ZMP
atp2a3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 (ATP2A1
Human Orthologue:
ATP2A3
Human Description:
ATPase, Ca++ transporting, ubiquitous [Source:HGNC Symbol;Acc:813]
Mouse Orthologue:
Atp2a3
Mouse Description:
ATPase, Ca++ transporting, ubiquitous Gene [Source:MGI Symbol;Acc:MGI:1194503]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33633 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12264 | Essential Splice Site | Available for shipment | Available now |
sa11614 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33633
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 |
---|---|---|---|---|---|
ENSDART00000086443 | Essential Splice Site | 211 | 849 | 3 | 16 |
ENSDART00000133432 | Essential Splice Site | 292 | 932 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 32868758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 30630990 |
GRCz11 | 5 | 31231143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGACAAGACTGGGACCCTGACAACCAACCAGATGTCTGTCTGCAGG[G/A]TAAGTGATGTGGCTGTTCCAGCTAGACACAGAGATGCTGTCTCATTCAGC
Long Flanking Sequence:
TGCTTATTTGTGCATCTGCTCATGTTTTCCGAAAGGGCACAAACATCGCTGCAGGCCGGGCAATCGGTGTCGTCGTCTCCACTGGGGTTTCCACCGAAATCGGCAAGATCCGTAACCAGATGGCGGCAACAGAGCAGGAGAAGACCCCACTGCAGCAGAAGCTGGATGAGTTTGGTCAACAGCTCTCCAAGGTCATCTCGCTCATCTGCATTGCCGTCTGGGTCATTAACATTGGCCATTTTGCTGACCCAGTCCACGGCGGGTCCTGGATCCGAGGTGCCATCTACTACTTCAAGATTGCTGTGGCCTTGGCAGTAGCAGCCATCCCTGAGGGTTTGCCAGCTGTCATCACCACCTGTCTGGCACTGGGCACCCGTCGCATGGCCAAGAAAAATGCCATTGTCCGTTCACTGCCCTCGGTGGAGACGCTGGGATGCACCTCCGTTATCTGTTCAGACAAGACTGGGACCCTGACAACCAACCAGATGTCTGTCTGCAGG[G/A]TAAGTGATGTGGCTGTTCCAGCTAGACACAGAGATGCTGTCTCATTCAGCATCGGAACTGATGTCTGCGGGCAGATTTCAATTTTTATGTCTGATACGATGACATCTTCATTTTTCATTTTGTTTTTCACTGAAATATGGTCCTATGTGAGCTTTCTTTTAATATAGATCTTAAAAGCACAGATTTAGAACTAGGTGGTTTATTGTGTGCTTTAACGAGAGCCAGAACTTTCAAATCTTCATGAGCCACTGGAGATTCCAAAATCATGATCCATGTGAGGAATCCCCCCTTTTATATACATAAAAAAAATCAAAAGAGACCCTTGAGGCCAGAGAGAGTCATGCTAATTCCTTTTATACCACATCTCAGGATTCTTTCCCACTGATTCCAGACCCGTGTGTAGGTCTTTACTGTGGTTTGTGGAGCACTGGCAGGTGGGTTTCACAGGCCTGAATATTACAGTGGTGTTTACCGTCAGAGCAGGTCTTTGATGCTGTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12264
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086443 | Essential Splice Site | 319 | 849 | 6 | 16 |
ENSDART00000133432 | Essential Splice Site | 400 | 932 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 32883885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 30646117 |
GRCz11 | 5 | 31246270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCTATCTGGACTCAGTAAAGTGGACAGAGCTGCAGCTTGCAACTTGG[T/A]AAGAAAGAGCCACAGGGTGCAGGAGGATATGAGACCRACTGMAATAAAAG
Long Flanking Sequence:
