ZMP
atp2b3a
Ensembl ID:
ZFIN ID:
Description:
plasma membrane calcium ATPase 3a [Source:RefSeq peptide;Acc:NP_001002472]
Human Orthologue:
ATP2B3
Human Description:
ATPase, Ca++ transporting, plasma membrane 3 [Source:HGNC Symbol;Acc:816]
Mouse Orthologue:
Atp2b3
Mouse Description:
ATPase, Ca++ transporting, plasma membrane 3 Gene [Source:MGI Symbol;Acc:MGI:1347353]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18912 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2421 | Nonsense | F2 line generated | Not yet available |
sa10745 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18912
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 |
---|---|---|---|---|---|
ENSDART00000045917 | Essential Splice Site | 320 | 723 | 7 | 13 |
ENSDART00000090252 | Essential Splice Site | 320 | 1245 | 7 | 22 |
ENSDART00000093117 | Essential Splice Site | 320 | 1176 | 7 | 20 |
ENSDART00000133922 | None | None | 177 | None | 4 |
ENSDART00000135811 | Essential Splice Site | 320 | 1248 | 8 | 21 |
The following transcripts of ENSDARG00000043474 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 14544251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13989595 |
GRCz11 | 8 | 14027300 |
KASP Assay ID:
2260-0280.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAGCTCTAATTCTACTTGCCTTGATCAATTTGTCTCCACCCTCCACA[G/A]CTAAGAAACAGGATGAGGCTGTTGCCATGGAGATGCAGCCTCTGAAGAGT
Long Flanking Sequence:
CTTGATTTCCAATTCCGGCTTAAGGACATTTCACGACCTTACCACCCTCGCTCTTTTCCACATCACTTCCTATCTCATTAATGTCCTATCTAATTAAGACAAAAGGGCCAAAAATAAATCTTAAAAAATAAAAAAGTAACTCAAATATTATTATTTTTAAATTTTTTTCAAGTCATTACTTTACTCCTTACTTAGAAAAGTAATATTATTACATAACTTGTCATGCGTTACCCTCAAGACTGTATAAACAGTAACTATACTTTCATTCCGGTGTATGTGCTATGGCAGCATTGATATTCTGCAGCACCTGAAAATAAGATTATAGTGTACTTTTAATGCATTTTATATATTTTTGCAAAATTTCACACAGAACAAATAAGGATAATGTACTTTTTATGCATAGTATACAGTAAGCATACAAGCCACGACATAGTGTCTCCTATTTCCTACTATTAGCTCTAATTCTACTTGCCTTGATCAATTTGTCTCCACCCTCCACA[G/A]CTAAGAAACAGGATGAGGCTGTTGCCATGGAGATGCAGCCTCTGAAGAGTGCAGAAGGTGGTGAAGTGGAGGAGAAAGAGAAGAAAAAAGCCAGTGTGCCCAAGAAGGAGAAATCCGTTCTTCAGGGCAAACTCACCAAGCTGGCAGTGCAAATTGGGAAAGCAGGTGAGGAGGTGTTAGACTCTTTTAGGACAAATTCTTCTTTTTATATTAGTATCAGTTTTGTTTTTACATTTACACTTCACTGAATTTCTGAATAATACATTTAAATATGTTTTAATCAAGTGATTACGCTGTCTGAATTCAGAAAATAAGCATTGGGCACTTTCATCTAAAGTTTGGTAACACTAAAAGAATAACTCAATATTTTGTTATAGGGATAGTTTACCCAAAACTGAAAACTGTCATCATTTACTCACCCCGGATTATTCCAAGTAAATTTGAGTGTTTTCTATTGAACGGAGGAGATTTTGAAGAACTGACATCCGTTGTAGCCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2421
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000045917 | None | None | 723 | None | 13 |
ENSDART00000090252 | Nonsense | 883 | 1245 | 16 | 22 |
ENSDART00000093117 | Nonsense | 883 | 1176 | 16 | 20 |
ENSDART00000133922 | None | None | 177 | None | 4 |
ENSDART00000135811 | Nonsense | 883 | 1248 | 17 | 21 |
The following transcripts of ENSDARG00000043474 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 14529650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13974994 |
GRCz11 | 8 | 14012699 |
KASP Assay ID:
554-2680.1 (used for ordering genotyping assays)
KASP Sequence:
CATTCAATTTTTTNATGCATTTGTGCATAGGATTCACCCCTGAAAKCTGTG[C/T]AGATGCTTTGGGTCAATCTGATCATGGACACATTTGCTTCTCTTGCTCTT
Long Flanking Sequence:
AATAACTGTTAATATACAGTAACTAACATTGGATAAGGTTAGGTTTAGGGGGAGGTTCAGGGGTTAATATTTAGTTAGTACCTAATTTGAGTACTTGAACTGGACTATAAAGTGCCGTTCTTAAGCATGTACACGTTTAGTTTTTTTTTTTGATAAATTTTGTTAAACTAAAACACATTTACTCTTGTGTTCCAGGAATCTGCCAAAGGTACACTGAGCCGTTAGTTACAAATGCCAAGGGATTAAACAGTCAGAAATGAATTCATTAAAAATAATAATAAATCAAGGTTTAAGCTAAAACACAGAAAAAAAAACTGAAAATGAAATGTTACATCACAGGAATAAACAACATTTTGAAAGATGTTTAGTTTTAAATAAATATTTTTTAATATAATAATTACATTTAATTTAATAAAAAATCTCATCCTAAAGATTTTAAATGATACCTGGCATTCAATTTTTTATGCATTTGTGCATAGGATTCACCCCTGAAAGCTGTG[C/T]AGATGCTTTGGGTCAATCTGATCATGGACACATTTGCTTCTCTTGCTCTTGCTACGGAGCCGCCAACGGAAGCTCTGCTCCTGAGGAAGCCTTATGGCCGAAACAACCCTCTCATCTCCAGAACGATGATGAAGAACATCCTTGGACATGCCGTCTACCAGCTCGTCATCATCTTTACCTTGCTCTTCGCCGGTATGTTCCTTCACTGCTTCTGTCAAAGGATTTGTTGGATACAAGTTCTGCTCTATTTCATCTCTTTTTATTCTTGTTAAATGTACCGGTATGTGATGAAGCTGTAATTTTTTTGCACAGGTGAGAGGATCTTTGACATTGACAGCGGCCGTGATGCTCCGCTTCACTCTCCTCCATCTGAGCACTACACCATCATCTTTAACACGTTTGTCCTCATGCAACTCTTCAACGAGATCAATGCCCGTAAGATTCACGGAGAGAGGAACGTGTTCGATGGGATATTCTCAAACCCCATATTCTGTTCGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10745
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 |
---|---|---|---|---|---|
ENSDART00000045917 | None | None | 723 | None | 13 |
ENSDART00000090252 | Nonsense | 916 | 1245 | 16 | 22 |
ENSDART00000093117 | Nonsense | 916 | 1176 | 16 | 20 |
ENSDART00000133922 | None | None | 177 | None | 4 |
ENSDART00000135811 | Nonsense | 916 | 1248 | 17 | 21 |
The following transcripts of ENSDARG00000043474 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 14529551)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13974895 |
GRCz11 | 8 | 14012600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCTACGGAGCCRCCAACGGAAGCTCTGCTCCTGAGGAAGCCTTATGGC[C/T]GAAACAACCCTCTCATCTCCAGAACRATGATGAAGAACATCCTTGGACAT
Long Flanking Sequence:
CTGGACTATAAAGTGCCGTTCTTAAGCATGTACACGTTTAGTTTTTTTTTTTGATAAATTTTGTTAAACTAAAACACATTTACTCTTGTGTTCCAGGAATCTGCCAAAGGTACACTGAGCCGTTAGTTACAAATGCCAAGGGATTAAACAGTCAGAAATGAATTCATTAAAAATAATAATAAATCAAGGTTTAAGCTAAAACACAGAAAAAAAAACTGAAAATGAAATGTTACATCACAGGAATAAACAACATTTTGAAAGATGTTTAGTTTTAAATAAATATTTTTTAATATAATAATTACATTTAATTTAATAAAAAATCTCATCCTAAAGATTTTAAATGATACCTGGCATTCAATTTTTTATGCATTTGTGCATAGGATTCACCCCTGAAAGCTGTGCAGATGCTTTGGGTCAATCTGATCATGGACACATTTGCTTCTCTTGCTCTTGCTACGGAGCCGCCAACGGAAGCTCTGCTCCTGAGGAAGCCTTATGGC[C/T]GAAACAACCCTCTCATCTCCAGAACGATGATGAAGAACATCCTTGGACATGCCGTCTACCAGCTCGTCATCATCTTTACCTTGCTCTTCGCCGGTATGTTCCTTCACTGCTTCTGTCAAAGGATTTGTTGGATACAAGTTCTGCTCTATTTCATCTCTTTTTATTCTTGTTAAATGTACCGGTATGTGATGAAGCTGTAATTTTTTTGCACAGGTGAGAGGATCTTTGACATTGACAGCGGCCGTGATGCTCCGCTTCACTCTCCTCCATCTGAGCACTACACCATCATCTTTAACACGTTTGTCCTCATGCAACTCTTCAACGAGATCAATGCCCGTAAGATTCACGGAGAGAGGAACGTGTTCGATGGGATATTCTCAAACCCCATATTCTGTTCGATCGTGCTGGGTACATTTGCAATACAGGTAAAAACGCACAAATCTCAAGATTTAGGCTTGATTTCTGGGTTTGATTTCTGGCTTATTTAATGTCTCTTAATT
Associated Phenotype:
Not determined