ZMP
adra2c
Ensembl ID:
ZFIN ID:
Description:
Alpha-2C adrenergic receptor [Source:UniProtKB/Swiss-Prot;Acc:Q90WY6]
Human Orthologue:
ADRA2C
Human Description:
adrenergic, alpha-2C-, receptor [Source:HGNC Symbol;Acc:283]
Mouse Orthologue:
Adra2c
Mouse Description:
adrenergic receptor, alpha 2c Gene [Source:MGI Symbol;Acc:MGI:87936]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30804 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39656 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39655 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19542 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30804
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101562 | Nonsense | 224 | 432 | 1 | 1 |
| ENSDART00000101562 | Nonsense | 224 | 432 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 1 (position 41374520)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40290761 |
| GRCz11 | 1 | 40993548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCATTATGATCCTCGTTTACATCCGAATCTATCAGGTGGCTAAAACA[A/T]GAACCCGAAATATGTCTGAAAAGCGGCGGGATCCTGATGGTGGCTCAGGA
Long Flanking Sequence:
TTATCGCCGTTTTAACGAGCAGAGCACTCAAGCCACCACAAAACCTTTTTCTCGTGTCTCTGGCCAGCGCGGACATTCTGGTGGCCACACTTATAATCCCCTTCTCCCTGGCCAATGAATTAATGGGCTACTGGTTTTTTGGGGAAGTTTGGTGTAATATCTATCTCGCTCTAGATGTTCTTTTCTGCACGTCTTCTATTGTTCACCTGTGTGCCATAAGTCTGGACAGGTACTGGTCTGTGACACAGGCGGTCGAGTATAACTTAAAAAGGACGCCTCGCAGGGTTAAGGGGATGATTGTGGTGGTGTGGTTGATTTCGGCTGTGATCTCCTTCCCACCGCTCATCTCCATGGATCGGAATACAGTTGATGAGAGGAGACCAATGTGCCAGCTGAATGACCACACATGGTACATCTTGTACTCCAGCATTGGGTCATTCTTTGCCCCGTGTGTCATTATGATCCTCGTTTACATCCGAATCTATCAGGTGGCTAAAACA[A/T]GAACCCGAAATATGTCTGAAAAGCGGCGGGATCCTGATGGTGGCTCAGGAACGCCACGCTTGGAGAACGGCTTAAGCCGTGAGGATTCTAGACGGGAAAATGGCCACTGTTCCTCATCGCCAGGCGAACGCAAACCAGCCGAGGATAACCCAGACGCTGACCTCGAGGACAGCAGCTCGTCCGACGAGAAGGCCAAGCGGTCACAAAATGAGACGGCCCCATCGAAAAAAGACCGCAGATCCAGCCGCAAGAACAGCTCCAGCTCCAAACACTCCAGCCGAAAGTCCCGAGCCAGCAGCAAATCCCTGGACTTGTTTTCATCTCGCAGAAAGAGGAGAAACACCATTTCCAGGAAAAAAATATCCCAGGCACGCGAGAAGCGGTTCACCTTTGTGCTGGCCGTGGTCATGGGCGTTTTTGTGGTCTGCTGGTTTCCCTTCTTCTTCAGCTACAGCCTGTATGGGATCTGCCGGGAGCCTTGCGCCATCCCTGACCCCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39656
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101562 | Nonsense | 224 | 432 | 1 | 1 |
| ENSDART00000101562 | Nonsense | 224 | 432 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 1 (position 41374520)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40290761 |
| GRCz11 | 1 | 40993548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCATTATGATCCTCGTTTACATCCGAATCTATCAGGTGGCTAAAACA[A/T]GAACCCGAAATATGTCTGAAAAGCGGCGGGATCCTGATGGTGGCTCAGGA
Long Flanking Sequence:
TTATCGCCGTTTTAACGAGCAGAGCACTCAAGCCACCACAAAACCTTTTTCTCGTGTCTCTGGCCAGCGCGGACATTCTGGTGGCCACACTTATAATCCCCTTCTCCCTGGCCAATGAATTAATGGGCTACTGGTTTTTTGGGGAAGTTTGGTGTAATATCTATCTCGCTCTAGATGTTCTTTTCTGCACGTCTTCTATTGTTCACCTGTGTGCCATAAGTCTGGACAGGTACTGGTCTGTGACACAGGCGGTCGAGTATAACTTAAAAAGGACGCCTCGCAGGGTTAAGGGGATGATTGTGGTGGTGTGGTTGATTTCGGCTGTGATCTCCTTCCCACCGCTCATCTCCATGGATCGGAATACAGTTGATGAGAGGAGACCAATGTGCCAGCTGAATGACCACACATGGTACATCTTGTACTCCAGCATTGGGTCATTCTTTGCCCCGTGTGTCATTATGATCCTCGTTTACATCCGAATCTATCAGGTGGCTAAAACA[A/T]GAACCCGAAATATGTCTGAAAAGCGGCGGGATCCTGATGGTGGCTCAGGAACGCCACGCTTGGAGAACGGCTTAAGCCGTGAGGATTCTAGACGGGAAAATGGCCACTGTTCCTCATCGCCAGGCGAACGCAAACCAGCCGAGGATAACCCAGACGCTGACCTCGAGGACAGCAGCTCGTCCGACGAGAAGGCCAAGCGGTCACAAAATGAGACGGCCCCATCGAAAAAAGACCGCAGATCCAGCCGCAAGAACAGCTCCAGCTCCAAACACTCCAGCCGAAAGTCCCGAGCCAGCAGCAAATCCCTGGACTTGTTTTCATCTCGCAGAAAGAGGAGAAACACCATTTCCAGGAAAAAAATATCCCAGGCACGCGAGAAGCGGTTCACCTTTGTGCTGGCCGTGGTCATGGGCGTTTTTGTGGTCTGCTGGTTTCCCTTCTTCTTCAGCTACAGCCTGTATGGGATCTGCCGGGAGCCTTGCGCCATCCCTGACCCCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39655
