ZMP
plg
Ensembl ID:
ZFIN ID:
Description:
plasminogen [Source:RefSeq peptide;Acc:NP_958880]
Human Orthologues:
LPA, PLG
Human Descriptions:
lipoprotein, Lp(a) [Source:HGNC Symbol;Acc:6667]
plasminogen [Source:HGNC Symbol;Acc:9071]
plasminogen [Source:HGNC Symbol;Acc:9071]
Mouse Orthologue:
Plg
Mouse Description:
plasminogen Gene [Source:MGI Symbol;Acc:MGI:97620]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16064 | Nonsense | Available for shipment | Available now |
| sa44949 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa37133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16767 | Nonsense | Available for shipment | Available now |
| sa37132 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39304 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39303 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16064
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 |
|---|---|---|---|---|---|
| ENSDART00000045816 | Nonsense | 179 | 818 | 6 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42732784)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42803943 |
| GRCz11 | 20 | 42701053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAYGGAGATAAGGGGGGTCCCTGGTGCTACACCACAGATCCTGAGAAA[C/T]GATGGGAGCACTGCAATATCCAAGACTGCACAGGTRCATTCAGCAATTAW
Long Flanking Sequence:
GGGTCACATTTCATCATTCGCATCTTTTTTACAAGACCAGTTTTTCTGTCACAAACCCTAGCGGACTATGCAGAATGTACAGTAACTACCATTATCCACAGTTCTACTGTATATCGACATCATTAGTAAACAAAGCGTTGTTAAGTATGCTGTAACCAATTGATTGAATTCCTTCATACAGAGTACTTACTGGAATGTGTAAATGGCATTGGCATGGACTACAGAGGGACAAAATCCAAGACAAAATCAGGGAAAACATGTCAGCGATGGGAGGGAACTTTCCCCCATGTACCCAAGTATGCTTCTTTATCAAATTTGTGTTTCAGGATGCTGTAAAAGACAAAATGTTTATCACAGTGAACAGCTAAATAACTTCAGTCATATCTTCCCGCAGCATAACACCAAGAGCTTACCCAAAAGCAGATTTGGAGTCCAACTTTTGTCGAAACCCAGATGGAGATAAGGGGGGTCCCTGGTGCTACACCACAGATCCTGAGAAA[C/T]GATGGGAGCACTGCAATATCCAAGACTGCACAGGTGCATTCAGCAATTAAACTTGTACATAATGATAAGAAATCATACAGATGGATGGAGAAATCCCATGCAAAATCTCACTGTTGCTTTCATTTAAAATGAGGGAGTAGACTATTTGCTTTATAAACAAATCCTACATCTAACCCCCTGGTAACATCATTACACTGATAACTATATGGTGTGATAAAATAAATTGAGAAGATTTGCTACTTAATCATGCAAATATTTAGAAATGATCTTGTACCTTTAACTAATGGCTCATTTTCACTGAGTGGTTACGGTGCGATACAGTTAAATACAGCACACATTAATTTCCATTTCCACTGTTATAAGTATCAAAATAGTGAAACATAGCATACATTTTGGGACCCTTTCGCAAGAGTACCTTGCACAACAGTATTGTAAAAGGTTGGAGCAATACTCGCAGCTGAATGCTATTGGTTTACAGAGAATCATTACTTGTGCATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44949
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 |
|---|---|---|---|---|---|
| ENSDART00000045816 | Essential Splice Site | 230 | 818 | 7 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42730597)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42801756 |
| GRCz11 | 20 | 42698866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACGCTGGGACTCTCAGCAACCCCAAAACCACGGTTACCTTCCTTCAGC[G/A]TAAGACCCTATTATTTAAAGCCCAATTGGCATATGGCCTATTTTGTGCAT
Long Flanking Sequence:
