ZMP
si:ch211-180b7.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
ATP8B1
Human Description:
ATPase, aminophospholipid transporter, class I, type 8B, member 1 [Source:HGNC Symbol;Acc:3706]
Mouse Orthologue:
Atp8b1
Mouse Description:
ATPase, class I, type 8B, member 1 Gene [Source:MGI Symbol;Acc:MGI:1859665]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23846 | Essential Splice Site | Available for shipment | Available now |
sa9801 | Nonsense | Available for shipment | Available now |
sa37211 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37210 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23845 | Nonsense | Available for shipment | Available now |
sa14588 | Nonsense | Available for shipment | Available now |
sa37209 | Essential Splice Site | Available for shipment | Available now |
sa43566 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23844 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23846
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Essential Splice Site | 87 | 1131 | 2 | 25 |
ENSDART00000137844 | Essential Splice Site | 87 | 847 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3919097)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3516353 |
GRCz11 | 21 | 3667774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTTTCAGAAGAAGGTCTTTCTGTGCATCAAGAAAAGCAGATACTCTG[T/A]AAGTGAATCCATCATTGTTTACAGTGAAACTCCAATCACCCATATCGCAC
Long Flanking Sequence:
TGAGAATTTTGGTAAAAATCTGCAGATTTCTTCGGAATTATTTTGGGAGTATCCAGCAGAGTATCATAACTAAAACCTTAATATATGAAATAAAAAGTAATAAATTACTGAATAAAAACTGAATAAATTTATATTTGCACATTTACTCAAGTAACTAAACATAATTAATGATGGGCTAAAAATCTGCAGAAATCTGCGAAAAATCAGCGAAATTCTGTGCGCGCAGATTCCGTGTGGGCCTAGCCATGGGATAGCGTAGCGTGCATCGGATGCACACTTCAGAATCTTGCCGGAAGTAGTAGGTCATTCGGGTACTTCTCGCATACAGTTTATTCTAACTAAATGCAAACTTACCTGAGTTAAACTATTTTGAATCTAATGATTTTTGTTTCCTTGTTCAGAGGCCGGTTGGAGCGTCCGAGCGAATGACAGGGAATATTGCAAACGGCCAGAGTTTCAGAAGAAGGTCTTTCTGTGCATCAAGAAAAGCAGATACTCTG[T/A]AAGTGAATCCATCATTGTTTACAGTGAAACTCCAATCACCCATATCGCACGCTAATTGGTTCACTCATGTTACCAAAGCCGCTTTACTGGAAAGAATTGTACAGTAATGACAGTAAAACAGTGAAATACTATCACCATTTAAAGTAACTGCTTTGTTTTTAAATATGTTGTAGAATATAATGTATTCATGTGATTCAGTGCTGAATGTTCAACATCTAGATTGTTATGTTATCCTTTAGAAATCTCTGATGTCAATGTTGAAAAAAGTTCTGGTGCATCATACTTTTGTCAACATTACAAAGTCAGATTTTTCCCTATTTCCCCAATGAGTTGAAAGAATTCTTAAGGATTGTTTTGAACAACTTAATTATTTACGTTCAGTCCACTTAAAATTGTATAAACGATCGCACTTAACTTGTGTTGGGACAGCATGAGGGAATTGTGTGTGTTTTTTTGCAGTGTATCGTGCAGCTCCACTGCAGGAATCTCAGGCAAAAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9801
