Busch Lab

ZMP

atp2b4

Ensembl ID:
ENSDARG00000044902
ZFIN ID:
ZDB-GENE-061027-60
Description:
ATPase, Ca++ transporting, plasma membrane 4 [Source:RefSeq peptide;Acc:NP_001070935]
Human Orthologue:
ATP2B4
Human Description:
ATPase, Ca++ transporting, plasma membrane 4 [Source:HGNC Symbol;Acc:817]
Mouse Orthologue:
Atp2b4
Mouse Description:
ATPase, Ca++ transporting, plasma membrane 4 Gene [Source:MGI Symbol;Acc:MGI:88111]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa10432 Essential Splice Site Available for shipment Available now
sa6208 Nonsense Mutation detected in F1 DNA Not yet available
sa21897 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10432
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046122 Essential Splice Site 682 1174 12 21
ENSDART00000127791 Essential Splice Site 682 1174 11 21

The following transcripts of ENSDARG00000044902 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 11 (position 23914231)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 22726828
GRCz11 11 22979852
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGACATGCATCTGTGTTGTYGGCATTGAAGACCCTGTCCGTCCTGAGG[T/C]GAGCAAAACCATCCAATTTGCTTGTTCCAAATAGTGACRTGCTTGTGCAT
Long Flanking Sequence:
AAAATCTAAATCAAGTAATTTTAGAATGTCAAAGTCAAATTTATACATATAAAATATATTTTCCCAACAACAAAATTGTGACAAGTGAAAATGGAGAGTGGCTAGTAATGTTGAAAAACTACTAGCCACAGTGGCTAGTGTTTAAAAAAAGTTAATGTCAAGCCCTGTTTGTCTGATATGTTGAGACATTTAATATGGTTTTAAAAAATGAAAGAAATTTGAGATGCAAATTTGTATATTTTCTTATTAAAGCTTTCTCTTGTCCATCAGGTGTTCCCATATCCTTGATGCTTCAGGCCAGCAACGTGTCTTCAAGGCCAAAGATCGGGATGAGATGGTGCAGAAAGTGATTGAGCCAATGGCCTGTGATGGGTTAAGGACCATTTGTGTAGCCATGAGGGACTTCTCAACAGAGCCAGACTGGGACAATGAGGCTGACATTTTGAATGACCTGACATGCATCTGTGTTGTTGGCATTGAAGACCCTGTCCGTCCTGAGG[T/C]GAGCAAAACCATCCAATTTGCTTGTTCCAAATAGTGACGTGCTTGTGCATACTGCACATGGACTGCAGATTTATATATTTCAGGCCTTTGTTCGTAATGAGACAAGACAAGCATTAAGGGGCATCTTGTCAGGAGTGGGGCAACCCGCCACTTTTTGTGTAATGAAAATGTATTGACCGTGATTATCATGTGATGATGATGGATTATTTGCAGAGTGTCGAGCACTATGTGGAAGTGTGGACAGGAATAGCCTCATCGACGGAGGGACAAACTGACCTAATTCCTTTGAAGGTGGTGAAATGAGTACATGACAGGCGATTGCGCTGTTCTTGATTATGAATATTGGATCAGTGCAGAATTTACATCAGCTTCTCTTAAATGAGGCAGCATGTATAATTCTATAATGAAACGCATTACTGATATTTAGGTTAAATTGATTCCTGCAGGCTTTAATTAAGTGGATTTTTTTAATCCATTGTATTGGCGTTCCATTTTTAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6208
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046122 Nonsense 910 1174 17 21
ENSDART00000127791 Nonsense 910 1174 16 21

