ZMP
esrrga
Ensembl ID:
ZFIN ID:
Description:
estrogen-related receptor gamma [Source:RefSeq peptide;Acc:NP_998119]
Human Orthologue:
ESRRG
Human Description:
estrogen-related receptor gamma [Source:HGNC Symbol;Acc:3474]
Mouse Orthologue:
Esrrg
Mouse Description:
estrogen-related receptor gamma Gene [Source:MGI Symbol;Acc:MGI:1347056]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32156 | Nonsense | Available for shipment | Available now |
sa7438 | Missense | Mutation detected in F1 DNA | Not yet available |
sa23108 | Missense, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32156
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 |
---|---|---|---|---|---|
ENSDART00000009104 | None | None | 435 | None | 7 |
ENSDART00000126966 | Nonsense | 19 | 508 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 29961046)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29884973 |
GRCz11 | 17 | 29901936 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCGGTAGAACTTTCGCTCCCTGAGTGTTTTTCCCTGCACTCCGATCAA[C/T]AGTAGGTACATTTTCATTTCTTCTACTTCTTGCTTGCACTTGTGTGTCCG
Long Flanking Sequence:
TCTCTCTCTCTCTCGCTCGCTCGCGCTTTGTCTTTCCCCTCCCCTCTCTCCCTGCTCCGTCTCTCTGTGGGCGCAGACACTACCCTGTCTCACTCCGATTGGCTGAGAAGCCACCAATCTGGCGTCCGGGAGGGCCGGGGGGACTGCATATGCAAAGCTCTGCTTCATATTAATGAGCAGCAATCGTGGCTTTAAGTCCTTGATTAGAAGAGTGCAAGAGCTTTTGGTCCCAACTGGCTGTGCCTATAGGCTGTCACCGGGAGAACGGTCCTGTTAATTGCACTGCTCAGTCACGGAAGGGAGAGAGAGGAGGAGGAGGTACAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGACAGAAAGAGGAGCGCAGACACAGAGAGAAAGAGAGAGAGAGAAAACTTTAATTTATAGAAGAGGTTTGCTCAAACGATGATCGCAGAGCGCACATGGATTCGGTAGAACTTTCGCTCCCTGAGTGTTTTTCCCTGCACTCCGATCAA[C/T]AGTAGGTACATTTTCATTTCTTCTACTTCTTGCTTGCACTTGTGTGTCCGGCTAGACTGTTTGTTCCTGTCCTGGCAGTGTGCTTGTGTTTATGTGTGCATGTGGTCAGCGTAGTCCTCATCTCAAGGTTGTTTTCGCTGTCAGATAGCAGTTTGGAGCCCAAACGTATATACTAAATGCTGTGACAGCTTATCCACTATTACAGCAATCTGCGTCCGCTTTGACAGTACATAGTGTGTTTTGTGTAAATCATTAGGAGTGTGTTATGGAAAACAACATGATAGAGAGAGTGTCGAGGGAGAGACGAAAGCAACGGGATAGAAGGGAGAAAAGGGTCTTAGGTGGCTTGAATCGCAGACCGGTCGCACAGCATGTGGCCCGCTAAATGTATTAAGACGGTGTGCTGGCTCAGAGAGAGAGAGAGATAGAGGGAGAGAGGGAAGGAGGGAGGGATTGAGTTCACTGAGCGAGCGAGTGAGCGGACGGTCCAGGAGCCGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7438
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009104 | Missense | 152 | 435 | 3 | 7 |
ENSDART00000126966 | Missense | 218 | 508 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 29932336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29856263 |
GRCz11 | 17 | 29873226 |
KASP Assay ID:
554-4274.1 (used for ordering genotyping assays)
KASP Sequence:
GAAACATCGAGTACAGCTGCCCCGCCACCAATGAATGTGAGWTCACCAAA[C/T]GTAGAAGGAAGTCCTGCCAAGCCTGCCGCTTCATGAAGTGTCTGACCGTC
