ZMP
pparg
Ensembl ID:
ZFIN ID:
Description:
peroxisome proliferator-activated receptor gamma [Source:RefSeq peptide;Acc:NP_571542]
Human Orthologue:
PPARG
Human Description:
peroxisome proliferator-activated receptor gamma [Source:HGNC Symbol;Acc:9236]
Mouse Orthologue:
Pparg
Mouse Description:
peroxisome proliferator activated receptor gamma Gene [Source:MGI Symbol;Acc:MGI:97747]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35000 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1220 | Nonsense | Available for shipment | Available now |
| sa27703 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1737 | Nonsense | Available for shipment | Available now |
| sa34999 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35000
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039950 | Essential Splice Site | 106 | 431 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 11 (position 627416)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 610248 |
| GRCz11 | 11 | 636746 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATAATCAGATGTGTTTAGTTTAATCGTCTTTCCGTTTGCTGTGTTTTCA[G/T]ACTCGATCAAGCTTGAGCCCGAATCTCCTCCACAGTTTGCAGAGAACAGC
Long Flanking Sequence:
TTATTTTAATGACAAATGTGTAATAATACTGATAATTTACGATGAATGCAATAAATGTAAGCCTGCTAACTGTGTGTGGTTCAAATTGTAGAATATGTAAACTTAGTTTATATATATATATAATTAATTAATAATAATTAAAAGCCTGGGTGCTGATCTGCAGAGGACTTTCATTTTGAGGGCCACATCACAAGCTCAGATTTGGTTGGCGAATCAGAAGGAAAAGGGGCATTTCAGCACCGCCTATGTGTGTATAAGGAATTTTAAAGTCATTTATCTGTTTTCCTGTGGCAACCTCAGATAAATAAGGGACTAGCCCAAAGCAAAATGAATAAATGAAAAATAAATGTATCCATAATAGTTTGTTCATGTTAGTGAATGCATTACCTAATGGACTGTTATTTTAAAGTGTTACCATCATTTCTACTCACCATAGTATGTAGTAGACTTTATAATCAGATGTGTTTAGTTTAATCGTCTTTCCGTTTGCTGTGTTTTCA[G/T]ACTCGATCAAGCTTGAGCCCGAATCTCCTCCACAGTTTGCAGAGAACAGCGTTTCATTCTCCAAAACTCCTGAAGATCCGTCTTCATCCTCACTGAACATCGAGTGCCGAGTGTGTGGAGACAAAGCTTCGGGGTTTCATTACGGCGTTCACGCCTGCGAGGGATGCAAGGTATTCAGCAGCAATACTTTTCAGTTATTGTGCCTGTAAATCAATAAAAATAGTCAGTCAAGTTTTATTTAGCTATTTAGGTCCGTGCATCAGATTTATTTTTTACATATTCATTTAAGAATAATAATAACTTGAGTCAGACAGCGAATATTTTTGCTATTTATAAGCAGAAATTTGTAAAAAAAAAATTATAATAATAATAAATAAAAATAATAATTATATTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1220
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039950 | Nonsense | 127 | 431 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 11 (position 627353)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 610185 |
| GRCz11 | 11 | 636683 |
KASP Assay ID:
554-1129.1 (used for ordering genotyping assays)
KASP Sequence:
TTGAGCCCGAATCTCCTCCACAGTTTGCAGAGAACAGCGTTTCATTCTCC[A/T]AAACWCCTGAAGATCCGTCTTCATCCTCACTGAACATCGAGTGCCGAGTG
