ZMP
atp1a1
Ensembl ID:
ZFIN ID:
Description:
Na+/K+ -ATPase alpha 1 subunit [Source:RefSeq peptide;Acc:NP_571761]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31185 | Essential Splice Site | Available for shipment | Available now |
sa13646 | Nonsense | Available for shipment | Available now |
sa19398 | Essential Splice Site | Available for shipment | Available now |
sa15598 | Nonsense | Available for shipment | Available now |
sa12184 | Essential Splice Site | Available for shipment | Available now |
sa38236 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31185
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 |
---|---|---|---|---|---|
ENSDART00000081047 | Essential Splice Site | 4 | 1028 | 1 | 22 |
The following transcripts of ENSDARG00000002791 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1469144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1564564 |
GRCz11 | 1 | 1712358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTCCCAGGTGGTCGATTTTAATCAAAAGCAGCAAAATGGGACGAGGAG[T/C]AAGTGTAAACCCAATTGTTGATTCACTTTTTATATCGGTTTGTCCAGTTC
Long Flanking Sequence:
GGCTTAACCTGGATATTCCAACAGGGTCTTAATGTTGAATGTACAGTCTAAAGGTCTCATTTCACAGATTAAAATCAAAGACGCCGGCTTCTGCTCTCTGATAGAGGAAAGCCACTGGTGGGCATTTTTCTCCAGCGTGATCAAAGTTCAGAGGTGAAAGTCTGTACTGTTCTGTTCTCCCGCGGCTCTTCTTCCCCGTAGACCCCGCCTCTTTTCCTCCGCGTTACCATGACGATCCGTGCATACGTCATACTGAAAAACCGCACTATATATAAGCTTTGAATGAACTGACTGTAACGCGGCTCGGATGCGTGTCTGGGTGGTACTACGCGTCCGGCGGTGACCAAGGAGAGAATACATTTGAAAAAGCCCCAAAAAGAGAGGAAACGGGATCGGGGACTTTTAATTTGTTGTTTTGAAAGAAAGCTCGGATTTGTTTTATTTTTTGGGAATTCCCAGGTGGTCGATTTTAATCAAAAGCAGCAAAATGGGACGAGGAG[T/C]AAGTGTAAACCCAATTGTTGATTCACTTTTTATATCGGTTTGTCCAGTTCTGTGTTTGAACGCAGTGTTTTTAAAGTAACCACAAGATGATCAACTGGTAAACGGCTTCTCGCCGTTCTAGACTTCCGCAGTTTTCATATTCAAATGAGTTTTAAATGAATGAAATGTGCGCAGATGTTCATCTAAACTACTTGTGAAGTCTGTTTTCGATAGTGGAGCAACAGGTTTTCCAGTCTGTGGCTTTAAAAGGGAGTCAAACTCCATTTTAAGACGTTCCTCGATCACTAGAAAGATTTGAGGAATGTAGCAGACACTAAACTTCCTCTATGGCCGCGGTGTTACACGGCCTGTTTGTCTAAGCAGATATAGTTGAAATCTCGTGACTTTTACACTGTAAAACTGAAGTAATCATGTGTGTCGCAATTGAGCTGCTAAGCAGTTCTTATGAGGGGGAAAACAAACTTAAAGCTCTTTATCTATTGCTACAGAACATAACTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13646
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 |
---|---|---|---|---|---|
ENSDART00000081047 | Nonsense | 114 | 1028 | 4 | 22 |
The following transcripts of ENSDARG00000002791 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1474627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1570047 |
