ZMP
zc4h2
Ensembl ID:
ZFIN ID:
Description:
zinc finger C4H2 domain-containing protein [Source:RefSeq peptide;Acc:NP_955936]
Human Orthologue:
ZC4H2
Human Description:
zinc finger, C4H2 domain containing [Source:HGNC Symbol;Acc:24931]
Mouse Orthologue:
Zc4h2
Mouse Description:
zinc finger, C4H2 domain containing Gene [Source:MGI Symbol;Acc:MGI:2679294]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38464 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33577 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38464
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020908 | Essential Splice Site | 187 | 224 | 4 | 5 |
The following transcripts of ENSDARG00000015314 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 23861229)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21574101 |
| GRCz11 | 5 | 22077901 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACGCCAGGCAGACGGCAACGTTCCGACAGCAGCCGCCACCAATGAAG[G/A]TACGCAGACTTTTACATTGTCTACAGTAGTCAACCATTTGAGTGGATTCA
Long Flanking Sequence:
ACGATGAATACAAGCCACTGAAAGAGCATGTGGACGCCCTGAGGATGACCCTCGGCTTACAGAGACTTCCAGACCTCAGCCAGGAAGAGGAGAAACTCTCGCTGGAGTCAGTAACACTGCTTCTGAGTGTGTGTGTTTGTGTGTGTGACTGGGGAAACTCCTCAAAATGAGTCACTGGCGTGTGGGAGTGTGTGTTTGCAACAGAGTAATTCTTAAAGCTGAGTCAGAGAAATTGCGAGAAGGAGAGTGTGTAATTGTGTACAGTGTGTGTGTGTGTGTGTGTATAGGAAAGCTAAACTGCTTACTGTCTGTTTGTGTGCTCTTTCTCGTGTTGCAGCTACTTTGAAAAGCAAAAGGCTGAGTGGCAGACAGAACCCCAAGAGCCCCCTATTCCAGAATCCCTGGCGGCGGCGGCAGCTGCAGCCCAGCAGCTTCAGGCTGCTCGAAAACAGGACGCCAGGCAGACGGCAACGTTCCGACAGCAGCCGCCACCAATGAAG[G/A]TACGCAGACTTTTACATTGTCTACAGTAGTCAACCATTTGAGTGGATTCACTTAGGACAAGAATGGGTGTTGGAGAGGTTTTTTTTCACACTTTTATTGTTTCTGAAAAATGTGATGCATACATACTGTATTGATAACCAAATACCAAATTAAAGAACACCCACCCCATCCCGACAGAGCCATAAAAAATGCATTCACATGCAAGGAAAATAATACATAAACAAATAAATAAATAGAAAATAAAAATAAACTAAAATAAGATAAAATAATACTAAAAAAATTAAAGAGCATTTGAAAGCACATGAAAGTGAAAAATATATTAAAGTTAGTCATTACAAACACAGTGCACATTAACACAGTCACATTGTTTGGGATTACTAAACAGTCAGTCCGTTTTTATTTAAAAAATGAAGAAAGAAGTCCCAAATCTTGTAAAATATGTGCATTTTTGTTTGATAGAGTAAGGCTACGTTCACACTGCGAGGCTTAGTGCTCAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33577
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020908 | Essential Splice Site | 187 | 224 | 4 | 5 |
The following transcripts of ENSDARG00000015314 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 23861228)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21574100 |
| GRCz11 | 5 | 22077900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACGCCAGGCAGACGGCAACGTTCCGACAGCAGCCGCCACCAATGAAGG[T/A]ACGCAGACTTTTACATTGTCTACAGTAGTCAACCATTTGAGTGGATTCAC
Long Flanking Sequence:
CGATGAATACAAGCCACTGAAAGAGCATGTGGACGCCCTGAGGATGACCCTCGGCTTACAGAGACTTCCAGACCTCAGCCAGGAAGAGGAGAAACTCTCGCTGGAGTCAGTAACACTGCTTCTGAGTGTGTGTGTTTGTGTGTGTGACTGGGGAAACTCCTCAAAATGAGTCACTGGCGTGTGGGAGTGTGTGTTTGCAACAGAGTAATTCTTAAAGCTGAGTCAGAGAAATTGCGAGAAGGAGAGTGTGTAATTGTGTACAGTGTGTGTGTGTGTGTGTGTATAGGAAAGCTAAACTGCTTACTGTCTGTTTGTGTGCTCTTTCTCGTGTTGCAGCTACTTTGAAAAGCAAAAGGCTGAGTGGCAGACAGAACCCCAAGAGCCCCCTATTCCAGAATCCCTGGCGGCGGCGGCAGCTGCAGCCCAGCAGCTTCAGGCTGCTCGAAAACAGGACGCCAGGCAGACGGCAACGTTCCGACAGCAGCCGCCACCAATGAAGG[T/A]ACGCAGACTTTTACATTGTCTACAGTAGTCAACCATTTGAGTGGATTCACTTAGGACAAGAATGGGTGTTGGAGAGGTTTTTTTTCACACTTTTATTGTTTCTGAAAAATGTGATGCATACATACTGTATTGATAACCAAATACCAAATTAAAGAACACCCACCCCATCCCGACAGAGCCATAAAAAATGCATTCACATGCAAGGAAAATAATACATAAACAAATAAATAAATAGAAAATAAAAATAAACTAAAATAAGATAAAATAATACTAAAAAAATTAAAGAGCATTTGAAAGCACATGAAAGTGAAAAATATATTAAAGTTAGTCATTACAAACACAGTGCACATTAACACAGTCACATTGTTTGGGATTACTAAACAGTCAGTCCGTTTTTATTTAAAAAATGAAGAAAGAAGTCCCAAATCTTGTAAAATATGTGCATTTTTGTTTGATAGAGTAAGGCTACGTTCACACTGCGAGGCTTAGTGCTCAAATCA
Associated Phenotype:
Not determined