ZMP
glra4b
Ensembl ID:
ZFIN ID:
Description:
Glycine receptor, alpha 4b [Source:UniProtKB/TrEMBL;Acc:A2BGE6]
Human Orthologue:
GLRA4
Human Description:
glycine receptor, alpha 4 [Source:HGNC Symbol;Acc:31715]
Mouse Orthologue:
Glra4
Mouse Description:
glycine receptor, alpha 4 subunit Gene [Source:MGI Symbol;Acc:MGI:95750]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30615 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40407 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40406 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13378 | Essential Splice Site | Available for shipment | Available now |
sa13466 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30615
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006474 | Essential Splice Site | 69 | 537 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 24327273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22040145 |
GRCz11 | 5 | 22543945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTACTGGAGCTCTTACTGGTTTGCTGGATGTTTGAAGGGGTCATCAGG[T/G]GAGTTTTCATCAAGTCTCTGTGTTTTTGTTGGTTAAAACACTATGCGTTA
Long Flanking Sequence:
GTACGCAGATATCAGGAGAGACGGATGGATGGCTGTTTGTCCTCTGCTAGAGTGCGTCTTGGGATGTGGATCTGGAGCCCCTCAGGTTAAGTTGTGTCACAGTTGTTTATTCTGATAAAAGTCTTTAAATGCATCTTACGCTTTGTTGCCTTCTCTCTTCTCCATGATAGAACTGCACCTCAGGCTAGCATGTGGCCAGAAAGAGAAAGAAAGAGCAGAAGACCCCCTCTACACACACACACACACACACACGCGCGCACACACACATAGTCGTCTCTCAGCCCGTCTCGGGATGCTGTGCTCAGTCAGATGGCAGTGGAGGAGAGACCAGAGTGCATCAGAATGGGCGTCCTGCCCCTCAAAAACACATCTGCTCATTGAGATTTAGCCACGGGACACCAGAAAAGCAGCTGCTGAACAGTGAAAGGATGTTTTCTGTGATCTGGAGGATCCTACTGGAGCTCTTACTGGTTTGCTGGATGTTTGAAGGGGTCATCAGG[T/G]GAGTTTTCATCAAGTCTCTGTGTTTTTGTTGGTTAAAACACTATGCGTTAAGCGTGAAAACACTTGTGGAGAGAGTGTCTTGAAATGAAGTGTCTTCCAAATTCAGTAGATCTACCTGTTTCTCCTCAATATTTGAGTTTTCGTATTTGTTTATGTGTCCAGTCATGCGTTTTCGGCTTGTGCGTTCAGTTCAGTAGACTTCATGGGTGATAGGTTTATTTTAATCCCGGAGAGCGTTCTTATGTTTCTGAGTGTGTGTTTGTGTGTGTGTTTGTTGGCTTTATGTATCTGGGTCTCTGAAGTATGAGGCTGACACGTAGAGACAGCTCTGTCTGAAGTCATTGTCACTGTTACTGAAATTGCAGATTTATTGAAGTTCACATAATGAGATTTAACTATTATTGGCCTGTTTGGGACTTGACGTTGCTTCATACTGACATAAAAGGATTGTGAGACTCACCTGAGGATGCGTTTGCTGTGTGCTATATTTCCATTTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40407
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006474 | Essential Splice Site | 209 | 537 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 24316874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22029746 |
GRCz11 | 5 | 22533546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGCTGCTGAGAATTTTCCAGAACGGAAACGTGCTGTATAGCATCAGG[T/C]GCAGTGTCAGCCCCTACAGTATATGTTACATAAATCCTTTCAAACTATTA
Long Flanking Sequence:
