ZMP
zgc:154169
Ensembl ID:
ZFIN ID:
Description:
all-trans-13,14-dihydroretinol saturase [Source:RefSeq peptide;Acc:NP_001071261]
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 |
|---|---|---|---|
| sa40126 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33258 | Nonsense | Available for shipment | Available now |
| sa31348 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40126
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 |
|---|---|---|---|---|---|
| ENSDART00000102690 | Essential Splice Site | 328 | 607 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 39190347)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39053707 |
| GRCz11 | 3 | 39195565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCACCTGTAAACCGCATTCTCCTCAATGATGCTAAAGAGGCTATTGG[T/C]AAAACGTTCCACTTTCTATAAAGATATACTGTATCCTCTTACTACACTTA
Long Flanking Sequence:
TCTAATGCATCTGTTAGAAAGTCGCACCTGGAATATGGTTCATGGTCCTGCTGAAGCTTGCCCCGGCTCCTTTTGCAAAGTTCCTGGTGCGCACGGGTCTGGCCAGTCGCTTAACATCCTTCTTCAGCTATGCGTCCCGCAGCCTGAAGGATGTGGTGAATGAGCTTACACAGAATAAGGACCTGAGAGCCGTGCTCTCCTACATCTTTTTGACCTATGGTGAGATCACCTGACTTGACTGGAGATCAAGGTGCATGTCGACACTTGTACACATTTGTAGTCAACTTTTTCTGTTAAACAGGCAATATTCCCAAAGAAGCAAGCTTTTCCATGCATAGTATACTTGTGTGCCACTTCATGAATGGTGCTTGGTACCCCAAGGGTGGTGCCAGCGAGATCGCCTACCACATGATTCCCATTATTGAGAAGGCAGGAGGTGCTGTGCTTGTTAGAGCACCTGTAAACCGCATTCTCCTCAATGATGCTAAAGAGGCTATTGG[T/C]AAAACGTTCCACTTTCTATAAAGATATACTGTATCCTCTTACTACACTTACTACACTCAACTCTTTAATAAGAATATTAGCACTGTGAAAAGGTCATTCAGCTAATAACTGACTTGTTTTTTGGCATTATTGCAGGTGTGAGTGTTCTGAAGGGACAGGAGGAAGTGCATGTACGAGCCCCCATTGTGATTTCAGATGCTGGAATCTTTAATACCTATGAACATCTCCTGCCCAAAGATGTGCAGACTATGCCTGGTGAGAGAGAGAAACTACATTTCTTTTGCTATTAAGAAACAATATTCTTTCAAATCTTCACAATATAGATTATTCTTATCAATAATAATATTATTAGTTGTAAATTCTACCTTAGTTGTTATGATCCTGTACAGCAATTCAGAAACAGTTGAGTATGCTAAAGCATGGAGAGAGTGGTCTCAGCATTTTCATTGGTTTAAATGGGACAAAAGAGGAGCTCGAGCTAAAAGCGGACAATTTCTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33258
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 |
|---|---|---|---|---|---|
| ENSDART00000102690 | Nonsense | 355 | 607 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 39190129)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39053489 |
| GRCz11 | 3 | 39195347 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTACGAGCCCCCATTGTGATTTCAGATGCTGGAATCTTTAATACCTA[T/A]GAACATCTCCTGCCCAAAGATGTGCAGACTATGCCTGGTGAGAGAGAGAA
Long Flanking Sequence:
