ZMP
pdcd6ip
Ensembl ID:
ZFIN ID:
Description:
programmed cell death 6 interacting protein [Source:RefSeq peptide;Acc:NP_998525]
Human Orthologues:
AC011767.1, AC055876.3, PDCD6IP
Human Description:
programmed cell death 6 interacting protein [Source:HGNC Symbol;Acc:8766]
Mouse Orthologue:
Pdcd6ip
Mouse Description:
programmed cell death 6 interacting protein Gene [Source:MGI Symbol;Acc:MGI:1333753]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5928 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43338 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9404 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5928
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028592 | Nonsense | 576 | 873 | 13 | 18 |
ENSDART00000122296 | None | None | 465 | None | 12 |
ENSDART00000135164 | Nonsense | 569 | 866 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 19 (position 44471185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43298953 |
GRCz11 | 19 | 42868390 |
KASP Assay ID:
554-3779.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTGGCGCAACTGGATGAGGTCAAGAGGGAACGAGAAGTTCTGGAAGGA[G/T]AGGTGAAGTCAGTGACCTTTGACCTGACGGCAAAGTTTCTTACAGCACTG
Long Flanking Sequence:
CAATTTAATTATTAGTTAAAAATGTATTCAATAAAAACCTGTTTAATTTTCATAAAAAACTGTTGAAAGTGATTCAAATATTTAGATACAGTCATTCATTCAATGCAATTACTCATTTTTAAAGTTAGTCATGGTACAATTTCTTGTGCTTGAGTGCTTTCAAAATCATTATACCGTCACAGGCATCAAAAGCACATACAAATGACAAGTTATAATACAGACTGAAGATTGCAGATAGTGTGATGTGACTATTGCGAATGATCACATTGCGATATCAGTGCTGAAACGATATATTGAACAACCCTAGTATAAACAATTATACTATTAAAATAGGTGTTAATATTAAAAATGCCTAAATGGTATATAACACCAAAAAACACACACTAACCAAGCTGTTATACTAATGCCAAGTCTCATCTCCTGCACAGGTGGTAAATGTGTTGAGGTCTCAGCTGGCGCAACTGGATGAGGTCAAGAGGGAACGAGAAGTTCTGGAAGGA[G/T]AGGTGAAGTCAGTGACCTTTGACCTGACGGCAAAGTTTCTTACAGCACTGGCTCAAGATGGCGCCATCAATGAGGAGGTCATGACCAGCAGTGAGCTTGACGCTCGATACGGCTCACACAATCAACGCGTTCAACAGAACTTACGCAGACAGGAAGAGCTGCTGTCACAGATACAGGTGCGTAATAAATAGATTATAAATAGCGTAATAAATCTCTTAAATAGATTCCGAGGTTACTTTATACATTACAAATATTCTGCTTGCATTGAACCTGAAATAATCATTATTAGTTAACTAAAAAAAGGTTTACGCAAATTACAAGAGTGTTCACAGTGAGTTATGTTTACATTAATATAATCTCTGCTGGTAAAAACTAGCCCAGAACCCCTTCTGCTGTTTAAAAACTACCCTTGAGCACCATCTGCTGTTATAAACCAGCCTAGAACGCCATTTGCTGTTAAAATCTAGCCTAGAACGCCATCCGCTGTTTAAAAACTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43338
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028592 | Nonsense | 799 | 873 | 17 | 18 |
ENSDART00000122296 | None | None | 465 | None | 12 |
ENSDART00000135164 | Nonsense | 792 | 866 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 19 (position 44475284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43303052 |
GRCz11 | 19 | 42872489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCCCCAATGGCTCCCGGCAGCTCTAATCCTCCACCTGTTGCACCCACT[G/T]GACCCTCACAGGCTCAAGGGCCACCATACCCCAGTTATCAAGGCTACCCA
