ZMP
ppargc1al
Ensembl ID:
ZFIN ID:
Description:
Proliferator-activated receptor gamma coactivator 1 alpha [Source:UniProtKB/TrEMBL;Acc:D7F2U9]
Human Orthologue:
PPARGC1A
Human Description:
peroxisome proliferator-activated receptor gamma, coactivator 1 alpha [Source:HGNC Symbol;Acc:9237]
Mouse Orthologue:
Ppargc1a
Mouse Description:
peroxisome proliferative activated receptor, gamma, coactivator 1 alpha Gene [Source:MGI Symbol;Acc:
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34243 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31621 | Nonsense | Available for shipment | Available now |
sa13186 | Nonsense | Available for shipment | Available now |
sa34242 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7107 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34243
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 |
---|---|---|---|---|---|
ENSDART00000097710 | Nonsense | 364 | 873 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 73167826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 70161594 |
GRCz11 | 7 | 70611859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCCTTTCAAAGTATCACTCAAAAACAAGCTGTCTTCATGCTCTCCCT[C/A]GGCCCTGACAAGCAAAAGGCCCAGGCTGAGTAATGGGGGCTCTTGCCCTC
Long Flanking Sequence:
AAGATGGTTGGGGTTCATGAGGAGAAAAGGTGGCAAAGATGAAGAGAATGATAACAGCTCCCGCATCACCGTGCTTTCATCGGAGTCCCATGAGGATAGCATTCGCGCATCTGTTGAAACCACCAGTCTTATCATTATAAGATCTGACTGTTTACTTTCTGATGAATTAGGATTGTTTACGGTCTGGAGGAAGTTTAATTGAGTAACTCTGTGTCTGTATCGCAGTGCAATCTGAGGTCACATTGATCTGTCAGGGTCGCAATAAAATGCGGATAAGGATTAGCCCTAAATGAAAGGGAATATTTTAATCAGGCTCGAGTGTTCAATCACTTAGAGACACTCTTGAGCACTGTTGAGGAATGAGAGTGATCCCGTTTGGTAAATCTTTTGTCTCTTCTTCCCTCCAGGTCTGACACCACCTACCACGCCTCCTCACAAAGCCAGTCAAGAGAACCCTTTCAAAGTATCACTCAAAAACAAGCTGTCTTCATGCTCTCCCT[C/A]GGCCCTGACAAGCAAAAGGCCCAGGCTGAGTAATGGGGGCTCTTGCCCTCAGCCAACCAGCGGCTCTATTCGGAAGGGCCCAGAGCAGACTGAGCTCTATGCCCAGCTGAGCAAGGCGTCCTCCACTATGCCCCAAGGGGGCTTGGAGGATCGTCGGGGCAAGCGGCCCATGCCCCGTGTCTTTGGCGATCATGACTATTGCCAATCTACAAGCACAAAACGAGACAGCACCACCCCAGCTGCAGTGGTACCCGGGCCAACAGAGGGCCGGCATGTGGAATGTAAAGACTTAAACATGCCAACCTCCACTACTACGACATCATCGTTGTCTTCCACCCCCCCTTCGTCTTCCTCACTGGCCAGGCAGCTTCAAGGCCTTTCCCCAACACCTCAGGAGGCTTGTCCGGACACATATGCTCACGTGCAGCACCACGACTCAAGCTCCAAAATGACAATGGACTGCAGTTCTGGTGGCAGGAAACTTCTTAGGGACCAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31621
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 |
---|---|---|---|---|---|
ENSDART00000097710 | Nonsense | 412 | 873 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 73167682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 70161450 |
GRCz11 | 7 | 70611715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTATGCCCAGCTGAGCAAGGCGTCCTCCACTATGCCCCAAGGGGGCT[T/A]GGAGGATCGTCGGGGCAAGCGGCCCATGCCCCGTGTCTTTGGCGATCATG
Long Flanking Sequence:
TGACTGTTTACTTTCTGATGAATTAGGATTGTTTACGGTCTGGAGGAAGTTTAATTGAGTAACTCTGTGTCTGTATCGCAGTGCAATCTGAGGTCACATTGATCTGTCAGGGTCGCAATAAAATGCGGATAAGGATTAGCCCTAAATGAAAGGGAATATTTTAATCAGGCTCGAGTGTTCAATCACTTAGAGACACTCTTGAGCACTGTTGAGGAATGAGAGTGATCCCGTTTGGTAAATCTTTTGTCTCTTCTTCCCTCCAGGTCTGACACCACCTACCACGCCTCCTCACAAAGCCAGTCAAGAGAACCCTTTCAAAGTATCACTCAAAAACAAGCTGTCTTCATGCTCTCCCTCGGCCCTGACAAGCAAAAGGCCCAGGCTGAGTAATGGGGGCTCTTGCCCTCAGCCAACCAGCGGCTCTATTCGGAAGGGCCCAGAGCAGACTGAGCTCTATGCCCAGCTGAGCAAGGCGTCCTCCACTATGCCCCAAGGGGGCT[T/A]GGAGGATCGTCGGGGCAAGCGGCCCATGCCCCGTGTCTTTGGCGATCATGACTATTGCCAATCTACAAGCACAAAACGAGACAGCACCACCCCAGCTGCAGTGGTACCCGGGCCAACAGAGGGCCGGCATGTGGAATGTAAAGACTTAAACATGCCAACCTCCACTACTACGACATCATCGTTGTCTTCCACCCCCCCTTCGTCTTCCTCACTGGCCAGGCAGCTTCAAGGCCTTTCCCCAACACCTCAGGAGGCTTGTCCGGACACATATGCTCACGTGCAGCACCACGACTCAAGCTCCAAAATGACAATGGACTGCAGTTCTGGTGGCAGGAAACTTCTTAGGGACCAGGAGATCCGGGACGAGCTCAACAAGCACTTTGGAAAGCCTCAGCAAGCCTTCTATAGCGGGGTAGTGGGAGAGCCGAGGGGCAAACAGCCAATTGAGGACAGTGACTCTGGGGATGAGTACCCGGGTCTACTCGGCGACTACATCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13186
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 |
---|---|---|---|---|---|
ENSDART00000097710 | Nonsense | 502 | 873 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 73167411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 70161179 |
GRCz11 | 7 | 70611444 |
KASP Assay ID:
2259-9833.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCTTCAAGGCCTTTCCCCAACACCTCAGGAGGCTTGTCCGGACACAWA[T/A]GCTCACGTGCAGCACCACGACTCAAGCTCCAAAATGACAATGGACTGCAG
Long Flanking Sequence:
CCACCTACCACGCCTCCTCACAAAGCCAGTCAAGAGAACCCTTTCAAAGTATCACTCAAAAACAAGCTGTCTTCATGCTCTCCCTCGGCCCTGACAAGCAAAAGGCCCAGGCTGAGTAATGGGGGCTCTTGCCCTCAGCCAACCAGCGGCTCTATTCGGAAGGGCCCAGAGCAGACTGAGCTCTATGCCCAGCTGAGCAAGGCGTCCTCCACTATGCCCCAAGGGGGCTTGGAGGATCGTCGGGGCAAGCGGCCCATGCCCCGTGTCTTTGGCGATCATGACTATTGCCAATCTACAAGCACAAAACGAGACAGCACCACCCCAGCTGCAGTGGTACCCGGGCCAACAGAGGGCCGGCATGTGGAATGTAAAGACTTAAACATGCCAACCTCCACTACTACGACATCATCGTTGTCTTCCACCCCCCCTTCGTCTTCCTCACTGGCCAGGCAGCTTCAAGGCCTTTCCCCAACACCTCAGGAGGCTTGTCCGGACACATA[T/A]GCTCACGTGCAGCACCACGACTCAAGCTCCAAAATGACAATGGACTGCAGTTCTGGTGGCAGGAAACTTCTTAGGGACCAGGAGATCCGGGACGAGCTCAACAAGCACTTTGGAAAGCCTCAGCAAGCCTTCTATAGCGGGGTAGTGGGAGAGCCGAGGGGCAAACAGCCAATTGAGGACAGTGACTCTGGGGATGAGTACCCGGGTCTACTCGGCGACTACATCCACCCAGGTCTGCCTGATTTCGAGGACCTGGAGGTAGGCCGGGAGCGCCTGTTCTACTTGGGGGAAGGTTCTCCACTCGAGCTGCTCCTCGAAGGGTCACCCTCCAGCTCCCCTTCCAGCAGTTCCTTTTCATGGTGCTCTGTCTCGCCTCCTTCCTCTCAGCTCTCCCCACAGCACCTCCGCTGGCCACGCTCCATCTCCCGCTCCCGTTCTCGTTCTTCATCTCACCACAGGCGCAGATCCCTCTCCAGGTCTCCCTACTCCCGCTCCGGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34242
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 |
---|---|---|---|---|---|
ENSDART00000097710 | Nonsense | 726 | 873 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 73157358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 70151126 |
