ZMP
ankrd12
Ensembl ID:
ZFIN ID:
Description:
ankyrin repeat domain 12 [Source:RefSeq peptide;Acc:NP_956444]
Human Orthologue:
ANKRD12
Human Description:
ankyrin repeat domain 12 [Source:HGNC Symbol;Acc:29135]
Mouse Orthologue:
Ankrd12
Mouse Description:
ankyrin repeat domain 12 Gene [Source:MGI Symbol;Acc:MGI:1914357]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8899 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19905 | Nonsense | Available for shipment | Available now |
sa25937 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa11738 | Nonsense | Available for shipment | Available now |
sa33058 | Nonsense | Available for shipment | Available now |
sa6870 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19906 | Nonsense | Available for shipment | Available now |
sa44551 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8899
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 |
---|---|---|---|---|---|
ENSDART00000074270 | Nonsense | 46 | 424 | 3 | 10 |
ENSDART00000097864 | Nonsense | 46 | 1987 | 2 | 12 |
ENSDART00000146037 | None | None | 71 | None | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55360326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55025325 |
GRCz11 | 2 | 54758264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAAACTCCGAAGCTGGATYGGAGTGAACTCTTGGGGAAAGAGGGGAAGT[C/A]GAAATCCTCCATGAAGCGGAAACTCTCYTTCACTGKCAGTCCATCCCGAA
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATATAAACAGTGAAAAACTTTGGCAGGACAAGTAAAAATCTGAACCACTGGCCCGATTGGGCCTGTAGAAAAAATCCTTAGCGTTGAACCCTGAATATAATCCAATATAATTTTAGTAAACTTAATAGCACAAAAATATTGCAACGCTTTTAAATTGAAATTGAAATTGAATTTTAAAATGGAAAACTTCAGTACAAACACGTTGTGCACATTTAAATGATCTGAGATATATCAATCATAATAAGCAATTCCAGCGTTATGGATGTGACATTTGCAGTAAAAACTCAAAACTTAAATTCACAGATATTAGTGATTCTTTTGTGTACAATTTTTTTTTGAATAAAATGTGTGTCCAATTCTTCCTGTCTCTCTCAGAGTAAAGAGAAAATCTCTCCGTTTGCTAAAACTCCGAAGCTGGATCGGAGTGAACTCTTGGGGAAAGAGGGGAAGT[C/A]GAAATCCTCCATGAAGCGGAAACTCTCCTTCACTGTCAGTCCATCCCGAAACGAGGAGCGCGACTCGGATGCAGGTCAGTTTCACACTCTCTAAAGGGTTTGTTTTTAATGTAATCTCTGTATGTACTCACTGAATGTTCTGGTAGCTCGTGTTCGTGCCTCACTGACGCCCCCTAGTGATCACTTTTTTATTGCACACACTGTACTGTTGAAGGGTTTTCGAGAGGGTTATATAACGGTTAGGCTAAACTTGCTTAATTCACGAGTCCACCTCGAAAATGCAGGAAAAATACAGTATGAGGGAGTGGTGAATGTTTATCTTTTTATTATTATATTTAAATGACTTAATTTAGTTGACTAATTTAAATGCAAATACTTTAATACTGGTGATTCACACAGTATAAGAATACATTCATTATATTATACAATACATACAATTATTATAGTAATGAAAGTAATTTTTTGTTTCATGTGAATGCAAATACTCTAATACTGTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19905
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 |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Nonsense | 793 | 1987 | 8 | 12 |
ENSDART00000146037 | None | None | 71 | None | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55377801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55042801 |
