ZMP
si:dkey-169l5.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate gamma-aminobutyric acid (GABA) A receptor, beta 3 (GABRB3) [Sour
Human Orthologue:
GABRQ
Human Description:
gamma-aminobutyric acid (GABA) receptor, theta [Source:HGNC Symbol;Acc:14454]
Mouse Orthologue:
Gabrq
Mouse Description:
gamma-aminobutyric acid (GABA) A receptor, subunit theta Gene [Source:MGI Symbol;Acc:MGI:1888498]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31063 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43691 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39341 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31063
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 |
|---|---|---|---|---|---|
| ENSDART00000064718 | Nonsense | 129 | 512 | 4 | 10 |
| ENSDART00000145280 | None | None | 203 | None | 2 |
| ENSDART00000064718 | Nonsense | 129 | 512 | 4 | 10 |
| ENSDART00000145280 | None | None | 203 | None | 2 |
Genomic Location (Zv9):
Chromosome 21 (position 35255987)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 36427294 |
| GRCz11 | 21 | 37822669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGGCGGATCAGTTGTGGCTCCCGGATACTTATTTCCTGAACGACAAG[A/T]AGAGTTTCTTGCACGGAGTGACGGTGAAAAACCGGATGATCCGCCTCCAT
Long Flanking Sequence:
ATTGTGTGCAACAGTTCTGCATGCAACACTTTTTTCAGTGTCTGAGGTATTGGGCGGGGCTAACATACTTAACCACGCCCCCTCCAGCTGTCAGTTTTGGCAACAAACAGAAATAGTGTGGAAGAGGAGTCTGTTAGGTTGTAATATCTCCTCCCAAACCCTTTTCCCTATCTTTGTGAATAAAAACGCCTATTTTACATCATCCAATCAGCTCGCAGTAGAAGAAAACAAGCCACGCCTACTGTTTTGTCATTTAATATTCCATTTCTCTAAGAAATGCGTCAAACTATGAAAAAAAAATGGTTGCAGCTTCCAGTTGATGCAGATTTTAATTCTCATGCTGTCTGTTGATTTTGCAGGACTACACCATCACCATGTATTTCCAACAGAGCTGGAGGGACAAGCGCTTGGCCTACGCCGAGATGGCGTTGAACCTGACTTTGGACAACCGTGTGGCGGATCAGTTGTGGCTCCCGGATACTTATTTCCTGAACGACAAG[A/T]AGAGTTTCTTGCACGGAGTGACGGTGAAAAACCGGATGATCCGCCTCCATCCGGACGGCACAGTTCTGTACGGACTGAGGTAAATGCCATCATTAATGCTGTGCTGGATAATGTACAGGGGTGTATTCCAGAAATCAACTGACTTACACCTTACTACATACAACCTTAACCATCTGCAATGTCGATGTGCAGAATATCTATTTTAGAAATGCTTTCTATTTCTGTGATGTCACAGCAGAACAACAGCATAAACTACTATGGCAATGATCACCTCAGGTACTGATTATGTGCGTTATTCAGTGTTAAGTGCTCCCAGTGTGAGTTTAAATAGCACTGTATGCAGTGTGCGAATTATACATGGACGATTGGGGGGTCAACTTAGTTACTTAGTTTGTGTAATACATGCTTCAGTGAATGTATTTATTTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43691
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 |
|---|---|---|---|---|---|
| ENSDART00000064718 | Nonsense | 129 | 512 | 4 | 10 |
| ENSDART00000145280 | None | None | 203 | None | 2 |
| ENSDART00000064718 | Nonsense | 129 | 512 | 4 | 10 |
| ENSDART00000145280 | None | None | 203 | None | 2 |
Genomic Location (Zv9):
Chromosome 21 (position 35255987)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 36427294 |
