ZMP
esr2a
Ensembl ID:
ZFIN ID:
Description:
estrogen receptor 2a [Source:RefSeq peptide;Acc:NP_851297]
Human Orthologue:
ESR2
Human Description:
estrogen receptor 2 (ER beta) [Source:HGNC Symbol;Acc:3468]
Mouse Orthologue:
Esr2
Mouse Description:
estrogen receptor 2 (beta) Gene [Source:MGI Symbol;Acc:MGI:109392]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37010 | Essential Splice Site | Available for shipment | Available now |
| sa25133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16405 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37010
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010643 | None | None | 553 | None | 10 |
| ENSDART00000129589 | None | None | 551 | None | 12 |
| ENSDART00000131069 | Essential Splice Site | None | 553 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 21667301)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 21695468 |
| GRCz11 | 20 | 21595141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTTATCCACTTTATCACATCATCCTTTTGTGCTTCTGTCATTCTGC[A/T]GGTGCTTGTTCTTGTTCTGTGCTCAGGGTATGTTTTGGCCGCTTGCCTGT
Long Flanking Sequence:
AGTCAGAATTATTAGCCCCCCTGTATTTTTTACTTTCTTATTTATGTTTAACTCAACACATTTCTAAAGAATAGTTTCTTTTGTAGGTAATCAGAAAAAAATGCTTAAAGGGCTTAATATTGACTTTAAGATGTTTTTTTAAACGGTTAACAACTGCTTTTTGTCTTGCAAAATAAAACAAATAAGACTTTCTCCGGAAGAAAAAAATATTACAGGAAATACAGTGAAAAATTCCTTGCTCTGAGAAATATTTAAAATAAATAATAAAGAAAAAAAAATCACAGGAGGGCTAATAATTTTGACCAAAACTGTATATTAATTAATTTTATTTCGCCTTAGTCCCTTTATTCATCAGAGGTCGCCACAGTGGAATGAACCGCCTACAACTGTATTTAATAAATGCTTGTTTTTCCCATTCAATGTTAAATTAGATTGTGTGCAGTTCAGTGCTTGTTTTATCCACTTTATCACATCATCCTTTTGTGCTTCTGTCATTCTGC[A/T]GGTGCTTGTTCTTGTTCTGTGCTCAGGGTATGTTTTGGCCGCTTGCCTGTCTGCACTGAACAAGAGTTCAAAAGTCCTCACTGAGTCACCGTTGCCGTCTGGAGAGACAGTGTGGTATACCGCCTTGCTCACTGTCTTGCTACAACACTGAGGAGGTAAGACTCACTTTAACAGACTTCTGTGTTAAAAAAAAGTGCTGAGTGAATACAACTGTGTCTCGACTGTGCATTGATTTTTTTTGTTTGGATTTTTAGTTTTAGAGAAGTGTAAGTTAGTAAGCAGTTTAGATTCAGGCCATCACTGTCTGTACACGACTGTCTGGAACTAAAATAGACAGCTATGCAAAACTCAAAGTATTTTTTTCAGTGTTCACAAGCTGCTATTTAAGTATTTGAAGCAAATATCTGTTATAAAACTGTAGTGAGAGCAGCATTTTTGAGCATTCCTGAATAGCGTGGCACTAGCAGTGTCGAGGTCGTAGGCTCATTCCTGGAAATGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25133
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010643 | Nonsense | 119 | 553 | 2 | 10 |
| ENSDART00000129589 | Nonsense | 117 | 551 | 4 | 12 |
| ENSDART00000131069 | Nonsense | 119 | 553 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 21673532)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 21701699 |
| GRCz11 | 20 | 21601372 |
KASP Assay ID:
554-7852.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCAACAACAGAGTCGACTTCAACAGAACCATGCTACTAGTGGGACTT[G/A]GACCGAACATACACCACATGATCATGTTGAAGAGGAAAACAGGTAGGTTT
