ZMP

fsd1

Ensembl ID:

ENSDARG00000062017

ZFIN ID:

ZDB-GENE-060503-218

Description:

Fibronectin type III and SPRY domain-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q1LY10]

Human Orthologue:

FSD1

Human Description:

fibronectin type III and SPRY domain containing 1 [Source:HGNC Symbol;Acc:13745]

Mouse Orthologue:

Fsd1

Mouse Description:

fibronectin type 3 and SPRY domain-containing protein Gene [Source:MGI Symbol;Acc:MGI:1934858]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15589	Nonsense	Available for shipment	Available now
sa7611	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15589

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089141	Nonsense	42	494	3	14

Genomic Location (Zv9):

Chromosome 8 (position 19152733)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	18597621
GRCz11	8	18628613

KASP Assay ID:

2260-0414.1 (used for ordering genotyping assays)

KASP Sequence:

RGACATGCTGCTTGAACTCTTGGTCACGGTGTGTGCAGGCGAATTCAAAC[C/T]GAGTGCAGGAAGACCWGGAGTCAGAGTTTAGTTCGCTGCATTCGGTCCTG

Long Flanking Sequence:

TTGTTTTTTTTTTCTTTGGTCACTTCTGCTACACTAAACGGTTACAAAAAAACAATGGTACAATTCTTCATTTATTAAGCACTTCATTTATTTAGAATATGCTTCCCAGAACAGGACATGTTTTACCCTTTTTATGATCAGGTATCCTCTAACCTATTGTTTTTTTTCTGGTTATGATGTGGCATTTCATGATTATTAAGATTGTGTTTCATGTTTCAGGAGTCACTGAGGAAGATTATCACTACACTGGCTCTGAAAAATGAGGAAATTCAAAATTTCATTTGCTCTCTAAAGCAGAGTCTGGAGAACCTAGAGGTAAACACTACAGGAGGCCAGTTCTCTTTACTCACACTTAGTTATCAAACTGTTTGATAAGTGAGAAGATGTCTTTGTCAGCTCTTAATATGTTTCAAGCACAGTGTTAATTTCGCAAAACATCAATAAGTTTGAGGACATGCTGCTTGAACTCTTGGTCACGGTGTGTGCAGGCGAATTCAAAC[C/T]GAGTGCAGGAAGACCTGGAGTCAGAGTTTAGTTCGCTGCATTCGGTCCTGGATGACCTGAAAGAGGGAATGGTTACACGGATCAAGCAAGAAAGAGCCAGTCGCACATATGAGCTACAGGTGAGAGCATCGTGAAGATTCCTGTCGTACTCTGACAGCCATTTATTACAATTCAAGTGAAACCACATTCACATGCTGAACCCCATTCAGATCAGTTTGTGACATCAGTGAATCGTTTACTGGAGACTCACTCTGAATGGATCACTTGAATCAGTGAGTCGTTTACCAGAAACCCACTCTGAATGAATCATTTGCATCAGAATTGTTTGTTGACGTCTGAACAGACACCAGTCCTATTCAAATACTAATTGTTCAGTGTAGTATGTAAACCGATTTAACAGGTTAACTGATAAAATACAGCTTGTTTACGAATTAAACAGCACTTTCTCGTCTCTGAAAAGGTCACAATTTCTCCTTTTCAACATACATTTTTACTCTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7611

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089141	Missense	211	494	8	14

Genomic Location (Zv9):

Chromosome 8 (position 19159410)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	18604298
GRCz11	8	18635291

KASP Assay ID:

554-4259.1 (used for ordering genotyping assays)

KASP Sequence:

TCGACCACTACATCCTGGAGCATCGRAAAACCAATCAYGAGGGTCCACCG[C/T]GGGYTCGTGAGGACTATCCCTGGATGGTGGTGGAGGGAATTAAAGAAACT

Long Flanking Sequence:

CAATGAAATGGTGTAAATTACCCAGATTTTGATTAAATACTGTCACCTGACAAAGACTTTGGTGAGCAAGTCAGTGGCAGATTCGGCTCACCTGTGTATTCAGCATTATTTTAAAAGTGATACTGCATTAGATAATACAATTTAACACAATATTTTCTTTTTTTAATATTATGAAATAAATTAGGAAATTACCCATGGCAATTTTAATGTAAAATAGTTTGCCATATTTACCCTTGGCCCACGGCTCTCAATGATATTTGGTTTTTGGCCACTCATACGGAAAAAGTAAAAAAAAAAAGTTCTGGTTAGTATGTGTGAAGCTCTATGATATCAGATCTCTGTGTTGTTCACCTTCAGTGCCAGCCACTCCCGAAATTCATGTTGCCGATTGCCAGGTGTTTGATAACACAGTGACAGTGGTGTGGACCTTACCGGAACCCGACTCCAAAATCGACCACTACATCCTGGAGCATCGGAAAACCAATCATGAGGGTCCACCG[C/T]GGGCTCGTGAGGACTATCCCTGGATGGTGGTGGAGGGAATTAAAGAAACTGAGTACACACTCACAGGTACAGTAAATGCTGACGCATGTTCTGGATCCGATAGTTTAAATGAAGATGTAATAATCATGATGTCATTTGTTTTTCCAGGCGTTCGTTTTGACACGCGCTACATGACCTTTAGAGTGAAGGCATGTAATAAAGCAGTGGCGGGTGAATTCTCAGAGCCGGTTACTCTAGAAACACATGGTTGGTAGCTTAATGTTTGCGCACACACACACACACACACACACACACACACACACACACACACAGAGGGTAATGAGGCATGAGGTTTCTTCTCACATAGAAAAAAAGAGTCTTACACGAGTTGCAAAGCACTAGCCCTACTAAACTAAAGCTGATTCAAAGGGCACAGATGTAGCACGTCTGCCCTTTTGTGAAATACTATTTATGGTTGTCAATTTAATGTATTTTTAGTGTAATTAACGCTAAAAGAACAA

Associated Phenotype:

Not determined