ZMP
atp1a1a.2
Ensembl ID:
ZFIN ID:
Description:
ATPase, Na+/K+ transporting, alpha 1a.2 polypeptide [Source:RefSeq peptide;Acc:NP_571762]
Human Orthologue:
ATP1A1
Human Description:
ATPase, Na+/K+ transporting, alpha 1 polypeptide [Source:HGNC Symbol;Acc:799]
Mouse Orthologue:
Atp1a1
Mouse Description:
ATPase, Na+/K+ transporting, alpha 1 polypeptide Gene [Source:MGI Symbol;Acc:MGI:88105]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31186 | Nonsense | Available for shipment | Available now |
| sa38237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31187 | Nonsense | Available for shipment | Available now |
| sa19399 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31186
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 |
|---|---|---|---|---|---|
| ENSDART00000006449 | Nonsense | 88 | 1023 | 4 | 22 |
The following transcripts of ENSDARG00000007739 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1547584)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 1643004 |
| GRCz11 | 1 | 1790798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGGACCGCGATGGGCCGAATGCATTGACCCCACCTCCTACAACTCCA[C/T]AATGGGTGAAGTTCTGCAAACAGCTCTTCGGTGGTTTCCAAACTCTGCTG
Long Flanking Sequence:
CTAATATGTACTTACACAGGAATTAATAGTTTGTTACAATGTACTTATTGTGTGAATACATGTATTTACTGTGTACTTATGCTTGATTAAATACCTGTATGTAATTATATCTGTGATTAACTTCTGTAATTACATTTGTAAATACACTGCTGACCATTCCCTACACCTTAACCCACCCTTAAACCTACCCATACCACCAAACCTGTCCATAACCCAACCTCTATCCCAACTCAAGAACACCACAAGTGTTCTCAAATACATTATAAACACAGTAAATACACTGCATTTATTTTTTGATGTAAGTACATAGTAGTTAAGGACACTTAATATAAAGTAGGACCAATGTAGGTTATTTGACTTTAAGTTGTGTTTTTGTTTCTTCTATATGTGTTTGAACTCCTCAATGCTCATACCCAATGCAGGGCTTGTCTTCTTTTCGTGCAAAAGAGGTCCTGGACCGCGATGGGCCGAATGCATTGACCCCACCTCCTACAACTCCA[C/T]AATGGGTGAAGTTCTGCAAACAGCTCTTCGGTGGTTTCCAAACTCTGCTGTGGTTCGGTGCATTCCTTTGTTTCTTAGCTTATGGAATCCAGGTGGCATCTGTGGAAGACGCGGCACATGACAATGTAAGAGAGAGAGAAAATATATCTACATAAATATCTACCTTCTTCCTACAGCCCATGATGCATTTTGAGATTTATGGGAGTTGGTTTCATTAAACTGCAAACAATCAGTGAAGTGTTTTGAAGAGGTGTCATTGTTCTCACAGTTCATCCATTCCAATACTACTGTACAAGGCAACTTAATAAATTACTTTCAGCACAGGATGAATGATCCCTATTGAGTCTTTTTGTGGCAAATTTACAATTATTTAACATTACGGTCCTGTGCAGAAATAATCTGAACAAGCAAAACTGTGAACAATTATACTCCTCAATCAGTTTTTACTTATGCAATCGGAGAATTCAACCCAGGCTCATTTTGGAAACATAGTCCCGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38237
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 |
