ZMP
zgc:171544
Ensembl ID:
ZFIN ID:
Description:
gamma-aminobutyric acid (GABA) A receptor, pi [Source:RefSeq peptide;Acc:NP_001108214]
Human Orthologue:
GABRP
Human Description:
gamma-aminobutyric acid (GABA) A receptor, pi [Source:HGNC Symbol;Acc:4089]
Mouse Orthologue:
Gabrp
Mouse Description:
gamma-aminobutyric acid (GABA) A receptor, pi Gene [Source:MGI Symbol;Acc:MGI:2387597]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42053 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30961 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10337 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42053
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076317 | None | None | 446 | None | 12 |
| ENSDART00000076322 | Essential Splice Site | None | 447 | 1 | 11 |
| ENSDART00000076317 | None | None | 446 | None | 12 |
| ENSDART00000076322 | Essential Splice Site | None | 447 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 30603494)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 28940431 |
| GRCz11 | 12 | 29055333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGATTCTATAAGCGTTTGGGAAATGCAAACGATTGTCCGGCTATAAAT[G/A]TAAGTACGCAGTGTGTCATGTGTGAGGCGATGGACATTCATTAATGTGAA
Long Flanking Sequence:
AAGTGGGCGAGCATGTGAAACTGCATTTTCATGCCTCCAAGGAAATAACCTCATGACCAAAGTGACAACGTAAAGAGATGACAGACGTGGTGGCATGAATAGCCTGTAAAGATTTGATGTGTGCGTGTGGCTATGTGTTAATTACATGCCATTGCGATTCAATGTTTCTTTTCTAAATATGCGAGATGTCACTTTCCGATCCTGCTCCCCCCAATCAGCACTAAATCATCAGTCTATCGCGGATAGGTTGGTTGTTCTGCTGTGAGCGCAGCGCGGAATGTGTCTGGGATGCAACCAGTAGTTTAGACTGACTGACTGACTGCTGTGAAGAAGTAGTTGCGCATCACTGACGGATTCCAGCGCCGCGGAAACCGCCGAAAGTCACGTCTTTCTTCTCACTGAGCTAAATGGCTCGGATTTACGACAGATACGACTTATGCAGATGAGTGATTCGATTCTATAAGCGTTTGGGAAATGCAAACGATTGTCCGGCTATAAAT[G/A]TAAGTACGCAGTGTGTCATGTGTGAGGCGATGGACATTCATTAATGTGAATGAAGTGTTTGAAAAAGTCGGGAGTGCACGTTTTATGTTTTTATTTTCGCTTACTCTTAATCATGCTTGTTTTTACCATTTGATTTGGAAAAATGATTCATTTTGTTGAATACAGCTTCTTTTATATGAAACAGTTTGTGTTGATATGCGTTTATGATTAGTTTCACTATATAGTATGCTGGGTTTGCTTTTATAATGAAGTTCAGGTGTGACAGGTCTTTAAACTTAACCCTTAAGGTTTTTAACCATTCATGGGGGGAAATTATTCAATTAGTTTAAAACTGCTTCTTTTATACTAAACAGTTTGTGTTAATGTGGGTTTTATGAATATTTTCACTGATATATGCTGGGTTTGCTTTTATAACGAAGTTCAGGTGTGACAGGTCGTCAAATTTAACTCGTTCATAGGTCCTTGTTCATGTTTTTTAGTGTAAATGCTGGCATAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30961
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076317 | None | None | 446 | None | 12 |
| ENSDART00000076322 | Essential Splice Site | None | 447 | 1 | 11 |
| ENSDART00000076317 | None | None | 446 | None | 12 |
| ENSDART00000076322 | Essential Splice Site | None | 447 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 30603494)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 28940431 |
