Busch Lab

ZMP

cu137686.1

Ensembl ID:
ENSDARG00000054028
ZFIN IDs:
ZDB-GENE-030131-7027, ZDB-GENE-081031-13, ZDB-GENE-081031-14
Description:
Wu:fk66a11 protein [Source:UniProtKB/TrEMBL;Acc:Q6AZB4]
Human Orthologue:
ATP11B
Human Description:
ATPase, class VI, type 11B [Source:HGNC Symbol;Acc:13553]
Mouse Orthologue:
Atp11b
Mouse Description:
ATPase, class VI, type 11B Gene [Source:MGI Symbol;Acc:MGI:1923545]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa16252 Essential Splice Site Available for shipment Available now
sa11368 Nonsense Available for shipment Available now
sa9669 Essential Splice Site Available for shipment Available now
sa39387 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa16252
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
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076151 Essential Splice Site 235 1149 8 30
ENSDART00000134544 Essential Splice Site 157 1000 5 25
Genomic Location (Zv9):
Chromosome 22 (position 39988048)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 37066353
GRCz11 22 37007098
KASP Assay ID:
2261-7098.1 (used for ordering genotyping assays)
KASP Sequence:
GGTTTRTCGGGAGAATAACAGTAACCCAGCATGGAGAGGAGATMGTCAGG[T/C]AAGGCTTYAGTTYACTCGATYAGAGGAAWTAAAATCATTTGTAGATGTAT
Long Flanking Sequence:
TGAAATCATTAATAATCAAGACATGATCATATTTTATTGTGGTAAAATAAGCGTCATCTAGAGGCCTTTGCCTTTCATATAAGGCACTTCAGATACCAAATGATCAACCAGAAGTCCAGTTAATATATGTTGCTCCTAAATCTTGGACTGGCGACAAGACTTTCGTCAGTTTGTGTAGTTCTAATATGTAACCTGGTCTTGACACTGGAAGTTTTCTCTGTGCGGATGTTTAGACCCACTATGCTGTGCCGGAAACAGCTGTGTCGCAGTCTGTGTCGCGGCTGGAGTCTCTGCAGGCGGTGGTGGAGTGCCAGCAGCCAGAGGCAGACTTATACAGGTACCTTTCACAGCTGACCACTGAAACACGGAGCTTTACAATCCTGCGCATCCACATTCGATTTTATGGCACTTTGGCTTTTATCCTGACGCAGCACATTCTCTCCCCTCTCAGGTTTGTCGGGAGAATAACAGTAACCCAGCATGGAGAGGAGATAGTCAGG[T/C]AAGGCTTTAGTTTACTCGATCAGAGGAATTAAAATCATTTGTAGATGTATGTTTTTATTTTTGTTTATTGTATGCATATTTAGGTTATTATTTGTGTTTTTTGTATGTTTGTGTTACTCATTTCAGACCATTAGGACCAGAGAACCTCCTGCTTCGAGGAGCAAGATTAAAAAACACCAAAGAAATATTTGGTACATCATCCACACCATTGTCTTGTGAACAACACAACACGAAATCCAAATCGCACGCATTTTCGCTCATAACACAAGTTCACAACTTGTTACGACACTGATAAGTTTGTGTTTGTAATCTTTAAACAAAATTGTGAACCTGCACCATCTATAAAGCCCTTCTTCAGTTGAATGGGTGAATGTTTTAGTATTTGTTACTAGAGCTCTGGTGAAAAACATTTGGGAAATTGATTCTTCCGATTGTCAAAACTCATCGTATTCTCTCATATTGGATTCTGAGTAGTTTTTAATAGGCGATGGAGCTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11368
