | Nonsense | Available for shipment | Available now |
| sa23593 | Nonsense | Available for shipment | Available now |
| sa31037 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43342 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43343 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36912
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 250 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 250 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44966537)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44021518 |
| GRCz11 | 19 | 43617115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAATCTGACATTGTACATTTTTTTTTTTCTCTTTTCCCAGCTTTATGT[G/A]GTCTTTTGAGAAGATCCACCGCTGTATCGCCCATTTATTCCTTGGAGAGC
Long Flanking Sequence:
TCAGAAATCACTCTAATATTAATGAATATTGTTATTATTATTAATGCTAATAGTAATATAAGCAATGATGACTAGAGTAATAATTTAATTTGAAACTACATACAATAAGTCAGGGATCACCAAACTTGTTCCTGGAGGGCCGGTGTCCGGCAGATTTTAGCTACAACCCTAATCAAACACACCTGAACAAGCTAATCAAGGTCTTACTAGGTATGCTTTAAACACTCAGGCAGGTGTGTTGAGGCAGGTTGGAGCTTAACCCTGCAGGGACACCGGCCCTCCAGGACTGAGATTGGTGACCCCTGCAATAAGTAATAAATATTTAAAAAAACTCTTTACATTTAATAAATGTTACCTTGATAATTAAAAAAAAAAAATGAAACAAAAATAAATGACCCCAAACTATTGACCAGTAGCGGACGTAATTAACTCTAAAGCATGCACTTTTAATGTAATCTGACATTGTACATTTTTTTTTTTCTCTTTTCCCAGCTTTATGT[G/A]GTCTTTTGAGAAGATCCACCGCTGTATCGCCCATTTATTCCTTGGAGAGCTTGTTGCCACTTTTGATGAGGAGTTTCGTATTTTGTTTGCTCAATCTCAGCCTCTTGTTGTTGAAAATGCCCTTGTGCCCATGCCACAAGATAGTTACCTCGGCAACCAGTTTGGCTTAAAAAGAACTCAGTCGCTAAGGAATCCCAGAGGATATCTTCGTCAACCTGAACTCGGTGGTTACCAATATGGAGATCGCCTTGACTCCATACTGCCTTTTCGGAGGGATGACCCTTTCCGCCATACAATTGAACCAAGTGCAGGTCCCATGCAGGTCACAAAATATGCAACACAGCAGTTCAGGATGCAACAGTCATTCTTGGATCAAGGGCGCTCAATGTTAGCCTCCCGGCAGTTGGAAATGAATGCTTTTAAAAGGCATAGCTATGCAGAAGGCACCCGCGAGACCTACGCCTCCTCCCGGCAGTACATGAAACAGCGTGTAATGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43341
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 403 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 403 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44966997)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44021058 |
| GRCz11 | 19 | 43616655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAATGCTTTTAAAAGGCATAGCTATGCAGAAGGCACCCGCGAGACCTA[C/A]GCCTCCTCCCGGCAGTACATGAAACAGCGTGTAATGAACAACTTGGAAGA
Long Flanking Sequence:
