ZMP
pdcd11
Ensembl ID:
ZFIN ID:
Description:
protein RRP5 homolog [Source:RefSeq peptide;Acc:NP_001082837]
Human Orthologue:
PDCD11
Human Description:
programmed cell death 11 [Source:HGNC Symbol;Acc:13408]
Mouse Orthologue:
Pdcd11
Mouse Description:
programmed cell death 11 Gene [Source:MGI Symbol;Acc:MGI:1341788]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10691 | Nonsense | Available for shipment | Available now |
sa9850 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10691
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 |
---|---|---|---|---|---|
ENSDART00000074342 | Nonsense | 416 | 1816 | 9 | 35 |
ENSDART00000108733 | Nonsense | 413 | 931 | 10 | 31 |
ENSDART00000124833 | Nonsense | 416 | 1816 | 10 | 36 |
The following transcripts of ENSDARG00000052480 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 49953986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 48803167 |
GRCz11 | 1 | 49447587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AMAAACCACCTGATGTCCCAGWCTCAGCATATTCTGAGGATCATAAATTA[C/A]AGTCCAATAGAGCAGATCTACCARGCCACGCTCCGCTGGTTGGTTTTGAG
Long Flanking Sequence:
TCTATCTCTCAGGAACACTATATTGTTTGACCGCCTGCTCCCGTTCAAATTACAAGATTTGCCAATCACCACCATGTTTTATTCAGAAATTTATTTCCGTGCCGCAAGAAATCTGTTTGGGTCCTCATGATTGAAGTCCAATGCAGACCTCAAGATTGCAACTACATTTAATTCAAAGTGATTCAAACTTGATTCAAGCACCATCTGCTGGTCAAAAAGAGAAATGCAACAATACATGTATGGGTCAACGACTAAAAGTGGCTTAACTGTGTTTTTTATACTGTTGCCGCTATCCTTTAAACCACTGCATCTTACGCATTCGTTGGATCACTCATTCTATTATATATTTTAAAGTGATTGTAATATGAAACATGAAAACTGGTCATTTACTCATCCTTTACTTTTCTCATGCAGAGAAACCTGCTGAAGGAGCCCAAAGAAGAGCTCGACACAAACCACCTGATGTCCCAGACTCAGCATATTCTGAGGATCATAAATTA[C/A]AGTCCAATAGAGCAGATCTACCAAGCCACGCTCCGCTGGTTGGTTTTGAGTAGAGCTGGGCAGAAAAATAGTTTGAATCAATTCTGAAAATTCCAAAATGCATCACTATTCTGAATTCTGAGCTTGATTTATTTATTTATTTTTTTACAGCAGATGGAGTTTTATGCTCGTTGTTAACAGAGGATGACGTTCTAAATTGGTTTTGATCAGCATATGGCACTCTAGGATAGTTTTGAACAGCAGATGGCGCTCTAGGATAGTTTTGAACAGCAGATGGCGCTCTAGGATAGTTTTGAACAGCAGATGGCGCTCTAGGATAGTTTTGAACAGCAGATGGCGCTCTAGGATAGTTTTAACAGTAGATGGCGCTCTAGGCTAGTTTTTAACACCGAAATCCTCTCAAGGAAGAGGTGTTGTGTGTTCGGCTGAGTCATGCAAGTCAGCTTTTATGTCATGAAATGACTAAACACGGCTCGCTATGAACATTTTTGTAATTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9850
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 |
---|---|---|---|---|---|
ENSDART00000074342 | Essential Splice Site | 1513 | 1816 | 30 | 35 |
ENSDART00000108733 | None | None | 931 | None | 31 |
ENSDART00000124833 | Essential Splice Site | 1513 | 1816 | 31 | 36 |
ENSDART00000074342 | Essential Splice Site | 1513 | 1816 | 30 | 35 |
ENSDART00000108733 | None | None | 931 | None | 31 |
ENSDART00000124833 | Essential Splice Site | 1513 | 1816 | 31 | 36 |
The following transcripts of ENSDARG00000052480 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 49981447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 48830628 |
GRCz11 | 1 | 49475048 |
KASP Assay ID:
2259-1063.1 (used for ordering genotyping assays)
KASP Sequence:
CAGACGACAACCAGAACTCCAGTGAGGATGAGGAGGAAGTCAAAAGCAAG[G/A]TGAGCTCAHGTGTCAATCAAAAGCTCMATTTCTTCTGTGTAGACTTTAGG
Long Flanking Sequence:
TAATTTATTTACTTTTATATATTATTTATTTTATTGTATTTTTTATCATTTATTTACTTTTTATTATGCATTTATCTTATTGTACTATTGTTTTATTTTATTGTATTGTGTATTTAATTTTTTTTTTTCCAGTAACAGACTCCTGAGAGTTTTGTATAAAAGTGTGCTCACTTAATTTTTCCTTTGCATCATGCTATACATTTGCCGTTTTCAAAACCATGCACATTATTCATGTCTATGCTTACTTGACCTTCACTGAGGATGATTTAAAAGAGGATTGATAACTTATTAATTCTCAGCTTTCCTAATCAAAATACACGATTTCCTCTGATATCTTACATTTTCTAAATGTTTAGGTTAAATGCAAGGAACAGGAACCAAACCGGCTTCAGGTGACATCCAGCTTCCCATGGGAGTCCACACTGGGCTCTTTAACACCTTTTGCTCCAGCAGACGACAACCAGAACTCCAGTGAGGATGAGGAGGAAGTCAAAAGCAAG[G/A]TGAGCTCAAGTGTCAATCAAAAGCTCCATTTCTTCTGTGTAGACTTTAGGATATACCATCAGAAATGTATGTTCTTCATTCCCCTATTAGCCATGATTTGCCAAAACTTTGCATTTACTTGCACATTTGCATTCCCTCAAGAAACAAACATGTTTTTTTTTACCTTTAGGATTCCTGTATATATAAGATTCTAAATATTTATGTTTTGTGTTTTGCACTCTCTACTACACAACAATATTCCAACGAGAGCTTTGCTTATTCTCACTCTTAAAGGGATAGTTTAAAAAAAAACTACTCACCCTCAAGTGGCTCCAAACCTTTGTGAGTTTCCTTTTTCTGTTGAACACTAAAGATATTTTAATGAAAACTGATAACTATTGACTTCCATAGTAAAGAAAAAACATATTATGGGAGTCAGTGATTACAGGATCAAAGAAACTTGAAGAGTAAATAATGAGTAAATGTATATTTTTGGATGAACTGTAACTAAGGTTATGGCC
Associated Phenotype:
Not determined