ZMP
wu:fc01d11
Ensembl ID:
ZFIN ID:
Human Orthologue:
FASN
Human Description:
fatty acid synthase [Source:HGNC Symbol;Acc:3594]
Mouse Orthologue:
Fasn
Mouse Description:
fatty acid synthase Gene [Source:MGI Symbol;Acc:MGI:95485]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16541 | Nonsense | Available for shipment | Available now |
sa8950 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11216 | Nonsense | Available for shipment | Available now |
sa44170 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8717 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16541
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 |
---|---|---|---|---|---|
ENSDART00000122088 | Nonsense | 31 | 1583 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 33757352)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 32637279 |
GRCz11 | 24 | 32551922 |
KASP Assay ID:
2261-8908.1 (used for ordering genotyping assays)
KASP Sequence:
TGGTTTTTGTATTTTGTGGGAATGGTRTTACCTATAGGGGAATGTGTAAA[C/T]AGCTGCTGAAAGAAGAACCTGTTTTTAGRAGCAAGGTCAAAGAGGTGGAA
Long Flanking Sequence:
TCTACTCGGCAGAAAATTCCAGCATAGATGCCAAAGCTCTCAATCTTAAAATCCCCACCAGAGCTGAGAAATGGCTTTACTCTGGGTCCAGGATAAAGATGGCTGGATTAAACAGCTTTGGGTTTGGTGGCACCAATGCCCATGCCATCATCACTGAGTATGTGCAAGCAGCAGTCTTTGATAGGCAGACTCTTGAACCTCTAAAACTACTCCCACTGTCTGCAGCCACGGATCAGTCTCTTCAATTGTGCATTGCTGACACATATCAGAGGATTTCAGCAGATGAGACAGTTGATCTACAAGCTCTTGCCTATACATCCGCCTGCCGAAGAAGCCACATTAGACACAAATTTAGAAAAGTCTTCGCTGCATCGTCTCTGTCAGAGTTAATCTCGCTTCTCAAAGCTAGCATGAATAAGAAATTAGCCCCAACAAAGCAGGACCAGAAATTGGTTTTTGTATTTTGTGGGAATGGTGTTACCTATAGGGGAATGTGTAAA[C/T]AGCTGCTGAAAGAAGAACCTGTTTTTAGGAGCAAGGTCAAAGAGGTGGAAAGCTACTTCCAGAAGTTCAAATGCAGTATTTCTCAAAAGATCTCAAGCAGCTACAAAGATGAAGATTTCTCTAAACCAGATGTTGTACAGCCACTTCTTTTTGCAATACAGGTTGGAATTGGACACCTTCTTAGGCACTGGGGAATCAGACCAGATATTGTTCTTGGGCATTCAGTAGGAGAGATTGCTGCAGCTCATTGCTCTGGTTTGCTGTCTCTTGAGGACGCAGTAAAGGTTGTATACCATCGTAGTTCTCTACAGACTAAAGTGACTGGTGGGAGGATGCTTGTTGTTGGCAACATTCCTGTTCTGGATGTTGTAGAAATTCTTCCTGCATACACAGGAAAGATTTGTCTAGCTGCTTTGAACAGTCCTATGTCTTGTGTACTGTCAGGTAACAAGCAAACTGTTGAGAATGTGCATCAAAAGCTTCAGTCTTTGTTTGAGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8950
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122088 | Nonsense | 666 | 1583 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 33759257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 32639184 |
GRCz11 | 24 | 32553827 |
KASP Assay ID:
2261-8909.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTTCTTGGAGCACATGGACATATCAGAGATYTGTGTTTCTTTAACAAT[C/T]AGAAGATTGACATTCACACTGAGAGCAGCTTCTCCAGGAGAATCAAGGCT
Long Flanking Sequence:
AGCAAACTATTCACCTCAGTAGTGTTTTGAAGAGATGCCAATCAGTAATTGAATCAAAGGATGTGTACGGCACTCTTAATGAAGTGGGATTTGAGTATGGGCCTAACTTTAAGCAACTTGAAGATATTCATTACGGACAAGAATTCAAAGAAGCAGTCACCAGAGTTGTGATTCCAGAAGGAGTACTCAACCATCTGTATGAGTATTGCTTGCACCCAGTAGTCCTAGATTACTTCTTGCAAATGTCTTCAGTTTTAGGATTAGTCTCTAGCACCATCAGGCCTGGATTTCCCTCTGCAATTGGTAGTATGGTTATATCTGCACCTCCCCATAAAGAGATGTTCATGTATATGAGATTGACCAAACAAATGTCAGACTACTTTGAGGTTTGTGGCTGCTTCACTGACAAAGATGGACATGTGTTGATTGAGCTAAGGGATGTGAGAATTACTTTTCTTGGAGCACATGGACATATCAGAGATCTGTGTTTCTTTAACAAT[C/T]AGAAGATTGACATTCACACTGAGAGCAGCTTCTCCAGGAGAATCAAGGCTTTGGTCTTTGAGGACACTTTTGGTATTGCTAAAGGTTTGAAGCCATATTTGCACCCAAAATCTGTATTTGTTCCTGAACCTGAATTAACAAAGAACTCAGCTTTCCTCGTACCAGAATTCAAGTCTACTTGCAGTGCAGCAGATATGGAACTTGACAAGATCCTGTTTATCTGGGGCATTCAGAGTATCAGTCACCTAAAATCTGAAGCTATTTTAGACTCCTTGGTCGACAGCTGTGAACTTTACCATCAGGTTGTTTTGTCTTTAAGAAACTGTGGCCGTGCATGCTCAATCCATGTCATTACCTACAGGTCAGCAGAAGGGATAGTTGACACTATAAGTCCTGCTTTTGTGTTGTCTGGCATGACAAGAGCATGTGCTGCAGAGTTGTCAGGCATTTCATTTCAGCTTATTGACCTTTCCACAGTGTCAAGAGAGGATATAGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11216
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 |
---|---|---|---|---|---|
ENSDART00000122088 | Nonsense | 1033 | 1583 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 33760358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 32640285 |
GRCz11 | 24 | 32554928 |
KASP Assay ID:
2261-8910.1 (used for ordering genotyping assays)
KASP Sequence:
TCCTGATCAGGGAGATACTSATTTGCATGTTACCAAACAYAACCARACAA[C/T]AGCAAAGTTTGAGCATCTTCTCGGCTGTTCGTGATTCAGCTCTGGTCAAG
Long Flanking Sequence:
CCACAATTGAAACAATGAATTCTAAATCAAAATGCCTACAGTACCACAACTTTACCTTGCAGACAACCAATCCCTACAGGATGACCAGCATATTAGCTTTGCCTTCAGAGAGTACAGTTAACACCATTGATAGGAAAAGCATTGAGATTCAGCTGAGTAAAGTATGTGTGCACTCATCAGATTATTTTCCAGTTAGTACTTCAGAGCTAAACTTTGGTCAGACAGTGTACTGGAATAAGCACAGTACTCAGAACCACCATCTCCTGGTACTCGATTTCTCCGGGATTGTTACGGCTGTGGGAAAGGATGTCAACAGACTTAAAGTGGGAGACCATGTGATTTGTTGTTATCCTGTAAAAGCTACTTCCAAGGTTGTTCTCCCTGAGGATGTGTGCTTCAAAATAAAAAGGTTTCCATTCCTGAAGGATGTGCCATGTGCTTCTTACCTTGTCCTGATCAGGGAGATACTCATTTGCATGTTACCAAACACAACCAAACAA[C/T]AGCAAAGTTTGAGCATCTTCTCGGCTGTTCGTGATTCAGCTCTGGTCAAGTTATTGACAATCATAGCAAGTAAATCAGGCTGGAGTGTTTTTACAGAAACTGAGATAAGTGGATTAGTCCAAAGTGCAAAGCAGTGCCATCTTTTAGTAATTATTCCCCCATTTGATTGTTCACTTTTGACAGAGATTGTCAGTGTTGCCAATGCATATCACACAATTGCACTGTGTGGCATCCGTGACCCAAGCTACTCTGCACTAGATGTATTTCAACAGGACTCTGAGAGGACTTGCTTCCAGACTCTTGAGATGTCCAAAATCTTCCAGAAGTCACGTCTCAAGGCACATGGTGCTTTTCTCCAGAAATGGCTAAAGGGAATGCACTTGCACAAAGTGTGGCCAACAATACAAAGCAGAACCTTTCAGATGGCACCCTCTGAAAGTATGCCTGCTCAGTATGTTGAGCATTCTGGATCTTATTTCAATGCAAGAACTGTGGATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44170
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122088 | Nonsense | 1331 | 1583 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 33761252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 32641179 |
