ZMP
atp9b
Ensembl ID:
ZFIN ID:
Description:
probable phospholipid-transporting ATPase IIB [Source:RefSeq peptide;Acc:NP_001038619]
Human Orthologue:
ATP9B
Human Description:
ATPase, class II, type 9B [Source:HGNC Symbol;Acc:13541]
Mouse Orthologue:
Atp9b
Mouse Description:
ATPase, class II, type 9B Gene [Source:MGI Symbol;Acc:MGI:1354757]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23507 | Nonsense | Available for shipment | Available now |
| sa8437 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43270 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23507
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:
Founder:
SL6_02_A2
KASP Assay Location:
Unknown
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090476 | Nonsense | 88 | 1125 | 3 | 29 |
| ENSDART00000136294 | Nonsense | 49 | 1108 | 2 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 22576421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 22507801 |
| GRCz11 | 19 | 22092124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGGATGATCTTTTTTCCTCTCCGTGGTCTCTGTCACGCAGCTGTTGC[G/T]AATGTCTGGTTCACACATGTCGCAGAAAGAAGGAGCTGAAAGCTCGGACA
Long Flanking Sequence:
CAAATGTACCCTCTTTTTGAGTGTTCTCCATTTACTGCTTCAACAATTTTAGTCTTCTTAGTGGAAGCACACCTTGTTTATCCACCTAAAGTTCAAGTGAATCTAGACTGAGCTAGTCTGCCTTTACTCTCAGTAACATCACTTACATTAATGTTGCATTAACGTCAGTTGTATTTCAAGTGGAATCAACTGGATACGCGCGACTGCTGATGAATTGCGCAAAAGGTCCCAGTGTTCGTTTTCAAGTGCGCTTTAAGTGATTGACGGAATGATAATTCAACTAAATCGCTGGTTTTCAGCGCAACCCTCAAATTAGGAGTAATGATCACTCTTGATATTTGTTCATTATTCGGTCGGGGGTATTTTTAAAATGAAGACCGTTTTTACTGGAAATCCGGGCCTGAATTATGCCTGTAGCACTGTGTCCTCCCTTAAATGAATTTATCTAATCACTGGATGATCTTTTTTCCTCTCCGTGGTCTCTGTCACGCAGCTGTTGC[G/T]AATGTCTGGTTCACACATGTCGCAGAAAGAAGGAGCTGAAAGCTCGGACAGTGTGGCTGGGACATCCCGAGAAATGTGAAGAGAAGTACCCCAAAAATGCCATCAAGAATCAGAAATACAACATTGTCACTTTTGTGCCAGGGGTAAGACTGTGTAATCAATCTCTCATGCATGTTATTGTTTTGATTTTCAAGTGTTATATTTGATTTCTTTGCCAAAAAATATTGATTAGTCTTATAAATGTTTGCAATTCAGGTTATTAGTGTTCATCTTTTAATATAAATTTTGATTGTACAATTCAATTAATTATATTTATACTTTAAAATGCTTGTGTATGCGTTTATTCCGCAGCTCTCGCTAGGCTGTTTAAAGTGAAATCTCTACCCATTGTCAGATTTGCTCAGTAATCAGGTTAATGTGTAACTAGCTGTGAAGTAAGGGGGTGTAACAGCAATCTAGCGTATCTTTTTCCACTGAGAGTGTAAGCGATCTACTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8437
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
Founder:
SL4_01_D1
KASP Assay Location:
Unknown
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090476 | Nonsense | 138 | 1125 | 4 | 29 |
| ENSDART00000136294 | Nonsense | 99 | 1108 | 3 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 22578576)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 22509956 |
| GRCz11 | 19 | 22094279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTNNTCTCTCTCTCTCTTTCTCTCTCTTTCTTTTCTTTTAGGTTCTTTA[C/A]CAGCAGTTTAAGTTCTTCCTCAACTTGTATTTTCTAGTAGTGGCCTGTTC
