ZMP
fn1
Ensembl ID:
ZFIN ID:
Description:
fibronectin [Source:RefSeq peptide;Acc:NP_571595]
Human Orthologue:
FN1
Human Description:
fibronectin 1 [Source:HGNC Symbol;Acc:3778]
Mouse Orthologue:
Fn1
Mouse Description:
fibronectin 1 Gene [Source:MGI Symbol;Acc:MGI:95566]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12585 | Nonsense | Available for shipment | Available now |
sa21453 | Essential Splice Site | Available for shipment | Available now |
sa21452 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12585
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010521 | Nonsense | 156 | 2477 | 4 | 51 |
ENSDART00000124346 | Nonsense | 156 | 2480 | 4 | 46 |
The following transcripts of ENSDARG00000019815 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 15698343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 15450908 |
GRCz11 | 9 | 15422111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTACAAGATTGGAGACAYATGGCAGAGACCTCATGACACTGGAGACTA[C/A]ATGCTGGAGTGTGTCTGCTTGGGAAATGGGAAGGGGGAGTGGACCTGTAA
Long Flanking Sequence:
AACTTAAAATCTCCTTTAGTGTTCTACTACAGAAAAAAAAAGCCAACTACATCTAGGATGATAAATCCTGAAGATAAATCAATAAACTGCCAGTTTTCATTTTTGGAAGCATTAACTATGCCTTTAAGTTTTGTATGTTTGTATTTATACCAACTGGTGTGAAGAACAAAGTCCATGTGTGTTCCCAGCTGAGGAGACCTGCTACGATAAAGTCAATTCTCGTTCCTACCGGGTTGGAGAGACTTACGAGAGGCCCAAGGACGGAATGATCTGGGACTGTACTTGCATTGGCTCTGCCCGAGGGAAAATCAGTTGCACCATTGCGAGTGGGTAGACTGGAACTTTCCTTTACTGTACTTAACCGCAAGTTGGGAATTAGACTTTTGGAAGTTGTGCTTGCTGTTTACCTACTTGGCCTCTGTTGTAGACCGCTGTCATGAGGGAGGGCACTCCTACAAGATTGGAGACACATGGCAGAGACCTCATGACACTGGAGACTA[C/A]ATGCTGGAGTGTGTCTGCTTGGGAAATGGGAAGGGGGAGTGGACCTGTAAACCTGTTGGTAAGTTTGGACTTTTTCATCCCATCATCAAGTTTTGTGGTTTGCTATACTCTTAAGCATTACATTTAACAGATTAATAATAAATAGATTTTTAAGGCTGGAAAACCAAATAAGTTCTAGATTAAGAAACTCCTTCTTCTGTCAGTTGGTGTGATTTTAAGTTAACCTGCCGGCAGCTAGCTCTCTGCAACTCTCACATGGTCGCCCACTGAAGCTAAGCAGGGCTGCGCCCAGTCAGTACCTGGATGGGAGACCACATGGGAAAGCTAGGTTGCTGCCGGAAGTGGTGTTAGTGAGGCCAGCAGGGGGCGCCCAACTTGCGGTCTGTGTGGGTCCTAATGCCCCAGTATAGTGACGGGGACTCTATACTGCTCTGTGAGCGCCGTCTTTCGGATGAGACGTTAAACTGAGGTCCCGACTCTCTGTGGTCATTAAAAATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21453
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010521 | Essential Splice Site | 341 | 2477 | None | 51 |
ENSDART00000124346 | Essential Splice Site | 341 | 2480 | None | 46 |
The following transcripts of ENSDARG00000019815 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 15693775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 15446340 |
GRCz11 | 9 | 15417543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTTAGACTGAATGGTTTTTATCTAAGTTTCTTACTGTCTTTTGTGT[A/T]GAGAGTCAATCTCAGGTGTATGGCGGGACCTCAGGTGGCGAACCGTGTGC
