ZMP
tmem8a
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 8A [Source:RefSeq peptide;Acc:NP_001139040]
Human Orthologue:
TMEM8A
Human Description:
transmembrane protein 8A [Source:HGNC Symbol;Acc:17205]
Mouse Orthologue:
Tmem8
Mouse Description:
transmembrane protein 8 (five membrane-spanning domains) Gene [Source:MGI Symbol;Acc:MGI:1926283]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1975 | Essential Splice Site | F2 line generated | Not yet available |
| sa39557 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39556 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25531 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38247 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10041 | Nonsense | Available for shipment | Available now |
| sa39555 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32598 | Nonsense | Available for shipment | Available now |
| sa39554 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1975
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000041849 | Essential Splice Site | 21 | 751 | 2 | 13 |
| ENSDART00000138726 | None | None | 692 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9016564)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9256369 |
| GRCz11 | 1 | 9940480 |
KASP Assay ID:
554-2692.1 (used for ordering genotyping assays)
KASP Sequence:
TTTGGGGTTGTTTACATCTGACGCAACCGTGACGTCACGCTCTCTTCCTA[G/T]ACCTCACTTACTTGAACGGGTTTTACTCCAAAACGCCTCAGAGGTTGTCC
Long Flanking Sequence:
CAACAGTCCGTAGACATTTGGAGAACACAACAATGGGCTGACTGAGGAGAATCTAAACAAAAAAATGGAGAAGTATTTTGTACTGTGCCTTTTACTGTATGCTACCGCTGGCTGTTTTGCTGACGGTGAGTCTCTGAAGTGATAGGCGTCTCTTGGGGTTAACGTTATATATTTAAGCATTTAATATGATGTATGTCGACAAATGAATGCGATTTGACCATGCTAGTCTTTTTTCAGGCATTTAATTAAATCGCTTTAATTTATTTGCATTATACTAAACTAGCAAGCTTATCTCATTCAGTGTTACAACATACAGCATAAGTTTAGTAAGTTACACATATTTACTCTGCTGGGTTGTATGTCGTTAATTGTGATATACGTTATCATGTTTACGTTATAAAATGTCAGTAAATATACTAGTCATACATGAATTAGGAGATTATCAAGCCATTTGGGGTTGTTTACATCTGACGCAACCGTGACGTCACGCTCTCTTCCTA[G/T]ACCTCACTTACTTGAACGGGTTTTACTCCAAAACGCCTCAGAGGTTGTCCAAATACAGCTGGTTCGGGAATGTTCGGCTCCATCACTTCAGGGTACCGGAGGATGCGGTGCTCGTGCGGTGGCTGCTCACGGTCTCACGGGGATCCGGACTCAACTGTGGCAACCAAAACATCACTGTGTATGTATATGCTGCTGAATTCATGACAACAAACTACCTGACAAATCTTGTCGTCAATCCTAGTTGTAAGAGCAATAAATAACTTGACTTCTAGCTGATCATTTGGAAATGTGGCAAAAGATAGATTTTACTGATGAATTATCTGTTGAACTGCATCCCAATCATCACAAATACTGCAGAAGACTTATTGGAACCCGTTTGGACCCAAGATTCTCAGAGAAATCAGTCAAGTTTGGTGAAGGAAAAGTCATGGTTGGGGGTTAAATTTAGTATGGGGCGTGCAAGAGATCTGCAGAGTGGATGGCAACATCAACAGACTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39557
