ZMP
ATP1A3 (2 of 2)
Ensembl ID:
Description:
ATPase, Na+/K+ transporting, alpha 3 polypeptide [Source:HGNC Symbol;Acc:801]
Human Orthologue:
ATP1A3
Human Description:
ATPase, Na+/K+ transporting, alpha 3 polypeptide [Source:HGNC Symbol;Acc:801]
Mouse Orthologue:
Atp1a3
Mouse Description:
ATPase, Na+/K+ transporting, alpha 3 polypeptide Gene [Source:MGI Symbol;Acc:MGI:88107]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36052 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8659 | Nonsense | Available for shipment | Available now |
sa9603 | Nonsense | Available for shipment | Available now |
sa22768 | Nonsense | Available for shipment | Available now |
sa6413 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36052
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011121 | Nonsense | 474 | 905 | 10 | 17 |
ENSDART00000124130 | Nonsense | 475 | 920 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 12414327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 10913993 |
GRCz11 | 16 | 10804895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTATCGAGCTGTCCAGTGGCTCAGTCAAAGCAATGAGAGAAAAGAAC[A/T]AGAAAGTAGCCGAAATCCCATTCAACTCCACCAACAAATATCAGGTTTGT
Long Flanking Sequence:
TGAATGTCTTTTTAATCTCAGGTGTGTCTCACTCTGACTGCCAAGCGAATGGCTCGCAAGAACTGCCTGGTTAAGAATCTGGAAGCCGTAGAGACGCTGGGATCCACCTCAACGATCTGCTCAGACAAGACTGGAACTCTGACCCAGAATCGAATGACTGTGGCACACATGTGGTTTGACAATCAGATCCACGAAGCCGACACCACTGAAGATCAGTCAGGTTTGTTCTTTTCTTCTGTTATGACTCAACATATGACACCTATTTTTCTATCCAGAGTCTAAGGTGATCTGTCTCTGCAGGTGCGTCGTTTGATAAGAGCTCTGTGACTTGGGTGGCTCTGGCCCGTGTGGCGGCTCTGTGTAACAGAGCTGTGTTTAAGGCGGGACAAGACTCTCTGCCCATTCTCAAGAGGGACGTAGCTGGTGACGCTTCTGAGTCTGCCCTGCTTAAGTGTATCGAGCTGTCCAGTGGCTCAGTCAAAGCAATGAGAGAAAAGAAC[A/T]AGAAAGTAGCCGAAATCCCATTCAACTCCACCAACAAATATCAGGTTTGTTATTAGTTAGACACCAAATATAAACCAAAAGAGAAGCTGAGGGATAATTCTACACACAACAATTATGAAGAAACACTCTATAAAGACGGCTGAGGTCTTGGAGTTGTTAAAAATTGTTAAATTCACTTCATTGTTATATTCACTTCATTGTTATATTCTCTGTGTACGAGCGGGTGCAGCCATTTGAATCTTTTTGGCTCGAGACTTCAGGTTTCATTCTCTTCCATTCATTTCCAGTTTTAGGCGTTAAAAACAGCTTGTTATGATGCTTGATGTTGCAAACTGATATTATCTTAGTTAATTATTCAACTCGGCCTGTTTAGTCATGCAAACACTTGTTTGTCGAGCAAGTTGTTTGACTGTTTTCTGCTGTTTATTATTCCTAGTCATTTCTCCCATAGGGAACTGAATCGGAAGTTCTAAAATATTCTTGAAAATGTGCGCACACGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8659
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 |
---|---|---|---|---|---|
ENSDART00000011121 | Nonsense | 635 | 905 | 12 | 17 |
ENSDART00000124130 | Nonsense | 636 | 920 | 12 | 17 |
ENSDART00000011121 | Nonsense | 635 | 905 | 12 | 17 |
ENSDART00000124130 | Nonsense | 636 | 920 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 12416892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 10916558 |
GRCz11 | 16 | 10807460 |
KASP Assay ID:
2260-9279.1 (used for ordering genotyping assays)
KASP Sequence:
ATCACCCYATCACTGCCAAGGCCATCGCCAAGGGTGTGGGCATCATCTCA[G/T]AGGGTAACGARACTGTGGAAGACATCGCTGCCCGTCTCAACATCCCTGWC
Long Flanking Sequence:
ATTTAGATCTTGTTATAATTTGAATAAATTGCATTTTAAAATACATCCAGATAGAGAACCCCAAAATATAATTTTAACTGCAATAATATTTTATGTTTTTGCTGTTTTTCATCAATAAATTTAGTTTGGTGAGCATACCAGACTTTTTTTGAAAGAAAAAAAAAACTGAAATATTCCAAACTTTTCACCCAGAGTCCATAATGACACTAGAGTCTACAATATTTAAGTATGTGTAAACCTGCGTTCTTTCAACAGGATTCTGCCATGTCTTAATGCCTGAGGACCAGTACCCGAAAGGTTTCGCCTTTGACACCGATGATGTCAATTTCCAGACAGACAACCTTTGCTTTGTGGGCTTGATGTCTATGATTGACCCTCCCCGTGCTGCCGTGCCTGATGCTGTGGGAAAGTGCCGTTCCGCTGGAATCAAAGTCATCATGGTGACAGGAGATCACCCCATCACTGCCAAGGCCATCGCCAAGGGTGTGGGCATCATCTCA[G/T]AGGGTAACGAAACTGTGGAAGACATCGCTGCCCGTCTCAACATCCCTGTCAGTCAGGTCAATCCCAGGTAAAACACTGAGCAGCACTGAAAACATCACATAGCACATCAACATGGTGCGGTGGTATAAGTTCAGTTTATGCTGACTACCAATGTGTGAATATAATCACAGGTCAGAAATAGATATTTAAGCAACTAAATACATGTAATACTACCCCTAAAGCACTTTTGGTTTGTTTTTGGATTATTAATATTGAACTTTTTTTTTTGTAGAAAAGTACTTTGGAGCATGCAAGAAGTTAAAGGCTCACTGTACAAAATACTGGGTTCCACACTAGTGATCTGTGTTGGGACAACTTAAAGGAAATAAGTTAACTTATTAAGTTTTACAGATTTTAGTTGATTGAACAAAACAAATGTCACAAAAAAAACAGGATTTGTGTTGTTTCAACTCCTTTTTAATAACTACTTTTAACAAACAGCAAACATGATCATTTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9603
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 |
---|---|---|---|---|---|
ENSDART00000011121 | Nonsense | 635 | 905 | 12 | 17 |
ENSDART00000124130 | Nonsense | 636 | 920 | 12 | 17 |
ENSDART00000011121 | Nonsense | 635 | 905 | 12 | 17 |
ENSDART00000124130 | Nonsense | 636 | 920 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 12416892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 10916558 |
GRCz11 | 16 | 10807460 |
KASP Assay ID:
2260-9279.1 (used for ordering genotyping assays)
KASP Sequence:
ATCACCCYATCACTGCCAAGGCCATCGCCAAGGGTGTGGGCATCATCTCA[G/T]AGGGTAACGARACTGTGGAAGACATCGCTGCCCGTCTCAACATCCCTGWC
Long Flanking Sequence:
ATTTAGATCTTGTTATAATTTGAATAAATTGCATTTTAAAATACATCCAGATAGAGAACCCCAAAATATAATTTTAACTGCAATAATATTTTATGTTTTTGCTGTTTTTCATCAATAAATTTAGTTTGGTGAGCATACCAGACTTTTTTTGAAAGAAAAAAAAAACTGAAATATTCCAAACTTTTCACCCAGAGTCCATAATGACACTAGAGTCTACAATATTTAAGTATGTGTAAACCTGCGTTCTTTCAACAGGATTCTGCCATGTCTTAATGCCTGAGGACCAGTACCCGAAAGGTTTCGCCTTTGACACCGATGATGTCAATTTCCAGACAGACAACCTTTGCTTTGTGGGCTTGATGTCTATGATTGACCCTCCCCGTGCTGCCGTGCCTGATGCTGTGGGAAAGTGCCGTTCCGCTGGAATCAAAGTCATCATGGTGACAGGAGATCACCCCATCACTGCCAAGGCCATCGCCAAGGGTGTGGGCATCATCTCA[G/T]AGGGTAACGAAACTGTGGAAGACATCGCTGCCCGTCTCAACATCCCTGTCAGTCAGGTCAATCCCAGGTAAAACACTGAGCAGCACTGAAAACATCACATAGCACATCAACATGGTGCGGTGGTATAAGTTCAGTTTATGCTGACTACCAATGTGTGAATATAATCACAGGTCAGAAATAGATATTTAAGCAACTAAATACATGTAATACTACCCCTAAAGCACTTTTGGTTTGTTTTTGGATTATTAATATTGAACTTTTTTTTTTGTAGAAAAGTACTTTGGAGCATGCAAGAAGTTAAAGGCTCACTGTACAAAATACTGGGTTCCACACTAGTGATCTGTGTTGGGACAACTTAAAGGAAATAAGTTAACTTATTAAGTTTTACAGATTTTAGTTGATTGAACAAAACAAATGTCACAAAAAAAACAGGATTTGTGTTGTTTCAACTCCTTTTTAATAACTACTTTTAACAAACAGCAAACATGATCATTTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22768
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 |
---|---|---|---|---|---|
ENSDART00000011121 | Nonsense | 662 | 905 | 13 | 17 |
