ZMP
atp13a
Ensembl ID:
ZFIN ID:
Description:
probable cation-transporting ATPase 13A1 [Source:RefSeq peptide;Acc:NP_001001403]
Human Orthologue:
ATP13A1
Human Description:
ATPase type 13A1 [Source:HGNC Symbol;Acc:24215]
Mouse Orthologue:
Atp13a1
Mouse Description:
ATPase type 13A1 Gene [Source:MGI Symbol;Acc:MGI:2180801]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20141 | Essential Splice Site | Available for shipment | Available now |
| sa13862 | Essential Splice Site | Available for shipment | Available now |
| sa31360 | Nonsense | Available for shipment | Available now |
| sa20142 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20141
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:
Founder:
SL6_02_G12
KASP Assay Location:
Unknown
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042147 | Essential Splice Site | 373 | 887 | 6 | 18 |
| ENSDART00000058958 | Essential Splice Site | 392 | 1242 | 6 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 53551441)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 52658756 |
| GRCz11 | 3 | 52913419 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTGTGGATGAAGCCATGCTTACAGGAGAGTCTGTGCCGCAGATGAAG[G/A]TGCGTCTGCTTGCTTTTTCCACTTCAAACTATTATACCATCAGCTTTCGG
Long Flanking Sequence:
TGATGGAAATTCAGCTTTGACATCACAGAAATAAATGACATTTCAAAATGAATTCATTAAAATATAATTATATTCAACTGCACTAGTATTTTGCCAAAATATATATATTTTTTTTACTCATATTTAGTCAAATAAATGCAGAAGTTTATTTTTAAAAAACACCTTAATAACCTCCAACAGTTGGATAATACTATTTAAAATTAAGAATAAAACTTAATAAACTTTTGTTTGTCACGTTTGTATTTAATGGGATGAACTTCACGTTACTTTAAATAGTAATGTTACAAAATAATGTTATAATAATTACAAAAAGGTAATAACAATAACCGTACAAAAGTAAATGCTACGCTCACTAGCATGAGTAATGAGCATCTATTTCCTGTGTCTTGACAGGACGTTCTCCTCAGGATAACCTGGTCCCATGTGACGTGCTGCTGCTGAGGGGCCGCTGCATTGTGGATGAAGCCATGCTTACAGGAGAGTCTGTGCCGCAGATGAAG[G/A]TGCGTCTGCTTGCTTTTTCCACTTCAAACTATTATACCATCAGCTTTCGGTAATTGCCTATGCTGTGTCTACAGGAACCTATAGAGGACCTGGACCCTAACAGGATCCTAGACCTGCAGACTGACTCCCGACTTCACATTATTTCAGGCGGCACCAAAGTGGTTCAGCACAGCCCACCACTGCGAGCCAGCGCAGGCCTAAAACGTTAGTACATGTGCTTCACCTGTAATGAATCATTTGACGTAATATGAAAGAATGTCAGACCAAACCAACCTGTTCAGTTCAATATATTTAAAACCGCTTGCCAAAGAAAGCTTTCAGATCAAGTTTGGTCTAGCTGTTAAACACCTTAAAAATGTTGTATTTTATATACAGTATGTGTGTATTTATACATATACATACATATAAACCGTACACATGTATAAATATTAAGTAAACTTTTGTATTGGGTGTGACTTAATTGTGATTAATAATTTGACAGCACTAATATTTGCATATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13862
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:
Founder:
SL4_06_H5
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042147 | Essential Splice Site | 373 | 887 | 6 | 18 |
| ENSDART00000058958 | Essential Splice Site | 392 | 1242 | 6 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 53551442)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 52658757 |
| GRCz11 | 3 | 52913420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTGTGGATGAAGCCATGCTYACAGGAGAGTCTGTGCCGCAGATGAARG[T/A]GCGTCTGCTBGCTTTTWCCACTTCHAWCTAYTATACCATCAGCTYTCGGT
Long Flanking Sequence:
GATGGAAATTCAGCTTTGACATCACAGAAATAAATGACATTTCAAAATGAATTCATTAAAATATAATTATATTCAACTGCACTAGTATTTTGCCAAAATATATATATTTTTTTTACTCATATTTAGTCAAATAAATGCAGAAGTTTATTTTTAAAAAACACCTTAATAACCTCCAACAGTTGGATAATACTATTTAAAATTAAGAATAAAACTTAATAAACTTTTGTTTGTCACGTTTGTATTTAATGGGATGAACTTCACGTTACTTTAAATAGTAATGTTACAAAATAATGTTATAATAATTACAAAAAGGTAATAACAATAACCGTACAAAAGTAAATGCTACGCTCACTAGCATGAGTAATGAGCATCTATTTCCTGTGTCTTGACAGGACGTTCTCCTCAGGATAACCTGGTCCCATGTGACGTGCTGCTGCTGAGGGGCCGCTGCATTGTGGATGAAGCCATGCTTACAGGAGAGTCTGTGCCGCAGATGAAGG[T/A]GCGTCTGCTTGCTTTTTCCACTTCAAACTATTATACCATCAGCTTTCGGTAATTGCCTATGCTGTGTCTACAGGAACCTATAGAGGACCTGGACCCTAACAGGATCCTAGACCTGCAGACTGACTCCCGACTTCACATTATTTCAGGCGGCACCAAAGTGGTTCAGCACAGCCCACCACTGCGAGCCAGCGCAGGCCTAAAACGTTAGTACATGTGCTTCACCTGTAATGAATCATTTGACGTAATATGAAAGAATGTCAGACCAAACCAACCTGTTCAGTTCAATATATTTAAAACCGCTTGCCAAAGAAAGCTTTCAGATCAAGTTTGGTCTAGCTGTTAAACACCTTAAAAATGTTGTATTTTATATACAGTATGTGTGTATTTATACATATACATACATATAAACCGTACACATGTATAAATATTAAGTAAACTTTTGTATTGGGTGTGACTTAATTGTGATTAATAATTTGACAGCACTAATATTTGCATATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31360