CATTGTACATTTTTTTTTTTCTCTTTTCCCAGCTTTATGTGGTCTTTTGAGAAGATCCACCGCTGTATCGCCCATTTATTCCTTGGAGAGCTTGTTGCCACTTTTGATGAGGAGTTTCGTATTTTGTTTGCTCAATCTCAGCCTCTTGTTGTTGAAAATGCCCTTGTGCCCATGCCACAAGATAGTTACCTCGGCAACCAGTTTGGCTTAAAAAGAACTCAGTCGCTAAGGAATCCCAGAGGATATCTTCGTCAACCTGAACTCGGTGGTTACCAATATGGAGATCGCCTTGACTCCATACTGCCTTTTCGGAGGGATGACCCTTTCCGCCATACAATTGAACCAAGTGCAGGTCCCATGCAGGTCACAAAATATGCAACACAGCAGTTCAGGATGCAACAGTCATTCTTGGATCAAGGGCGCTCAATGTTAGCCTCCCGGCAGTTGGAAATGAATGCTTTTAAAAGGCATAGCTATGCAGAAGGCACCCGCGAGACCTA[C/A]GCCTCCTCCCGGCAGTACATGAAACAGCGTGTAATGAACAACTTGGAAGAGACTGAATCGCATTACCAGCGAGAACAACATTATTATCAGAGTGAAGGCATGGGACATGATGACCGTGGACACTACGACCGATTTAACTATGGCTTGGCAGATCAACACTCAGATTCTGGATATCCCCCTGAACTTGAGGCACCAGGAAATATAAATGTTTTATCCTCGGATGACCTCAAAAGTGATTCAGAAAAACAGTATAACATAGGAGGTCGCTATGATCCACAAGGCCACAAGAGGCCTGCTGCGGGCCATGCATACGCATGTCAGAGTTCGCCGACTCAGCCCCATCCTCCAGACCAAAAGCAGTTGTTCTCCACTGGAGATCAGGTACGGCAGTCGCAGGACCCCAGCGTGAAGCAGGGGTTGCGGAGCTGGAGGATCAACTCTTATCTCAGCACTTATGAAGATGGAGGAGAGGAAGGCCTGCATCAGCCCATGGGCTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23591
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 427 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 427 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44967067)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44020988 |
| GRCz11 | 19 | 43616585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAACAGCGTGTAATGAACAACTTGGAAGAGACTGAATCGCATTACCAG[C/T]GAGAACAACATTATTATCAGAGTGAAGGCATGGGACATGATGACCGTGGA
Long Flanking Sequence:
CCCATTTATTCCTTGGAGAGCTTGTTGCCACTTTTGATGAGGAGTTTCGTATTTTGTTTGCTCAATCTCAGCCTCTTGTTGTTGAAAATGCCCTTGTGCCCATGCCACAAGATAGTTACCTCGGCAACCAGTTTGGCTTAAAAAGAACTCAGTCGCTAAGGAATCCCAGAGGATATCTTCGTCAACCTGAACTCGGTGGTTACCAATATGGAGATCGCCTTGACTCCATACTGCCTTTTCGGAGGGATGACCCTTTCCGCCATACAATTGAACCAAGTGCAGGTCCCATGCAGGTCACAAAATATGCAACACAGCAGTTCAGGATGCAACAGTCATTCTTGGATCAAGGGCGCTCAATGTTAGCCTCCCGGCAGTTGGAAATGAATGCTTTTAAAAGGCATAGCTATGCAGAAGGCACCCGCGAGACCTACGCCTCCTCCCGGCAGTACATGAAACAGCGTGTAATGAACAACTTGGAAGAGACTGAATCGCATTACCAG[C/T]GAGAACAACATTATTATCAGAGTGAAGGCATGGGACATGATGACCGTGGACACTACGACCGATTTAACTATGGCTTGGCAGATCAACACTCAGATTCTGGATATCCCCCTGAACTTGAGGCACCAGGAAATATAAATGTTTTATCCTCGGATGACCTCAAAAGTGATTCAGAAAAACAGTATAACATAGGAGGTCGCTATGATCCACAAGGCCACAAGAGGCCTGCTGCGGGCCATGCATACGCATGTCAGAGTTCGCCGACTCAGCCCCATCCTCCAGACCAAAAGCAGTTGTTCTCCACTGGAGATCAGGTACGGCAGTCGCAGGACCCCAGCGTGAAGCAGGGGTTGCGGAGCTGGAGGATCAACTCTTATCTCAGCACTTATGAAGATGGAGGAGAGGAAGGCCTGCATCAGCCCATGGGCTCAGATGCTTTTGAAGACTCACATCAACAACCTGACAGCAGACTTTATGGCTCTGAAGGACCAGGTATTCATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32261
