ZMP
atp1b2b
Ensembl ID:
ZFIN ID:
Description:
ATPase, Na+/K+ transporting, beta 2b polypeptide [Source:RefSeq peptide;Acc:NP_571913]
Human Orthologue:
ATP1B2
Human Description:
ATPase, Na+/K+ transporting, beta 2 polypeptide [Source:HGNC Symbol;Acc:805]
Mouse Orthologue:
Atp1b2
Mouse Description:
ATPase, Na+/K+ transporting, beta 2 polypeptide Gene [Source:MGI Symbol;Acc:MGI:88109]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13292 | Nonsense | Available for shipment | Available now |
| sa12906 | Nonsense | Available for shipment | Available now |
| sa20490 | Nonsense | Available for shipment | Available now |
| sa12895 | Essential Splice Site | Available for shipment | Available now |
| sa2197 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa13292
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097822 | Nonsense | 9 | 292 | 1 | 8 |
The following transcripts of ENSDARG00000034424 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40107099)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37906489 |
| GRCz11 | 5 | 38506642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGYGCACATTTAGTCCAGGAAAATGGCCAAGGATGACAAGAACGGCTG[G/A]AAGGAGTWCTTCTGGAACCCGAGGAYCCGCGAGTTCTGCGGGAGGACCGC
Long Flanking Sequence:
GTCGTTTTACTGGGGGGCGGGGCTAAGAGTGCCGCATAGCGCTGCTATTGGCCAAAGAAGTCACTTGAGTTTTGCAGAAGGAGGGCTATGTGTTTAGGGGTGGGGGTGAGCAGGCAGAGCTTGTTTTGCTGCAGTGTCTTTACATTATTGCTGCACTGGTCTCTCTCTCTCTCTCTCTCTCCCTCTCTCTCTGCGGAATGCGCACTGCACTGGCGGGTGAGCAGAGATTCGGGCGTTACAGTGGGATCGAGATCTTCTCTCACTCAGTCCTCGCTTGACTGCTCAGGTTTAGGCAGAGTGCCTTCGGAATCAATCTTAAGCAGTCTTTCATTTAAAAAAACTTTCTGTAGAGCCACAAAAGATCGTTTAACCCTTTCCACACAGTATTTAAGGCTTGAATAGCTCTTTATTACTCTCAAAGAGAGTGCTAGCCCCGAGGAGTTGTCTCTGTGAGCGCACATTTAGTCCAGGAAAATGGCCAAGGATGACAAGAACGGCTG[G/A]AAGGAGTTCTTCTGGAACCCGAGGACCCGCGAGTTCTGCGGGAGGACCGCGAGCAGTTGGGGTAAGACTAGCTAACACTGACTAACAGGATGCCAATTAGTATCACATATTGGTAAATTATATATATATATATACACTGATGAGCTGCAGTCGTTAGTACTTCTGTGTGAGTGCAGAGAAGTTACAGTGAAGAAGATCGCTGTCCGCGGTGCTGAAACTCCAGTTGCCGGTTACCGGCTCTATGCGTCGCATGCGTTTCTGTTCGTCGCCTGTTTTAGCTGTAAAACTTTATACAAAACCATTCGAGTGTGTTTATATCAGTCAACTGACGCAAATTTACCTCAGCTGTAACTGTGATCACTAATTGCTCGGTTTTGCTGGTGTTTGCAGATAAAATGTTGAATGTGCTTCTTGAGCCAATGAACAGCGTGGAGAAATGCAGTGTCGAGTCACTGCACAACTCCACAATGCGCTTCAGGCACAGTGCCTAAATACAGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12906
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097822 | Nonsense | 36 | 292 | 2 | 8 |
The following transcripts of ENSDARG00000034424 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40091397)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37890787 |
| GRCz11 | 5 | 38490940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTTTTTTTTTTTTKTTTTTTTTTTKCAGGTCTGATTYTGCTGTTTTW[T/A]CTGGCATTCTACATATTCCTGGCTGGATTRTTTACTCTCACCATGTAYGT
Long Flanking Sequence:
GTATGACCTATACTACATGTTACTATTATTAATGTTTTTAATTGATTTGATGTATTTCAAAAATGCTGTTCCACTTGGACTGTAGTTAGTGATATAACAGTGGTAGTAATTGTTTTTAAAAAGCTACCTGAAAAGTATCTGACTGTCAAAAATGCTCAGTGGCATCTAAAATATGGGTTATTTTTGTTTAAGTGTGATGTTTAGGTTGCAAGCTGTAAGTTGTAATAATAATAATAATAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAATTATCTTCATATAAATATAATAATATAGCCAGCAGTCCAGGTGAAATAATTATATATTTAAGTGTTAAGTTTGACCAGTATTTCAGAGATATTTATTATTTTGCATAAGTCTCCATTTCTCTTTTTATTGTTTGCCTTTGCTGTGTGTTTATTTGATTGTGTGTGTGTGTTTTTTTTTTTTTTGTTTTTTTTTTGCAGGTCTGATTCTGCTGTTTTA[T/A]CTGGCATTCTACATATTCCTGGCTGGATTGTTTACTCTCACCATGTACGTAATGCTGCAGACCCTCGATGACCACAGACCAACATACCAGGACAGACTTTCAACTCCAGGTACACACACACACAAACACACATATGCATATAATATGTGTTCCACTTGATCACTATATTAATTATAACCACAATAAATCTGTTTCTGCACACCTTTTACCATATTTAAATTGCAGTGAAATGACCATTTACTATTTGGGCCATTAATCAACCTCTTTGACTTTCAAAAATATAATAAATGTAAGCAAGCAGACACTCATAGCCGCTGCCTGTTCCTTCTCCTCCTCTCTTTTGTTTATTTGATGTTTTGCAGGGATGATGATCAGACCTAAAGGAGAGCAGCTGGAGATTGCTTATACCACCGAGTACACAGAGACCTGGGAAAGATACGTGCAGGCTCTCAATAACTTCCTCTCACGTGCGTTTATTTAACAACCCTAATGCTGCATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20490
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097822 | Nonsense | 77 | 292 | 3 | 8 |
The following transcripts of ENSDARG00000034424 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40091023)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37890413 |
| GRCz11 | 5 | 38490566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCTCCTCCTCTCTTTTGTTTATTTGATGTTTTGCAGGGATGATGATC[A/T]GACCTAAAGGAGAGCAGCTGGAGATTGCTTATACCACCGAGTACACAGAG
Long Flanking Sequence:
TTTATTATTTTGCATAAGTCTCCATTTCTCTTTTTATTGTTTGCCTTTGCTGTGTGTTTATTTGATTGTGTGTGTGTGTTTTTTTTTTTTTTGTTTTTTTTTTGCAGGTCTGATTCTGCTGTTTTATCTGGCATTCTACATATTCCTGGCTGGATTGTTTACTCTCACCATGTACGTAATGCTGCAGACCCTCGATGACCACAGACCAACATACCAGGACAGACTTTCAACTCCAGGTACACACACACACAAACACACATATGCATATAATATGTGTTCCACTTGATCACTATATTAATTATAACCACAATAAATCTGTTTCTGCACACCTTTTACCATATTTAAATTGCAGTGAAATGACCATTTACTATTTGGGCCATTAATCAACCTCTTTGACTTTCAAAAATATAATAAATGTAAGCAAGCAGACACTCATAGCCGCTGCCTGTTCCTTCTCCTCCTCTCTTTTGTTTATTTGATGTTTTGCAGGGATGATGATC[A/T]GACCTAAAGGAGAGCAGCTGGAGATTGCTTATACCACCGAGTACACAGAGACCTGGGAAAGATACGTGCAGGCTCTCAATAACTTCCTCTCACGTGCGTTTATTTAACAACCCTAATGCTGCATGTATTGCACAGTAAATATAGACATTAGGCATTTGATTAAAGCTACGGTATCTAACTTCTGAAAATCTAGTGGTTAATAAATGAAGAGCTTACAGGCAAAAACCTAAAATTTTTCTCCAAAATGAGCATTTTTATCAGGCTCTTGTGTGTATCCCAATTCATCCCAAAGAAAAGAAGTCCTTTTCCTGCACTGTCAGAAAAAATGTGCAAAATTTGTACCTTTAGGGGTACAATGGCTTGTCACTGGGGCAGTACCCTCAAGGGTACACCTGTTGTACCCTTTCACATGGGTACATATTTGTACCCTAGCAGTATGTACCTTAATGGGTCAAATATGTACCTCTGCTGACTAATTTGTACCTTACTTGGGCTATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12895
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097822 | Essential Splice Site | 107 | 292 | 3 | 8 |
The following transcripts of ENSDARG00000034424 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40090929)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37890319 |