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:
Founder:
SL6_05_D2
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042147 | Nonsense | 439 | 887 | 9 | 18 |
| ENSDART00000058958 | Nonsense | 458 | 1242 | 9 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 53555991)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 52663306 |
| GRCz11 | 3 | 52917969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTATTAACATCTTAAACTTTGCTGTGTCTATATTTAGGGCAAATTAT[T/A]GAGAACGATTCTGTTTGGTGTGAAAAGGGTAACGGCCAACAACCTGGAGA
Long Flanking Sequence:
CTTTAACATTACAGCGCCTCTGGCCATGCCTCTTTGCTGTGAGAGTTGTGTGCGTGAGGTGAATGCACTTAACCAGAAGCCTTTCCTGATCTCAATAGCCCGGATGTATTTTTTATTTTTTTTGTCCCCAATTTCGTTCGCTGTATGCTTTGCTAAGCTAACTCTGTAAAAGCCAATGTCTCCTTTTGCAATGAACTTTGAGCGTCTTACATTCAGAGATGTTGTTTATATTTACACAGCTTTATTACACGTAAACTAAAGTTTAAAATACGATATTGTAGTGGATCACCCCTTTAAGATTTGCATGTGTTATTATGTAATGTCTTATTCTGTCTTTTCACAGCTGTAGACAACGGCTGTGTTGCTTATGTTTTAAGAACGGGCTTCTACACCTCTCAGGTGAGGCATTGAATCAAGGAGATGGCGTTTTACTTTTTCTTTCAGGTTGGTTTATTATTAACATCTTAAACTTTGCTGTGTCTATATTTAGGGCAAATTAT[T/A]GAGAACGATTCTGTTTGGTGTGAAAAGGGTAACGGCCAACAACCTGGAGACTTTCATCTTCATTCTGTTCTTATTGGTTTTTGCCATTGCGGCTGCTGTGTATGTTTGGGTCGAAGGTAAGTTATCTGCACATTTCTTCTTATTGTCAATGTTCAAAACAGTTTCTGTGGATAATATGATAACACGTTTTACCTTCAGCAATATTTGAAAAATAAAATCAGTAGTGTATATCTTAATTCTGTTTAAGTGATATGCCGACAAGTTTTCATTTCACTTGCTTTAATTTGATACAGTTTTACTCTGATCATAAAGAAGAATTATACATATACGCATACCCATATACGCATACCCATGCGCGAGAGATAATAAACATTTTGCCTTGCTAATCATTGACAGATCCTAAAGTAATACAAATGCTTAGGGCAGTGTCTGGCTGATACTTTCATGCCATTCAGAATCTATACAAGACCTTGAACAAGACTTTCAACTAAACTTGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20142
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:
Founder:
SL6_01_D6
KASP Assay Location:
Unknown
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042147 | Essential Splice Site | 616 | 887 | 12 | 18 |
| ENSDART00000058958 | Essential Splice Site | 635 | 1242 | 12 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 53561834)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 52669149 |
| GRCz11 | 3 | 52923812 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCCTGGAGAAGGCTATGCTGACCGCAGCAGACTGGACGCTCACTAAAG[G/A]TCTGATTAATACACTGCACAAGACAAAGGCTGAGCCACACACCATCATCT
Long Flanking Sequence:
ATAATTCTGACTTTAACTGTACACAGAGACATTGTTTTTAATAGATAGCATGATTTACTTTGTTTTATTTATTTATTTGTTTATTTTAAGTTTTATTAAAGTAAAATAACAGAGGGTTTATCTTGGTCATGCCAAATGTACCCACATATCAAATAATATGTTTTTAAAAAATGTACATTTCTAATAGGGGTCTAATGTCACAAACCCCGAATGGGAAAGCGAATATTACATTTACTATAGTTTGGTTTTACAAGTGTATAAGTTTACCCAAATATGACAGCTTCTGCATCTGTGAAGGCCAAAAATGTGAAATGTGTGTAATCGTGTTCCTCTTTTCCTCAGAGAGGGGAAACAAGTGATGCCAGTATCAGAGATTCCAGTGGACACTCATCGGGTGGTGGCCACATGTCATTCGCTGGTCACTCTAGATGATGGTCAGCTGGTGGGGGATCCCCTGGAGAAGGCTATGCTGACCGCAGCAGACTGGACGCTCACTAAAG[G/A]TCTGATTAATACACTGCACAAGACAAAGGCTGAGCCACACACCATCATCTTTTAGGCTTTATGATTTCCACATTGCTGGACATTTGGATTTTATTGAGGAGATTTATTACTGTGCACTTGCAGTGGCAGGCCTTAGGCTTTAAAACACTCTGCCTTTACATTAGATATGCACAATGTTTTGGTGGTCATATCGATATGGGCTGAAAAATTCTATTTTTAATGTTATCGTTATTGGTCCGATATTAAAATTAGGCCGATATCTTCAAGCCAATAAATTACTTAATTGTACAGAACTGCCTGCCTTGTAAGCAGGATAGAATCTTGTGAGAGTGCGGTTATGAAAACGTCAAATGACTAACAATTGTACATTACTGTAACACAGGGGTGGCCAACCCTGTTCCTGCTTTCAGTTCTTAGTTCTTTCATTTTATTTAAAAATATGTTTAAATTAATTGAATCCAGTTTTGTCATTTAACCTATTATTTTTACACAACAGTTAA
Associated Phenotype:
Not determined