CAAGATGCACTTTCAGATTTAAGACCTTGGCTGGATGTTTTTATTCATTTAGAGCTGTTATGCACTGCATGGAAGGTCATTTTCAAAAACCCATTATATGGGCTCTTTAAAGAAAGCTTTTCTTCTTGTGACAAACAGCCACATGCCAAGAAGTAAGAGTACTGTTGGCAGTGGAAAAGCAAGCCTGGTCAAGGTGACCTGTTTGAATCGCATTGAACAGTACCGTACTTCTTAGAGAAAACAAGGCATTATGTTCTTGTGGAAAAGCCTTTTCATAAAGGGATTAAGTTGCTCAATTTTATTTGTAAAATTGGAAAAAAGTAATGTACAAGGAAACAAAAAGGAATTGTCCTTTAAATGTGCCCTTCAATATCTGCAGAGGAATGTATGCAGTGCAGTGGAGAAAACTACAGAGGGAAAATCTCCACCACTGTGAGTGGATTCACCTGCCAACGCTGGGACTCTCAGCAACCCCAAAACCACGGTTACCTTCCTTCAGC[G/A]TAAGACCCTATTATTTAAAGCCCAATTGGCATATGGCCTATTTTGTGCATTTTTAACTGTGGTCTGTCTTTTGTAGTCTTCCTGATAAGTACTTGGAAGAGAACTACTGCAGGAACCCCGATGGAGAGCCCAGGCCCTGGTGCTTCACCACCAGTCCATCCAAACGCTGGGAAGCTTGTGCCATCCCTCGATGCAGTAAGCAATGTTCTCGTTAATATGAAACTTCAAGTTTTGTTTTAATTGTTGACTTCTCATTTATTTCTTTTAGCAACTGAACCACCGACAATTGTACCGGAGCTTACCTGTGCAAGTGGAGAAGGTAGTTCCTACAGAGGCACAATTTCAGTCACAATCACAGGGAAAACATGCCAGCAATGGACATCCCAAAGTCCTCACAAACATTCCAGATCTCCAGAAAATTACCCATGCAAGTAAGTATCAACATGTTGGGTGTTATGGGACAGATTCTGCTTGAATATGTGGTGTTTTTTTCCTACGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37133
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 |
|---|---|---|---|---|---|
| ENSDART00000045816 | Nonsense | 330 | 818 | 10 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42729301)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42800460 |
| GRCz11 | 20 | 42697570 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACAAACCTTAAACTGTATTTCTATCGCAGAGGCCTTGATGGGAACTA[C/A]TGCAGAAATCCTGATAATGAAAGAAGTCCATGGTGTTACACTACAGATCC
Long Flanking Sequence:
AATCAAAGCACAATAAGTAAAGCACAATAAATACGGCAAATAAATGTGCATTACATTATGGAGCAGCTAATTAAGATATTCAAGATAACAGTAAAATTACAGGCTGGTTTTGAGAAGTGGCAGAATGAAGCTCTGAAAACAATAATAAAAAGGCACTCCAAGAACAGAATTTGGAACCCTTGAATAACATGTCCACTCCTGCTCTTCAAGAGTTTTACTCTACCCATAATTTAACATTCTGAAACAGCTAATTGAGGCCTTCAGGGTTACTAGAAACACGAGTTGAAGCTAAACTCCACAACACTGGGCCATCCATGTACAGGGATTTACATAAATGAACTAGAAGAACAAAACAGACAGATTTTACATAGCTTAAGCTATCCTTTACAACACAACTATGACTTGCTTTAGTATGCCAAACATAAAGGGAATATTTACAGCACAGAGAATGCAACAAACCTTAAACTGTATTTCTATCGCAGAGGCCTTGATGGGAACTA[C/A]TGCAGAAATCCTGATAATGAAAGAAGTCCATGGTGTTACACTACAGATCCTGAGACCCGCTGGGAATACTGCAGTGTGCCTAGTTGTGGAGATCAACCTAGACCTGGTCTGTTTTGAAGGACTTATTACAAAAAACATTTACAATTAAATGTAGATTCTGCTGTTATGTCATATTACATTACATTATATACTCCTAGTACTGATAAAAGAGCCATAAGTAATGTAAATATATGATCCCCAGAGGAGCCCGTGATCCCCCAGGGTGAGGAATGTTATGAGGGTGATGGAAGTTCATACCGAGGTGTCATGTCTGAGACCATAAGTGGAAAGAAATGCCAGTTCTGGACATCCATGGAGCCTCATCGACATTCCAAAACACCTCAGAACTTTCCCAAAGCGTAAGAAACTACATCAAACTGTGCCAACTGTTGCAAACTTTAGTTTTACTGATTTCCCCTCTGGCGCATGTCGTGATTTATGCAGAGATCTAAGGAGAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16767
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 |
|---|---|---|---|---|---|
| ENSDART00000045816 | Nonsense | 473 | 818 | 12 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42728654)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42799813 |
| GRCz11 | 20 | 42696923 |
KASP Assay ID:
