ZMP
ANKRD11
Ensembl ID:
Description:
ankyrin repeat domain 11 [Source:HGNC Symbol;Acc:21316]
Human Orthologue:
ANKRD11
Human Description:
ankyrin repeat domain 11 [Source:HGNC Symbol;Acc:21316]
Mouse Orthologue:
Ankrd11
Mouse Description:
ankyrin repeat domain 11 Gene [Source:MGI Symbol;Acc:MGI:1924337]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16144 | Essential Splice Site | Available for shipment | Available now |
| sa17722 | Nonsense | Available for shipment | Available now |
| sa31604 | Nonsense | Available for shipment | Available now |
| sa31605 | Nonsense | Available for shipment | Available now |
| sa41040 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31606 | Nonsense | Available for shipment | Available now |
| sa7090 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11367 | Nonsense | Available for shipment | Available now |
| sa21093 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16144
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073594 | Essential Splice Site | 248 | 2820 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57657759)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56093085 |
| GRCz11 | 7 | 56394496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATGACGACACGCCTCTACATGATGCATCTAACAATGGCCATCTCAAAG[T/C]AAGTGACTCAGAAATKATACWTTACAKTTTTTTACACAAGATAGCAMACA
Long Flanking Sequence:
CACAGTCAAGTCTGGGTCAGAAGGGAACGCCAAACTCTGCCTCAAAAACCAAAGACAAAGTTAACAAGAGGAACGAGAGGGGTGAGACAAGGTTGCACCGGGCAGCCATTCGTGGAGAGGCACGCCGCATAAAGGAGCTCATCAATGAGGGGGCTGACGTGAATGTAAAAGACTTTGCAGGTAAGTGCAGCTTTCAGAGATCAGTTTCAGAGATCAGTTGCTTTTTTTCCATCGTTTCATGTTGATGTGTGCTGTTAATATCGAATAGGACAGAATGATATAGATTATTGCAGTTTGGAACTATTTGAAATGCACATGAAATTCTTCCAGTAATGTAGGAATGCTTTTTATTTTAGGCTGGACCGCACTACATGAGGCTTGTAACAGAGGGTATTATGATGTGGCCAAACAGCTGCTGGCAGCCGGGGCCGAGGTTAACACCAAGGGCCTGGATGACGACACGCCTCTACATGATGCATCTAACAATGGCCATCTCAAAG[T/C]AAGTGACTCAGAAATTATACATTACATTTTTTTACACAAGATAGCACACAATTTTAGGACCTTGTTTTTATTGATTATGTCACACCTACATTCTGGTTTTGTAGGTAGTGAAGCTGCTGTTACGATATGGAGGTGATCCTTGTCAAAGCAACAGAAGAGGAGAGACTCCGTTAAAAGTGGCAAATTCACAAACAATGCTTAATTTGTTGTTGGGGAAAATCACCTACTCCTCCAGTGAGGAGAGTTCCTCTGGTATGTATCATGAAGTGCATCTGTTTGCATGTATTCCAGAAAGTGCTTAACAGGAAATGTTACTAATAAAAGTTCTTGTGCTTCTCAGCAGATTCTTCTGAAGAGGAAGATTCCCCATCGTTTGCCCCATCTAGCTCTGTCGATGGCAATAATACGGACTCAGAGTTTGAGAAGGGCTTAAAATTAAAAGGGAAGGGCATGGACCCACCCAAATCCACCACCACTCCAGTCAAGGATGAGTATGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17722