GRCz11 | 7 | 70601391 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACAGCTATGAGGAATACCAGCACGAGCGTCTGAAGCGAGAGGAGTAC[C/T]GACGCGACTATGAGAAACGGGAATGTGAGAGGGCCGAGCAGAGGGAGAGA
Long Flanking Sequence:
TCATGTCATTTGAGAAATATTTTTGTTTTTCACACAATAATGCCTCTTGTACATAGTCGTGTTATCCTTTAGGAGAAGCCTGTGTCATTTTCAGTCAATTGCTGGTTGAATAAAAGTAATTTAAGTAAGAATTGAAGAAGGTATGAATAATTTAGGGCTTGGAAATATATTTAAATAATAAAATATATATATAAATAATAAACTGTTTGATTGGGAAAATGAAAACTGAAGATCTGCATTTTATTTCTGGGAAAATATTTACACATTATTTCACATTTTAGATGTTTTCTGAAACTCTAGAGGAGACTCTTGATATTACTGTGGAGTTTTTCTAAGAAAGAATCGTCAGAGGAGCAGGAGACTGCTTTCTGTTCCTTGTTTCTTATTGTGTGTTTAGAGAACACTTGATGTGATTTCGTTCTGCAATGTTTTGTCATTTCAATTCTAGGTATGACAGCTATGAGGAATACCAGCACGAGCGTCTGAAGCGAGAGGAGTAC[C/T]GACGCGACTATGAGAAACGGGAATGTGAGAGGGCCGAGCAGAGGGAGAGACAACGGCAAAAAGCAATAGTGAGTACGCCCACCTATTTTATTCAATTATAGAATGCTTCTTCAACTACGGACACTGTTATATCCCTGTGGTTGTTTGTTATTAAACTTACAGGTTTAAACTTTTGTTAAATAAAGGGGCATAGAAAACTTTCCTGGAAACTTTTACTGCACAATTAGTTTTTGTGTCCAGAATTGAAGCAGAATCTATCATAAGGCTGAAACATGCTCATGTAAAATAAGGAGTGTAATCAGAATCAATAATAATAGTATGAGTCAAATCCATCTATCAAACAACTGGGTTTTGCTCATTTGTTACTAAGAACAATTTAAAATACAATCACATGCATTATGATTGCTGAATGAATTATTAATAAATCAATGAATAATTAAAAATGAAACAATACATCTATGTACTCTGCAAAATATTTTTCTGTTGCTCAGAGGTTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7107
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 |
---|---|---|---|---|---|
ENSDART00000097710 | Nonsense | 734 | 873 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 73157332)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 70151100 |
GRCz11 | 7 | 70601365 |
KASP Assay ID:
554-5312.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCGTCTGAAGCGAGAGGAGTACCGACGCGACTATGARAAACGGGAATG[T/A]GAGAGGGCCGAGCAGAGGGAGAGACAACGGCAAAAAGCAATAGTGAGTAC
Long Flanking Sequence:
TTTTCACACAATAATGCCTCTTGTACATAGTCGTGTTATCCTTTAGGAGAAGCCTGTGTCATTTTCAGTCAATTGCTGGTTGAATAAAAGTAATTTAAGTAAGAATTGAAGAAGGTATGAATAATTTAGGGCTTGGAAATATATTTAAATAATAAAATATATATATAAATAATAAACTGTTTGATTGGGAAAATGAAAACTGAAGATCTGCATTTTATTTCTGGGAAAATATTTACACATTATTTCACATTTTAGATGTTTTCTGAAACTCTAGAGGAGACTCTTGATATTACTGTGGAGTTTTTCTAAGAAAGAATCGTCAGAGGAGCAGGAGACTGCTTTCTGTTCCTTGTTTCTTATTGTGTGTTTAGAGAACACTTGATGTGATTTCGTTCTGCAATGTTTTGTCATTTCAATTCTAGGTATGACAGCTATGAGGAATACCAGCACGAGCGTCTGAAGCGAGAGGAGTACCGACGCGACTATGAGAAACGGGAATG[T/A]GAGAGGGCCGAGCAGAGGGAGAGACAACGGCAAAAAGCAATAGTGAGTACGCCCACCTATTTTATTCAATTATAGAATGCTTCTTCAACTACGGACACTGTTATATCCCTGTGGTTGTTTGTTATTAAACTTACAGGTTTAAACTTTTGTTAAATAAAGGGGCATAGAAAACTTTCCTGGAAACTTTTACTGCACAATTAGTTTTTGTGTCCAGAATTGAAGCAGAATCTATCATAAGGCTGAAACATGCTCATGTAAAATAAGGAGTGTAATCAGAATCAATAATAATAGTATGAGTCAAATCCATCTATCAAACAACTGGGTTTTGCTCATTTGTTACTAAGAACAATTTAAAATACAATCACATGCATTATGATTGCTGAATGAATTATTAATAAATCAATGAATAATTAAAAATGAAACAATACATCTATGTACTCTGCAAAATATTTTTCTGTTGCTCAGAGGTTGCTATTTTTTGTAAGCGTTTTATATCAGTT
Associated Phenotype:
Not determined