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
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076151 Nonsense 300 1149 11 30
ENSDART00000134544 Nonsense 222 1000 8 25
Genomic Location (Zv9):
Chromosome 22 (position 39986257)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 37063877
GRCz11 22 37004622
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGATCAATGAATAYATTTCTCATCATCTACTTGGGCATCCTGCWGTTT[G/T]AAGCCATCCTCAGCACCAYTTTAAAGTACGCCTGGCAGGCGGAGGACAAG
Long Flanking Sequence:
TAGCCTAGAGCACTGTCTGCTGTTTAAAACTAGCCTAGAGCACCGTCTCCTGTTTAAAACTGGCCTAGAGCGCCGTCTGCTGTTCAAAACTAGCCTAGAGCACAATCTACTGTTTAAAACTAGCCTACAGCTCCATCAACTTTTCAAAACTAGCCTAGAGCGCTAGTTATTGTTATTTCTAACAATGCGGATATTTTGAATGGTTTTGCAGCAGTGTAGTCAGTATTTCTGTTCTATAATCCTGCAGGTGTGGCTGTGTACACGGGCATGGAGTCCAAGATGGCTCTGAACTACAAGTGTAAATCTCAGAAGCGCTCTGCAGTGGAGAAGTAGGTGTTTCTTCATTTTACTGTCCACCTTTACATTCCCTCAGCGTTTCTTTACTGCTCCATTATGGCTACATCATCGCTCTCTCTCTCTCTCGCTCTCTCTCTCTCTCTCTCTGTCTGTGCAGATCAATGAATACATTTCTCATCATCTACTTGGGCATCCTGCTGTTT[G/T]AAGCCATCCTCAGCACCATTTTAAAGTACGCCTGGCAGGCGGAGGACAAGTGGAACGAACCGTTTTACAACCAGAAGACCGATCAGGAGAGAAACAGCAGCCAGGTCACTAGAAAGCGCTTATGATGGTTATTGTTTCTCAATTAAAAGGCACACTGATAAAATAATAGTATCTGAGATAGATAATAAATATCTGTTTAGTTTAGATCTGTTTTGTTGAGTTCAGATCTATTTAGCTTAGTTTAGTTCAGAATGGTTTAGTTTAGTTTAGTTCCATTTAGTTCAGTTCCATTTGTTGAGTTTAGTTCAGATCAGTTTAGTTCACTTTTGTTTTATTCAGATCTGTTTAGTTTAGTTCAGATCCTTGTAGTTCAGTTGAGCTTCATTTGGTTCAGTTCAGTTTAGTTTAGATACATTTAGTGTAGTTCGGATACATTTTGTTCAATTTCATTTCGTTCAATTCAGCTTAACTTAGTTTAGTTCAGTTTCATTAAGTTCAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9669
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076151 Essential Splice Site 723 1149 19 30
ENSDART00000134544 Essential Splice Site 645 1000 16 25
Genomic Location (Zv9):
Chromosome 22 (position 39969077)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 37047443
GRCz11 22 36988188
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAATCAGACAACGAGTGCGCAGAGCAGCTCCGCAGGCTGGCCCGGAG[G/A]TACACAGATTCACACASCATTCAAGTGTATTTWTTTYACTCAGCAGTGGT
Long Flanking Sequence:
CATCAATACTGACAAATCCTTCAGCAATATTTAAGTGTTGCTAAAAAATAACATATCGTATTACTTAGTCTACTTCATGTGACCTGTTAATGCGAAGAAAATAAAAGTTGTCATTGCTTTTTCAAATCAAAAGGTCTGAGATTTTGTGGGACTGATTTGATTAGGAAGATTTTCAATTCACCTTTTCAGTTTGCAGTTTCAACACAAGGGAACACATCTGTTGTGCAATTTACTGCAACACGCCTAATAATGTTTACATTGAACTGAACTGATTTTCTGTGTTTGTGTGTATGCAGGCTTCAGGATAAGGTCCAGGAGACAATCGAAGCTCTGCGATTGGCTGGAATCAAAGTGTGGGTGTTGACAGGAGACAAGCACGAGACGGCGGTCAGCGTGAGCCTCTCCTGTGGTCATTTCCATCGCACCATGAACATCCTGGAACTCGTGCAGCAGAAATCAGACAACGAGTGCGCAGAGCAGCTCCGCAGGCTGGCCCGGAG[G/A]TACACAGATTCACACACCATTCAAGTGTATTTATTTCACTCAGCAGTGGTCTGACAGTGACGCTATTTGAGTTAAGATGCACTCAAAATAAATACAATTCTGGGGCAAATACTGGCGGCACGGTAGCTCAGTGGTTAACACTGTAGCAAGAAGGTTGCTTGTTCAGCGTCGGCTGGGTCAGTTGGTATTTCAGTGTGGAGTTTCCATGTTCTCCCCGCGTTCACGTGGGTTTCCTCCAGGTGCTCTGGTTTCCCCTACACTGGGTAGGCTATATTGTCCGTAGTGTATGTGTGTGAATAGGAGTGTATGGATGTTTCCCAGGGACGGGTTGCAGCTGGAAGGGCATCCACTGCGTAAAACATATGCTGGATAAGTTGGTGTTTTTTCTCCGCTGTGGCGACCCCAGATTAATAAAGGGGCTAAGCCTTAAAGAAAGTGAATGAATGAATGAGCATATCTGTCTTGGCCATCTTTATTAATTCTGGGTGACTCATGTTACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39387
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076151 Essential Splice Site 877 1149 23 30
ENSDART00000134544 Essential Splice Site 799 1000 20 25
Genomic Location (Zv9):
Chromosome 22 (position 39962522)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 37040829
GRCz11 22 36981574
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCACTCCCCAGTTTTTATACCAGTTCTTCTGTCTGTTCTCTCAGCAAG[T/C]AAGTGTCTCCTGATGCTACCGTTTTTGTTGATACAGGATATTTTTTAAAG
Long Flanking Sequence:
CATTGGTGACGGAGCCAATGACGTCAGCATGATCCAAGAGGCTCACGTTGGTATTGGTAGGTGCCACACTCTCAAAGGGGCTGATTGAGGTTATTTAAATTAAGAGAAATCTTTTAGTGTTGTATGATATCTTGAGCATATCTGTGCTGTAATAATTCAGGGTGTTCGCAGATCCTTAAAAAGACTTGAAATGTCCCGTCTGTGCAGGAATCATGGGAAAAGAAGGAAGGCAAGCCGTGCGAAACAGCGACTATGCAATCGCGAGGTTTAAATTCCTCGCCAAATTGCTGCTTGTGCACGGCCATTTCTACTACATTAGAATAGCAACCCTCGTGCAATACTTTTTCTACAAGGTACGTGTTCTCAGATTGAGAGATGTGTTGTGTTGTGTTTATGAGCTGGCTGTGTTTATAATGCTCTCTGTGTTTTTCTTCTGCAGAATGTGTGCTTTATCACTCCCCAGTTTTTATACCAGTTCTTCTGTCTGTTCTCTCAGCAAG[T/C]AAGTGTCTCCTGATGCTACCGTTTTTGTTGATACAGGATATTTTTTAAAGGAATGCTGCGGCCAAAAATGAAAAAAATAAACCTTTATTGGGTGGGTTTTCTTTTGTTGAACACAAAAGAGGATATTTTGCAGAATGTTGGTTGCTGGCACCCCATGACTTCCATAGTAAATGAAAATAACCTCATTGTTAATTGGTTTTAAACCTTTATGGTTTTTTTTTCTCTTCTATTTAACACAAAAGAAGATATTTTGAAGAATGTTGGTGGCTGGCAGCCATCGACTTCCATAGTAAAATGAAAATTACTACATTGTTTATTAGTTTTAAGTCTTTATAGGTTTTTTTTTTTCTCTTCTGTTGAACACAAAAGAGGATATTTTGCAGAATGTTGGTGGCTGGCACCCCATGACTTCCATAGTAAATGAAAACTACCTCATTGTTTATTGGTTTTGAACCTTTATGAGTATTTTTTTTCTTTATTGAACAAAAAGAAGAAGATAT
Associated Phenotype:
Not determined