ZMP
adrbk2
Ensembl ID:
ZFIN ID:
Description:
beta-adrenergic receptor kinase 2 [Source:RefSeq peptide;Acc:NP_001128197]
Human Orthologue:
ADRBK1
Human Description:
adrenergic, beta, receptor kinase 1 [Source:HGNC Symbol;Acc:289]
Mouse Orthologue:
Adrbk1
Mouse Description:
adrenergic receptor kinase, beta 1 Gene [Source:MGI Symbol;Acc:MGI:87940]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2558 | Nonsense | F2 line generated | Not yet available |
| sa5588 | Nonsense | F2 line generated | Not yet available |
| sa2560 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa2558
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000022369 | Nonsense | 462 | 688 | 16 | 21 |
| ENSDART00000134164 | Nonsense | 143 | 278 | 5 | 8 |
| ENSDART00000022369 | Nonsense | 462 | 688 | 16 | 21 |
| ENSDART00000134164 | Nonsense | 143 | 278 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 45894608)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44323835 |
| GRCz11 | 10 | 44170632 |
KASP Assay ID:
554-3099.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGTGAAGGAKCACGTGTTCTTCAAGGGAATCGATTGGCAGCAGGTTTA[T/A]CTCCAGAAGGTGAGACCTTTGCCCTTTTTCTTTTCTTTTATCGAGCCTAA
Long Flanking Sequence:
CTTGGTCAGACTTTATTTTGATGGTCTCTACTGCACGTTTTGTTGACTAAAAGCTGCATTGCTACATGCCAATGACTTCTCATTTGAGTATGAGTAGACTGTCTGCTTCATATCTGCTGATACCGCTCCTTCAACAGACATTTAACTGACCATAAGAACCTTTGCAAGTACATGTCAACTTACACTAACCCTAACCTGACAGTCTACTTATAATCTAATGAGAATGAGTTGCCATATAGATGCAATGTAACCCAAATTCAACTAAATGCATTAAAGGGACCATCAAAATAAAGTGAGAGCGATTACTTTTGTTATTTAAAAACCTGAAGTGTATTACCAGCCTTCTCTAATATTTAAAATACAACTGTATTGCATTACAATGTGGCTAATATATGTTATTGATAAACACTAGATTGATTTCCTGCTTTTAAATAATCCACTAGGGCGTCAGAGGTGAAGGAGCACGTGTTCTTCAAGGGAATCGATTGGCAGCAGGTTTA[T/A]CTCCAGAAGGTGAGACCTTTGCCCTTTTTCTTTTCTTTTATCGAGCCTAAAGGGGTAGTTCACCCAAAGTTCAAATGTACTCACTATTTACTCATCCTTAAAGTCTGAATATCGGTAACCATTGACTTCCATTGTAGGATAAACAAATACTACAGAAGTGAATGGCTACAGGTTTGTGGCATTTTTCAAAATGTCTTCTTTTGTGTGCAACAGAAGAATGAAATCTGTAAAGGTTTTAAACGTGAAGTGAGAGTGACAGATTTTTCATTTTTGGGTGAACTGTCTCTATATATAAATATAAGACGACGATAATAACACTAATGCTGATGTTGTTGAATAAAACACAAAAATCTGAATTTCTATAGGTTGTTTTCACGTGGTTCTGGTGATGTGTGAAATTCAGATGGAGGGCAGGAAGGAAAACTGAATGGGAAAGTCCATATTTTAGCGATTTAAACCATATTTCCAAGGAGATATAAATATAAAATATCCACATATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5588
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000022369 | Nonsense | 462 | 688 | 16 | 21 |
| ENSDART00000134164 | Nonsense | 143 | 278 | 5 | 8 |
| ENSDART00000022369 | Nonsense | 462 | 688 | 16 | 21 |
| ENSDART00000134164 | Nonsense | 143 | 278 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 45894608)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44323835 |
| GRCz11 | 10 | 44170632 |
KASP Assay ID:
554-3099.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGTGAAGGAKCACGTGTTCTTCAAGGGAATCGATTGGCAGCAGGTTTA[T/A]CTCCAGAAGGTGAGACCTTTGCCCTTTTTCTTTTCTTTTATCGAGCCTAA
