ZMP
ENSDARG00000076710
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 |
---|---|---|---|
sa19124 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11017 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19124
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 |
---|---|---|---|---|---|
ENSDART00000115178 | Nonsense | 77 | 320 | 2 | 2 |
ENSDART00000115178 | Nonsense | 77 | 320 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 36430848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 37830852 |
GRCz11 | 15 | 37732437 |
KASP Assay ID:
2260-8868.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACTCCATTTGGTTTCTGAATTTGGCGATTACAGACTTCATCTTTTTTT[T/A]ACTTTCAATCACAAATTATTTCTTAATCGTGAGTAATCAGCACAGTGTCT
Long Flanking Sequence:
GCACAGAGATAATGTAAAATCCATATAATTAAGCACAAGATACACATTTACTTTGTCAAACAAATGACCCTTCATACAAAGATGTGCTTCTAATGAATCCACACACTGCAAATGCAAAATTATTCAATATAAAAGACTAATTATTGGTTTTATTCTAATGAGGTTTTATTAAAATGTTTGAGAGGAGCATGATCAGATATACTCTAATAGCTAATAGTTCAGAAATTTGCAGCACAATGACACACTGACAGTCCTTTCTGTGTTCCCTTGTTTAGAAAACAGCAGTTTTGGGCTTAAAAATGTGACTGGAAACTCAACAGACAAGAGCACTGTGGATAACAAGGGATTTGATATTTTTTTTGCCTGCATTTTCACTGTAACCGTGGTAGTGGGTGTCATTGGAAATGGGCTGGTCATATTTCTGGCCGGCTGCAGAATGAAGACGACTGTCAACTCCATTTGGTTTCTGAATTTGGCGATTACAGACTTCATCTTTTTTT[T/A]ACTTTCAATCACAAATTATTTCTTAATCGTGAGTAATCAGCACAGTGTCTTCACAGGCAGCCTTTTTAGCATTTCATTTACACAAAATGTGTTTGTTAGCGTTTGGACTCTTGTAGTTATTAGTCTGGATCGATGCCTGTGCACATGGATGGCTGTTTGGGCTCAAAATAACAGAACTTTGCGTAAAGCCAGAATCATCTGCATCATCATCTTTGTTTCATCCATAGTCTACATTTTACCTTACTTCAACCTTTTTGAGACTACATTTACAATTCGTGCCACATATGGATTTATATTGTCCTTTCTCATCCCCTTCCTGATCATTGCATCTTCATACATCGCTATTGGAGTAAAAATCAATCGCCTCAAAAAGAGGAAGCAGCTCAAGCCATACAGACTCATTATAACTGTAATCCTGACTTTCTTCATCTGTTCATTTCCACAACATGTTTGCTATTTTTTGATGGCAAAAGCAGAAAAGAATAATTGGACTCTCCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11017
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115178 | Nonsense | 77 | 320 | 2 | 2 |
ENSDART00000115178 | Nonsense | 77 | 320 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 36430848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 37830852 |
GRCz11 | 15 | 37732437 |
KASP Assay ID:
2260-8868.1 (used for ordering genotyping assays)
KASP Sequence:
CAACTCCATTTGGTTTCTGAATTTGGCGATTACAGACTTCATCTTTTTTT[T/A]ACTTTCAATCACAAATTATTTCTTAATYGTGARTAATCAGCACAGTGTCT
Long Flanking Sequence:
GCACAGAGATAATGTAAAATCCATATAATTAAGCACAAGATACACATTTACTTTGTCAAACAAATGACCCTTCATACAAAGATGTGCTTCTAATGAATCCACACACTGCAAATGCAAAATTATTCAATATAAAAGACTAATTATTGGTTTTATTCTAATGAGGTTTTATTAAAATGTTTGAGAGGAGCATGATCAGATATACTCTAATAGCTAATAGTTCAGAAATTTGCAGCACAATGACACACTGACAGTCCTTTCTGTGTTCCCTTGTTTAGAAAACAGCAGTTTTGGGCTTAAAAATGTGACTGGAAACTCAACAGACAAGAGCACTGTGGATAACAAGGGATTTGATATTTTTTTTGCCTGCATTTTCACTGTAACCGTGGTAGTGGGTGTCATTGGAAATGGGCTGGTCATATTTCTGGCCGGCTGCAGAATGAAGACGACTGTCAACTCCATTTGGTTTCTGAATTTGGCGATTACAGACTTCATCTTTTTTT[T/A]ACTTTCAATCACAAATTATTTCTTAATCGTGAGTAATCAGCACAGTGTCTTCACAGGCAGCCTTTTTAGCATTTCATTTACACAAAATGTGTTTGTTAGCGTTTGGACTCTTGTAGTTATTAGTCTGGATCGATGCCTGTGCACATGGATGGCTGTTTGGGCTCAAAATAACAGAACTTTGCGTAAAGCCAGAATCATCTGCATCATCATCTTTGTTTCATCCATAGTCTACATTTTACCTTACTTCAACCTTTTTGAGACTACATTTACAATTCGTGCCACATATGGATTTATATTGTCCTTTCTCATCCCCTTCCTGATCATTGCATCTTCATACATCGCTATTGGAGTAAAAATCAATCGCCTCAAAAAGAGGAAGCAGCTCAAGCCATACAGACTCATTATAACTGTAATCCTGACTTTCTTCATCTGTTCATTTCCACAACATGTTTGCTATTTTTTGATGGCAAAAGCAGAAAAGAATAATTGGACTCTCCCTT
Associated Phenotype:
Not determined