Busch Lab

ZMP

dhrs1

Ensembl ID:
ENSDARG00000054300
ZFIN ID:
ZDB-GENE-030616-591
Description:
dehydrogenase/reductase SDR family member 1 [Source:RefSeq peptide;Acc:NP_001002205]
Human Orthologue:
DHRS1
Human Description:
dehydrogenase/reductase (SDR family) member 1 [Source:HGNC Symbol;Acc:16445]
Mouse Orthologue:
Dhrs1
Mouse Description:
dehydrogenase/reductase (SDR family) member 1 Gene [Source:MGI Symbol;Acc:MGI:1196314]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa12544 Nonsense Available for shipment Available now
sa18735 Nonsense Mutation detected in F1 DNA Not yet available
sa32983 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12544
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076478 Nonsense 235 310 7 9
ENSDART00000076478 Nonsense 235 310 7 9
Genomic Location (Zv9):
Chromosome 2 (position 37971676)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 38286590
GRCz11 2 38268918
KASP Assay ID:
2259-2407.1 (used for ordering genotyping assays)
KASP Sequence:
ACGTTTTCACTAATGGTGAGACGACGGAGCTTAGTGGACGATGCATAGTT[G/T]AGCTAGCRAAAGGTTAGATATTATTGWTATTATTSTAATTTTATTATTGA
Long Flanking Sequence:
TCAGACTATTTACAGTTTCTCAAAATAGCAACGCGTCAAAACACACCTGCTTTTTTAGATCAGAACGCCTATGGGCGCACATTTGAGCGCAAATGCATTTGCTATTTAAACAGCGTGGCGCAACACCTCAAAATGACTCTTGCGCTGAGCTAAAAGTAGCAAAAGAGTATTGCGCCGTGCCTTGCGCCACATTGTGCCGGGTGTATGATAGGACCCATAAAATGTTTGGATGAACCATCCCTTCATTTGGGAATCTTACTCCAGTTAAACGTTTGCTTCTTAAGTTAATCTGGAATAAATTGATAACACAAAAGGGTGGTATTTGACTGTTCAAGTCTATTCAATAAGTGCAAACTGGGAGTGACCTTAACAACACCATGCCTTAGGTATTTTAGTACAACAAGCCACTCATTTAATAACTTTATACAATCTGTCTTTCTCAGTACAAGGACGTTTTCACTAATGGTGAGACGACGGAGCTTAGTGGACGATGCATAGTT[G/T]AGCTAGCGAAAGGTTAGATATTATTGTTATTATTGTAATTTTATTATTGATTTAATGAGAACTGAAAGTTAAAAGTAATGAGATTATCTTAAAAATCTAATGGATGAAATGTGAACTGCTTATGAATGTGTTAACTTTTTTGTGACAAACAGATAAAGGTCTGATGTCAATGACTGGACAAGTGTTGATGACCTGTGAACTGGCCCGGCGCTATGGATTTAAGGATGTTGATGGTATGATTCTTATAAAAAAAGATACATGCCGTAGATGTAAGGGTTCCAAAATAAAACTGCACTGTATTTGATGAACTCTTTCTCTGTTTAGGTCGCAGTATTGTGGATTACACCTCTCTGAAGTTTGCCATTTCCCAGATACCCTACGTGTCCTGGCTATCCATTTTTACTCCTTCATTCATCAGAGTGCCTCGGTCCTTGCTGAGTCTTGGCAGTGGTAATTTCTAACCTGCATTGGTGCAGAGACAGAGCCTGCTTTTTTGGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18735
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076478 Nonsense 235 310 7 9
ENSDART00000076478 Nonsense 235 310 7 9
Genomic Location (Zv9):
Chromosome 2 (position 37971676)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 38286590
GRCz11 2 38268918
KASP Assay ID:
2259-2407.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTTTCACTAATGGTGAGACGACGGAGCTTAGTGGACGATGCATAGTT[G/T]AGCTAGCGAAAGGTTAGATATTATTGTTATTATTGTAATTTTATTATTGA
