ZMP
si:ch211-11m18.3
Ensembl ID:
ZFIN ID:
Description:
Protein zyg-11 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q5TYQ1]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31042 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43405 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31042
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104112 | Essential Splice Site | 445 | 746 | None | 16 |
ENSDART00000129633 | None | 446 | 445 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 16227463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 16287416 |
GRCz11 | 20 | 16186999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCTCTCTGTGCAGTGATCGTATCTTGCAGGAGGTTCCCTTTAACAGG[T/C]GACACATTGCACATGATCTATAATTCATTGCACACACATAAACATGAGTT
Long Flanking Sequence:
TTTACTTAATTACTAGTTTAATAAATTAAGCAAATGATCATGAAAATCAGAAGTGATTATGAAATGAGAAGATCTTTTTGGAAACTTGGATGAGCTTATTAACAATTAAAATGCACATCAAAATCAACCTTGGTTTAGAATGTTGCTTATTATTATATTGCAAGTCATCGCATTACATAACATTTTGCTTATTTAATACATATTTTTTTCACCTAACTAGAGCAGTAGATGAAATGAATATGACTGAATTGTATAATGATGGTTTAATGCTGCCAGGTTGTGTACTCGGTTACAGGAAACATAACTGCACACAAAAGAGCATTTGTAACATAGTGTTCCCCATGTCATGGTGATGCAGAACTTCTTGTGGTGAATGAGGAAGAGAATTCTAGAGGGTTTCACAGGTGCTTTGATTTCCTCTATTTTTTTTTCAGCTTCAGAAGAACTGTCTGCTCTCTCTGTGCAGTGATCGTATCTTGCAGGAGGTTCCCTTTAACAGG[T/C]GACACATTGCACATGATCTATAATTCATTGCACACACATAAACATGAGTTTATTTATATAGCACATTTCACACACAATAGTAATTCAAAGTGCTTTACATGAACAAGAAGAAAAGTAATAATAAATACAAAAAGTTTGAGAATTAAAAATGGGTTCAAATTACATAGGATTGATTTATAAATATATGAAGAGTTCAGATGCAAAAGCTGCGAAACGCCACTTCTGTCAAAAATGAGCTAATGGCATTGAGCGAATGATTAAGGAACGTAGTACATGTTAAACCAATATTTTCACTTCAAAGCATCAGCGCTTTCAGAAATGACAGTTTGTTTGCAAAAGCCTCTGAACGGCACTTGCCTTTGACCCCAAAAGCCACTGTGTCCCGACGACCAATCAAAAGAGGTAGAATGTTTTCAATGTAGCAGTGTGCTGATGCGCCAGCTTTTATGAGGAGACTGTTTTATTCAGATTTATATTTTAAAAGACAGAGTTTGATGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43405
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104112 | Essential Splice Site | 549 | 746 | 10 | 16 |
ENSDART00000129633 | None | None | 445 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 16234377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 16294330 |
GRCz11 | 20 | 16193913 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTTCATCGAGAACCAGGGGCTGGAGCTCTTCATCAAAGTGCTGGAGG[T/C]GAACATTGATTAAATGTGATTGTAATCTGATAAAGCTGTCCTGAACGAAG
Long Flanking Sequence:
TCCACATTAACATGCAGATTTTTTTTTTTTTAACAAAATACTGTGCAGAAATAGTAAAAAATGTCTGCAGATTCTGTCTGGCCCTACTGATATCACAACAACTATATTAATAACTATTAATAAGCAGGAGTTTATTAAGGCCAAACTTAATAACAGCGAGAATTGCATCCTAAAATAAAACATAATCCAATTTGTCTTTGACAGTTGTCCACTGAGCAAACCGCACAGTTGGGAGCCGAGCTTTTTATCGTCAAGGTATGTTTTTTGGAAGAGACTTTTTCTAATACCCTTGAATGGTAAAACTAGCAAACACTCACTCTCAAACTGTCTGCTTCAGCAACTCCTGCATATCGTGCGTCAGAAAACGTGTCAGTCGACGGTGGACGCCACGCTGAAGTTTACCCTCAGTGCCCTGTGGAACCTCACAGACGAGTCTCCGACCACATGCAGACACTTCATCGAGAACCAGGGGCTGGAGCTCTTCATCAAAGTGCTGGAGG[T/C]GAACATTGATTAAATGTGATTGTAATCTGATAAAGCTGTCCTGAACGAAGCCCTCATTCCTGAATCTCTCTGTTTTTTATAGTCTTTTCCATCAGAGTCATCCATTCAGCAGAAGGTGCTGGGGTTACTGGTAAGAAATGTATCTTGTGTAGTTGTGTCTAGCATAAAAATACATCAAAATAGCCTAAAGTGACCTTAAATAAAAGATTACTTTATTAACTTTCACGAACTAATCATAAAAAAAATGTATTATGGATTCATGTTTACCTTTTTATTTAAAATCAAATCATCATGTTTAAATGATTTCCAGAGGTTTGTGTAACCCTAAAGTTTGCTGTAATGTGCTAAAAAATCTACTTTGCTTCACACAAATAAACATTTAAAATGTATTAAGATAGGCAGCAAACTGGCTCAGTGGTTAACACTGTCGCCTCCCAGCAAGAAGTTCGATGGTTTAAGTCCTGGCTAGGTCAGTTGGCATTTCTTTGTGGAGTTTGCAT
Associated Phenotype:
Not determined