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Nonsense | 150 | 751 | 3 | 13 |
| ENSDART00000138726 | Nonsense | 106 | 692 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9012883)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9252688 |
| GRCz11 | 1 | 9936799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGTTCCTCGCTGCACACCTGCCTAAGGACGACGGCAAGATTGAGCAG[C/T]AGGTATGTTTTTGGTGTCTTATGCCTGTTAATAGTGTTTGTTTGATTTTT
Long Flanking Sequence:
TCTCTGCTAGGAGACTACTGAATACAGAAGATTCTGTTCATTCTCTTGAGAAAGCCCAAGATTATTGTCTACTGTGTCAATACCAGGAGACTAAAACACATAAACAAATAGTTCATCAAACTATTTTACTGGTTCTTTAACCCCAAGTCACCCCAGATGGACTTTTTCATTATACTGCAGATTGTTATACTGTAAAAGTAGATAAAAGCATGCAAATAAATAGCCAAGTAGTGATTTCTTTATAATTGCTTGGCTTCACATTGACATTTGTTCATCTTGCTTCCATTAACAGGCACTTTAGGGCAGGAGCGCCCCCAGTAATTAACCCTATTCAAACAGCCTTTCCGAACTCTACATCAGCTTCTCTTGCTCATAATTTGACGCTGATTGTTCCCAGTGGACAAAGTTCTAATGTGACACTGTTCAATGTGACGCACCCCAAACCAGGAGACTGGTTCCTCGCTGCACACCTGCCTAAGGACGACGGCAAGATTGAGCAG[C/T]AGGTATGTTTTTGGTGTCTTATGCCTGTTAATAGTGTTTGTTTGATTTTTCTCGGTTAAAAACGACATGCTTTGTAAAAATAAGTGTTATTTCTTGTCATTAAATTATTTATTTTATTTTTATCGCTCTGTTTTTGATGACACATTGGCTGTTTCTCAATTCCAAGAATGCAGAGAACGGACTTGCGTTCTCGTGGAGAGTGGTCTTGCCAGGTTAACTCGGAAGAACAAACTAGGAAGACCGCAAGAAAACAGAACATGTCCTTCGAGAAATGAGATGCTGCATTTTCCCTGATAATCACATGACCTTCACGCATTTTTGACAGAAAATTATTTCAACTTTACAGCATTCATACAATGATTTTTTGTTTTTCCCTTTTGCAAAATATATATTTAACATGCACAAAAACCCTACGAATATACTTTGCGCAATAGAAAATAAAAAAAATGTTTATTACTAATGTCAGCAAATAAACACCTTAATGTGTTTATGCCCTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39556
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Essential Splice Site | 150 | 751 | 3 | 13 |
| ENSDART00000138726 | Essential Splice Site | 106 | 692 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9012880)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9252685 |
| GRCz11 | 1 | 9936796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTCCTCGCTGCACACCTGCCTAAGGACGACGGCAAGATTGAGCAGCAG[G/A]TATGTTTTTGGTGTCTTATGCCTGTTAATAGTGTTTGTTTGATTTTTCTC
Long Flanking Sequence:
CTGCTAGGAGACTACTGAATACAGAAGATTCTGTTCATTCTCTTGAGAAAGCCCAAGATTATTGTCTACTGTGTCAATACCAGGAGACTAAAACACATAAACAAATAGTTCATCAAACTATTTTACTGGTTCTTTAACCCCAAGTCACCCCAGATGGACTTTTTCATTATACTGCAGATTGTTATACTGTAAAAGTAGATAAAAGCATGCAAATAAATAGCCAAGTAGTGATTTCTTTATAATTGCTTGGCTTCACATTGACATTTGTTCATCTTGCTTCCATTAACAGGCACTTTAGGGCAGGAGCGCCCCCAGTAATTAACCCTATTCAAACAGCCTTTCCGAACTCTACATCAGCTTCTCTTGCTCATAATTTGACGCTGATTGTTCCCAGTGGACAAAGTTCTAATGTGACACTGTTCAATGTGACGCACCCCAAACCAGGAGACTGGTTCCTCGCTGCACACCTGCCTAAGGACGACGGCAAGATTGAGCAGCAG[G/A]TATGTTTTTGGTGTCTTATGCCTGTTAATAGTGTTTGTTTGATTTTTCTCGGTTAAAAACGACATGCTTTGTAAAAATAAGTGTTATTTCTTGTCATTAAATTATTTATTTTATTTTTATCGCTCTGTTTTTGATGACACATTGGCTGTTTCTCAATTCCAAGAATGCAGAGAACGGACTTGCGTTCTCGTGGAGAGTGGTCTTGCCAGGTTAACTCGGAAGAACAAACTAGGAAGACCGCAAGAAAACAGAACATGTCCTTCGAGAAATGAGATGCTGCATTTTCCCTGATAATCACATGACCTTCACGCATTTTTGACAGAAAATTATTTCAACTTTACAGCATTCATACAATGATTTTTTGTTTTTCCCTTTTGCAAAATATATATTTAACATGCACAAAAACCCTACGAATATACTTTGCGCAATAGAAAATAAAAAAAATGTTTATTACTAATGTCAGCAAATAAACACCTTAATGTGTTTATGCCCTTATTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25531
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000041849 | Nonsense | 253 | 751 | 5 | 13 |
| ENSDART00000138726 | Nonsense | 209 | 692 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9009660)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9249465 |
| GRCz11 | 1 | 9933576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGTTCAGGCTTAAAGATCTGCCACGCATCTGTTCTCATTCCCCCATG[G/A]AACACCTGGTTACTGGTTACCGTTGAGACCAATCAACCAAACACCTCAGT
Long Flanking Sequence:
TTGTAAAAAATGATGAAACTGCTTTTATTCCAGCAAGAATAAAACAAATAAGACTTTTTCCAGAAAAAAAAAAATATTATTGAAAATACTGTCAAAATGTTCAAATATCACCTGAGAAATATTTGAAAAAGAATGCACATTTCAGAGGAGGGCTAACAACTTTAATATTTACATATTAAAAAATGTATTTATGTTATGGCATACATAAATTATTCCAGTTTATAGCATCACATGATCCCTCAGAAATTGGATTACAAAAGGAAAAATGCTAAATGTCTTCTCATATAAATTCTAAAGTATTTTGATTTGGTTTGTAGGGTTTTTGTTCCCGAATTTTCCTCCAGTTTGGATGTTTTCATCTCAAATTGTTCTGCAAATGTGGGAAATGATTGCGGGCTCTCGATCACTGTTGGCTCCAGCACTTTGCGGCAGGGTTCAGAGGTGAAACAGAACTGTTCAGGCTTAAAGATCTGCCACGCATCTGTTCTCATTCCCCCATG[G/A]AACACCTGGTTACTGGTTACCGTTGAGACCAATCAACCAAACACCTCAGTACCTTTCTACATCGCTGCCAATGTCACAGGTCTGTTTTAACTTTACTACACTCCCACACTTCTTGAATTTCAGAAAATATGGATTCAAGTTTTGGAAAGTACTTAAAAACAAACACAGGTCCTTAAAATGGTTGAATTAAATTTGAAATGAAATTAGTTTTTCGTGTTATTTCAACAATTGTCATGCCACTGTCAAAAACAGAATGAAAATACAAAAAATCTTAATTTAAAAATCTTAAATTGCAATCTTGTACAAGAACTATGACAAATAAAGCATATTTGTTTTATAAAAAATTCAGAAACCAGTTTTATAATATATATCACCAGAATATTACATCATTTTTCAGACATTTTTAATGTAAATATTAAGTGTAAGTAAAATCTTAAGTACAGTAAGGACTTTCATGGCACTACATAGAGCGGGGGAAATAAGTATTGAACACTATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38247
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Nonsense | 257 | 751 | 5 | 13 |
| ENSDART00000138726 | Nonsense | 213 | 692 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9009649)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9249454 |
