ZMP
si:dkey-208c22.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
GPR124
Human Description:
G protein-coupled receptor 124 [Source:HGNC Symbol;Acc:17849]
Mouse Orthologue:
Gpr124
Mouse Description:
G protein-coupled receptor 124 Gene [Source:MGI Symbol;Acc:MGI:1925810]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31669 | Essential Splice Site | Available for shipment | Available now |
| sa8749 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31669
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112331 | Essential Splice Site | 354 | 1115 | 8 | 19 |
| ENSDART00000131546 | Essential Splice Site | 278 | 973 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 39139946)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 38018749 |
| GRCz11 | 8 | 38051688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCTTCTGTCCGGAGCAGAAAGTGAACAACAATCGAGGGGAGTTCAGG[T/G]AGGGGAGGTGTCCTAATGCTTTATCTGTATCCAAATAAGAATTCTCAACA
Long Flanking Sequence:
TTTAGTATATTTATCTTCGGCCCACCGCTCTCAATGATGTTTGGTTTTTGGCACTTCATACAAAAACATTTAGCCACCTCTGCTTTAGACATTCTTGACTATTAACAATACTGAAACTACATATCAACAACTTTTATTTTAAAAGTAGTTAAAGTAGTAGTTTTTTCTCACTTTTAAGCAGCTTAACAAATCACAACAGAATCACAGTATGGCATAATTATATATCAAATGCTGTAAATTAATTGCTTAAAATATGCGCAGCTGGTTTTCGACCATACTGTTCATGCTGAGCAACAGTACACTTAAATAATAACATGGTTCTGTTTATTTTTAGTGAACTGATCCTGTCAAACGTCCATGTTGAGGCAAGCGGTGAGTGGGAATGTGTGGTGTCTACAGGCCGTGGGAACACCTCTTGCAGTGTGGAGATAGTGGTGCTAGAGAACAGTGCCTCCTTCTGTCCGGAGCAGAAAGTGAACAACAATCGAGGGGAGTTCAGG[T/G]AGGGGAGGTGTCCTAATGCTTTATCTGTATCCAAATAAGAATTCTCAACAAATGCATGAACTGTCTTCTGTTTGATCTTCAGATGGCCTAGAACTCTAGCTGGCATCACCTCCTACCAGCACTGTCTGCAGCTACGCTATCCTTCCCTAACTCTAGGGGGTGGTGTGGAGCAGAAGAAGGCTTCACGTAACTGTGACCGGTCTGGACGCTGGGAGGAGGCAGACTACTCTCAGTGCCTTTATACCAATGACATCACACGCATACTACATACATTCATACTGGTTAGTGCAAAGTTCTGGTTTATTAACATAATTTTAAAAGCTGCAAGCTCCCACTGGTTAGAAGGTAACGCACTTTAGCTTTCTTTCGAAAACTTATTATGAAAATAAGATTTGTCATTGATTGACACATAACTACTGATAGTTAGGTTCCTTTTTTGACTCACTTTATTATACAGATGTTACTACTTCAATGTGTTCCTTTTGCCGCCATTCATACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8749
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112331 | Nonsense | 998 | 1115 | 19 | 19 |
| ENSDART00000131546 | Nonsense | 922 | 973 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 39116051)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 37994854 |
| GRCz11 | 8 | 38027793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTGGCACTGATGGCAACCCAGTTTGTGTTTGTTGGGCTGTGGTGCTG[C/A]GGCGCTATGGCARTTTGGCATGTGGATAGAGAGCGGAAACTCTTCARTTG
Long Flanking Sequence:
TTTCACTGTCTGATACTTGTAGCAGATTTACTGCACATGCTGGACCGCTTCTTTACAGGCTCTTTAAAAAAGTGTCTGTTTCGTACAGAGCTTTCTTTGTGTTTCTGCTATTTGACTAATTACTGCCCTGCCCTCCCTGACCTTTTTCATTGCTCTTGACCTTTTGACAGCTGCTGGTTGGTATGGCAACCCAGTTTCGGAGCTTTCTACATTCCAGCTGGATTGATCATTCTTGTGACCTGGATCTACTTCCTGTGCACTGTTTTCTGCCTGAGGCAGCGAAACTTCCAGGAGTCTAAAGATCTTCAATGCTCTGCATCCGACCCTTCAAATTTGCCAGAGAGTCAACCGGCACTCAGCGGCAGCACCAGTCTTCTTTCCACAGACTCTGGGGTCAGCCCGGTGCATGCTGGAACAACAGTGGAGGACCAGTACTCATTGAAGGTCCAGTGTCTGGCACTGATGGCAACCCAGTTTGTGTTTGTTGGGCTGTGGTGCTG[C/A]GGCGCTATGGCAGTTTGGCATGTGGATAGAGAGCGGAAACTCTTCAGTTGCCTATATGGAGGAACAGCTACCGGTTTAGGCATCTTTTTAGTGCTCCATCACTGTTTCAAGCGTTTGGATGTCCAGGCAGCTTGGCTAGGGTGTTGTCCAGGCTATCATCGCTCTCAACCCATGCCAGCCTATTCCCACCCCTGCACTGTCACAGTGGGTGTTCAGAGTGCCTCAGAAAGGGGCTCCCAGCTTTTTGTAGCATGCCATCCACCTACGGACCCAAACCATTACTCTTCTTCTGCCAGGTCATCTTCAACTCAGAGTGGAACAGCAAGTATCACTGTTGTACCTAGCAAGCTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCGCCAACAGTGGCGGATCTGTCCGGTAAAATCTCTGACTGCGTGTCACC
Associated Phenotype:
Not determined