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 289 | 2820 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57657986)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56093312 |
| GRCz11 | 7 | 56394723 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGCAAATTCACAAACAATGCTTAATTTGTTGTTGGGGAAAATCACCTA[C/A]TCCTCCAGTGAGGAGAGTTCCTCWGGTATGTATCATGAAGTGCATCTGTT
Long Flanking Sequence:
TCCATCGTTTCATGTTGATGTGTGCTGTTAATATCGAATAGGACAGAATGATATAGATTATTGCAGTTTGGAACTATTTGAAATGCACATGAAATTCTTCCAGTAATGTAGGAATGCTTTTTATTTTAGGCTGGACCGCACTACATGAGGCTTGTAACAGAGGGTATTATGATGTGGCCAAACAGCTGCTGGCAGCCGGGGCCGAGGTTAACACCAAGGGCCTGGATGACGACACGCCTCTACATGATGCATCTAACAATGGCCATCTCAAAGTAAGTGACTCAGAAATTATACATTACATTTTTTTACACAAGATAGCACACAATTTTAGGACCTTGTTTTTATTGATTATGTCACACCTACATTCTGGTTTTGTAGGTAGTGAAGCTGCTGTTACGATATGGAGGTGATCCTTGTCAAAGCAACAGAAGAGGAGAGACTCCGTTAAAAGTGGCAAATTCACAAACAATGCTTAATTTGTTGTTGGGGAAAATCACCTA[C/A]TCCTCCAGTGAGGAGAGTTCCTCTGGTATGTATCATGAAGTGCATCTGTTTGCATGTATTCCAGAAAGTGCTTAACAGGAAATGTTACTAATAAAAGTTCTTGTGCTTCTCAGCAGATTCTTCTGAAGAGGAAGATTCCCCATCGTTTGCCCCATCTAGCTCTGTCGATGGCAATAATACGGACTCAGAGTTTGAGAAGGGCTTAAAATTAAAAGGGAAGGGCATGGACCCACCCAAATCCACCACCACTCCAGTCAAGGATGAGTATGAGTTTGACGAGGACGATGAGGAGGAGCGTGTCCCACCTGTGGATGACAAGCACCTGCTCAAGAAAGAGTTCCGCAAGGAGCCTGTCAGCAAAACAAACAACTTAATCTCCATACCCAAGATGGAGGTCAAAACCTATTCCAAAAGCAACTCGCTAACACCAAAGAAGGCTGTGCGCAGGATCCTGTCAGACAGCAACAGCTCGGACGAAGATGACAGAACATTGTGTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31604
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 599 | 2820 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57659002)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56094328 |
| GRCz11 | 7 | 56395739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTGAGTCAGACTACTCATCTGCAGACTCCAGTGTTGAGTCTGTGAAA[C/T]AGGTAAAAAAGAAAGTGCAAGACAGCAGAAAGAAAAACAACACGCATGTC
Long Flanking Sequence:
CAAGGCAACCTGCACCTCAAACTAACATCAAGAGCAGAGACTCGACGTCACTGAATTCCAAGCAGCAGAAAGAGAAAAGTAAAGTCAAAAAGAAAAGGAAGAAGGAGACAAAAAATAATGTTAACAAGGAGGTGCGCTTTAATAAAGTGAATAAGTTCTGCACCTCAGACTCAGAGATTGGGGACCTCGAGAGTGAAGACGATAAAGGGTCCATTCAGAATACAAATTGTGTAAAGGACTCTTCTACATTGAGCCTTAAAGACCCCTCTGTCTTTACCTCTTTGTCAGTCACGTCTTCCTCCTCGCATGGGAGTTTGAACTCACAAAAACACACACAGTCTTTGGCAGAGCAGCACCCAAAGCAGTGGAGGACAGATGGCTGGAAAACAGTATCTTCTCCGACAATGTCTGATGTCAGCTCCCTTTCGGACTCGGTCAGAACACGGCTCTCCAGTGAGTCAGACTACTCATCTGCAGACTCCAGTGTTGAGTCTGTGAAA[C/T]AGGTAAAAAAGAAAGTGCAAGACAGCAGAAAGAAAAACAACACGCATGTCAATGCGGTAGACAAAAAGAACTCTGAGCTTTATAAGACTTCAAACACTGAGGGAGCCATTTCGAAAGCAGACAAAGATGGAAAAGTGTTAAAGAAACACAAAGTGAAACACAAACACAAAAGTAAGGAAAAAGATAAGGCTCCAAGTGTGGTGTTGAGTCAGGACATGAATGAAAAATTTGTCAAGAGCTTCTCTTTTGACTTTGACGATACACGGCAGAAGTCGCTCATTGTTGAGACAGAGTCTCCTTCAGAAAACAGAGTCAAACTCTCCAAACATGAAAAAGATCATTTCAAGAAGGAAGACAGACTGTCTAAGGGTAAATCTGAAGACAAGGACTGGCCAGTTAAGGAAACTCAAAGGGTGGTTAAAGAGGAGAAGTCAAAAAAGACAAAGGAGTCAAACAAGGAAAAGGTGAACAAAGAAGAGCGGGACAAACCTTTAAAGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31605
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 1548 | 2820 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57661851)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56097177 |
| GRCz11 | 7 | 56398588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAAAACACTCAAATATCAAGTATTAAAGAGAAATCAAAAGAAGACTG[T/A]TCTAAATTTGACGGCAAAAATAAGGACAGGATTAAAGATATAGTGGATAA
Long Flanking Sequence:
CTGTCTATCACTAATCCACAGGACAGGTTCAAAGAGAAAGAGAGACATAGACATTCCTCGTCTTCATCATCCAAAAAGAGTCATGACAAAGAAAAGGAGAAAGTCAAGAAAGAAAAGAGTGAGAAAAAAGACAAGTCAGAGGAGATAAGAGAAAGTTATGGTCGCAGAGAAAGCTTGCCCTTTGACAAAGAGCCCATGCCTTTAGAGGCTGATCCTTACACTTTTCCATATGGCTCCAAAGTTGATGGCGAAGATGACTTGGACAAGACTCTAGAGTTTGAGAAGGAGATGTCCAAAAAAGACAAGACAAACAGTATCATGAACAGTGATAAATTAAAAGACAAAAAGAAGAAAGAGAAACACAAGGAAAAAATAAAAGAGGAAAAGCATAAATATTCGGATGGATTGGGGTCCTTCAGACACTCAAAAGAAGAACAAAAATCAGGACTGAAGGAAAACACTCAAATATCAAGTATTAAAGAGAAATCAAAAGAAGACTG[T/A]TCTAAATTTGACGGCAAAAATAAGGACAGGATTAAAGATATAGTGGATAAAGACAGAACAGACAGCAAGTCAAAAGTCAAAGATGAGAACGACAAATTCAGCCAGTCAAAGGAGACAATAAGAAAGGACAACCGCCCTCGTGAAAAGCTTTTAGTTGATGGCGATTTAAGACTAACAAGTTTTGGTAAAATGCTAAGCTTGAAAGATCAGGAGATAGAAGAACGCCATAAGAGACACAAAGAGAGAATGAAACAGATGGAAAAATTGAGGCATCGATCAGGCGACCCAAAACTCAAAGATAAAACAAAGTCAAATGAAGAACTAAAGAAAAATCGCAGTGAACTCTCCAAAAAAACTGGTTCGGTGGATGCTGCTTTAAAAGAGAAGAAGATTAAAGAGATTGGCCTCCCAACCCAAATGATGTCACCTGATAGAAAGCCACAACCTATTGACAGTCAGAACTCAAAAGACTGGCTTGCTGGTCACCAAATGAAGGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41040
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 1768 | 2820 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57662509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56097835 |
| GRCz11 | 7 | 56399246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCATCCTGCAGTGCAGAGGACTATTCAGATATCATGTTTGATGGTCTT[G/T]AGTGTCATAATTCCTCAGCCACCACAATGTCCATGAATGCTTGTTCCCCC
