ZMP

ENSDARG00000019093

Ensembl ID:

ENSDARG00000019093

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]

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]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15172	Nonsense	Available for shipment	Available now
sa25087	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15172

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091926	Nonsense	29	318	1	2

Genomic Location (Zv9):

Chromosome 19 (position 11141140)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	10599642
GRCz11	19	10518567

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TMTAAAATCTCAACCGACTTTGAGAAAACGACAGTGGATATGGTCTTTTA[C/A]GCTATCATYGTTCTCCTCGGCACCACCGGGAACTCTGTGGTCATCTGGGT

Long Flanking Sequence:

ATGCTATTAATTCCCAGATTTATTTCACCTTTTTATTTTACCTCACAATTGAGTTTTACAATATACGATTATGGACAATCTTAAACCTATTTTAATATATATAACATCAATAATATATTCAAAAAATGTGTAAAATTCTAAATGTATAGCTGAAATCAATGTCCCTATTATGATATCCAAGTATAGGCTATCAGTTCAATCACCTAGAACCTCTTGGTTGCCAGACAACTGCAATAATGTTTATCGTACTGTGTGATGAAGCTCGTGAGACTAGCATGGTAACCACACGCTTATGATGTACAGAACATGTGGGCAGATCAAAGTTAAGTGCTTAAGTGTACGAAAGTTGCTGTTAACCAACAGAGAAAAATCTGAGAAAGCACATTTTAAGGATTCATCTTTCTTGCTTGCAGAATGACCGACAATACGACTCTTTCTCCTCCCTCCAACTCTAAAATCTCAACCGACTTTGAGAAAACGACAGTGGATATGGTCTTTTA[C/A]GCTATCATCGTTCTCCTCGGCACCACCGGGAACTCTGTGGTCATCTGGGTGGCTGGTTTCTGCATGAAACCCAACGTCACCAATGTTTGGTTGGTCAACCTTGCAGTAGCAGATCTGATCTTCAGCATGACAAGAATCATTTCACTCATCAAAAATCTTTTCTTTGATTACTGGCCTTTTGGAATTTTTCTCTGCAAGTTCAATGGTTTCTTCAAGTACGCCAACATGTTCTGCAGTGTTTTTCTTCTGGCTGTCATTAGTGTGGATCGAGTGCTCTGCGTCTGGCGTCCGGTGTTCACCAGGAAACGACGGACAGTATGTGCTGCTCGTGTGGTCAGTGTGGGAGTTTGGATCGTGGCTGTGATCTTTAGTTCTCCATACTTTGTTTACCGGGAGGTCTTTGTGCGTTCGAACAACTTGAGTCATTGCTCACTGGGGGTCAGAATGGCTTTAAAACTTACTGCATATATTACAGTATATTGAGGTTAGTAAAAATGTAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25087

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091926	Nonsense	300	318	2	2

Genomic Location (Zv9):

Chromosome 19 (position 11142025)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	10600527
GRCz11	19	10519452

KASP Assay ID:

554-7684.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTGCATTAACCCAATCTTGTACTTCTTCATGGGACTGGATGTTAGTCGA[C/T]GATGCAACCAAAGTTTGTCTGGGATTTTTCATAGAGCACTTATGGAGGAA

Long Flanking Sequence:

GTTTACCGGGAGGTCTTTGTGCGTTCGAACAACTTGAGTCATTGCTCACTGGGGGTCAGAATGGCTTTAAAACTTACTGCATATATTACAGTATATTGAGGTTAGTAAAAATGTATTTCTAATTTTATTTATAACTTCACTTGCAGGGTAAAGATGGTGCTGAGGGTGGCAATTTGCCAAAGTACGTCTACTACTTTGTTCGTTTCATCTGTGGATTCCTGTTGCCCTTTCTGGTCATCTTTATCTGCTACACACTGGCTGCTATTGGGATCCGCAGAACGAGATTCTCCGGCAAATCAAGACCTCTTCGCATTCTTGCTGTTTTGGTCTGTGCCTTTTTCCTATGCTGGGCTCCATATCACTTTCTAGGGCTGGTCAAATTGGTGAATAAAGACAATGAGGTGGTAAAAATAGGATGGAATATGGCTTCAAACTTAGCCTATTTCAACAGCTGCATTAACCCAATCTTGTACTTCTTCATGGGACTGGATGTTAGTCGA[C/T]GATGCAACCAAAGTTTGTCTGGGATTTTTCATAGAGCACTTATGGAGGAAGGCCAAAGTCTATCCCAGCAAGGAACTGAAGAAAGCTGTAATTCTTTTCCAAAGACTGCAGGTGATGAGTGTGTCGCTAAAATTTAGGCGTTTTCACTCATTTTCCTTTATTTTCAGGGTGCGAATTACAGGGGGGTTTGGGGAGGATTGACGCCCTTAATTATTGCTTGATCCCCCCTGAAGGACATCAAAACAAGATGTATGGGGGGTCAGCCCTGAAATAGTAAGAAATAACTTTCTCCAATCTCTGATTTTTATCTGAAATATTAATAATTATAAATAGAAATATACATTTGACCCCCTAGAACTGAAACAGTTCTAGAGCACTGATAGACATCTTAAGTGTTCACAAAACATGTTTATTGTAAAATAGGTGTTTTTCAGTAACCTCTTAAATAGTCACTAATACCCTCAAAACACTGAAAATGTATACATTTTATTAATAAACGA

Associated Phenotype:

Not determined