ZMP
si:ch211-195m2.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LY58]
Human Orthologue:
ATP8B3
Human Description:
ATPase, aminophospholipid transporter, class I, type 8B, member 3 [Source:HGNC Symbol;Acc:13535]
Mouse Orthologue:
Atp8b3
Mouse Description:
ATPase, class I, type 8B, member 3 Gene [Source:MGI Symbol;Acc:MGI:1914581]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37500 | Nonsense | Available for shipment | Available now |
| sa43824 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12857 | Essential Splice Site | Available for shipment | Available now |
| sa43823 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43822 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37500
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088890 | Nonsense | 319 | 1198 | 10 | 30 |
| ENSDART00000137371 | Nonsense | 288 | 1033 | 9 | 24 |
Genomic Location (Zv9):
Chromosome 22 (position 20817871)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 20472547 |
| GRCz11 | 22 | 20497525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATTTTCGAGTACAGGATTTCTCCGAATTATGATGTTGTCTCCATTGTA[C/T]AACGCGACTCGTCTCCTGCCTATCAGGGCTTCCTAACATTTTGGGGCTAC
Long Flanking Sequence:
AAAAAACTCCTTTTAATATGGAAAATTGTCACCTATTGTGTGCCGTTGCTTTTATTTAGGACATAACATTCAGTCGTTAGGTTTGAGACTTGCTGCTGTTGGTCTGATCAGGCAACCTGCGCTTGCGCTTGCTTTGATCCAGGAATGCAATACCTAGTTCAACCACTGGGTGTCAGACTTACACACTTCACCTTTAACTGCATATAGCAATTTAAATATTAAATTTTTTTTATGTATTTGACATTTATATTGTAAATTTTATATATGATTAATTGTAGTATAAAATATTTTTTGTACAATATTTTTTTATTTTGTTTTGTTCTTTGACATATTATATATAACACTTGTGTCTTTATTATTATTCTGTCAGTAAATGTTGTCTCCCTCCTCTTTGTATCCAGATTCTGCTCTTCATGCTGACCACAGCTCTCCTCCTGGCCATTGGCGCTGGGATTTTCGAGTACAGGATTTCTCCGAATTATGATGTTGTCTCCATTGTA[C/T]AACGCGACTCGTCTCCTGCCTATCAGGGCTTCCTAACATTTTGGGGCTACATCATTTTACTGAGTCCCTCTATGCCCATGTCTCTCTATATCACGTAAAAACCAGCTCTCCATATTTTGATTATGTCTTTCTTTGAGGTTTTAAGTCCTCATATTTGAGTGCAAAAACAAACAAACAAACAAAAAAAAACTTTTTCTTTACTCAAGGAGTTATAAAAATGTGTTCTCATTCCCAGTGGTACAATCAAAACGCTGCATAATATATGCAAATAAAATTGCTAATTGCTGAGCTCTACTGTAAGTTTAGATACGCAGAGTTATTTGCTGTTAATACCATAAAAAATATAAGGTCTTGTTACAATAGTTTACTTGAATTACTGGGTTAACCAACATAACAGGTTATTTCAATAAGCTCACTAGTATATTGGTGCCATGTTTTCCTTGTTGACATTGTTTGAATTGTATTTCATTGTGTCAAACCAGGTTTGAAGTGATCCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43824
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 |
|---|---|---|---|---|---|
| ENSDART00000088890 | Nonsense | 534 | 1198 | 15 | 30 |
| ENSDART00000137371 | Nonsense | 489 | 1033 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 22 (position 20814606)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 20469282 |
| GRCz11 | 22 | 20494260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGACACGTGACACTCTCACCATCAGCGAGATGGGCCTCACTCGAAACTA[T/A]CAGCTCCTGGCCCTTCTAGACTTCACCAGCAAGAGAAGACGCATGTCAGT
Long Flanking Sequence:
