ZMP
NM_001077563.1
Ensembl ID:
Description:
zinc finger, DHHC-type containing 18 (zdhhc18), mRNA [Source:RefSeq DNA;Acc:NM_001077563]
Human Orthologue:
PIGV
Human Description:
phosphatidylinositol glycan anchor biosynthesis, class V [Source:HGNC Symbol;Acc:26031]
Mouse Orthologue:
Pigv
Mouse Description:
phosphatidylinositol glycan anchor biosynthesis, class V Gene [Source:MGI Symbol;Acc:MGI:2442480]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45582 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22895 | Nonsense | Available for shipment | Available now |
sa36202 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13974 | Essential Splice Site | Available for shipment | Available now |
sa6440 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45582
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 |
---|---|---|---|---|---|
ENSDART00000130540 | Essential Splice Site | 41 | 523 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 36404407)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34034190 |
GRCz11 | 16 | 33988220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCTACGCTGTGCAACGTTTACACGACTCATTTCGCTATTCCTACAGG[T/C]AAGCAACTGACAGAAACTATGAATTTCTTGTTTGTATTTTTGGAGGAAAT
Long Flanking Sequence:
TGTATATACATTAGCATTACTTTAATAAAATAAAATAAAATGAAAAAGAATTGTTTACCTAGGTGTTCAGATATGTCTGAATGGAGGTCAATAAGCCGTTTAAAGCTTGGGGACTTTTATTTTGGTACTACTAAAATTGCATACCGGAAGTACATGTAGCCTGTCGTTAGTTCTATCGTTCGTGTCTGTGTTAATGCAATGAATTGTAAAAACGTGAATATAATAATTCCTTGAATTGTTATTCATCTGCGGACCCGATGTTTTTATGGTGGATAGAAACTCCAAGGAAGAACGCAAATTTCAGCTTTGGTTAATGTCAATGATGCCTCTACCATCCTACACGCTAATCCATTTAGAATAATACAGCGTTCAGCAAATGTCCTGTTGTCATTGTCCTCAATTAAAGTTGTCAAGTATGACTCTATTTAACAAAAATGAAGACATACAGACTGTTCTACGCTGTGCAACGTTTACACGACTCATTTCGCTATTCCTACAGG[T/C]AAGCAACTGACAGAAACTATGAATTTCTTGTTTGTATTTTTGGAGGAAATGCCGAAAATACAACCCGTTAACTTCTACGATTTAAAAAAAATACATAAAGATGGTTAAATTGTATTACTTAAACCCCTCTGAACAAAGGTAGCATTTTCTGCTTATAACCCTAACAGGAATAAATAGATGAAGCCACCCTCTGAAGACTTTGAGAACAGTCTTTAGCAGGGGTGCCCAAACTCCAACCCCAATTAAACACACATGAACCAGCTAATCAAGCTCTTTCTAGGTATACTAGAAACTTCCAGGCAGGTGTGTTGAGAGAAGTTGAAGTTAAACTATGCAGGACACCTGTCCTCCTGGACCGAGTTTGGACACCCCTGGTCTTAAGCAGTACACAAACTGTTCTTATTTACAGTAATGATCAGATTACTTCATTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22895
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130540 | Nonsense | 296 | 523 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 36405972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34035755 |
GRCz11 | 16 | 33989785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTCTTTCAGTTTTATGGCTTTCAAACATTTTGCCATCCAACTTCAAAC[C/T]AAATTCCTCCTGCGCTGGTTAATTTAGCTCAGCACAAAGGATATCGTGTG
Long Flanking Sequence:
GCCGGTTAATCATAACTGTGGTTATAGGGAATAGTTTCCTCTTTGTCTTAAGTGCAGTGGCTCTATATAGTCTGAGTCGAATAGTGCTACAAGAAAGAAAGCTTGCATTTGTTGCAGTCATGATGTACTGTTTGACACCAGCTAATGTGTTTATGCTAGCAGGCTACTCGGAGACACTCTTTGCAACTCTTACTTTTGCAGGCCTCTGGATGCTTGAGAGAAGATACACAGTTGGAGCTTGCCTCCTGTTTGGCTTTGCTACTGGCGCTCGAGCCAATGGGCTTGTGAATGTTGGGTTTTTGCTGTATCTCACGCTTCAGCGGTGTTTAGCTCGTGCTCGTGCTTTTAATAAAGTAGCTGAGGGCGTTCAATATCACAATTATATTTGGGAACTTGTTCGATTTGCCTTCACAGGAGCAGTTTACGCAGCCCTTGTTGCTCTTCCGTTTGGTCTCTTTCAGTTTTATGGCTTTCAAACATTTTGCCATCCAACTTCAAAC[C/T]AAATTCCTCCTGCGCTGGTTAATTTAGCTCAGCACAAAGGATATCGTGTGGCTGACGCAGCATCTCCAAAACCAAAATGGTGCCATTGGCAGATTCCACTTTTATATTCGTATATACAGGATGTTTATTGGGATGTGGGTTTCCTTCGATACTTCCAGTGGAAGCAGATACCCAACTTTATTTTGGCATTGCCTGTTGCAACTCTGGGATTTAAAGCCTTGTTTATATACATTACAGATAACCCAGTGTTTTGTATGTATTTGGGGTTGGGAGAGAAAGGAAATAGCAAGAAGATTTATGGGTTTTGTAACCCAAGAGTCTTTGTTTATATTGTGCACAATACCGTCTTGCTTCTGTTTGGGATATTCTGCATGCACGTGCAGGTAAGACTCATACAGTTGGATGTTGTTATTATTATGGGATTTGTAATGTATGCTTAATAAGCATGCCTGTAATGTGTCTCCTTTTAGGTTTTGACTCGGTTTCTTGCTTCCTCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36202
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130540 | Essential Splice Site | None | 523 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 36408608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34038391 |
GRCz11 | 16 | 33992421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCGCTTTCTTCAGGTAATAATCATCGGCTAGGGAAGTGAACGCTGAG[G/A]TAAATGTTGCTCTTCATTGGTAGATGTACGCTCGCTTTCTTTAGCATTTG
Long Flanking Sequence:
CAAAATAGTGACACTTTTAAAAGCCTATTTCCCAAACACTCATTGTTTGTTACAGTTCCAGTGTCATTTAATGAAATGTATATACTATAATGGGATTTATTTATTAACATTTTCAGTAAAAGTAATACCTAAGTTACTTAGCCTTTGTCTGTTGGGCTTATTTTCAATTTGTAGTTTTAGCAAATAAACACTTAGGTTAGTTTTTAAAGTAACGTTTTAATACCAGCTTTATAAAAGTGTATTTTAAACTGGAAATATTTAAGTGAAAACTAGTTGAAGTTAGTTCAATTGAACTGGTTTTATTGAATTTAGTTTGAGCCTAGCAAGTTAATTAAACAGACTAATTAAAACATCGGAATGGATATGCATGTATCACTTGCAGCAGGATCAGTTAAAAAGGCGGAGCTCAGCGTGTCGGAAGTGAACGCGCATCATCACTCTTCGAGTCATTGGTCGCTTTCTTCAGGTAATAATCATCGGCTAGGGAAGTGAACGCTGAG[G/A]TAAATGTTGCTCTTCATTGGTAGATGTACGCTCGCTTTCTTTAGCATTTGCAGCTTTGAAAACAACACTAACCTAACAATCCTTAACCCACAGATTAAACTCGGACGGGGAGCAGCGCGAGGAGCCGACTGTCGTTCAGATGACGGTTGAGCAGCGCGTGAGGAGTAATGTCCTCCGCTGAGATAGTTGACAGCTAACGTTAGTCAACAAGCTAACACGATTAGCTTAGCCTAGAAGCTCCTAATTTATCGAAATCAACAACATGGCATGACAGTATAACAATTACACGTTAATATGTTACCAATAAGGGTTATTTAGCTGCATACTTTTCCACAGAGCAACATATTATTTGTTTACGTCCGTTCTAATTAGCTTAACGTAGTTCTAGCTTTGTTTACATATTCATTTTTACCACCCAAGTGATTTATTGGTGTTACAGAAGCTTCACGGCTGATAACTAACGTTAATGAGTGTCGTGGTAGCTTCCCCTTTTGACTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13974
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 |
---|---|---|---|---|---|
ENSDART00000130540 | Essential Splice Site | None | 523 | None | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 36408609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34038392 |
