Busch Lab

ZMP

retsat

Ensembl ID:
ENSDARG00000018600
ZFIN ID:
ZDB-GENE-050320-11
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.
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.
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.
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