ZMP
atp1a1a.4
Ensembl ID:
ZFIN ID:
Description:
ATPase, Na+/K+ transporting, alpha 1a.4 polypeptide [Source:RefSeq peptide;Acc:NP_571764]
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 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19396 | Nonsense | Available for shipment | Available now |
sa19397 | Nonsense | Available for shipment | Available now |
sa17542 | Nonsense | Available for shipment | Available now |
sa14454 | Nonsense | Available for shipment | Available now |
sa13870 | Nonsense | Available for shipment | Available now |
sa14079 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19396
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 |
---|---|---|---|---|---|
ENSDART00000048828 | Nonsense | 505 | 1024 | 11 | 22 |
The following transcripts of ENSDARG00000001870 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1456708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1552128 |
GRCz11 | 1 | 1699922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTAGCTTTCAATCCACAAGAATCCCAATTCCTCAGAGCCAAAACACT[T/A]GCTTGTGATGAAGGGAGCACCTGAGAGGATCTTGGATCGATGCTCCACCA
Long Flanking Sequence:
TCGACAGCCAGATTCATGAAGCAGACACCACTGAGAACCAGAGTGGAACCACCTTTGACAGGAGCTCTCCTACGTGGTCTGCACTTGCACGTGTTGCTGGCCTTTGCAATCGTGCCGTCTTCCTAGCTGATCAGCGCAATGTGCCTATCCTCAAGGTGGGTTGATTTATGTTTAAAGGTGTTGTAGTAAACAAATGTCCATCAAGATGCTCTTTATAAAAGACAGAATCAATGCATTGCAGAGAGACACAGCTGGTGATGCCTCCGAGTCTGCCCTCCTGAAGTGTATTGAGCTGTGCTGCGGTTCAGTCAATGAAATGAGAGAGAAGTACACAAAGATTGCAGAAATCCCTTTCAACTCCACCAACAAGTATCAGGTATTGTGTATATGTTGTGTTGGTTTTCTATTTGCTGATTTGACTAGCCTTGCTAACAGTGCTGATTCTGCCTTGCTCTAGCTTTCAATCCACAAGAATCCCAATTCCTCAGAGCCAAAACACT[T/A]GCTTGTGATGAAGGGAGCACCTGAGAGGATCTTGGATCGATGCTCCACCATTTTAATTCAGGGAAAACAGCAGCCCTTAGATGAAGAAATGAAAGATGCTTTTCAGAATGCTTATGTTGAACTTGGAGGTCTTGGAGAAAGAGTCCTGGGTAAATTCCCCAAATGAGGTTTATCATTGGAAGTTTTCTGTGTATTAATAACTGAGACTTTTCACACAAGTAAATGTGTTATTTCTCACAGGTTTCTGCCACTTCTGCCTTCCTGATGATCAGTTTCCTGAGGGTTTTGCATTTGATACTGAAGAAGTGAACTTCCCCACTGAGAACCTGTGCTTTGTTGGCCTCATGTCCATGATTGATCCTCCTCGTGCCGCTGTACCAGATGCTGTGGGCAAGTGCAGGAGTGCTGGAATCAAGGTGTTTTTTTCACCTTGATTCAAGACTGATGCCTTGATTATTTTATTCCTGTATTAAATTAATTAGATGATCAAGCATCTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19397
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 |
---|---|---|---|---|---|
ENSDART00000048828 | Nonsense | 543 | 1024 | 11 | 22 |
The following transcripts of ENSDARG00000001870 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1456823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1552243 |
