ZMP
dmrt1
Ensembl ID:
ZFIN ID:
Description:
doublesex- and mab-3-related transcription factor 1 isoform 1 [Source:RefSeq peptide;Acc:NP_991191]
Human Orthologue:
DMRT1
Human Description:
doublesex and mab-3 related transcription factor 1 [Source:HGNC Symbol;Acc:2934]
Mouse Orthologue:
Dmrt1
Mouse Description:
doublesex and mab-3 related transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:1354733]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31472 | Nonsense | Available for shipment | Available now |
| sa26559 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31472
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 |
|---|---|---|---|---|---|
| ENSDART00000044361 | Nonsense | 48 | 267 | 1 | 5 |
| ENSDART00000124637 | Nonsense | 48 | 268 | 1 | 5 |
| ENSDART00000126066 | Nonsense | 48 | 256 | 1 | 5 |
| ENSDART00000128825 | Nonsense | 48 | 191 | 1 | 4 |
| ENSDART00000130428 | Nonsense | 48 | 190 | 1 | 4 |
The following transcripts of ENSDARG00000007349 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46563669)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 44344934 |
| GRCz11 | 5 | 44945087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCGCTGAAGGGCCACAAACGCTTCTGTAATTGGAGAGACTGCCAGTG[T/A]CAGAAATGCAGACTCATCGCCGAGAGACAGCGGGTCATGGCTGCCCAGGT
Long Flanking Sequence:
GTGACGGGCAGGACATTTTAAAATCAAATCAGGCAGGATTAAAACAAGCTAATATGAACCAAAATATAACAAATGGGCTGCAGCTTTTATAAAACAATAGCAGCCTTAAACACCCTTTATTGTGGTGTTTGCTCGATGTGTTGTGATATCATGAGGCGCTTTGGGAGTCTCAGTGTGAAGGAGCGGACATCATCATCATCATCATCCTCCTCGTCTCCCACGAGCTCTGGAATGCACAGGTTCCTCGTGCCAACACATGCGCCCATTGTAACGTTATCAAACCTCAGACCCTATTTATAAGCGCCGATAATCCCCATTCAGAGCAGAGCAGACTGGCCATCACCATTAGCTGTCAGGATGAGTGAAGAAGAGCAGACTAACGGGTCGCTGTCCATCAGGAAACCGTCCCGGATGCCGAAGTGCTCTCGCTGCAGAAACCACGGCTTCGTGTCACCGCTGAAGGGCCACAAACGCTTCTGTAATTGGAGAGACTGCCAGTG[T/A]CAGAAATGCAGACTCATCGCCGAGAGACAGCGGGTCATGGCTGCCCAGGTAACTTAGACATCCTCGACAAGGCCATGAGAGGTCATTTTGTATTTTGTATAACGTTTTAAATTATTAAATATTATTACCTCGTATCTACAGCCATCACGTGTTTAATTTCGTGTGCGTTGTTTACAAACACAAGTTGTATTTAAGTATTACTATAACACCGCCGTCGAGTTTACAAATAATTTAATTGTTTGCTACAATTGTCTTGATAAATTGTTTATATTCATAGTAAAGTTTGGTCGGTTAGCTACATTGTTGACTGCTTTGGCTAGCTGCAGTTTGGCGCCGTTTTTATCAAGACAGTGACGTTACAAAAACACCATTTATTTTCATGTAAAGTTAACTTATTACAATTTATTTAAACCACGTTTAAATGCCTCGTGCTAATTTTGTTACCTAGAGGGTGAATTTGGGGACTTCATTTGACTTATTTTGTCGTGTTAGGTGGCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26559
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 > A
Consequence:
Essential Splice Site, Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044361 | Splice Site | None | 267 | None | 5 |
| ENSDART00000124637 | Essential Splice Site | 224 | 268 | None | 5 |
| ENSDART00000126066 | None | None | 256 | None | 5 |
| ENSDART00000128825 | Essential Splice Site | 177 | 191 | None | 4 |
| ENSDART00000130428 | Splice Site | None | 190 | None | 4 |
The following transcripts of ENSDARG00000007349 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46608090)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 44389355 |
| GRCz11 | 5 | 44989508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCGCCAATAATAAACACCAAATAGTTCATGTTTCATGATCCATCCCAT[T/A]TCAGCTTTCTCCGATGGAGCTCAAGACTCTGTGTCCATCAGCTCGATGAT
Long Flanking Sequence:
AAATGGCTGCTGTTTTTTAACATTCTTTAGAAAATCTTGTTTCGTGCTCAACAGAAAACTAAAAAATGCATAGATGTTTAAAACCATTTAAGGGTAATTACATGGTGAAGTTTTTGTTTTTGGGTGAACTACACCTTTAATCTTGAATGATGCCTCTATTGTTTATTGTTAAGTCTTAACCAGATTTCTTTTACTTGGAAAAAAACATGCCTGAGATTTCTGAATCTCAGGTATAAACACTTCTTGGCTTGATATTTTGTTTCTAATGCAAAGACATTTTCAAGTGTAGCTCAAGTTTCCAAATACTTTTTGGCACCATTGTACTTTACTGTGCATGCCATTAGATGAGAAAATGACAGGAACCCAAAAAAGCTCATGTTACAGTACATGCATGCGTCAGGTGTTCTTTATCACAGATGCCCAAACCAGATTACGCTCTGGCATAAAAGAAGTCGCCAATAATAAACACCAAATAGTTCATGTTTCATGATCCATCCCAT[T/A]TCAGCTTTCTCCGATGGAGCTCAAGACTCTGTGTCCATCAGCTCGATGATCAACGCTGAGAACAAGCTGGAGTGTGAAAGCAGTTCAGAGTCTGGAAGCTTCTCAGTCGACTCCATCATAGAGGGGGCCACCAAATGAAAGACCATCTCCAGCTGCCAGTTACAACAACTTGAATTTTTTGTTAAATGAGAAGTTACTGTTATTTTCAGCCAAATGTGTAATGATTCTGTAACCAACATGTTTCCAATAATACTGATCAGGTTGATCACAGTGCTGTTTTTTTTCTCTTTTTAGGGGTCGTTCTATAAGGTTTTGACTTTTATTGTTAACTCGATTGTTGTCATCGATGACAAGAAATGCTGTTTACATAGTTTACTAATATGTTTCACACAGTTTGATAGCTTAGCTTTGTTCACTTTACTGCTGCAGATTTTAAAGGTTAAAATGATTTACTTCCACTATCTAGAAGAACACTATTGAAAGAAATGGCAGAGCAGAAC
Associated Phenotype:
Not determined