ZMP
adra2a
Ensembl ID:
ZFIN ID:
Description:
Alpha-2A adrenergic receptor [Source:UniProtKB/Swiss-Prot;Acc:Q90WY4]
Human Orthologue:
ADRA2A
Human Description:
adrenergic, alpha-2A-, receptor [Source:HGNC Symbol;Acc:281]
Mouse Orthologue:
Adra2a
Mouse Description:
adrenergic receptor, alpha 2a Gene [Source:MGI Symbol;Acc:MGI:87934]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43873 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45776 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24199 | Nonsense | Available for shipment | Available now |
sa39378 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43873
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 |
---|---|---|---|---|---|
ENSDART00000059869 | Essential Splice Site | None | 388 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 32276130)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29637260 |
GRCz11 | 22 | 29586455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAGATGCCTTAATAAGTTTGTGGAAAGCTTCAGGCTTATTTCATTAAG[G/A]TAAGGTACATCCCTGTCTTACTTTTTTTTTGGTTGTGTAATTTTGTGGTG
Long Flanking Sequence:
GTTATGTTGTCTTCTCCAAGTAAAAGATAGAGCAAATAAACGTTTTTATTGGTTTAAACCACTCAGAAACATACAAAAAGTTATTTATTTATTAATTTTTTGGCGTTTTTACAGAGCCTCTCAAGGCTGCTGCTTAGCAACGTCAATCGGAGGCTGGAGTTAAGAGAAAGTGGGCGTGGCTCAGAATAGTCATTATTATAATTTCCTGTGCGCGTCTCCCACAACACACACACACACACTCCAGCGCGCTCACGGCAAGCTAAAGTGATCACGCCTCTATTAGCTGTGCGCGCTCACGGCAGATCCTGCGCGCGCACAGCCGAGTCGAGCGCTGATGATGATGATGCGCGGTCTTCACACGCTCCATCGACGAGATGCGAGAGATTAACCATGCAGTTTTTCTCATGCTGAGCGACTTTAAACAGAGAAGTTGCACTCCGAGGGACGTTTCTTAGATGCCTTAATAAGTTTGTGGAAAGCTTCAGGCTTATTTCATTAAG[G/A]TAAGGTACATCCCTGTCTTACTTTTTTTTTGGTTGTGTAATTTTGTGGTGTTTTATATAAGAGTGAGAAACAAATGTATAGTTTTACCATAATTATTTAAATGTTTGAAATTAGTGTAATTGTTTTGTTTAATTACAATCAATTGCTTGTAAAATAAAACTTTGCATCTGTATGTTGTGTGTACTGTGTATGTTATGTATAAACTTGATAAAAACATGTTTATATATAATGCAAAATATATGTTAATACATTTGTTTAATATATATTTAAAATTTTTACTTGTTTATTATTGTTGTAGCCTATATATACACAATAAACATACAGTACACATTTCATCTATTTTCATCTAATAATACATTTTCCAATTTCTTTTTAGATGTCAGAATGATTAGAATCGTCTCTGTTTGTCAGTAATATGGAAAAAGTGAAGTGTCATCAACCAAAAACATAATTTCACTCGTGTGGAGAAGAGACTGTAACTGTCAGCTATGATTTGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45776
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 |
---|---|---|---|---|---|
ENSDART00000059869 | Nonsense | 80 | 388 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 32275403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29636533 |
GRCz11 | 22 | 29585728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGCCTCAGCTGACATACTGGTGGCCACTCTGGTGATGCCGTTCTCAT[T/A]GGCGAATGAGCTGATGGGTATGTGGACGTTTGGGGGAGTTTGGTGTGAAA
Long Flanking Sequence:
TAATGCAAAATATATGTTAATACATTTGTTTAATATATATTTAAAATTTTTACTTGTTTATTATTGTTGTAGCCTATATATACACAATAAACATACAGTACACATTTCATCTATTTTCATCTAATAATACATTTTCCAATTTCTTTTTAGATGTCAGAATGATTAGAATCGTCTCTGTTTGTCAGTAATATGGAAAAAGTGAAGTGTCATCAACCAAAAACATAATTTCACTCGTGTGGAGAAGAGACTGTAACTGTCAGCTATGATTTGTGGGGCCAATGCAACCAATGGGACCAATGCAACAAAGGAGTACACCCTGCTGGTGGCCCTACCACTGAGCGTTGCAGTGGGGCTCCTCATCCTCCTCATCATCTTCGGCAATGTCCTGGTGATCATCGCCGTGTTCACGAGCCGAGCACTCCGGGCTCCCCAGAACCTCTTTCTGGTCTCGCTGGCCTCAGCTGACATACTGGTGGCCACTCTGGTGATGCCGTTCTCAT[T/A]GGCGAATGAGCTGATGGGTATGTGGACGTTTGGGGGAGTTTGGTGTGAAATCTACCTGGCCTTGGACGTTCTTTTCTGCACAGCTTCAATTACTCACCTGTGCGCCATCAGTCTGGACAGGTACTGGTCAATTACGCAAGCCATCGAGTACAACCTGAAGCGAACACCGCAACGTATTAAGCGTATCATTTTTATCGTTTGGATCATCGCCGCCGTGATCTCCTGCCCCCCTCTTATAACAATGAAGAAATCTGAGGGGGATATCTGTGACATCAATAAGGAAAAATGGTACATAGTCTCATCTTGCATTGGCTCGTTTTTCCTGCCTTGCATCATCATGGTCCTCGTCTACATCCGGATCTATCAAATTGCCAAGAAGAGAACTAGAGCACCTCCTGGGGACCACAGGAAAAACGAAGTGGGAAAGAAGGAAAACGACCCGCATGAGAAGCTCAATGGAATTCAGAATGCAGAACCGGACGACAAGGATGAAATAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24199