GRCz11 | 2 | 54775740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATGAGCGGACTGATGGTACTTTCTCTGTACGAATTCCTGATGGCTCA[C/T]AACACTTGTCAGAAGAAGTGGATGAGAAACCAGCAACTTGTAATTCGGCT
Long Flanking Sequence:
TAAGCAACAGTATAGACAGCTCTGAGGGTGCGTTTAGGAAGACTGACAAAGATGGGAAAGTTGTAAAAAAGCACAAGCTAAAACACAAGGAGAAGGAAAAGGAGAAATATAGGAAAGAGTACGAGGCAGAGAGGAATCGCCACCGGCAGAAAGAGCCACGCAAGGACGGACATAGAAACCTCGAGTTTGATCGAGAGTTCTGGAAGGAGAACTTCTTCAAAAGTGATGAAAATGAGGAACCTGTGGGCAAAGGTGAGATACCTGCTGGTGGATCTCCAGTAAAATCCTCAGATTCGTCACCTGTTAAAGAGGAAAAAGGGGCATCAAAAGACAAACATTCAACTAGTAGCAGTAACAAGGACAGGAGGCCAAAAGAGGAAAGAGATAAAACCATTAAAAAGGAGAAAAAAGAGATTCCTCTTAAAGAGGAGCGAGGAAAAGAAGATGAAACAGATGAGCGGACTGATGGTACTTTCTCTGTACGAATTCCTGATGGCTCA[C/T]AACACTTGTCAGAAGAAGTGGATGAGAAACCAGCAACTTGTAATTCGGCTGACCAAGAGCAACTGGAGTCTCCAGAGAAGAACTCTCGAGAAAAAACTGATAAGCGACCACCAACAAAGGATCGGGAATCTGAGAAGTCTGATAAGAGACACTCGGATAAAGATAAGAAGGTAAAATCTGAGCATTTAGCTGACAAGCCTGAGCTCCACAACTCTACAGATCGATGGAAGGAAAAGGAGAAATTAACAAATGTTTCATATTCGCCCAATGATAAGAGCCATAAAGAGGGTGAAAAACTCAAACCAATGACTCCAGTGAAAAAGCATGAGGAGAACAAGAAGAATAAGGACAAGCTTGATAAAAAAGCGGAGAAAGAGCACGCTTCTGGTGACCACAGAGACAAAGATAAAACAACTTCTGAAAAGAAAGGAAAAGCTCCTGAGAAAACTGCTGATCATGGAAAATCTGACCGCAGTAAAGACAAAGAACGGGACAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25937
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Missense | 799 | 1987 | 8 | 12 |
ENSDART00000146037 | Essential Splice Site | 21 | 71 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55377819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55042819 |
GRCz11 | 2 | 54775758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACTTTCTCTGTACGAATTCCTGATGGCTCACAACACTTGTCAGAAGAA[G/A]TGGATGAGAAACCAGCAACTTGTAATTCGGCTGACCAAGAGCAACTGGAG
Long Flanking Sequence:
GCTCTGAGGGTGCGTTTAGGAAGACTGACAAAGATGGGAAAGTTGTAAAAAAGCACAAGCTAAAACACAAGGAGAAGGAAAAGGAGAAATATAGGAAAGAGTACGAGGCAGAGAGGAATCGCCACCGGCAGAAAGAGCCACGCAAGGACGGACATAGAAACCTCGAGTTTGATCGAGAGTTCTGGAAGGAGAACTTCTTCAAAAGTGATGAAAATGAGGAACCTGTGGGCAAAGGTGAGATACCTGCTGGTGGATCTCCAGTAAAATCCTCAGATTCGTCACCTGTTAAAGAGGAAAAAGGGGCATCAAAAGACAAACATTCAACTAGTAGCAGTAACAAGGACAGGAGGCCAAAAGAGGAAAGAGATAAAACCATTAAAAAGGAGAAAAAAGAGATTCCTCTTAAAGAGGAGCGAGGAAAAGAAGATGAAACAGATGAGCGGACTGATGGTACTTTCTCTGTACGAATTCCTGATGGCTCACAACACTTGTCAGAAGAA[G/A]TGGATGAGAAACCAGCAACTTGTAATTCGGCTGACCAAGAGCAACTGGAGTCTCCAGAGAAGAACTCTCGAGAAAAAACTGATAAGCGACCACCAACAAAGGATCGGGAATCTGAGAAGTCTGATAAGAGACACTCGGATAAAGATAAGAAGGTAAAATCTGAGCATTTAGCTGACAAGCCTGAGCTCCACAACTCTACAGATCGATGGAAGGAAAAGGAGAAATTAACAAATGTTTCATATTCGCCCAATGATAAGAGCCATAAAGAGGGTGAAAAACTCAAACCAATGACTCCAGTGAAAAAGCATGAGGAGAACAAGAAGAATAAGGACAAGCTTGATAAAAAAGCGGAGAAAGAGCACGCTTCTGGTGACCACAGAGACAAAGATAAAACAACTTCTGAAAAGAAAGGAAAAGCTCCTGAGAAAACTGCTGATCATGGAAAATCTGACCGCAGTAAAGACAAAGAACGGGACAAAGATTCTGACAAGAGGAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11738