Long Flanking Sequence:
TGCTAACTGTGTGTGGTTCAAATTGTAGAATATGTAAACTTAGTTTATATATATATATAATTAATTAATAATAATTAAAAGCCTGGGTGCTGATCTGCAGAGGACTTTCATTTTGAGGGCCACATCACAAGCTCAGATTTGGTTGGCGAATCAGAAGGAAAAGGGGCATTTCAGCACCGCCTATGTGTGTATAAGGAATTTTAAAGTCATTTATCTGTTTTCCTGTGGCAACCTCAGATAAATAAGGGACTAGCCCAAAGCAAAATGAATAAATGAAAAATAAATGTATCCATAATAGTTTGTTCATGTTAGTGAATGCATTACCTAATGGACTGTTATTTTAAAGTGTTACCATCATTTCTACTCACCATAGTATGTAGTAGACTTTATAATCAGATGTGTTTAGTTTAATCGTCTTTCCGTTTGCTGTGTTTTCAGACTCGATCAAGCTTGAGCCCGAATCTCCTCCACAGTTTGCAGAGAACAGCGTTTCATTCTCC[A/T]AAACTCCTGAAGATCCGTCTTCATCCTCACTGAACATCGAGTGCCGAGTGTGTGGAGACAAAGCTTCGGGGTTTCATTACGGCGTTCACGCCTGCGAGGGATGCAAGGTATTCAGCAGCAATACTTTTCAGTTATTGTGCCTGTAAATCAATAAAAATAGTCAGTCAAGTTTTATTTAGCTATTTAGGTCCGTGCATCAGATTTATTTTTTACATATTCATTTAAGAATAATAATAACTTGAGTCAGACAGCGAATATTTTTGCTATTTATAAGCAGAAATTTGTAAAAAAAAAATTATAATAATAATAAATAAAAATAATAATTATATTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa27703
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039950 | Nonsense | 142 | 431 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 11 (position 627308)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 610140 |
| GRCz11 | 11 | 636638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCAAAACTCCTGAAGATCCGTCTTCATCCTCACTGAACATCGAGTGC[C/T]GAGTGTGTGGAGACAAAGCTTCGGGGTTTCATTACGGCGTTCACGCCTGC
Long Flanking Sequence:
TATATATATATATAATTAATTAATAATAATTAAAAGCCTGGGTGCTGATCTGCAGAGGACTTTCATTTTGAGGGCCACATCACAAGCTCAGATTTGGTTGGCGAATCAGAAGGAAAAGGGGCATTTCAGCACCGCCTATGTGTGTATAAGGAATTTTAAAGTCATTTATCTGTTTTCCTGTGGCAACCTCAGATAAATAAGGGACTAGCCCAAAGCAAAATGAATAAATGAAAAATAAATGTATCCATAATAGTTTGTTCATGTTAGTGAATGCATTACCTAATGGACTGTTATTTTAAAGTGTTACCATCATTTCTACTCACCATAGTATGTAGTAGACTTTATAATCAGATGTGTTTAGTTTAATCGTCTTTCCGTTTGCTGTGTTTTCAGACTCGATCAAGCTTGAGCCCGAATCTCCTCCACAGTTTGCAGAGAACAGCGTTTCATTCTCCAAAACTCCTGAAGATCCGTCTTCATCCTCACTGAACATCGAGTGC[C/T]GAGTGTGTGGAGACAAAGCTTCGGGGTTTCATTACGGCGTTCACGCCTGCGAGGGATGCAAGGTATTCAGCAGCAATACTTTTCAGTTATTGTGCCTGTAAATCAATAAAAATAGTCAGTCAAGTTTTATTTAGCTATTTAGGTCCGTGCATCAGATTTATTTTTTACATATTCATTTAAGAATAATAATAACTTGAGTCAGACAGCGAATATTTTTGCTATTTATAAGCAGAAATTTGTAAAAAAAAAATTATAATAATAATAAATAAAAATAATAATTATATTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAATGTAAATTATAAATCTTTTTAAAATTTTTAAAAAGAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1737
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039950 | Nonsense | 162 | 431 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 11 (position 627248)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 610080 |
| GRCz11 | 11 | 636578 |
KASP Assay ID:
554-1682.1 (used for ordering genotyping assays)
