ZMP

fgl2

Ensembl ID:

ENSDARG00000019861

ZFIN ID:

ZDB-GENE-030131-9506

Description:

fibroleukin [Source:RefSeq peptide;Acc:NP_001020710]

Human Orthologue:

FGL2

Human Description:

fibrinogen-like 2 [Source:HGNC Symbol;Acc:3696]

Mouse Orthologue:

Fgl2

Mouse Description:

fibrinogen-like protein 2 Gene [Source:MGI Symbol;Acc:MGI:103266]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14776	Nonsense	Available for shipment	Available now
sa15081	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa14776

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
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Mutation:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022539	Nonsense	294	451	2	2

Genomic Location (Zv9):

Chromosome 4 (position 19115993)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	20459328
GRCz11	4	20180303

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACCTGGGCTGACTACAAGAAGGGCTTCGGGAACCTTAACAGTGAATTCTG[G/A]CTTGGTAMTGATAAAATCCACCTGCTCACCAAAGCCAAGGACATGATCCT

Long Flanking Sequence:

AAATCAAATGTGGAATGAAAACAAATGATGTCAGTGTTTGCATTTCAAAAATTCAAACCTGCAGAGGCGATGAACCCTGACCACAGAATCACATGATGATTAAAGGAATGCAATAAGCCCCACTAAACCAAATTATACATAGTTATTGAAACATAAAACATACTCTATATTTAAAAAAAATTGTTATACATTGTAATATTGCAAAACTTTTTAAATGTATGAAATGATAAAGCATGCTTAAAGGTCATCTCTCTCTACACAGACCTCACAAACATCCCTCCAAGAGACTGCTCAGACATCAGCATGCTGGGGCAAAGGATAAACAAGGTGTACCAGGTGACTCCTGATCCCAGGAATGGCAGCTTTGCGGTTTACTGTGACATGGAGTCATTTGGAGGTGGGTGGACCGTCATACAACATCGAATAAACGGCAGCGTGAGCTTCAACCGCACCTGGGCTGACTACAAGAAGGGCTTCGGGAACCTTAACAGTGAATTCTG[G/A]CTTGGTAATGATAAAATCCACCTGCTCACCAAAGCCAAGGACATGATCCTACGCATTGAGCTGGAAGACTCAGAGGGCACACGTGGATATGCCAAATATGATCAGTTCTATGTGTCCAATGAGTTCCTTCATTATCGGCTGTCTGTGAGCGGGTATTCGGGGACAGCTGGAAACGCTTTGCAGTTTAGCAAACACTTCAACCATGATCAGAAGTTCTTCACTACGCCGGATAAAGATAACGACAGATACCCCTCAGGCAACTGTGGGGCGTATTATGGTTCGGGATGGTGGTTTGATGCCTGCATGTCAGCAAACCTTAATGGCAAATACTACAAAACAAAGTACAAAGGGAAAAGGGATGGGATTTTTTGGGGAACGTGGCCCAATGCGACTTCTGAGTACTATCCGACAAGCTTCAGGCAAGCTTATAAAAATGTTAAAATGATGATAAGGCCGAAGAACTATGCACCCTAAGGCAACTCACAATAATAATAATTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15081

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022539	Nonsense	323	451	2	2

Genomic Location (Zv9):

Chromosome 4 (position 19115908)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	20459243
GRCz11	4	20180218

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCAAGGACATGATCCTACGCATTGMGCTGGAAGACTCAGAGGGCACACGT[G/T]GATATGCCAAATATGATCAGTTCTATGTGTCCAATGAGTTCCTTCATTAT

Long Flanking Sequence:

GAATCACATGATGATTAAAGGAATGCAATAAGCCCCACTAAACCAAATTATACATAGTTATTGAAACATAAAACATACTCTATATTTAAAAAAAATTGTTATACATTGTAATATTGCAAAACTTTTTAAATGTATGAAATGATAAAGCATGCTTAAAGGTCATCTCTCTCTACACAGACCTCACAAACATCCCTCCAAGAGACTGCTCAGACATCAGCATGCTGGGGCAAAGGATAAACAAGGTGTACCAGGTGACTCCTGATCCCAGGAATGGCAGCTTTGCGGTTTACTGTGACATGGAGTCATTTGGAGGTGGGTGGACCGTCATACAACATCGAATAAACGGCAGCGTGAGCTTCAACCGCACCTGGGCTGACTACAAGAAGGGCTTCGGGAACCTTAACAGTGAATTCTGGCTTGGTAATGATAAAATCCACCTGCTCACCAAAGCCAAGGACATGATCCTACGCATTGAGCTGGAAGACTCAGAGGGCACACGT[G/T]GATATGCCAAATATGATCAGTTCTATGTGTCCAATGAGTTCCTTCATTATCGGCTGTCTGTGAGCGGGTATTCGGGGACAGCTGGAAACGCTTTGCAGTTTAGCAAACACTTCAACCATGATCAGAAGTTCTTCACTACGCCGGATAAAGATAACGACAGATACCCCTCAGGCAACTGTGGGGCGTATTATGGTTCGGGATGGTGGTTTGATGCCTGCATGTCAGCAAACCTTAATGGCAAATACTACAAAACAAAGTACAAAGGGAAAAGGGATGGGATTTTTTGGGGAACGTGGCCCAATGCGACTTCTGAGTACTATCCGACAAGCTTCAGGCAAGCTTATAAAAATGTTAAAATGATGATAAGGCCGAAGAACTATGCACCCTAAGGCAACTCACAATAATAATAATTAATTATTTTTTGGGGGAACTTTTCCTCAAGACCAAATTGTGATGCAAATCCACAGACATTAACAGAACTGCCTTAAAAATATAAACCT

Associated Phenotype:

Not determined