Long Flanking Sequence:
GTTCAAAATGAGTCTGCTCAATGCTAATTCACACTGTAATTCTTCCTGCTTTTCTCCCAGTATCGAGGACTGAGAAGTTCACCATGACACACATCAACAGTCCCCCGTTACTGATGCGACAGCTCTGAACTCATCCGCCTTCACCATGTCCGAGTATCCCGAAGGAGACAGTCCTCTTCTTCAGCTGCAGGAAGTGGACTCAGGCCGGGTGGGAGGTCACATCCTCTCCCCCATCTTCAACTCATCCTCTCCATCTCTGCCAGTGGAGAATCACCCCATCTGCATCCCATCGCCCTACACAGACCTTGGCCACGACTTCAGCACTCTGCCCTTTTACAGTCCCGCTCTGCTGGGGTACAGCACATCGCCTTTATCGGACTGCTCGTCTGTGCGCCAGTCGCTAAGCCCGACTTTATTTTGGCCACCTCACAGCCATGTTTCCTCACTCACATTGCAACAACAGAGTCGACTTCAACAGAACCATGCTACTAGTGGGACTT[G/A]GACCGAACATACACCACATGATCATGTTGAAGAGGAAAACAGGTAGGTTTAAGCTTAATAGTCCATATGTAATGTTCTTAAAGGAATAGTTCACATAATTTAATTTCTGTCACTGTTTACTCACCCTTCACAAGCCTTTATGACTTTCTATTGTCTAAACACAAAATGAGATATCTTGAAGAATGCTTGGAATTCAGTAATTATTGAATTCCATTGTATTTTTTTCTACAATAAATGTCAGTGTTTTCCAGCGTTCTTTAAAATATCTTCTTTTTTGTTGAACATATAATAGCAACATAAAAATTTGGAATCACTTGAGGGTGAGTAAATGATAACAAAACTTTCTCTTTTTTTTCTTACTTTTTAATACTAAAAAACACCTTCTCTTCCTTGAACTATCCCTTTAAGTCAGCATGATAACGTCTGGTGAAAGGTTGGTGTGACTATATCATCAGGGATTCTTTAACAGTTGTAGTTCATATTCAAGTTTATAATAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16405
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 |
|---|---|---|---|---|---|
| ENSDART00000010643 | Nonsense | 411 | 553 | 7 | 10 |
| ENSDART00000129589 | Nonsense | 409 | 551 | 9 | 12 |
| ENSDART00000131069 | Nonsense | 411 | 553 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 21697722)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 21725889 |
| GRCz11 | 20 | 21625562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTTGATATGCTGCTGGCAGCCACGTCCAGATTCAGAGAGYTGAAGTTA[C/T]AGAGAGAAGAGTACGTGTGTCTCAAAGCCATGATCCTCCTGAACTCCAGT
Long Flanking Sequence:
TTTTGTTTCTTAGTGTAAACGGGACACTCCTGAGGCTCACAGTAATGAAGTACATCCACTCAATTATTTCTAACCTCTAGTGTTAATGTTGCGAAAAAGTCTTGTTTAAAGCTAAATACAAGTAACTCTATCTTTTTTCTATCTGTCCTCACAAGTTTTAATGAAGTGTTAGTGACTGTCCAGGTCACATTCACTGTCGCAGCTCCAATTGTAGCACCTCTTGGCGTCCCAAAAAGCTCTAGTACGCTTTTTTCCATCGACACTTTGTGCTAAAATGACCATTGATGCTGTCAGCAGGTGCCAGGTTTGGAATAGGGCGAGCTTGAGATGAAGGCCTGCTCTCTTGTTTCTGATGAGGTGAAGCTAATTTGTTAGGCTGAAAATGTGTGTGTGTGTGCGTGTGTGTGTTTGGCAGGGATGAAAGCAGCTGTGTGCAGGGGTTGGTGGAGATCTTTGATATGCTGCTGGCAGCCACGTCCAGATTCAGAGAGTTGAAGTTA[C/T]AGAGAGAAGAGTACGTGTGTCTCAAAGCCATGATCCTCCTGAACTCCAGTAAGTGCTCTTCTTATTGTAGAGTTTATGAAGCATATGCGTCTCTATTTTTGTAGATAAATTATTGGGTATTTTTTTTAGTTGAGCCTCTACATACAGTACAACAACAGTACAGAAAAATACATTTGTCCGCAGTGAAATGAAGCAAAGTGTAAATGAAGACTTTAGCATTGACATTCTGATTTTTCATACGTTTATAAAATTAAAGAGCTCATATTATACATGAAATAGGATCATATCTTGGTTGTAAGGGTCTCCAACAACAGTCTAATATGCATGCAAGGTCAAAAAACACTTTCATGGTCTCATAATCTGCATTTATTTTTACCTAATTATTCCAGAGACTCCGGTAAGAATCGTCCAGTGATTCATTTGTTCCCAAACCCATATACCCATATATATATGGTAAGGATTTGGTTATGAATTGACGGGTAGAGATCTGTAGATTTCAC
Associated Phenotype:
Not determined