ZMP
si:dkey-287h13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate epidermal growth factor receptor pathway substrate 8 (EPS8) [Sou
Human Orthologue:
EPS8L2
Human Description:
EPS8-like 2 [Source:HGNC Symbol;Acc:21296]
Mouse Orthologue:
Eps8l2
Mouse Description:
EPS8-like 2 Gene [Source:MGI Symbol;Acc:MGI:2138828]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32197 | Essential Splice Site | Available for shipment | Available now |
sa8563 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32197
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100057 | None | None | 121 | None | 3 |
ENSDART00000127636 | Essential Splice Site | 36 | 70 | None | 3 |
ENSDART00000136626 | Essential Splice Site | 39 | 242 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 16094668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16446434 |
GRCz11 | 18 | 16435500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTACTGTGATAATGCTAGACATAAATTAGATGAGTGTCTTGTACTGC[A/G]GGTCTTGGAAAACAACCAACAGTGGTGGTTATTGAGGAACCGCAGTGGTC
Long Flanking Sequence:
ATAATGAATGTAATTTGTGAAAGAAAAGCAAACTTGGAAAGAAAATGAGGTCCCTAATTATAAGGTTAATTAGCAAATGCAGAATACATATAATGCAGGAAAGAACAGTCCTTTCAACTTGTCACTTTCAGATGTCTGTGGTTTCAGCCTGCGACCCTGAAGCACTCTATTTACATGAGAACTACAGAAGTGATCAGGAGGGATTACCCCCGATTGGCTAATCCATCTGGAAACACGGATAATCGTGTTTCTAGACATGCCCAGCCTGAGCCTGGTATCACTGGGATTTAATTCAAGCATCCCAATGGTAGGATGCATCACTGAGACTGAGTACGACAACAACAAACGCTGTACCAAAACCTTTTAGCTAAAATTAGACAACATGTTGAATAAACAGACACAAGCCTCAAAAATAGATTTGTCCCAGAAAAAGTGATTGCACACTCATGCGATTTACTGTGATAATGCTAGACATAAATTAGATGAGTGTCTTGTACTGC[A/G]GGTCTTGGAAAACAACCAACAGTGGTGGTTATTGAGGAACCGCAGTGGTCAGTCAGGCTATGTGCCATGTAATGTGCTGGAAGAGGTCAAACCAGAAGAGCAGCAGTACAACCGAGCAGCTCTATTCAGCAGCCAGGTAAACTACTTCACTGTTCACCCAACAGTCCATATATAGTATATATTTCTGCTTATAATTCTATCTACCTTTCTGTAATGCCATGATGCATCGCATGAATTATGAGAGTAACTTATGCTGAACTGAAAACAATCATTTGAAGGAGACCTATTATGTCCCTTTTTACAAGAAGTAAAATGAGTCTCTGGAGCTTTCTCAGGAGATCAGGTTTTTATAGCACAACCTTATTATTTGAAGTGACTTGTTTAGAGCTCCCTACACCAAAAGTGCAGCCTTTCCTTAAAAGTAATTCTAAACTGAAAATATTAGCAAAGTCTATATCATAACTATAAAGATAAACACTCAAACGAATGAAATCATCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8563
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 |
---|---|---|---|---|---|
ENSDART00000100057 | Essential Splice Site | 69 | 121 | 2 | 3 |
ENSDART00000127636 | None | None | 70 | None | 3 |
ENSDART00000136626 | Essential Splice Site | 174 | 242 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 16097091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16448857 |
GRCz11 | 18 | 16437923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGYCCTTTGAGGTCCACGCTTGGCTCAATGCGAAGGGATTTTCTAGGCC[G/A]TGAGTGAMACATGTGACACTTTAGAATTAGATGATATATGAGTGGTSTGA
Long Flanking Sequence:
CAGGCTGTGAATCCTTACAAAGGTACCACCACCAGCCCTGTACCTGTAAATCACGCCGTGGTTTTGGAGATGAATAAATCCTCCCGGGATAAAGATAGTACGTATACCTCTTATCGGCCTCGCTGTATTTGCTGAGAGATGGAGAGCGCGGAGAGTCTGCCGGAAAAAAAAAAAATGCAGAGAAGTGGGAAATGAATTTGGTGTGCAAGTGCTCTTATGTACATAGATTGCAGATCGCTCCTGTCTTGGCCAATCTTATTCACTGTGTCTCTGTCCCAGTGCTTGTTTCTCCATCTCCAGCTTCTCCTGTCTGTCTCTATAGACCGCGACCAGCAAAAGGAGGTAAACGATGAGCTGCTGAAGAGGATAACAGACAATAAAGCTCAACCTCCGGCTCGAAACTTCCGGGTGGAACGCTCTAGCAGATCCATTCGCATCACAGATGAATCGCAGCCCTTTGAGGTCCACGCTTGGCTCAATGCGAAGGGATTTTCTAGGCC[G/A]TGAGTGACACATGTGACACTTTAGAATTAGATGATATATGAGTGGTGTGACCTAGTGGTTAAACGTGAGGGTTGTTAACCGAGGTGGCAAGTCCAAAGCTCAGAAGCAATGATCCATGTACCCTTGAACAAGGTACTTACTCTGCAGGTGACTCCAGGGGACTGTGGTTGAGATGTTCTGAATATAAAGCTTATTGTACAGAGGTCATAATAAAACTTGGGAAATATAAGTATATTTATTACCCATATGTAATTTAATAGGGAGGTACGGTGGCTCAGTGGTTAGCACTGTCACCGCACAGCAAGAAGGTCGCTTGTTAGAGTTCTGGCTGAACCTGTTGACATTTCTGTGTGGAGTTTGCATGTGCTCCCCGTGTTTGTGTGTGTTTCCTCTGGGTGCTCTGGTTTACCCTACAGCCCAAAGACATGCACAATAAGTGAATTAGAGAACCTAAATTGGCCATAGGGTATGAGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined