ZMP
atp1b3a
Ensembl ID:
ZFIN ID:
Description:
ATPase, Na+/K+ transporting, beta 3a polypeptide [Source:RefSeq peptide;Acc:NP_571296]
Human Orthologue:
ATP1B3
Human Description:
ATPase, Na+/K+ transporting, beta 3 polypeptide [Source:HGNC Symbol;Acc:806]
Mouse Orthologue:
Atp1b3
Mouse Description:
ATPase, Na+/K+ transporting, beta 3 polypeptide Gene [Source:MGI Symbol;Acc:MGI:107788]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31268 | Nonsense | Available for shipment | Available now |
sa32871 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25786 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31268
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022549 | Nonsense | 111 | 278 | 3 | 7 |
ENSDART00000100282 | Nonsense | 108 | 275 | 5 | 9 |
The following transcripts of ENSDARG00000015790 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 16383293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16894120 |
GRCz11 | 2 | 16562710 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACAGATCAGATCCTCTTGAATATGGCCAGTATGTCCAGCATCTAGAAT[C/A]GTTTCTGCATCGTAAGTGCTCAGCATACATCCTTTGAAACATTTCTGAAC
Long Flanking Sequence:
TATGTTTATATTTTACAGTGTTAACACAGATATTTAATTTGAATAAAAATTATTAGAAAATATATGATTTGTATAAGATATTTTTAAAAATGTAAGCTCTATAGCAAAAGTCTAATCAGTTTAAATCTGCTGATCAAAAGCTAATCATCAAAGGTACTACTTTCCAGGCCTCATCCTGCTCTTTTACTTGGTCTTCTATGGCTTCTTGGCTGCCATGTTTGTCTTCACTTTGTGGGTGATGCTTCAGACACTGAATGACGACACACCAAAGTATCGAGATCGTGTTGCGTCCCCAGGTAAGTTTGTTAGTGTGCAGTTTTTATTATCGAGCTGTTTTTTACATGACTGTAGTGCAACAAAACTGTAAACGTTCATTTAAAACGCATTTAATGTCAGTTTAAATTTTGTTGCAGGGTTGGTTATCAGGCCAAATTCTTTGAATATAGAGTTTAACAGATCAGATCCTCTTGAATATGGCCAGTATGTCCAGCATCTAGAAT[C/A]GTTTCTGCATCGTAAGTGCTCAGCATACATCCTTTGAAACATTTCTGAACTGGTTACATAATATTGTACTTGTATATTTATAGTGTCTCTATGTTCCGTTTCCAGAATATAATGACTCGGAACAAGCCAAAAATGACTTGTGTATGGCGGGACAGTACTCTGAGCAGGATGGGGAATCTCTGAAAAAGGTTTGCCAGTTCAAGAGGAGTTTACTTTATAGTTGCTCTGGGATGGAGGATACCACCTTCGGCTATGCTAAAGGACAGCCATGTGTTATTGTTAAGATGAATAGGGTGAGTAACCTTTGGGGTCAGAACCATTTTTACCTTTTATTTTGTTTTATAGTGAACCAGAAACATATGATCAGTGATTTTTACAAAAATGTAATTACAAAAATAATAATTACAAGAAATATTAACTGTGTTCCAAATCATAATATTAGATTGATTTCTGATGAATTATGTGACACTTAAGACTGGAGTAATGATGCTAAAAATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32871
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 |
---|---|---|---|---|---|
ENSDART00000022549 | Nonsense | 127 | 278 | 4 | 7 |
ENSDART00000100282 | Nonsense | 124 | 275 | 6 | 9 |
The following transcripts of ENSDARG00000015790 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 16383150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16893977 |
GRCz11 | 2 | 16562567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCGTTTCCAGAATATAATGACTCGGAACAAGCCAAAAATGACTTGTG[T/A]ATGGCGGGACAGTACTCTGAGCAGGATGGGGAATCTCTGAAAAAGGTTTG
