Busch Lab

ZMP

atp9b

Ensembl ID:
ENSDARG00000062521
ZFIN ID:
ZDB-GENE-060503-583
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Not yet available
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.
Availability:
Not yet available
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