ZMP
si:dkeyp-192m14.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate epidermal growth factor receptor pathway substrate 15 (EP15) [So
Human Orthologue:
EPS15L1
Human Description:
epidermal growth factor receptor pathway substrate 15-like 1 [Source:HGNC Symbol;Acc:24634]
Mouse Orthologue:
Eps15l1
Mouse Description:
epidermal growth factor receptor pathway substrate 15-like 1 Gene [Source:MGI Symbol;Acc:MGI:104582]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24121 | Nonsense | Available for shipment | Available now |
sa14244 | Nonsense | Available for shipment | Available now |
sa43801 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa820 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24121
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080047 | Nonsense | 295 | 929 | 10 | 26 |
Genomic Location (Zv9):
Chromosome 22 (position 16092724)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15920294 |
GRCz11 | 22 | 15946564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGGTTGCAGACAGGGGGCGCTATGATGACATCTTCCTCAAAACAGACT[C/A]AGATCTGGATGGTTTCGTCAGCGGACTAGAAGTTAAAGACATCTTCATGC
Long Flanking Sequence:
TTTCACTACTGTATTGTTTTTAAACAGAGAAAATACAGGTGTGAATCACCAAATGCGACCAATATTAAAATGAATTTGAATACTATTTTTCTTTTGTTGTTATCCATGAATTTTCAAATGTACTTAATGTGGTTATTATGACCATCAGGCAATCTAGTTCAGCTAAACTTGTGCTTAAAATGTCACTAAAATGCAGTATTTAAATCTCATAAATAAGTAGTAGCTCAAATAAGGCCTATCTTATTTAAAAAGATCCACTTTTTGGGAAAAAAGAACCACCCCTTTTACCAGGTTGACACCAGATGCATATTTAATTAAAGAATGCCTCATTTGCATATTTAAATATCACATGTTTAAATAACTTTATTCGCTTTTTCACCACCTGCATTGTTTTTATGCCTTAAAGATGAATGTTTTATTCATCCCTCAGCATTCAGTAAACTGGGTAGTGCCGGTTGCAGACAGGGGGCGCTATGATGACATCTTCCTCAAAACAGACT[C/A]AGATCTGGATGGTTTCGTCAGCGGACTAGAAGTTAAAGACATCTTCATGCAGTCTGGACTTCATCAGAACCTTCTGGCACACATTTGGTAACAACAAAATTTTAACATTTGAATTTTTTGTCGTGGTTGCCAGATTCATCACTTCATCACTCTGCTGTGTTTGTCAGGGCTTTGGCGGACACCAGGCAGATGGGCAAACTCACACGCGAGCAGTTCTCCTTAGCCATGTATCTAATTCAGCAGAAAGTGAGCAAAGGTCTGGATCCTCCGCAGGCTTTGACACCAGACATGATCCCACCATCTGAACGCGGCACACCGGGACCTGTGAGTCTCATGTTTACCACTTTACACTTATGGAAATGCATGATAGGCTTCTGCATTGGACTGATAGGTTGATGTTTTAAATCTGAAGGAAGTGAGCCACTGAACATGTATAATTTAGCCACATTTTTACCATAAGTCTAGAATAACTAGAACTAAAACAATTAAATGAGCTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14244
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080047 | Nonsense | 345 | 929 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 22 (position 16092493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15920063 |
GRCz11 | 22 | 15946333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAGGCAGATGGGCAAACTCACACGCGAGCAGTTCTCCTTAGCCATGTA[T/A]CTAATTCAGCAGAAAGTGAGCAAAGGTCTGGATCCTCCGCAGGCTTTGAC
Long Flanking Sequence:
AGGCCTATCTTATTTAAAAAGATCCACTTTTTGGGAAAAAAGAACCACCCCTTTTACCAGGTTGACACCAGATGCATATTTAATTAAAGAATGCCTCATTTGCATATTTAAATATCACATGTTTAAATAACTTTATTCGCTTTTTCACCACCTGCATTGTTTTTATGCCTTAAAGATGAATGTTTTATTCATCCCTCAGCATTCAGTAAACTGGGTAGTGCCGGTTGCAGACAGGGGGCGCTATGATGACATCTTCCTCAAAACAGACTCAGATCTGGATGGTTTCGTCAGCGGACTAGAAGTTAAAGACATCTTCATGCAGTCTGGACTTCATCAGAACCTTCTGGCACACATTTGGTAACAACAAAATTTTAACATTTGAATTTTTTGTCGTGGTTGCCAGATTCATCACTTCATCACTCTGCTGTGTTTGTCAGGGCTTTGGCGGACACCAGGCAGATGGGCAAACTCACACGCGAGCAGTTCTCCTTAGCCATGTA[T/A]CTAATTCAGCAGAAAGTGAGCAAAGGTCTGGATCCTCCGCAGGCTTTGACACCAGACATGATCCCACCATCTGAACGCGGCACACCGGGACCTGTGAGTCTCATGTTTACCACTTTACACTTATGGAAATGCATGATAGGCTTCTGCATTGGACTGATAGGTTGATGTTTTAAATCTGAAGGAAGTGAGCCACTGAACATGTATAATTTAGCCACATTTTTACCATAAGTCTAGAATAACTAGAACTAAAACAATTAAATGAGCTAATAATAAAAACAAATATATTATTTGATAAAGTTTTAGATTCAAATAAAAAGACAATTGCATTAAATAAATAACGTTCCCTTAACCCTTGTGTGCTGTGCGGGATGTTTTCATCCATTCTGGAGTGATTTTGAGTCCTAATTTGGCCACAGTATTCTCTGTGTTTCAGCAAAGGGAATAATATTTCTTATTTTGACACATATTTGGGCAAAATGCTTTGAAAAAAAAAAAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43801