GRCz11 | 16 | 33992422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCGCTTTCTTCAGGTAATAATCATCRGCTAGGGAAGTGAACRCTGAGG[T/A]AAAYGTTGCTCWTCATTGGTAGATGTACGCTCGCTTTCTTTAGCATTTGC
Long Flanking Sequence:
AAAATAGTGACACTTTTAAAAGCCTATTTCCCAAACACTCATTGTTTGTTACAGTTCCAGTGTCATTTAATGAAATGTATATACTATAATGGGATTTATTTATTAACATTTTCAGTAAAAGTAATACCTAAGTTACTTAGCCTTTGTCTGTTGGGCTTATTTTCAATTTGTAGTTTTAGCAAATAAACACTTAGGTTAGTTTTTAAAGTAACGTTTTAATACCAGCTTTATAAAAGTGTATTTTAAACTGGAAATATTTAAGTGAAAACTAGTTGAAGTTAGTTCAATTGAACTGGTTTTATTGAATTTAGTTTGAGCCTAGCAAGTTAATTAAACAGACTAATTAAAACATCGGAATGGATATGCATGTATCACTTGCAGCAGGATCAGTTAAAAAGGCGGAGCTCAGCGTGTCGGAAGTGAACGCGCATCATCACTCTTCGAGTCATTGGTCGCTTTCTTCAGGTAATAATCATCGGCTAGGGAAGTGAACGCTGAGG[T/A]AAATGTTGCTCTTCATTGGTAGATGTACGCTCGCTTTCTTTAGCATTTGCAGCTTTGAAAACAACACTAACCTAACAATCCTTAACCCACAGATTAAACTCGGACGGGGAGCAGCGCGAGGAGCCGACTGTCGTTCAGATGACGGTTGAGCAGCGCGTGAGGAGTAATGTCCTCCGCTGAGATAGTTGACAGCTAACGTTAGTCAACAAGCTAACACGATTAGCTTAGCCTAGAAGCTCCTAATTTATCGAAATCAACAACATGGCATGACAGTATAACAATTACACGTTAATATGTTACCAATAAGGGTTATTTAGCTGCATACTTTTCCACAGAGCAACATATTATTTGTTTACGTCCGTTCTAATTAGCTTAACGTAGTTCTAGCTTTGTTTACATATTCATTTTTACCACCCAAGTGATTTATTGGTGTTACAGAAGCTTCACGGCTGATAACTAACGTTAATGAGTGTCGTGGTAGCTTCCCCTTTTGACTGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6440
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 |
---|---|---|---|---|---|
ENSDART00000130540 | Essential Splice Site | None | 523 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 36411992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 34041775 |
GRCz11 | 16 | 33995805 |
KASP Assay ID:
554-5125.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCTGACTTCCTTTATCTTTGGCTGTGTGATCACTCACCTCACTTTGCG[T/C]AAGTTTCAACAGTCACTTTTATACAAWTATAATGTGCCTGCATATRTATT
Long Flanking Sequence:
CTTCTAACTAATTTTATAAATCATTTTTGATATCTGGAATTATATAATACAATAATATGCACAAGTCATATGGAAATTTGTTTGATCATATTTTTTACTGTGCTTCTGCTTTTTTGGAGCTTTAAAATCTCAACTAATTATTTATTGTAATGCCAAAGAAGGAACTTATACATATTTGAAAGCATAAACAATGTTTGTTTTGGGTGAAATATTTCTATAAAGCTTTCGAAGTATTACAGTGTTTTGATAAGTAATGTGCAATAGTTAATTACAGTAACACAGATCACTTCCTCAAAGTAATTTCTTGAGAATTTATTAAAGTGTCCCCCTCTCTCTCTCTCTCTCTCTCTCTTCCTACTAGAGCGCTTCGATCATCACTGTCCTTGGGTGGGAAACTGTGTGGGGAAGCGCAACTATCGCTTTTTTTATGCCTTCATAGTGTCGCTGTCGTTTCTGACTTCCTTTATCTTTGGCTGTGTGATCACTCACCTCACTTTGCG[T/C]AAGTTTCAACAGTCACTTTTATACAAATATAATGTGCCTGCATATGTATTATATGTTTTTATAGACACTACACAACATTTTATGGTTTTTACCATTGATGATAATGATAATAACAAAAAACGTCTTAAACGCCAAATTTTCATGATAGAAAGGATCAACACCAAAGACAGCTTATTTTAAAATTACACTTAAAATTAAAATATTGGCATATTTAATCATTTAATATTTATATATTTATTATATTTGATTATTTTAAATTATAAAATAAAAAAAACATTTATTCTTAACATATTAAAATATATAATTTTTATTTATGTACAATAAAAATATATATTCATTTGTATAAAAGCAAAAGATCATTGTCTTTGTTGTATTTTGATATTTGATAACTTTTTGTAAGCTGTTTCATTTTTTTTCTTTCTCATCAACAGGATCACAAGGTGGGAATGGTTTCATCCAGGCAATACAGGACAGCCCCGCCAGATATCCTTTAAAAGAAA
Associated Phenotype:
Not determined