ZMP
frem2b
Ensembl ID:
ZFIN ID:
Description:
Fras1 related extracellular matrix protein 2b [Source:RefSeq peptide;Acc:NP_001131133]
Human Orthologue:
FREM2
Human Description:
FRAS1 related extracellular matrix protein 2 [Source:HGNC Symbol;Acc:25396]
Mouse Orthologue:
Frem2
Mouse Description:
Fras1 related extracellular matrix protein 2 Gene [Source:MGI Symbol;Acc:MGI:2444465]
Alleles
There are 16 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35951 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa22690 | Nonsense | Available for shipment | Available now |
| sa12619 | Nonsense | Available for shipment | Available now |
| sa11529 | Nonsense | Available for shipment | Available now |
| sa10377 | Nonsense | Available for shipment | Available now |
| sa42593 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13551 | Nonsense | Available for shipment | Available now |
| sa39061 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12519 | Nonsense | Available for shipment | Available now |
| sa12912 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35951
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 680 | 3116 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33280586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32735965 |
| GRCz11 | 15 | 32593944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATACCATCTCACTTTTTTCCGAAAGAAATTCTTGCGCTACACAGATT[T/A]GGATTCTGACGACAGGGATTTGAAGTACACAATTACCCAACCACCCGCTG
Long Flanking Sequence:
TATAATCAATGCCAACACCGGTTTGGTTTTGTTTAAAAACCAAATGATGCCTATTTCTTCTTTAACGCTTAGTGCGGCAGATATAGACTCTGAGGATTCAACTATCAAATTCATCATGGTGCCTCCTTACTCTAACATCGGAGAAGTGATACTTCGTCAATCAGATGCACCAGAGGATCCGTCCACATGGAGGTTCAACGCAGAGGATGAGATGTATGAGAAAGTAGTGACCGAATGGCTCCAGCATGATATCACAGAAGGCAAGTTGTTTTATAGACATATCGGACCACACAATACAAAAACCATCATGGATCAGTTTGTTTTCCGTGTGCAAGATGACAATGATCCACCAAACCAGTCAGGAGAGAACTCTTTCATCATCAAAGTTCTCCCCATTGATGATATCCCCCCTGATATGTATCCTGGGACCACCTTGCAAATGACTGTTCATGAATACCATCTCACTTTTTTCCGAAAGAAATTCTTGCGCTACACAGATT[T/A]GGATTCTGACGACAGGGATTTGAAGTACACAATTACCCAACCACCCGCTGACACAGATGAGAACAGCCCTGGCATTCTGGGAAGCATCGTTTTAACCGAGAGTCCAACTTTGGAGGTCAATGAGTTCACTCAGGCGCAGATAAATCATCACAAGATTGCCTACAAGCCTCCCGATCTAGAACTTGGAATAACCCCACACGTGGTGCAGTTCCAATACAAAGTCGAGGATACAGCAGGAAACAGCGCCAGTGGAGTTTTCACCATATTTTTACAGCCTGTGGACAACAAACCTCCGCAGATCACCAACACGGGCTTTACTTTGCAAGAACGAGGGATGCACGTCATCACACGCGCTGAGCTGGACACCACAGATGCCGACACGGACAGCTCACAGATTTTGTTTACAATCACCCAGCCTCCACAGCATGGTCAGGTCAAGTACACATTCACCGACATGACTAAAGGGAATTCGTTTAATTTGGATGACATATCGAATGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22690