GRCz11 | 1 | 1700037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAGCAGCCCTTAGATGAAGAAATGAAAGATGCTTTTCAGAATGCTTA[T/A]GTTGAACTTGGAGGTCTTGGAGAAAGAGTCCTGGGTAAATTCCCCAAATG
Long Flanking Sequence:
CGTCTTCCTAGCTGATCAGCGCAATGTGCCTATCCTCAAGGTGGGTTGATTTATGTTTAAAGGTGTTGTAGTAAACAAATGTCCATCAAGATGCTCTTTATAAAAGACAGAATCAATGCATTGCAGAGAGACACAGCTGGTGATGCCTCCGAGTCTGCCCTCCTGAAGTGTATTGAGCTGTGCTGCGGTTCAGTCAATGAAATGAGAGAGAAGTACACAAAGATTGCAGAAATCCCTTTCAACTCCACCAACAAGTATCAGGTATTGTGTATATGTTGTGTTGGTTTTCTATTTGCTGATTTGACTAGCCTTGCTAACAGTGCTGATTCTGCCTTGCTCTAGCTTTCAATCCACAAGAATCCCAATTCCTCAGAGCCAAAACACTTGCTTGTGATGAAGGGAGCACCTGAGAGGATCTTGGATCGATGCTCCACCATTTTAATTCAGGGAAAACAGCAGCCCTTAGATGAAGAAATGAAAGATGCTTTTCAGAATGCTTA[T/A]GTTGAACTTGGAGGTCTTGGAGAAAGAGTCCTGGGTAAATTCCCCAAATGAGGTTTATCATTGGAAGTTTTCTGTGTATTAATAACTGAGACTTTTCACACAAGTAAATGTGTTATTTCTCACAGGTTTCTGCCACTTCTGCCTTCCTGATGATCAGTTTCCTGAGGGTTTTGCATTTGATACTGAAGAAGTGAACTTCCCCACTGAGAACCTGTGCTTTGTTGGCCTCATGTCCATGATTGATCCTCCTCGTGCCGCTGTACCAGATGCTGTGGGCAAGTGCAGGAGTGCTGGAATCAAGGTGTTTTTTTCACCTTGATTCAAGACTGATGCCTTGATTATTTTATTCCTGTATTAAATTAATTAGATGATCAAGCATCTATGTCTTCTATCACAGGTTACTTGTGACCATCGATTTACAGCCAAGACTATTGTAAAGGATCTTGAATCAAGATTCAAGTAGTTCTTGATTCAAGATCCGCTGATTGAATATGTCGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17542
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 |
---|---|---|---|---|---|
ENSDART00000048828 | Nonsense | 672 | 1024 | 14 | 22 |
The following transcripts of ENSDARG00000001870 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1457650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1553070 |
GRCz11 | 1 | 1700864 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGTGCCTTTAGAGATGCGAAGGCATGTGTGGTCCATGGAGGAGAACTG[A/T]AAAGTATGAGYGAAGAAGAGCTAGATGATATCCTGAAACACCATACWGAA
Long Flanking Sequence:
CTGATGCCTTGATTATTTTATTCCTGTATTAAATTAATTAGATGATCAAGCATCTATGTCTTCTATCACAGGTTACTTGTGACCATCGATTTACAGCCAAGACTATTGTAAAGGATCTTGAATCAAGATTCAAGTAGTTCTTGATTCAAGATCCGCTGATTGAATATGTCGCACCTTAGTTGCAGCATATTCACTGTGGTTCATACTGGTTGAATTTCTTTCAGTTAATCAAATAATAACTCTGAATCTTATTTACAGGTGATCATGGTTACTGGTGACCATCCAATTACAGCTAAAGCTATTGCAAAAGGTGTCGGCATCATCTCAGAAGGCAATGAGACTGTTGAAGACATTGCCGCTCGTTTGAACATCCCGGTTGGAGAGGTTAATCCAAGGTATGTTAAAGCAAAACTTATGGAGAAGTTTGAATCTAAATGTTTGCTAATACATAGTGTGCCTTTAGAGATGCGAAGGCATGTGTGGTCCATGGAGGAGAACTG[A/T]AAAGTATGAGTGAAGAAGAGCTAGATGATATCCTGAAACACCATACAGAAATTGTGTTCGCCAGAACTTCTCCACAACAAAAGCTGATCATTGTGGAAGGATGTCAGCGACAGGTACCATCAGATATATTCAATTCCTGCTGAGAGTATTTATGCTGCATGAACTCAACGTAATTATTATTTTGTTTACTCTTTCAGGGTGCCATTGTAGCCGTAACCGGTGATGGAGTCAATGATTCTCCAGCTCTGAAGAAGGCTGACATTGGTGTGGCTATGGGTATTGCTGGATCTGACGTATCCAAGCAGGCTGCTGACATGATCCTTCTGGACGACAACTTTGCCTCAATTGTCACTGGAGTAGAAGAAGGTACGACGACCTAAATTAAAAAAAAAATTTAAATGTTACTTTGAAGGTTACTTATTCCTCAAATGTGTCTTTAACTATAGGACGTCTGATCTTTGATAACTTGAAGAAGTCCATTGCCTACACCCTGACAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14454
