Busch Lab

ZMP

atp2b3a

Ensembl ID:
ENSDARG00000043474
ZFIN ID:
ZDB-GENE-040718-174
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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