ZMP
adra2b
Ensembl ID:
ZFIN ID:
Description:
Alpha-2B adrenergic receptor [Source:UniProtKB/Swiss-Prot;Acc:Q90WY5]
Human Orthologue:
ADRA2B
Human Description:
adrenergic, alpha-2B-, receptor [Source:HGNC Symbol;Acc:282]
Mouse Orthologue:
Adra2b
Mouse Description:
adrenergic receptor, alpha 2b Gene [Source:MGI Symbol;Acc:MGI:87935]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7617 | Missense | Mutation detected in F1 DNA | Not yet available |
sa34462 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7617
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018663 | Missense | 121 | 509 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 8 (position 42260215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 40605667 |
GRCz11 | 8 | 40645232 |
KASP Assay ID:
554-4020.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCTACTGGTATTTCCGCTCTGTATGGTGTGAGATCTACCTGGCGCTGG[A/T]TGTGTTGTTCTGCACTTCCTCCATAGTACATCTGTGYGCCATCAGTCTAG
Long Flanking Sequence:
GTAATATTTAATAAAATATTGAACACTTAGTTTTTAGAACATAAAATAAACACCAAAACCATATTATTTAACTTATTCTACCCACATACGGATTGCCATAGAGAAGAACTGCCCACGTGCACTTTCTGCATTTGCAGTCATGGATAGCCCGTGCCCTGTTGCCGTGGGTCTGCCTGGCCACACTAATGGCACTGGAGGCACGTCTTCACCGACTTGTAACCAGAGCATGATAAAACTCGCCCCGTACTCTCCTGAAGCCACAGCAGCCTTTGCAACAGCCATCACATTGATGATGCTTATTACAATAGTAGGCAATATCCTGGTCATCATTGCTGTTTTAACAAGTCGCTCATTAAGAGGACCCCAAAATCTTTTTTTGGTCTCCCTTGCTGCTGCAGACATTTTGGTGGCCACCCTCATCATCCCCTTTTCCCTAGCCAATGAACTGATGGGCTACTGGTATTTCCGCTCTGTATGGTGTGAGATCTACCTGGCGCTGG[A/T]TGTGTTGTTCTGCACTTCCTCCATAGTACATCTGTGCGCCATCAGTCTAGACCGCTACATGTCTATCTCACGTGCTGTCACGTACGGTCCCAAGCGGACACCGAAACGAATCAAGTGTGCCATTTTGGTGGTGTGGTTGATCTCAGCGGTAATCTCATTTCCGCCACTACTATCTATGAACAAGAATAAAGGTGGTGGCGAGTCAGGTGCGCTGCCTCAGTGTCAGCTCAACGATGAGCGCTGGTACATCCTGTACTCTACTATTGGTTCCTTCTTTGCTCCTTGTCTAATAATGATCTTAGTCTACATGCGGATCTATCAGATCGCCAAGCAGCGCACACGGTGTCCACCAGGGGAGCCCCGCAAAGAAGCCCCAGCTAATGCTACGACTCCTCAGCACAAGATCCAAAATGGAAGAGGAGATGAAACGCCAGGCACCCTTCAGAAAAAAGCCAGGCCTCCAACTTTGGCTGTGTCCCAAGTGGAGTCTGTCCAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34462
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 |
---|---|---|---|---|---|
ENSDART00000018663 | Nonsense | 409 | 509 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 8 (position 42259352)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 40606530 |
GRCz11 | 8 | 40646095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGATCGCCACCGCTAAAGGTGCCAAGCTGGTGGCCCGAAAGGCCAAG[C/T]AAGATGGAACGCCCAACTCTGCACGCCGCAAAGCGATGGTGAACCGAGAG
Long Flanking Sequence:
GCAAAGAAGCCCCAGCTAATGCTACGACTCCTCAGCACAAGATCCAAAATGGAAGAGGAGATGAAACGCCAGGCACCCTTCAGAAAAAAGCCAGGCCTCCAACTTTGGCTGTGTCCCAAGTGGAGTCTGTCCAGCAGGCAGCAAACACCCCGATCGCCAACAACCTTCTGCAAGCCCCTTCAACAACCTTGACACCAACCACCCCATGCCCCTCGCCATCTCCTTCGAATTCATCTGAAGTGGCTCCCAGTAAAAGTAAAGAGGGGAAAAAGGAGAAGAAGAAGAAGAACAACAAAAACAAGAACAAGAAAGAGCCTGACAACAATAATGGAGAAAGCATGAGCTCTGATTCGGACACTGAGCAAGGTGGGAGGGGGTTAGAGGTCCCTTGCACCCCGACTATGACCCCCAGTGGCATTCATTCTCCTGCCACTATGCAGAAATACAGAGACATGATCGCCACCGCTAAAGGTGCCAAGCTGGTGGCCCGAAAGGCCAAG[C/T]AAGATGGAACGCCCAACTCTGCACGCCGCAAAGCGATGGTGAACCGAGAGAAACGATTCACCTTTGTGTTGGCGGTAGTGATTGGTGTCTTTGTCATTTGCTGGTTTCCCTTCTTCTTCTCATACAGCCTACAGGCTGTGTGCCCAGAGTCGTGCGCCCTGCCAGAGCCACTCTTCAAGTTCTTCTTCTGGATCGGCTACTGCAACAGCTGCCTCAACCCGGTCATCTACACCATCTTCAACAAAGACTTCCGCAGAGCCTTCAAAAAGATCCTCTGCAAGAACACCAAAGGCACATTCTTCTGAAGCTCCTGAGGTGCATCGTCTCCTCAGATTTAAAACAAAAAAAAACACTTACATCTATTCAGAACACGAGTGTCAGAAAGAACACTAAAATAAGCACAATAATGGCGTTGTTGTGATGTAAATGAAGGGCTTTTTGTGCTGCCGGGTGAACCGAGGAGACCACGCGACTCAAATGACTCTATTCTGTCCAGGTTA
Associated Phenotype:
Not determined