ZMP
pgap1
Ensembl ID:
ZFIN ID:
Human Orthologue:
PGAP1
Human Description:
post-GPI attachment to proteins 1 [Source:HGNC Symbol;Acc:25712]
Mouse Orthologue:
Pgap1
Mouse Description:
post-GPI attachment to proteins 1 Gene [Source:MGI Symbol;Acc:MGI:2443342]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14116 | Essential Splice Site | Available for shipment | Available now |
sa34641 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21488 | Splice Site, Nonsense | Available for shipment | Available now |
sa21489 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14116
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 |
---|---|---|---|---|---|
ENSDART00000090346 | None | 49 | 943 | None | 27 |
ENSDART00000132045 | Essential Splice Site | 44 | 952 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 25159701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24315487 |
GRCz11 | 9 | 24126356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGAACCGATGCAGCATGACATACATGTTCGAGTACCCAGAATATCGAG[T/A]GAGTATCAGCGCTAACAGNNTCCATCGCCGTTGTTTTCTTCTCACGTTTG
Long Flanking Sequence:
TACATACACTTTCACCTCCCTTCACTTTAAACTGAAGGTGACGTAATGGTCTTTATTTTTTGCCAATTTTTTTTTTGCGTTTAGGTAGAAGGTAGTAAATGCACGATGATCCCACTGTTTTCATTTCGTTTTCCCCTCCCACTGACAATTTTAATTGGTCAAATCACAAACCTGTCTTCCCTCTCCATAGGCTCATTCCTCTGTCTGCGTCGTGACGTCAGCCCAGAAGCTGGCTGCGTGAGCGTGACAGGTCCATACGAGGTTCCTGAAGGTTTGAACAGGCAGTGAGTGTTGGGTGTACAATAAGGAAAGCGGAGACACGATTAAAATGAATCTGTAAATAAAGTCAAGCTCAATTTCTGGAGACATGAGACTCGTTGTATACGCGTTTTTTGCCTTCGCTCTTGGGCTTCTGCTCGTGGGTTTGCGAGAATTATTATTTGGTTTTGAGGAGAACCGATGCAGCATGACATACATGTTCGAGTACCCAGAATATCGAG[T/A]GAGTATCAGCGCTAACAGTCTCCATCGCCGTTGTTTTCTTCTCACGTTTGGTTTGCGATTAACAAAATGCACATTGTTTTGTATTGGACACAATTCATTGGCAGGCCATGTATCAGTTCCTCATACCTGTCTATCTACCTGTTGTAATGGCAACAACAAACATTGGCAAGCCGCAAGCAGCATTAGTCTTTAAACAACATCTCTTCAATATACATCAACCCTCTTTTTGTCGATATTGACAGTAAATACAGAAAAAAGACTAATCATATTAAGTAGGAATTTGTATCTCTAAATGTAGTATATTTTGTTTAAATTTTTTATCTTTTAACTTTGTGTTTTTAGTCAATGCCATTGACTGTTCATCGTTAAATTCTGCACATTGTGCTTATATGTAAACTAATCCAACTGTTAGGGAAAAAGTATTTTAGAGTAGAAAAGTGATTAACTTTTAATTCTTCTCCTGTCATTTCTGATCCCGAAGATCAGTCAAGTGTGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34641
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090346 | Nonsense | 623 | 943 | 20 | 27 |
ENSDART00000132045 | Nonsense | 630 | 952 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 25170223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24326009 |
GRCz11 | 9 | 24136878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGCACTTCTCCTGATGATCAGAGTCCAGCTGAGCTCTGTCAGAAGAT[C/A]AGGACGTCCTGTCGAATTGCAAGAGGCCATGAGTAAATCCTTAGAGATCC
Long Flanking Sequence:
TTTTGTCTTAACTCTCTTTAATAAGCCAGCTGTCTCATTCTCTCCGCAGTCATTATTTATGCTAAAGTACTGATGAATATGTCTTTTTGTTTTTTGTTTTTCTCACTGAAGTACTCCTTCGGTCTCTGAGATCTTCAGCATGCTTCACAGCAGCCGACCAGACAACACATCCAGTGCCATGCTGCAGCTCCACACTGCCCCCAACTGCCAGTACAAGGTGTTTAATTCACAACTTCTGTTTCTTTATAGAAAACGGAAAGACAACTTAAATGATCTTTTTCTCTCTCTCTACAGGTGTCGATACGGACATCATTTCCTAAAGTGCTTGGGCAGGTGAGCTTACATTTGTGGTTTTTCATCTGTCATGCTTTTAAACTCATATTCAAATGGAGTTGTTGTTGTTCTCCAGATTCTGCGTTTCTGTGGTCCGCTTCTGCCCGTCTACTGTGCTTTAGCACTTCTCCTGATGATCAGAGTCCAGCTGAGCTCTGTCAGAAGAT[C/A]AGGACGTCCTGTCGAATTGCAAGAGGCCATGAGTAAATCCTTAGAGATCCACAAACTGGAGCTGCCGGTCCTCTTGCTGATGCTGCTGCTCCGGTGAGTTCTGACATCAACATCTCAAAGGCCTAATAGTTTGCTGCAATTGCCAGTGTAAATATTCCTAAACATCAGTATTTTGTTTATCTAGCAATAGGACTGGATGTCCATTATTTAATTAAAGTGCTCAGCAAATATTTGTACACCCCTCACAAATATTTTAAATTCATAATTCATAATTTTTTAATAGAAAGCTATACAATATTATACTTAAGCATATACATTAGATTATTCGAAATTAAAGCCAAATCTGGAGCTTATCTAACAAAATAATTTACAATAACAGTCCAAAAACTTGTACAGCCAAATTTATGTTAAAAAAAGATTAAATACAATTTTAAAAATCAAGAAAAGCAAAAAAACTGAAAAAAATTGTTGAAATTTTGTTGGTTGTAAAACAACAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21488