| GRCz11 | 1 | 9933565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAAAGATCTGCCACGCATCTGTTCTCATTCCCCCATGGAACACCTGGT[T/A]ACTGGTTACCGTTGAGACCAATCAACCAAACACCTCAGTACCTTTCTACA
Long Flanking Sequence:
GATGAAACTGCTTTTATTCCAGCAAGAATAAAACAAATAAGACTTTTTCCAGAAAAAAAAAAATATTATTGAAAATACTGTCAAAATGTTCAAATATCACCTGAGAAATATTTGAAAAAGAATGCACATTTCAGAGGAGGGCTAACAACTTTAATATTTACATATTAAAAAATGTATTTATGTTATGGCATACATAAATTATTCCAGTTTATAGCATCACATGATCCCTCAGAAATTGGATTACAAAAGGAAAAATGCTAAATGTCTTCTCATATAAATTCTAAAGTATTTTGATTTGGTTTGTAGGGTTTTTGTTCCCGAATTTTCCTCCAGTTTGGATGTTTTCATCTCAAATTGTTCTGCAAATGTGGGAAATGATTGCGGGCTCTCGATCACTGTTGGCTCCAGCACTTTGCGGCAGGGTTCAGAGGTGAAACAGAACTGTTCAGGCTTAAAGATCTGCCACGCATCTGTTCTCATTCCCCCATGGAACACCTGGT[T/A]ACTGGTTACCGTTGAGACCAATCAACCAAACACCTCAGTACCTTTCTACATCGCTGCCAATGTCACAGGTCTGTTTTAACTTTACTACACTCCCACACTTCTTGAATTTCAGAAAATATGGATTCAAGTTTTGGAAAGTACTTAAAAACAAACACAGGTCCTTAAAATGGTTGAATTAAATTTGAAATGAAATTAGTTTTTCGTGTTATTTCAACAATTGTCATGCCACTGTCAAAAACAGAATGAAAATACAAAAAATCTTAATTTAAAAATCTTAAATTGCAATCTTGTACAAGAACTATGACAAATAAAGCATATTTGTTTTATAAAAAATTCAGAAACCAGTTTTATAATATATATCACCAGAATATTACATCATTTTTCAGACATTTTTAATGTAAATATTAAGTGTAAGTAAAATCTTAAGTACAGTAAGGACTTTCATGGCACTACATAGAGCGGGGGAAATAAGTATTGAACACTATTTTTCTCAGAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10041
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Nonsense | 304 | 751 | 6 | 13 |
| ENSDART00000138726 | Nonsense | 245 | 692 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9008154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9247959 |
| GRCz11 | 1 | 9932070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTTCAGATTTCAAYGCTGYAGCCTTCATTCGTACCATCATTGCTCCA[C/T]AAAGCAACAGCTCAGGTGTTTTCGGTAACTCGTCTRCTKCAGCAAAGAAC
Long Flanking Sequence:
TTAAGCTGCCATCACCAAAAAAAAGCCTTTTAAATGAAATATTAAATACATTTCAGTAGTTCAGTACTTTCTCCTTGTGTCATTCCGTTGTTATTATACATAAGTCATTTTTCAGATGTTTTTTTCTGTTTTGTTTTGTTTATTTTTATAATTGTATTGTTTGGGTTTTTACCAAAATCTGGTTCAATGGCATATCAATAGCTCCTTTAGAAATGTTATTTCCAGGAATAAGCATAATGTGTTCAATACTTATTTCCCCAACTGTATGCTGAGGTGTGAATTACAAAGGTGCTTGATTTGAAATTAACAGTGCTTTAAAAAGTTCTTGAATTGACTCTTTATGAAAGATTGGTAACACTGAATGCTTTTTTCCCCAGTTTTTACTCGACTTTTAAATGTCTTTCTCTCTCTTTTTCTTCAAACACATAGTTGGTTGTAAACCCCTGAGCTCCTCTTCAGATTTCAATGCTGCAGCCTTCATTCGTACCATCATTGCTCCA[C/T]AAAGCAACAGCTCAGGTGTTTTCGGTAACTCGTCTACTTCAGCAAAGAACCAGTCAGGCCTTCGTTCTAACAGCTCTGAGCCAATGTGCATGAGAAGCCCGTCAGTGTTCAGAGATGAGCAGGACGTACTTTCTTTTCGATACATTGTGTCCGGCAACAACCTCACTGTGACCTCTGACCTTCCAACTGTGCTCGCACTCGAACACTCACCTGGAGACAGTGGAGGCACACTTGTTGTACAGCTCCAGCTTAATACTGTAAGTGTAATAACATTTCTGCTTCTTCATATATTATTGTAAAAAATGAACTGTTAGTACCTATTGAACATATCAATAAGTCTGTTGTAACATTATAAATATTCATGTAATGAATTCTTGCTCACTAAAACTGTAATTTTATTTTATAAATAATTGACTGATCCTAATCGTTTGGTAGTATAATAAATAGTTAAATAATCAATAGTTTAATTTAATTAAATCACTTTTATTTATTATTAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39555
