ZMP
wu:fi26e04
Ensembl ID:
ZFIN ID:
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]
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]
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 |
---|---|---|---|
sa13583 | Essential Splice Site | Available for shipment | Available now |
sa13217 | Nonsense | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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