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Nonsense | 94 | 1131 | 3 | 25 |
ENSDART00000137844 | Nonsense | 94 | 847 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3913013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3510269 |
GRCz11 | 21 | 3661690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATAATTTTGRATGTCTTTTKATTTRTAGGGAAACGCAATCAAGACCTA[C/A]AAATACAATGTGTTAACCTTCCTGCCGCTGAATCTGTATGAGCAGTTCAA
Long Flanking Sequence:
ATTGTATAGCAGTGGTTTGCTCTGTAGACAATTAAAAGCGAATATTGCTTAAGAGGGCTAATAATATTGAGCTTAAAATGCTTTTAAAAAAAATTAAAAACTGCTTTTATCCTAGTTGAAATTAAACAAGACTTTCTCCAGAAGAAAAAATATTATCAGAATTACTGTGAAAATATCTTTATTCCATTAAATATCACTATATAAATACTTGAAAAAGAATAAATATTACTCAGGAGGGCTAATAATTTAGCCTTCATCTGTGTATATAACCAGACTAAAAGAAATAAACCTTATTCAGAGGAAAAATACAATAAGAAATACTATGAAAAAGTGTCCTTGCTCTGTTAGACAGGAAATATATATTTTTAAATAATTAACATTTCTAATAATCTTGCTCTTATCTGTACAGTTTGTTCTATAATGACCTTTAGAGATGTTAAAGTGATGGATTTATAATTTTGGATGTCTTTTTATTTATAGGGAAACGCAATCAAGACCTA[C/A]AAATACAATGTGTTAACCTTCCTGCCGCTGAATCTGTATGAGCAGTTCAAGAGAGCTGCTAACCTCTACTTTCTGTGTCTGCTGGTCCTGCAGGTCTGAACCAACAACACACCAACACACTGATGCTTATGATGATGGACAAACTACACTGTAGATTATACGTAATAGGATAGTTATCTAAAAAATTTACAAACTTAAAAAAATGTAAAACAATAGAATTAGAGTAAACAAAATGTGAGAGAGTGTGTGTAAGAACTTTACGAAAGACTAAAAATAAAAAAAAATTAAATGTAAAAAATTTATAAATAATTAATATAATATATTATTTTTTTTAAATGTGATTATTTTAGTATTCTATTTATTATTTATATTTATTATTATATAATATTTATTTATTTTATAATTTTATTTTATATGTAATTTTTGTTGATTATATAAACGAGCAATATCACATGAGTAGCAATGCGATGTGGCTGTAAATCGGCAATGGTGGGAGGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37211
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Nonsense | 399 | 1131 | 11 | 25 |
ENSDART00000137844 | Nonsense | 398 | 847 | 12 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3903751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3501007 |
GRCz11 | 21 | 3652428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGGGGCTACATCATCATCCTCAACACCATGGTGCCCATCTCGCTTTA[C/A]GTCAGGTATAGTTATGGATGCTTCATTTACATCTGATGCTTTGAAATAGT
Long Flanking Sequence:
GACATTCCCAGATAACAACCGCTAAATAACATATGCTCGTCTGGTATTTTCTGTCAGCTTTGCGTCTAATTAAAGAATAAATAAACTATTATGATTCAGAACAGTGTGTCTAATTTTTAAGTTTTGTGGCAAGTAGCCTTGTAATAAGCAGGATAAAGTATATCCTGGTAGTTTTTTTCACAGAATAAAGCCCTTCAGCCTTATTAAAACTGCCTTGGCTTTGCTTCGGGCTGCCGATAAGCCTGTCAGGCTTTATTCTGTGATAACCTTCTGGATGTACTTTATTACTTACTTATCCTATTGTTCTTTCTGTAGATCTTTGTTTTGTTGGTGTTGTTGTGTGCTGGTCTGGCCATCGGACACACATACTGGTACGAGAGCATCGGCTCCAAGGCCTGGTATTTGATTGACGGACTGGACTACACTTCATCCTACAGAGGTTTCCTCAGTTTCTGGGGCTACATCATCATCCTCAACACCATGGTGCCCATCTCGCTTTA[C/A]GTCAGGTATAGTTATGGATGCTTCATTTACATCTGATGCTTTGAAATAGTTGTCAATCATTTGTTTTCAGTTAGCTATTCAGGGGTGTGTTTCCCAAACCATTGTCAGTCAACTAAGATCACAATTCCGTTCTTACGAATAGAGTTCAGCAATTCTGTATTTCCAGAATCCATTGTTACAATTAGGGCCAGGAGATTTAATCAAGATGATTTTGTCAGTAAAGCCCGTTCTTGTAAACATCCATCATGTACGTTTAGTCCTAGTTCACTGCTAGTAGTCTTAGATGGAATCTGCATGCAGAAGTCTGCTCATTTACAGATTTATTTTACCCATCATTGAATCTGTTCACATGCATTGAAAATTGAAAAGGGGAACAAAAACCTATTTGGGACTTGTGTGTGAATATTTTGACGACAAAACATATTTTAATAAAATGTGTATTCTTAAATGATATTAGAGAACGTTTTTATTTGGGAAATATTTTAATTCTTCAGGAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37210
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Essential Splice Site | 401 | 1131 | 11 | 25 |
ENSDART00000137844 | Essential Splice Site | 400 | 847 | 12 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3903745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3501001 |
GRCz11 | 21 | 3652422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTACATCATCATCCTCAACACCATGGTGCCCATCTCGCTTTACGTCAG[G/T]TATAGTTATGGATGCTTCATTTACATCTGATGCTTTGAAATAGTTGTCAA
Long Flanking Sequence:
CCCAGATAACAACCGCTAAATAACATATGCTCGTCTGGTATTTTCTGTCAGCTTTGCGTCTAATTAAAGAATAAATAAACTATTATGATTCAGAACAGTGTGTCTAATTTTTAAGTTTTGTGGCAAGTAGCCTTGTAATAAGCAGGATAAAGTATATCCTGGTAGTTTTTTTCACAGAATAAAGCCCTTCAGCCTTATTAAAACTGCCTTGGCTTTGCTTCGGGCTGCCGATAAGCCTGTCAGGCTTTATTCTGTGATAACCTTCTGGATGTACTTTATTACTTACTTATCCTATTGTTCTTTCTGTAGATCTTTGTTTTGTTGGTGTTGTTGTGTGCTGGTCTGGCCATCGGACACACATACTGGTACGAGAGCATCGGCTCCAAGGCCTGGTATTTGATTGACGGACTGGACTACACTTCATCCTACAGAGGTTTCCTCAGTTTCTGGGGCTACATCATCATCCTCAACACCATGGTGCCCATCTCGCTTTACGTCAG[G/T]TATAGTTATGGATGCTTCATTTACATCTGATGCTTTGAAATAGTTGTCAATCATTTGTTTTCAGTTAGCTATTCAGGGGTGTGTTTCCCAAACCATTGTCAGTCAACTAAGATCACAATTCCGTTCTTACGAATAGAGTTCAGCAATTCTGTATTTCCAGAATCCATTGTTACAATTAGGGCCAGGAGATTTAATCAAGATGATTTTGTCAGTAAAGCCCGTTCTTGTAAACATCCATCATGTACGTTTAGTCCTAGTTCACTGCTAGTAGTCTTAGATGGAATCTGCATGCAGAAGTCTGCTCATTTACAGATTTATTTTACCCATCATTGAATCTGTTCACATGCATTGAAAATTGAAAAGGGGAACAAAAACCTATTTGGGACTTGTGTGTGAATATTTTGACGACAAAACATATTTTAATAAAATGTGTATTCTTAAATGATATTAGAGAACGTTTTTATTTGGGAAATATTTTAATTCTTCAGGAGGAAGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23845
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Nonsense | 438 | 1131 | 12 | 25 |
ENSDART00000137844 | Nonsense | 437 | 847 | 13 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3901600)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3498856 |