Long Flanking Sequence:
ATGGCGATTTAAGACTAACAAGTTTTGGTAAAATGCTAAGCTTGAAAGATCAGGAGATAGAAGAACGCCATAAGAGACACAAAGAGAGAATGAAACAGATGGAAAAATTGAGGCATCGATCAGGCGACCCAAAACTCAAAGATAAAACAAAGTCAAATGAAGAACTAAAGAAAAATCGCAGTGAACTCTCCAAAAAAACTGGTTCGGTGGATGCTGCTTTAAAAGAGAAGAAGATTAAAGAGATTGGCCTCCCAACCCAAATGATGTCACCTGATAGAAAGCCACAACCTATTGACAGTCAGAACTCAAAAGACTGGCTTGCTGGTCACCAAATGAAGGAAAGTCTTCCTGCATCTCCACGACCTGACCAGAACAGACCAACAGGTGTTCCCACCCCAACATCTGTGATCTCATGTCCAAGCTATGAGGAAGTCATGCAAACTCCACGCACGCCATCCTGCAGTGCAGAGGACTATTCAGATATCATGTTTGATGGTCTT[G/T]AGTGTCATAATTCCTCAGCCACCACAATGTCCATGAATGCTTGTTCCCCCTCCTTCTTTGATAGATTTTCTAACTCATCAAATACTTTCCAGGAGGGAACGTGTATAACACCAGCAAAGAACATGCAGTTACCCCTTGTAAGTCGCTCTGTCACCTCTGACGTCAGAAGACCACTTGATGTTGAGTTCAAAGCAGAAGCAGACAAGTTACTACGACAACACGTTCAAGAAGGCACAGAATTTGAGTCTTCAGCCTCACAACTTTCTGAGGACAAGATGGCAGCAGACAGACTTAATTGCCTTTCCTCGTGTTTTTCACCCACTGCTGACATGTCTCCCAGGCCTGACCTATTGCAACATGAAAGATTACAAGATGAAGTGTCTGCTGTAAATTCCATCAGTGATGGTAATGAATACTCAGGGTGTGTGTATAACAACTATCTCATGAAGCCCTCAACTCCAGTCCATAGACCTGACCCCCAAGAGCCTTGTCTGGATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31606
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 2170 | 2820 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57663715)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56099041 |
| GRCz11 | 7 | 56400452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACACTGGAGTCCGAATCACCTCAGCTAGAAAATTTCTTCACTGATTGT[A/T]AACCAACCCCTGAGGAAAATCAGATGGACCTAGAGTTGCCATGCATGATT
Long Flanking Sequence:
AGGACCCCACAGAAAGTCACCATGCTCCAGAGGAGAGCATGCAGGCTAGAAACAATCCCACTTATTTACTCGGGATCGAAGAATCTGACAAAAAGGCTTGGCTTGAATGTTCAGATAGAAGAGATCCTGATGTGCTTCCCATTACACCAGCCCATCCACAAGACAACTACATGGAAAACTCATGTGATCAGTCTTTAGGCTGGAATTCAGAAGCACTCATGAAGTCACCTCATGAGAGTTACAGAGAGGTTGAGGCAGCAGTCTCAAAAATTAGCAGTCCATATTCACATTCTGATTGCGATTTGCAGCACATCCCAAATGTAATCCCTGTGACGCCACCTCATTCTACTTACTCCAGAGCATACTGTCCATCGCAGATTCCTGACTCTCATTATGAGGACCCCAAAGACACAGTGGAAGACCTTCCATCACCTGGAAGACCTGTAGCAGAGACACTGGAGTCCGAATCACCTCAGCTAGAAAATTTCTTCACTGATTGT[A/T]AACCAACCCCTGAGGAAAATCAGATGGACCTAGAGTTGCCATGCATGATTAAAGACAATAGACAAGAGTCTCCCACCTATCCTGCAGAGATCAGCATGCCTGTAGCCCCACCAGTCAGCGAAGATCCTGTTGTTTCATGGGCAGATCCATTTTCTGGTGCAGCTGATGAAATGGATGACATGGGTCCCTTCTCTATACCAGAACTTCCTTTTCAAGAGAAGGAGATGCAGGACCCTGATATAACAGCCCCAGAAATTGCAGAGAATAAGCATTCCCCTACTCTGACGAGACCGCCAGTTATTGAGACAAGCGAAAATGTTGAAATGATCAATGTTGACCTGTCAAGTTTGTCTAAAGCTCCATGTTCTCCTACAGTTGTGCCTCATGATGAATCTAGTCAGGATTTGGTTCCTCCAGTAAGTAAGGATGACTATACACCTCAATGCGAGTTGGAGCCAGAGCCTCAGAACATCCCAGATGTTCTTCCCATCAAAGAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7090