GRCz11 | 1 | 1717841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCTCTTTGGAGGATTCWCAACTCTCCTGTGGATTGGAGCCATCCTTTG[T/A]TTTCTTGCCTACGGCATCCTGGCGGCCTCTGAGGAGGARCCTGCCAATRA
Long Flanking Sequence:
AGGAAGGCCGAGAACAATATGAGCTGGCAGCCACCTCAGAGCAGGGGGGCAAGAAGTCAAAGTCCAAGGGCAAGAAAGAGAAGGATAAAGACATGGATGAACTCAAAAAAGAAGTGGACTTGGTGAGTTAGTTTATGAGCATAAATCCTATAATGGCTATCGTAACTTTTGATAGGATGGTAAAATGCTGTTTTTATTACATCTTTGTAGGACGATCACAAACTGTCCCTGGATGAGCTCACCAGGAAATATAACACTGATTTGACAAGGGTAAGACTGTATTGGATGAACAGCTTTGGAAATGTAAGTCTCAGTTTGGATCTTCATTATCTAACCCATCACTTTATCTAGGGATTGTCAGGCACTCGTGCTAAGGAGATCTTGGCACGTGATGGACCCAACGCTTTGACTCCACCTCCCACAACCCCAGAATGGGTCAAGTTCTGCAAGCAGCTCTTTGGAGGATTCTCAACTCTCCTGTGGATTGGAGCCATCCTTTG[T/A]TTTCTTGCCTACGGCATCCTGGCGGCCTCTGAGGAGGAGCCTGCCAATGATAATGTAAGGAGAAAACCCTGTTTGTGTGTCTTAAGGATTTGCCTTCTTAAGATCATGTTGTTTTAGCACCAATCCTAACATCTCCTTCATTGTCTTGCACAGTTGTATCTGGGTATTGTGCTTTCTGCTGTCGTGATGATCACTGGATGCTTCTCGTACTATCAAGAAGCCAAGAGCTCCAAGATCATGGACTCTTTCAAGAATTTGGTTCCCCAGGTACTTATTGATATTATATTGCATAGATTGTTTTATAAGTGTTATATTTTCCTGACTCTGACGAATGTGAATTCCCACTTTGTCTTATAGCAAGCCTTGGTTATCCGTGATGGTGAGAAGAAGAACATCAACGCTGAAGAAGTTGCTGTCGGAGATCTTGTGGAAGTCAAAGGTGGTGACAGAATTCCTGCTGATTTGCGTATCATTTCTGCTCATGGATGCAAGGTAAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19398
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 |
---|---|---|---|---|---|
ENSDART00000081047 | Essential Splice Site | 344 | 1028 | 8 | 22 |
The following transcripts of ENSDARG00000002791 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1475668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1571088 |
GRCz11 | 1 | 1718882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGTATCATTGTTGCGAATGTACCAGAGGGTCTCTTGGCTACTGTAACT[G/A]TAAGTGTCAGAGGAATTGCTACAGATTTAGTTAAATTTAGTTCTACACGT
Long Flanking Sequence:
CAAGCATTTACAAATAATTGTTGTCTTCCTAGGTGGACAACTCCTCCCTCACTGGAGAATCTGAACCCCAGACTCGTACTCCTGACTTTTCCAATGATAACCCACTGGAGACCAGGAACATTGCGTTCTTCTCTACCAACTGTGTTGAAGGTACAAAAAGAGGTCTTTTGGGGATTAAGCATGGTGTTAATCAACAGTAGATGTTTTCATTGCCTTATGCTTTACATCTAGGTACTGCCAGAGGAATTGTCATCAACACTGGTGACCGCACAGTCATGGGTCGCATCGCCACTCTCGCTTCTGGCCTTGAAGTTGGTCGCACCCCCATCTCTATTGAGATCGAGCACTTCATCCACATCATCACTGGTGTAGCTGTCTTCCTGGGTGTGTCCTTCTTCATCCTCTCCCTCATCCTTGGGTACAGTTGGTTGGAGGCTGTCATCTTCCTGATTGGTATCATTGTTGCGAATGTACCAGAGGGTCTCTTGGCTACTGTAACT[G/A]TAAGTGTCAGAGGAATTGCTACAGATTTAGTTAAATTTAGTTCTACACGTAGACAAACCTCATTCTTGTCGTGTTCAGGTGTGTTTGACTCTCACCGCCAAACGAATGGCAAAGAAGAACTGCCTGGTGAAGAATCTTGAAGCTGTGGAGACTCTTGGCTCGACCTCCACCATCTGCTCTGACAAGACTGGAACTTTGACCCAGAACCGGATGACCGTCGCTCACATGTGGTTCGACAACCAGATTCATGAAGCAGACACCACAGAGAACCAGAGTGGAACGTCTTTTGACAGGAGCTCTGCTACTTGGGCCGCCCTCGCTCGTGTTGCTGGCCTCTGCAACCGCGCCGTCTTCCTTGCTGAGCAAGAAAACATCCCAATTCTTAAGGTCTGTGTTTATGCGTTGTCTGTCAAAAGATTTACCGGTCCTTGCAGTGTATGGAGAAGTAGTTTTTCATCTTGCGCCCTGTTCACACAAATACGTGTATTTTCAAAACCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15598
