ZMP
far1
Ensembl ID:
ZFIN ID:
Description:
fatty acyl CoA reductase 1 [Source:RefSeq peptide;Acc:NP_998673]
Human Orthologue:
FAR1
Human Description:
fatty acyl CoA reductase 1 [Source:HGNC Symbol;Acc:26222]
Mouse Orthologue:
Far1
Mouse Description:
fatty acyl CoA reductase 1 Gene [Source:MGI Symbol;Acc:MGI:1914670]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13327 | Essential Splice Site | Available for shipment | Available now |
| sa39476 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13327
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061753 | Essential Splice Site | None | 432 | 1 | 11 |
| ENSDART00000139778 | None | None | 197 | None | 4 |
| ENSDART00000142564 | None | None | 181 | None | 3 |
| ENSDART00000146350 | Essential Splice Site | None | 464 | 1 | 11 |
| ENSDART00000146604 | None | None | 197 | None | 4 |
Genomic Location (Zv9):
Chromosome 25 (position 16437367)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 15983911 |
| GRCz11 | 25 | 16080311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGACCGACACGCAAAAAATAGTGCGGGGAAAATATATTCAACATCCAAG[G/A]TAAGCGTACGTGTGCTTCGCGATTGTATCTGAGGTTACCTCCNTTTTTTC
Long Flanking Sequence:
GTTAGCATGCAAATATAAGCTCCTGCCCAGTGAGGTCACACATTTTGATGCCATACATCTGTTCATAGGATTGACCTATAAGCTACAACATTGGTGCTTAATGCAAATGGATTTTACATTAGAGTGGCACTACTGTCCCTTTGGGGATTATAGGGAGAAATCCTTCAATCCTGCTCGGAGATCCTTAAATCCTGCATCCTATAATTTCCCCGTGTGATCTCTTTCCAGAACTCTCACTAGAGAATATACGTTGGATGTGAATTGTCATACAATTCGTTTTTTTCCACACAGGATTATTATTTTGCGCTTGGTGGTGGTGGATTGTGACGTCGGTTCTCTTCTGATAGGCATCACGATCTGGCAACCCATCACAGTTCCTCTCCAGCGAAGCTAAGCTACATCCCCTCTGCGTTTCCCATCACTGCTGAATAGAGTACTAGACCCTTCGTATCGACCGACACGCAAAAAATAGTGCGGGGAAAATATATTCAACATCCAAG[G/A]TAAGCGTACGTGTGCTTCGCGATTGTATCTGAGGTTACCTCCTTTTTTTCTGAGCGCAAAATTGAGTTTGCGCGTTTTTAGAGAGTGAAATGCTAGCCGTCGTTAGCACTTTCGCATGCTGGGGTTTTCACCGGTGTGTTGTAAATCTTGAAAGAAGCACAGCTGGAAAGTAGAGCTTGAGCTCATGATTTTAACAGTGATTAAAAAAATACACAATTTTATGTGTACCTGCGTTTTGTTTGCTTGTACAAATGGTGTCCATTCTCCTTTTTTTGCGTAAAGATCTGGAGATTTGATATAAAATAAATACATGAACGTCTGTTGAAACTTGCAAGACTTTTATTGACGTATGTATACACTGTTAATAATGTAATACGTGCTTATTTAATAACCGCAAAACGAACTGTCCTAATAGTTATGTACAACATGTAATATGCATCTTTTCCATATGCTTGAAAATACATTAAGGAAAAGTCAAGCACATCAACGTGAGTACAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39476
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061753 | Essential Splice Site | 256 | 432 | 6 | 11 |
| ENSDART00000139778 | None | None | 197 | None | 4 |
| ENSDART00000142564 | None | None | 181 | None | 3 |
| ENSDART00000146350 | Essential Splice Site | 256 | 464 | 6 | 11 |
| ENSDART00000146604 | None | None | 197 | None | 4 |
Genomic Location (Zv9):
Chromosome 25 (position 16467013)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 16013557 |
| GRCz11 | 25 | 16109957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGGCTGGATTGACAATTTCAACGGGCCTAGCGGGATATTCATCGCTG[T/C]GAGTATCAGTGTGCTGCTTTTGATGTAAAAATTTAGGTGCTGTTTGCTTA
Long Flanking Sequence:
ACTCGGCAGATGCCTGTATATGTTATTGATGAACAAACAAAATTGTCACTAATAAAAATAAAAATTTATTTTCCATAATACAGCTCAGAAATAACAAACTAATGCAAAATATATTAAAGAAATTTCAAGAAAGATTATCCACCTTTTTCTTTCAACTTCCTGTACGTGTTCACTTCTGACAGGTGGATGGATGACAAACTGGTGTCTTTGATGACACCTAGGCTGTTGGGTGAGCGGCCGAACACATACACCTACACTAAAGCGCTGGCAGAGCAGCTGGTCCAGCAAGAGTGTGGAAACCTCAACATCGCCATCATAAGACCCTCTATAGTAGGAGCCAGCTGGAAAGAGCCGTTCCCCGTAAGTGTGTGCTTTTACAAATGCCAACCTAACATTAAACAATACCACCTCCATATTAAACAGGCCATCTTCTTTCTTCTTTTGTTTTTTAAAGGGCTGGATTGACAATTTCAACGGGCCTAGCGGGATATTCATCGCTG[T/C]GAGTATCAGTGTGCTGCTTTTGATGTAAAAATTTAGGTGCTGTTTGCTTATCCATATAATGCTAGTGAACAGTGTCCAAGATTACGCCTTTAAAAGGTTTGTCAGATTTTATTTTTCATATTTATTTTTTTGAGTGATAAAGATCCAAAACACACTGCCAATGTAATGAAATCATATTTGGAGGGTAAAACAGCTGATGAAACAAAGACTTTCATGAAATGGCCTTCACAGAGTCCAGACCTGAATATTATATGCAGTATGTTTAAGCAATATTATATGACACTATACTCAATACAATATTGAACCATTTAGTATGACTTCCATGGTTTAATACGCATATACAGTACTGTGCAAAAGTTTTAAGACCCCAGTTACATTTGTAGTTTTAGTGAGGGTGTAATGACATTATATATTATTTCTCTTAACTAAAATACAACCAGAAAACACAGGCTCTAGTCAGATTTCTTTGGGTCACATTGTGAAGGACATATGAAAGAAAG
Associated Phenotype:
Not determined