ZMP
si:dkey-251i8.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ATPase, class VI, type 11A (ATP11A) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
ATP11A
Human Description:
ATPase, class VI, type 11A [Source:HGNC Symbol;Acc:13552]
Mouse Orthologue:
Atp11a
Mouse Description:
ATPase, class VI, type 11A Gene [Source:MGI Symbol;Acc:MGI:1354735]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32744 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31231 | Essential Splice Site | Available for shipment | Available now |
sa25650 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32744
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040284 | Essential Splice Site | 14 | 1169 | 2 | 30 |
ENSDART00000145117 | None | 1 | 1124 | 1 | 28 |
The following transcripts of ENSDARG00000008413 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 46841108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 45652769 |
GRCz11 | 1 | 46344001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATATATCTGAATAAATAAATAATGCATGCTGTCTGTCTGTTTGTTTC[A/G]GTGTACAGGAGAGGAGAACTGGGTGGACAGCAGGACGGTTTATATTGGGC
Long Flanking Sequence:
CAGACAAACACTGGGAACCAATGTGTCATCTTTGCACCCGGCTTTTTTTTTTTTTACAGGAAATGTAAAAGTCTAGTATTGCACTCTTCTTTTCTTCTGTCTGTTCCTCTCTTGGTCTCCTTTCTCTGCCTCTCGCTCTTTGTTATGAAACTATGGTCGCTCTGCCTTTGAGAGTCAAATCAAGCATGACGGGGACCATAAGTTCTCTATCTGTTCTCTTTCTCATCAGACTAAACTCTGCAGTTGTAGCTCAAAGCGGGTTCCTCTTTTTGTGCACCTGTTTTCTCTGACCTGTGAACTCACATGACAACACACTGGAGGCAAAAACACCCTTTTCATCCATCTGTCAGTTTTTAGATTTGGGGCTTTTGGGCTTCTTTTAAAGTGATTTTTAAATGTAATTTAAAGAGAATAGTTTTACATACATATATATATATATATATATATATATATATATATCTGAATAAATAAATAATGCATGCTGTCTGTCTGTTTGTTTC[A/G]GTGTACAGGAGAGGAGAACTGGGTGGACAGCAGGACGGTTTATATTGGGCATAAAGAGCCTCCACCAGGAACAGAAGCCTACATTCCACAGAGATTTCCTGACAACAGAATCGTCTCCTCGAAGGTCAGATGTGAACTACGACAAGCAGTTTTGTATAACCATGACAAGCTGACTAAGAATATTTTATATAATAATAATATTAATAATAATAACAATAATAGTAATAATAATAATAATAATAATAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTATATTTTCATTTTTTTTATATTATTAATAATAAATATTTTTGGTATGTTCTTTGGTACTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31231
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040284 | Essential Splice Site | 54 | 1169 | 2 | 30 |
ENSDART00000145117 | Essential Splice Site | 41 | 1124 | 1 | 28 |
The following transcripts of ENSDARG00000008413 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 46840982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 45652643 |
GRCz11 | 1 | 46343875 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCTACATTCCACAGAGATTTCCTGACAACAGAATCGTCTCCTCGAAGG[T/G]CAGATGTGAACTACGACAAGCAGTTTTGTATAACCATGACAAGCTGACTA
Long Flanking Sequence:
TGCCTCTCGCTCTTTGTTATGAAACTATGGTCGCTCTGCCTTTGAGAGTCAAATCAAGCATGACGGGGACCATAAGTTCTCTATCTGTTCTCTTTCTCATCAGACTAAACTCTGCAGTTGTAGCTCAAAGCGGGTTCCTCTTTTTGTGCACCTGTTTTCTCTGACCTGTGAACTCACATGACAACACACTGGAGGCAAAAACACCCTTTTCATCCATCTGTCAGTTTTTAGATTTGGGGCTTTTGGGCTTCTTTTAAAGTGATTTTTAAATGTAATTTAAAGAGAATAGTTTTACATACATATATATATATATATATATATATATATATATATCTGAATAAATAAATAATGCATGCTGTCTGTCTGTTTGTTTCAGTGTACAGGAGAGGAGAACTGGGTGGACAGCAGGACGGTTTATATTGGGCATAAAGAGCCTCCACCAGGAACAGAAGCCTACATTCCACAGAGATTTCCTGACAACAGAATCGTCTCCTCGAAGG[T/G]CAGATGTGAACTACGACAAGCAGTTTTGTATAACCATGACAAGCTGACTAAGAATATTTTATATAATAATAATATTAATAATAATAACAATAATAGTAATAATAATAATAATAATAATAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTATATTTTCATTTTTTTTATATTATTAATAATAAATATTTTTGGTATGTTCTTTGGTACTATATAGCAAAAAACATTTAATAGGATCATCTACACTTTAATATATTATAATAAGTAAAGGTCAGAATAAATATGTTTTAAGATTTTATTTTTATATATAAATAAGTTTTACACTGAATGCTGAATTTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25650
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040284 | Nonsense | 891 | 1169 | 22 | 30 |
ENSDART00000145117 | Nonsense | 878 | 1124 | 21 | 28 |
The following transcripts of ENSDARG00000008413 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 46798358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 45610019 |
GRCz11 | 1 | 46301251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACACTACTATTACATCAGAATCGCTGAGCTGGTCCAGTATTTCTTCTA[T/G]AAGGTGAACCCAAACACTCACAATACAACATACTTCTCCCTACACATATG
Long Flanking Sequence:
CTGATCATCTTTGAATTAAACTCAGGCTCTACTTTCCTCCCACATAAAATGGACGTTAGAAATTTGACTAAGGTTTTACTGTTTTTTTCCTTGATTTTACAATAAACTACTGGCAGTTGTGGTTGCCAGATAATCTTCAGTTTAAAAAAAAACAATAATGTTTTAGTTTAAAAATGTATTTAACTGTAAATCTAGATTTCTTTACAGCAATTGTTTACGGTATAGGTTTCATTTTTTTACAGTAAAGATTAAAAATTTCACAGGAATTTCACAATCATTTAATCTTCAAATGTATATTTAACAGCGACGTCAATAATGTCTTCCATGCAGTTACTGTTTTTCTTTTTTCTGCCTCTAGGTATCATGGGTAAAGAGGGACGTCAGGCGGCTCGTAACAGCGACTATGCAATTACCAAGTTCAAACACCTGAAGAAGATGCTGCTGGTTCATGGACACTACTATTACATCAGAATCGCTGAGCTGGTCCAGTATTTCTTCTA[T/G]AAGGTGAACCCAAACACTCACAATACAACATACTTCTCCCTACACATATGATGCTTTGTGTAAATTATAGGAGTAAATCTTTAACAAAATTTTATCAATATACAATCAGATGACCAATTACTCTAATTAACATAGTCAAGCTCTTAAATTGCACTTTAAGCTGAATACTAGTATCTTGAAAAATATCTTGAAAAATATGATGTGCTGTCATCATGGCAAAGATAAAATAAATTAGTTATTAAAACTATTATCTTTAGAAATGTGTTGAAAAATCATCTTATTGACACTTTTTAATGATTCTATTAATTCTGATTTTAACTGTATGTTTGTGATACTAGGCAAGGCAAGGCAAGTATATTTATATAGCACATTTCATACACAATGGTAATTCAAAGTGCTTTACATAAACAGGAATAAAAGAAACAAGTATAAGAAAAGAATTACAACAGAATAAAATTGTGAAAAGCAGATTAAAATGTGTTTAACATGTTTTAAAGGAA
Associated Phenotype:
Not determined