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 |
---|---|---|---|---|---|
ENSDART00000048828 | Nonsense | 822 | 1024 | 17 | 22 |
The following transcripts of ENSDARG00000001870 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1459898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1555318 |
GRCz11 | 1 | 1703112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTGCAAATGTTAAYTATTGTTTAATGTTTCCTCAGGTTCCTGCGATCT[C/A]KTTGGCCTMTGAAAGTGCWGAAAGTRACATCATGAAGWGACAACCCAGAA
Long Flanking Sequence:
ATATTATTTCTTAAAACAAGACAATATGTTTTGCTTGTCCATAAAACGCTTCTTGATTTAAGAACTTTCAGATATTTGGACTAGAAAAGGGGACAAAAAAAATCTCGGTAAGAAAAGCATTTTTTGCAGTTCAGACACCAACATTGTTTGTCAAAATTTGCTCATAGCACATTTAATGTGTTGTACGCAATGATTATTTTTATAGATATCCACTAAATGTCATTCCAGCAAGGAAGTGTGAGCTTATATTGGCAACCTTTGGATGTCTAAAAGAAAACCTTGTAAAAGGAAATCCAAAGCAATCCCTTTATCTTCCCTAGATGATCTTTGATCCATGCACATGAATTCCTGATGGCTCCCTCGAGTGGTATAAAAGATTAAAGAAATGGTTCACATAATTTCCTTTGAAGCAGCTTGCTTAAATTTGCTGTGATTCCTCCTGCAATGCTGGATTGCAAATGTTAACTATTGTTTAATGTTTCCTCAGGTTCCTGCGATCT[C/A]GTTGGCCTATGAAAGTGCTGAAAGTGACATCATGAAGAGACAACCCAGAAATGCTAAAACAGATAAACTGGTGAACGAGAGGCTGATCAGTATGGCCTATGGTCAAATAGGTAAGAGCTTGGTTAATCTAAACAGATGTTTATAGCGGTTTGCTCTGTGTTCAGTCTTTGATCTGGTTCTGAAAAGTAGTACTCTACGGTTCTGTCTGCTTGTTAATTGTGACGTCACGTGAAGCAACTTCCGGGTCCAATCGATATATCAAACTGTATGGGGACACTCAACAAATGCTAATACTAAATGTTTACCAGAAACATTTATGGTAAATGTGCTCAGGTGCTCTGGTTTCCCCCACAATCCAAACGCATGCTCTATAGGGGAATTGAATGAGCTAATTCAGTCGTAGTGTATGTGTGTGAATGTGAGCGTGTATGGATGTTTCCTAGTACTGGGTTGCAGCTGGAAGGGCATCAGCTGCGTAAAACATATGCTAGATAAGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13870
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 |
---|---|---|---|---|---|
ENSDART00000048828 | Nonsense | 835 | 1024 | 17 | 22 |
ENSDART00000048828 | Nonsense | 835 | 1024 | 17 | 22 |
The following transcripts of ENSDARG00000001870 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1459936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1555356 |
GRCz11 | 1 | 1703150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTGCGATCTMKTTGGCCTMTGAAAGTGCWGAAAGTRACATCATGAAG[A/T]GACAACCCAGAAATGCTAAAACAGATAAACTGGTGAACGAGAGGCTGATC
Long Flanking Sequence:
CCATAAAACGCTTCTTGATTTAAGAACTTTCAGATATTTGGACTAGAAAAGGGGACAAAAAAAATCTCGGTAAGAAAAGCATTTTTTGCAGTTCAGACACCAACATTGTTTGTCAAAATTTGCTCATAGCACATTTAATGTGTTGTACGCAATGATTATTTTTATAGATATCCACTAAATGTCATTCCAGCAAGGAAGTGTGAGCTTATATTGGCAACCTTTGGATGTCTAAAAGAAAACCTTGTAAAAGGAAATCCAAAGCAATCCCTTTATCTTCCCTAGATGATCTTTGATCCATGCACATGAATTCCTGATGGCTCCCTCGAGTGGTATAAAAGATTAAAGAAATGGTTCACATAATTTCCTTTGAAGCAGCTTGCTTAAATTTGCTGTGATTCCTCCTGCAATGCTGGATTGCAAATGTTAACTATTGTTTAATGTTTCCTCAGGTTCCTGCGATCTCGTTGGCCTATGAAAGTGCTGAAAGTGACATCATGAAG[A/T]GACAACCCAGAAATGCTAAAACAGATAAACTGGTGAACGAGAGGCTGATCAGTATGGCCTATGGTCAAATAGGTAAGAGCTTGGTTAATCTAAACAGATGTTTATAGCGGTTTGCTCTGTGTTCAGTCTTTGATCTGGTTCTGAAAAGTAGTACTCTACGGTTCTGTCTGCTTGTTAATTGTGACGTCACGTGAAGCAACTTCCGGGTCCAATCGATATATCAAACTGTATGGGGACACTCAACAAATGCTAATACTAAATGTTTACCAGAAACATTTATGGTAAATGTGCTCAGGTGCTCTGGTTTCCCCCACAATCCAAACGCATGCTCTATAGGGGAATTGAATGAGCTAATTCAGTCGTAGTGTATGTGTGTGAATGTGAGCGTGTATGGATGTTTCCTAGTACTGGGTTGCAGCTGGAAGGGCATCAGCTGCGTAAAACATATGCTAGATAAGTTGGTGGTTCATTCCGCTGTGGCGATCCCTGATAAATAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14079
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 |
---|---|---|---|---|---|
ENSDART00000048828 | Nonsense | 835 | 1024 | 17 | 22 |
ENSDART00000048828 | Nonsense | 835 | 1024 | 17 | 22 |
The following transcripts of ENSDARG00000001870 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 1459936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 1555356 |
GRCz11 | 1 | 1703150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTGCGATCTMKTTGGCCTMTGAAAGTGCWGAAAGTRACATCATGAAG[A/T]GACAACCCAGAAATGCTAAAACAGATAAACTGGTGAACGAGAGGCTGATC
Long Flanking Sequence:
CCATAAAACGCTTCTTGATTTAAGAACTTTCAGATATTTGGACTAGAAAAGGGGACAAAAAAAATCTCGGTAAGAAAAGCATTTTTTGCAGTTCAGACACCAACATTGTTTGTCAAAATTTGCTCATAGCACATTTAATGTGTTGTACGCAATGATTATTTTTATAGATATCCACTAAATGTCATTCCAGCAAGGAAGTGTGAGCTTATATTGGCAACCTTTGGATGTCTAAAAGAAAACCTTGTAAAAGGAAATCCAAAGCAATCCCTTTATCTTCCCTAGATGATCTTTGATCCATGCACATGAATTCCTGATGGCTCCCTCGAGTGGTATAAAAGATTAAAGAAATGGTTCACATAATTTCCTTTGAAGCAGCTTGCTTAAATTTGCTGTGATTCCTCCTGCAATGCTGGATTGCAAATGTTAACTATTGTTTAATGTTTCCTCAGGTTCCTGCGATCTCGTTGGCCTATGAAAGTGCTGAAAGTGACATCATGAAG[A/T]GACAACCCAGAAATGCTAAAACAGATAAACTGGTGAACGAGAGGCTGATCAGTATGGCCTATGGTCAAATAGGTAAGAGCTTGGTTAATCTAAACAGATGTTTATAGCGGTTTGCTCTGTGTTCAGTCTTTGATCTGGTTCTGAAAAGTAGTACTCTACGGTTCTGTCTGCTTGTTAATTGTGACGTCACGTGAAGCAACTTCCGGGTCCAATCGATATATCAAACTGTATGGGGACACTCAACAAATGCTAATACTAAATGTTTACCAGAAACATTTATGGTAAATGTGCTCAGGTGCTCTGGTTTCCCCCACAATCCAAACGCATGCTCTATAGGGGAATTGAATGAGCTAATTCAGTCGTAGTGTATGTGTGTGAATGTGAGCGTGTATGGATGTTTCCTAGTACTGGGTTGCAGCTGGAAGGGCATCAGCTGCGTAAAACATATGCTAGATAAGTTGGTGGTTCATTCCGCTGTGGCGATCCCTGATAAATAAAGG
Associated Phenotype:
Not determined