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 |
|---|---|---|---|---|---|
| ENSDART00000101562 | Nonsense | 263 | 432 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 1 (position 41374402)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40290643 |
| GRCz11 | 1 | 40993430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCTTAAGCCGTGAGGATTCTAGACGGGAAAATGGCCACTGTTCCTCAT[C/A]GCCAGGCGAACGCAAACCAGCCGAGGATAACCCAGACGCTGACCTCGAGG
Long Flanking Sequence:
ATTAATGGGCTACTGGTTTTTTGGGGAAGTTTGGTGTAATATCTATCTCGCTCTAGATGTTCTTTTCTGCACGTCTTCTATTGTTCACCTGTGTGCCATAAGTCTGGACAGGTACTGGTCTGTGACACAGGCGGTCGAGTATAACTTAAAAAGGACGCCTCGCAGGGTTAAGGGGATGATTGTGGTGGTGTGGTTGATTTCGGCTGTGATCTCCTTCCCACCGCTCATCTCCATGGATCGGAATACAGTTGATGAGAGGAGACCAATGTGCCAGCTGAATGACCACACATGGTACATCTTGTACTCCAGCATTGGGTCATTCTTTGCCCCGTGTGTCATTATGATCCTCGTTTACATCCGAATCTATCAGGTGGCTAAAACAAGAACCCGAAATATGTCTGAAAAGCGGCGGGATCCTGATGGTGGCTCAGGAACGCCACGCTTGGAGAACGGCTTAAGCCGTGAGGATTCTAGACGGGAAAATGGCCACTGTTCCTCAT[C/A]GCCAGGCGAACGCAAACCAGCCGAGGATAACCCAGACGCTGACCTCGAGGACAGCAGCTCGTCCGACGAGAAGGCCAAGCGGTCACAAAATGAGACGGCCCCATCGAAAAAAGACCGCAGATCCAGCCGCAAGAACAGCTCCAGCTCCAAACACTCCAGCCGAAAGTCCCGAGCCAGCAGCAAATCCCTGGACTTGTTTTCATCTCGCAGAAAGAGGAGAAACACCATTTCCAGGAAAAAAATATCCCAGGCACGCGAGAAGCGGTTCACCTTTGTGCTGGCCGTGGTCATGGGCGTTTTTGTGGTCTGCTGGTTTCCCTTCTTCTTCAGCTACAGCCTGTATGGGATCTGCCGGGAGCCTTGCGCCATCCCTGACCCCCTTTTCAAGTTTTTCTTCTGGATCGGTTACTGCAACAGCTCCCTCAACCCCGTCATCTACACCATCTTCAACCAGGACTTCCGGCGAGCTTTTCAAAAGATCCTGTGCAAGTCCTGGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19542
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 |
|---|---|---|---|---|---|
| ENSDART00000101562 | Nonsense | 426 | 432 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 1 (position 41373914)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40290155 |
| GRCz11 | 1 | 40992942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCATCTTCAACCAGGACTTCCGGCGAGCTTTTCAAAAGATCCTGTGC[A/T]AGTCCTGGAAAAGGTCTTTCTAGAGGCACCAATTTGCAGCGTCCAGTGCA
Long Flanking Sequence:
ACTGTTCCTCATCGCCAGGCGAACGCAAACCAGCCGAGGATAACCCAGACGCTGACCTCGAGGACAGCAGCTCGTCCGACGAGAAGGCCAAGCGGTCACAAAATGAGACGGCCCCATCGAAAAAAGACCGCAGATCCAGCCGCAAGAACAGCTCCAGCTCCAAACACTCCAGCCGAAAGTCCCGAGCCAGCAGCAAATCCCTGGACTTGTTTTCATCTCGCAGAAAGAGGAGAAACACCATTTCCAGGAAAAAAATATCCCAGGCACGCGAGAAGCGGTTCACCTTTGTGCTGGCCGTGGTCATGGGCGTTTTTGTGGTCTGCTGGTTTCCCTTCTTCTTCAGCTACAGCCTGTATGGGATCTGCCGGGAGCCTTGCGCCATCCCTGACCCCCTTTTCAAGTTTTTCTTCTGGATCGGTTACTGCAACAGCTCCCTCAACCCCGTCATCTACACCATCTTCAACCAGGACTTCCGGCGAGCTTTTCAAAAGATCCTGTGC[A/T]AGTCCTGGAAAAGGTCTTTCTAGAGGCACCAATTTGCAGCGTCCAGTGCAATTTTTACAGGTGGTTGACAAGGAAGAGACGTTTCGTTTTCAACAATACCACTGCCTCTATCTTTGCATTGACAATCTGTACACAACAAAGACATTGATATTTTTTCCTACTTCGTTGTGTAATGCTCTTCATGAGTCTGCGAGGACAACAGATGTTGGTGGTACAAAAGATGCTAGGAGAAAAAAAAAACCCTCAGCACTGTACTGCATTAGAGGAAACAGGCTTATCTTTATTATGGCTGCAGGCACTCTGAAGATATCAAGAGATATTTTTATGATGAGTTAGCACATATGGCTTGTGTCATTGTGACTAGAGAGCTATGTAACATGAAAGGTTGTCTCCTTTTTATGGTGACCCCAAAAAAAAAAGAAGTGACTTCTCAGAAAGCATGCTGTTCCTTTCTAGCTGAGAGAGACAAAACGGACACTGCTGGATAGGGAGTATGAGAA
Associated Phenotype:
Not determined