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 447 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 447 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44967127)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44020928 |
| GRCz11 | 19 | 43616525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTATCAGAGTGAAGGCATGGGACATGATGACCGTGGACACTACGAC[C/T]GATTTAACTATGGCTTGGCAGATCAACACTCAGATTCTGGATATCCCCCT
Long Flanking Sequence:
CTCAATCTCAGCCTCTTGTTGTTGAAAATGCCCTTGTGCCCATGCCACAAGATAGTTACCTCGGCAACCAGTTTGGCTTAAAAAGAACTCAGTCGCTAAGGAATCCCAGAGGATATCTTCGTCAACCTGAACTCGGTGGTTACCAATATGGAGATCGCCTTGACTCCATACTGCCTTTTCGGAGGGATGACCCTTTCCGCCATACAATTGAACCAAGTGCAGGTCCCATGCAGGTCACAAAATATGCAACACAGCAGTTCAGGATGCAACAGTCATTCTTGGATCAAGGGCGCTCAATGTTAGCCTCCCGGCAGTTGGAAATGAATGCTTTTAAAAGGCATAGCTATGCAGAAGGCACCCGCGAGACCTACGCCTCCTCCCGGCAGTACATGAAACAGCGTGTAATGAACAACTTGGAAGAGACTGAATCGCATTACCAGCGAGAACAACATTATTATCAGAGTGAAGGCATGGGACATGATGACCGTGGACACTACGAC[C/T]GATTTAACTATGGCTTGGCAGATCAACACTCAGATTCTGGATATCCCCCTGAACTTGAGGCACCAGGAAATATAAATGTTTTATCCTCGGATGACCTCAAAAGTGATTCAGAAAAACAGTATAACATAGGAGGTCGCTATGATCCACAAGGCCACAAGAGGCCTGCTGCGGGCCATGCATACGCATGTCAGAGTTCGCCGACTCAGCCCCATCCTCCAGACCAAAAGCAGTTGTTCTCCACTGGAGATCAGGTACGGCAGTCGCAGGACCCCAGCGTGAAGCAGGGGTTGCGGAGCTGGAGGATCAACTCTTATCTCAGCACTTATGAAGATGGAGGAGAGGAAGGCCTGCATCAGCCCATGGGCTCAGATGCTTTTGAAGACTCACATCAACAACCTGACAGCAGACTTTATGGCTCTGAAGGACCAGGTATTCATTCAAACATTAGAGAACGTCCAAATATCCCAACTAAGCCAAACCTTGATTTGCGGCCACGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23592
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 485 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 485 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44967241)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44020814 |
| GRCz11 | 19 | 43616411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAAATATAAATGTTTTATCCTCGGATGACCTCAAAAGTGATTCAGAA[A/T]AACAGTATAACATAGGAGGTCGCTATGATCCACAAGGCCACAAGAGGCCT
Long Flanking Sequence:
