ZMP
ep300b
Ensembl ID:
ZFIN ID:
Description:
P300-B [Source:UniProtKB/TrEMBL;Acc:Q1L664]
Human Orthologue:
EP300
Human Description:
E1A binding protein p300 [Source:HGNC Symbol;Acc:3373]
Mouse Orthologue:
Ep300
Mouse Description:
E1A binding protein p300 Gene [Source:MGI Symbol;Acc:MGI:1276116]
Alleles
There are 12 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6889 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31328 | Essential Splice Site | Available for shipment | Available now |
| sa38388 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33173 | Nonsense | Available for shipment | Available now |
| sa33172 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6888 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20005 | Nonsense | Available for shipment | Available now |
| sa26061 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33171 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31327 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6889
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086768 | Essential Splice Site | 281 | 2573 | 4 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25142193)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24910378 |
| GRCz11 | 3 | 25040926 |
KASP Assay ID:
554-5038.1 (used for ordering genotyping assays)
KASP Sequence:
CATCTRGAACTGCAGGAGCATGAAAACACTCTTYGGTCTGTCTKTCTCCA[G/T]CAGGGCCCAGGTGTGGTGGGTGGTGTATCGGGRCCAGGTGGGACGGCAGC
Long Flanking Sequence:
AAGTGACCGGTGAGTATATAATACTTCAGAGAGAAACAAAGCAGAAGGAAAAAAAGTCTAAACAAATTAATCAAAAGCGACAGTTTGACGTTACCAATATCATTTGTTTAAAAAATGCTGTTCTTATGACCTTTACACTCATCAAAGAGTCTTGGAAAAACTCAAAGCATCACATTTCCCCAAATCAGCATATTAGCATGATTTCTGATGGATCCAGTGTCAACGAAGGCTGCAGAAATGACTGCTGTATATGCTTTGGCATCACAGGAATAACTAGCTTTTTTTTTTTTTAATGTACAGCAATACTGCTGCAATACTGATAATAAACGCACCTTTGGTGAGAAGAAGAATGTTTAAAATCTTCTTTAAATTTGTGTACATGTTGCCATATTTGCTAATGCTAATGGACCCTCCAGTCTGCTGACTTCCTGATCTTTAAATCTTAATTTCCATCTGGAACTGCAGGAGCATGAAAACACTCTTCGGTCTGTCTTTCTCCA[G/T]CAGGGCCCAGGTGTGGTGGGTGGTGTATCGGGGCCAGGTGGGACGGCAGCGCCCCCTGCCGCGGACCCAGAGAAGCGTAAACTGATTCAGCAGCAGCTGGTGCTGTTACTGCACGCTCACAAGTGCCATCGCAGAGAGCAGGCCAACGGAGAGGTCCGCCAGTGCAACCTGCCTCACTGCAGAACCATGAAGAACGTCCTCAATCACATGACGCACTGTCAGGCCGGCAAATCCTGCCAGGGTAAGCAGAGCCAGCTTTTTTAAATCTTTGATTTGTGTTTTATGTTTTCAACCCTAAACAAGATGACATGGTGTCTTACTGGTGGCTCACTAATGTGCTTGTGTTTTTTTGACAGTGGCTCACTGCGCGTCCTCCAGACAGATCATCTCTCATTGGAAGAACTGCACACGGCATGACTGTCCTGTCTGCCTGCCGCTAAAGAGCGCCGGAGACAAAAGAAACCAGCAATGTGAGTTAACATGCAGAAATGTCTGGAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31328
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086768 | Essential Splice Site | 679 | 2573 | 12 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25131679)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24899864 |