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 |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Nonsense | 1106 | 1987 | 8 | 12 |
ENSDART00000146037 | None | None | 71 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55378741)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55043741 |
GRCz11 | 2 | 54776680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGCTCAGTCTCAAAGATCAGGAAATCGAACAGTGGCACAAAAAGCACT[T/A]GGAGAAAATCAAGCAGAAGGAACGGGAGCGGCTAAAACAGCGTCCTGGAA
Long Flanking Sequence:
TGAGAAAACTGCTGATCATGGAAAATCTGACCGCAGTAAAGACAAAGAACGGGACAAAGATTCTGACAAGAGGAAAAAAGATAAATCAACCACTCCATCTTCCTCTTCCTACTCGAATCTAAAGTCGTTATTGGAAGAAAAGAAAGGCTATGTTTGTGAGAATAATAAGGTTGTCTCATCTAAATCAAAGGAAGAGGTAACCAAGCCTTCAGAGAAAGACCGAGATCGAAGAGAGAGGGACCGGGAGTCTGAAAGACATCGAGATCGGGAACGAGATCGGCACAAGGAAAAGGACAAAGATCGATCCCAGTTTAACAGGGATGGCAAAATTAACAAACCGAAACCAAGTGAAGTGGACTCCAAATCTAAGGTTACACCTATTCTAAAGGATACTCGTCCCAAAGAAAAGAGGCTGGTGAATGATGACCTCATGAAGACCAGCTTTGAACGCATGCTCAGTCTCAAAGATCAGGAAATCGAACAGTGGCACAAAAAGCACT[T/A]GGAGAAAATCAAGCAGAAGGAACGGGAGCGGCTAAAACAGCGTCCTGGAATTGACCCTGCGAAACAACAAAAAAACAAGGAAAAAATTAAATCATCCTCTACGTCCACTGAGCCATGTCTAACCAAGGAACTAACTCGGTCAAAGAGCTCAGAAGCGCCAGATGGACAACGTGAAAAGATCTTAAAGGACGCCACTAGTGTGAGAACTCTCTCGCTAGATGCAAAAACCTTGGGGAAGAACGGTCCTATAATTGAAAACAATCTAAGTCGATCTCCGAGACCAGAAAGTGAAAAATCTGGTCTTATGTCAAGATCAATATCAATGATCTCTGTGGCAAGTTCAGAAGACTCCTGCCAGGCAACTATTTTGACACCTAGACCAACTGACCAATATGATTCTGACATGAACGTGGAAGCCTTAGATTCGCAGCCACCTTTACTTCAGTCTTCCCTTGTTGCACAGTCCTCCAGGTCGCCTAGTGTTCATGATAAAGATATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33058
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 |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Nonsense | 1143 | 1987 | 8 | 12 |
ENSDART00000146037 | None | None | 71 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55378851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55043851 |
GRCz11 | 2 | 54776790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAACAACAAAAAAACAAGGAAAAAATTAAATCATCCTCTACGTCCACT[G/T]AGCCATGTCTAACCAAGGAACTAACTCGGTCAAAGAGCTCAGAAGCGCCA
Long Flanking Sequence:
ACTCGAATCTAAAGTCGTTATTGGAAGAAAAGAAAGGCTATGTTTGTGAGAATAATAAGGTTGTCTCATCTAAATCAAAGGAAGAGGTAACCAAGCCTTCAGAGAAAGACCGAGATCGAAGAGAGAGGGACCGGGAGTCTGAAAGACATCGAGATCGGGAACGAGATCGGCACAAGGAAAAGGACAAAGATCGATCCCAGTTTAACAGGGATGGCAAAATTAACAAACCGAAACCAAGTGAAGTGGACTCCAAATCTAAGGTTACACCTATTCTAAAGGATACTCGTCCCAAAGAAAAGAGGCTGGTGAATGATGACCTCATGAAGACCAGCTTTGAACGCATGCTCAGTCTCAAAGATCAGGAAATCGAACAGTGGCACAAAAAGCACTTGGAGAAAATCAAGCAGAAGGAACGGGAGCGGCTAAAACAGCGTCCTGGAATTGACCCTGCGAAACAACAAAAAAACAAGGAAAAAATTAAATCATCCTCTACGTCCACT[G/T]AGCCATGTCTAACCAAGGAACTAACTCGGTCAAAGAGCTCAGAAGCGCCAGATGGACAACGTGAAAAGATCTTAAAGGACGCCACTAGTGTGAGAACTCTCTCGCTAGATGCAAAAACCTTGGGGAAGAACGGTCCTATAATTGAAAACAATCTAAGTCGATCTCCGAGACCAGAAAGTGAAAAATCTGGTCTTATGTCAAGATCAATATCAATGATCTCTGTGGCAAGTTCAGAAGACTCCTGCCAGGCAACTATTTTGACACCTAGACCAACTGACCAATATGATTCTGACATGAACGTGGAAGCCTTAGATTCGCAGCCACCTTTACTTCAGTCTTCCCTTGTTGCACAGTCCTCCAGGTCGCCTAGTGTTCATGATAAAGATATTAGCAGTCTTCCCGAATCATCGGCTCTCTGCAATCGCACACCATTGGCAAGCAGGCATGCATCACCATGCTTAAGGGCTATTCTGGATGAAGAAGCCAAGGTACCAACAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6870
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 |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Nonsense | 1211 | 1987 | 8 | 12 |
ENSDART00000146037 | None | None | 71 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55379056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55044056 |
GRCz11 | 2 | 54776995 |
KASP Assay ID:
554-4684.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTCGATCTCCGAGACCAGARAGTGAAAAATCTGGTCTTATGTCAAGAT[C/A]AATATCAATGATCTCTGTGGCAAGTTCAGAAGACTCCTGCCAGGCAACTA
Long Flanking Sequence:
CAGGGATGGCAAAATTAACAAACCGAAACCAAGTGAAGTGGACTCCAAATCTAAGGTTACACCTATTCTAAAGGATACTCGTCCCAAAGAAAAGAGGCTGGTGAATGATGACCTCATGAAGACCAGCTTTGAACGCATGCTCAGTCTCAAAGATCAGGAAATCGAACAGTGGCACAAAAAGCACTTGGAGAAAATCAAGCAGAAGGAACGGGAGCGGCTAAAACAGCGTCCTGGAATTGACCCTGCGAAACAACAAAAAAACAAGGAAAAAATTAAATCATCCTCTACGTCCACTGAGCCATGTCTAACCAAGGAACTAACTCGGTCAAAGAGCTCAGAAGCGCCAGATGGACAACGTGAAAAGATCTTAAAGGACGCCACTAGTGTGAGAACTCTCTCGCTAGATGCAAAAACCTTGGGGAAGAACGGTCCTATAATTGAAAACAATCTAAGTCGATCTCCGAGACCAGAAAGTGAAAAATCTGGTCTTATGTCAAGAT[C/A]AATATCAATGATCTCTGTGGCAAGTTCAGAAGACTCCTGCCAGGCAACTATTTTGACACCTAGACCAACTGACCAATATGATTCTGACATGAACGTGGAAGCCTTAGATTCGCAGCCACCTTTACTTCAGTCTTCCCTTGTTGCACAGTCCTCCAGGTCGCCTAGTGTTCATGATAAAGATATTAGCAGTCTTCCCGAATCATCGGCTCTCTGCAATCGCACACCATTGGCAAGCAGGCATGCATCACCATGCTTAAGGGCTATTCTGGATGAAGAAGCCAAGGTACCAACAACTGAAACAAAACCCACAGAAGAGTCTCCGGTAATCAGTATTGCATCACAACCAACCAGCGAGCAATCTCAAGTTCATCTAACTGAGATTAGTGTCCCCCCTGTTCAGGAGACTCGGAGCAGTCAAAGTCTTACAAACTCTTTTCCAGAAAATGAAATTCTGTCTAGTAATGAAGCCGAAGTCGTCAGTTCCACATGTCAAGTACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19906
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 |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Nonsense | 1330 | 1987 | 8 | 12 |
ENSDART00000146037 | None | None | 71 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55379412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55044412 |
GRCz11 | 2 | 54777351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAGAAGAGTCTCCGGTAATCAGTATTGCATCACAACCAACCAGCGAG[C/T]AATCTCAAGTTCATCTAACTGAGATTAGTGTCCCCCCTGTTCAGGAGACT
Long Flanking Sequence:
