ZMP
dhcr24
Ensembl ID:
ZFIN ID:
Description:
24-dehydrocholesterol reductase [Source:RefSeq peptide;Acc:NP_001008645]
Human Orthologue:
DHCR24
Human Description:
24-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:2859]
Mouse Orthologue:
Dhcr24
Mouse Description:
24-dehydrocholesterol reductase Gene [Source:MGI Symbol;Acc:MGI:1922004]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15847 | Nonsense | Available for shipment | Available now |
| sa3089 | Nonsense | F2 line generated | Not yet available |
| sa5668 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa15847
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 |
|---|---|---|---|---|---|
| ENSDART00000125019 | Nonsense | 50 | 516 | 1 | 9 |
The following transcripts of ENSDARG00000013236 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 7351270)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 7186663 |
| GRCz11 | 20 | 7176542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCGTGTGCCTGTTTCTCCTGCCCTTGTCCGTCGTGTTTGATGTRTACTA[T/A]CAYCTGCGCGCCTGGATCATCTTCAAGATGTGCTCCGCGCCCAAACAGCA
Long Flanking Sequence:
CAGACAGAAAGAACAAGTATCTGCTATATCAGTAAATTTTAACAGCAGCATAGTAATGAACATCGCACTGTCAATGGTGTGACGGTGTTCCTTTCTTGTGATTGGCCGATGAGACTCCACGCAGCCACTGGCGTCATCTGATTTGACGTCCTACCGACCAATCAGCGCACGCAGGGGGCGGTGCCTTGACCACCTGGGCATGTTTCTAAACACCACGCAAATGATAGATGTCAAATCGTACGCGTGCAAGCGGGGAAACTGTGCTCAAGGGAAACGAGGAGACGCATGAAATAACTGTTTATTAAGCTTCATGCGTTTTTAAAGTGCTTGCAAATTCAAAACGTCGTCGGCATGGATCCGTTATTGTATTTGGGAGGGTTAGCTGTGTTGTTTTTGATATGGATCAAAGTGAAAGGCTTGGAGTACGTGATTATACACCAGAGATGGATCTTCGTGTGCCTGTTTCTCCTGCCCTTGTCCGTCGTGTTTGATGTGTACTA[T/A]CACCTGCGCGCCTGGATCATCTTCAAGATGTGCTCCGCGCCCAAACAGCACGACCAGCGGGTCAGAGACATTCAGAGACAGGTAAAGTTAAAAGCACCAAACCTGCAGCGTGGACGACCCTTGTTACTTAATGATAGACAACTTTTACTGAATATGGCATGCGAATATACTTTAATATTGGACTCAAAGGAATTTATGACAGTTTTATGTAGTAGGTATATTAATATGATTATAATATTATGAATATGCATGTACAGTCTATTTGAGAATTGTTTAGAGTTTTTAAAAGAAATGCTGTTTTAAAAAAATGTTAATAAATGTTATTTCTGTGGCAGTTACGTTGTGGTACAGGTAGGGGCGTGACAAAGTTGTATGGACACGCCCCTTACTTTTTTATTGATTAACAGGAAAGTACAGAGTTATACATAAAACAGTATATAAGGGAATTAACAACAGAAATTAATCATGCACATTAAGTATATTATTCAGCAGTGGGGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3089
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125019 | Nonsense | 482 | 516 | 9 | 9 |
| ENSDART00000125019 | Nonsense | 482 | 516 | 9 | 9 |
The following transcripts of ENSDARG00000013236 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 7324091)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 7159484 |
| GRCz11 | 20 | 7149363 |
KASP Assay ID:
554-3402.1 (used for ordering genotyping assays)
KASP Sequence:
AGATTCCAGATGTTGTATGCTGATGTATACATGGAACRCAAKGAATTCTG[G/A]GAGATGTTTGACGGCACTTTGTATCACAAACTCAGAGAGGAGCTCGGCTG