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 776 | 3116 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33280873)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32735678 |
| GRCz11 | 15 | 32593657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACAGCGCCAGTGGAGTTTTCACCATATTTTTACAGCCTGTGGACAAC[A/T]AACCTCCGCAGATCACCAACACGGGCTTTACTTTGCAAGAACGAGGGATG
Long Flanking Sequence:
CACACAATACAAAAACCATCATGGATCAGTTTGTTTTCCGTGTGCAAGATGACAATGATCCACCAAACCAGTCAGGAGAGAACTCTTTCATCATCAAAGTTCTCCCCATTGATGATATCCCCCCTGATATGTATCCTGGGACCACCTTGCAAATGACTGTTCATGAATACCATCTCACTTTTTTCCGAAAGAAATTCTTGCGCTACACAGATTTGGATTCTGACGACAGGGATTTGAAGTACACAATTACCCAACCACCCGCTGACACAGATGAGAACAGCCCTGGCATTCTGGGAAGCATCGTTTTAACCGAGAGTCCAACTTTGGAGGTCAATGAGTTCACTCAGGCGCAGATAAATCATCACAAGATTGCCTACAAGCCTCCCGATCTAGAACTTGGAATAACCCCACACGTGGTGCAGTTCCAATACAAAGTCGAGGATACAGCAGGAAACAGCGCCAGTGGAGTTTTCACCATATTTTTACAGCCTGTGGACAAC[A/T]AACCTCCGCAGATCACCAACACGGGCTTTACTTTGCAAGAACGAGGGATGCACGTCATCACACGCGCTGAGCTGGACACCACAGATGCCGACACGGACAGCTCACAGATTTTGTTTACAATCACCCAGCCTCCACAGCATGGTCAGGTCAAGTACACATTCACCGACATGACTAAAGGGAATTCGTTTAATTTGGATGACATATCGAATGGCAGAATATCTTACATTCATAATGGGGATGAGTCAACTAGTGATTTCTTTCAGCTGGATGTCAGTGATGGTGTCCATGTTGTCACAATCACCGTCAGGATCAGCGTAAAGCCTATTGACGATGAAGCGCCAATCATCAGCCTTCCAGAGGGAACTATTGGCTCCTATATAGATGTTTTAGAGAACGGAGCGACTGAGATCACAACCAATGTTATTCAAGGTCGAGATGAGGACACCGATGACCTAAGGCTGACCTTTATTGTGGAGGATCCCCCAGTGTTTGGTGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12619
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 1102 | 3116 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33281851)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32734700 |
| GRCz11 | 15 | 32592679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATCAAAGACATTCGGGAAAACCACATTTATTATGTGCAAAGTATTCAT[A/T]AAGGAGTCGAGCCAGTTGAAGATAGGTTTACTTTCAGGTGTTCAGATGGG
Long Flanking Sequence:
ATCCCCCAGTGTTTGGTGAAATATTAGTAAATGGTGTGCCATCCAATAGGTTTACTCAAGCAGATATCATCAGTGGTTTGGTAGTGTATGCGCATAATACTGGAGAAATTGGCTTGGCAACAAAACAAGACTTTTTCAATCTGACACTCACCGATATGTCTGATGAATGGACAGTTGGGGGGAATAAAATCAAAGGGGTTCGCGTGCAGGTCACCATTCTGCCATTGGACAGTCAGGCTCCGGAGGTGTTCGTGGGCCCCCAGTTCATCGTCGTAGAGGGTGAGAAAAATGTTATAGCAATTTCGCACATTAGCGCCAATGACATTGACACCCCTAATGATGATCTCCTTTGCACAATTATTGTGCAGCCCACTTCAGGTTATGTAGAAAACATTTCCCCCGCACCAGGATCTGAAAAATCCAGATCAGGGATTGCCATCAGTGCTTTCACCATCAAAGACATTCGGGAAAACCACATTTATTATGTGCAAAGTATTCAT[A/T]AAGGAGTCGAGCCAGTTGAAGATAGGTTTACTTTCAGGTGTTCAGATGGGATCAACTTTTCCGAGAGACACTTTTTCCCAATCGTCATAATCCCATCCAATGATGAGAAGCCTGAGATCTATATGAGAGAGTTTGTTGTGATGGAGGGCATGAACATTGTGATTGACACTCCAATATTAAATGGCGCCGATGCTGACGTTCCAGCGGATGAGCTCACATTTATTATTTCAAAACCTCCGAAACATGGATTTATCCTTAATCAGCTAACCTCAGGCACAATTCCTGTCACAAACTTCACTCTCGAACAGATACGAGAGGCTTCAAGTATTGTCTACGAACATGATGATTCAGAAACCACAGAGGATAGCTTTGAAATTCTTCTTACTGATGGTAAATTCACAGTGGAGAAAACCGTTATGATCATGGTCATATTGGTGGATGATGAAACACCAAGGATGGCGATTAATGATGGCCTTGAAATAGAAATCGGAGAGGTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11529
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 1142 | 3116 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33281973)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32734578 |
| GRCz11 | 15 | 32592557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTCCCAATCGTSATAATCCCATCCAATGATGAGAAGCCTGAGATCTA[T/A]ATGAGAGAGTTTGTTGTGATGGAGGGCATGAACATTGTGATTGACACTCC
Long Flanking Sequence:
AAACAAGACTTTTTCAATCTGACACTCACCGATATGTCTGATGAATGGACAGTTGGGGGGAATAAAATCAAAGGGGTTCGCGTGCAGGTCACCATTCTGCCATTGGACAGTCAGGCTCCGGAGGTGTTCGTGGGCCCCCAGTTCATCGTCGTAGAGGGTGAGAAAAATGTTATAGCAATTTCGCACATTAGCGCCAATGACATTGACACCCCTAATGATGATCTCCTTTGCACAATTATTGTGCAGCCCACTTCAGGTTATGTAGAAAACATTTCCCCCGCACCAGGATCTGAAAAATCCAGATCAGGGATTGCCATCAGTGCTTTCACCATCAAAGACATTCGGGAAAACCACATTTATTATGTGCAAAGTATTCATAAAGGAGTCGAGCCAGTTGAAGATAGGTTTACTTTCAGGTGTTCAGATGGGATCAACTTTTCCGAGAGACACTTTTTCCCAATCGTCATAATCCCATCCAATGATGAGAAGCCTGAGATCTA[T/A]ATGAGAGAGTTTGTTGTGATGGAGGGCATGAACATTGTGATTGACACTCCAATATTAAATGGCGCCGATGCTGACGTTCCAGCGGATGAGCTCACATTTATTATTTCAAAACCTCCGAAACATGGATTTATCCTTAATCAGCTAACCTCAGGCACAATTCCTGTCACAAACTTCACTCTCGAACAGATACGAGAGGCTTCAAGTATTGTCTACGAACATGATGATTCAGAAACCACAGAGGATAGCTTTGAAATTCTTCTTACTGATGGTAAATTCACAGTGGAGAAAACCGTTATGATCATGGTCATATTGGTGGATGATGAAACACCAAGGATGGCGATTAATGATGGCCTTGAAATAGAAATCGGAGAGGTCAAAATCATCAACAATAAAGTGTTAAAAGCCACTGATTTGGATACAGAAGACAGCACTCTGACCTACATCATCCGTTATGGTCCGAATCAAGGTATTTTACAAAAGCGAACACCATTTGGACTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10377
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 1856 | 3116 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33380908)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32635643 |
| GRCz11 | 15 | 32493622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCGATTGAGGAGGATATTGGAGAACTTTTGATTCCTGTGCGAAGATCT[G/T]GAGATGTCAGTCAGGAGCTCATGGTGGTCTGCTTCACACAAYAAGGTGAA
Long Flanking Sequence:
CTTGAAATTAGTTTAGATTAATACAATGTTCTGAATACACAAGCGAAAAGAAAACAATTTTTTTGACAGGACCCTTCACTTTGTATAGAATGAACATTTTCGGGTTTGTAGATGTTGAAAGCATTTTAATTTTTGGGTGAAATGCAGTATGCGATTCTGAACTGTTTGACAGCTACTGTGTGAGATCAATCCTGCATTAAAAATACAGAAACAGAAACTTAAATTGCGCATGCATTTTTAAACGGCTAGAAACTTACTATATAAATGTCATGCTGAAAGAACTTTAGGTCTGAAATGAAACTGATTCCACCTGGACCCATGAAGTTCCTCACACAATGATGATTCCTTTAACTCTTTTATTTCTCAGTCTCTAAAGTTATGTGCATATAAATGAAATGTGATGCTTGCCGTTTGCCCTAGAGTCCACAGTGTTCATCCCGTTGACTGCATACTCGATTGAGGAGGATATTGGAGAACTTTTGATTCCTGTGCGAAGATCT[G/T]GAGATGTCAGTCAGGAGCTCATGGTGGTCTGCTTCACACAACAAGGTGAATTATGAATGATGCTAAAATTATTCTCATTGGTAACACTTTACAATAAGATTTCATTAGTTATTTCATTAGTTAAGTATGAGCAATACTTGTACGGCATTTATTAATCGTAGTTTAACATTTAATAATGTCTCATTAAAATTTTAATTCTCATTTGTTAACATTAGTTAATGCACTCTGAGTTAACTAAAAACGCCTCACAGCAAGAAGGTCGCTGGTTCGAGTCCCAACTGGGTCAGTTTGCATGTTCTCCTTGTGTTCACGTGGGTTTCCTCCGGGTGCTTTGGTTTCCCCCATAGTCCAAAGACATGTACTGTAGGTGAATTGGGTAAGCTAAATTGTCCATAGTGTATATGTGTTTGTCCTGATCCTCCAGGTTGGGGGTTAAGCATTGAGCTAGCAACCAACCTCGTAAAAACTAGATGTTACGAAACTCCAATATGGTGCGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42593
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 1890 | 3116 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33382783)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32633768 |
| GRCz11 | 15 | 32491747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAGGCACGGTTCCCACTACGGTGCTTTCCTATTCGGACTATATTTCC[C/T]GAGCTGAGGAGCACCACAGTGTGCTGCGTTTCGATAAGGGTGAGACTGAG
Long Flanking Sequence:
ATGATCTAAAGCATTAAAGTGTAATGAACATAACTAAAAAATAAATTAGTAGGGGCAAACACTTATTCACAACACATATATAACTGGCAGTCAAACTGAAAGGGAATACTGTGAAAATGTCTTTGCTCTGTTAAACATCCCTTGTGAAATACTTGAAAAAATAAATTTCACTTAAGGACTAAGAATTTTCCCATCAACTGTATATGTGCATGTGTATGTATAACCTATTGGTTATTATTATTACTTATAAAAAATCAACAGTTCTTGAATTAAAGAAAAGAAAATTCTTGTTATAATGTTATAATTTATTGAAGGTCTTATTTTTCATAATATACGCTACATGATTAGACTTTAAAATGACCTTTAACCTTTACCTTCAAGTGTTAAAATAAATGTGAATGGTCAAAACTTTCTCCAAGCTTTGCTTTATTCTTATCTGTGTAGGTACAGCCAAAGGCACGGTTCCCACTACGGTGCTTTCCTATTCGGACTATATTTCC[C/T]GAGCTGAGGAGCACCACAGTGTGCTGCGTTTCGATAAGGGTGAGACTGAGAAGCAGTGCCGTGTAGTCATCATTGATGACTCCCTCTACGAGCCAGAGGAAAGCTTCAATGTAACTCTCAGCATGGCCATGGGTGGCCGTCTTGGACAAGAGTTCAGCACCGCTAGAGTCACCATCCTACCTGATGCAGATGACGGTGAGAGGCTTCACTTTGCTCCATGTGTTTAGTTTATTTGGTTTGCTTGCTGTTTTGATTTTTGCCTGGGGTGTCTATGCATGCAAATAGTCTATCCTGCTGGCAGATGCTATTTCCAATGGTTCTGCTCACCAGTGCCTGATTTAAACAGTCAAAAGGATGATCAATGCATCCTTGCCATTGCAGTAGGGGACACTTAAGTTTTTTTATTATATAGGAGATCACAAATGTGTTTATTTTAACTCAAAATTATTAAAACATTGAAAAGTGTAAATATAATAATATTTAATAATAAGTGCCATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13551
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 2037 | 3116 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33405091)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32611460 |