AAGTTTAATTGGTTTAATTGTTTAATTGTCATAATTATATTTGAATGTTTTGTAAATGTGTTTGTGAAGGTTTTGTTTATTTTATTTGAATATATAAAATTTAAAATGCTATTTATTCCTCTGATGGGAATGCTGAACTTTCTGCAAAATTACTTTTAGTTTTGGATGATCATAAACGGAGAAGGAGGAATATTTCAGTTTCTTTTGACCACTTTCTGATTTTTTAGGAAAGAATGTATTTTGTATATGTATATTGAGTCATTATATGTGTATACATCTTTTTCTTTAATCTTGCGCTCTATTTGTAAAAATGTAGACAAATAAAACCAGAGGAACGTATAATTGACCTTCTGTTTTATAAATGCAGGTTTACCTCACTACCAGGCTGCGTCACCAGATGAAGAAGCTCTGGTTTGTGCAGCTCGAGAGCTGGGCTGGGTGTTCCTCTCCCGGACACGTGACACTCTCACCATCAGCGAGATGGGCCTCACTCGAAACTA[T/A]CAGCTCCTGGCCCTTCTAGACTTCACCAGCAAGAGAAGACGCATGTCAGTGCTGGGTGAGATTCAGATGGAAAGTTTCATCCTTGTTGTCTCCCTCACACTAGTTCTCACCAGTTTAGCTGTAAATTGTTGAGTCTCAGCAGAAACTTTGTAGCCATTTCAAGACTCATGATGTGAATTGTTACAAAAGTGCAACTTTCGGGAAACCTCAATGAGGCAGTTTGCCACAACGTTAAATAGTTACAAATTGTTGCAATTTTCAGTAGTGTGTTTGTTCTATGTCATGTTTTTCTTTTCTGACTTTGGATTAACTTTTTATATGTAACTTTGAACTAACCGTCCTAATGTTTCTGTCTTGCTAATAAACTAATTAGCTGGGAAAAAATTAGCATATGCGTTTGGAAGAATCAAGCAGTGCAGAGCTTTTACACAGTGGTTCTCCATAACCGTTTTCACCACCCACCGCTCTGCATATTTTGCCTGTCTCGCCTAATTAACGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12857
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 |
|---|---|---|---|---|---|
| ENSDART00000088890 | None | None | 1198 | None | 30 |
| ENSDART00000137371 | Essential Splice Site | 508 | 1033 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 22 (position 20812711)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz11 | 22 | 20492365 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGTNGTGTGTGTNGTNGTNGTGTGTGTGTGTGTGTGTGTGTGTKTGTGTA[G/A]TGCGTAGCCCTGGAGGACAGTTAAAGCTGTACAGTAAGGGWGCAGATATC
Long Flanking Sequence:
TTCACTCTGAAATAGCATGTCAGTTTGGCTTAGTAATGAGTGTAATTCCTGCATGCCGCCAGACAAGCACTAGTCGCTTTTAACACGAGAGGGTTCTTTTGCTGCGCTCGTGTTTCTGGAGGCGTGGCTCTAGACGGCAGGGGAGGGACTGTGATTCAGAGATTTATGCTAAGCTGTTAGCATTGTGGAAGATCACCTACTGCACCTTTAACTATGCACAGTTTTAAAGATAAAAAAATACCTTCCTTGCAGTTGTAATGACCGCCAATATTAGCTATTTAAACCATTTTTGTATCGCTTTTTACTACTTATGGTAGTCTGAAGCAATTAGAGAAACATAAAATGGGTAGAGCAATGGGTCGTGAGGACTGCGATTAAAAGCTACTGTACTAGCTTCAGCATAAAAACCATAATTTAACTCTATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTA[G/A]TGCGTAGCCCTGGAGGACAGTTAAAGCTGTACAGTAAGGGTGCAGATATCGTCATTCTGGAGAGGCTTCAGAAGGACTGGCCGCTTCAGGAGAGCACAGACAGAGCTCTAGAGGTAAGGCGACTGGACACAATCACCACTTTTGACCACTTCCCTGATGAGAGAGGGTCTGTGGGTGTTTATTAGCTTTTAAAGCTAGCACCATTTCATTCATTCATTTTGCTTCAGCTTAGTCCCTTATTTATTAATTTAATGCACCCCCAACTATTCCAACATAAGTTTTACACTGTGGATGCTCTTCTAGCCTCAACCCAGTACTGGGAAACAGCTAGCACAATTTTCATAATGTGAAAACAACCTTATTAATAGTTTCAGATCAATTAAACACACTACTGTATGAATAGGCTACTCAATGCATCTGTAATGGCGGTCTATTCCTTTCAATTCTCCGCCATTTCCATAGGGACTCGGCACAAAGGATTTGATGCAAAAAAACACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43823
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088890 | Essential Splice Site | 767 | 1198 | 22 | 30 |
| ENSDART00000137371 | None | None | 1033 | None | 24 |
Genomic Location (Zv9):
