ZMP
dhrs1
Ensembl ID:
ZFIN ID:
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 |
|---|---|---|---|
| sa18735 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12544 | Nonsense | Available for shipment | Available now |
| sa32983 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
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.
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:
sa12544
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:
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:
sa32983
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:
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