GRCz11 | 24 | 32555822 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCCACAGTGCTGCTGTTCTCCATGATGGGTTACTGGAAACCCTTGAT[C/T]GATCTCTTTTCCGGAAAGTCCTGCAACCTAAAGTCTGCGGTGCTCTTAAT
Long Flanking Sequence:
GGCCAACAATACAAAGCAGAACCTTTCAGATGGCACCCTCTGAAAGTATGCCTGCTCAGTATGTTGAGCATTCTGGATCTTATTTCAATGCAAGAACTGTGGATGTGATCACTCTGGCCGCAGATGACCCCAGGACCAAGATATCTGCCATCCCTTTGCGTCCAAGAGCAAGGCAGCTATTCTCGAAGGAAGGTGTGTACATAATTTCAGGGGGTCTTTCTGGTTTGGGATTTGAAACTGTTAAGTTTGTTGCACAGAAAGGTGGAGGATGCATTGCCACTCTTTCAAGGAGTGCACCATCTGAGAAGGTACAAGATGACATTAATGGTCTCAAAAGAAGATACGGAGTAAGAATTCTTACTCTTCAGTGTGACGTCTCTGCACAGAAGCAAGTTATGGAAGCCATTACCATGATTGCCAATCATTTTTCCTGCCATCCAATCAGAGGGGTTTTCCACAGTGCTGCTGTTCTCCATGATGGGTTACTGGAAACCCTTGAT[C/T]GATCTCTTTTCCGGAAAGTCCTGCAACCTAAAGTCTGCGGTGCTCTTAATCTCCATCTTGCCACTCTGCACAGCAAGACACTCGATTACTTTGTGTGCTATTCCTCCATCTCCTCTTTCATCGGAAATGCTGCACAAGCTAACTACGCAGCAGCTAACTCATTTCTGGATACTTTTTGCCACTACCGACGTAATATCGGACTTCCAGGACAGTCTATCAATTGGGGTCCCCTTAAACTTGGCCTGCTAATGAACAAAGACAATTTTCAAAAGTTCCTGGAAACAAAAGGACTGATGATCATGGATGTGGCTGAGATCCATGAAGCACTAGAGCACTGCCTTTTGCTTGACAATCCCCAGCAAGTGGTGTGCAGATTTAATTTCAGAAACCTGAACAACCACGTCCTCTCCCAGAACATGTCTCTGAAGTTTCGTCTGTCTGCTTTAGTTGAGGAAGGACTAAAAAACAAAGATGCTGAGGATTCTGGCATAAGTGTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8717
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122088 | Nonsense | 1401 | 1583 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 33761462)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 32641389 |
GRCz11 | 24 | 32556032 |
KASP Assay ID:
2261-8911.1 (used for ordering genotyping assays)
KASP Sequence:
CATTTCTGGATAYTTTTTGCCACTACCGACGYAATATCGGACTTCCAGGA[C/T]AGTCTATCAATTGGGGTCCCCTTAAACTTGGCCTGCTAATGAACAAAGAC
Long Flanking Sequence:
GGGGTCTTTCTGGTTTGGGATTTGAAACTGTTAAGTTTGTTGCACAGAAAGGTGGAGGATGCATTGCCACTCTTTCAAGGAGTGCACCATCTGAGAAGGTACAAGATGACATTAATGGTCTCAAAAGAAGATACGGAGTAAGAATTCTTACTCTTCAGTGTGACGTCTCTGCACAGAAGCAAGTTATGGAAGCCATTACCATGATTGCCAATCATTTTTCCTGCCATCCAATCAGAGGGGTTTTCCACAGTGCTGCTGTTCTCCATGATGGGTTACTGGAAACCCTTGATCGATCTCTTTTCCGGAAAGTCCTGCAACCTAAAGTCTGCGGTGCTCTTAATCTCCATCTTGCCACTCTGCACAGCAAGACACTCGATTACTTTGTGTGCTATTCCTCCATCTCCTCTTTCATCGGAAATGCTGCACAAGCTAACTACGCAGCAGCTAACTCATTTCTGGATACTTTTTGCCACTACCGACGTAATATCGGACTTCCAGGA[C/T]AGTCTATCAATTGGGGTCCCCTTAAACTTGGCCTGCTAATGAACAAAGACAATTTTCAAAAGTTCCTGGAAACAAAAGGACTGATGATCATGGATGTGGCTGAGATCCATGAAGCACTAGAGCACTGCCTTTTGCTTGACAATCCCCAGCAAGTGGTGTGCAGATTTAATTTCAGAAACCTGAACAACCACGTCCTCTCCCAGAACATGTCTCTGAAGTTTCGTCTGTCTGCTTTAGTTGAGGAAGGACTAAAAAACAAAGATGCTGAGGATTCTGGCATAAGTGTTCAGTCATCAGTCGATGATTGTGTTCGAGTGATTCTGACTGAAATTTGCAGTGTTGATAGTGATGAGCTAAGTGATGAGACTACGCTTACTGCACTAGGGATTGACTCGATGTTGGCCATGACGCTGCAGAATCGCTTCTTTCAAGAGATGGGTGTAAATATTCCTCTTGTCGCTTTGCTCGATCCAAATTGTACGTTGTTGTCATTGACTGAA
Associated Phenotype:
Not determined