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 2570 | 2820 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57664915)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56100241 |
| GRCz11 | 7 | 56401652 |
KASP Assay ID:
554-4997.1 (used for ordering genotyping assays)
KASP Sequence:
AGGTTCAGTTGGTGAACACAGCAATGAAGCAGACTCGGGAGATGATCCAA[C/T]AAACTCTAGCAGTCATTGTGAAYGCCATCAAATTGGATGAAATCGAGCCA
Long Flanking Sequence:
GGCCTTCCTGTAGCCCTCATCTTACTGTTCATATTCCAGCCGTGTCAATGCCTACCAGCACCCATGTATCAGAGACTCTTGAGACAACTGCCAAGTTGTCAGTGACTATACCGGTGTCTGAGGCACCCAAGAAAATTGAGGAAATACCTCAGAGAATTACCCGGAAAAAGGCTCAGATGCTGGCCAATCAAAACAAGCAGAGCGCCACACTAAGCTCATCAAGCATCACTCATTCAGTATCCTCATCACCAATTACAACGAGTGTTACCACCTCTTGTGTCACAGTAGAAAAGGAGAAAGAGACCATCAGCTCAAGTAATGTTCAAACATCCGCACCCTCTGCACCTGCATTAATCACAAAAACAAAAGGCAGGCCCATTGAGGATGATGACAACCAGTCCCAACATCCACGCAAGAGAAAGTTTCCAAAATCAGGCCAGCAGCAGGTGCAGGTTCAGTTGGTGAACACAGCAATGAAGCAGACTCGGGAGATGATCCAA[C/T]AAACTCTAGCAGTCATTGTGAACGCCATCAAATTGGATGAAATCGAGCCATACCACAGTGACCGTTCCAACCCCTATTTTGAATACCTTCAGATCCGCAAGAAAATCGAAGAGAAGAGGAAGATCTTGTGTTACATAACCCCTCAAGCCCCTCAGTGTTATGCAGATTATGTGACATACACGGGCTCCTATCTGCTTGATGGCAAGCCTCTTAGCAAGCTTCATATTCCTGTGGTAAGACATTTGTTTTTATAAAGACCCCTTAACAGTGTTCTAACCAATTTAGCATACCATTTTGGACCATATTAAGACATTATATGTTTAAGCTGTAGGTATGCTTAGCTAAACAAAATTAAAATTCCGAGATTTCCTAAATAAAAAGTTGTGGCATATTTCCTTGTTATTTTAGATTGCTCCACCACCATCTTTGTCAGAACCCCTGAAGGAGTTGTTCAGACAGCAAGAGGCCGTGAGAGGAAAACTAAGACTACAACACAGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11367
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Nonsense | 2664 | 2820 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57665372)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56100698 |
| GRCz11 | 7 | 56402109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATTGCTCCACCACCATCTTTGTCAGARCCCCTGAAGGAGTTGTTCAGA[C/T]AGCAAGAGGCCGTGAGAGGAAAACTAAGACTACAACACAGCATTGAGAGG
Long Flanking Sequence:
GTTGGTGAACACAGCAATGAAGCAGACTCGGGAGATGATCCAACAAACTCTAGCAGTCATTGTGAACGCCATCAAATTGGATGAAATCGAGCCATACCACAGTGACCGTTCCAACCCCTATTTTGAATACCTTCAGATCCGCAAGAAAATCGAAGAGAAGAGGAAGATCTTGTGTTACATAACCCCTCAAGCCCCTCAGTGTTATGCAGATTATGTGACATACACGGGCTCCTATCTGCTTGATGGCAAGCCTCTTAGCAAGCTTCATATTCCTGTGGTAAGACATTTGTTTTTATAAAGACCCCTTAACAGTGTTCTAACCAATTTAGCATACCATTTTGGACCATATTAAGACATTATATGTTTAAGCTGTAGGTATGCTTAGCTAAACAAAATTAAAATTCCGAGATTTCCTAAATAAAAAGTTGTGGCATATTTCCTTGTTATTTTAGATTGCTCCACCACCATCTTTGTCAGAACCCCTGAAGGAGTTGTTCAGA[C/T]AGCAAGAGGCCGTGAGAGGAAAACTAAGACTACAACACAGCATTGAGAGGGTAAACTTTTACTCTTTGCCTTTAGACTTTTTTTGTTTTCTCCCCTCTATGCATCCCAGAGCTCATTTCAGAAGTCACCCCATTAGGATGCAATGATCACACTGCACAAATCCTTTGATGAATCATCAAAGGCTTTGTGTAATAGAATAGCAACTTATTTGAAATACACTTCCACTTCCAACTAAACAAGTGTATTTCAGTATGATCAGTCTCCTCATTTCATCTCATTTTCTTCTGATGTTCTTACTGCGACTACCAGACCTTGATCCCTTTAAAAGACCGGCTTTGTCCCTGGATTAGATGAATAGGGTATCACTGAATCAGTCGAATGTCCAGTCTAACTATAATTTTATGTCCCCTTACAGGAGAAGCTGATTGTATCCTGTGAGCAGGAAGTGCTACGTGTTCACTGTAGAGCAGCAAGAACGATCGCAAATCAGGCCGTTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21093
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 |
|---|---|---|---|---|---|
| ENSDART00000073594 | Essential Splice Site | 2680 | 2820 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 57665424)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 56100750 |
| GRCz11 | 7 | 56402161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGAGGCCGTGAGAGGAAAACTAAGACTACAACACAGCATTGAGAGGG[T/A]AAACTTTTACTCTTTGCCTTTAGACTTTTTTTGTTTTCTCCCCTCTATGC
Long Flanking Sequence:
GCAGTCATTGTGAACGCCATCAAATTGGATGAAATCGAGCCATACCACAGTGACCGTTCCAACCCCTATTTTGAATACCTTCAGATCCGCAAGAAAATCGAAGAGAAGAGGAAGATCTTGTGTTACATAACCCCTCAAGCCCCTCAGTGTTATGCAGATTATGTGACATACACGGGCTCCTATCTGCTTGATGGCAAGCCTCTTAGCAAGCTTCATATTCCTGTGGTAAGACATTTGTTTTTATAAAGACCCCTTAACAGTGTTCTAACCAATTTAGCATACCATTTTGGACCATATTAAGACATTATATGTTTAAGCTGTAGGTATGCTTAGCTAAACAAAATTAAAATTCCGAGATTTCCTAAATAAAAAGTTGTGGCATATTTCCTTGTTATTTTAGATTGCTCCACCACCATCTTTGTCAGAACCCCTGAAGGAGTTGTTCAGACAGCAAGAGGCCGTGAGAGGAAAACTAAGACTACAACACAGCATTGAGAGGG[T/A]AAACTTTTACTCTTTGCCTTTAGACTTTTTTTGTTTTCTCCCCTCTATGCATCCCAGAGCTCATTTCAGAAGTCACCCCATTAGGATGCAATGATCACACTGCACAAATCCTTTGATGAATCATCAAAGGCTTTGTGTAATAGAATAGCAACTTATTTGAAATACACTTCCACTTCCAACTAAACAAGTGTATTTCAGTATGATCAGTCTCCTCATTTCATCTCATTTTCTTCTGATGTTCTTACTGCGACTACCAGACCTTGATCCCTTTAAAAGACCGGCTTTGTCCCTGGATTAGATGAATAGGGTATCACTGAATCAGTCGAATGTCCAGTCTAACTATAATTTTATGTCCCCTTACAGGAGAAGCTGATTGTATCCTGTGAGCAGGAAGTGCTACGTGTTCACTGTAGAGCAGCAAGAACGATCGCAAATCAGGCCGTTCCTTTTAGTGCTTGCACAATGCTGCTGGATTCAGAAGTCTACAACATGCCATCAGA
Associated Phenotype:
Not determined