| GRCz11 | 5 | 38490472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACAGAGACCTGGGAAAGATACGTGCAGGCTCTCAATAACTTCCTCTCAC[G/A]TGCGTTTATTTAACAACCCTAATGCTGCATGTATTGCACAGTAAATATAG
Long Flanking Sequence:
TTTTTTTTTGCAGGTCTGATTCTGCTGTTTTATCTGGCATTCTACATATTCCTGGCTGGATTGTTTACTCTCACCATGTACGTAATGCTGCAGACCCTCGATGACCACAGACCAACATACCAGGACAGACTTTCAACTCCAGGTACACACACACACAAACACACATATGCATATAATATGTGTTCCACTTGATCACTATATTAATTATAACCACAATAAATCTGTTTCTGCACACCTTTTACCATATTTAAATTGCAGTGAAATGACCATTTACTATTTGGGCCATTAATCAACCTCTTTGACTTTCAAAAATATAATAAATGTAAGCAAGCAGACACTCATAGCCGCTGCCTGTTCCTTCTCCTCCTCTCTTTTGTTTATTTGATGTTTTGCAGGGATGATGATCAGACCTAAAGGAGAGCAGCTGGAGATTGCTTATACCACCGAGTACACAGAGACCTGGGAAAGATACGTGCAGGCTCTCAATAACTTCCTCTCAC[G/A]TGCGTTTATTTAACAACCCTAATGCTGCATGTATTGCACAGTAAATATAGACATTAGGCATTTGATTAAAGCTACGGTATCTAACTTCTGAAAATCTAGTGGTTAATAAATGAAGAGCTTACAGGCAAAAACCTAAAATTTTTCTCCAAAATGAGCATTTTTATCAGGCTCTTGTGTGTATCCCAATTCATCCCAAAGAAAAGAAGTCCTTTTCCTGCACTGTCAGAAAAAATGTGCAAAATTTGTACCTTTAGGGGTACAATGGCTTGTCACTGGGGCAGTACCCTCAAGGGTACACCTGTTGTACCCTTTCACATGGGTACATATTTGTACCCTAGCAGTATGTACCTTAATGGGTCAAATATGTACCTCTGCTGACTAATTTGTACCTTACTTGGGCTATGGTGCAAAAATGTACCTTTAAAAAAGGTACAATTTTTCCTCCATAGGGATGAATTTTGTACCCTTTCATTTCAGACTTGTACTCCATAAACAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2197
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097822 | Nonsense | 291 | 292 | 8 | 8 |
The following transcripts of ENSDARG00000034424 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 40077236)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37876626 |
| GRCz11 | 5 | 38476779 |
KASP Assay ID:
554-2491.1 (used for ordering genotyping assays)
KASP Sequence:
AACGAGACAAGTTTGCTGGACGAGTTTCCTTCACACTGAGGATCAACTCC[A/T]GAGATTGAACAGACAAGAGTGTTTGTTTNTTTTTTTNGCACGCACACACAT
Long Flanking Sequence:
TCCAATAAAAGTAGAACACTGACTTATAAAACAAGATAGCTTTTATTAGACTAGCTTTACTAGCCCTTTTTGGAGTAAAGAACCATATATGGTAACTTCATTGACACCGATTACAGTATATAAATGTATGTACACAAATCTTTGCCCTACACTTTAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAACAAATTGTGTGGCACCTTGCATTTTTTACAATGTATAAAGGGAAAATAAAACAGCCTATAATGATTGTTCTCACAAAGTTTCCCTCTGGTATCTTCTTCTTCTGCAGGTGAACTACTCTCAGCCTCTAGTGGCCGTTAAGTTCCTCAACATCACCAGGAATGAGGACGTCAATGTGGAGTGCAAAATCAACTCCAACAACATTCCCGAAGGCAGTGAACGAGACAAGTTTGCTGGACGAGTTTCCTTCACACTGAGGATCAACTCC[A/T]GAGATTGAACAGACAAGAGTGTTTGTTTGTTTTTTTGCACGCACACACATACATATGCACACACCGGTCCTCCCATCTAATAGTTTACAACAACGTGTGGAAGGAACAGCTAGTAGTCCGACAGAACAAAGAATAATAGTACTCTTTTAGACTTTGAGACTAGTAAGGTTGCAAATAGTAAGCAGGATTTTTTGTGCATATTAAATCAGTGTGTGTGTGTGTGTGCGTGTGAGTTCAGAGTACAGTATTTATTTTTTGAACCAAAATTTGAATTGCATGCTCAGCTAGCAGAGCTGGTGATTAAAAAAATAATATACTATTCTGGTCAAGCAACCTTACCTAGTATCTTTTAAAAAATACCTTTTTCTTTACTAAGTATCTGTTCATTTTGTTCAATTTTTAATTTCGGAGCAGGCGTCAATGAGGTAATGTGCTTGGCTGGCATAATCTCATGTGTGTTTGGAGAATCTCTAGAGTTCTGGGACTGTTTGGCACTTGTG
Associated Phenotype:
Not determined