Long Flanking Sequence:
TATTATTTTTTTTTGTTGTTGTTTTTTCTCTTATCGAATCCTGAATTTGTTATTATTATGCAATATGGTTTTATTTGTCTTGATCTTACCATTAAAAAGCCATAAGCTGTGGCAATAAACAAACAAACAAAATTGTTGTTCATGTTAGTAAATATATTTAAAGTAAAATTATTTGTAAAATTTGTATTAACATTATTATTATTGTATTATAACATTTATTATGTACTGTAATATAACCTTATTTTAAAGTCCTGGTTAATTTAATTTAATTTGAATTTAATTTTGTTTTCATTTATAATTTAATTTTGTTTTGTTTTGTTTTGTTTTCTTTTTCTTTTTATGTTATTTTACAACTAGAGAGAGTGTACCAGAATCATTCCTCAAACATTCCTCAAGAAAGTAAATGTACCCAAATTATCCTACCCTTTTGGCAGATGTTATAGGCAAAAAATTTCTCTCTCTCTCTCTTTCTCTCTCTTTCTTTTCTTTTAGGTTCTTTA[C/A]CAGCAGTTTAAGTTCTTCCTCAACTTGTATTTTCTAGTAGTGGCCTGTTCTCAGTTTGTTCCTTCACTAAAGATAGGATATTTGTACACCTACTGGGCCCCATTGGTGAGTACGTCTGACCACACAAAGCTACTCAATAATGTTAATTCATTCATCACTTTTGTTGTTACTTGTGTTTTTTCTTCTTCTTTTTCTTGTCGTCCAGGGCTTTGTGTTGGCTGTCACCATGGTGAGAGAGGCGGTTGACGAAGTTCGCCGCTGCAGGAGAGATAAAGAGATGAACTCCCAGCTGTACAGTAAACTCACAGTGAGAGGTGACCACAATATGACACATCACAAATCCTGATGTTATTAGACATGCTGTGTATCATTCACAGATCATCATATTTTGAGCTCCGTTCTCTAACTATAAGAGTTGCAGCATTTGGAAACTATTAAGATGATTTAGTTCATAATGATATTTAGCTGATATACATTTAAATTGTACAGTTCACATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43270
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
Founder:
SL7_02_D3
KASP Assay Location:
Unknown
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090476 | Nonsense | 1078 | 1125 | 28 | 29 |
| ENSDART00000136294 | Nonsense | 1061 | 1108 | 27 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 22657579)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 22588959 |
| GRCz11 | 19 | 22173282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCTCATCAGTCTGGCCTGCTACCTCGCCTCCCTCGCCTTCCTCAAT[G/T]AATACTTTGGTAAGAACTGACAACACATTTGACATCTTCTAATTTTTTAT
Long Flanking Sequence:
TTTTTATTATTTAATTTTTTCATTCTTTAAAATGCTGTTTTTTTTTTTTTTGTTTTGTTGGGTTTTTTTTTCCTTTACTGAAGAAAAAAACTCAAACAGGGATAGGGTGCCAACTTACAGTAAATAAAATACAATTCCTCTAGTACATTAATAAAGTACAATCTTTCATCAAGTGCTATCACATACTCAAGCATTTTATGATCCATGTTTGAGGCACGTGTTTTATTCTCTTCTCAATGCTAAAGTGACCGCGTTATCTTAGTCCTTGTTAGCCTGTCTGAAACACGTCCTCTGTGCGTCCACCAGGGGGCATCCTGATGTACGGAGCGCTGGTGCTGTTTGATCAGGAGTTTGTTCATGTGGTTGCGATCTCCTTCACTGCTCTAATCCTCACTGAGCTCCTGATGGTGGCGCTGACTATCCGCACGTGGCACTGGCTCATGGTCGTAGCACAGCTCATCAGTCTGGCCTGCTACCTCGCCTCCCTCGCCTTCCTCAAT[G/T]AATACTTTGGTAAGAACTGACAACACATTTGACATCTTCTAATTTTTTATAATATATAATAATTGCATTTACTGCATTTTATTTAGGTATAACTATTGATATTAGCTGAATTTTAACAAATTAAGTTTAACATTACTCAATTTAATTTATTTGTTTAAATGCAGCCCATTTAAATAGTTTGCAGTCACTTACCTTAATTTTTTTAGTTAATCCAATTATTATTTGATTTTAGTGATTTTTTTTGTTTATTTAAATGTGTTATATAACTACAGTACATGTCTACCAATTGATTAATTGAGTTTTGAAGGTTTTTATTTTTCCAATATTTCTTATTATTCACCTGCCTACATATTTGTTTCATTTTATTTAAACGTAAATGTCTATTTACTTACTTATTTGTTTAATTTGTTTGCGTTTGTTTGTTCATATATTTTTGCAATTTGTTTATGAATAGTGCTGTGCAAAAAATGTTGTTTTGACATAATTTAAGTGTGTACTGT
Associated Phenotype:
Not determined