| GRCz11 | 15 | 32469439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGCGTCAACATGCAGACTTTYAAGGYTACAATCCTGGATGACCTGGGA[C/T]AGCCGGTGCTGGAGGGCCCGGAGAAGTTTGAGCTGGTTCTCCGAATGCCC
Long Flanking Sequence:
AAAAATATATACAAATGTATTCTAAAGTAATTCTGATATTTTGATCGCAGTTGTGACATAAAGTCACTGATCTATGTTATAAAGTGGGAATTAGTCATTTTCCCTTCAGAATTGGGCTATATGACTTACAAGTGTTCGATTAAGAGCAAATAAGTTAGAATTCAAAATAGAAAAGTGAGATTTGCTGGTTTATATTTGCCAGTTATGACTATTTTTGTAAATTGTGACATAAAAAATTATCTTTCAAGCTTAGTATTTTAGCCCATACATTTAACACAATAGAATCACGCAGTTCTTTGTTGTTTGTTTTGTGTCTCAAGTGCTAACTTTACTTGTGAGAACTGACCTATTATTATTATTTCTGCAATATTCTCTCCACTAACTCTCTGTAAACCTTTAACACAGCTGGTGTGGACTACGTTGGAATTAGCAAGAACTTGGACTTTTCCCCAGGCGTCAACATGCAGACTTTCAAGGTTACAATCCTGGATGACCTGGGA[C/T]AGCCGGTGCTGGAGGGCCCGGAGAAGTTTGAGCTGGTTCTCCGAATGCCCATGAACGGCATATTAGGAGAACCAGGAAAAGCTACAATCTACATCAACGACTCCATCTCAGATTGTGCGTTGCCTTGAACTAAACCCTAATATGGATACAATCAATGTCCTTTAAATGACACTGTAAAAAATTCTTGCTGCCTTAACGTTTTTAGTTGAATCAAATGAACTTTTCTAGTCATCTTAACTTATATCAATCAAACTGACTAACTTTGCACAACTTAAAAATGTAGTTAAAACGTCATTAACATGTCAAAATAAGCTAAAAAATAACATAAAACATTTATAGTCATGACTTTTTGCCATATAATTTTTTAAAATGTATGAAAATGATCTTATGCAAGAAAAAAATCTGTAAGAATAATGATTATTTTGAACATAAAACATTTTTGTTTGTTTTTTAGTGCCCAAAATGCAATTCCGGGATCCTACATACACAGGTAATGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39061
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 2262 | 3116 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33411170)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32605381 |
| GRCz11 | 15 | 32463360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACATGTGATAAAAATGACAATTTTCTACCTGCAGATGTGGAGTTTAAA[G/T]AGGGAGAGACTGAGCACATCGTGGAGGTAGAGATTCTGTACGATGGAGTT
Long Flanking Sequence:
ACTATTATAAATAACGTTACAATGCAAACGATTGACTCACTTATGTCACCAATGTCAAGCAGAAGCACTTTGACCATCTTTGGGAATCATATAGGAATATTATTTAAATTGTGTGTTTTTAAATATGTATTTTTATTTTTTTAATGTATTTTTTTTATTATTGAATTAATTTATTATTTATTTTTCAATGTTTCCATTAATTATTATTTCTATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATGTTATAATATAATTATATATATATAATATATATAATATATAATATATATATAATAATATATATATATGTTATTGTACGCCATATATTTTTTTGTCCCATCACACTTTATAAAAAAAGGATTTGTCAAAAAAAACATATGAGTTACTCAGTCACATGTGATAAAAATGACAATTTTCTACCTGCAGATGTGGAGTTTAAA[G/T]AGGGAGAGACTGAGCACATCGTGGAGGTAGAGATTCTGTACGATGGAGTTCGAGAGATGAGAGAAGCCTTCACCATCCACCTCAAACCTGATGACAACATGATAGCGGAGATTCAAGTATGACAATATGCTGAAATAAGAACAAAATGCTGAAATAATCTGCCTGTGCTACAATCGAAATAGCAGGCCTGTTTTTATTAGATCCACTCTGTGCTTAATGTTTGCTGCTTCTCCAAACCTTCAGGTCACCAAAGCCATCATCTACATTGAGGAAACCAACAGTATGGCTGATGTGACCTTTCCCTCGGTGCCGGTGGTGGTGTCTCTCTTACAGTATGATGATACCAGCAGGACTAGAGAAACTCAACCAGCTGCTGGATATCCTGTCGTCTGTGTCACGGTGTGTTCACTATATGTAACACTCCTTCAATCCTGTATGATTTGTATTCATTTATTAAATAGAGCATACATTTTTTTTTTATTTCTATATTTATTATAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35952