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Essential Splice Site | 460 | 751 | 9 | 13 |
| ENSDART00000138726 | Essential Splice Site | 401 | 692 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9004706)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9244511 |
| GRCz11 | 1 | 9928622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCATTAAAGCAGCTTATGAGCATTACTTACACTTGTATTGTCTTTCCA[G/A]TGTTGACTGCACGAATGCATCGGCTACAGTGAGTGCATCTGTGAGTGTTA
Long Flanking Sequence:
GGCTAAAAGCAAGTCAAGTTTGTAATCATGTGTAATTCTTTTGTCTAGCATTTTAAGAAATACTTATTACATGTTTTTATGCCTTTTGTCATATGTAACTTTACTGTTTTTGTATGTGTGATGATGTGTTTTTTTATTTTAGGTTCCCTTTTAAAATCTGGCAGGGGGCAACAGATAAATATTAGCCCTTGTGGCTAACTCTGGCTAAAACTTACAGTTTTACTGTTTATTAATGAGCATTGTCCCTGTTAAATAAAATAAATTCAAAATTAGTACTCAACTGGAAGGTACAGACTAAAAGGGCAACCATTCAGTCTGCAGTCACTGCTTTCAATCTGTTAGAACCAGATGTTAGAATACTTTCAAAGTGTTTAACAAGTCTAAAACTGCACCTAGAAGTGCTTGAAAAGAGCTTAAATTTGATTTTGAAAAAGGTGTAAGAACCATGGTCTGCATTAAAGCAGCTTATGAGCATTACTTACACTTGTATTGTCTTTCCA[G/A]TGTTGACTGCACGAATGCATCGGCTACAGTGAGTGCATCTGTGAGTGTTAGCGCCTGCATTGATGAGTGCGGGCCGTACGGAGAGTGCAGACTTCTGCGCACATACAACTACCTTTACGGTGCTTGTGTGTGCAAAGCAGGTAAACCTACATAAACTCACCAACCAATGGACAGAAACATAATTGATGCTGAGATGTGCATTTGGTTGTTTGTTTGTGTGCTTTTGATCAATGACAGGATGGCAGGGATGGGGTTGTACGGATGGAGTGTCTGCGCTCTCGTACTCTCGACAGATGACTGCAGCTCTGCTTCTCACCCTCAGTAACTTTTTCTTCATCCCACCCATCATCGTAGCACTTTACAGAGGATACCTCATCGAGGCTGCCATCTACTTATTTACCATGTTTTTTTCCACGGTGTGTTTTAACTTTACAGCTTTCTGTTTATCTTTCTGTTTATCCACTGTTAAAGGCAGGGGTTCCCATTCTTTTCAGCCTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32598
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Nonsense | 573 | 751 | 11 | 13 |
| ENSDART00000138726 | Nonsense | 514 | 692 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9002932)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9242737 |
| GRCz11 | 1 | 9926848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTACTCATAATGATTGTGTGTTTTGCAGTTTTACCATGCGTGTGAT[C/T]AGCCCGGTGTGACTGTGATGTGTATCATGGACTACGACACTCTCCAGTTC
Long Flanking Sequence:
