ZMP
atp2b1a
Ensembl ID:
ZFIN ID:
Description:
plasma membrane calcium-transporting ATPase 1 [Source:RefSeq peptide;Acc:NP_001038222]
Human Orthologue:
ATP2B1
Human Description:
ATPase, Ca++ transporting, plasma membrane 1 [Source:HGNC Symbol;Acc:814]
Mouse Orthologue:
Atp2b1
Mouse Description:
ATPase, Ca++ transporting, plasma membrane 1 Gene [Source:MGI Symbol;Acc:MGI:104653]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40264 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33434 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40264
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014257 | Nonsense | 122 | 1215 | 3 | 20 |
ENSDART00000077664 | Nonsense | 122 | 1228 | 3 | 21 |
ENSDART00000123224 | Nonsense | 125 | 1226 | 2 | 21 |
ENSDART00000126958 | Nonsense | 122 | 334 | 3 | 9 |
ENSDART00000128079 | Nonsense | 122 | 1228 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 15164504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16100357 |
GRCz11 | 4 | 16099112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGATTATTTTGGAAGTGGCAGCAATAGTTTCTTTAGGCCTTTCTTTTTA[T/A]AAACCTCCAGATGCAGGAGATAAAAGTAAGTAACCTGTTTATTTCCTTCT
Long Flanking Sequence:
TTTTATAGTGCAATATTATTTCACAGTTTACACTGTATTTTTAATGAAATAAATGCAGCCTTGGTGAGCAGGAGAAGCTTATTTAAAAACATTTCAAAATCCTACTGACCCCAATCGACTTTTGAACAGTAGTGTACCTCCGCCACTTAGTACTGGTTTTGTGGTCCAGACTTGCATTTAATGCTGCATTGGATGAAAATAATAGATTTTCTAATCAAAAAAAAAAAAAAAAAGATTGCATTCAATAGCATGAAACGTAATTTCTTGTCCTAATCAGTATATAATTGAACGATTAATTGTTGCCTTTTCACTTCCTTTTTCCTTCCAGGTTTAAGTGGGCAGCCCTCAGATATTGAAAAAAGAAAAGCAGCATTTGGACAGAACTTTATACCTCCGAAAAAGCCAAAAACCTTTCTTCAGTTAGTATGGGAAGCATTGCAGGATGTAACATTGATTATTTTGGAAGTGGCAGCAATAGTTTCTTTAGGCCTTTCTTTTTA[T/A]AAACCTCCAGATGCAGGAGATAAAAGTAAGTAACCTGTTTATTTCCTTCTACCTTATTTATTGTTTATCCTCTCAGTTTTAGGTTGTTCTGAGCTGAGTTTTTTTTTTGTGTGCGTGTTTGTGTATGTGTAGATTGTGTGAAGGGAACGGGTGGAGAACCTGAGGAAGAAGGAGAGACAGGGTGGATAGAAGGTGCAGCTATCCTGCTTTCTGTTGTTTGTGTGGTGCTCGTGACTGCGTTTAATGACTGGAGTAAAGAGAAGCAGTTCCGTGGCTTACAGAGCCGCATTGAACAAGAGCAGAAGTTTTCGGTGGTTCGTGGAGGGCAAGTCATTCAGATCCATGTGGCCGAGATTGTCGTCGGGGACATTGCACAAATAAAATATGGTAAGATTGAGATTTTCTTTTTAAGATAATGAGATTTTTGAATTATAATGTTTAAAAAAGAAATTAAACTGTACAAGTTTGATGGTTGGGTAACGAGTAGGGCTTTGCAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33434
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014257 | Nonsense | 420 | 1215 | 8 | 20 |
ENSDART00000077664 | Nonsense | 433 | 1228 | 9 | 21 |
ENSDART00000123224 | Nonsense | 430 | 1226 | 9 | 21 |
ENSDART00000126958 | None | None | 334 | None | 9 |
ENSDART00000128079 | Nonsense | 433 | 1228 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 15154451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16090304 |
GRCz11 | 4 | 16089059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTAAGTTTTTCATCATTGGTGTGACCGTACTGGTGGTGGCCGTTCCT[G/T]AGGGTCTTCCGCTGGCTGTTACCATCTCATTGGCTTACTCTGTCAAAGTA
Long Flanking Sequence:
GATGACTCATCCTGCACTACACAGATTCTCACCCAGTCAGATTCTCTCTATAATAATAAAATCCTGCTGCCTCCTGGTACTTCTTGTGATTGACTAGTCTTCATGGCTGTGGCATTACTAAAGCCTTTTGGCTATTAAAAAATGGATGTCTCTTCAAAATGTTGGGTTTTAATAGGAAATATGTCAGCACAGGACACAAAGCTGCATTTGTCAAATGGCTTGCTGAGGTCTTGAGGGCTAACAGTCAATCTCACACTGGTAATGGTTTTTGCTGGGACATCAGATGCATTTAGCGTGGGCTCCAGAGGTGCTAATGTATGTGTCCTTTCGCAGGTTTGTTGATGTCAGCCATCACCGTGATCATCTTGGTGGTGCTGTTCGTGGTGGACACTTTCTGGGTGGATAAGATTCCTTGGGATTCAGGATGTATACCCATCTACATCCAGTTCTTTGTTAAGTTTTTCATCATTGGTGTGACCGTACTGGTGGTGGCCGTTCCT[G/T]AGGGTCTTCCGCTGGCTGTTACCATCTCATTGGCTTACTCTGTCAAAGTATGACTTCGCTTTTCTGTTTTAATGTTTCGATTTTTCATGACTAACTTCTTCTATCTTAGAAGTGAGCCCTGTTTGTTGAGCCAAACAATATGTTGATCCAATGAAGATGATCTGCTATTTCCATTCATGTATATTTTTTACTGCAATTATCGCTCATCTCATACAGTAGCATCACTTCTGGATGTTGTTTAATTGGGGATTAGTGGACATTCCTGTTTAATCTTGCATTCAAGCTGTTTATTGTTTTGTGTGTCTGTCTACCAGCCTCTTATCCCAAACCAATTGTTTCACTTTGCTTCTGTGTTTCAGAAAATGATGAAGGACAATAATTTAGTGAGGCATCTTGACGCCTGCGAAACCATGGGCAATGCCACAGCCATCTGTTCAGATAAGACAGGAACTCTGACTATGAATCGGATGACAGTAGTTCAGGTTTTTATTGCTGACAAG
Associated Phenotype:
Not determined