Long Flanking Sequence:
AGTTTTCACTCTTTTCCATTTGGTTAGATGAACAATGTTAAAAACACCATACATTTACATGCATTTTATTTCACTGGAATTACACAGATATACCTAAATATACCAGTTCCAGCTGAAATGAACAGTTATTTTAATTAGCTGAGTTTAAGAAAACCATGATTATATCTGAATTTATTTAACGACAGAGTCACAATTTAATCATTAATCACTTGTTTGGTCATTTTTATTTTCTCGTTGTATTAAAATTGTACCAAACTGACTTTTTATTTATTTATTTATTTATTTTTGTCAGATTTGTAATAACCCTTCATTTTAATTACTGTTACGAAAAACACTGCTGTAATACTTAACAACCAGCTTTTAAAATCCAGTTAATTTGTTTTAAATTCTTTAGAAGTATACAATATTCTAGTATTTCCTTCACAGCAATAACACAACACCTCCTTTTGTAGATTCCAGATGTTGTATGCTGATGTATACATGGAACGCAAGGAATTCTG[G/A]GAGATGTTTGACGGCACTTTGTATCACAAACTCAGAGAGGAGCTCGGCTGTAAAGATGCATTCCCTGAAGTCTTTGACAAAATCTGCAAGTCTGCAAGACATTGAATCCAAATGAACCTGAGACATGGCCAAAACAATAAACAAAACATATGATATATTGCTGACAACATTGGGGTCAGACACACTTAAAACATAGATACTCTTATTCACAATGGAGCACCAGCAAATGTGACAATATTTTATAAAAATAATTTTTATTCCTTTATTTTTGGGCCCTTTTTATTTTTTACGGTTTAAACACTATTCATATAAACAATAAATATTGCTTAAAGGATTTTGAATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATGTATATATGTATGTATATATATACACACACACACACACACACACACACACACAGTTGAAGTCAGAATTATTAGCACCCTTTTGATTTTTATTTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5668
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125019 | Nonsense | 482 | 516 | 9 | 9 |
| ENSDART00000125019 | Nonsense | 482 | 516 | 9 | 9 |
The following transcripts of ENSDARG00000013236 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 7324091)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 7159484 |
| GRCz11 | 20 | 7149363 |
KASP Assay ID:
554-3402.1 (used for ordering genotyping assays)
KASP Sequence:
AGATTCCAGATGTTGTATGCTGATGTATACATGGAACRCAAKGAATTCTG[G/A]GAGATGTTTGACGGCACTTTGTATCACAAACTCAGAGAGGAGCTCGGCTG
Long Flanking Sequence:
AGTTTTCACTCTTTTCCATTTGGTTAGATGAACAATGTTAAAAACACCATACATTTACATGCATTTTATTTCACTGGAATTACACAGATATACCTAAATATACCAGTTCCAGCTGAAATGAACAGTTATTTTAATTAGCTGAGTTTAAGAAAACCATGATTATATCTGAATTTATTTAACGACAGAGTCACAATTTAATCATTAATCACTTGTTTGGTCATTTTTATTTTCTCGTTGTATTAAAATTGTACCAAACTGACTTTTTATTTATTTATTTATTTATTTTTGTCAGATTTGTAATAACCCTTCATTTTAATTACTGTTACGAAAAACACTGCTGTAATACTTAACAACCAGCTTTTAAAATCCAGTTAATTTGTTTTAAATTCTTTAGAAGTATACAATATTCTAGTATTTCCTTCACAGCAATAACACAACACCTCCTTTTGTAGATTCCAGATGTTGTATGCTGATGTATACATGGAACGCAAGGAATTCTG[G/A]GAGATGTTTGACGGCACTTTGTATCACAAACTCAGAGAGGAGCTCGGCTGTAAAGATGCATTCCCTGAAGTCTTTGACAAAATCTGCAAGTCTGCAAGACATTGAATCCAAATGAACCTGAGACATGGCCAAAACAATAAACAAAACATATGATATATTGCTGACAACATTGGGGTCAGACACACTTAAAACATAGATACTCTTATTCACAATGGAGCACCAGCAAATGTGACAATATTTTATAAAAATAATTTTTATTCCTTTATTTTTGGGCCCTTTTTATTTTTTACGGTTTAAACACTATTCATATAAACAATAAATATTGCTTAAAGGATTTTGAATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATGTATATATGTATGTATATATATACACACACACACACACACACACACACACACAGTTGAAGTCAGAATTATTAGCACCCTTTTGATTTTTATTTTCTTT
Associated Phenotype:
Not determined