Chromosome 22 (position 20807388)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 20462064 |
| GRCz11 | 22 | 20487042 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAGTTTTTTTTTTTTTTTTTTTAGAAATTATTACTTTAATTCAGCAAG[G/T]ATGGGGTTAGTTCACCCAAAATTTAAATTCTGTTATCAATTACTGATCAT
Long Flanking Sequence:
GGTTCACTCAGTTAAACATCATTTGGGAAATGTTTTAAAAGGAAAAAAATTCAAAGGGGGGCTAATATTTCTGACTTTTACTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGTGTATCTGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGAATATAACACATTATGACCTCTGTCAACATCTTCAGGCAGCTCCTAGAGTCTCCATCTTCAAATGTTGATGTCAAATCTAAAGAGCCAGAGGTTTGGATCACAGACAAAAAAGCAGTGATGAGCAAAGCTGCGCTAGTCATCTCAGGTCCAGAACTGGTGAGAATATCAATACTATGAAAAAAATAAATCTTAAAAAATAAAATAAAATGTTTAAATGCTTGAATAATTATACAAAGGTTTTGTGCCAGTAAGTTTTTTTTTTTTTTTTTTTAGAAATTATTACTTTAATTCAGCAAG[G/T]ATGGGGTTAGTTCACCCAAAATTTAAATTCTGTTATCAATTACTGATCATGATGTCAGTACAAACCCCCAAGATCTTTGTTCATCTTTGGAACACAAATCAAGTTGTTTTCTCATCCTCCATAGACAGAAATATTCCTAACTCATTTAAAGAAAAAATACCCCAAAACATCTTCAAAACAGACTATAGACATTCAATGGTTCAATCTGAATATTATCAAGCTTCAAGCATACTTTTTTTACATATAAAACAAAAATAACCACGTTATTCAACAGGTTCCTCTCCACAGTGTCTGCATAGGTGCATTTATGCGTCACAGAATGTCATTTGCTGGCATCTGGGGTATACATCAGTGCACAGTACTCATGAACATGCGCAATATACTGACACTGAAGAGAAAAAACTGTTGAGTAAATTCATTATTTGTGTTTTATGAGTATATGACACAAAAGTATACTTGCAGCTATTCTTGCAGATTACTGCAGGCATATGGTCTGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43822
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088890 | Nonsense | 1169 | 1198 | 30 | 30 |
| ENSDART00000137371 | None | None | 1033 | None | 24 |
Genomic Location (Zv9):
Chromosome 22 (position 20799856)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 20454532 |
| GRCz11 | 22 | 20479510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGGGAAAGGTTTCGGAAAGTTAATTACCACAGGAGTTGGTCTTCCCT[C/A]AGCAGCGCCTCGACAGGATGGGAGAGTTACAGCAGAAAGCCTGAAGAATG
Long Flanking Sequence:
TTGTGACTACCCTTTTTAAAATAAGAATTAATGTAGTCCACCAGGTGGCAGTGTTAACAGACTGTTTATCACCAAAAAAATTGCAAAAGGCATTTGCAATGAATTCAAATCACATTCCCTGAATGCTACAATCCCATCTGTATTTTTTATTTTCAGGAGCATCGCAAAATGCTTACAGCACTCCTGAGGTTTGGCTGACCATATTTGTGACCACCTGTGTTGCAGTCCTTCCCTCAATAACAACACGAGCCTTGGGTGTTGTGCTAGCAAACCCCAACAAACACAAGGTTGCTCCTTACTTTTGTCCCAGTTTACATGAAATAAGCATTGACATTGTTTATGCTCACCTTATTTGTTGTTGCAGATTCACAGCTCAGCGAATGAACCCGTAGAGCTTCAGTCGTGGTTTCAAAGAGGTACTGTTCAGCGTCGATCATCCTACGCTGTTTCCCAAGGGAAAGGTTTCGGAAAGTTAATTACCACAGGAGTTGGTCTTCCCT[C/A]AGCAGCGCCTCGACAGGATGGGAGAGTTACAGCAGAAAGCCTGAAGAATGAATCTCCACAGGGTTTACACATAGAAATGAATAGTGCTGGTGTGTCATGCTAGCATCTTTAGTCATGACAGGATTGGGATTAGCGAATGTAGCATCAAGAATCTGTGCTAAACAATCATTGTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAACCCACTGATAGGGAACTTTTTGTCAATATAAATTTTTATATGCATTTTTTTTTTTATTAAAATACAAATAAGTAAAGCCAGTTTTGTGATTTTAGATAAATAAAATAAAAATTACAATAAATAAATACAATACAATTTAATCAAAAATCTATTATTTTACTCTTTATTGCTGCAAACAAATCCAGGCTAGGTAAATAAAGAGACTGTAGCATGAAAATGTTCAACAATGGTTGTATTTT
Associated Phenotype:
Not determined