Long Flanking Sequence:
CTCTATTTACTGAAAAATTTATAAAAATATTAATTTTCAAAATGCGGTGTACTCTATTAGGCTGAGCACTGTGTATGATATTTTTATCTTTCATAGAATGATTTTTGTTGTGTTTAATTCATGTAACGTAGTACACTAAATGCATTTATGATGCACCCCCCCCCCACACACACACATATATACAAAAATAAGTGACACTTTGCAATATGCTAAAATTGTCATTTTAAATGTTAACCATATTTAACAGTATTACTGTTTTAGTATTTTTTTTTTTTACTGTTTTAGTATTTATATTAAACAAATATGGCTTTGGTGGACATAAACATAAAAAAACACAAAATCACCAGTATCTAAAATAGTATGATATAATGTAATTAAATGGATTAATAAAGTTTGGGTTGTCAGTCATTAAACACTCTCTGTTCCTTCTCTCTACATGCCTCGCCACAGGAAACATCGAGTACAGCTGCCCCGCCACCAATGAATGTGAGATCACCAAA[C/T]GTAGAAGGAAGTCCTGCCAAGCCTGCCGCTTCATGAAGTGTCTGACCGTCGGCATGATGCGAGAAGGTGAGCGAATTATTTTAAAAAAGCAGAAAAAGAACATTTCATCCATTTCCCGACTACAACTCTCAGCCTTCTGAGGAAAATACAGGTTTCCAAGAGAGAAAAAAAAGTAGAACAGGTCTTAAATGAAGTCAAGGTTGAAACTGAAGGGCCGGTTGGCCTCCTGCCCCGAGGGCCACTCACGGTCAGCCAAACACCATCTTTTGTCTCGGCCTCCAGGCCCATTTCTAACTAACAAGACTGGTTATTATTTAGAGAGCCGGCCTGTGAGGCATTTTCTCAGAGGTCTGCCAAATGGACAAGCAGTTATTTTCAAACCGCCGCTCTCCTGTGGAAACACAGACTCTGGCTTTCTGGGCTTTCCCGCTTTTGATGTTAAAAGTTTACAGAAGAGCTAGCCTTTAACCTTCATGCAGGGAAAAAAAGTCCTTTCTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23108
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009104 | Nonsense | 211 | 435 | 5 | 7 |
ENSDART00000126966 | Missense | 284 | 508 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 29895687)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29819614 |
GRCz11 | 17 | 29836577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTCTCCCCTCGGTGTTCAAATACAGTCCCCTTTGGCTGCCTTGCAGA[T/A]AACAAGATTGTGTCTCACTTGCTGGTGGCGGAGCCGGAGAAGATCTACGC
Long Flanking Sequence:
TCTTTTCTTTTTAGTACTTTTGTAAACTGTGCTTATCTGTAATTCTTAATAGTAAATAATTATTAAACATATGTATATATCCTTTTGTATTGTTCATTTATTTTTAATTATTCATATATAATCTAAAAGTGATTAAACCTTTGATCTGGCTAACAGAACAGCTTACAAAATCACCATCTTGTTTTTGAAGCAGAACTGGTTGAAAACCACTGCTGGACACCATAAAACCCTCCCCCCTAACTAAATGCCTAAGAAACCAACGCTTTATTTTCAATTATAAATGACTCCGGGCATTTATTCTTGTCCAAAAAATAGCATTTTCAAACCACAAACATCATCTTTTCTGTCCAAAGAACACACCTCTGCCAATATTTCATGTTATCTGATTGCTTTTTTTGCTGCTGAAGCAAACACTACATGACCTTGCTGGTATAATCCCAATCTGTTTCTTTGTTCTCCCCTCGGTGTTCAAATACAGTCCCCTTTGGCTGCCTTGCAGA[T/A]AACAAGATTGTGTCTCACTTGCTGGTGGCGGAGCCGGAGAAGATCTACGCCATGCCTGACCCGACAGTGCCCGACAGCGACATCAAAGCCCTGACCACGCTCTGCGACCTGGCAGACCGAGAGCTGGTGGTCAACATAGGCTGGGCCAAGCATATCCCAGGTAGGACATGAGCAAAGATCCAAATACTGACCAGCTCCAAGAGTATAGTGTGGATTGGATAACACATTTAATATAAATGCCTAAAAGGAATAAAACAAACTGTCAAAAAAACAAATCTCTAACTATAGGGCACAATGTGTTGTATTTATTTATCTCTTTATTTAATTATTTACTGGTATTTTACCTGTATTTGGAATTTAGCACTGCTTTTGCATTGTGTTTAGAAGCTACTTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTGAGCGTGTTTAGAGTATAGATTAAAAAATAGCTAATTATATTATTATGTGCTGCTTACAAACTTTATAGT
Associated Phenotype:
Not determined