GTGAAAAGATCTTAAAGGACGCCACTAGTGTGAGAACTCTCTCGCTAGATGCAAAAACCTTGGGGAAGAACGGTCCTATAATTGAAAACAATCTAAGTCGATCTCCGAGACCAGAAAGTGAAAAATCTGGTCTTATGTCAAGATCAATATCAATGATCTCTGTGGCAAGTTCAGAAGACTCCTGCCAGGCAACTATTTTGACACCTAGACCAACTGACCAATATGATTCTGACATGAACGTGGAAGCCTTAGATTCGCAGCCACCTTTACTTCAGTCTTCCCTTGTTGCACAGTCCTCCAGGTCGCCTAGTGTTCATGATAAAGATATTAGCAGTCTTCCCGAATCATCGGCTCTCTGCAATCGCACACCATTGGCAAGCAGGCATGCATCACCATGCTTAAGGGCTATTCTGGATGAAGAAGCCAAGGTACCAACAACTGAAACAAAACCCACAGAAGAGTCTCCGGTAATCAGTATTGCATCACAACCAACCAGCGAG[C/T]AATCTCAAGTTCATCTAACTGAGATTAGTGTCCCCCCTGTTCAGGAGACTCGGAGCAGTCAAAGTCTTACAAACTCTTTTCCAGAAAATGAAATTCTGTCTAGTAATGAAGCCGAAGTCGTCAGTTCCACATGTCAAGTACAACCTTCGCAGGCTAGTGCTAAAGACAGTGTAACACAAGCAAACAGTGTGTTTCCGAGCCATTTGGAAGAGCAGAACAAGTTTTGCACCACTAGTAGTCAAATAGAGCATGCAAGTCTAGGTCAGCTTGATGTCCCTGGTGCAGAGGGAGTAAAAAAGGAGGCTTCACTTGCTGTTGCATCATTACAGTCATCTCATACATCAACTTCATCATCAGATTCCAATGCACATTTGCCTTCGAGTAGTCAGCATTGTGAGATTAGCTCTGCTTCCAGTGGTGAACAGACAATGACAACAGACTCTAGTTTGAGAACAGAGCAAAGAGACAAACCATTGGTTGCTTCAGAGGACAAGATTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44551
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 |
---|---|---|---|---|---|
ENSDART00000074270 | None | None | 424 | None | 10 |
ENSDART00000097864 | Essential Splice Site | 1846 | 1987 | None | 12 |
ENSDART00000146037 | Essential Splice Site | None | 71 | None | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55381053)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 55046053 |
GRCz11 | 2 | 54778992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGAGATGGTGCGGATGAAGCTGAGACTGCAGCACAGCATCGAAAGGG[T/C]GAGTGGAAATCAAGAATGGGTGACGTTTCTTTTTTGCAATTCAGTTTTTA
Long Flanking Sequence:
GAAAACGAAAAATGCCTAGAGCTTCTCCGCTAGCCCAAGCAAATCTTACAGCTCAGCAGGTCAGAGAAAAGACACAGCAGTCCCTCGCTGCGATTGTAGATGCACTGAAGCTTGAGGAGATTCAGCCTTACCAGACAGAGAGAGCCAACCCATATTATGAGTACTTGCACATTCGCAAAAAGATCGAAGAGAAGAGGAAAGTCCTTTGTAGTGTCATTCCTCAAGCGCCTCAGTACTACGACGAGTATGTGACATTCAATGGGTCCTATCTGCTGGATGGAAACCCTCTCAGCAAACTCTGCATCCCAACAGTAAGTGATCTCCACTAACAGTATGTGAAAGTAATATTTACTCAAGAAAGACTAAGGCAAAAATGTCTCACTGTTCTTCCGTTTTGTAGATAACGCCTCCACCCTCTTTACCTGAACCACTGAAGGAGATGTTCAAACAGCAAGAGATGGTGCGGATGAAGCTGAGACTGCAGCACAGCATCGAAAGGG[T/C]GAGTGGAAATCAAGAATGGGTGACGTTTCTTTTTTGCAATTCAGTTTTTATTTTATTTTTCAAAAATAATATATAAAGTTTTACAATAACCAGAAGGATTGTTACCACTCTATATATTTTACAAACCCAGTACACATCAGGAATTACAACATAAATATAATATAGGCCAAGTAGTTCACTAACATTGACTCAATTGACATTCCTAATATTAGATAAGGGCAAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACTGCAAGAAGGTCGCTGGTTCGAACCTCGGCTCCTTTGCATGGGTTTCCTCAGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTAAATTGGGTAGGCTAAATTGACCGTAGTGTATGAGTGGGTGTGTGAACGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGTATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCAACC
Associated Phenotype:
Not determined