| GRCz11 | 3 | 25030412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGACAGAGGGCCACGCCTCCCCTGCCAATGGGTGCAAACCTCAATCAGG[T/A]AATTTCACTTGCCACCCAAAGGTCGGCGACTGATGTAAATGTACCTGATT
Long Flanking Sequence:
TGTTATTGATCATGTGGAGTGATTATAAAGGATCTTCTGGTCTTTCCTAGATGGTCCTCATTCAGATCCGTCTTTAGTTCAAGCCACTGGTCCCAGTCAGATGGTCAATCGCATGCAGAATCCTGCTGGTATGCCACACTCACTAAATGGTCTGTAGTTGATGCACTATTGCTACATATATATGAAGGGTTTATGTGCAAAGACAGATTAGTCCATTTTTAGACATCATGTTTTGTACAATTGCCAAAAAAGAAATCATATTTTCACCTTGAGTGTTAAAGAGTACATTTGCAAAAAAAACTCATATATAACTGTTGATTTATCTGTTTTTATATGAACTCTTCATATATATAAAAGTCATAGTTTTGTTTTTGACTTATGTTTTAAACTTTGTAATTGCTTTCATCCAGGTATGAATCAATTTGGCCAGGTGGGGATGCAGCAACCAATGGGACAGAGGGCCACGCCTCCCCTGCCAATGGGTGCAAACCTCAATCAGG[T/A]AATTTCACTTGCCACCCAAAGGTCGGCGACTGATGTAAATGTACCTGATTGAAGCATTTATTTGGCATCTTTATTGTCTGTATTTAGATGAGCATGCAGGGAACACCTCGAATGGCTCAGCCCAATGTACCCCAGTTACAAAACCAGTACATGCAGAACCAGTTTACAGGAACGGGTGCTGGATTGGGACAGGGTGCGGTTGGCCTGAATCAACCTGCAGGGCAGGGAGCCATGCCGCAGGTCAGCTATTAAACCACATTCATATCTTGTTACTCAGAACAATGTGATGTCTCTAATATTTCTGTATGATAGTGTGTAGTGGTGCTGATAAGAGTGTTTCTCTTCTGAACTCTCGTGAAAGACAATAGCATAAACAGTTTTTAAAAAACAACCTTTATTTATTGAAATGTAAGCCTCACTCAAATTTAAATTTAAATCTCTTTAGATTCATTATTAGACATAGGTTTATTATTAAACATTCATAGAATTTAATGTTAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38388
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Essential Splice Site | 1144 | 2573 | 18 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25118842)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24887027 |
| GRCz11 | 3 | 25017575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAATAGACCCTGTTATGCAGGAGTTGGGCTACTGCTGTGGAAGGAAGG[T/C]CAGTGTGTCGCTTGAGGGCTTTATTTATTTATTTATTTATTTATTTTGCA
Long Flanking Sequence:
CCATCCTACCCCAGTATGTCAGCCTTTTCCCCTCATTGACCCCAAGAATCCATGTATGTGTTTTGTGTGTTTCTGGGAGACCGGAGGTGAACTAGGGTACAGATTTGAGTGAGGCAGTGGGAGTCTGTTACGGTTTTCTCTGTTTGTGCATGTGAACCTCTTCTACAGCGCTCAACATTGTCCCCCTGCACCCTCTTCTCTCCCCCTGACTCTCCACCATCCATTGTCTCGACCGCGATGGTGACCATTCATCTTCCAGGACTACTTTGACATTGTGAAAAACCCCATAGACTTGTCCACTATCAAGCGTAAGCTGGACACGGGGCAGTACCAGGAGCCCTGGCAGTATGTGGATGACGTGTGGCTGATGTTCAATAACGCCTGGCTGTATAACAGAAAGACGTCACGGGTTTATAAATACTGCTCCAAACTGGCCGAGGTCTTCGAACAGGAAATAGACCCTGTTATGCAGGAGTTGGGCTACTGCTGTGGAAGGAAGG[T/C]CAGTGTGTCGCTTGAGGGCTTTATTTATTTATTTATTTATTTATTTTGCATGTTCAAGTGGGTTTTAGTAAAGGAATGTGGCTCAACAATATGATTTAATCCCTTTAAAAGAAGCCATATTAGGGCTGGGCGATATGGCTAAAATGTAGTCTCGATAAATTATTTTCTATATTGAAAAATACCGATGTATATTTTAATATCAGTTGTTAATGCATCCAGATTTAAGTGTATACCAGCAATGTCTGAAGCATTATAAATGAGAGGGTCCGTTAAAATAACACAACCTATTTTCGGTGGCCGAAAATTTTTTGCATCCTTAATAGCAAACACTTCTAGATTCTAGGGTTGCACGATACTGGAATTCGGAACCAATCGATAGTGATATTTGAAAAATGTTCATTTACCCCTGTTTAGCATGTTCATAAACAGCACTGATTTGCCTTTGGGTTTGGTGAACTGATGACCTTCATGGCCAATCACAGTCCTTTTCTGTTGAGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33173