ATCTTCGTCAACCTGAACTCGGTGGTTACCAATATGGAGATCGCCTTGACTCCATACTGCCTTTTCGGAGGGATGACCCTTTCCGCCATACAATTGAACCAAGTGCAGGTCCCATGCAGGTCACAAAATATGCAACACAGCAGTTCAGGATGCAACAGTCATTCTTGGATCAAGGGCGCTCAATGTTAGCCTCCCGGCAGTTGGAAATGAATGCTTTTAAAAGGCATAGCTATGCAGAAGGCACCCGCGAGACCTACGCCTCCTCCCGGCAGTACATGAAACAGCGTGTAATGAACAACTTGGAAGAGACTGAATCGCATTACCAGCGAGAACAACATTATTATCAGAGTGAAGGCATGGGACATGATGACCGTGGACACTACGACCGATTTAACTATGGCTTGGCAGATCAACACTCAGATTCTGGATATCCCCCTGAACTTGAGGCACCAGGAAATATAAATGTTTTATCCTCGGATGACCTCAAAAGTGATTCAGAA[A/T]AACAGTATAACATAGGAGGTCGCTATGATCCACAAGGCCACAAGAGGCCTGCTGCGGGCCATGCATACGCATGTCAGAGTTCGCCGACTCAGCCCCATCCTCCAGACCAAAAGCAGTTGTTCTCCACTGGAGATCAGGTACGGCAGTCGCAGGACCCCAGCGTGAAGCAGGGGTTGCGGAGCTGGAGGATCAACTCTTATCTCAGCACTTATGAAGATGGAGGAGAGGAAGGCCTGCATCAGCCCATGGGCTCAGATGCTTTTGAAGACTCACATCAACAACCTGACAGCAGACTTTATGGCTCTGAAGGACCAGGTATTCATTCAAACATTAGAGAACGTCCAAATATCCCAACTAAGCCAAACCTTGATTTGCGGCCACGTTTTGGTAAACCCATCATACAAGATAGAAATCAAGTAAAGGATAATACCTCTGATTTGGGTCCCACAAGTACTGACACATTAAAGCCAGCGATTTCAGCGTCATCACTAGCATCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23593
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 761 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 761 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44968069)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44019986 |
| GRCz11 | 19 | 43615583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATAAACATAAAAAAGCAGATGAAAAAGATGTTAAACACGCTTCAACC[G/T]GAGATCTGACTACGATCCAAGACACCAAAGAAGAGCCCATCAAAGAGAAG
Long Flanking Sequence:
ACATTAGAGAACGTCCAAATATCCCAACTAAGCCAAACCTTGATTTGCGGCCACGTTTTGGTAAACCCATCATACAAGATAGAAATCAAGTAAAGGATAATACCTCTGATTTGGGTCCCACAAGTACTGACACATTAAAGCCAGCGATTTCAGCGTCATCACTAGCATCTTCAACAGACAACGAGAAAGAGTTGGCAGAACCAAGGGAAATCAGCATTACCAAGCACGAGTCTTTCCGAACTCGAATTAACCCCATGCTTCAGAGGAGCTCAAGATTAAGGTCTTCTTTAATCTTCAGCTCTTCGAAGCTGGAACAACACAACTCATCGCAAGCCAAGTCCGGTGGAGAGTTACAAGAGGAGAAAGAAGAGAGTGAGCCCATTCGATACTCATCAATTGTGGCAGAGATTCTTGAGAAGAGGAGATCTCTGTCAAGAGAGCCCTTCGATTGGAATAAACATAAAAAAGCAGATGAAAAAGATGTTAAACACGCTTCAACC[G/T]GAGATCTGACTACGATCCAAGACACCAAAGAAGAGCCCATCAAAGAGAAGGAGAAACCAGACAACCCTAAACCTGAGGAAAACAAAGTTACACAGCCAACAGTGCCTTCAGCGTCTCAGCAAATAACTTCTTCGCTAAACATGAATGATCCAGCAAGCCGACTTCAGTACTTCAAAGATCAGCAAGAAAAGAGGAAGACCTCCAAATTAGAGTTAGATTTGGGTACAAAAAGTCAAGAAGCAGCCATTAAAAAGCCAGAAACCTTGGATACAGCAACCAAAGTTCCAGATGTGCTTTTAACATCAGAGCAGTCCACTGTAAAGGCACAAGAACCAACAGTTTCGCAAACAGATCCTGTACCACATCGCCCGGTGATTGAAACAAAACCAAAACCATCAGAAGTCTCTGTGGACAGACCCTACACCACCAACAAAACTCTAACGGAGAGCATAGCTGATGCACCAAAGAAAGAGCCTGTTAAGGAACCAACTAAATCACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31037
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 844 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 844 | 1192 | 5 | 5 |