|---|---|---|---|---|---|
| ENSDART00000006449 | Nonsense | 437 | 1023 | 9 | 22 |
The following transcripts of ENSDARG00000007739 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1550401)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 1645821 |
| GRCz11 | 1 | 1793615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCGCTCGTGTTGCTGGCCTCTGCAATCGCGCCGTCTTCCGTGCTGAA[C/T]AAAGCCATCTCCCAGTCCTTAATGTGAGCTTGTCTCCAGATTTCCTATTA
Long Flanking Sequence:
TGTCTATTTTCTTGGGTGTGACCTTCTTCGTCCTGTCCCTGATCCTTGGATATGCGTGGATTGAAGCAGTTGTTTTCCTTATTGGAATCATTGTCGCTAATGTGCCTGAAGGTCTCCCTGCTACTGTAACTGTAAGTTAGAGAGGTTATTGATGATTCCTGGTTGTATTTTAGGCTGCTTGATGCTAAATGATTGGCTCTTGTCTGTTCATGTAGGTGTGTCTGACTCTCACTGCCAAACGAATGGCAAAGAAGAACTGCCTGGTGAAGAATCTTGAAGCTGTGGAGACTCTTGGATCAACCACCACTATTTGCTCAGACAAAACAGGAACTTTGACTCAGAACCGGATGACTGTTGCTCATATGTGGTTCGACAGCCAGATTCATGAAGCAGACACCACAGAGAACCAGAGTGGAACCTCCTTTGACAGAAGCTCTCCTACTTGGGCGGCCCTCGCTCGTGTTGCTGGCCTCTGCAATCGCGCCGTCTTCCGTGCTGAA[C/T]AAAGCCATCTCCCAGTCCTTAATGTGAGCTTGTCTCCAGATTTCCTATTATCTAAATGAGCTTCATTCAATCTTGCAACTTGTGCTACTTCAATATAGCTCTATTATTTTGAGTACAATTAAATCTGTTCTGCAGAGAGAGACAGCTGGTGATGCCTCCGAGTCTGCCCTCCTAAAGTGTATTGAGCTGTGCTGCGGATCAGTCATTGAAATGAGAGAGAAGTACAGAAAGATTTGTGAGATTCCTTTCAACTCCACCAACAAGTATCAGGTATTTTTGCTGAGATGTTCTTTGAAGGTGAGATGATGTAAATTTGACATTAGATCCTAATCGATCTTTGTTATACTTATTTCTAGCTCTCGGTCCACAAGGATCCCAGTTCCTCAGGTACTAAACACCTGCTGGTGATGAAGGGAGCACCTGAGAGAATCTTGGACCGATGCTCCACCATTTTAATTAATGGAAAAGAGCAGCCTATGGACGACGAAAATAAAGATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31187
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 |
|---|---|---|---|---|---|
| ENSDART00000006449 | Nonsense | 625 | 1023 | 13 | 22 |
The following transcripts of ENSDARG00000007739 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1551400)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 1646820 |
| GRCz11 | 1 | 1794614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTTCAATACAGGTCATCATGGTTACTGGTGACCATCCAATTACAGCT[A/T]AAGCTATTGCAAAAGGTGTTGGCATCATCTCAGAAGGCAATGAGACTGTT
Long Flanking Sequence:
CTTTTCAAAGTGCTTATGTGGAACTCGGAGGTCTTGGAGAAAGAGTCCTGGGTAAATGCACCTATGGAATTTCATTTTATGAAAAGCATTAGATTTTAAGGCTACAGAAGAAATTACAGATCATTAAAATAACAATACATTTTCTGTAACAGGTTTCTGCCAATTTAACCTGCCTGATGACCAGTTTCCTGAGGGTTTTGCATTTGATCCTGAGGATGTTAACTTCCCCACTGAGAACCTGTGCTTTCTTGGCCTCATGTCCATGATTGATCCTCCTCGTGCCGCTGTACCAGATGCTGTAGCCAAGTGCCGGAGTGCTGGAATCAAGGTTTAACCTTTATTTAACCTTTTAACCTTTATTCAAGTTCAACTACTTGAACATGCTGAATATGTAGTTAAATTGTTCAAATAATAAGCAACTGTTTAAATAAAGCTAATTTAAATGAATGCCTCTTTCAATACAGGTCATCATGGTTACTGGTGACCATCCAATTACAGCT[A/T]AAGCTATTGCAAAAGGTGTTGGCATCATCTCAGAAGGCAATGAGACTGTTGAAGACATTGCCGCTCGCATGAACATCCCTGTTGGAGAGGTTAATCCGAGGTAAACCCAACCACCTAAAACACAGCAACAATTTAAATAAATATATTGCAAAAAATACAGGACTTGCTGGTCTTCTAATACAAATTTGTCTCTATAGAGAAGCTAAGGCCTGTGTGGTCCATGGTGGAGAGCTGAAGAATATGAATGACAGTGACCTGGATGAGATCCTCCGTTATCATACAGAAATTGTGTTCGCCAGAACGTCTCCACAACAAAAGCTGATCATTGTGGAAGGTTGTCAAAGACAGGTGCTGCCAGAGAAATCTATCCAATCGTACAGATGTACAGTTTTACACCTGTACGTAAACTTTAATGTCTCTTTACTCTTATCAGGGTGCCATTGTAGCCGTAACCGGTGATGGAGTCAATGATTCTCCAGCTCTGAAGAAGGCTGACATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19399
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006449 | Splice Site, Nonsense | 658 | 1023 | 13 | 22 |
The following transcripts of ENSDARG00000007739 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1551499)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 1646919 |
| GRCz11 | 1 | 1794713 |
KASP Assay ID:
2259-0051.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAGACATTGCCGCTCGCATGAACATCCCTGTTGGAGAGGTTAATCCG[A/T]GGTAAACCCAACCACCTAAAACACAGCAACAATTTAAATAAATATATTGC
Long Flanking Sequence:
GGCTACAGAAGAAATTACAGATCATTAAAATAACAATACATTTTCTGTAACAGGTTTCTGCCAATTTAACCTGCCTGATGACCAGTTTCCTGAGGGTTTTGCATTTGATCCTGAGGATGTTAACTTCCCCACTGAGAACCTGTGCTTTCTTGGCCTCATGTCCATGATTGATCCTCCTCGTGCCGCTGTACCAGATGCTGTAGCCAAGTGCCGGAGTGCTGGAATCAAGGTTTAACCTTTATTTAACCTTTTAACCTTTATTCAAGTTCAACTACTTGAACATGCTGAATATGTAGTTAAATTGTTCAAATAATAAGCAACTGTTTAAATAAAGCTAATTTAAATGAATGCCTCTTTCAATACAGGTCATCATGGTTACTGGTGACCATCCAATTACAGCTAAAGCTATTGCAAAAGGTGTTGGCATCATCTCAGAAGGCAATGAGACTGTTGAAGACATTGCCGCTCGCATGAACATCCCTGTTGGAGAGGTTAATCCG[A/T]GGTAAACCCAACCACCTAAAACACAGCAACAATTTAAATAAATATATTGCAAAAAATACAGGACTTGCTGGTCTTCTAATACAAATTTGTCTCTATAGAGAAGCTAAGGCCTGTGTGGTCCATGGTGGAGAGCTGAAGAATATGAATGACAGTGACCTGGATGAGATCCTCCGTTATCATACAGAAATTGTGTTCGCCAGAACGTCTCCACAACAAAAGCTGATCATTGTGGAAGGTTGTCAAAGACAGGTGCTGCCAGAGAAATCTATCCAATCGTACAGATGTACAGTTTTACACCTGTACGTAAACTTTAATGTCTCTTTACTCTTATCAGGGTGCCATTGTAGCCGTAACCGGTGATGGAGTCAATGATTCTCCAGCTCTGAAGAAGGCTGACATTGGTGTGGCTATGGGTATTTCTGGATCTGACGTATCCAAACAGGCTGCTGACATGATCCTTCTGGACGACAACTTTGCCTCTATTGTCACTGGAGTAGAGG
Associated Phenotype:
Not determined