ZMP

f2rl1

Ensembl ID:

ENSDARG00000068856

ZFIN ID:

ZDB-GENE-061215-140

Description:

coagulation factor II (thrombin) receptor-like 1 [Source:RefSeq peptide;Acc:NP_001073273]

Human Orthologue:

F2RL1

Human Description:

coagulation factor II (thrombin) receptor-like 1 [Source:HGNC Symbol;Acc:3538]

Mouse Orthologue:

F2rl1

Mouse Description:

coagulation factor II (thrombin) receptor-like 1 Gene [Source:MGI Symbol;Acc:MGI:101910]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23853	Nonsense	Available for shipment	Available now
sa29513	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23853

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

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099733	Nonsense	330	380	2	2
ENSDART00000136671	None	None	270	None	3

Genomic Location (Zv9):

Chromosome 21 (position 7208676)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	7329889
GRCz11	21	7935110

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTGGCCAGTCTGAACAGCTGTGTTGATCCATTCGTGTATTATTTTATCT[C/A]GGATGAATTCAGGGAGCATGTTAGAAACACTTTTCTTTGCCGAAGTGAGC

Long Flanking Sequence:

ACTTTCCCAGCAGAAGAGGAACAACAGGTTGGCGGTGTGTGTGTCAGTGTGCGTGTGGCTGGTCGTGTGGGCTTTAACCGTGCCTCTGTATCTTTACGACCAGACCGTGAAGGTCACCAACATGGATATAGTCACCTGCCATGATGTCACTCGACCCAGCCAATCACTTTACCCCTGCATCTACTTCCTGACCATGGGAGTTGTGGGATTTGTAGTTCCCTGCCTAGTGTGTATAGTGTCAAACGTGCAGATGCTGCGCGCCCTGAAGAGCTCGATGAATGATCCCAGCATCGTTCAGAAGAGAAAAAAGGCTATCATCCTTATTGTGACGGTGCTGGTGATGTTTCTAGTGTGCTTCACGCCTAGTAACATCATGGTGATGGTGCATTACGCTCTGCTGTTTAATGGAGTGAAGAACAGCGGTTATGGTTTCTACATCACCACGCTGTGCTTGGCCAGTCTGAACAGCTGTGTTGATCCATTCGTGTATTATTTTATCT[C/A]GGATGAATTCAGGGAGCATGTTAGAAACACTTTTCTTTGCCGAAGTGAGCGCACTGCCCAGAGAATGCGAGTTTCTTTTAGTGCGCTGAAGTATTCGAAGAAAAGCAGCACGTACACATCAGACTCTGGAAACACACAGAGCAGTTCCTATTGAGAGTGACTAGAGAGAGTGTGAACTGTTTTTAAAATCTCAGGTGGAAATTCTGAGCTTGTTTTGTAGTATGCTTGAAAGGACCTGAGGGATACGTTTCTGAAACATGCACTGTCTGAAGGAAAAATGAATTAATTAACCAATAAATGTCTTTTTCTATGATTTTTACCTCTGTTTTTATATTTACGCTGTGAATAATATGCGTAAATTTACTTAATTTTTATTTTGTGACCATGTTTTTCGCCACATTTTTTTATGCTTTTGAGTTGCATTATGGAATCGGATTGCATCCTTTTCCTCTAGGAAAGTAGCTTTTATTAAAATTTTTAACAGTTTACATTGTACGATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29513

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099733	Nonsense	361	380	2	2
ENSDART00000136671	None	None	270	None	3

Genomic Location (Zv9):

Chromosome 21 (position 7208582)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	7329795
GRCz11	21	7935016

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTGAGCGCACTGCCCAGAGAATGCGAGTTTCTTTTAGTGCGCTGAAGTA[T/G]TCGAAGAAAAGCAGCACGTACACATCAGACTCTGGAAACACACAGAGCAG

Long Flanking Sequence:

TACGACCAGACCGTGAAGGTCACCAACATGGATATAGTCACCTGCCATGATGTCACTCGACCCAGCCAATCACTTTACCCCTGCATCTACTTCCTGACCATGGGAGTTGTGGGATTTGTAGTTCCCTGCCTAGTGTGTATAGTGTCAAACGTGCAGATGCTGCGCGCCCTGAAGAGCTCGATGAATGATCCCAGCATCGTTCAGAAGAGAAAAAAGGCTATCATCCTTATTGTGACGGTGCTGGTGATGTTTCTAGTGTGCTTCACGCCTAGTAACATCATGGTGATGGTGCATTACGCTCTGCTGTTTAATGGAGTGAAGAACAGCGGTTATGGTTTCTACATCACCACGCTGTGCTTGGCCAGTCTGAACAGCTGTGTTGATCCATTCGTGTATTATTTTATCTCGGATGAATTCAGGGAGCATGTTAGAAACACTTTTCTTTGCCGAAGTGAGCGCACTGCCCAGAGAATGCGAGTTTCTTTTAGTGCGCTGAAGTA[T/G]TCGAAGAAAAGCAGCACGTACACATCAGACTCTGGAAACACACAGAGCAGTTCCTATTGAGAGTGACTAGAGAGAGTGTGAACTGTTTTTAAAATCTCAGGTGGAAATTCTGAGCTTGTTTTGTAGTATGCTTGAAAGGACCTGAGGGATACGTTTCTGAAACATGCACTGTCTGAAGGAAAAATGAATTAATTAACCAATAAATGTCTTTTTCTATGATTTTTACCTCTGTTTTTATATTTACGCTGTGAATAATATGCGTAAATTTACTTAATTTTTATTTTGTGACCATGTTTTTCGCCACATTTTTTTATGCTTTTGAGTTGCATTATGGAATCGGATTGCATCCTTTTCCTCTAGGAAAGTAGCTTTTATTAAAATTTTTAACAGTTTACATTGTACGATGTTATAAATTATGGTACATAAACGGCACACTGTAAAAATTATGTGTTTCTTGGATTTTTTTTTGTTCTGATTTTAGTCCAAATATCTAAACATTC

Associated Phenotype:

Not determined