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090346 | Splice Site, Nonsense | 655 | 943 | 21 | 27 |
ENSDART00000132045 | Splice Site, Nonsense | 662 | 952 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 25172659)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24328445 |
GRCz11 | 9 | 24139314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTAAATAAATGTCTAATCGTTTAAATTGATTTTCTTTCTACCACAGG[C/T]AAAGCTGGTTTCAGGATGTCTGGACATCTTTGGGCCTCCCTGGGGTGGAT
Long Flanking Sequence:
CAAGAACTCCAAATTTTTTAAAATGGTTAGCTGAAATGGTTTCTGCCCTCTAGCTGGAAAGGCTACATTTCTCTAGATTTGGCAAACAGAAGTTGTATGACAAAATATGGGGCCCTACCTTAGATATTCTATTTCGTTTCTTATTCCATTAGTCTGGCTGAGATTTTTTAGTATTTTTGATGGTGCTGTATAATTGCTGTATTGTCTGCTAGTGTTTTGGTGTATGTTCTAGTTAGTATCAGGTAATAACACCTATATAATTTTGTTACATATATACATGATGTACACTAGGGTGTTAAGTTTTTATAAAAAACGTCAAAACAGTCGTTTGGTGCTTGGCTGTTCATTCTAGTCTTATTCTGAAAGTGTCTGTGTGCTGTATTAAAATGCTGAGTCTCTTTTGCAGCAAATCTTGACAGCCTTGTCAGACAACACAGCGCTAATTTTGACCATTTAAATAAATGTCTAATCGTTTAAATTGATTTTCTTTCTACCACAGG[C/T]AAAGCTGGTTTCAGGATGTCTGGACATCTTTGGGCCTCCCTGGGGTGGATGCACTTCCTCTAAACACGGTGGAGGACCTGTCCCATGAAAAAGCTTCTGTGCAGGAATGGCCTCGTCTCGTGTCTCCACTGCTGTGTGTGTTCGGTGCAGCCATTGCATTCTGGGGCAGCACAGTCCTCCGAATGTCTGTCTGCTTCCTGTCCTTTATTGTTGCTCCACTACACAGGTGAAAATCACATTAATAATAGCATTGTAGTTGGAGCTTTTTTACTTTTTATGGGAACATAAAATGTTTGATATATTATTTCATGCTATTTTACAGTTCTGTTAAAGTATATGTGCATAATATGTAATAACCTTAGTATGTAAACAGTTTAATAACTACGCACACCAGTTATTAGAACTCTTTTTAAAAGCATATTTTATTAGAATGTGAAATTTCAAAGACATTTAGAAAAGATTATTTTACACCAAGTACTTTGATGGATGTTTTTAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21489
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 |
---|---|---|---|---|---|
ENSDART00000090346 | Nonsense | 785 | 943 | 23 | 27 |
ENSDART00000132045 | None | None | 952 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 25175485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24331271 |
GRCz11 | 9 | 24142140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAAATTACCAACTTTTTAATATATACACTTAACTATGTCTTTCGACT[T/A]AGCTAAGGGCAGAGCTTTATAATCACAGTGTCTTCACATTGAATTTTTTT
Long Flanking Sequence:
TTGCTCTCACTTCAAACATATCTTCACATGAAGTCCTTGTTTTCAAGGTTATTGGACTCGGAAAGTCTCTGGATTTTGCTTGAATTTGAAGTAACCATTGGTGTGAGAATCCTGCAGTATTATTACAGGGTTCATCTCTAAAAATGCACATGTAGCTGTAGCTTCAGTTGAGAGCAGCAGGACTTTACATGTGTTGTGGAAAAAAGATTCTGGTCTGCAAAAATATTCTAAGTCTCTAAGTCAAACTTTTCAAAAAATGACAAAGTCTGAGATCTCCGAAGTCTTTATAGACAATAGCATCTGCCATTTTTGGAGGGTGCAGATCACCAAAAATGCATGTAGCATGTCCTCAAGTTGCATCATTCACCTGTCCTGATCTTGTCTAATGCTCTGCCCTTCCTTTTCAGATCACAAAAGAATGTAAAAAAAAAGTCTCTTGCACTCATCCAGTCAAAAATTACCAACTTTTTAATATATACACTTAACTATGTCTTTCGACT[T/A]AGCTAAGGGCAGAGCTTTATAATCACAGTGTCTTCACATTGAATTTTTTTACAGCGTTGGTGTCTTGAATGTATTAAAGGAGGACATGCTACATGTGTTGGGGAATTCATTGTGTCTTGATGAATTTCTAATGAATGTATTACTCTCATTTATATGCTTATTTGAGTGATTTCAGTATTATCATCTATTATATTATAACCCATACCTATGGCATTATTTTCAGGTATGTGTGTTTTGGTACATAAAAAAGTCATTTTGTGTAAATGCAGTCAGAGATGAGAAGATAAATTAGAAGAGCAGAATTAATGTCACAATGAGGGCTGATTTATGGAAGCAAGGCTAAAAGGACACCTGCTTTCTGTTCTGTAACTCATGATAAAGTGCACCTGCAGGTGCGCCCACACTCACTTTTATTGACATCTAAAGAATTATGAGTACATATGAACTTCAGCTGAACTTACAGTTGACAGCTCAGTGGACAGTGAACAAGACATATTGTT
Associated Phenotype:
Not determined