2261-4832.1 (used for ordering genotyping assays)
KASP Sequence:
RGCCCAACATACAGGAACCTCCYGCCAAACCAGCAGCTACAACTCCAACA[C/T]AGTCTACTCCAGCTCAGTCTACTCCAGATCAATCTGCTYCYTCAGAAAAA
Long Flanking Sequence:
AAATGTAGATTCTGCTGTTATGTCATATTACATTACATTATATACTCCTAGTACTGATAAAAGAGCCATAAGTAATGTAAATATATGATCCCCAGAGGAGCCCGTGATCCCCCAGGGTGAGGAATGTTATGAGGGTGATGGAAGTTCATACCGAGGTGTCATGTCTGAGACCATAAGTGGAAAGAAATGCCAGTTCTGGACATCCATGGAGCCTCATCGACATTCCAAAACACCTCAGAACTTTCCCAAAGCGTAAGAAACTACATCAAACTGTGCCAACTGTTGCAAACTTTAGTTTTACTGATTTCCCCTCTGGCGCATGTCGTGATTTATGCAGAGATCTAAGGAGAAACCTGTGCAGAAACCCAGATGGAGACAGAGCCCCTTGGTGTTACACCACAGATCCCACAGTTCGGTGGGAGTACTGCAATATTGAGCGGTGTGACAACAGGCCCAACATACAGGAACCTCCTGCCAAACCAGCAGCTACAACTCCAACA[C/T]AGTCTACTCCAGCTCAGTCTACTCCAGATCAATCTGCTCCCTCAGAAAAAGGTGCATCCACCTAGAAGCTAAAAAATTATGTTAGATGTAAAAAGTACCATAGACTAATTTCACGCCAAGTCATTAAAAAAGCTAAATCAAGGCAGAAAAAGAAACTTGGAAGTATCGCCTGAGTCACACAGGAACGTTGTGTACCTGGCTGTATATCTTATCAGCGAAGAGAAAGTGACACAATTTTATCTGAACGGAAAGTGAAAATAAAGAGGATGTCAGAACTCATTTTTATCTAAGTTAAGGGAAAAGGCACTAGTTAGCTAACGTTTTCTTTCCCAAACACACGGTTTAGATGCCATTGAACAAACTCTTCCTCTTTCACTATATTAGACTTGTCACGATACTGAATTTCGGTACTGAAATAAAAAAACTGTCAATTTCCCGTTAACATTTAAGCGCTGTTAAATTCAACACCACTGATTTGCCATTTGCCGCACTTCACTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37132
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 |
|---|---|---|---|---|---|
| ENSDART00000045816 | Essential Splice Site | 489 | 818 | 12 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42728602)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42799761 |
| GRCz11 | 20 | 42696871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTACTCCAGCTCAGTCTACTCCAGATCAATCTGCTCCCTCAGAAAAAG[G/A]TGCATCCACCTAGAAGCTAAAAAATTATGTTAGATGTAAAAAGTACCATA
Long Flanking Sequence:
ACTGATAAAAGAGCCATAAGTAATGTAAATATATGATCCCCAGAGGAGCCCGTGATCCCCCAGGGTGAGGAATGTTATGAGGGTGATGGAAGTTCATACCGAGGTGTCATGTCTGAGACCATAAGTGGAAAGAAATGCCAGTTCTGGACATCCATGGAGCCTCATCGACATTCCAAAACACCTCAGAACTTTCCCAAAGCGTAAGAAACTACATCAAACTGTGCCAACTGTTGCAAACTTTAGTTTTACTGATTTCCCCTCTGGCGCATGTCGTGATTTATGCAGAGATCTAAGGAGAAACCTGTGCAGAAACCCAGATGGAGACAGAGCCCCTTGGTGTTACACCACAGATCCCACAGTTCGGTGGGAGTACTGCAATATTGAGCGGTGTGACAACAGGCCCAACATACAGGAACCTCCTGCCAAACCAGCAGCTACAACTCCAACACAGTCTACTCCAGCTCAGTCTACTCCAGATCAATCTGCTCCCTCAGAAAAAG[G/A]TGCATCCACCTAGAAGCTAAAAAATTATGTTAGATGTAAAAAGTACCATAGACTAATTTCACGCCAAGTCATTAAAAAAGCTAAATCAAGGCAGAAAAAGAAACTTGGAAGTATCGCCTGAGTCACACAGGAACGTTGTGTACCTGGCTGTATATCTTATCAGCGAAGAGAAAGTGACACAATTTTATCTGAACGGAAAGTGAAAATAAAGAGGATGTCAGAACTCATTTTTATCTAAGTTAAGGGAAAAGGCACTAGTTAGCTAACGTTTTCTTTCCCAAACACACGGTTTAGATGCCATTGAACAAACTCTTCCTCTTTCACTATATTAGACTTGTCACGATACTGAATTTCGGTACTGAAATAAAAAAACTGTCAATTTCCCGTTAACATTTAAGCGCTGTTAAATTCAACACCACTGATTTGCCATTTGCCGCACTTCACTGCCGTTTAAGAGCGCAAACACAGATGAACAATCGACTTTGAATGCTCCAATGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39304