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080047 | Nonsense | 671 | 929 | 19 | 26 |
Genomic Location (Zv9):
Chromosome 22 (position 16078515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15906085 |
GRCz11 | 22 | 15932355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACACAGACCCCTTCCAGTCTGAAGACCCCTTTAAAACAGACCCTTTC[A/T]AAGGTTTGTCATGGCTGTTTCCTTTTCTTTTTCTTCTTTTAAACTTATTC
Long Flanking Sequence:
TAAACCCAGCACTTTTAACAGAGGTTCTTATGTTACTTTAAACAGCTAAGATTGGCTGAAAATGAAAAACGACTGACACTTATAGAGACGTGGTTTTGGACCTTTCGGCCAAAGCTGACAGTACACATTTATCGTAAAAGGGATATTGTACACAAAAAATAAGTAAATCTGTCATCAATTACTCATTTTTAAAAATAACAGAAGATATTTTGAAGAATGTTGGAACCCGGTAGCCATTGACTTCCATAGTAAGGTTTTTCTACTGTGGAAGTCAGTGTTTTTAACATTCTTCAAAATATCTTTTTTTGGTTTAACATAACCTAACTTAACCCAAATGTTACCTTAATGTTACTTTTCGAGTGAACTATGCCTTTAAGTGTTTATTTGAATTGTTACAGGAAGACCCGTTTAAGGTAAAGCCCACTGTGTTCAACAGCGCCCCTCAGGAGATGCACACAGACCCCTTCCAGTCTGAAGACCCCTTTAAAACAGACCCTTTC[A/T]AAGGTTTGTCATGGCTGTTTCCTTTTCTTTTTCTTCTTTTAAACTTATTCACAATTTACACACTCTCAAGTAATTTCAAACCTTTATGACTTTCTTCAGTTGTACATAAAAGAAGATATTTTGATGAATGTTGAAAATCAGCATCCATAAAACAGTACTATGTAAGTCAATGGTTACCAGTTTCATTCTTCAAAATATCTTCTTTTGTGTTCAACAGAAGAAAGACTCTCAAACAGGTTTGTGAAAAGTGGAGGTGAGTAAATGAAGACAGAAGTTTCAGTTTGGGTGTCTATCCCTTTAATTATGGTTTATTGTGACAAAATGTAGTTTTAGATTTCTATTTTGTGGCACATTTTCGGGATTAGGCTTTGGGTTGGCTACTAAAAGCATCTCCTTGTTTGCTTTTGTATGTTTTGTAGGCGATCCGTTCCAGAATGACCCTTTCTCAAAACCGGCCACCACAGTCCCAGGTATGCGGCTTTCAGGTTTTGAGCTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa820
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080047 | Essential Splice Site | 813 | 929 | 24 | 26 |
Genomic Location (Zv9):
Chromosome 22 (position 16071789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15899359 |
GRCz11 | 22 | 15925629 |
KASP Assay ID:
554-0724.1 (used for ordering genotyping assays)
KASP Sequence:
GCACTCCCGCCCAAAAAAAGTATACCACCACGACCCAAACCACCCAGCGG[T/C]AAGACTTTAAGAGRCACACAAACAAACTGTGACAAAATTTATATACACAA
Long Flanking Sequence:
TCTAAAATACATTTATTATTTTTGCTAATTATTGTTTAAGTGTTTATTGAGTGTTTTATTAAAGTTTATTGTTGAATAAACCTATGAACAAAATTACTTTAAAAAGATGCTTCATTGTTTTTCCTATTTCCAATTTCAGATTTCTTCGGCACTTTAGACCCATTCGGTAGTAGTACGTTTGGCAGCAACAGCGGCTTTGCAGACTTCAGCCAAATGTCAAAGGTAGTTAACACCTTTTTCATCTGTTACACTTGCATCATAAGCACAGTGGAGCTCCAGTTTCTCACACGTTTGCAACATGACTTTCATAAGATGTGGTTTTGATAGAGATCCCACTCATAATTCATGTTCTTTGCACCTTACTGATTATGGCCCACCACTTCTTCTGCCTTCTGAAATTCAATTTAGGGCTTTGTAGAAGACCCCTTCAGCCGAAAACAAGACATGCCAGCACTCCCGCCCAAAAAAAGTATACCACCACGACCCAAACCACCCAGCGG[T/C]AAGACTTTAAGAGACACACAAACAAACTGTGACAAAATTTATATACACAACCATATAAGGTGTTTAATCAAACTAGTGTTCAGTTTCTACAAGTAAACGTTTACTAAAGCTACACAGCTGTTGTGTCTGGAAAAAGGGTTAGTAGACAAAACAGGTAATGCAAACAGCCAACATGAAAGACCAGGAGAAATGTTGTTTAGGTGGATAACTATACATTTTTTTTTGATATGCAATGAGAAAAATCAGCTGTAGCTTTGCAGTGAAAGCAAAGCAGCTTTGAGTAGAAATTTGGTGTCCTCCTTTCACACATTTATGTTGTGGACATTTATGTGTTATTTTACATGCATTTAAGCATGCCAGATAAGAAAAACTTAATGGAAACCCCAAAATGCACATACATTGTAAGATTTGTATTTTTTTTGACGATAAGTAGATTGTAATCTAGATTGACGATAAGTATTTTGAATAAACTACAAAATAAACACATTTATCAAATACAG
Associated Phenotype:
Not determined