AATTACAATTTGTATCTAGTTATAAATTAGTTACTATAATGTTACTAATAATTAAAAGTAACATAGACTGTGGAGTAATTATACACACACTGGGCAGTTTATTAGCTTCAACTGTTAGTTAATGCAAGTATCTCAGCCAATCACATTACAGCAATGCGTTTAGGATGCGTTTAAGATGATCTACTAAAGTTCAAACCGAGCATCAGAATGCAATGTATTATTGACTTTGCTGCTGTGAACGTCATCTAATTCATTTCTGAACATAACTTCATTAGGATTACCGGCTGAACGTTTTTCTACGGCAGCAGTGGAATGACCCACGACTAGCTTATAAAGAATACCCAGACGATTCCCTGGATCTGGACCCATCCATGCTGGACTCCATCTGGAAGCCAGACTTGTTCTTCGCCAATGAGAAAGGCGCCAACTTTCATGAGGTCACCACAGACAACAAGCTGCTGAGAATTTTCCAGAACGGAAACGTGCTGTATAGCATCAGG[T/C]GCAGTGTCAGCCCCTACAGTATATGTTACATAAATCCTTTCAAACTATTACATGAACGATACTCAGAAATGTCTCTTCTTTAGACTCACGCTGATTCTGTCGTGTCCTATGGATCTGAAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGTTAGAGAGCTGTAAGACTCAACATCAACAACTCATTTAAATATCATTTCTTCTTTGTATGCTTATTATTCTCCCTGTTGTTCTTTTCTTCTAGTTGGCTACACTATGAATGATCTGATATTTCAGTGGTTGGACGAAGGCCCGGTGCAAGTAGCTGATGACCTTATGCTGCCCCAGTTTGTCCTCAAAGAAGAGAAAGACTTGGGATACTGTACAAAGCACTACAACACTGGTAGAGCACTGAACACCACAGTACTAATGCTTCAGTACAACACTATTTGGGTTCTTGCGATTTCTGTTTTAAGGGGTTGTCTGGGGGTTACTCTGTATTTGCTAACATGATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40406
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006474 | Nonsense | 234 | 537 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 24316716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22029588 |
GRCz11 | 5 | 22533388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGGATCTGAAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGT[T/A]AGAGAGCTGTAAGACTCAACATCAACAACTCATTTAAATATCATTTCTTC
Long Flanking Sequence:
TTTAGGATGCGTTTAAGATGATCTACTAAAGTTCAAACCGAGCATCAGAATGCAATGTATTATTGACTTTGCTGCTGTGAACGTCATCTAATTCATTTCTGAACATAACTTCATTAGGATTACCGGCTGAACGTTTTTCTACGGCAGCAGTGGAATGACCCACGACTAGCTTATAAAGAATACCCAGACGATTCCCTGGATCTGGACCCATCCATGCTGGACTCCATCTGGAAGCCAGACTTGTTCTTCGCCAATGAGAAAGGCGCCAACTTTCATGAGGTCACCACAGACAACAAGCTGCTGAGAATTTTCCAGAACGGAAACGTGCTGTATAGCATCAGGTGCAGTGTCAGCCCCTACAGTATATGTTACATAAATCCTTTCAAACTATTACATGAACGATACTCAGAAATGTCTCTTCTTTAGACTCACGCTGATTCTGTCGTGTCCTATGGATCTGAAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGT[T/A]AGAGAGCTGTAAGACTCAACATCAACAACTCATTTAAATATCATTTCTTCTTTGTATGCTTATTATTCTCCCTGTTGTTCTTTTCTTCTAGTTGGCTACACTATGAATGATCTGATATTTCAGTGGTTGGACGAAGGCCCGGTGCAAGTAGCTGATGACCTTATGCTGCCCCAGTTTGTCCTCAAAGAAGAGAAAGACTTGGGATACTGTACAAAGCACTACAACACTGGTAGAGCACTGAACACCACAGTACTAATGCTTCAGTACAACACTATTTGGGTTCTTGCGATTTCTGTTTTAAGGGGTTGTCTGGGGGTTACTCTGTATTTGCTAACATGATCATAGTAATGGTACTGGTAACTATTGGTAAGTTGAATAAATTATTATTATTTCTGAAAAGATGGTAATTTATAAATTTATGCATGGTCATTATTTTTTACTTCAGATTGAACAGGATTATCCAAACTCAGTCCTGCATATTTTAGTTCCAACCCCAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13378
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006474 | Essential Splice Site | 237 | 537 | 5 | 10 |
ENSDART00000006474 | Essential Splice Site | 237 | 537 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 24316706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22029578 |