Long Flanking Sequence:
TTATTATCATTAAACCAGCACAAATATACACTCAGGAAATATTAAATGTTTTACAAAAAAACATTAAACACTCCTGGTGTCCACAGAATAACAAATCATAATGGCTTCAAAATCCTCATTTCTCACCAGGCAAATGATTGGCTGATAATTGTCTCATTTTACAGGGAGCTGCAGCAGAGTATTGCTCGAGAGCCAAGCGCTCCTTCATTCAGCGTCCCGTCATACCAGTCCAACACCCCTGCCCCTGCAGGAGGCCCGACCCCTGCGCCCAGGACTGTGTTTGTGAGTTCACACGCACTGATGACAGATATAACACTTGATCGCATGCAATAGTCTGATGTATATCTGTTTTCCAGTCACAGCAGCAGCCTCAGGCTAAGCCCCAGCCGCCGGCGAGACCCCCACCCCCCAGCATCGCTCCTCAGGCAGCCAGTGCTGCCGTTCCAGTCAGCGCCCCAATGGCTCCCGGCAGCTCTAATCCTCCACCTGTTGCACCCACT[G/T]GACCCTCACAGGCTCAAGGGCCACCATACCCCAGTTATCAAGGCTACCCAGGGTAAATAAAGACATTCAAGAGTGCATGTGTCCTCAGTGTTAGGTACAGTTGAAGTCAAAATTATTAGCCCTTCTGAATTATTAGCCCCTTTGAATGTTTTTTTTTCTCCAATTTCTATTTAAATTAATTGGGTTAATTAGGCAAATTATGGTAATGAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTAGACAATTGAAAGAAAACATTGCTTAAGAGAGCCAATAATATTAACCTTAAAGTGGTTTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAGACTTATAAGGCAAGGCAAATAAGTTTTCAACTCGATGGGTGTTATAGTCTATGCTTTAAACTAGCGTTTCTCAACCATGTTCCTGAAGGACCACCAGCTCTGCACATTTTCCATGTCTCTTTAAGCATACACACCAGATTCAGATCATCAGCTCATTAGCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9404
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028592 | Nonsense | 839 | 873 | 18 | 18 |
ENSDART00000122296 | None | None | 465 | None | 12 |
ENSDART00000135164 | Nonsense | 832 | 866 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 19 (position 44476418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43304186 |
GRCz11 | 19 | 42873623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCYTATAATCCCTATGCATACGGGCAGTATAATATGCCCTACATGCCCTA[T/A]CAAGCTCAGGGCCAGGCTGGATACCCTGGAGCCCCTGCAAYACAGCAACC
Long Flanking Sequence:
AGGGTGTAAATACACAGTACAGTTACGATCTTATTGCCAAATTATATTGTTATAATAGCATAATATAGGCCTTCAGTGATTTCCTGAAGATAAATGACAAAAAATAACACAACTGTAATAAGTACAGCAGGCGCGATCGATCATCTGATCTCATATGAGGCAAGAGCTCACGATGACATATGATGGCCTGTGCAGGTGCTGTAGTGATGTCCCAATTTCTTAGGGGTAAATTTTAAAGCTCTTCCCCTTCACACTCTTTTTCAAGGGCCAAAGGCAAGAGGAAGGGGTACAAAAATAGAACTGGGATTGGGCCTTAATAATTACTACTTAATCAAATTTTTCAGCAGCAGAAAGCTCACTAGGTTTTACAACACTCTGCATATTACAGAAGCATGACTTTTGTATATTTCTCTTTTTCTCCTCTCTTTTAGGTATTACCAGATGCCAATGGCCTATAATCCCTATGCATACGGGCAGTATAATATGCCCTACATGCCCTA[T/A]CAAGCTCAGGGCCAGGCTGGATACCCTGGAGCCCCTGCAACACAGCAACCCTACCCCTACCCTCAACAACCACCCCAACAACAGCCCTATTACCCCCAACAGTAGAGCAACAACCTCCGCGACTACAGCCACACTCATTCCTGTAAACTAGCACTCTTCTTACTGCACTTATCTATTAACACTCCTGCACTCACACGCACTCGATCTCTACTTAACATCCCATTGGATCTGGGCGGGGTTTAAGACACAAGCCACACCTTTTATACAGTAGGGCGGAGTTTAGAATGTAAGCCACACCCTTTAAATAGGAGGGCAGTTTAGAATGCAAGCACTGCGTCTTCTATGGGAGGGTGGGGTTTAGATCTTAAACCACACCCCTTGTATAGGAGGGCGGAGTTTAGAATGCTAGCTCTGCCTCTTGTTTGGGGGCGGGTTTAGACAATAAATCACACCCCTTGTATAGAAAGGCGGGGTTTAGAATACGAACTCTGCCTATTGTA
Associated Phenotype:
Not determined