| GRCz11 | 12 | 29055333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGATTCTATAAGCGTTTGGGAAATGCAAACGATTGTCCGGCTATAAAT[G/A]TAAGTACGCAGTGTGTCATGTGTGAGGCGATGGACATTCATTAATGTGAA
Long Flanking Sequence:
AAGTGGGCGAGCATGTGAAACTGCATTTTCATGCCTCCAAGGAAATAACCTCATGACCAAAGTGACAACGTAAAGAGATGACAGACGTGGTGGCATGAATAGCCTGTAAAGATTTGATGTGTGCGTGTGGCTATGTGTTAATTACATGCCATTGCGATTCAATGTTTCTTTTCTAAATATGCGAGATGTCACTTTCCGATCCTGCTCCCCCCAATCAGCACTAAATCATCAGTCTATCGCGGATAGGTTGGTTGTTCTGCTGTGAGCGCAGCGCGGAATGTGTCTGGGATGCAACCAGTAGTTTAGACTGACTGACTGACTGCTGTGAAGAAGTAGTTGCGCATCACTGACGGATTCCAGCGCCGCGGAAACCGCCGAAAGTCACGTCTTTCTTCTCACTGAGCTAAATGGCTCGGATTTACGACAGATACGACTTATGCAGATGAGTGATTCGATTCTATAAGCGTTTGGGAAATGCAAACGATTGTCCGGCTATAAAT[G/A]TAAGTACGCAGTGTGTCATGTGTGAGGCGATGGACATTCATTAATGTGAATGAAGTGTTTGAAAAAGTCGGGAGTGCACGTTTTATGTTTTTATTTTCGCTTACTCTTAATCATGCTTGTTTTTACCATTTGATTTGGAAAAATGATTCATTTTGTTGAATACAGCTTCTTTTATATGAAACAGTTTGTGTTGATATGCGTTTATGATTAGTTTCACTATATAGTATGCTGGGTTTGCTTTTATAATGAAGTTCAGGTGTGACAGGTCTTTAAACTTAACCCTTAAGGTTTTTAACCATTCATGGGGGGAAATTATTCAATTAGTTTAAAACTGCTTCTTTTATACTAAACAGTTTGTGTTAATGTGGGTTTTATGAATATTTTCACTGATATATGCTGGGTTTGCTTTTATAACGAAGTTCAGGTGTGACAGGTCGTCAAATTTAACTCGTTCATAGGTCCTTGTTCATGTTTTTTAGTGTAAATGCTGGCATAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10337
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076317 | Essential Splice Site | 174 | 446 | 7 | 12 |
| ENSDART00000076322 | Essential Splice Site | 175 | 447 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 30644058)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 28980995 |
| GRCz11 | 12 | 29095897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTATTCTGTGGTGATAATTGGCTCTTGGATTTATATTATGTTCTCCAC[A/T]GGGGGATATAACGTGAAAGATGTTGTTTTCTATTGGACACGGGGAAACCA
Long Flanking Sequence:
CCTTGTAGAAAATCTCCAGTATAATAATGATCAATGACATGTAAAAAAATCAATTAGTTTTTTTCCCCATAAGTTATTCTATGCTTGCGATTGTTAAAGTATATTCACTAACCCCTCATTCAGTAACCTAATTAAAGGCTCAGCACAAAGTGTGTGCTTCCAGCAAATGTAATTCTTGCATGTTTAACTGCTTCAGGACTTCTTTTTAATATAGATTGCTAACAAGCATGTTATTTCACATGCTTGGCCGATTGTACAATTGTTTTTAAATTCCACAGGGATCCCATGGTAAATCAGCATTACCCTAAAAAAACACTGAATAGCTCCATTTAGAATTATTGATATTATGCTAATGCCTGCTTTACAGTATAGAGCTCTAGCAGCATATAAGATTAGTGGTAACCGAATGCGTAATTCAGCGGAAATATAGTAGCTCTCAGCACTGAAATGACTTATTCTGTGGTGATAATTGGCTCTTGGATTTATATTATGTTCTCCAC[A/T]GGGGGATATAACGTGAAAGATGTTGTTTTCTATTGGACACGGGGAAACCAATCGGTTAGCGGCCTGGATCATTTACAGCTGGCACAGTACACCCTTGAGGATCATTACACCTCTGAATCTGAAGCTGTTTATGAGACTGGTATGTTCACAAACACACACACAATGATATTTTGGGGACATTCTCAGTGTGTATACTTATAAATTTAATCCTAATGTAACAGGTAACTACCCGAAGTTGATCTTCCACTTCAAACTCAAGCGAAGCATCCTGTATTTTATTCTGGAGACGTACGTTCCCTCCAGTGCTCTGGTGGTCTTGTCCTGGGTCTCCTTCTGGATCAGTCAGTCCTCAGTACCTGCTCGCATCTGCATAGGTAGGAACGCAATGCAATCATTAGCACATTCAAATAGGACTATTTATTTCAAATATGTGCTTTAGTATTCGGAAGCTTGGCCTAATGGATGACACAAAAGCCAATAAAAGCGTATTACATTAGTGT
Associated Phenotype:
Not determined