Long Flanking Sequence:
ATCATCAAAGGTACTACTTTCCAGGCCTCATCCTGCTCTTTTACTTGGTCTTCTATGGCTTCTTGGCTGCCATGTTTGTCTTCACTTTGTGGGTGATGCTTCAGACACTGAATGACGACACACCAAAGTATCGAGATCGTGTTGCGTCCCCAGGTAAGTTTGTTAGTGTGCAGTTTTTATTATCGAGCTGTTTTTTACATGACTGTAGTGCAACAAAACTGTAAACGTTCATTTAAAACGCATTTAATGTCAGTTTAAATTTTGTTGCAGGGTTGGTTATCAGGCCAAATTCTTTGAATATAGAGTTTAACAGATCAGATCCTCTTGAATATGGCCAGTATGTCCAGCATCTAGAATCGTTTCTGCATCGTAAGTGCTCAGCATACATCCTTTGAAACATTTCTGAACTGGTTACATAATATTGTACTTGTATATTTATAGTGTCTCTATGTTCCGTTTCCAGAATATAATGACTCGGAACAAGCCAAAAATGACTTGTG[T/A]ATGGCGGGACAGTACTCTGAGCAGGATGGGGAATCTCTGAAAAAGGTTTGCCAGTTCAAGAGGAGTTTACTTTATAGTTGCTCTGGGATGGAGGATACCACCTTCGGCTATGCTAAAGGACAGCCATGTGTTATTGTTAAGATGAATAGGGTGAGTAACCTTTGGGGTCAGAACCATTTTTACCTTTTATTTTGTTTTATAGTGAACCAGAAACATATGATCAGTGATTTTTACAAAAATGTAATTACAAAAATAATAATTACAAGAAATATTAACTGTGTTCCAAATCATAATATTAGATTGATTTCTGATGAATTATGTGACACTTAAGACTGGAGTAATGATGCTAAAAATGCAGGAATACATTTACATTTTAACTGTACTTTGATGAAACTAATATACAACGGAGGTGAGGATCCAATTGCAGATTCTTTATTAATAACAGAAGTCAGGCAGGCAAGGGTCTATGGAGACAGATTAGACTCAATAATAATTCACGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25786
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 |
---|---|---|---|---|---|
ENSDART00000022549 | Nonsense | 218 | 278 | 6 | 7 |
ENSDART00000100282 | Nonsense | 215 | 275 | 8 | 9 |
The following transcripts of ENSDARG00000015790 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 16374394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16885221 |
GRCz11 | 2 | 16553811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTATTTCCCCCATGAGGGGACTATTGATAGGATGTACTTCCCTTACTA[T/A]GGGAAAAAGACACATGTAAGTATGGCAGTCAGCACATGCTTTAAAGGATT
Long Flanking Sequence:
ATTCGTGGTGGTGTAATTGTAAAAATAGAGGAAATTTGTTATTTACTTTAAAAAATCTAATAAAAGTTCATACAAAAGTCTGTAATGTTGGCCGATATCTTATGCATCCCTAATCAGAATTAAAAAAATTGTCCATTCTCCTATTGGTCATCATTTGAATATTTTTGCTAATGCTATTTTTGAATAAGCAACAAGTCTAATATTAGGCCAAATATTAGCTCATTTAGCATGGCAAAGCTGCTGCATGTCATTCAGCGCTTGTTTTCTCAAAAGGAGCCTTACAAATACATTTCTATGCCGCAGGAGCTGTTTACACGGCATATTGATGATTTATACTAGTGTTACAGCTACATCAAACCTCATCATCTCTCACCCGGTGATGGTCTGCTGTCTGCACTTGTCTGATGCTATTTTCTCTATTCTCTTCAGAGTGTGAAACCTCTCCAGATGCAGTATTTCCCCCATGAGGGGACTATTGATAGGATGTACTTCCCTTACTA[T/A]GGGAAAAAGACACATGTAAGTATGGCAGTCAGCACATGCTTTAAAGGATTGTTACAGGTTTAATAAAAGCTCAGGTGCTGGTGTTTGTAATGCTGGGTTCACACCAAATGCAAAGAGATCACGTCGAATGCGTCACTCGCTTTTGTTTCAACCCAGGCTCATTCTGAAAACAAACCTCTATATACATTTCTGGAGAGCGCCAAATACGTCCCAGGAGCTATGTTTTTTTTTTGCAGTTTTTGTTTTCGTGAACCCACCAGAGGCCGCTGTGAGCATTTTAAGATCTCAAATTTTTCTTTTCACGCCTGCTGTTCTTGCGTAAATCCACCAGAAGCTGCTGTCGACTGACTGAATGACTAACTGACTGACTAATCGATCCTCCTCCTTCCCTAAACCCAACCAATAGTGTTTTCAAAAGCGCCGATTGACCCGTCCACCCAATTCCCTAAACCCAACAAACAGTTTTAAAAAGCAATCCAGAAAAAGAAAAGATTTTACCA
Associated Phenotype:
Not determined