GRCz11 | 21 | 3650277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCTGATAAAGACACTCCGGCCAAATCCAGAACCACCACCCTGAACGAG[C/T]AGCTGGGCCAGATCGAGTACATCTTCTCGGATAAAACCGGCACGCTCACA
Long Flanking Sequence:
GTGTCTTGTTAATTCAATGCCATGAAGGATTAAGGCAGTTCTGAAGAGAAAAGGGGGTCCAACCTGATACTCGTGAGGTGTACCTAATAAAGTGGCCGGTGAGTGTGTATATACAAATTACAACAACACTGATAAAAGGTTACATAAGTTATGTGAGCTTTTATCAGTGTTGTTGTTATTTCTGTTTTTTTGTACAATGAATGATTAAGAAACATGATTGTACATTCTGCAATGAATATTTACTACAAGTGTTGCCATCAATATAGCCAATGCTGCTGATATGAAAAAATAAAAAATAAATAAATAAAACATCTCTGCATTTGTTCCTGCACATATAGAAGGTAATAGATCTAATGATTGATCAATTGTTGTGTTTGTTGTTGTGTGTCAGTGTGGAGGTGATCCGGCTGGGTCAGAGTAAGTTCATTAACTGGGATCTGCAGATGTACTACGCTGATAAAGACACTCCGGCCAAATCCAGAACCACCACCCTGAACGAG[C/T]AGCTGGGCCAGATCGAGTACATCTTCTCGGATAAAACCGGCACGCTCACACAGAACATCATGGCCTTCAAGAAGTGCACCATTTCTGGACGAACTTACGGTGAGGCTTTGACTGACTGATAACCTTACACCTAGGCCTTACTCACACTAGGTACAGTTGCCTCGAACCGGGCCAGAGCACGCTTGTCCTCCCTCCCGTCTCCCCCGATGGCCCGCGCTCACACCATATCGGGCCTCGGCACGCTTACGTCATCGCTGCTACTCTGTTCAGTGAGAAGCGCTCTCTATGGCAAGCCTTTTTAGCATTTAAATCTTTGTTCTGACTCCATAAATATATTTAGAGATATCTCTAATTATATTTCGACTAGTCATAATTATAATTCCACTACTCAGAATGACAATTAGAGATATCTGCAATTGCAATTGTACTAGTACGAAATCAGATTGGAGATATCTGCAAATATATTATGACTAGTCATATTCCTCCATTGAAAAATATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14588
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Nonsense | 566 | 1131 | 15 | 25 |
ENSDART00000137844 | Nonsense | 565 | 847 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3894086)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3491342 |
GRCz11 | 21 | 3642763 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGCGCTCTGGTCAYAGCAGCACGAAAYTTCGGMTTTGTCTTCCTGTCG[C/T]GAACWCAAGAYACCATCACCATCCAGGAGATGGACAAACCACAGACCTAC
Long Flanking Sequence:
GTTTGAAGATCATTTCCTCATTTCCTGTATCCGCTCGAAGAAGGACCCACAGGTTCTGGAGTTCTTCAAACTGCTGTCTTTGTGTCACACCGTCATGGTGGAGGAGAAAGAGGGTGAGCAGAAAAAACTACACACATTTCCCAGTGCTAGAAAACACCCATACACACTCATTCACACTCATACACTATGGCCATTTTAGTTTGTTCAATTCAACTGTACTGCATGTGTTTGGACTGTGGAGGAAACCGACACACCATCACACCAACCGGAAGAAACTCACACCAACACAGGGAGAACATGCAAACTCTTGCTGTGAGGCGACAGTGCTAACCATTCTTCATGCGTCCTTTATTCTTTACACGACGTCCTCCACGTTTTCCCCTGTAAATGACTCCGTTTTCCCTGTGTTGCGTTCAGGTGAGCTGGTGTACCAGGCGGCGTCTCCAGATGAGGGCGCTCTGGTCACAGCAGCACGAAACTTCGGCTTTGTCTTCCTGTCG[C/T]GAACTCAAGACACCATCACCATCCAGGAGATGGACAAACCACAGACCTACACCATGCTGGCGCTGCTGGACTTCAACAGTGACCGCAAACGCATGTCCATCATCTGTGAGTATCACACAATATGCAGACAGTGTACATTATTACTGTTATTATTATTATTATTATTCATTTATTATTACTTTTATTATTATTATTTTTATTGCTACTACTTAACTTAAAATTTTAGTGCGTCGACACATGACACCCCAGTTCGATTCCACCTTGTAGTCCTTTACAGATCCTTCCCCTCTTTCTGCTCCCAATGCTTTCCTGTAAATTTTCTCTACTTTCCTATCCAAAATAAAAGTGAACCCCCCCCCCCATTCAATTTTTTTTTAGCATTTTAATCAACAGTGAATCATTTTGTTTTGTTTTTTGTTTTTTGTTTTATTTTGTATTTTATTTTATATTTAAAATTTTACAATATATTGTATATTGTATTGTTTTTTTTAATTTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37209