ENSDART00000124130 | Nonsense | 663 | 920 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 12418903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 10918569 |
GRCz11 | 16 | 10809471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTTATCAAGAATTTCTTGTTTGTATGTTTTAGGGATGCCAAAGCCTG[T/A]GTTATACATGGAACAGATCTGAAAGACTATTCTCAGGAGCAAATAGATGA
Long Flanking Sequence:
AGAACTCTGGGATCAGTTTAACTTTTTAAAAAGCATTTTAAGACACACCTTTTTGGTCAAGCTTTTAATTAACAGTATTAGTGTTTTTGTATTTTAAATTTTAATTAGTCTTAATATGTTTTGACATGCCTTCTTTTATTGTCATGTGTTCTTTTACTTGTTTTCACTTATTGTAAAGCACTTTGCGACTCAATGTCTGGGAAAGGTGCTATATAAATAAAATTTACTTACTTACTTACTTACTTACTTACTTACTTACTTACTTACTTACTTACACAGAAAACGCTTTTAATCCAAGCAACTTTTGTTAGTAAAATCTGTACAATTGCAAAAACAGCTTCATTGCATTGCAAAAAGTCAATCACCTAGATTCCTATTGAAACAACTGTATTTAACCCAAAAATGTACCAGGCAATGTGTGCACCTTTACTTAAACCAACAAATACTTCTGTATTTATCAAGAATTTCTTGTTTGTATGTTTTAGGGATGCCAAAGCCTG[T/A]GTTATACATGGAACAGATCTGAAAGACTATTCTCAGGAGCAAATAGATGAAGTTCTGCGAAACCACACTGAGATTGTGTTTGCCAGGACGTCTCCCCAGCAAAAACTTATCATTGTAGAAGGCTGCCAGCGACAGGTAAACACACATACAGGCATTCAAGTCTACTGTCTTCAAAAGCCCCATTTACACCTGATACTAAATTGATAGTTCACCTGAAAATGAAAATTCTGTCATCATTTACTCATCCTCTACTTGTTCCAAAACTCTCTCACAGATACAGATATTCTGAAGAATGCTGGAAAAAACAACTACTGACTTCCATGGTATTTTTTGTTCCTACTAAGTATGGCTGCTTTTTACCAGCATTCATCAGAATATCTTATTTTTTGTTCAAAAGAAAAAAGAAATTCATAAAAGTTTAGAACCGCTTGAGCGTAAGTAAATCATAAGGAAATTTACTATTCCTTACTATGATTTTTTGTCAAAATAATCACAAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6413
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011121 | Essential Splice Site | 815 | 905 | 15 | 17 |
ENSDART00000124130 | Essential Splice Site | 816 | 920 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 12422653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 10922319 |
GRCz11 | 16 | 10813221 |
KASP Assay ID:
554-4031.1 (used for ordering genotyping assays)
KASP Sequence:
GCCCCTCGGCACCATMACCATCCTCTGTATCGACCTGGGAACTGACATGG[T/G]GAGCATTAGTATTAGCCTTAGTATAGAAATAYTATGTTCTGATATCCTRA
Long Flanking Sequence:
ATGTAATCTCAACACTGGTGGTCACAAGAGACACATCTGAACACGTGTTAATCCCATGTTTCACCCCTGTCCTGTTTCTCGTTCTGTCTCTCAGGGGGCCATCGTGGCTGTAACAGGTGATGGTGTGAATGACTCTCCAGCCCTGAAGAAGGCTGATATCGGCGTCGCTATGGGCATTTCTGGCTCTGATGTGTCTAAACAGGCTGCTGACATGATTTTGCTGGATGACAACTTCGCCTCCATCGTCACTGGAGTAGAAGAAGGTGAGTCAGACAGTGAAGTACATGGAAAGGCAGGAGACAAGTTGTCAAACACAATGTATAAATCCATTTCTCCTCTCGCAGGTCGACTCATCTTTGATAATTTGAAGAAGTCTATTGCGTACACCCTGACCAGCAATATCCCTGAGATCACCCCATTCCTGCTGTTTATTATTGTCAATATTCCCCTGCCCCTCGGCACCATCACCATCCTCTGTATCGACCTGGGAACTGACATGG[T/G]GAGCATTAGTATTAGCCTTAGTATAGAAATATTATGTTCTGATATCCTGATGCTTAAGTTTATACACTTTCTTTTTCTTCTGCCTCTTTAGGTACCTGCAATTTCTTTAGCTTATGAAGCAGCTGAGAGTGACATCATGAAGAGGCAGCCCAGGAACCCTATGAGAGACAAACTTGTGAACGAACGTCTCATCAGCATCGCTTATGGACAGATCGGTTGGTCTCATTCTGCATGAAACTGTAGATTTGGCTTCATTTTAAGTCAATGTGCCATATTAAAAAGGGTAGTTAGCTTTGTTAGCAAGTTATTTTTATTTATTAATTTTTTTTATTCATTGAAATCATGGAAATGAAGAAAATTCTGGGGGAAAATCATACTTCTACGCTGATTTAATAGATTTTTTTTCATTATAAAAGTTCAGTTGTTTACTTATTTACTACTTTATAGTCAGATATTATATCTTTAAACACTGAACAGATTTTATTTATAGATTTAATCAC
Associated Phenotype:
Not determined