Busch Lab

ZMP

adra2b

Ensembl ID:
ENSDARG00000019819
ZFIN ID:
ZDB-GENE-021010-2
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.
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.
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