ZMP
zgc:73328
Ensembl ID:
Description:
zinc finger CCCH type containing 11A-like [Source:RefSeq peptide;Acc:NP_955980]
Human Orthologue:
ZC3H11A
Human Description:
zinc finger CCCH-type containing 11A [Source:HGNC Symbol;Acc:29093]
Mouse Orthologue:
Zc3h11a
Mouse Description:
zinc finger CCCH type containing 11A Gene [Source:MGI Symbol;Acc:MGI:1917829]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11501 | Essential Splice Site | Available for shipment | Available now |
| sa2592 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa11501
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034027 | None | None | 794 | None | 15 |
| ENSDART00000103766 | Essential Splice Site | None | 358 | 1 | 13 |
| ENSDART00000128309 | Essential Splice Site | None | 794 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 25023082)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 23796640 |
| GRCz11 | 11 | 24034497 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTACGTGCATCAACCCGAACATACTTAATTCCACTCGGTATAAACTGG[T/G]AATTGTGCTAGATTAATTTAAAGTAAATGTTNTTAAACRTTTTATTTAWT
Long Flanking Sequence:
ACGTTTTTGAACTGTGCAGAGCTGTACTGTAGCTGCTTTACTGGGCTTACTACGCTACAGTATTTCAATATTGCTCATGGTGGTACTTGATGAAAAAAGTTTGAGAACCACTGCAGTAGAGCATCTGAACACAAGACATTGAGGTAGAAGGGCTACAGCATCATCTGATTAACATGTCAAGCACATGATTGACACTGTTGTTAAGCTAACATAAACTTAAGACTGGACCAAAATTTCTGAGTTGTTATTTAAACAATTAAAAGTAAGTCCAACCTGTCTGTACCCATTTAATTGAGAAGGGTGTGATTTAAGTGGTGAACTGTCCCTTTAACGAGTCTCGCCGTCACACTGACGTTTACAGTCATTTGTGTAAGCACTTTCCTGCTGGGCAGCGCGGGCGCCATTTTGTTCGTCTGTAAAACCGAGAAGAGAAAAGTCCTGTACTGGAGAGCCTACGTGCATCAACCCGAACATACTTAATTCCACTCGGTATAAACTGG[T/G]AATTGTGCTAGATTAATTTAAAGTAAATGTTATTAAACATTTTATTTATTTATCATTCAACATATTTTAGTACAGTCTAGTAGTTGTGTTAAAGTTAGAATGCTAACTTACTCGAAGTTAGCAACATGCTATGCTAAGCCGTAGAATAAGCTACCGTGTTGTTTGTCACGTAACGCTAAACAGCTATTGGATTTAAAATATACTCATTTGGTCTTTACACGTTGTTTGTCTGTGTTTTTCATATGAAGATTTGCATAGTAAATCGAGTCAAATAAAACAATGACACCACGGCCTAACTCGACAATCTTGCATAACGCGACAATCATTTGAGTAACGTTAGTGGATTTCGAAGATTACGGTAATGTAATACAGCTATGGGAATATAATTATTGACTCTTATTACATTCAAAACGTTTTTGCTTCGGCTTTGATTTATGATCGTGGTGATATTTGCTTTTTGTTCATCTGTAAAAATGTGCTTTAAACCTTTACACTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2592
Status:
F2 line generated
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034027 | Nonsense | 40 | 794 | 2 | 15 |
| ENSDART00000103766 | Nonsense | 40 | 358 | 4 | 13 |
| ENSDART00000128309 | Nonsense | 40 | 794 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 25020448)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 23799274 |
| GRCz11 | 11 | 24037131 |
KASP Assay ID:
554-2701.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCGACACTGTGAGGCTGCCATGGGTAGTGAAACGGTTTGCAACCTGTG[G/A]CAAGAGCAAAGATGCTTCCGTAACGTCTGCAAGTTTCGACACATGGAAAT
Long Flanking Sequence:
AACATTGAAACAATTTTTGACCACTTCATAAACCTAATTTGGTTGAAAAAATGCTCTTTTTGTAATGAATTTCATTTGGTAAAATTTTCATCTTTATTTTAATGTATTTTTCGTCGGTCAGTTATTTACAAACTAAACAAAAAAAAAACGTTCAAATACTTTTTTCAATAATAAAGCAATGGTTAATTAGATTTAAGTAGGCCTATTATAACGTAAATTGTAGTGTTTCTGAATTTTTTTTTATATCATGGGTTTGAGTTATTAATTACAATATCGCAATACTACTTAGTATCACGATGCTTCAGCTGGTATAGTATCGTAACATGAATTAATGATATCGCAGCAACCCTATTATTAACAATAGAACACTTTTTTATGATTTTTGTAAATAAAAAATTGTATAGTGAATTAAAAATGTTTTGTGTCCTTTTTAAGGGTGACAGTTGCCCTTTTCGACACTGTGAGGCTGCCATGGGTAGTGAAACGGTTTGCAACCTGTG[G/A]CAAGAGCAAAGATGCTTCCGTAACGTCTGCAAGTTTCGACACATGGAAATAGATGTAGGTCACTTTTTAAATCCCTCAAATGTTAAGATTTTTTTCTTTCTGAAATTAGACCTCATTAGTGATGACTTTGTTGATGCCATTTATAGAAAAACCGAAAGGAAATTGCCTGCTATTGGGAGAATCAGCCGGCTGGATGCCAGAAGCCTCATTGTGCTTTCCATCATGAGAAGCCACGCATCATCAATGGCAACTACTTGGCTCCAGATAAGGGTATTTGATCCTCTTTAGAGGATTTTTAAACATTACTGGTCTCCATAGGAATTTCTAATTGATGAATTGTCTTTTTTTTTTTTTTTTTTTTTTTTACAGGGCAGGTAGCGCGAAAGGACAATGAAGAGGCCCCGCTTGAGGAGAAGGTGAACCAAGTCCCTGCACCCAGTGCAAACCCCACTAACCCACAGCTCAGAGGAGTCAAGAGAACTGAGACCCAAGAGAATGTG
Associated Phenotype:
Not determined