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 2346 | 3116 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33411551)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32605000 |
| GRCz11 | 15 | 32462979 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTATGATGATACCAGCAGGACTAGAGAAACTCAACCAGCTGCTGGATA[T/A]CCTGTCGTCTGTGTCACGGTGTGTTCACTATATGTAACACTCCTTCAATC
Long Flanking Sequence:
ATATATTTTTTTGTCCCATCACACTTTATAAAAAAAGGATTTGTCAAAAAAAACATATGAGTTACTCAGTCACATGTGATAAAAATGACAATTTTCTACCTGCAGATGTGGAGTTTAAAGAGGGAGAGACTGAGCACATCGTGGAGGTAGAGATTCTGTACGATGGAGTTCGAGAGATGAGAGAAGCCTTCACCATCCACCTCAAACCTGATGACAACATGATAGCGGAGATTCAAGTATGACAATATGCTGAAATAAGAACAAAATGCTGAAATAATCTGCCTGTGCTACAATCGAAATAGCAGGCCTGTTTTTATTAGATCCACTCTGTGCTTAATGTTTGCTGCTTCTCCAAACCTTCAGGTCACCAAAGCCATCATCTACATTGAGGAAACCAACAGTATGGCTGATGTGACCTTTCCCTCGGTGCCGGTGGTGGTGTCTCTCTTACAGTATGATGATACCAGCAGGACTAGAGAAACTCAACCAGCTGCTGGATA[T/A]CCTGTCGTCTGTGTCACGGTGTGTTCACTATATGTAACACTCCTTCAATCCTGTATGATTTGTATTCATTTATTAAATAGAGCATACATTTTTTTTTTATTTCTATATTTATTATAGTCATGCAACCCCAAGTATCCTGACTTTGACCGAACGGGCTCTATCTGTGTTGCGGAGAACATCAACAACACCCTGACCCGGTACCGTTGGCTAGTCAGTGCCCCGACAGGGCCCGACGGTGTGACCAGCCCCATGAAGGAGGTGGATTTCGACACCTTCTTCACCTCCTCCAAGACCATCACATTGGACTCGGTGTATTTCCATGCAGGCTCACGTGTGCAGTGCGCAGCTCGAGCTGTCAACTCTAATGGGGATGAAGGCCTGGAGCTCAGCAGTCCCATCATCTCCATCAGCCAGGAGGACGGTGAGTTTAGCACAGCATACAGTACAGAATTAGTGCTGATATTAAGACAGTTTCTGGGCAAATAAATGAGGTGGAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12519
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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 2653 | 3116 | 17 | 24 |
| ENSDART00000114905 | Nonsense | 2653 | 3116 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33421103)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32595448 |
| GRCz11 | 15 | 32453427 |
KASP Assay ID:
2260-8791.1 (used for ordering genotyping assays)
KASP Sequence:
GGCTGGCAGCACTTTGACCTGCAGTCTGAGCTGCGTCTCACTTTTGTGTA[T/A]GACACCGCCATCTTGTGGAGAGACGGCATCGGCAGTCCACCAGAGGCTGA
Long Flanking Sequence:
