ZMP

LOC799082

Ensembl ID:

ENSDARG00000059507

Human Orthologue:

F2R

Human Description:

coagulation factor II (thrombin) receptor [Source:HGNC Symbol;Acc:3537]

Mouse Orthologue:

F2r

Mouse Description:

coagulation factor II (thrombin) receptor Gene [Source:MGI Symbol;Acc:MGI:101802]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa17453	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa17453

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082790	Nonsense	350	462	4	4

Genomic Location (Zv9):

Chromosome 21 (position 7350763)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	7471976
GRCz11	21	8077197

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCCGTGCAAAGTCCAACCGATTATCGAAATCTCCATCATGGTTGRAAAAA[C/T]GACGGAGAGCTGCGATTATGCTTATCGCCAWGTTGTCTGAGTTTATGGTG

Long Flanking Sequence:

TGGATCTGCTCTTCGCCCTGCTGCTGCCTCTGAAGATCCACTACCAGCTGAACGCTTCTGATTGGCTGTTTGGTGAGGCGGCGTGTCGTGTGCTCACTGCAGCGTATTACTGCTACATGTACTGCTCCATACTGCTGATGATGTGCATGAGTGTGGACAGACTGCTGGCCGTGGTGTTTCCAGTCGCCTCTTTAACCTGGAGAAATGCAAGGAAAGCCTCGCTTATATGCGCATTAGTCTGGCTGCTGGCGCTCGCTGGTACTGTGCCACTACTATTAATGAGACAAACATTCCAGATTGAGGATGTGGGCGTCACATGCCATGATGCGCTGATTCATAACAACCCTAAAGATCAGCAATATTTGTATGTGTTCTTCATCCTTTCGTGCTTTTACTACTTCGTACCACTCATTATCACCATAGTGAGCTACTCCACCATCATATATGTGCTCCGTGCAAAGTCCAACCGATTATCGAAATCTCCATCATGGTTGAAAAAA[C/T]GACGGAGAGCTGCGATTATGCTTATCGCCATGTTGTCTGAGTTTATGGTGTGTTTTGCTCCAATCAACGGCATCCTGTTGTATCACTGCATTCGATTGGCTGTTGGAGGAAACAGTGGCGAGGGAGATTCATCTTATAGTGCATACATGTTGGCTGTGTGTTTGGGGAGCGCAAGTGTTTTTCTGGATCCTCTGCTATACTATTATGGCTCGTCTCAATGCAGACAGAAGATCAGCTCTCTGTTTTGGTGGAAAAAGTCAAAAGCCCTCTTATCAAAAGGAAGCAGGTCAGGATCCTCTTTTGTAAGTATTGAGTACACTAAGGCGTCAGTTAAGATGTAAATTAGTGAACACTTTCTTTTTTTAGTTGTGTATATAATACTGCTTATTGGCTAAATTGTACATGAATATGTGATTATCACTTAAATTGTGAAGTTCTCTGATATTCGATATGCAGAAGTGTAGATAAATCATGAATTAAAGGGGACCTATTATGCGAAA

Associated Phenotype:

Not determined