TTTTATTTAATGTTAACAATGCAAATCCAATCAGACCCTATATTTGGTAAACAAAGCTAGTCTCTTATATAATATATCTACTAAATATATCTACTAAAAGACTGTATTGTAAATAAATCATATGAGCATTTTCATATTAATCAATAATGCTACTGAAATGCCTTAAAAAACTAAATAAATTGAAATATTAATTTAAAATACATTTATAATAATATTGACCTCAAAAATAATTTTAAAAATTGTATTTATTCCAGCAGATACTAAAGAAAAAAAGACTTTCTCCAGAAGAAACATATTAGAGGAAATACTGTGAAAATGTTTTTTTTTTTTTTTTTAAACATCATTTGGGAGATATTTGAAAGAGAATTAAAAATTTTAAATTTCACAGGAGGGATAATAATTTTGCTTTCAACTCTTCATCTGTCTGTTTAATCAATAATATACACATTTTTTTGTACTCATAATGATTGTGTGTTTTGCAGTTTTACCATGCGTGTGAT[C/T]AGCCCGGTGTGACTGTGATGTGTATCATGGACTACGACACTCTCCAGTTCTGTGATTTCTTGGGATCTGTCGTGTCCGTCTGGGTGACCATTGTCTGCATGGCACGGCTGCAGGAGCCAATAAAATACGTAAGTACTATAGTATGCAGGGTTGCACAACATTGGAAAAATCTGACATTGTAATATTTTGTTTTGCTGCAATGTGAACATTATTTCACTTGAAGATTTAAATAGTACTGTATTCGGAAAGATTTCATAAATTTAGATTATCTGGGGTGATCAAGTCTTTTTCTCTGCAGTGCATTTGCATAAAATGTAATAAATTACAAGCATAAATAAATATGACAGAGTAAAAGTAAAAATGAAATAAATCATGCTTTATGGTTTTCTGGGGAGTCTATCAGTATTCAAATACAAAAATTGAACAATCAAACATAAAATAACATGGTCATCAAATAATTTTATGAAATAATATAAAAGTAATATTTAATAATATCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39554
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 |
|---|---|---|---|---|---|
| ENSDART00000041849 | Nonsense | 657 | 751 | 13 | 13 |
| ENSDART00000138726 | Nonsense | 598 | 692 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 8996451)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9236256 |
| GRCz11 | 1 | 9920367 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGTAGTTTTGAAATATTTCTTGTCCTCTTGTCCCCCGCCAGGTTTAT[C/T]GAGGTGTCAAACGCCATCAGTGCTACCCTCCATTATGGCGCCGCTGGGTT
Long Flanking Sequence:
TTAAGGACAATTGAGACTTACATCTTTTGAAAAGGACCTAATAGAACCCTTTTAAAAAGGGGTTAGACTACTTAAGCATGCCAATGCACAAAATTGTGTTGCATGTCAGTTTTAAGAGCTTGTATTCTTGTATTCCAGCTGTTGTTTATGATGGGCACTCTGGTCATTTCCATGGCGATGCAGTTGGACCGGAGGGGTCTATGGAACCTTCTGGGTCCCGTCCTGTTTGCTTTAGTCATTATGGTCACTTCTTGGGTGAGTTTGACTTTTTTCGTTACTCCAAAACATTATGTAATCATTGAGTGTTTGTTTTCTCTTTGTCTGTTTGTTTATTATTGTTAAATCAAGTATTTTATTGCATTTTAAGATCTTAACATTTTAATATTTTAAGATCATTTTAATATTTTTATCTCAATTCAATTGTTTCACTAAAATCCTCAGTTCACCTGTCAAAGTAGTTTTGAAATATTTCTTGTCCTCTTGTCCCCCGCCAGGTTTAT[C/T]GAGGTGTCAAACGCCATCAGTGCTACCCTCCATTATGGCGCCGCTGGGTTTTGTTCCTGCTGCCAGGCATCGTATCCGCTCTGATTGGAGTATGTGTGTACGTCTTCGCTCAGACCGACAGCAACTACTACTACACACACTCCATATGGCATGTCATGGTGGCCACAAGCGTGGTCTTCCTCCTCCCGCCACGAGAGAAGCACGTCCCCCCTTGGGGCTGGACCAACAAAATCTGCAGCTACAGCAGGTGCAAAAATGAGAAAGTGCAGCTTTACACTGTCACCTAAACACACTGCTGTTGATATTGATGTGGAGATTCATGTGCAATTTGTACCGTTTTACAAAACCAAGCAACTAGCTTTAAGTATCACGATCAAGCTTTACATTCACCAGTATGAGTTACATGTAAGTTCACAAATACTTCTAGGAATAGTTTATGCAGAATTCATTTTTTGGTCTATTCAAACCCATAAACTAAAACAGGAGATTTTTTTTAGAAA
Associated Phenotype:
Not determined