CTCTGCTATACTAAAAACACGTTTAGCAGAGCTGCTCATGTAAAATGATTTCTGTGTAACATATTACATATTTTTACACAGTTTATTTTACCTTAGTCATATCATAATCATAAACCAGACGGTTAGCTGCCTTGAGAATTAATAACAACTAACTGACCAAACTTTTTAGCACCTGGTAAATGTTTATTTTAGGCCTTTAAAAAATTACCAAAATGTAAGCTTTTCTAAACCTAAAAGCAATGTTTTATTTGCATTAATAGAACATTCTTGGCTATAACAAACAAAGGAACATTAGAATGTATATTGGAATTACTAAAGATTGTTATGTAGTAGTTATTATGCGCTAAAGTGTTGTTCTTTGTGCAGGTGCTGAATCTGGTGCAGTCTTACGTGACGCTGCGTGTTCCTCTACATGTCTCATATGTGTTTCATTCACCCGTCGGCGCTGGAGGCTGGCAGCACTTTGACCTGCAGTCTGAGCTGCGTCTCACTTTTGTGTA[T/A]GACACCGCCATCTTGTGGAGAGACGGCATCGGCAGTCCACCAGAGGCTGAATTACAAGGCAAGTGCTTCAGTCTTTCTGACCAATCAAAAAAATGATATAATTAATATGATGACATTTTATTACCAAAATTGTTATTTCAAATTGAAATAACTATTTTCAGAAGCAAATACTTCTGAAAAATGTATGTGTTTAGCCATAGGGACTTTATGGTCCTGTGTGGGTATGTGTTTTGTTTTGTTTTAAATTATGTAAAATATGTATATTGTAGGTGCTCTCTACCCTACCAGCATGCGCATCAATGAGCAAGGCCGTCTGGTCGTCAACTTCCGTACAGAAGCACGTTTTCGAGGGCTCTTTGTCACAGCACATTCAGGTTTGTTATTAAACATTCATTCATTTATTTATTAATTATTATTGATAATTATTATTATTAATATTAATAATTGTTTATAAATTATTATTTATTTATTAGGTCATATTATCTATTTTGATGATGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12912
Status:
Available for shipment
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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 |
|---|---|---|---|---|---|
| ENSDART00000114905 | Nonsense | 2653 | 3116 | 17 | 24 |
| ENSDART00000114905 | Nonsense | 2653 | 3116 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 15 (position 33421103)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32595448 |
| GRCz11 | 15 | 32453427 |
KASP Assay ID:
2260-8791.1 (used for ordering genotyping assays)
KASP Sequence:
GGCTGGCAGCACTTTGACCTGCAGTCTGAGCTGCGTCTCACTTTTGTGTA[T/A]GACACCGCCATCTTGTGGAGAGACGGCATCGGCAGTCCACCAGAGGCTGA
Long Flanking Sequence:
CTCTGCTATACTAAAAACACGTTTAGCAGAGCTGCTCATGTAAAATGATTTCTGTGTAACATATTACATATTTTTACACAGTTTATTTTACCTTAGTCATATCATAATCATAAACCAGACGGTTAGCTGCCTTGAGAATTAATAACAACTAACTGACCAAACTTTTTAGCACCTGGTAAATGTTTATTTTAGGCCTTTAAAAAATTACCAAAATGTAAGCTTTTCTAAACCTAAAAGCAATGTTTTATTTGCATTAATAGAACATTCTTGGCTATAACAAACAAAGGAACATTAGAATGTATATTGGAATTACTAAAGATTGTTATGTAGTAGTTATTATGCGCTAAAGTGTTGTTCTTTGTGCAGGTGCTGAATCTGGTGCAGTCTTACGTGACGCTGCGTGTTCCTCTACATGTCTCATATGTGTTTCATTCACCCGTCGGCGCTGGAGGCTGGCAGCACTTTGACCTGCAGTCTGAGCTGCGTCTCACTTTTGTGTA[T/A]GACACCGCCATCTTGTGGAGAGACGGCATCGGCAGTCCACCAGAGGCTGAATTACAAGGCAAGTGCTTCAGTCTTTCTGACCAATCAAAAAAATGATATAATTAATATGATGACATTTTATTACCAAAATTGTTATTTCAAATTGAAATAACTATTTTCAGAAGCAAATACTTCTGAAAAATGTATGTGTTTAGCCATAGGGACTTTATGGTCCTGTGTGGGTATGTGTTTTGTTTTGTTTTAAATTATGTAAAATATGTATATTGTAGGTGCTCTCTACCCTACCAGCATGCGCATCAATGAGCAAGGCCGTCTGGTCGTCAACTTCCGTACAGAAGCACGTTTTCGAGGGCTCTTTGTCACAGCACATTCAGGTTTGTTATTAAACATTCATTCATTTATTTATTAATTATTATTGATAATTATTATTATTAATATTAATAATTGTTTATAAATTATTATTTATTTATTAGGTCATATTATCTATTTTGATGATGATG
Associated Phenotype:
Not determined