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086492 | Essential Splice Site | 756 | 1131 | 19 | 25 |
ENSDART00000137844 | Essential Splice Site | 755 | 847 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3889694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3486950 |
GRCz11 | 21 | 3638371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGCTGCTGACAGACGACATGAAGATCCACTATGGAGAAGACGTCAA[G/A]TATGATTCATTCATTTATTCATTCCCCGTTCATTCATCTATATATTTATT
Long Flanking Sequence:
CCGGGCCGCAGCGCACATTACTTTCGGGCCGATTCGGGCAGTGAGTCTGTATTTAAGATCTGCAAAAAAATTACTATGTTTAAATTTTTTTACATTTATTCAGACTCTTTAATGACAAAATGATAATAGTGTAATATGTTTAATGTCAAAGTATGTTATTTATAGTTGTGTATGTATTTATTGTATGTTTTTATTGATTGCTAATTGAAAAATTGTGTGATTTGTTTAGCTGATTGGGGCGACGGCCATTGAAGACAAACTTCAGGACGGCGTTCCTGAAACCATCGCAAAACTGGCCAAAGCGGATATTAAGATCTGGGTTCTGACCGGAGACAAGAAAGGTGAGCGATGGACATGTAGAATATTAATGTATTTTACAGCAGATGGATTTTTATTAACGTTAATTGTGTTTTTATGTGTTTAGAAACAGCGGAGAACATCGGCTACTCCTGTCAGCTGCTGACAGACGACATGAAGATCCACTATGGAGAAGACGTCAA[G/A]TATGATTCATTCATTTATTCATTCCCCGTTCATTCATCTATATATTTATTCATTGATTTTCTTTATTTATCCATTCATGAATTCTTCCATTCATTCGTCCATTAATTAATTCATTCATTCCATCCTGTATCCATCCATTCATGATCCATCATTCATTCATTCATTCATTCATCCATCTATTCTGTCTTTTTTCATCCGTTGAATTTTTTCATTCATCATTCATCAATTTATTCATCCATTAATTAATTAATTCATTCATTCTATCCTCCATTTATCCATCCATCCACCCATTTGTCCATCATTCGTTCACCTATCCATCCATCCATCCATCTATTCTTTCAGTCATTCATTAATTTCATCCTCCATCCATCATTCATCTGTTTGTTCATTCATTCACTCATTTATGTTCATACATTCATTGATCCATTGATTTCTTCCTTCCTTCCTTCCTTCCTTTCTTCCTACCTTCCTTCCTTCCTTCATTCATCCATCCATCCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43566
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 |
---|---|---|---|---|---|
ENSDART00000086492 | Nonsense | 856 | 1131 | 21 | 25 |
ENSDART00000137844 | Nonsense | 804 | 847 | 22 | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3887527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3484783 |
GRCz11 | 21 | 3636204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAGAAGGAGAAGCGGCAGGAGGATTTCGTGGATATGGCCTGTGAATG[C/A]AGCGCCGTCATCTGCTGCCGCGTCACGCCCAAGCAGAAGGCCAACGTCGT
Long Flanking Sequence:
AAGGAGTCGTTCTTCAATGAGCCGGGCAAAAACGCTCTCATCATCACTGGAGGATGGCTGGTACGATCAGCACACACATACACTCAACAGCTCTTCTTTACAGTGTACATCATGCTTTTTAAGTGTGTACATCACATAATCTAAAATATATAGACAAAAACACTAGTAATATTTGAGCAATTATGGTGAAGTTTAGGGTCTGATTGATTGATTGATATATGAAAATAATCATTCAAATATTTGATAATATGATAATAATTATACTTAACATAAATGTCAAAGTCATGTCGAAAATCTAAAAGAATATATCATTGATGATGTCAGAATGAGATCCTGTATGAGAAGAAGAAGAAGCGTCGTCGTCTGCGTCTGAAGAAGCTGCGGCTGCGGCAGAATAACCAGCAGTCCAGCAGCAGCACGGCTCCAGACAGCAGCCAGCCGGTGGACGACTGGGAGAAGGAGAAGCGGCAGGAGGATTTCGTGGATATGGCCTGTGAATG[C/A]AGCGCCGTCATCTGCTGCCGCGTCACGCCCAAGCAGAAGGCCAACGTCGTCAGCCTTGTCAAGAAGTACAAGAAAGCTGTGACTCTGTCTATCGGAGACGGAGCTAATGACGTCAACATGATCAAGAGTGAGTCTAGTCTAGTGAGACTAATGTTGTATAGGTGTATGTTTCTAGCAAAAGACATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATGTATGTATGTATGTATATATATATATATATATATATGTATGTATGTATATATATATATATGTATTTATGTATATATATATATATATATATGTATGTATGTATATATATACAGCGGGGAAAATAAGTATTTGACACATCAGCATTTTTATCAGTAAGGGGATTTCTAAGTGGGCTACTGACACAAAATTCCTACCAGATGTAGCCATCAAGCCAAATATTGAATTCATACAAAGAAATCAGAACATTTAAGTATACAAGTTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23844
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086492 | Nonsense | 984 | 1131 | 23 | 25 |
ENSDART00000137844 | None | None | 847 | None | 22 |
Genomic Location (Zv9):
Chromosome 21 (position 3880408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3477664 |
GRCz11 | 21 | 3629085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTGTTGTGTTTCAGACAGCGTATGAAGACTGGTTCATCACTCTATA[T/G]AACGTCTGCTACAGCAGTTTACCGGTTCTCCTCGTCGGCCTTCTGGATCA
Long Flanking Sequence:
CATCCCCCATCCGGACACTTGTATTTGAATGTCTTCTGGGTTGATTCTGAACCTATTATTCTTCTGTGCAGCCGCAGACATCGGCGTGGGCATCAGTGGTCAGGAAGGCATGCAGGCGGTGATGTCCAGCGATTACGCCTTCGCTCAATTCTGCTTCCTGCAGCGCCTCCTGCTGGTGCACGGCCGCTGGTCCTACATCCGCATGTGCAAGTTCCTGCGCTACTTCTTCTACAAGAACTTCGCCTTCACGCTCGTCCACTTCTGGTTCTCCTTCTTCAACGGCTTCTCCGCGCAGGTCAGAAAACCACACCTACACTCACAGATCATGCGTTTGTGCAATGCAGTACAGTAATCATATGGTTAGACAAAATTTAAAGGGATAGTACATACAAAACTGAACTCTAAGAGCAGTATATGAAGTTAATTGAAGCAGATTAAAGTGAATGCTGAGGTGTTGTTGTGTTTCAGACAGCGTATGAAGACTGGTTCATCACTCTATA[T/G]AACGTCTGCTACAGCAGTTTACCGGTTCTCCTCGTCGGCCTTCTGGATCAGGTATCATTAACACACAATAACAATATAGTAATATTATCTTCTCCCATAATAAAAATAAGAGAATTCAGCTCATCACTGCAGACTCGAACAAATGGCATAATGCAGGAAAACACTCACTAACTAACTGTTAAATAGGTTTCGTTTTAAGTATTAGGTCTAATAGTATAGAGAAATGTGTCTTTTCCCTGTTAAGCATCACTCGTGCATTATTTTAAAAGATGGATAGATAAAAGATTTTATCTGCAACTTAATGTTTTTTTTTTTAAAGAAGTTTATTGAGAGCCAAATACGCTAAGGCACTAAAATTCAAAGTTTGCATGAACTAGAAGCTGCGTCTGTATTTTTGTAGTATGATGCAGTTCACAAAGAAACTAGAACAGGGGTAGGGAACCTGTGGCTTGGGAGCCACATGTGGCTCTTTGACCAAAAATATGTGGCTCTCCAGTTGT
Associated Phenotype:
Not determined