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059869 | Nonsense | 130 | 388 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 32275252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29636382 |
GRCz11 | 22 | 29585577 |
KASP Assay ID:
2261-6996.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCCATCAGTCTGGACAGGTACTGGTCAATTACGCAAGCCATCGAGTA[C/A]AACCTGAAGCGAACACCGCAACGTATTAAGCGTATCATTTTTATCGTTTG
Long Flanking Sequence:
TGTCAGAATGATTAGAATCGTCTCTGTTTGTCAGTAATATGGAAAAAGTGAAGTGTCATCAACCAAAAACATAATTTCACTCGTGTGGAGAAGAGACTGTAACTGTCAGCTATGATTTGTGGGGCCAATGCAACCAATGGGACCAATGCAACAAAGGAGTACACCCTGCTGGTGGCCCTACCACTGAGCGTTGCAGTGGGGCTCCTCATCCTCCTCATCATCTTCGGCAATGTCCTGGTGATCATCGCCGTGTTCACGAGCCGAGCACTCCGGGCTCCCCAGAACCTCTTTCTGGTCTCGCTGGCCTCAGCTGACATACTGGTGGCCACTCTGGTGATGCCGTTCTCATTGGCGAATGAGCTGATGGGTATGTGGACGTTTGGGGGAGTTTGGTGTGAAATCTACCTGGCCTTGGACGTTCTTTTCTGCACAGCTTCAATTACTCACCTGTGCGCCATCAGTCTGGACAGGTACTGGTCAATTACGCAAGCCATCGAGTA[C/A]AACCTGAAGCGAACACCGCAACGTATTAAGCGTATCATTTTTATCGTTTGGATCATCGCCGCCGTGATCTCCTGCCCCCCTCTTATAACAATGAAGAAATCTGAGGGGGATATCTGTGACATCAATAAGGAAAAATGGTACATAGTCTCATCTTGCATTGGCTCGTTTTTCCTGCCTTGCATCATCATGGTCCTCGTCTACATCCGGATCTATCAAATTGCCAAGAAGAGAACTAGAGCACCTCCTGGGGACCACAGGAAAAACGAAGTGGGAAAGAAGGAAAACGACCCGCATGAGAAGCTCAATGGAATTCAGAATGCAGAACCGGACGACAAGGATGAAATAAATGGTGTGGACATGGAGGAATCCTCCTCCTCAGACCACAAGGTCTCCAATCCTTGCTCCCTCAAGAAGAAAAGCTCAAAAGGAAAGACCAAGTTGAGCCAAATCAAACCAGGCGATGGAGACAAAACCGAGGCCTGCCAGACTACCAAAGCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39378
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 |
---|---|---|---|---|---|
ENSDART00000059869 | Nonsense | 277 | 388 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 32274812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 29635942 |
GRCz11 | 22 | 29585137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAATCCTTGCTCCCTCAAGAAGAAAAGCTCAAAAGGAAAGACCAAGT[T/A]GAGCCAAATCAAACCAGGCGATGGAGACAAAACCGAGGCCTGCCAGACTA
Long Flanking Sequence:
TACTCACCTGTGCGCCATCAGTCTGGACAGGTACTGGTCAATTACGCAAGCCATCGAGTACAACCTGAAGCGAACACCGCAACGTATTAAGCGTATCATTTTTATCGTTTGGATCATCGCCGCCGTGATCTCCTGCCCCCCTCTTATAACAATGAAGAAATCTGAGGGGGATATCTGTGACATCAATAAGGAAAAATGGTACATAGTCTCATCTTGCATTGGCTCGTTTTTCCTGCCTTGCATCATCATGGTCCTCGTCTACATCCGGATCTATCAAATTGCCAAGAAGAGAACTAGAGCACCTCCTGGGGACCACAGGAAAAACGAAGTGGGAAAGAAGGAAAACGACCCGCATGAGAAGCTCAATGGAATTCAGAATGCAGAACCGGACGACAAGGATGAAATAAATGGTGTGGACATGGAGGAATCCTCCTCCTCAGACCACAAGGTCTCCAATCCTTGCTCCCTCAAGAAGAAAAGCTCAAAAGGAAAGACCAAGT[T/A]GAGCCAAATCAAACCAGGCGATGGAGACAAAACCGAGGCCTGCCAGACTACCAAAGCAAGCAGATGGAAGGGCCGTCAAAACCGAGAGAAGCGGTTCACATTTGTTCTGGCGGTGGTCATAGGCGTGTTCGTCATTTGTTGGTTCCCGTTCTTCTTCACCTACACATTCACAGCGTTTTGTGACTGCTGTGTGCCTGAAACACTTTTTAAGTTCTTCTTCTGGTTCGGCTACTGCAACAGCTCCCTCAATCCCATTATATACACTATCTTCAATAACGACTTCCGAAGATCCTTTAAAAAGATCCTCTGCCGGAGAGATAAGAGGAGAGTGGTGTGAACGGGCTGCTGTGTTGTCCGTTTCTCTATCAAATGTAATATATCACCTGCAGTTTACGGGAAGCACTTGTTTACAGTAAGCCAACATGTTGTGTGTCATTATACAACAAGTCCAAGCGGGGCTAAAAATAAAAAAAGACTTTCACATTCTTTGTACAAATGCA
Associated Phenotype:
Not determined