ZMP
pigx
Ensembl ID:
ZFIN ID:
Description:
phosphatidylinositol-glycan biosynthesis class X protein [Source:RefSeq peptide;Acc:NP_001119908]
Human Orthologue:
PIGX
Human Description:
phosphatidylinositol glycan anchor biosynthesis, class X [Source:HGNC Symbol;Acc:26046]
Mouse Orthologue:
Pigx
Mouse Description:
phosphatidylinositol glycan anchor biosynthesis, class X Gene [Source:MGI Symbol;Acc:MGI:1919334]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37405 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14619 | Essential Splice Site | Available for shipment | Available now |
sa18479 | Nonsense | Available for shipment | Available now |
sa6688 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37405
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 |
---|---|---|---|---|---|
ENSDART00000092991 | Nonsense | 6 | 243 | 1 | 6 |
ENSDART00000131110 | Nonsense | 6 | 232 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 2180099)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 2921189 |
GRCz11 | 22 | 2937455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGTTGGGATTAGAGCATGAGCGCGGATCAATGATGGTTTATTTATA[T/A]TTATTAGCAACGGTGTTGTGTTTTATTCATCATGGAAATGCGCAAGAAGG
Long Flanking Sequence:
ATAAAGGGACTAAGCTGACAAGAAAATGAATAAATTTTATAAATTACACTTGTTTAAAATATATAATAAAAACTGTTATATAAGTACATGTATTTATAATAATATTTTAAAAAACGCTATTAAAATCTGTCTAGAGTTAACTATTTGTGTGTAGTGTAACTATAGCAACCGCGAGCGTTTCAATTGTTGAAATGTACGTTTATATTTACCATTGCTCAATTCGCGCTGAATGTTTTCTTAAAGACACAGGCTCGCATTGACCACACGACGGACGAGCTCGTAAATAAGCCATTAATTAAATGTAACCCGAATAAAACCTTTGTTGTGGTCATTTGTCTGAGGTTTCCATGTTTCTTCTCTGTCGTTTTCTTCTACTGAGAGAGGGAGTTTAGCGCGACGCTCATTGGCGCCCTCCACCAGAAAGACGTCATCGGACACGGAAGTAAACACTTGGAGTTGGGATTAGAGCATGAGCGCGGATCAATGATGGTTTATTTATA[T/A]TTATTAGCAACGGTGTTGTGTTTTATTCATCATGGAAATGCGCAAGAAGGTATTTATGATGCTAAACATACTGGTTAATGTTGGTTTATGTATGAGTTATCGTTATAAGTGACAACTTTGTGCATATTTTGTTCCTATTTAGCAGATGATTGTTTTCCCACTGAATGGCTGAAGTCTCTGGTCATTTCTGTGAACATTTCCAAAGCTGGATTTCACAGGTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCATTGGTTTATTCATGTTTTAATTGTGATGTGTTGTATAGAGATCTGGAGTACAGTGTTTACTGGAGTGAAACAGATCATGACGTGAAAGCTTTACTAGTGCAGAAGATGCCGAGTGGAGTTTACATGGATGAATATCAGCTGGAGACTCTGAGACATGACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14619
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092991 | Essential Splice Site | 23 | 243 | None | 6 |
ENSDART00000131110 | Essential Splice Site | 23 | 232 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 2180048)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 2921138 |
GRCz11 | 22 | 2937404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTAGCRACGGTGTTGTGTTTTATYCATCATGGAAATGCGCAAGAAGG[T/A]ATTTATGATGCTAAACATACTGGTTAATGTTGGTTTATGTATGAGTTATC
Long Flanking Sequence:
GTTTAAAATATATAATAAAAACTGTTATATAAGTACATGTATTTATAATAATATTTTAAAAAACGCTATTAAAATCTGTCTAGAGTTAACTATTTGTGTGTAGTGTAACTATAGCAACCGCGAGCGTTTCAATTGTTGAAATGTACGTTTATATTTACCATTGCTCAATTCGCGCTGAATGTTTTCTTAAAGACACAGGCTCGCATTGACCACACGACGGACGAGCTCGTAAATAAGCCATTAATTAAATGTAACCCGAATAAAACCTTTGTTGTGGTCATTTGTCTGAGGTTTCCATGTTTCTTCTCTGTCGTTTTCTTCTACTGAGAGAGGGAGTTTAGCGCGACGCTCATTGGCGCCCTCCACCAGAAAGACGTCATCGGACACGGAAGTAAACACTTGGAGTTGGGATTAGAGCATGAGCGCGGATCAATGATGGTTTATTTATATTTATTAGCAACGGTGTTGTGTTTTATTCATCATGGAAATGCGCAAGAAGG[T/A]ATTTATGATGCTAAACATACTGGTTAATGTTGGTTTATGTATGAGTTATCGTTATAAGTGACAACTTTGTGCATATTTTGTTCCTATTTAGCAGATGATTGTTTTCCCACTGAATGGCTGAAGTCTCTGGTCATTTCTGTGAACATTTCCAAAGCTGGATTTCACAGGTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCATTGGTTTATTCATGTTTTAATTGTGATGTGTTGTATAGAGATCTGGAGTACAGTGTTTACTGGAGTGAAACAGATCATGACGTGAAAGCTTTACTAGTGCAGAAGATGCCGAGTGGAGTTTACATGGATGAATATCAGCTGGAGACTCTGAGACATGACACAGGCTTGGAGGTATGTTTTTTTTTTCCAGTGATATCATGTTAAAACCGTGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18479
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 |
---|---|---|---|---|---|
ENSDART00000092991 | Nonsense | 80 | 243 | 3 | 6 |
ENSDART00000131110 | Nonsense | 80 | 232 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 2179627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 2920717 |
GRCz11 | 22 | 2936983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNCNNCCAGCTTTACTAGTGCASAAGATGCCGAGKGGAGTTTACATGGATGAATA[T/A]CAGCTGGAGACTCTGAGACAKGACACRGGCTTGGAGGTATGTTTTTTTTT
Long Flanking Sequence:
AGCGCGGATCAATGATGGTTTATTTATATTTATTAGCAACGGTGTTGTGTTTTATTCATCATGGAAATGCGCAAGAAGGTATTTATGATGCTAAACATACTGGTTAATGTTGGTTTATGTATGAGTTATCGTTATAAGTGACAACTTTGTGCATATTTTGTTCCTATTTAGCAGATGATTGTTTTCCCACTGAATGGCTGAAGTCTCTGGTCATTTCTGTGAACATTTCCAAAGCTGGATTTCACAGGTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCATTGGTTTATTCATGTTTTAATTGTGATGTGTTGTATAGAGATCTGGAGTACAGTGTTTACTGGAGTGAAACAGATCATGACGTGAAAGCTTTACTAGTGCAGAAGATGCCGAGTGGAGTTTACATGGATGAATA[T/A]CAGCTGGAGACTCTGAGACATGACACAGGCTTGGAGGTATGTTTTTTTTTTCCAGTGATATCATGTTAAAACCGTGGCTTAAACACCTGTTTGGTTCCCATTTGGCTCTTCTTTGGGTATCAAATATAAAGGTTCTGGGAACATTTCGGTAACCAAAAACTAACCTTCTTCAGAATGTCATGGCTGATTTGGAAACATTCTCCTAACCTTGAGGGAATGTAATGTATTTGTGTAAAGTAGGGTTTGGCGATATGGGCAAAATATATCCCGGTATTTTTAGGGAGAATGACGGTATACAATATATATCCGGTATTTTCCCATAAATGGTTAATTGAGAGTTAAAGCCTTTATTAAAACTTTATTAAAAAAATTTTAAGCAAAATATAATTTAAACACTAGGGTTTCCCTCTCTGTTTATGTAAAGTAACTCCTACATAAAGTTGTGGTCGGTCTGAAAACCGCTCCAATTGGTCCACCGTTTTTATGTTGTTAAATTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6688
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092991 | Essential Splice Site | 167 | 243 | 4 | 6 |
ENSDART00000131110 | None | None | 232 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 2176391)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 2917481 |
GRCz11 | 22 | 2933747 |
KASP Assay ID:
554-4826.1 (used for ordering genotyping assays)
KASP Sequence:
CTGAGATCAGACCAGTGTACGTCAATCCTCATATCAAYAGATTCAGAAGG[T/C]GGAGAGCAGTTGTTACTACTACACCGTGATGTTCACCTTCATTGTGTTCA
Long Flanking Sequence:
TAAAACATGCTGGATAGGTTTGCGGTTCATTCTGCTGTGGCGACCCCTGATGAATAAAGGGACTAAGCCGAAGGAAAATGAATGAATATAAGTGAAATCTAACAGGGCTTAGCACAAAAGTAATCTAAATGTAATCCGAAAGTAGTCCAATTACATTACATGTGTAATCAAAGCGGTTATATTACTGACTACACTTTTGGTCATGTAGAGTAACTGATTACAAATAAGTAATCTACTTCTGACGTCTGATTTAAATCTTGGCTTTTGTTTTCGCAGGTTCTCCTGGACTCAAAGGTGGATCTGGAAGCTCCGGAGTATTTGTCGTCTGGTTTCACGGCGCTGGTTTTTCTCTCTGGTAATGCGGTGACTGTTCCGGTTCACGGCCGCTATCACAGACCCTCAGACACACACAGCCATGTGACGGTGGACATCCAGCCGCCCAGACTCCTGCTGAGATCAGACCAGTGTACGTCAATCCTCATATCAACAGATTCAGAAGG[T/C]GGAGAGCAGTTGTTACTACTACACCGTGATGTTCACCTTCATTGTGTTCATGTGTGTGTGTGTGTGTGTGTGTGTTCATCACAGGTGAGACTCCCAATGCTCAACATACAGTGGTTGAAGCTCCATGTACATTCAGAAACGAGAGCTTCTGCTTATGGCTGGAGATACAGGACCTGAAGGTAACTAGTCTAAAGATGTATAACTAGGTATCTTGGTAAAGAACATAGCTAGGTTCAATGGTAGCACTTTTAGCTTAGCTTAGCATAAATCATTGAATCAGATTAGACCATTAGCATCTAGCTGTGACACAAATTAAATCATTCAGCGTAGTGATGTGGAGCTGTATTGCAATGCTCTCAAAACCTGCCGGAACTACTTTAGCTGTGCGTTTATATGAAAATAACGGCACACTTTAGAGTGCTCATCAGCCAATCAGAATCAAGCATTCGGCAGAAATATAGCCAGGTCGGATGGGAGCATATTTAGCTTAGCTTAGCATA
Associated Phenotype:
Not determined