Long Flanking Sequence:
CTTGGTCAGACTTTATTTTGATGGTCTCTACTGCACGTTTTGTTGACTAAAAGCTGCATTGCTACATGCCAATGACTTCTCATTTGAGTATGAGTAGACTGTCTGCTTCATATCTGCTGATACCGCTCCTTCAACAGACATTTAACTGACCATAAGAACCTTTGCAAGTACATGTCAACTTACACTAACCCTAACCTGACAGTCTACTTATAATCTAATGAGAATGAGTTGCCATATAGATGCAATGTAACCCAAATTCAACTAAATGCATTAAAGGGACCATCAAAATAAAGTGAGAGCGATTACTTTTGTTATTTAAAAACCTGAAGTGTATTACCAGCCTTCTCTAATATTTAAAATACAACTGTATTGCATTACAATGTGGCTAATATATGTTATTGATAAACACTAGATTGATTTCCTGCTTTTAAATAATCCACTAGGGCGTCAGAGGTGAAGGAGCACGTGTTCTTCAAGGGAATCGATTGGCAGCAGGTTTA[T/A]CTCCAGAAGGTGAGACCTTTGCCCTTTTTCTTTTCTTTTATCGAGCCTAAAGGGGTAGTTCACCCAAAGTTCAAATGTACTCACTATTTACTCATCCTTAAAGTCTGAATATCGGTAACCATTGACTTCCATTGTAGGATAAACAAATACTACAGAAGTGAATGGCTACAGGTTTGTGGCATTTTTCAAAATGTCTTCTTTTGTGTGCAACAGAAGAATGAAATCTGTAAAGGTTTTAAACGTGAAGTGAGAGTGACAGATTTTTCATTTTTGGGTGAACTGTCTCTATATATAAATATAAGACGACGATAATAACACTAATGCTGATGTTGTTGAATAAAACACAAAAATCTGAATTTCTATAGGTTGTTTTCACGTGGTTCTGGTGATGTGTGAAATTCAGATGGAGGGCAGGAAGGAAAACTGAATGGGAAAGTCCATATTTTAGCGATTTAAACCATATTTCCAAGGAGATATAAATATAAAATATCCACATATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2560
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000022369 | Nonsense | 582 | 688 | 19 | 21 |
| ENSDART00000134164 | Nonsense | 263 | 278 | 8 | 8 |
| ENSDART00000022369 | Nonsense | 582 | 688 | 19 | 21 |
| ENSDART00000134164 | Nonsense | 263 | 278 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 45913280)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44342507 |
| GRCz11 | 10 | 44189304 |
KASP Assay ID:
554-3153.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAAGCTAGGAAACCCCTTCCTGACGCAGTGGCAGCGGCGCTATTTCTA[T/A]CTGTTCCCCAACCGTGTRGAGTGGAGAGGTGAAGGAGAGTCTCGGGTAAG
Long Flanking Sequence:
ATGATTAGATCATTGGTTCCGACGCATTTGTATCTTGAACAGTTCGATAATAAAATGAAATGTCCGTGTCTTTGAGAATAAAGTTAGATGTCCCAATCTATTTATTGTCCATTTAGTCAAAAGTAAACATCCAAATAAACATGAACTCATTCTCAAGTCCATCATAGTCAAAAGGTTTGTTTGACCTTCTTTTACGCCCCGCAGGTCATCAATAGGAGAGCATAAATACATTAAAATACATTATACACCCTCTAGTGGTGTGAAAGAAAATTACACAAAAAATGGCTCCTACAGTAATAATTAAAAATAGATGTAAATTAATTCAGCTTTTTTTTTCAATTTGGATATAATACTCAGCATTCAACTGTCAAGCATATGATCATTCTCCTTGTGTGTGACTTTTGTGCAGATTACGCGCTGGGGAAGGACTGCATCATGCACGGCTACATGCTAAAGCTAGGAAACCCCTTCCTGACGCAGTGGCAGCGGCGCTATTTCTA[T/A]CTGTTCCCCAACCGTGTGGAGTGGAGAGGTGAAGGAGAGTCTCGGGTAAGAGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTTTTTTGTGACATATCAGGACACAAATCTGTATAATGGCATGGGTATGACACAGGTATTACAAAAAGGAGGTGAAATATGAGGACATCGGTGACGTCCTCATTTCTCAAAATGCTTATAAATCCTACAGGATGAGTTTAATCAGAGAGTAAAGCTGCACACAGTCTCCTGTGATGGTTGGGTTTAGGGGTGGGGTGAGGGTGAGGGCAATACAATATACGGTTTGGACAGTATAAAATGAATGGAAACCTATGTAATGTCCCCACTTTTCACAAAAACAAATGTGTCTGTGTGGTGTGTGTGTGTTGTCACTGCTGTTTATATCAATATAATTGGTTAACCGACAGATTTCTGAGATTGAATGTTGCCTGTTTGTCCATACGCTGTAGGAATGTTGGACTAAAACGT
Associated Phenotype:
Not determined