ZMP
LOC793256
Ensembl ID:
Human Orthologues:
C3AR1, C5AR1
Human Descriptions:
complement component 3a receptor 1 [Source:HGNC Symbol;Acc:1319]
complement component 5a receptor 1 [Source:HGNC Symbol;Acc:1338]
complement component 5a receptor 1 [Source:HGNC Symbol;Acc:1338]
Mouse Orthologues:
C3ar1, C5ar1, Gpr33
Mouse Descriptions:
G protein-coupled receptor 33 Gene [Source:MGI Symbol;Acc:MGI:1277106]
complement component 3a receptor 1 Gene [Source:MGI Symbol;Acc:MGI:1097680]
complement component 5a receptor 1 Gene [Source:MGI Symbol;Acc:MGI:88232]
complement component 3a receptor 1 Gene [Source:MGI Symbol;Acc:MGI:1097680]
complement component 5a receptor 1 Gene [Source:MGI Symbol;Acc:MGI:88232]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25086 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17050 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25086
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053336 | Essential Splice Site | 187 | 350 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 11131537)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10589977 |
GRCz11 | 19 | 10508902 |
KASP Assay ID:
554-7522.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAATGGCATTAAGAATCACTGTATGTTCACCTTGTATGAAAATGATA[T/A]ATGTATTTATAATTTATTTGATTTTACTTGCAGGTGAATGGGTCATCCGA
Long Flanking Sequence:
TGGTCTTCTACACCATCGTCATTCTCCTCGGCACCACCGGGAACTCTGTGGTCATCTGGGTGGCTGGTTTCCACATGAAATCCAACGTCACTAAAGTATGGTTGGTCAACCTCGCAGTAGCAGATTTGATTTTCTGCTTGACACGAATTTCTTCACTCATCTCTAAAGTCTTCTTTGATTACTGGCCTTTTGGAGTCTTTCTCTGCAAGTTCAATGGTTTCATTAAATATGCCAACATGTTCTGCAGTGTTTTTCTTCTGGCTGTCATCAGTGTGGATCGAGCGCTTTGCATATGGCATCCATTTTTCACCAGGGAACGACGGACAGTATGTGCTGCTCGTGTGGTCAGTGTGGGAGTTTGGATCGTGGCTGTGATCTTTAGTTCTCCATACTTTGTTTACCGGCAGGTCTTTCCTGGCAAGAACAACTTAAGCCACTGCTCACTGAAGGTCAGAATGGCATTAAGAATCACTGTATGTTCACCTTGTATGAAAATGATA[T/A]ATGTATTTATAATTTATTTGATTTTACTTGCAGGTGAATGGGTCATCCGAGACTGGCATTTCAACAAAGTATGTCTACTACTTCATTCGTTTCATCTGTGGATTCCTGTTGCCCTTTCTGATCATCTTTATCTGCTACACACTGGCTGCTATTGGGATCCGCAGATCAAGGCTCTCCAGAAAAGCAAAGCCTCTTCGCATTCTTGCTGTTTTGGTCTGTGCCTTTTTCCTATGCTGGGCTCCATATCACTTTCTAGGGCTGGTCAAATTGGTGAATAAAGACAATGAGGTGGTAAAAATAGGATGGAATATGGCTTCAAACTTAGCCTATTTCAACAGCTGCATTAACCCAATATTGTACTTCTTCATGGGACTGGATGTTAGTCGACGATGCAACCAAAGTTTGTCTGGGATTTTTCGCAGAGCACTTATGGAGGAAGGCCAAAGTCTATCCCAGCAAGGTATTGGGGAAGATATCAGCAATTCATTTCTAAAGACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17050
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053336 | Nonsense | 306 | 350 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 11131925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10590365 |
GRCz11 | 19 | 10509290 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGCATTAACCCAATMTTGTACTTCTTCATGGGWCTGGATGTTAGTCGA[C/T]GATGCARCCAAAGTTTGTCTGGGATTTTTCKMAGAGCACTTAYGGAGGAA
Long Flanking Sequence:
ATACTTTGTTTACCGGCAGGTCTTTCCTGGCAAGAACAACTTAAGCCACTGCTCACTGAAGGTCAGAATGGCATTAAGAATCACTGTATGTTCACCTTGTATGAAAATGATATATGTATTTATAATTTATTTGATTTTACTTGCAGGTGAATGGGTCATCCGAGACTGGCATTTCAACAAAGTATGTCTACTACTTCATTCGTTTCATCTGTGGATTCCTGTTGCCCTTTCTGATCATCTTTATCTGCTACACACTGGCTGCTATTGGGATCCGCAGATCAAGGCTCTCCAGAAAAGCAAAGCCTCTTCGCATTCTTGCTGTTTTGGTCTGTGCCTTTTTCCTATGCTGGGCTCCATATCACTTTCTAGGGCTGGTCAAATTGGTGAATAAAGACAATGAGGTGGTAAAAATAGGATGGAATATGGCTTCAAACTTAGCCTATTTCAACAGCTGCATTAACCCAATATTGTACTTCTTCATGGGACTGGATGTTAGTCGA[C/T]GATGCAACCAAAGTTTGTCTGGGATTTTTCGCAGAGCACTTATGGAGGAAGGCCAAAGTCTATCCCAGCAAGGTATTGGGGAAGATATCAGCAATTCATTTCTAAAGACCATAGGTGTTGAGTGTGAAACTAAAGTTTAGGAGTTTTTACTCTCTTTTTCTTGTTAATTTATCAGATCATGCAAACTGTAAACGTGTCTTACTATGTATTTCTTACAAAACAGGTCTTGGATATTACCTGAAAAAACAGTATATGTTAAGTCTCAACTCAAAAATACCTCATATATATATAAAATAATGCTTTTTTGGTGTTCTTTTTTAAAATGTAAATAAGCTACTGCTCACAGCCTTTCTAGAACTGGAATGTGCCTTAAGGCTGATTTATACTTCTGCGTCAAACACCGGCGTATGCTACGGCGCTGACGCATAGCCCTTCGCCGTGGCCGTCGCCGTCACTGACGTGCACCTCTCAAAAAATGTAACTACACGTCGCAACAACGC
Associated Phenotype:
Not determined