Busch Lab

ZMP

wu:fi26e04

Ensembl ID:
ENSDARG00000045828
ZFIN ID:
ZDB-GENE-030131-5941
Human Orthologues:
ZYG11A, ZYG11B
Human Descriptions:
zyg-11 homolog A (C. elegans) [Source:HGNC Symbol;Acc:32058]
zyg-11 homolog B (C. elegans) [Source:HGNC Symbol;Acc:25820]
Mouse Orthologues:
Zyg11a, Zyg11b
Mouse Descriptions:
zyg-11 homolog A (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2446208]
zyg-ll homolog B (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2685277]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa38308 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa13583 Essential Splice Site Available for shipment Available now
sa13217 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa38308
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067356 Essential Splice Site 370 735 3 14
Genomic Location (Zv9):
Chromosome 2 (position 3521655)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 3101024
GRCz11 2 2942913
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACAGTCACACCAGTGAATTAGAAGAACCTCAGCCAAACATTTTAAAG[G/T]TATTTACCAGTTTATTTAACAGTTTGTTTTATTATTATTATCTGTGTTTG
Long Flanking Sequence:
TCCCCTTTATACATTTTATTTACTTGATTATAATGATTCTTAACTCTGTTAAAACTGACACATGAACAAAGAGTCAGAATATTCCTTTTTTTTTTTTTTTTTGGAACTGAGATGTTTATTAATCCTAATATTAAGATCTATTTTTTCCCATATATGTGTTTTATACATTTATTATGTATCATAATGATACATCAGGTCTTTTGGTAACGTTTTTTGCTCAGAACTATTTCAATTTAGTTACAAAAAAAAACATTTTGTCAGAACTCGCATGCCCCTCAGTAAATGTGTTGTTGCGCCTCTGGGTCAAACCCACCTGCTGTGGGTTTTATATCCTGAATATAGCACTTCTATATCTGCAGGTGGCTGGAGAGGCTAATTTGCAGCAACTGTGTGAAGCCTTGAGGAGATACAGCGAGCGGGAGAGTTTCATACGGGAGACTCTTGCTCATCTTTACAGTCACACCAGTGAATTAGAAGAACCTCAGCCAAACATTTTAAAG[G/T]TATTTACCAGTTTATTTAACAGTTTGTTTTATTATTATTATCTGTGTTTGCGCAATCCCTAATCAGTTAAGCTATAAAAGTCACTTTAAGCTGAATACTAGTATCTAGAGAAATATCTAGTCAAATATTATGTGCTGTCATCATGGCAAAGATAAAATAATCAGCTATTAGAGATGAGTTATTAAAACTATTATGAATAATGTGTTAATCTAATTTCTGTTAAACAGAAATTAAGGAAAAATGTAGAGGGGTGCTAATAATTCTGACTTCAGCTGTATATGTGACTGTGCTGCAGCTGGTTTTAGCAGGGATGCGACGGCACACAGATTCTCTCCATGTTCAGCTCGTGGCCTCTGCATGTGTGTTTAACCTGACGGTTCAGGAGCTGGTGCTGGGGATGCCACTACACCTGCTGGGAACTGTGGTAAAACAGCTACTTATAGCCATGAAGAACTTCCCAAAACACGAGCAGGTATGTTTGCTTGTTTGTTTGTTTGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13583
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067356 Essential Splice Site 502 735 8 14
Genomic Location (Zv9):
Chromosome 2 (position 3516224)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 3095593
GRCz11 2 2937482
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATCTGTGAATTGTTGTCAAATGWAAATGATTGKTATTGTGTGTRAATGC[A/T]GCAGCTGCTGAGTATCGTCCAGCAGAAAGCGTCTCTGGGTCTGGTGGACT