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 |
---|---|---|---|---|---|
ENSDART00000081047 | Nonsense | 569 | 1028 | 12 | 22 |
The following transcripts of ENSDARG00000002791 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1478569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1573989 |
GRCz11 | 1 | 1721783 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MAACRTGTTGTTTCTCCACAGGATTCTGCCACTTCAATCTTCCCGATGAA[C/T]AGTTTCCTGAGGACTTCCAGTTCGATACTGAAGAAGTGAACTTCCCCACT
Long Flanking Sequence:
TTTCAGAGATCCCATTCAACTCCACCAACAAATACCAGGTATAACTGTCTTTGGCTTAGGATGTCACTTTAAAATTTACCAGTGTACACAGAATGAAACGTCATTGCATTGGCTAGGCAGTTTTAAAAATAACAATAGCGACTTTGACTTTGGATGAATATCAGATTTCTAATAGCTTCTTTTTGTGAATCTCCTTTTTTAGCTCTCCATCCACCAGAACCCCAACAGCAATAACACTGAAAGCAAACACCTGCTAGTAATGAAAGGCGCTCCTGAGAGGATCCTGGACCGGTGCTCCTCTATTTTAATCCAAGGAAAAGAGCAGCCTTTGGATGATGAGATGAAGGATGCTTTCCAGAATGCCTACCTGGAACTTGGTGGTCTTGGAGAGAGAGTACTGGGTGAGTACTGGCATTGCTATACTACGCATTTCCATGCGACGCGTTCCTTCAACGTGTTGTTTCTCCACAGGATTCTGCCACTTCAATCTTCCCGATGAA[C/T]AGTTTCCTGAGGACTTCCAGTTCGATACTGAAGAAGTGAACTTCCCCACTGAGAACCTGTGCTTTATTGGCCTCATGTCCATGATTGATCCTCCTCGTGCCGCTGTACCAGATGCTGTGGGCAAATGCAGGAGCGCTGGAATCAAGGTATGATTTAAAAACTGCTCATCTTAAAGAAACAGAAATGCATTGGCTACAAATTAAAAATCTCTTTTCTAGGTTATCATGGTTACCGGTGACCATCCAATCACAGCCAAGGCCATTGCCAAGGGGGTGGGTATCATCTCAGAGGGCAATGAAACTGTTGAAGACATCGCTGCTCGCTTGAACATCCCTATTAATGAGGTCAACCCAAGGTAATTGGTTCCTCTTCTTCAATTCGAATGTTTTCTTGCTGGATATTTATAGTGTCTAGCTTTTAATTCCATTTAATGTGCAACATGTAATCACTGTCAAGCCTCTCTCATCTTAAAAAATGTGAAATTTTAAAGATTACTAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12184
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081047 | Essential Splice Site | 821 | 1028 | 16 | 22 |
The following transcripts of ENSDARG00000002791 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1480295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1575715 |
GRCz11 | 1 | 1723509 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCTTTGGGCACCGTCACCATTCKCTGTATTGATCTGGGTACCGACATG[G/T]TRAGCACTGCATTTRATTGGTTCTATTTAATAGYTGGTTGGTGAGGTTAA
Long Flanking Sequence:
