ZMP
PELI3
Ensembl ID:
Description:
pellino homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:30010]
Human Orthologue:
PELI3
Human Description:
pellino homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:30010]
Mouse Orthologue:
Peli3
Mouse Description:
pellino 3 Gene [Source:MGI Symbol;Acc:MGI:1924963]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16556 | Nonsense | Available for shipment | Available now |
sa30885 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40857 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16556
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 |
---|---|---|---|---|---|
ENSDART00000127428 | Nonsense | 181 | 477 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 19412112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17884971 |
GRCz11 | 7 | 18137238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGGAGAAGGAGGACAGTCGGCCCAGAGCACCATCTCCCGCTATGCCTG[T/A]CGTATCATGTGTGAGCGCAGCGCCCCRTACACAGCRCGAATATATGCAGC
Long Flanking Sequence:
ACAGTAGTACTGTGAAATTTATAATTAAATATTTTAAAATAGGAATTATTTTTGTGATGTCAATGTTTAAAAGGTTTTCTAGGATCAGTTGAAAGTTCGAGACAACATAATTTATTTGAAAAATAATACTTTTATGACAATTTAAATGCTTTTATAGTTTTATTATGTATCTTTTCTGAATAAATTTAAATTTATTTAAAAACAAAAGAAGCTAAAACAGAACTAGTTACATAGATAAAAACAAGTCATCGATTTTTTGTATATATACCCTCAAATGTCATATACTGTAGGTTTGGAAAGGTAAAGCTTATTTAAGTGAATAAATCCTAAACATCTCACTTTCTCTCGTCGCTGTGTCTCTAGATCGGCCGTTCCACAGAGAGCATGATAGATTTCGTGGTGACAGACACAGCGAGCAGTGGCGGTGGAGGACAGGGCCAGGGTGGTGCAGGTGGAGAAGGAGGACAGTCGGCCCAGAGCACCATCTCCCGCTATGCCTG[T/A]CGTATCATGTGTGAGCGCAGCGCCCCATACACAGCGCGAATATATGCAGCCGGCTTTGACTCTTCCAAAAACATCTTTCTTGGGGTGAGTCATGACAAACTACTGAGTCATAACTACATTTACTGATGCAGAATCTCTGCCAAGGCGCCGAGGAAGACAACACAGCTCAATAGGATCATTTACACTGATATCTAGGAAGCAGCAGAGAGGAAAAGGGCGCATCATTTCCATACTGTTTTGCCTGTTAAAGTCTGTTTGTATTGCTTTTAAATGGAGGAAAATAAATGTTTGAAATGGGAGCTGCCTACTTCAAACCTAAGCACATAAAAACACATGATTCTTCCTCAAAGTCATAAATATAACAATGTAACAGCCAAAATATATCTACACAGCCATTTACAGTAGTGTTTTTTATTTTTAGAACTCATTTTGTTACTTATCATTTTGAACTCATTTTATGCTACTCTGACATCCTCGACCTGCAAAAAAAAAAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30885
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127428 | Nonsense | 309 | 477 | 6 | 6 |
ENSDART00000127428 | Nonsense | 309 | 477 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 19397915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17870774 |
GRCz11 | 7 | 18123041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCTTTGGCGGACTCCTAGCGGTCTTCGCCACACCCCGACTCTTAAA[C/T]AGCTGGAGTCTCTTCGCCAGGAGTTAAACGCTGCCCGTCCCCAGTGCCCC
Long Flanking Sequence:
AATAGCACAAATTCTGAAATGAGTTGGATGTTTTGACTAGTTATGTGCACATTATGTGCCCGTTTCTCTAAAACCAGCCTGGTAGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGAACCAAAAAAAATTATCATCATTTACTCAACCTTGTTGTCCCTTCTTATATTTTTGTGTGTCCTGCTGAGTTTAGCTTCAACTTGCTTAAAAAACACCTGTCTGGAATTTTCTAGTGTACCTAGTAAGCACGTGACCTAGTTGGGGTTGGAGCTAAACTCTGCAGGACACTGGCCCTCCAGGACCGAGCTTGGGCATCTATTATTCATGTTTTGAATAAACGTACATGTTTTTGTTGTCTTACCTCACAGGTAGAGAACGAGTCCAACATGCTCCAGGATGGTTCCCTCATCGATCTCTGTGGAGCCACTCTGCTTTGGCGGACTCCTAGCGGTCTTCGCCACACCCCGACTCTTAAA[C/T]AGCTGGAGTCTCTTCGCCAGGAGTTAAACGCTGCCCGTCCCCAGTGCCCCGTGGGCTTCAATACACTCGCCTTCCCCAGCCTGGCACAGCGAGCCACCATTGACAAGAAGCAGCCCTGGGTCTACATGAACTGCGGCCACGTACACGGCTACCACAACTGGGGCTTCCGCAAGGAGAAAGCGGGAGTCGCTGCGGTGGCGTTAACTGGGGGTGGAGGCACGGCTCCGGCTACGACTGGAGAGCGCGAATGTCCCATGTGTAGAGGGGTGGGTCCTTACGTGCCCCTTTGGCTCGGGTGCGAAGGGGGCTTATATCTGGATGCAGGGCCCCCAACACATGCGTTCTGCCCCTGCGGTCACGTGTGCTCGGAAAAGACGGTGCAAGGCTGGAGTCAGATCCCACTGCCGCACGGAACGCATGCCTTCCACGCTGCTTGTCCTTTCTGTGGAACGTGGCTGACCGGGGAACAAGGCTACATCAAACTCATCTTCCAAGGGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40857
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127428 | Nonsense | 309 | 477 | 6 | 6 |
ENSDART00000127428 | Nonsense | 309 | 477 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 19397915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17870774 |
GRCz11 | 7 | 18123041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCTTTGGCGGACTCCTAGCGGTCTTCGCCACACCCCGACTCTTAAA[C/T]AGCTGGAGTCTCTTCGCCAGGAGTTAAACGCTGCCCGTCCCCAGTGCCCC
Long Flanking Sequence:
AATAGCACAAATTCTGAAATGAGTTGGATGTTTTGACTAGTTATGTGCACATTATGTGCCCGTTTCTCTAAAACCAGCCTGGTAGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGAACCAAAAAAAATTATCATCATTTACTCAACCTTGTTGTCCCTTCTTATATTTTTGTGTGTCCTGCTGAGTTTAGCTTCAACTTGCTTAAAAAACACCTGTCTGGAATTTTCTAGTGTACCTAGTAAGCACGTGACCTAGTTGGGGTTGGAGCTAAACTCTGCAGGACACTGGCCCTCCAGGACCGAGCTTGGGCATCTATTATTCATGTTTTGAATAAACGTACATGTTTTTGTTGTCTTACCTCACAGGTAGAGAACGAGTCCAACATGCTCCAGGATGGTTCCCTCATCGATCTCTGTGGAGCCACTCTGCTTTGGCGGACTCCTAGCGGTCTTCGCCACACCCCGACTCTTAAA[C/T]AGCTGGAGTCTCTTCGCCAGGAGTTAAACGCTGCCCGTCCCCAGTGCCCCGTGGGCTTCAATACACTCGCCTTCCCCAGCCTGGCACAGCGAGCCACCATTGACAAGAAGCAGCCCTGGGTCTACATGAACTGCGGCCACGTACACGGCTACCACAACTGGGGCTTCCGCAAGGAGAAAGCGGGAGTCGCTGCGGTGGCGTTAACTGGGGGTGGAGGCACGGCTCCGGCTACGACTGGAGAGCGCGAATGTCCCATGTGTAGAGGGGTGGGTCCTTACGTGCCCCTTTGGCTCGGGTGCGAAGGGGGCTTATATCTGGATGCAGGGCCCCCAACACATGCGTTCTGCCCCTGCGGTCACGTGTGCTCGGAAAAGACGGTGCAAGGCTGGAGTCAGATCCCACTGCCGCACGGAACGCATGCCTTCCACGCTGCTTGTCCTTTCTGTGGAACGTGGCTGACCGGGGAACAAGGCTACATCAAACTCATCTTCCAAGGGCCC
Associated Phenotype:
Not determined