ZMP
zfpm2a
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein ZFPM2 [Source:RefSeq peptide;Acc:NP_001034724]
Human Orthologue:
ZFPM2
Human Description:
zinc finger protein, multitype 2 [Source:HGNC Symbol;Acc:16700]
Mouse Orthologue:
Zfpm2
Mouse Description:
zinc finger protein, multitype 2 Gene [Source:MGI Symbol;Acc:MGI:1334444]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36240 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42806 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36240
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 |
|---|---|---|---|---|---|
| ENSDART00000058685 | Essential Splice Site | 140 | 1142 | None | 8 |
| ENSDART00000102414 | Essential Splice Site | 139 | 194 | None | 6 |
| ENSDART00000104583 | Essential Splice Site | 140 | 195 | None | 5 |
| ENSDART00000141941 | Essential Splice Site | 41 | 1042 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 46823920)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 44023690 |
| GRCz11 | 16 | 43971138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATGGGGGCCTTTCGAGGGCAAAATTGAGCTGAACACAGACGCACAGG[T/C]ACAGTCCATCTCGTTTAAATGTTGATGAGGGTTAAAGGCCAAACATGCAA
Long Flanking Sequence:
GCCAAAGTATTCGATAGCTCAACTGTTTCATTTAGTCAACTTAAAATAGAAAATAAATCGTTATGTTAACTTAATCAATTTGTGTTGGGATGACATGAAGGGATTGGGTGGAACTCAGCATTTTTTTGGTGTATGGTATTTGTATGCTTTAGAAGTGTCAAAAACTTACACACAGCACTTGTAAAATTGTGTAAAAATGTCTCTAAATTCGAACATTCTTTGAAACATTTGGGATAATGTAAGTAAACAAGTCAGCAAAAAAAAATTGTTCTATGAATCTTTGCATATTTTAATGATACAATCTTACATATTGTGCCTTTAAATCCCCTTGAAGCATTTATTACACCTCCTAACACTGACTATCCTGTTCTGTCACACAGGAGAGCTGGACCTATTCAACAAAGATGGAGAACGGCGGATTCACAGCCGCCAGCAGCTTCCTGTAGGAACCACATGGGGGCCTTTCGAGGGCAAAATTGAGCTGAACACAGACGCACAGG[T/C]ACAGTCCATCTCGTTTAAATGTTGATGAGGGTTAAAGGCCAAACATGCAATTTATGCACTACTTAAAGGAAACTGCACCAACTTCATTTAATACGTGTGTTTAAAAGCGATCGATCTGTTTACTTGCTGAATCAATGGGATGGATTTGGTAAGGTTATTTGTTTTTATCAACTTTTTGCTATACTGTTGAAGCACACATTACATACTTCACCTTTAATAGAGTCTCTATATTTGTAAGTCCGTCCATGAAGCGGTTCATTATTAGAGGTGAAGCTTATTATCTTTGAAGACCTTTATTTGCATATTGACAAAGGAGAAAGTTTACTGAACATCAACAGATGTTAATAGTGTTATATACAGATCGTAACCCAGGGCTTCTTGAACATCCCAGTATCACACCGACCTGCTTTGTGAATTTAACTGTTTATTTGCATATTTTATTGCTAAAATTGATGGGTTTTACATATATACAGTTGAAGTCACTATTATTAGCCTTCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42806
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058685 | Nonsense | 1069 | 1142 | 8 | 8 |
| ENSDART00000102414 | None | None | 194 | None | 6 |
| ENSDART00000104583 | None | None | 195 | None | 5 |
| ENSDART00000141941 | Nonsense | 969 | 1042 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 46672917)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 43872687 |
| GRCz11 | 16 | 43820135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAGCCTCACAATACCTCATTGCCAGAGGAACAAACATCTCCCACATG[G/A]GGAGCCGAGAACCCTCCCGACCCAAACGAGAATGTATCACCAACTTCTAA
Long Flanking Sequence:
AGTTCTGTGAAATGCGAGAAAAATGGAGGCAACAAATTGATGCAAAATGGAGGCATGTTCCCACCACACCTCGGCTCCGCACCGGATCTGAAAGCTTTCGCTGATGCACAGCTAATGTCCTCGAAAGATGAGAACAAGAACATGTTTTTGCCTCACTCTCTCTATCCTGGAGCAATAAAGAAGGTGAAAGGTACCGAGCAAATATCACCGTATTTCGGGATTAAGAGTGGCGACTACATGGCAGGGAGTCTCGTCGTGCAGGCTGAGGCAGCCGAACAGGAGCAAAGCAGCAATGGTGCAGGTGAGCCAGGCACAGAATCACTTGCAGCCAATGGCTGTCCCCATCCCAACAAAGATCCACTGCCCCTGCTACCTAAAAATAGGAGCATGGTGATTGTCAATGGTGGTCATAAAGAGGATCGCCAGACACCAGCAACTCCCCAGCAAGAGAATCAGCCTCACAATACCTCATTGCCAGAGGAACAAACATCTCCCACATG[G/A]GGAGCCGAGAACCCTCCCGACCCAAACGAGAATGTATCACCAACTTCTAAATCACCCGTGGAGGATTCGGCACCCGCCGGGAAAGGTATTAATGGGTCGGCGTCGCCAGCAGGCAGTGGGAAGTACTGCCGCCTCTGTGACATCCAGTTCAATAACTTGTCAAACTTTATCACTCATAAGAAGTTTTACTGCTCGTCACATGCTGCCGAGCATGTGAAATGAAACTGCAGTCTTTTCCCCTTGTTCTCCCCTCTTTTTTGGGTACACGGTTGTGAAATAGTGCATCATGCAGTTTTATATACTGCTTGTGGACAATCAAGAGAAGCTTCTTCTTTCGTTATTTGAAGACTTAATGCAAAACGATGAAAAAACAAAAAAATCCAAGTGTAATATTGGTGCCACTTTCACCTTTTATTTATTTTACAATCAGTATTATTAGGAGTAGTGCTCTTAATTTAAATTCAAAGAAAGTTTATATCAGAGTTGTTTGTAATGTTAAT
Associated Phenotype:
Not determined