AATTAATGCTCTGAAATACAACTAAGACAAGTTTGGTTTGGACAAGACTTTGGACGTGTCACAACACTGGCTTACATTCATTTGCGTTTATCCACAGGGTGCCATTGTAGCCGTAACCGGTGATGGTGTCAATGATTCTCCAGCTCTGAAGAAGGCTGACATTGGTGTGGCTATGGGTATTGCTGGATCTGACGTATCCAAACAGGCTGCTGACATGATCCTTCTGGACGACAACTTTGCCTCAATTGTCACTGGAGTAGAAGAAGGTATGTCATATTTTGGGAACTTGCTTTGACTGAATAATTCTGAAGAGTCAAATCTCAAACATATCTTCCATATGTTTAGGTCGTCTGATCTTCGACAACTTAAAGAAGTCCATTGCCTACACACTGACCAGTAACATCCCCGAGATCACCCCTTTCCTTCTGTTCATCATTGCTAATATTCCTCTACCTTTGGGCACCGTCACCATTCTCTGTATTGATCTGGGTACCGACATG[G/T]TAAGCACTGCATTTGATTGGTTCTATTTAATAGCTGGTTGGTGAGGTTAATAAATGATATTGTCCTGTTATCGTCAAGGTTCCTGCCATCTCATTGGCCTATGAAGCTGCCGAGAGTGACATCATGAAGCGTCAACCCAGAAACCCCAAAACAGACAAACTTGTGAATGAGAGGCTCATTAGCATAGCCTACGGTCAGATCGGTAAGCATCTCAGATGCTCTATTAAAGGCATGGTTCACCCAAAAACTCGTCGTTTACTCAACCTTCTCTGGTCACTATTTGACTTTCTTTCTGCTGTTGAACACCGAAGAAGATATTGTAAAGAAATCTGGAACCATTTAACCATTGACTTCCATAGTAGGATTAACAAATACTATTGAAGTCAATGGTTGGTTTCTCTTCTTTCTTCAAAATACCATATTTAAAAGGTTCCCAATTGAAGTTGGGTAAATCTTTCATTTTTGGGTGGACTTGATCTGTTGGTGTTCACCAGGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38236
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081047 | Essential Splice Site | 955 | 1028 | 19 | 22 |
The following transcripts of ENSDARG00000002791 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1481207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1576627 |
GRCz11 | 1 | 1724421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGATCATCTGCAAGACCAGAAGAAACTCTGTCTTCCAGCAGGGAATGAA[G/A]TAAGTGGATGGGTAATAATTCAGTATGTTTCTGAGCGTCTTGTATCAGAG
Long Flanking Sequence:
AAATACCATATTTAAAAGGTTCCCAATTGAAGTTGGGTAAATCTTTCATTTTTGGGTGGACTTGATCTGTTGGTGTTCACCAGGTGTGTACTGTAGACTTTGAGGATTGAATCCCAATGCTTCTGCTTTCCCCACAGGTATGATTCAAGCTCTGGCTGGGTTCTTCACATATTTTGTCATCTTGGCTGAAAATGGCTTCCTACCATCATCACTGCTGGGCATTCGAGTGTTTTGGGATGACAAATACGTCAACGATCTGGAGGACAGTTATGGCCAGCAATGGGTGAGTGTTGTCAATCATCCAATAAGCAGATGACATCTCTGCTTGTCCAGCATCTAATCTGAATATTGTGTTCCTGGCCATCCCAGACGTACGAGCAGAGGAAGATTGTGGAGTTCACATGCCACACTGCCTTCTTCACCAGTATAGTGATTGTACAGTGGGCAGATTTGATCATCTGCAAGACCAGAAGAAACTCTGTCTTCCAGCAGGGAATGAA[G/A]TAAGTGGATGGGTAATAATTCAGTATGTTTCTGAGCGTCTTGTATCAGAGGTCTTACGTGTTTGCTGTTGTCTTGCAGAAATAAGATTCTAATCTTTGGATTGTTCGAAGAAACCGCTCTTGCAGCTTTCCTGTCCTACTGCCCGGGCATGGACGTAGCCCTCAGAATGTACCCACTTAAGTAAGTCAAGCCTCTTTACCAGTATTTGTTAATCATCTAGACATGTTTTGTTATGACGTTTGGGAATGTTTTTTAACATAAACTGCAAAAAATCCTTTTCTATCTTTGAGTTTTGTCTGGTTTCTTGTCCAAATATCCCAAAAAAAAAATCCTAATTCTCTTTCGGATAAGATGTTAAAGGGCCAGGAAATCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTCTGTTTAGGGGGGAGTGTCGAAGGAAGAAAAGTGGGAGGGTGTGGGAGTGTCTATTTGG
Associated Phenotype:
Not determined