KASP Sequence:
GAGACAAAGCTTCGGGGTTTCATTACGGCGTTCACGCCTGCGAGGGATGC[A/T]AGGTATTCAGCAGCAATACTTTTCAGTTATTGTGCCTGTAAATCAATAAA
Long Flanking Sequence:
TTTCATTTTGAGGGCCACATCACAAGCTCAGATTTGGTTGGCGAATCAGAAGGAAAAGGGGCATTTCAGCACCGCCTATGTGTGTATAAGGAATTTTAAAGTCATTTATCTGTTTTCCTGTGGCAACCTCAGATAAATAAGGGACTAGCCCAAAGCAAAATGAATAAATGAAAAATAAATGTATCCATAATAGTTTGTTCATGTTAGTGAATGCATTACCTAATGGACTGTTATTTTAAAGTGTTACCATCATTTCTACTCACCATAGTATGTAGTAGACTTTATAATCAGATGTGTTTAGTTTAATCGTCTTTCCGTTTGCTGTGTTTTCAGACTCGATCAAGCTTGAGCCCGAATCTCCTCCACAGTTTGCAGAGAACAGCGTTTCATTCTCCAAAACTCCTGAAGATCCGTCTTCATCCTCACTGAACATCGAGTGCCGAGTGTGTGGAGACAAAGCTTCGGGGTTTCATTACGGCGTTCACGCCTGCGAGGGATGC[A/T]AGGTATTCAGCAGCAATACTTTTCAGTTATTGTGCCTGTAAATCAATAAAAATAGTCAGTCAAGTTTTATTTAGCTATTTAGGTCCGTGCATCAGATTTATTTTTTACATATTCATTTAAGAATAATAATAACTTGAGTCAGACAGCGAATATTTTTGCTATTTATAAGCAGAAATTTGTAAAAAAAAAATTATAATAATAATAAATAAAAATAATAATTATATTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAATGTAAATTATAAATCTTTTTAAAATTTTTAAAAAGAAAAAAAAAAATTAAATGGGGGCTAATAATTCTGACTTCAACTGTGTGTGTGTGTATATATATATA
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa34999
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039950 | Nonsense | 193 | 431 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 11 (position 615815)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 598647 |
| GRCz11 | 11 | 625145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACTGCGACCTGCACTGCCGCATACACAAGAAGAGCCGCAACAAGTGC[C/T]AATACTGCCGCTTCCAGAAGTGCCTGATGGTGGGCATGTCACACAACGGT
Long Flanking Sequence:
AACACCAACTGACACAGCTAAGACTCGAACCAGTGATCTTCTTGCTGTGATGAGATTATGCTACCCACTGCGCCACCGTGACGCCCCGATTCTGATCATATCATTAATAAAAAACTACAAATGTATTCTGGTGTACAGTATGTTCACTTTTAGGAAGGTTTTTATAGCTTGAGCTGTCAGTGTTGTTAGCAGAGATGGAGTTGAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGCCTTATAGGAACTGCTATTGTGATTGTTGACAATGAGTTGAATAGATCAGATATGTTTTTAAAGAAATCTAGCGAGGCATCAGGAAAACCTTTTTTCCCTCTTCCTTCCTGACGACATTCCTCCTCCTCATGTGTGTGTGTGTGTGTGTTTCTGCAGGGTTTTTTCCGCAGGACGATTCGCCTGAAGCTGGTGTACGATCACTGCGACCTGCACTGCCGCATACACAAGAAGAGCCGCAACAAGTGC[C/T]AATACTGCCGCTTCCAGAAGTGCCTGATGGTGGGCATGTCACACAACGGTGAGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATGACAGAACCCTGATGTATTCCTGATATCAAGGATGCATTGATGCAGACTTGAGCGCAAAACTCACTCTAGAAGTCACAGAAGTCATCGCGGCTAAATAAAGCAGGTGGGAAGCGCAGGAGTTTCTCTAAATGAGAAGCTGAACGTAAACATTCAAATTAAAATCTTGTTTATTTGCTGAAATTCATTTTAAAGGTGCTGTGTGTGAGTTTTTGACTCTTCTAAAGTATAAACACACCATCATCTGTGTGCAGATATTCAGATCATGCTCAGGGAACATTCTTGTTTATCTGAAACACAATGCTGAAGTCAGATATTCTGCTGTGAACATGTGCATTACATATCTTTGTTTTGGTCTCTGTAACCCGCCCAATGCC
Associated Phenotype:
Not determined