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Nonsense | 1377 | 2573 | 25 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25103758)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24871943 |
| GRCz11 | 3 | 25002491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTGGAATGCATGTTCAAGAATACGGCTCTGATTGCCCTCCACCTAAT[C/T]AAAGGTTAAAAATAACAAAGACTCAGTCACACATCTTCAGGCACACACTG
Long Flanking Sequence:
TGCGTAATTCCTCATAGCATGACCAACATGAATGTTTATCATTGCATAAATGCCCACACGTTTCCATACATTTTGTATTAATATTGATGTATGTGGGCAGATGAATTGTAAACATTTGTCTTGCTAGCTCTCACTATTGGGTCTCAGAAAAGACTTCTCATGGATCAGTCACACTGTGACTTTTTCTTTTTAAACCAATGTAAATATACTATGCATCTATCACCATTGTGAGATAACAGTTCTCAAGTTGCGTATTTTATGGATATTTTATGAATACTCGTGCTAGCTTAATTAAAATTTTTTAAGACAGCACAACTGAAATGAAATAATCTAAGAATTAACTGTGTTTCTTTTCCAGATTTGTTGATAGCGGCGAGATGTCAGAATCATTCCCATATAGGACAAAAGCTCTGTTTGCATTTGAGGAGATTGACGGAACAGATGTCTGCTTCTTTGGAATGCATGTTCAAGAATACGGCTCTGATTGCCCTCCACCTAAT[C/T]AAAGGTTAAAAATAACAAAGACTCAGTCACACATCTTCAGGCACACACTGATTCTTCACTCACGTGCACATGTATGGCATTACAAAGTGGTATGAGAAACACAAGTAACTTGATGGTATCTCCTGTCTCTCTCTCTCTCTCCCCATGCAGACGTGTGTATATATCCTATCTAGACAGTGTGCACTTTTTCCAACCCCGTCATTTGAGAACAGGAGTCTACCATGAAATTCTCATAGGATACTTAGAGTACGTTAAGAAAATGGGGTTTGTCATGGGCCACATCTGGGCTTGTCCACCGAGTGAAGGTGATGACTACATCTTTCACTGCCATCCATCTGATCAGAAGATTCCCAAACCAAAACGCTTACAAGAGTGGTACAAGAAGATGCTTGACAAAGCAGTAACTGAGAGAATTGTACATGACTACAAGGTACAGCGACAGCTGACTATAATGAAAGTTTACACTAACGTCAGCATACTGCTCTATAGTACACATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33172
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Essential Splice Site | 1471 | 2573 | 26 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25103327)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24871512 |
| GRCz11 | 3 | 25002060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGATGCTTGACAAAGCAGTAACTGAGAGAATTGTACATGACTACAAG[G/A]TACAGCGACAGCTGACTATAATGAAAGTTTACACTAACGTCAGCATACTG
Long Flanking Sequence:
GACGGAACAGATGTCTGCTTCTTTGGAATGCATGTTCAAGAATACGGCTCTGATTGCCCTCCACCTAATCAAAGGTTAAAAATAACAAAGACTCAGTCACACATCTTCAGGCACACACTGATTCTTCACTCACGTGCACATGTATGGCATTACAAAGTGGTATGAGAAACACAAGTAACTTGATGGTATCTCCTGTCTCTCTCTCTCTCTCCCCATGCAGACGTGTGTATATATCCTATCTAGACAGTGTGCACTTTTTCCAACCCCGTCATTTGAGAACAGGAGTCTACCATGAAATTCTCATAGGATACTTAGAGTACGTTAAGAAAATGGGGTTTGTCATGGGCCACATCTGGGCTTGTCCACCGAGTGAAGGTGATGACTACATCTTTCACTGCCATCCATCTGATCAGAAGATTCCCAAACCAAAACGCTTACAAGAGTGGTACAAGAAGATGCTTGACAAAGCAGTAACTGAGAGAATTGTACATGACTACAAG[G/A]TACAGCGACAGCTGACTATAATGAAAGTTTACACTAACGTCAGCATACTGCTCTATAGTACACATTGTTTTTGATGGCCATGTGTCTTTTATTAACTGCTGCATGTTTCTTCTCACCCCAGGACATTTTTAAGCAGGCAACTGAGGATCGTCTGACCAGTGCGAAGGAGCTCCCTTATTTTGAGGGTGACTTTTGGCCTAACGTATTGGAGGAGAGCATCAAAGAGCTGGAACAGGAGGAGGAAGAACGGAAGAGAGAGGAAAATAACACCTCTAGTGAAAGTATTGATGTGAGTGATTGACTCAAATTTGCAAGCGCTGTGTGGTATTGGGGAAAACATGCAAAATGAAAACATTAGTTATGCATAATATTTCTACGTAGTCTTTTAAAAGTGTGGGTGATTTGCTATTTATTCTTAAAACCAATGTATTATTTTAATACCTTTTTTAATGATCTAGGCGACCAATGGTGACAGCAAAAATGCCAAAAAGAAGAACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6888
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Nonsense | 2092 | 2573 | 30 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25100993)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24869178 |
| GRCz11 | 3 | 24999726 |
KASP Assay ID:
554-5022.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCTCAACAGGTCGCTGTGCAAGGTCAGATGCCCCCACAAATGCATCCA[C/T]AGCAGCCGAGAATGAATCCACCACTTCAGCCTCAACAGCAACAGTGGCCA
Long Flanking Sequence:
TGGGACAAGTGCCACATCCACACAATCAATATGGCCCCCACCCCACAGGTCCCTCCCCAAATACCCAGTCCCAGGGTAAACCAGGCCTTGGTCCTGCAACTCCTCCGCAACTCCCCAGCAACCCAGGCACTGTACCTATGGCCCAGCAACAACAACCTACAGGTCCTCCGGCAGCCGCTGTGGAGATTGCCATGAAGATTCAGCAAGTGGCAGATGCACAGCGGAAAATGGCACAGGTTCAGTTGCTACAAAGACAAGCTGCCCAAGCAGGAATGATGCCACAGCACCATCAGCAGCCACAGGGACAGATTGGAGTGGCCCATCCTGGAATTGGTATGGTAGGGCCACAAGGCTTAGCCTCGCAGGCACAAACATCAGCGAACAGGGTGCAGATGGAGCAGCAACAAGGACCTCAGGGAATGATGGGAGCCGGGCCCATGCAGCAACAGCAGCCTCAACAGGTCGCTGTGCAAGGTCAGATGCCCCCACAAATGCATCCA[C/T]AGCAGCCGAGAATGAATCCACCACTTCAGCCTCAACAGCAACAGTGGCCAGGGCAGGGCATGCCTACCCAGCAGAGACCTGCTATGATGTCTCAGCAGGGAATGGTTTCAATGCAGCCCCAACCGCAGCCGCAACAACCATCACAACAAACGCAACAGCAGCAAGCACCCCAAATGCCAAATCGAAATGCCTTGATGAGTATGGTACAGGCTGGTCTACAGAGTGGCGTAGCAAGTGGGGCTGCAGCTAGCAATTTGCCCCAGGGAGCCTTGCAGCAGCTTTTGCGGACTCTGCGATCTCCAAGCTCTCCTCAACAGCAACAGCAAGTTCTCAACATTCTCCGGTCTAGCCCACTTCTAATGGCAGCATTTATCAAGCAACGGGTTCACAAGTATAAAGGAGGTACAGGTGGCCCCTCTGGACCGCAGGGAGGGCCAGGACCTATGGGAGGCCAACCTGTGGGTGTCAATACTGGGGTTCCCCAACCTGGTATGCATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20005
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Nonsense | 2260 | 2573 | 30 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25100489)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24868674 |
| GRCz11 | 3 | 24999222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTGTGGGTGTCAATACTGGGGTTCCCCAACCTGGTATGCATCTTGGA[C/T]AAGGTGTTAACATGCAGAGTCAACTTCTGAGTCAACAACAGAGCCAACAG
Long Flanking Sequence:
AGCCGAGAATGAATCCACCACTTCAGCCTCAACAGCAACAGTGGCCAGGGCAGGGCATGCCTACCCAGCAGAGACCTGCTATGATGTCTCAGCAGGGAATGGTTTCAATGCAGCCCCAACCGCAGCCGCAACAACCATCACAACAAACGCAACAGCAGCAAGCACCCCAAATGCCAAATCGAAATGCCTTGATGAGTATGGTACAGGCTGGTCTACAGAGTGGCGTAGCAAGTGGGGCTGCAGCTAGCAATTTGCCCCAGGGAGCCTTGCAGCAGCTTTTGCGGACTCTGCGATCTCCAAGCTCTCCTCAACAGCAACAGCAAGTTCTCAACATTCTCCGGTCTAGCCCACTTCTAATGGCAGCATTTATCAAGCAACGGGTTCACAAGTATAAAGGAGGTACAGGTGGCCCCTCTGGACCGCAGGGAGGGCCAGGACCTATGGGAGGCCAACCTGTGGGTGTCAATACTGGGGTTCCCCAACCTGGTATGCATCTTGGA[C/T]AAGGTGTTAACATGCAGAGTCAACTTCTGAGTCAACAACAGAGCCAACAGCAGCAGCAAATGCAACAACGACCGCTCCTGCAACAACAGCAAGTTGCTGCCTTGCAGCAGCAGCAACAACAACAACAACAGCAGCAGCAACAACAACAGCAGCAGCAGCACCAACAACAACAACAGCAGCAGCAGCACCAACAACAACAGCAGCAGCAGCAAGGGATTCAAGGACAGGGGACCCCAAACATGGCCAATCCACACTTCCGAGAACTAGTCATGAGAAGGCAACAGCAATTACAGTTTCAGCAGCAACAGCAGCAACAACAGCAACAACAACAACAACAAATGAGCAATCATGCGGCATTCCAGCAGCAGCAAGGTTACATGAGTCAGCAGGGTAACATGCAAGTCCCGCCAGGAGGTCAGCCACTGCAAGGAGTACAACCTGGCCAACAGCAGAATTTTCCTGGAAATCCTGCACAGCAACAAGCTGCAGCTGCTTTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26061
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Nonsense | 2303 | 2573 | 31 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25100162)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24868347 |
| GRCz11 | 3 | 24998895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAACAGCAATTACAGTTTCAGCAGCAACAGCAGCAACAACAGCAACAA[C/T]AACAACAACAAATGAGCAATCATGCGGCATTCCAGCAGCAGCAAGGTTAC
Long Flanking Sequence:
TCAACATTCTCCGGTCTAGCCCACTTCTAATGGCAGCATTTATCAAGCAACGGGTTCACAAGTATAAAGGAGGTACAGGTGGCCCCTCTGGACCGCAGGGAGGGCCAGGACCTATGGGAGGCCAACCTGTGGGTGTCAATACTGGGGTTCCCCAACCTGGTATGCATCTTGGACAAGGTGTTAACATGCAGAGTCAACTTCTGAGTCAACAACAGAGCCAACAGCAGCAGCAAATGCAACAACGACCGCTCCTGCAACAACAGCAAGTTGCTGCCTTGCAGCAGCAGCAACAACAACAACAACAGCAGCAGCAACAACAACAGCAGCAGCAGCACCAACAACAACAACAGCAGCAGCAGCACCAACAACAACAGCAGCAGCAGCAAGGGATTCAAGGACAGGGGACCCCAAACATGGCCAATCCACACTTCCGAGAACTAGTCATGAGAAGGCAACAGCAATTACAGTTTCAGCAGCAACAGCAGCAACAACAGCAACAA[C/T]AACAACAACAAATGAGCAATCATGCGGCATTCCAGCAGCAGCAAGGTTACATGAGTCAGCAGGGTAACATGCAAGTCCCGCCAGGAGGTCAGCCACTGCAAGGAGTACAACCTGGCCAACAGCAGAATTTTCCTGGAAATCCTGCACAGCAACAAGCTGCAGCTGCTTTGCAACAGAGGCTTGCGCAGCAGCAACATCAGCTACAGATGCAACAGCAGCAGAATGCTGCAACACAAGGTCCTGACATGGGACCTGGAGGAGGTCCACAGCCCACACAACTAGGTCCAGGTCTTCAGTCACCACAGGCATTATTGCAACAGGCTTTGCATCAGCGTCTATTTCCGCAGCAGCAGCATCTTAGTGGCACCTCTCCGGCACAGCAAAACAACCCAATGAGTCCACAGCAGCAACAGATATCTCAGTCGCCCCACTTGCAGGGCCAGCAGCTCCCATCCTCCCTCAGCAACCAGGTCTGTTCACCACAGCCATCTCCACGACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33171
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Nonsense | 2439 | 2573 | 31 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25099754)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24867939 |
| GRCz11 | 3 | 24998487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGTGGCACCTCTCCGGCACAGCAAAACAACCCAATGAGTCCACAGCAG[C/T]AACAGATATCTCAGTCGCCCCACTTGCAGGGCCAGCAGCTCCCATCCTCC