GRCz11 | 5 | 22533378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGTTAGAGAGCTG[T/A]AAGACTCAACATCAACAACTCATTTAAATATCATTTCTTCTTTGTATGCT
Long Flanking Sequence:
GTTTAAGATGATCTACTAAAGTTCAAACCGAGCATCAGAATGCAATGTATTATTGACTTTGCTGCTGTGAACGTCATCTAATTCATTTCTGAACATAACTTCATTAGGATTACCGGCTGAACGTTTTTCTACGGCAGCAGTGGAATGACCCACGACTAGCTTATAAAGAATACCCAGACGATTCCCTGGATCTGGACCCATCCATGCTGGACTCCATCTGGAAGCCAGACTTGTTCTTCGCCAATGAGAAAGGCGCCAACTTTCATGAGGTCACCACAGACAACAAGCTGCTGAGAATTTTCCAGAACGGAAACGTGCTGTATAGCATCAGGTGCAGTGTCAGCCCCTACAGTATATGTTACATAAATCCTTTCAAACTATTACATGAACGATACTCAGAAATGTCTCTTCTTTAGACTCACGCTGATTCTGTCGTGTCCTATGGATCTGAAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGTTAGAGAGCTG[T/A]AAGACTCAACATCAACAACTCATTTAAATATCATTTCTTCTTTGTATGCTTATTATTCTCCCTGTTGTTCTTTTCTTCTAGTTGGCTACACTATGAATGATCTGATATTTCAGTGGTTGGACGAAGGCCCGGTGCAAGTAGCTGATGACCTTATGCTGCCCCAGTTTGTCCTCAAAGAAGAGAAAGACTTGGGATACTGTACAAAGCACTACAACACTGGTAGAGCACTGAACACCACAGTACTAATGCTTCAGTACAACACTATTTGGGTTCTTGCGATTTCTGTTTTAAGGGGTTGTCTGGGGGTTACTCTGTATTTGCTAACATGATCATAGTAATGGTACTGGTAACTATTGGTAAGTTGAATAAATTATTATTATTTCTGAAAAGATGGTAATTTATAAATTTATGCATGGTCATTATTTTTTACTTCAGATTGAACAGGATTATCCAAACTCAGTCCTGCATATTTTAGTTCCAACCCCAATTAAACACACCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13466
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006474 | Essential Splice Site | 237 | 537 | 5 | 10 |
ENSDART00000006474 | Essential Splice Site | 237 | 537 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 24316706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22029578 |
GRCz11 | 5 | 22533378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGTTAGAGAGCTG[T/A]AAGACTCAACATCAACAACTCATTTAAATATCATTTCTTCTTTGTATGCT
Long Flanking Sequence:
GTTTAAGATGATCTACTAAAGTTCAAACCGAGCATCAGAATGCAATGTATTATTGACTTTGCTGCTGTGAACGTCATCTAATTCATTTCTGAACATAACTTCATTAGGATTACCGGCTGAACGTTTTTCTACGGCAGCAGTGGAATGACCCACGACTAGCTTATAAAGAATACCCAGACGATTCCCTGGATCTGGACCCATCCATGCTGGACTCCATCTGGAAGCCAGACTTGTTCTTCGCCAATGAGAAAGGCGCCAACTTTCATGAGGTCACCACAGACAACAAGCTGCTGAGAATTTTCCAGAACGGAAACGTGCTGTATAGCATCAGGTGCAGTGTCAGCCCCTACAGTATATGTTACATAAATCCTTTCAAACTATTACATGAACGATACTCAGAAATGTCTCTTCTTTAGACTCACGCTGATTCTGTCGTGTCCTATGGATCTGAAGAATTTCCCAATGGACACTCAGACCTGCACTATGCAGTTAGAGAGCTG[T/A]AAGACTCAACATCAACAACTCATTTAAATATCATTTCTTCTTTGTATGCTTATTATTCTCCCTGTTGTTCTTTTCTTCTAGTTGGCTACACTATGAATGATCTGATATTTCAGTGGTTGGACGAAGGCCCGGTGCAAGTAGCTGATGACCTTATGCTGCCCCAGTTTGTCCTCAAAGAAGAGAAAGACTTGGGATACTGTACAAAGCACTACAACACTGGTAGAGCACTGAACACCACAGTACTAATGCTTCAGTACAACACTATTTGGGTTCTTGCGATTTCTGTTTTAAGGGGTTGTCTGGGGGTTACTCTGTATTTGCTAACATGATCATAGTAATGGTACTGGTAACTATTGGTAAGTTGAATAAATTATTATTATTTCTGAAAAGATGGTAATTTATAAATTTATGCATGGTCATTATTTTTTACTTCAGATTGAACAGGATTATCCAAACTCAGTCCTGCATATTTTAGTTCCAACCCCAATTAAACACACCTG
Associated Phenotype:
Not determined