Busch Lab

ZMP

epc2

Ensembl ID:
ENSDARG00000007485
ZFIN ID:
ZDB-GENE-040426-802
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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