ZMP
retsat
Ensembl ID:
ZFIN ID:
Description:
Putative all-trans-retinol 13,14-reductase [Source:UniProtKB/Swiss-Prot;Acc:Q5BLE8]
Human Orthologue:
RETSAT
Human Description:
retinol saturase (all-trans-retinol 13,14-reductase) [Source:HGNC Symbol;Acc:25991]
Mouse Orthologue:
Retsat
Mouse Description:
retinol saturase (all trans retinol 13,14 reductase) Gene [Source:MGI Symbol;Acc:MGI:1914692]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33257 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44567 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1025 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa33257
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000013167 | Nonsense | 127 | 607 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 39184112)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39047472 |
| GRCz11 | 3 | 39189330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTTTCAGGCATCCACTATATTGGGGAACTGTCGAATCACAAGCCGT[T/G]ACGCTGTATTATTGACCAAATGACCAATGGGCAGCTGCAGTGGGATCCGC
Long Flanking Sequence:
TAACTTTAGTGGTTTTAATATGCACCCATAGAATGCAAAACTTCTCATTATAGACTTCTCATTATTATTGTTACAAAATAAAGTCTGTAGGCTGTACTACGTTACTGACCTTTGAATATTTTGCTCTTTATGAAACATCTGTTGTGTAACCTATCGTACATGTGTTTCCATATCCAGGTTTCTTGGCCAGTAGGGTTCCTGAGGATTTGGATGCAGTAGTGGTTGGCAGTGGGATTGGTGGACTGGCAATTGCTGTCCTGTTGGCCAAAGTGGGCAAGAAAGTTCTGGTTCTGGAGCAACATGACCGGGCTGGAGGATGCTGTCACACCTTTAAGGAGCAAGGCTTTGAGTTTGATGTTGGTGAGATGGACTTTTGTACCTCAGCATACAAACCTGCAAAATAGTGCTGTATGATCACCCAATAGGCAGTTTTGTTGTGGTCTGATTGCCTCTTTTTTCAGGCATCCACTATATTGGGGAACTGTCGAATCACAAGCCGT[T/G]ACGCTGTATTATTGACCAAATGACCAATGGGCAGCTGCAGTGGGATCCGCTGGAAAACCCCTTTGACAATGTGGTCATTGGTCCACCTGAAAACCGGCGCATATACCAAATCTACAGTGGCCGAAAACGCTACATGGACGAACTAAAGAAGTGCTTCCCAGGAGAGGAAAAGGCCATTGATGAATACGTGAGACTTTGCAAGGTGAGAAACAAGGATTGTGTTTAGTGGCTTTGACAAGGAAATATGAGGTTGTCTATCAGGTGTCAGTTGGGTGCTGGTTTAAATTTTTAAAAGGTTTTAGGTTAGCTCGAGCAATATTATTTTTTTTGAAATATTTAACATTTGTGGAAATTGCTTTTTTTATTGTAATAAATTTTCTATGTAAATGTCTGTGCTGACTGCTGAATATTCAGGTACTACTTCATTATCACATTCTTCAGAAATAATTCTGTTAAGTTACTTAGGGCCAATCCCAATTCCTTAATTTACTAAAATACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44567
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000013167 | Nonsense | 373 | 607 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 39179786)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39043146 |
| GRCz11 | 3 | 39185004 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGGGTGTTGTTTTTATTCTCATCCTCTACAGCAATTCAGAAACAGT[T/A]GAGTATGCTGCAGCATGGAGACAGTGGTCTCAGCATTTTCATTGGCCTGG
Long Flanking Sequence:
AGATTTAAAGAGAAACACAAGTCAATAGGGATATTGCAAACGACCAGCTTCTGCTCTAAACTGGACTGACTGAATATCTACTATTGTGTCTACTATTGAATAAACACAAATGTAAAATACAGTAAAACACCCTTAATCTGTTGAAACGGAATATGTGAATATATTAAATAGTTCACACAAAAATAGACAAAGAAATGCTTTCACTTTCACTTCACGCATACAGTAGTTTGTGAATGAACAGACTTACGTGTGCGTGTTGCAGAAGCGATCATGAGTCTGTTCTTGCGCTGAGTTTGAAGCAATCAGTCAGAGATCAGGAGAAAGTGCATTACTTTGATCATTTTAATATAGCATATTATAATGAAATCCAAAAATGATGCTATAATATTGAGAGTTAACTTTAATCTCGCGGCCCACCTGTATTATTATTACTGATGTGAATTGACAACCTTTTTGGGTGTTGTTTTTATTCTCATCCTCTACAGCAATTCAGAAACAGT[T/A]GAGTATGCTGCAGCATGGAGACAGTGGTCTCAGCATTTTCATTGGCCTGGATGGGACAAAAGAGGAGTTGGGCTTAAAAGCAGACAATTACTTTATCTACCCTGAGAACAATATAGACGAGCTGTGAGTGCAAATTTACCAGTCCTGAATAAACTAAAAGTGCTCTGTTTATTTGTATACAGATTTTCATTTTGTGTTCATGTCTGCTGTTATTCCAGGTTGGAGGATTATAGGAGCGGAAACAGGGAAGAATCTGCTAAAAAGAATCCTCTGATTTTTGTGGCCTCACCCTCTGCCAAAGACTCAACCTGGCCAGAAAGAACACCAGGTAAAGAGACAAACTAAAGATAAATCAATGCCCTGTTAACATCTGGAACTGTTATCAAATAGACTAAGTTGTTTGTAGCTTGTCCATATCTAGAAATCAGTAATCAAATCAGCTATCCATTATAATAACTGACAGTTCTGCTTGCTAAATCCAAATATTCTTCGCCTACAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1025
Status:
F2 line generated
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000013167 | Nonsense | 530 | 607 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 39178950)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39042310 |
| GRCz11 | 3 | 39184168 |
KASP Assay ID:
554-0929.1 (used for ordering genotyping assays)
KASP Sequence:
ACCCCAATCACTAATCAGCATTACATTGCCGCACCTAGGGGAGAGATTTA[T/A]GGCGCTGATCATGGAATTCCTCGCTTCAGTGCTGAACTGAATGCCACCAT
Long Flanking Sequence:
GACAAACTAAAGATAAATCAATGCCCTGTTAACATCTGGAACTGTTATCAAATAGACTAAGTTGTTTGTAGCTTGTCCATATCTAGAAATCAGTAATCAAATCAGCTATCCATTATAATAACTGACAGTTCTGCTTGCTAAATCCAAATATTCTTCGCCTACAGGTAAATCCACCCTGACTGTTGTTAGTTTTGCTAACTATGAATGGTTTGAAGAATGGAAAGATGACAAAGTGAAGAACAGAAGCACAGATTATAAGCAGTTGAAGGAGTTGTTCATCAATTACATATTAGAGGCAGTGACTGAGATCTATCCGAAGATCAAGGACAGGGTATAAATTCTCCAAACTGGAATTTTAACTCTAAATTGCAAATATTTCATGCACTTATCTTGTTTTCTCTTTGTTTTTCTCCATCTCTCTGTTTGTAGATTGAATATGTGGATGCAGGCACCCCAATCACTAATCAGCATTACATTGCCGCACCTAGGGGAGAGATTTA[T/A]GGCGCTGATCATGGAATTCCTCGCTTCAGTGCTGAACTGAATGCCACCATTAGAGCACAGACACCCATTAAAAACCTCTACCTTACAGGTGAGTGTTAAAAGTGGTGTTTAGAATGATGATAACTTCAGGTTAAGCCCATTTAAAATGGTTAAAGTATCATAAAACACAAAATTACAGATATTAACAGATCTCTTTGTATTGTACATCATGTTTTTTTTCCAGTCGGTGTAATTCTACTTGAAAAAGCAGTTTATTTTAAACTTTTTCACAGTATGTACATCTTCAAGACTTAAAGGTGCCATATAATGAATACTTGGATATACCTTGGCGTAGCTTAATAATAAGTTTCTAGTGCATTGTAATAGCATACAATGGACCTCAAACATCATTGTTTTTATCATTCCCCTTTAAATTTGTGTTCACATAAGATGATATGACTGGAATATGGATATGTCAGCAAGTCACACATCTCCATTGAAAATAACAAACTTGCGCAAAC
Associated Phenotype:
Not determined