Long Flanking Sequence:
TCAGACTATTTACAGTTTCTCAAAATAGCAACGCGTCAAAACACACCTGCTTTTTTAGATCAGAACGCCTATGGGCGCACATTTGAGCGCAAATGCATTTGCTATTTAAACAGCGTGGCGCAACACCTCAAAATGACTCTTGCGCTGAGCTAAAAGTAGCAAAAGAGTATTGCGCCGTGCCTTGCGCCACATTGTGCCGGGTGTATGATAGGACCCATAAAATGTTTGGATGAACCATCCCTTCATTTGGGAATCTTACTCCAGTTAAACGTTTGCTTCTTAAGTTAATCTGGAATAAATTGATAACACAAAAGGGTGGTATTTGACTGTTCAAGTCTATTCAATAAGTGCAAACTGGGAGTGACCTTAACAACACCATGCCTTAGGTATTTTAGTACAACAAGCCACTCATTTAATAACTTTATACAATCTGTCTTTCTCAGTACAAGGACGTTTTCACTAATGGTGAGACGACGGAGCTTAGTGGACGATGCATAGTT[G/T]AGCTAGCGAAAGGTTAGATATTATTGTTATTATTGTAATTTTATTATTGATTTAATGAGAACTGAAAGTTAAAAGTAATGAGATTATCTTAAAAATCTAATGGATGAAATGTGAACTGCTTATGAATGTGTTAACTTTTTTGTGACAAACAGATAAAGGTCTGATGTCAATGACTGGACAAGTGTTGATGACCTGTGAACTGGCCCGGCGCTATGGATTTAAGGATGTTGATGGTATGATTCTTATAAAAAAAGATACATGCCGTAGATGTAAGGGTTCCAAAATAAAACTGCACTGTATTTGATGAACTCTTTCTCTGTTTAGGTCGCAGTATTGTGGATTACACCTCTCTGAAGTTTGCCATTTCCCAGATACCCTACGTGTCCTGGCTATCCATTTTTACTCCTTCATTCATCAGAGTGCCTCGGTCCTTGCTGAGTCTTGGCAGTGGTAATTTCTAACCTGCATTGGTGCAGAGACAGAGCCTGCTTTTTTGGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32983
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076478 Essential Splice Site 238 310 7 9
Genomic Location (Zv9):
Chromosome 2 (position 37971689)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 38286603
GRCz11 2 38268931
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGAGACGACGGAGCTTAGTGGACGATGCATAGTTGAGCTAGCGAAAG[G/A]TTAGATATTATTGTTATTATTGTAATTTTATTATTGATTTAATGAGAACT
Long Flanking Sequence:
AGTTTCTCAAAATAGCAACGCGTCAAAACACACCTGCTTTTTTAGATCAGAACGCCTATGGGCGCACATTTGAGCGCAAATGCATTTGCTATTTAAACAGCGTGGCGCAACACCTCAAAATGACTCTTGCGCTGAGCTAAAAGTAGCAAAAGAGTATTGCGCCGTGCCTTGCGCCACATTGTGCCGGGTGTATGATAGGACCCATAAAATGTTTGGATGAACCATCCCTTCATTTGGGAATCTTACTCCAGTTAAACGTTTGCTTCTTAAGTTAATCTGGAATAAATTGATAACACAAAAGGGTGGTATTTGACTGTTCAAGTCTATTCAATAAGTGCAAACTGGGAGTGACCTTAACAACACCATGCCTTAGGTATTTTAGTACAACAAGCCACTCATTTAATAACTTTATACAATCTGTCTTTCTCAGTACAAGGACGTTTTCACTAATGGTGAGACGACGGAGCTTAGTGGACGATGCATAGTTGAGCTAGCGAAAG[G/A]TTAGATATTATTGTTATTATTGTAATTTTATTATTGATTTAATGAGAACTGAAAGTTAAAAGTAATGAGATTATCTTAAAAATCTAATGGATGAAATGTGAACTGCTTATGAATGTGTTAACTTTTTTGTGACAAACAGATAAAGGTCTGATGTCAATGACTGGACAAGTGTTGATGACCTGTGAACTGGCCCGGCGCTATGGATTTAAGGATGTTGATGGTATGATTCTTATAAAAAAAGATACATGCCGTAGATGTAAGGGTTCCAAAATAAAACTGCACTGTATTTGATGAACTCTTTCTCTGTTTAGGTCGCAGTATTGTGGATTACACCTCTCTGAAGTTTGCCATTTCCCAGATACCCTACGTGTCCTGGCTATCCATTTTTACTCCTTCATTCATCAGAGTGCCTCGGTCCTTGCTGAGTCTTGGCAGTGGTAATTTCTAACCTGCATTGGTGCAGAGACAGAGCCTGCTTTTTTGGTTAATTCTCTCTTCTC
Associated Phenotype:
Not determined