ACTACTTAAAATGACATGAAAATTGACGGTAACACTTTTGATGTTTAAAAATGTAACAATTTTGATGGTAAAAACCATCAATGACAATGACAATTAGTTGCAATGTAACTTAAATTCAACAAACAGACCATCAAAATAAAGTGTGACCAAATTGACTGACCCCTAATTTTAATGTTATACAGTTATACAGTATGAGGTTGCATTGCTTTTTACTTGCTTATTTGCTTTATTGCTTTCGTTTGACATTTAAAGTGCAAAGCAACTATCATTTCAAAAGTGGGTGCTTGACTCCAGGCTTGTGTTTAAAATGAATATACCAGTACTGTATATTTTGTTTACACACTTATGTTCTTATTCTGTACCACAGGCCAAAGGAGTGTATGAGAAAGTGGGAGAAGCCACGGAAACCGCACTCACCACGCTGGTGGAGAAGATGAACGTGTTTAAAACAGACCTATCTGGACTCAGTAAAGTGGACAGAGCTGCAGCTTGCAACTTGG[T/A]AAGAAAGAGCCACAGGGTGCAGGAGGATATGAGACCAACTGAAATAAAAGAGCACATTACTTCTGCTGAAAGTGATGAGAAATGATAGATATATATAGAGAGAGGTATAGTTGAGGCTTTAGACAAAGTGTTTTTTCTTTGTGTTTTTTTTAGTTATTCTACTACTGCTACTAATACAATACTACAGTAACTATGTAGTAAATATTTATGATGTTTTAGTTTAGTTTATCATTGCTTAACTTAAAAAAATGAATAAATAAAAAACAAGCAGATTAATGGATTTCTTAACTGTTTTTTTTTTCAGTTTCTTTGAATGGTGAATTAATTCATTTTATTAACTGAGGGTTTTGTTGACTTCTTGTTGCACGTTTACTAAAATACTATTGTATTTACTTGTACTTATAATTAATATTTGTAATTAATGACTTTTTTCTGCTTTTTATTTATTGGAAATTGGTTATTGAAATTTCTTTTACACTGGTTGTCTTGTCTGCTCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11614
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 |
---|---|---|---|---|---|
ENSDART00000086443 | Nonsense | 594 | 849 | 10 | 16 |
ENSDART00000133432 | Nonsense | 675 | 932 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 32893728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 30655960 |
GRCz11 | 5 | 31256113 |
KASP Assay ID:
2259-6004.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTCTCTGATGATAACTTCTCCACCATCGTGGCYGCCGTGGAAGAGGGA[C/T]GAGCTATCTATAACAACATGAAGCAGTTYATTCGTTAWCTCATCTCCTCC
Long Flanking Sequence:
CAAAACCTTTGAATAAATAAAATAATAATAAATTTTGAATAAATAATACAATAGTAATAACTTGAATATATTTTTTAAGAATGACCATTTTTATCCTTAGCATTTAGACTTGGTTTAAAACCTTCATGAAAATAAATGTAATTGAGTACTTTTTCAAAATTTGTTCAGTTTTAAATTGAAATGAGATAAGAAGCAAATGCTTGTAGAACAATATTCTAAAATTGAAATTGTTCAGCAATTTAGTTAAAGGTTAAAGATGATTTAAATGTTAAACGCATCATGTAAACAGCTCATTATTGTCTTTTAAGCCCTTACCCTTACTCCGTTCTTTCCTCCAATCTAATTTTTAGACAGGTGATGGTGTGAATGACGCCCCTGCTTTAAAAAAGGCTGAAATTGGCATCGCCATGGGCTCGGGCACAGCAGTAGCCAAATCTGCCTCCGAGATGGTGCTCTCTGATGATAACTTCTCCACCATCGTGGCTGCCGTGGAAGAGGGA[C/T]GAGCTATCTATAACAACATGAAGCAGTTTATTCGTTATCTCATCTCCTCCAACGTGGGAGAGGTGGTGTGGTGAGTAGTGCAGCGTGTCCATTCAGATGTTCACAAATTATCTATTCCATTATTGATTCAATTCTCTATTCGGTTCAGTAAATAAAAAGTTAATATCAATGCTATTGATATTTCTAAGAATGCACAATGAAAACTTTACTGTATGTCAAATGCATTAAATAAGTATTCAAAAAATGAAATATGGCCATGTATTTTCAGTGAGCGGATTATCTATTTATACTGTACTGTATATAGGCACAAACATACAGTATAGATGTACAAAGATTCTGAATAGATGCAATAAATTTGACATATTAAAGCTTATTAAGCATATGGTATGCTTATTTCTTTTGTTCTTTGTTTAATACGTTTAATATTGCCGACACAGTATATCATTAGGTGGCTGTCACTTTAAAATGATAGATAGATAGATAGATAGATAGATAGATAG
Associated Phenotype:
Not determined