ZMP
si:dkey-211g8.1
Ensembl ID:
ZFIN ID:
Description:
si:dkey-211g8.1 [Source:RefSeq peptide;Acc:NP_001076360]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16466 | Nonsense | Available for shipment | Available now |
sa31031 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16466
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003031 | Nonsense | 198 | 364 | 3 | 5 |
ENSDART00000138706 | Nonsense | 178 | 345 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 11158472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10617701 |
GRCz11 | 19 | 10536626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KACTTTGTGTACCGACAAGTCTTTCCTGATAAGAAGAACTTCAGCCAATG[C/A]TTTTTCAAGGTTTGTTTTACTTTCAGTCTTAAATACTAACWTATTATCAT
Long Flanking Sequence:
GACCCAAACCAGCATGTGAACATGACGGTGGACATTGAAGCCATTATGAATAAGGTCAGCACTGTTTTCCTCACCATCATCATTCTTTTCGGCACCACTGGGAACTCTGTGGTCATCTGGGTGGCTGGTTTTCGTATGAAGCCCAACGTCACCAATGTATTTTTGGTCAACCTCGCAGCAGCAGATCTGATCTTCTGTTTGACACAAATCTCTTGGCTAATCAAAGATATTTTCTTTGACCACTGGCCTTTTGGACTCTTTGTCTGCAAGTTTAATGGGTTCGTCAAGTATGCCAACATGTTCTGCAGTGTTTTTCTTCTGGCTGTCATCAGTGTGGATAGAGCGCTCTGCGTCTGGTGTCCGGTGTTCACCAGGAAACGACGGACAGTATGTGCTGCTCGTATGGTCAGTGTGGGAGTTTGGATCATGGCTGGGATCTTTAGTTTACCATACTTTGTGTACCGACAAGTCTTTCCTGATAAGAAGAACTTCAGCCAATG[C/A]TTTTTCAAGGTTTGTTTTACTTTCAGTCTTAAATACTAACATATTATCATTAAATACATTGGTGTGAAAAAGTGTTTGATTAGAAACACTAGAAATTTCAAGAATCTAAATTTCCCGCCACTTCTAAATAGCTGAAAGAAAACAAAATGAAGACTTTGGAGTGGCCTAGTCAAAGTCCTGAACTGAATCTAATTAAGATGCTGTGGTGCCGCATGACCTTAAAAAGGTTCTTGCTCAAAGACTCTCCAGTGTGGCTGAATTATAACAATTCTCCAAGGATGAGAAGGTTGAAATTCCTCCACAACACTGTAATAGACTCAATGGCAATTGTATAAAGCAATGGTATAAAGTAACAAATTACAAATACACAAATCACTGTAATTGAGTAGTTTTTCTCAGGAATTGTAATTTACTAAGTAGTTTCAAAAATGTGTACTTTTACTTTCCCTAAAAGTATCGGTACTTTTACTCCACTACTTTCCTTCAACCTGCAGTCACGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31031
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003031 | None | None | 364 | None | 5 |
ENSDART00000138706 | Nonsense | 344 | 345 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 11159820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10619049 |
GRCz11 | 19 | 10537974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAAGTTGTAATTCCTTTCCAAAGGCTGCAGTTGTTGAGTGTGTAAAT[A/T]GATTTTAAGAGTTTTTACTTTGTTTTTCTCTCTTGTTTGTTTGTCTGGTC
Long Flanking Sequence:
CTTTTCATTTGCAGGTGAATGAAACAGCTGAGGGTAACAATTCAGCAAAGTATGTGTACTACTTCATTCGTTTCATCTGTGGATTCCTGTTGCCCTTTCTGGTCATCTTTATCTGCTACACACTGGCTGCTATTGGGATCCGCAGGACGAGACTCTCTGGCAAATCAAGGCCTCTTCGCATTCTTGCTGTTTTGGTCTGTGCCTTTTTCCTATGCTGGGCTCCATATCACTTTCTAAGGCTGGTCAGGTTTGTAAATGAAGACAATGAGGTGGTAAAATTAGGATGGAGAATGGTTTCAGACTTAACCTATTTTAACAGCTGCATTAACCCAGTGTTGTACCTCTTCATGGGACTGGATGTTAGGCAGCTCTGTAAGCAAAGTTTGTTTGGGATTTTTCATAGAGCACTTACGGAGGAAGGTCAAAATCGGTCCCAGCTGTCCACTAAAGAAGAAAGTTGTAATTCCTTTCCAAAGGCTGCAGTTGTTGAGTGTGTAAAT[A/T]GATTTTAAGAGTTTTTACTTTGTTTTTCTCTCTTGTTTGTTTGTCTGGTCCATTAAATAGCACAAAGTGTTTAATGGGGAAAGGGGAAAAATCTATCACTGTGCCTGGTCTTCTGGTTAATTTCAGAGGACGTTCATATATTGCACCTTTTGTGCATGCAAGTTCATAAATTTTAATGCAAATGTGCAGCGCAATGCTTGTTTTTTCCTGGCATATCTAGAACATTATGAGTTAAAAACATCTCAACTTTTCAGAATGCCTTAAGCGAACCACAAGTCAAGTGACAAGAACCAATCAGCTTCACACATTGTATGGAATATACACATTTCAGTAATAACAGTAGACTATTTACCTCAGAAAAATACACTGCAAGGCTTTATACTTTTCACCTTAAGTAAGACTTGTATCAGAGCTACAGTAAGGGATTGTCAGTGGCGGAACCTCATAGAGCACTTATGATGGCAGCATAATAATCAATGCCACTGGTGCTCAAGCTCAAA
Associated Phenotype:
Not determined