Long Flanking Sequence:
AAAACAGATTAATTAGCATTTACTTCTTAGAAGCTGGTTATATCCACACACGGTTTCACACACATGTTGTTTAAACCCCTTATAAAAGTCATTTTTGCATAATAAGGTCGCCTTAAATGTCTAAACGCTTTTGAGGCTGGAGAACTGAACTCTCTCACTCTTTGTTCCAGTTGAGCACAGAGGAGATCTCAAAACTGGGGGCAGAAGAATTCATCATGAAGGTCAGTGCTAATGTTCACGTGTGTTAGCCGCGGCCAATACCTCAGACAGACCTAACAGAAAGTGCATTTTCAGATTTACATTTTAAGATTACAAGGGCAAACTATGGTTTTTATCTCAATGACATGCACAGATGAATTGTTCAGCACAAAACTAGCAATGCGAGCTAACAAAACCAACATGTTTAGTTTAGATTAAATCTGTACTTTAAGGATAAAATAAGGTGTTTAGGATCTGTGAATTGTTGTCAAATGTAAATGATTGTTATTGTGTGTAAATGC[A/T]GCAGCTGCTGAGTATCGTCCAGCAGAAAGCGTCTCTGGGTCTGGTGGACTCCACGCTGAAGTTTGCACTGAGCGCTCTGTGGAACCTGACGGATGAGACGCCCACAGCCTGCACACACTTCATACAGTGCAGAGGAGTGGAGCTCTACCTGGAACTGCTGGAGGTGCGCGCACACACACACACACACACACACACACACATAGACACACACACACTCATTCTCATTGATTCCTCATTCTCTCTTCTCTTCCACAGACGTATTATTCCGAGTCCTCCATCCAGCAGAAGCTCCTGGGCCTTTTGGTAATTTCTTGGTTTTCATGTCATGTGTGAAATGTACACATTTACAGAGAAAACAGCACTAATACAGGGCGGCTTGGTGGCGCAGTGGGTAGTGATGTCACCTCACAGCAAGAAGGTCACAGGTTCGAGCCATACACATGTTTGCTTACAAAGCGACTTCTGGCTTTGCTCCTTCTTATCTGCAGATGTATGTGCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13217
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
ENSDART00000067356 Nonsense 611 735 10 14
Genomic Location (Zv9):
Chromosome 2 (position 3512965)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 3092334
GRCz11 2 2934223
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WCCAGCTGCTGGTCCTGCCGCTGGTRGAGGTGGAYGTCAGCTACTTTGCT[G/T]GAGGGATTTTGRCTCATCTGGTGTCCGTCAGRGGGCCCGTGTGGAGTCTG
Long Flanking Sequence:
TCTAACCTGCCTAGTTACCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAATATCTGGTAAAATATTATTTACTGTCATCATGACAAAGATAAAATAAATCCATTATTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAGAAATCTGCTCTCCATTAAATAGAAATTGGGGTAAGAAATAAACGGGGTCTAATAATTCAGGGGGGCTATTAATTCTGACTTCAACTGTATGCTGAGCACTGTAGATATCCTAAAATCTAGCATCTAAAACATGTCTTTTAATTTCACAGGACCTTTAGATTCTGTGACAGTCGCTCAGCGCTGACGGTGTGTTTTCCCTCCAGAATAATGTGGCGGAGGTGGAGGATCTGCGGCCGGAGCTGATGAACGAGGAGCTGCTGGAGCACATTCTCCAGCTGCTGGTCCTGCCGCTGGTGGAGGTGGATGTCAGCTACTTTGCT[G/T]GAGGGATTTTGGCTCATCTGGTGTCCGTCAGGGGGCCCGTGTGGAGTCTGGATGAGGAGCTGCGCTGCACAGTACAGGACCAACTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGTTGAAGTCAGAATTCTGAGCCCACCTCTATATATTCCCTCAATTTCTGTTTGAAGGAGAGAAGATTTTTCCAACACATTTCTAATCATGATAGTTTTAATAACTCATTTCTAATGTCTTATTTTATCTTTGTCATGATGACGGCACATAATATATCACTAGATGTTTGTTAAGACACTATTACTAGCTTAAATTGAGATTTTAAGGCTTAACTAGGTTAATTAGGGTAAAGTTAGTGTAAGTCATTGCATAACAGTGGCTTGTTGTAGACAATCCAAAAAATATATTGCTAATATGTGCTAATAATTCTGTCTTCAAGCATATATTGTGCAAATGTCTCCTCTGGAAATCTCGCTGTCTCCCTGATGCTGTCTGTTTTAT
Associated Phenotype:
Not determined