ZMP
fsd1
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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