| GRCz11 | 21 | 37822669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGGCGGATCAGTTGTGGCTCCCGGATACTTATTTCCTGAACGACAAG[A/T]AGAGTTTCTTGCACGGAGTGACGGTGAAAAACCGGATGATCCGCCTCCAT
Long Flanking Sequence:
ATTGTGTGCAACAGTTCTGCATGCAACACTTTTTTCAGTGTCTGAGGTATTGGGCGGGGCTAACATACTTAACCACGCCCCCTCCAGCTGTCAGTTTTGGCAACAAACAGAAATAGTGTGGAAGAGGAGTCTGTTAGGTTGTAATATCTCCTCCCAAACCCTTTTCCCTATCTTTGTGAATAAAAACGCCTATTTTACATCATCCAATCAGCTCGCAGTAGAAGAAAACAAGCCACGCCTACTGTTTTGTCATTTAATATTCCATTTCTCTAAGAAATGCGTCAAACTATGAAAAAAAAATGGTTGCAGCTTCCAGTTGATGCAGATTTTAATTCTCATGCTGTCTGTTGATTTTGCAGGACTACACCATCACCATGTATTTCCAACAGAGCTGGAGGGACAAGCGCTTGGCCTACGCCGAGATGGCGTTGAACCTGACTTTGGACAACCGTGTGGCGGATCAGTTGTGGCTCCCGGATACTTATTTCCTGAACGACAAG[A/T]AGAGTTTCTTGCACGGAGTGACGGTGAAAAACCGGATGATCCGCCTCCATCCGGACGGCACAGTTCTGTACGGACTGAGGTAAATGCCATCATTAATGCTGTGCTGGATAATGTACAGGGGTGTATTCCAGAAATCAACTGACTTACACCTTACTACATACAACCTTAACCATCTGCAATGTCGATGTGCAGAATATCTATTTTAGAAATGCTTTCTATTTCTGTGATGTCACAGCAGAACAACAGCATAAACTACTATGGCAATGATCACCTCAGGTACTGATTATGTGCGTTATTCAGTGTTAAGTGCTCCCAGTGTGAGTTTAAATAGCACTGTATGCAGTGTGCGAATTATACATGGACGATTGGGGGGTCAACTTAGTTACTTAGTTTGTGTAATACATGCTTCAGTGAATGTATTTATTTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39341
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 |
|---|---|---|---|---|---|
| ENSDART00000064718 | Nonsense | 250 | 512 | 7 | 10 |
| ENSDART00000145280 | None | None | 203 | None | 2 |
Genomic Location (Zv9):
Chromosome 21 (position 35281961)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 36401320 |
| GRCz11 | 21 | 37795675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGTCGTTGAGTTTCCGCATCAAGAGAAACATCGGCTACTTTATCCTG[C/T]AGACTTACATGCCCTCCATCCTGATCACAATCTTGTCCTGGGTCTCCTTC
Long Flanking Sequence:
CTTACAGTTTTATTAATTTGCACACCAGATTTTACACATTAACTGAACTTATTTTTCAGTTACATATTTTTTTTTCGTCTTAAATACCCTGTATCTAGAGTCTAAATGGGGAAAAAAAAGACACTGCGGGCTTTTGTGACAATTCTCAGAGGGATGTAGACGCTGCCTGCTGAGAAGGGGCTTTCAGAAAAATCTGCCATGTTTGCGACTTTCTGCCATGTTTAATTGGAATGGAACTAGTCCCTGGGAAGGAATCCATTGCTTTGGGGAAATTAAACGCTCCGTCTGAACAAATGGGAAAATGACTATCTGTTGTCAAAGTGCAGACTATGACAATTGCAAATTGTAGATCTATTTTTCCTGCGCTTGCTCTTTTGTGTTTTCACTTGCATGTTGACATCTCTCTCTCTCTCTCTTTGGCTACTTGTGTCTCCCCAGGTTCATACCCTCGGCTGTCGTTGAGTTTCCGCATCAAGAGAAACATCGGCTACTTTATCCTG[C/T]AGACTTACATGCCCTCCATCCTGATCACAATCTTGTCCTGGGTCTCCTTCTGGATTAACTACGATGCCTCTGCGGCTCGGGTGGCCCTGGGTAACCTTTAGTGTTTTGTTCAAAAATCATACCATCTTTTTTTTACAGGAAGCAAATCCCACTGTGATTTCGAGCACTTGCGTGTGTGTGTCTGTGTGTGCGTGCAGAATACACACTGAATATCTTTTGCTCCAAATACTCTTCTTGTCAACCATGATTAAAGAACTGCCCTTTTTCATGACCATTGATGTGTCTCTTAAACAGTTATATACAGTTGAAGTCAGAATTATTAGCCCCCCTGAATTATTAGCCCCCCTTTAGTTTTTCCACAATTTCTGATTACAGTAATTTCTAAGTACATATTAGTTAAGGCCACTTAATATAAAGTGGGAACGAATAAGTGTATTTTATTTTTTTATATTAAGCTCTTGAAAGCAGCAGGACTGTGGGTGCACAATGTTATCGTCACT
Associated Phenotype:
Not determined