Long Flanking Sequence:
TCAAAAATGATACAGGAATATTGTAGAGCAGAACATTTTTCGTTTGTCTGAAACCTTTTTAAAGGCCTTCTTATGCTAAAAATGGTACTAATACATTCAAATGTAAATGTATTATTGGCGTCCATTCATATAAACTTGCATAAGACCCCTAGTGTTCCCCGCCCACCTAATGAATGTAGAAACTAAATGTGTATCCTATGTTTTATTTTTAACTGCAGGTACTGGGTCTCGTGTTGTGACCAATGTCCAGCCAGCAGTGTACCACCCACAAGGGGTGCCTGAACACCCTGTGGAGGGATCCTGTCTGACTGAAGCAGGTGTTTCCTATGCTCCAGGCATGCGCTGGAGCAAGGCTCAAGGTAGCAAGCAGATGTTGTGTACCTGCTTAGGAAACGGTGTCAGCTGTGAAGAGTCAGGTTTGTGTCTTTTATTCAAACAAGTCTGTCATTTTTCATTTAGACTGAATGGTTTTTATCTAAGTTTCTTACTGTCTTTTGTGT[A/T]GAGAGTCAATCTCAGGTGTATGGCGGGACCTCAGGTGGCGAACCGTGTGCTTTCCCTTTTGTGTTCATGGGGAAAACGTTTTACTCCTGCACGTCTGAGGGACGCAATGATGGACAGCTTTGGTGCAGCACCTCATCTGACTTTGAGAAAGACTACAAGTATTCCTTCTGTACCAGCAACAATGGTAAGTTCATAACAGAGTTTGTAAGATTTTATTTGTTGAAAGACTTCTTTTATACTGTCTATATACGAGTGATTGTATTTTATCAGAGTTAAAGTATGTTTTTAAACATATTTTTAACAATTTATTATGAATGTTATATATTTTAATATGTTAATTTGGCATCCAATAAAGCTTTGTATGTTAAATCAATGTTGAATAAAGTTGTGCAGCATGATATTTTTGTGGAAGCTTTTCAAATGATTAATTTATACAGTAAATGTGACCCTAAATCCTAGTCTTACGTTGCATAAGTAAACATATACAATAATATTTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21452
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010521 | Nonsense | 787 | 2477 | 16 | 51 |
ENSDART00000124346 | Nonsense | 787 | 2480 | 16 | 46 |
The following transcripts of ENSDARG00000019815 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 15675924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 15428489 |
GRCz11 | 9 | 15399692 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAACATCAGTGAACTTCTGCCAGGAAGGAAGTACACTGTGAATGTATA[T/A]GAAGTGACAGGAGAAGGAGAACCTAACCTCATCCTCACCACTTCCCAGAC
Long Flanking Sequence:
TGTAGGTCATCCAGCTTTGTCTCGTTAACTAAATGTGTATCCATGTTTTAGTGCAGAAATTATTATTCTTATTATGCAAGTTCATGAATGGGACACAATATATCCAACATCTCTCTAGTGGAGACCTCTGAGGGTGAGACCACCCAGCCCCCTCGAATGGTGGACACCTCTGAGTCAGTGACTGAAATCACCTCAAGCAGTTTCGTCATCTCCTGGGTGTCTGCGTCTGACACCGTGTCTGGTTTTAGGGTGGAATATGAGCTGAGTGAAGAGGGAGGCCAGACTGGACAGCCCATGATCTTGGGTCAGTATCTTCACCTCAAGTATGGTGTCATCAGCTTAGACTAGTAAACCTCATAATACTGATTTGCAAAAATTGTATGCTCCAATTTTCATAATACCGGTCAACTTGATGATCTGTTTCCAGACCTCCCTCATAGCGCTACGTCCGTGAACATCAGTGAACTTCTGCCAGGAAGGAAGTACACTGTGAATGTATA[T/A]GAAGTGACAGGAGAAGGAGAACCTAACCTCATCCTCACCACTTCCCAGACTACTGGTGAGCCTTTTCTCTCCGTCTTTTTTCTCTTTTACAAAAAAATGGCTTGAAATATCTCTAAATGTGTATATATATATATATATATATATATATATATATATACATACATACATACATACATACATACATACATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACATATATATATAAAAAAATTAAAACATTAAAAAAACCTAACAAAACAAACTAGTGTTTTGACATTAAAATATGTGGCTAAGAAATAAAAAAAACTTTGTTTTTTTCTGTTGTGGCAAGCAAAAAAAGAAAAGAAAAGAAAATAGCCAGGAAATTAGAAAAAATCCTTAGTGTTTAGCTCTGTATAAGTCTAAAATTTATGATGGTCTTAAAAGGGTTTTAAAAAGTCTTATATTTGACATGATGATGGCTGCAGA
Associated Phenotype:
Not determined