ZMP
si:ch73-107c13.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate farnesyl-diphosphate farnesyltransferase 1 (FDFT1) [Source:UniPr
Human Orthologue:
FDFT1
Human Description:
farnesyl-diphosphate farnesyltransferase 1 [Source:HGNC Symbol;Acc:3629]
Mouse Orthologue:
Fdft1
Mouse Description:
farnesyl diphosphate farnesyl transferase 1 Gene [Source:MGI Symbol;Acc:MGI:102706]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6657 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6657
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084724 | Essential Splice Site | 127 | 418 | 3 | 8 |
ENSDART00000133280 | Essential Splice Site | 156 | 179 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53557855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53118247 |
GRCz11 | 20 | 52923664 |
KASP Assay ID:
554-5382.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCCAGAGCAGAGAGAAGGACCGGCGCGTGCTGGAGGATTTCCCCACMG[T/A]CAGTACAACATCAACAACACACTCGAAACACTGCAGAACTTTTATTTCTT
Long Flanking Sequence:
TACGGATGATCTGAGTGCAGGAATACAGGCATGACCTTGAGGAACGCAAGACTATATTATTTGCTTGAAAATGCTAATTGATATTGCAGCTAAAAATGAGATAAAAACATTTCACAAATAAAAACAAATCATAGATTCACCCGTCTGAGGTGATGTCCTAAATAGATCCATTTATTTGTTATTTCAATGTAGACTGAAGAATATTCTAAGCAGGCGTAGCTGCGTACTCCACACAATAGCCTTCATACCCAATGCATGTTATGCAAATTGTATATATAATGAAAGTGCATTTAAATGTGTGAGTGTGTGTGTCAGGCATGCGGTGTGTATCTTCTACCTGGTTCTGCGAGCGCTGGATACGGTGGAGGATGATATGAGCATCCCGCTGGAGCAGAAGCTGCCGCTGCTGCAGGACTTCCACACGTTCCTCTACCAGCCCGAGTGGAGCTTCAGCCAGAGCAGAGAGAAGGACCGGCGCGTGCTGGAGGATTTCCCCACCG[T/A]CAGTACAACATCAACAACACACTCGAAACACTGCAGAACTTTTATTTCTTACTACTAAATATACAGTTATTAAAAAAAAAAAAACGATGCATGTAGTTTTGGGGCGACGCAGTGGCGCAGTGGGTAGTGCTGTCGCCTACATGTGGTACAGGTGAATTGGGTAGGCTAAATTGTCCATAGTGTATAAGTGTGTATAGATTTTTCCCAGTGATGGGTTGCAGCTGGATAGGCATCCTCTGTGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAACGAATGCATGTAGAATTATATACATTTATGCAACAGTGCAATATTTTGCCATAGTCAGCAACAAGCAGAGGACTCTCTACAGTTTGACAAATATTGCAGCTATTGGGCAACGTAATGTACTTTTAAGGCTTTTTTAGTTGAGAATGTCATTGTTTAGATTAGAGATCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37183
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 |
---|---|---|---|---|---|
ENSDART00000084724 | Nonsense | 191 | 418 | 5 | 8 |
ENSDART00000133280 | None | None | 179 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53551633)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53112025 |
GRCz11 | 20 | 52917442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGGCGGGGCTGGTGGGCATCGGGCTCTCCCGGCTGTTCTCCGCATCC[C/T]AGCTGGAGGAGCCGGAGGTGGGCCGGGACACAGAGCTGGCCAACTCTATG
Long Flanking Sequence:
AGGTGTCCTAATAGTGTTTTTAGCAGTGTGGGACACATATACCACTGTCAACAGCTCAAACACATGTGTTTTGGTGTTTCGTGACGCTTTAATGCAACCTAACAGACTCCTCCTCCCCACCAAAACTGTTTGTTGTCATGGCACTGACAAAGAGGCGTGGTTAAGTATGTTAGCCACGCCCAATACATAATCTGACAATTGAACTGAACACTAACAGGAAGTGCATTTTCAGATTGCAATTAATGATTACAAGGACAAGCTATTTATTTTTCTTAATGACATGCACAGATGAATTGTTCAGCACAAAACTGGCAATGTGAGCTGACCAAATCAATATGGTTAGATTTGATGTCATGTGTACTTTAAATGTGGCTTTGGAAAAGGTGGAATGCTATCTCTTTAATTATTTGTGTTTGACGTGTCTGCATGTGTCTCCGCAGTACTGTCATTATGTGGCGGGGCTGGTGGGCATCGGGCTCTCCCGGCTGTTCTCCGCATCC[C/T]AGCTGGAGGAGCCGGAGGTGGGCCGGGACACAGAGCTGGCCAACTCTATGGGTCTGTTCCTGCAGAAGACCAACATCATCAGAGATTATCTGGAGGACCAGCAGCAGGGGAGAGCGTTCTGGCCAGAGGAGGTACACACACACACACACACATCAACATATACACTGCGGATGAGCTGAAATGACACCCGAATCCACGGCGTCATATTAATCATCCACCTGCCAGCGCATATAGTTTTATCTGATAAATGTATCCGCACCCGATCGTCACTTTAATAATTTAATTCTTAGTTTTAGGCATGATGATTATGGAAGCATACGAGTAGCATAATTCAATTCAAAATGTAATATGCAAAATGGCAATGCAATATGTTAAATGGCAATGTATTTCTGTATTTGAATTTGCATTTTCCAAGACATATGAGCAATGTTTGGTGCAGAATGAAAATGTAAATTAAATTACATTGTTTGCATTTCTCATTTCAAACACTGTTTTAATAT
Associated Phenotype:
Not determined