| ENSDART00000086138 | Nonsense | 844 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 844 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44968318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44019737 |
| GRCz11 | 19 | 43615334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCAAATTAGAGTTAGATTTGGGTACAAAAAGTCAAGAAGCAGCCATT[A/T]AAAAGCCAGAAACCTTGGATACAGCAACCAAAGTTCCAGATGTGCTTTTA
Long Flanking Sequence:
ACCCCATGCTTCAGAGGAGCTCAAGATTAAGGTCTTCTTTAATCTTCAGCTCTTCGAAGCTGGAACAACACAACTCATCGCAAGCCAAGTCCGGTGGAGAGTTACAAGAGGAGAAAGAAGAGAGTGAGCCCATTCGATACTCATCAATTGTGGCAGAGATTCTTGAGAAGAGGAGATCTCTGTCAAGAGAGCCCTTCGATTGGAATAAACATAAAAAAGCAGATGAAAAAGATGTTAAACACGCTTCAACCGGAGATCTGACTACGATCCAAGACACCAAAGAAGAGCCCATCAAAGAGAAGGAGAAACCAGACAACCCTAAACCTGAGGAAAACAAAGTTACACAGCCAACAGTGCCTTCAGCGTCTCAGCAAATAACTTCTTCGCTAAACATGAATGATCCAGCAAGCCGACTTCAGTACTTCAAAGATCAGCAAGAAAAGAGGAAGACCTCCAAATTAGAGTTAGATTTGGGTACAAAAAGTCAAGAAGCAGCCATT[A/T]AAAAGCCAGAAACCTTGGATACAGCAACCAAAGTTCCAGATGTGCTTTTAACATCAGAGCAGTCCACTGTAAAGGCACAAGAACCAACAGTTTCGCAAACAGATCCTGTACCACATCGCCCGGTGATTGAAACAAAACCAAAACCATCAGAAGTCTCTGTGGACAGACCCTACACCACCAACAAAACTCTAACGGAGAGCATAGCTGATGCACCAAAGAAAGAGCCTGTTAAGGAACCAACTAAATCACTCAAGCCATTCCCTTCACCCAAGTTCTTAAAACCCTTCAAAAGCTCTCAATCTTCTAGTCGGCGGATATCATGTGGTGAGGAGATTCTCACAGATGCAACAGATGCTGAAAAGAGTGAGCTCAAAAAGTCTCGCAGCTTCAGCACATCAGGAATGTCCCGCACGGAGTCCAGAGAAAGCTTGAGCTCCCTTGGAAACTCTGAAAGCAAGGATACAAAGGCCCTGGACTTCCTCAAGAAACAAACGCAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43342
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 844 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 844 | 1192 | 5 | 5 |
| ENSDART00000086138 | Nonsense | 844 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 844 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44968318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44019737 |
| GRCz11 | 19 | 43615334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCAAATTAGAGTTAGATTTGGGTACAAAAAGTCAAGAAGCAGCCATT[A/T]AAAAGCCAGAAACCTTGGATACAGCAACCAAAGTTCCAGATGTGCTTTTA
Long Flanking Sequence:
ACCCCATGCTTCAGAGGAGCTCAAGATTAAGGTCTTCTTTAATCTTCAGCTCTTCGAAGCTGGAACAACACAACTCATCGCAAGCCAAGTCCGGTGGAGAGTTACAAGAGGAGAAAGAAGAGAGTGAGCCCATTCGATACTCATCAATTGTGGCAGAGATTCTTGAGAAGAGGAGATCTCTGTCAAGAGAGCCCTTCGATTGGAATAAACATAAAAAAGCAGATGAAAAAGATGTTAAACACGCTTCAACCGGAGATCTGACTACGATCCAAGACACCAAAGAAGAGCCCATCAAAGAGAAGGAGAAACCAGACAACCCTAAACCTGAGGAAAACAAAGTTACACAGCCAACAGTGCCTTCAGCGTCTCAGCAAATAACTTCTTCGCTAAACATGAATGATCCAGCAAGCCGACTTCAGTACTTCAAAGATCAGCAAGAAAAGAGGAAGACCTCCAAATTAGAGTTAGATTTGGGTACAAAAAGTCAAGAAGCAGCCATT[A/T]AAAAGCCAGAAACCTTGGATACAGCAACCAAAGTTCCAGATGTGCTTTTAACATCAGAGCAGTCCACTGTAAAGGCACAAGAACCAACAGTTTCGCAAACAGATCCTGTACCACATCGCCCGGTGATTGAAACAAAACCAAAACCATCAGAAGTCTCTGTGGACAGACCCTACACCACCAACAAAACTCTAACGGAGAGCATAGCTGATGCACCAAAGAAAGAGCCTGTTAAGGAACCAACTAAATCACTCAAGCCATTCCCTTCACCCAAGTTCTTAAAACCCTTCAAAAGCTCTCAATCTTCTAGTCGGCGGATATCATGTGGTGAGGAGATTCTCACAGATGCAACAGATGCTGAAAAGAGTGAGCTCAAAAAGTCTCGCAGCTTCAGCACATCAGGAATGTCCCGCACGGAGTCCAGAGAAAGCTTGAGCTCCCTTGGAAACTCTGAAAGCAAGGATACAAAGGCCCTGGACTTCCTCAAGAAACAAACGCAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43343
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 |
|---|---|---|---|---|---|
| ENSDART00000086138 | Nonsense | 901 | 1170 | 4 | 5 |
| ENSDART00000138009 | Nonsense | 901 | 1192 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 44968491)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44019564 |
| GRCz11 | 19 | 43615161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATTGAAACAAAACCAAAACCATCAGAAGTCTCTGTGGACAGACCCTA[C/A]ACCACCAACAAAACTCTAACGGAGAGCATAGCTGATGCACCAAAGAAAGA
Long Flanking Sequence:
AGATCTCTGTCAAGAGAGCCCTTCGATTGGAATAAACATAAAAAAGCAGATGAAAAAGATGTTAAACACGCTTCAACCGGAGATCTGACTACGATCCAAGACACCAAAGAAGAGCCCATCAAAGAGAAGGAGAAACCAGACAACCCTAAACCTGAGGAAAACAAAGTTACACAGCCAACAGTGCCTTCAGCGTCTCAGCAAATAACTTCTTCGCTAAACATGAATGATCCAGCAAGCCGACTTCAGTACTTCAAAGATCAGCAAGAAAAGAGGAAGACCTCCAAATTAGAGTTAGATTTGGGTACAAAAAGTCAAGAAGCAGCCATTAAAAAGCCAGAAACCTTGGATACAGCAACCAAAGTTCCAGATGTGCTTTTAACATCAGAGCAGTCCACTGTAAAGGCACAAGAACCAACAGTTTCGCAAACAGATCCTGTACCACATCGCCCGGTGATTGAAACAAAACCAAAACCATCAGAAGTCTCTGTGGACAGACCCTA[C/A]ACCACCAACAAAACTCTAACGGAGAGCATAGCTGATGCACCAAAGAAAGAGCCTGTTAAGGAACCAACTAAATCACTCAAGCCATTCCCTTCACCCAAGTTCTTAAAACCCTTCAAAAGCTCTCAATCTTCTAGTCGGCGGATATCATGTGGTGAGGAGATTCTCACAGATGCAACAGATGCTGAAAAGAGTGAGCTCAAAAAGTCTCGCAGCTTCAGCACATCAGGAATGTCCCGCACGGAGTCCAGAGAAAGCTTGAGCTCCCTTGGAAACTCTGAAAGCAAGGATACAAAGGCCCTGGACTTCCTCAAGAAACAAACGCAGAGATTGAAGGGTATCCTTGGGCCAAAGGGAGATAAGAAGCACTCAGGAGTGTCCAACTCCCAAGAGGACAAATCAATGAAAACAGTCCCAGAGGTGCAAGAGGAGATTTCAGACAAAGGCAAACCCTCTGAATCCATTTCATCTTCAACCGCAGTAGAGAACAAGCCCAGTGCTAA
Associated Phenotype:
Not determined