GGTGAGATCACCTGACTTGACTGGAGATCAAGGTGCATGTCGACACTTGTACACATTTGTAGTCAACTTTTTCTGTTAAACAGGCAATATTCCCAAAGAAGCAAGCTTTTCCATGCATAGTATACTTGTGTGCCACTTCATGAATGGTGCTTGGTACCCCAAGGGTGGTGCCAGCGAGATCGCCTACCACATGATTCCCATTATTGAGAAGGCAGGAGGTGCTGTGCTTGTTAGAGCACCTGTAAACCGCATTCTCCTCAATGATGCTAAAGAGGCTATTGGTAAAACGTTCCACTTTCTATAAAGATATACTGTATCCTCTTACTACACTTACTACACTCAACTCTTTAATAAGAATATTAGCACTGTGAAAAGGTCATTCAGCTAATAACTGACTTGTTTTTTGGCATTATTGCAGGTGTGAGTGTTCTGAAGGGACAGGAGGAAGTGCATGTACGAGCCCCCATTGTGATTTCAGATGCTGGAATCTTTAATACCTA[T/A]GAACATCTCCTGCCCAAAGATGTGCAGACTATGCCTGGTGAGAGAGAGAAACTACATTTCTTTTGCTATTAAGAAACAATATTCTTTCAAATCTTCACAATATAGATTATTCTTATCAATAATAATATTATTAGTTGTAAATTCTACCTTAGTTGTTATGATCCTGTACAGCAATTCAGAAACAGTTGAGTATGCTAAAGCATGGAGAGAGTGGTCTCAGCATTTTCATTGGTTTAAATGGGACAAAAGAGGAGCTCGAGCTAAAAGCGGACAATTTCTATGTCTTTCCTGAGAACAATTTTGATGAGCTGTGAGTGCAGAATCACCAGCTTCAATAGAATTGCTCTGTTTATTTGGTAAAAATATCTTTTAACTTGTGTTCATGTCTGCTGTTCTTCCAGGTTTGAGGCTTACAGGAAAGGAAACAGGGAAGACTCTGCTAAAAAGTTGCCTGTAATTTTTGTGGCCTCACCTTCTGCCAAAGACTCAACCTGGCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31348
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 |
|---|---|---|---|---|---|
| ENSDART00000102690 | Nonsense | 443 | 607 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 39189641)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39053001 |
| GRCz11 | 3 | 39194859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTAAAAAGTTGCCTGTAATTTTTGTGGCCTCACCTTCTGCCAAAGACT[C/A]AACCTGGCCAGAAAGGGAACCAGGTAAAGAGAAAAATGAAAAACACTTGA
Long Flanking Sequence:
CTTTAATACCTATGAACATCTCCTGCCCAAAGATGTGCAGACTATGCCTGGTGAGAGAGAGAAACTACATTTCTTTTGCTATTAAGAAACAATATTCTTTCAAATCTTCACAATATAGATTATTCTTATCAATAATAATATTATTAGTTGTAAATTCTACCTTAGTTGTTATGATCCTGTACAGCAATTCAGAAACAGTTGAGTATGCTAAAGCATGGAGAGAGTGGTCTCAGCATTTTCATTGGTTTAAATGGGACAAAAGAGGAGCTCGAGCTAAAAGCGGACAATTTCTATGTCTTTCCTGAGAACAATTTTGATGAGCTGTGAGTGCAGAATCACCAGCTTCAATAGAATTGCTCTGTTTATTTGGTAAAAATATCTTTTAACTTGTGTTCATGTCTGCTGTTCTTCCAGGTTTGAGGCTTACAGGAAAGGAAACAGGGAAGACTCTGCTAAAAAGTTGCCTGTAATTTTTGTGGCCTCACCTTCTGCCAAAGACT[C/A]AACCTGGCCAGAAAGGGAACCAGGTAAAGAGAAAAATGAAAAACACTTGAGGTCCTGTTTACATCTGGACTTAGGATTTTTATTGATCTGATCACATATCGACAAAGCTAATAAAGTAAATAGAGACACAATAGAGGAGGATTTAAGCGCTGCAGAATATATATATATATATATATATATATATATATATATATATATATATATAAATGTTAACAGAGAAATAGCTACATATAATCTTCATAAATCAAATCCAGGATGAATGAAAACACAAGTTTAAATACAAGACGTGTTAAATGAGTGACACTGAGTGTAGGACATAATGTATAGACTACTTTTGTGGTTTTATTTTGTGGAATAATTAAAAAGTATGCCATTATAACAGTATAAATATACCAGGGAACACACACTGTGTCCATAACAAGTCATGCTGTTTAGTTAAACCACCTTTAGCTTTGATTATAGCATGCATTGGCTGTGGCATCATTTCAATATGCTTCTGC
Associated Phenotype:
Not determined