ZMP

LOC793315

Ensembl ID:

ENSDARG00000079399

Human Orthologue:

F2RL3

Human Description:

coagulation factor II (thrombin) receptor-like 3 [Source:HGNC Symbol;Acc:3540]

Mouse Orthologue:

F2rl3

Mouse Description:

coagulation factor II (thrombin) receptor-like 3 Gene [Source:MGI Symbol;Acc:MGI:1298207]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12331	Nonsense	Available for shipment	Available now
sa42429	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12331

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
ENSDART00000111674	Nonsense	293	373	2	2

Genomic Location (Zv9):

Chromosome 14 (position 38196708)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	36535019
GRCz11	14	36875333

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTTTTCTTGTTGCCTAGCAATATTCTSATGCTGTGGCATTATTCTAAAT[C/A]AAGTTCGGTCAACAATCTTTATATGCCGTACCTGATYGCTTTGTCTCTCA

Long Flanking Sequence:

TTTCGGAGAGCCGTTTTGTCGTGTTGTGGTTGGATTCTTCTATGGAAACATGTACGGCTCAGTGGTTTGTCTGGCACTGATTGCCTTGGATCGCTATATAGCTCTGGTTCACCCTTTTGGTGCCAAAGTGCTCCGAAGTAAAAAGAACTCTGTCTATATGAGTGTGTTGGTCTGGATAGTGGTTTTAGCAGCTGCTGTGCCCTTATTAGCCTCAAAACAGACTCATGAGATAAATAACCTATCGATAACAACCTGCCATGATGCACTGCCTGTTGAAGAGCAGGAAAATTACTTTCTGCCATATTTTACCACTCTTTTCTCCCTTTGCTTTTTGCTTCCACTATTAGTGGTGCTGTTCTGCTATTCTGCAGTGTTACGGACACTTATGGCTGAAGGGCAGCGTTTTGCCCATGCGGTTAGAGTCACTGTGCTGATGTTGATTGTTTTTGTTGTTTTCTTGTTGCCTAGCAATATTCTCATGCTGTGGCATTATTCTAAAT[C/A]AAGTTCGGTCAACAATCTTTATATGCCGTACCTGATCGCTTTGTCTCTCAGCACATTCAACAGCTGCATCGACCCTTTTATTTTTTATTACGTGTCTAAGGATTTCCGAAAGAGGTCATGGGAGGCTCTCAGGTGTTTGAAGTCTGATTTAGAGTCTTCTTCAGATTCTAGGACAAAGGTCACCTTACTTTCAAAGATAAGCAAGACTGAAAGACCTTTAAATGGGGAATCAACTCATTTGTGATGCTAGGATGACCATTTCGAAATACGTAAGTTATCAGGTTATTTCTTGAATTTTAGGGGTATTGAAGGACTGAAGGCCCACTCATACCAAAGATGATAACTATAACAATTTAGATAAAAAATCTCTTAATTGAAAAGGATAGCACACCACAACTACAGTGCTCAGCATAAATGAGTACACCCCATTTGAAAATGAATATTTTCATCCATATCTCAGTCAATATATGCAATTCATTTTGGTGTAGTTAAACAAAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42429

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111674	Nonsense	300	373	2	2

Genomic Location (Zv9):

Chromosome 14 (position 38196730)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	36535041
GRCz11	14	36875355

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTCTCATGCTGTGGCATTATTCTAAATCAAGTTCGGTCAACAATCTTTA[T/A]ATGCCGTACCTGATCGCTTTGTCTCTCAGCACATTCAACAGCTGCATCGA

Long Flanking Sequence:

GTTGTGGTTGGATTCTTCTATGGAAACATGTACGGCTCAGTGGTTTGTCTGGCACTGATTGCCTTGGATCGCTATATAGCTCTGGTTCACCCTTTTGGTGCCAAAGTGCTCCGAAGTAAAAAGAACTCTGTCTATATGAGTGTGTTGGTCTGGATAGTGGTTTTAGCAGCTGCTGTGCCCTTATTAGCCTCAAAACAGACTCATGAGATAAATAACCTATCGATAACAACCTGCCATGATGCACTGCCTGTTGAAGAGCAGGAAAATTACTTTCTGCCATATTTTACCACTCTTTTCTCCCTTTGCTTTTTGCTTCCACTATTAGTGGTGCTGTTCTGCTATTCTGCAGTGTTACGGACACTTATGGCTGAAGGGCAGCGTTTTGCCCATGCGGTTAGAGTCACTGTGCTGATGTTGATTGTTTTTGTTGTTTTCTTGTTGCCTAGCAATATTCTCATGCTGTGGCATTATTCTAAATCAAGTTCGGTCAACAATCTTTA[T/A]ATGCCGTACCTGATCGCTTTGTCTCTCAGCACATTCAACAGCTGCATCGACCCTTTTATTTTTTATTACGTGTCTAAGGATTTCCGAAAGAGGTCATGGGAGGCTCTCAGGTGTTTGAAGTCTGATTTAGAGTCTTCTTCAGATTCTAGGACAAAGGTCACCTTACTTTCAAAGATAAGCAAGACTGAAAGACCTTTAAATGGGGAATCAACTCATTTGTGATGCTAGGATGACCATTTCGAAATACGTAAGTTATCAGGTTATTTCTTGAATTTTAGGGGTATTGAAGGACTGAAGGCCCACTCATACCAAAGATGATAACTATAACAATTTAGATAAAAAATCTCTTAATTGAAAAGGATAGCACACCACAACTACAGTGCTCAGCATAAATGAGTACACCCCATTTGAAAATGAATATTTTCATCCATATCTCAGTCAATATATGCAATTCATTTTGGTGTAGTTAAACAAAACAGGTTTATTAAACAGATGTATTT

Associated Phenotype:

Not determined