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045816 | Essential Splice Site | 490 | 818 | 12 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42728601)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42799760 |
| GRCz11 | 20 | 42696870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACTCCAGCTCAGTCTACTCCAGATCAATCTGCTCCCTCAGAAAAAGG[T/A]GCATCCACCTAGAAGCTAAAAAATTATGTTAGATGTAAAAAGTACCATAG
Long Flanking Sequence:
CTGATAAAAGAGCCATAAGTAATGTAAATATATGATCCCCAGAGGAGCCCGTGATCCCCCAGGGTGAGGAATGTTATGAGGGTGATGGAAGTTCATACCGAGGTGTCATGTCTGAGACCATAAGTGGAAAGAAATGCCAGTTCTGGACATCCATGGAGCCTCATCGACATTCCAAAACACCTCAGAACTTTCCCAAAGCGTAAGAAACTACATCAAACTGTGCCAACTGTTGCAAACTTTAGTTTTACTGATTTCCCCTCTGGCGCATGTCGTGATTTATGCAGAGATCTAAGGAGAAACCTGTGCAGAAACCCAGATGGAGACAGAGCCCCTTGGTGTTACACCACAGATCCCACAGTTCGGTGGGAGTACTGCAATATTGAGCGGTGTGACAACAGGCCCAACATACAGGAACCTCCTGCCAAACCAGCAGCTACAACTCCAACACAGTCTACTCCAGCTCAGTCTACTCCAGATCAATCTGCTCCCTCAGAAAAAGG[T/A]GCATCCACCTAGAAGCTAAAAAATTATGTTAGATGTAAAAAGTACCATAGACTAATTTCACGCCAAGTCATTAAAAAAGCTAAATCAAGGCAGAAAAAGAAACTTGGAAGTATCGCCTGAGTCACACAGGAACGTTGTGTACCTGGCTGTATATCTTATCAGCGAAGAGAAAGTGACACAATTTTATCTGAACGGAAAGTGAAAATAAAGAGGATGTCAGAACTCATTTTTATCTAAGTTAAGGGAAAAGGCACTAGTTAGCTAACGTTTTCTTTCCCAAACACACGGTTTAGATGCCATTGAACAAACTCTTCCTCTTTCACTATATTAGACTTGTCACGATACTGAATTTCGGTACTGAAATAAAAAAACTGTCAATTTCCCGTTAACATTTAAGCGCTGTTAAATTCAACACCACTGATTTGCCATTTGCCGCACTTCACTGCCGTTTAAGAGCGCAAACACAGATGAACAATCGACTTTGAATGCTCCAATGTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39303
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 |
|---|---|---|---|---|---|
| ENSDART00000045816 | Nonsense | 706 | 818 | 18 | 20 |
| ENSDART00000134689 | None | None | 148 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42723583)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42794742 |
| GRCz11 | 20 | 42691852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCACCTGTATGTCTACCAGAAAAAGACTACATTGTACCCAGCAATACT[G/T]AATGCTATGTAACAGGATGGGGGGAGACACAGGGTAAGTACTGTATAAGA
Long Flanking Sequence:
GATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGGCAGGCAGGCAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGAACGATAGACGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATAGGCAGGCAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAACAACCTTATTTCTAATAAACGTGATATCAAGACAGCTAATGGTTTTGTCTGATTTCAGGCCTGCATTAATAAATGATAAGGTGTCACCTGTATGTCTACCAGAAAAAGACTACATTGTACCCAGCAATACT[G/T]AATGCTATGTAACAGGATGGGGGGAGACACAGGGTAAGTACTGTATAAGAAAATGGATGCACTGCCACAATTTGACCTAAAAACACAAATAACTAACAATGAATAAAGATTATACAATGTACTTATCTGCAAGCTCTTCTGTCTCTTAGATACTGGTGGAGAAGGCTACCTGAAAGAGACCGGTTTCCCTGTAATTGAGAACAAAGTCTGTAACCGTCCATCATTTCTGAATGGCCGTGTGAAGGACCATGAAATGTGTGCTGGGAACATAGAAGGTGGAAATGACAGTTGCCAGGTACAGTATGAGAGCATTCAGGACATTTTAACCTGCCTAGTTAACCTCATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATGGAAGTGCCCTGAAAAATAATTAGTAAAATATTATGTACTTTCATCATGGCAATGATAAAATAAATCAGTTATTAGAAATGAGTTAATAAAACTATTCTCTTTAGAAATGTGTTGA
Associated Phenotype:
Not determined