ZMP
epc2
Ensembl ID:
ZFIN ID:
Description:
enhancer of polycomb homolog 2 [Source:RefSeq peptide;Acc:NP_957369]
Human Orthologue:
EPC2
Human Description:
enhancer of polycomb homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:24543]
Mouse Orthologue:
Epc2
Mouse Description:
enhancer of polycomb homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1278321]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12299 | Essential Splice Site | Available for shipment | Available now |
sa41428 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12299
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021672 | Essential Splice Site | 272 | 751 | 5 | 14 |
The following transcripts of ENSDARG00000007485 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 26391475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25547261 |
GRCz11 | 9 | 25358130 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGCAAACGAGAGCTGCTGCATCTGACGCTGGAAGTCTTTGAAAAAAG[G/A]TGTGTGAACATTTCTATTTTTAAAGTTTCTTTTAAAAGAGTTTGTTGTTA
Long Flanking Sequence:
AATTGGTATATAAACACTGATACCCGTGGTAGTGATCAAAATGATATTTCCTAATTAACTATTCAAATGATGATTGTATTGTATTGGTGGGCCAATAGGTGGCAACATGTAACCATTAAATGAATAAAAAAACCTTTCTCGATGACATTCATTGAAGTGACTTAACATGCAGATTTATACACAATTGAACTTTGAAAAAATTATGAAAGAATTTTGGCTCAAACGTTTTAACAAATGTTAATAAAATCTTTTAAACAGATATTTAGGGATGTTATTTATTGGATTTTTATTAAACAGCTACTAGAACCCTACTAGAATTTGGTCTCTGATCTGTAACCTCTCTCTCTATAGAATCGCAAGAATGACGAGGCATCTTATGAGAAGATGCTGAAGCTGAGGAGAGAGTTCAGCCGAACCATAAGCATCCTGGAAATGATCAAGAAAAGAGAAAAGAGCAAACGAGAGCTGCTGCATCTGACGCTGGAAGTCTTTGAAAAAAG[G/A]TGTGTGAACATTTCTATTTTTAAAGTTTCTTTTAAAAGAGTTTGTTGTTAAATAATTCATAAAATCAGTACTCAAAGTATAAATGTTTTTAGATCATGTTGATATTCTTGAGATAAACAATTGATTCATGCTAGTTAAAAAATGTATTGATTATCTTAATGGCATTCCTTCTGTGAAATCAGCATTTTATTCATTAATAAACGTAATCTCAGCTGTAACAGGAAGACAGGTCGAGACATAGAGCAGCCTTTTATAGATAGCAAATACACACATTCCCTGTACATTGACTAAGAATGTGTGTGCACTGTGCAATGTATTTTTCACATCTGGGCTTCCCGTAGAGTGGTGCTGAGCACAGCATATTTTAAAATGAATAGGGAATTCATATCAGCATAGCTTGGTTAAAATTTATCATTTTCTAAAATTGCAAGTATTTAGGCAAACCCTTGGGATTAAAAACACCTATTGACTGGAACAAATGACTAATTTTATTATGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41428
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021672 | Nonsense | 437 | 751 | 9 | 14 |
The following transcripts of ENSDARG00000007485 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 26387720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25543506 |
GRCz11 | 9 | 25354375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCTCATTGGCAGCAGACGGGTCAGGATCAGCTGTGGCAGCGGAACTG[T/A]CTCACTGCCCTCTCTGTGCCTAGACGGTGCATCGCAGTGGCTTGTAGGAG
Long Flanking Sequence:
CCTCCCCTATCCTATGCTAATCTACCCTACTCTACATTCTACCTTACCTACTTTCACTTCTTTACCCTACAATGTTCTACCCCAGTGGTTTCCAGCTCCAGTTTTTAGGACCCCTCCCATGCTGGAAATTTTTTATGTCTTATATGTCCTGAGGAACGGAATTGGGAATCACTGCTCTACCCTTCGCTATTCTTCACCACTCTACTCCACTCTACCCACCCTTACTCTACTCTAGTTTTCTTGTATGTTGCACATGGCTAATAATGCTGCACGTGAGACGTGCGTCACTTGAGACCAAACCATAGTTTTTTGTTCTCATTTCCTATAGATTGTGCCATACTTCAGTATTAAGTTAACTCGGTGGTGTTGACTCAGTGGTGCTTTTAAAATTTTGTTTGTGATTGTTAAATGTGTGTTATGTGTCCTCAGCCGGTGGTGGATCAGAGCTGTTCTCCTCATTGGCAGCAGACGGGTCAGGATCAGCTGTGGCAGCGGAACTG[T/A]CTCACTGCCCTCTCTGTGCCTAGACGGTGCATCGCAGTGGCTTGTAGGAGAGTGGGCAGAGGTGGCAGGTATGGCCCTGTTTACACTTTTTGCATATGGCTTTTTAGCTTTTTCTTGCTGAGTTGTTCTGAGTTTATTTGTTTTTTATTATTTGTAATTCACAGTATTTCTTGCGATTTTAAGATTTTTTTTCTGAAACATTGAAACGTTTTTCTGAAACGTTGCGTAAACATCTCATGGCTTTTATCCTCTGAAAATTGTGACTTGCAATGACAAGTTTATTTGCTTTCCAACCTAAAAAATATACATATGTTTAAATGTATTTAATAGTCTTTAAACAAATTTCTCAAAATGATTTCTCTCTGAATTGAGTTAACATTTAGTTGATTTCCTGCAAAAAAGTTTTTCTCCCAATTCAAAATTAAGATCTCACTGTTCTGTCGTTCTCAGAGTTGCAATCTTTATAAAAACAAAGTCAGTTGTGAGAGGGAAAAAAAAGG
Associated Phenotype:
Not determined