ZMP
LOC798235
Ensembl ID:
Human Orthologue:
ZC3H12A
Human Description:
zinc finger CCCH-type containing 12A [Source:HGNC Symbol;Acc:26259]
Mouse Orthologue:
Zc3h12a
Mouse Description:
zinc finger CCCH type containing 12A Gene [Source:MGI Symbol;Acc:MGI:2385891]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30998 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42648 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30998
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061720 | Nonsense | 14 | 579 | 1 | 5 |
| ENSDART00000061720 | Nonsense | 14 | 579 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 4968325)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 4186127 |
| GRCz11 | 16 | 3985180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGCATCAATATGCAGTCCAGGTGTTTCCATCAACCCACAGGCCTGGGC[C/T]AGGACTCACACGACCTCCTCAACCTGCAGATGAAGGTGGACTTCTTCCGA
Long Flanking Sequence:
GAATGAAATTGTGGAGTGGATAATTAACTTATGTAAAGTCAAAAATAAATAGGGGTCGAAGATCAACAGGCGGTTCAGGCTAAATCTGTAATGCAGATTTAGTTTTTCTCTATACATTTGAATGTGTCCTGGTTGATTTATTGCATGTGGGTGTTAATTCTGTGCAAAATTATACTGATAAAAAACTGAAAAGAAAATGAAAGGATGAATGAAATGCGATGGATAGTGATACTAGCCACAGTGACTGGTGGTCAAAAACGTTAATGTCAAGCCCTGCTGTCAAAAGACCAGGCCAAATTTAGGATTGAACATGCTTCTGTGATGTGGCGCACGTTTGAAGAATGCGTTTGTATTTCAGTCTTTTTCACAGACGGGAACAGCATGTCAGAGCAGCATATGGACCACGCAGAAGCTCATGCACTGATAACCCCCAAAACATCACACATCCATCCGGCATCAATATGCAGTCCAGGTGTTTCCATCAACCCACAGGCCTGGGC[C/T]AGGACTCACACGACCTCCTCAACCTGCAGATGAAGGTGGACTTCTTCCGAAAGCTGGGTTACTCTCCGCAAGAAGTGAAAGCTGCTTTGAGGAAGCTCGGCCTAGGGACGGACACTAATGCGGTTCTGGGGGAGCTGGTTCGTTCAGGGGCGAAGGCTGTCCCCCCTTCTGTTTCTAATAGTGATGATGGGGGCTCAGGATCATCCCATCGGGGAGGGGGCTCATCTAGAGGACAGGGATCTACGTTGGATGACGCCACTGAAGCTGAAAGTGACCTGAAGCCTATAGTTATTGATGGCAGCAATGTGGCTATGAGGTAAAGACTTTATTTTTTTTTTTTAGTCTTTTCTTAGAAAGAGGATTATCGGAAAGAGTGTTTGCATAATCATCTCTGTTGGTTTAACAAGTATGAACAAGTCACAAAGGGAAATTCAGGACAATGAGCTCTGGTTGTGAACAGAATGTAAACCCTTTCACTTTGGTTTTCTGTTGGATAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42648
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061720 | Nonsense | 14 | 579 | 1 | 5 |
| ENSDART00000061720 | Nonsense | 14 | 579 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 4968325)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 4186127 |
| GRCz11 | 16 | 3985180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGCATCAATATGCAGTCCAGGTGTTTCCATCAACCCACAGGCCTGGGC[C/T]AGGACTCACACGACCTCCTCAACCTGCAGATGAAGGTGGACTTCTTCCGA
Long Flanking Sequence:
GAATGAAATTGTGGAGTGGATAATTAACTTATGTAAAGTCAAAAATAAATAGGGGTCGAAGATCAACAGGCGGTTCAGGCTAAATCTGTAATGCAGATTTAGTTTTTCTCTATACATTTGAATGTGTCCTGGTTGATTTATTGCATGTGGGTGTTAATTCTGTGCAAAATTATACTGATAAAAAACTGAAAAGAAAATGAAAGGATGAATGAAATGCGATGGATAGTGATACTAGCCACAGTGACTGGTGGTCAAAAACGTTAATGTCAAGCCCTGCTGTCAAAAGACCAGGCCAAATTTAGGATTGAACATGCTTCTGTGATGTGGCGCACGTTTGAAGAATGCGTTTGTATTTCAGTCTTTTTCACAGACGGGAACAGCATGTCAGAGCAGCATATGGACCACGCAGAAGCTCATGCACTGATAACCCCCAAAACATCACACATCCATCCGGCATCAATATGCAGTCCAGGTGTTTCCATCAACCCACAGGCCTGGGC[C/T]AGGACTCACACGACCTCCTCAACCTGCAGATGAAGGTGGACTTCTTCCGAAAGCTGGGTTACTCTCCGCAAGAAGTGAAAGCTGCTTTGAGGAAGCTCGGCCTAGGGACGGACACTAATGCGGTTCTGGGGGAGCTGGTTCGTTCAGGGGCGAAGGCTGTCCCCCCTTCTGTTTCTAATAGTGATGATGGGGGCTCAGGATCATCCCATCGGGGAGGGGGCTCATCTAGAGGACAGGGATCTACGTTGGATGACGCCACTGAAGCTGAAAGTGACCTGAAGCCTATAGTTATTGATGGCAGCAATGTGGCTATGAGGTAAAGACTTTATTTTTTTTTTTTAGTCTTTTCTTAGAAAGAGGATTATCGGAAAGAGTGTTTGCATAATCATCTCTGTTGGTTTAACAAGTATGAACAAGTCACAAAGGGAAATTCAGGACAATGAGCTCTGGTTGTGAACAGAATGTAAACCCTTTCACTTTGGTTTTCTGTTGGATAATAT
Associated Phenotype:
Not determined