Busch Lab

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