Long Flanking Sequence:
CAAACATGGCCAATCCACACTTCCGAGAACTAGTCATGAGAAGGCAACAGCAATTACAGTTTCAGCAGCAACAGCAGCAACAACAGCAACAACAACAACAACAAATGAGCAATCATGCGGCATTCCAGCAGCAGCAAGGTTACATGAGTCAGCAGGGTAACATGCAAGTCCCGCCAGGAGGTCAGCCACTGCAAGGAGTACAACCTGGCCAACAGCAGAATTTTCCTGGAAATCCTGCACAGCAACAAGCTGCAGCTGCTTTGCAACAGAGGCTTGCGCAGCAGCAACATCAGCTACAGATGCAACAGCAGCAGAATGCTGCAACACAAGGTCCTGACATGGGACCTGGAGGAGGTCCACAGCCCACACAACTAGGTCCAGGTCTTCAGTCACCACAGGCATTATTGCAACAGGCTTTGCATCAGCGTCTATTTCCGCAGCAGCAGCATCTTAGTGGCACCTCTCCGGCACAGCAAAACAACCCAATGAGTCCACAGCAG[C/T]AACAGATATCTCAGTCGCCCCACTTGCAGGGCCAGCAGCTCCCATCCTCCCTCAGCAACCAGGTCTGTTCACCACAGCCATCTCCACGACCCCAGTCCCAGCCACCTCACTCAAGTCCGTCCCCACGCCTGCAACCTCAGCCCTCACCTCACCACATCTCGCCTCAAACCCAAACAGGTTCTCCGCATCCCAGCCATCTTCAGCAGCATCACTCAGGCATGGCTCCACCTCCTCCACCCCACCAACAGCCACAGCACAACTCTAAGGACCCAAGCGGATTTGGCGCAGATCAGAATGCCATGCTTTCTCAACTCAGTGGCATGGCGGGACTCCACGGACCAGGAGCGAATGATATGCTGCCTCCTAGTGGCCAGGACCTTGGCATTAACATGAATCTAACCCTTTAGATCATATAGTTATTAGGAAATTTACAAAACCTCGCCAGAGAGTGTTAGCATTTTTTACAAGGGTGAATTTAGTGTTTTTCAACATTAATGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31327
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 |
|---|---|---|---|---|---|
| ENSDART00000086768 | Nonsense | 2483 | 2573 | 31 | 31 |
Genomic Location (Zv9):
Chromosome 3 (position 25099622)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24867807 |
| GRCz11 | 3 | 24998355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCACGACCCCAGTCCCAGCCACCTCACTCAAGTCCGTCCCCACGCCTG[C/T]AACCTCAGCCCTCACCTCACCACATCTCGCCTCAAACCCAAACAGGTTCT
Long Flanking Sequence:
AGCAAGGTTACATGAGTCAGCAGGGTAACATGCAAGTCCCGCCAGGAGGTCAGCCACTGCAAGGAGTACAACCTGGCCAACAGCAGAATTTTCCTGGAAATCCTGCACAGCAACAAGCTGCAGCTGCTTTGCAACAGAGGCTTGCGCAGCAGCAACATCAGCTACAGATGCAACAGCAGCAGAATGCTGCAACACAAGGTCCTGACATGGGACCTGGAGGAGGTCCACAGCCCACACAACTAGGTCCAGGTCTTCAGTCACCACAGGCATTATTGCAACAGGCTTTGCATCAGCGTCTATTTCCGCAGCAGCAGCATCTTAGTGGCACCTCTCCGGCACAGCAAAACAACCCAATGAGTCCACAGCAGCAACAGATATCTCAGTCGCCCCACTTGCAGGGCCAGCAGCTCCCATCCTCCCTCAGCAACCAGGTCTGTTCACCACAGCCATCTCCACGACCCCAGTCCCAGCCACCTCACTCAAGTCCGTCCCCACGCCTG[C/T]AACCTCAGCCCTCACCTCACCACATCTCGCCTCAAACCCAAACAGGTTCTCCGCATCCCAGCCATCTTCAGCAGCATCACTCAGGCATGGCTCCACCTCCTCCACCCCACCAACAGCCACAGCACAACTCTAAGGACCCAAGCGGATTTGGCGCAGATCAGAATGCCATGCTTTCTCAACTCAGTGGCATGGCGGGACTCCACGGACCAGGAGCGAATGATATGCTGCCTCCTAGTGGCCAGGACCTTGGCATTAACATGAATCTAACCCTTTAGATCATATAGTTATTAGGAAATTTACAAAACCTCGCCAGAGAGTGTTAGCATTTTTTACAAGGGTGAATTTAGTGTTTTTCAACATTAATGCTTTGAGAACGGGCCCTTCTATGAGAGAGATCTCTTATATTCAACACAAATAAGTATATGGGGGTGTTTTTTTTTTCCTTTTGCCAGATATGTACAAAGAGAGGATTGTTTCTCAGCCTCAGAGAACAAACCACA
Associated Phenotype:
Not determined