The following transcripts of ENSDARG00000044902 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 11 (position 23900935)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 22713532
GRCz11 11 22966556
KASP Assay ID:
554-5190.1 (used for ordering genotyping assays)
KASP Sequence:
GCTTTGGCAACAGAACCCCCAAYAGAATCGCTCCTTCTGAGAAAACCGTA[C/A]GGTCGCGACAAGCCACTCATTTCTAGGACTATGATGAAGAATATATTGGG
Long Flanking Sequence:
AAAGATTGACGCAGCTTCTCCTACCATTTTTAAACATTTTTTTACTGTTGATATTTGGCACCAGTTTATCAGGAAGTGACTATTTAGTTTTCTTTGACTCGTTGGATGGAAATGCTGCTTTATTCGCATGTCTTATATGCGATAATCCGGTTTTGCGCATTTTTAGATGGAAACATAGCTAATGTTCCATAATAAAAGAACTCAAATCTGTGTATTTCATATTTAGTGATGCATACTGTACTGTGGCCATTTAGTGCCGGTGCCAGACTTGTATAATATGGGGCCGGCCAGTCTTTCTGTGACGCTGTCTAATTACATTAAGTATGACAATACTGTAGTAATGTCCTTTCTATGGAGTCACGCATAAGTTTGTTTTGTCTGCAGGACTCCCCACTTAAAGCCGTTCAGATGTTGTGGGTAAATCTAATTATGGATACACTGGCTTCTTTGGCTTTGGCAACAGAACCCCCAACAGAATCGCTCCTTCTGAGAAAACCGTA[C/A]GGTCGCGACAAGCCACTCATTTCTAGGACTATGATGAAGAATATATTGGGTCATGCTATCTACCAACTCGTCATCACATTTACTCTTCTATTCGCTGGTAAGAGACTTCTGTTTTCATGATGATGTTTAAGCAAATTTTGTGAAATGTGTTTAGCATTGAACTGGTGGAAACTTTGCATTTCAGGAATAGGCTCTGGTTAATTGCATTTTATGGATGGGACTGATGGTTTGTTGAGATGTATGGTTGCTTAGCAACTAGCGTTTATATTTGCAGTATTCAAAGCAGCCATAAGAACAGAGGGATGTTTTACAGTATAAGATGTTTTAGGTTAAAATCATAAAAAATTTTATGAATCTAAGCATTGTATTTTGTCTATTGAAAGACATAAAATGCACATTTGCACTAATTTATTTTATTTTATTTTTTATTTTTATGTAAATGTTAACATTTAACATTAACATAATGAGGGGGTGGGGGGGTCTTGCTAGGAAACCATCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21897
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046122 Nonsense 1102 1174 20 21
ENSDART00000127791 Nonsense 1102 1174 19 21

The following transcripts of ENSDARG00000044902 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 11 (position 23885293)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 22697890
GRCz11 11 22950914
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTGACCACGCTGAGATGGAGCTGCGCAGAGGACAGATCCTGTGGTTC[A/T]GAGGACTCAACCGTATCCAGACTCAGGCAAGCTCACCTTTTATGGTTCTT
Long Flanking Sequence:
AATGTTTGAAGGGTGAGTAAATGATGACATAGTTTTCAGTTCTGGTTGTACAATCCTTTTTTAATAGTACGCGAGAAACATTTTGTCAGGAAATCCTACAAAGCTTTTTATACAGTTTGGACAGAAAACATACAGAAACTAAAAGCCCTTTTTGCATTACATGCAAGCATTTTGCGGTCAGATGCCATAAGGATGTAGATTATAGAATCTCCATTTGTGCACCACATATAAAGCATCCTGTTCTCGGAAAATTGTTCACAATCCCAACCACTGTGCTAATGACTATTTTATGAGTTACAGTTCCCATCATTTGACCTTTTTTTTCTCCCTCTTTATCCCCCCAGTTGATCACTGCTATCCCCACACATCGCCTCAAATTCCTGAAGGAGGCCGGTCACGGCATTCCCAAAGAGGACATCGCAGAGGAGGTGCTGATTGAAGGTGCTGATGAAATTGACCACGCTGAGATGGAGCTGCGCAGAGGACAGATCCTGTGGTTC[A/T]GAGGACTCAACCGTATCCAGACTCAGGCAAGCTCACCTTTTATGGTTCTTTACTTGCTGTCTCTTCCAGCAAATGTCTCTGGAGGGAATATTTATATAATGTTAATGTATAATAGCAGTGAACAGTGTTGGGGAAAGTTACTTTTGAAAGTAATGCATTATAAAAAAAAGTAACTAATTGCTTACTGAGTTACTTTTTATGCAAAGTAATTCATTACATTACTTTTGAGTTACTTTTGCGTTAGATTTCTTTGCCTAGCTGAGGTTTGATCTCTTTCGGAACTTGCAGGTGTTTTTACCTGTTTTATAGAGAAGCATATTTATACATATTCATTTTCCTTTAAACATGTAGGATAATATTATATTTTGAGAATCTTCTGAGCCCAGAGCTATACATGCTACATATACAGAGTAATGACAGCATGTAAAGTAGTGTGTTTGTTACTTTTGTACATTTTGTGTTATTAATTAAGTAAATTCTCTGGCCATTAAGGTAAACAT
Associated Phenotype:
Not determined