ZMP
dram2
Ensembl ID:
ZFIN ID:
Description:
DNA damage-regulated autophagy modulator protein 2 [Source:RefSeq peptide;Acc:NP_001002135]
Human Orthologue:
DRAM2
Human Description:
DNA-damage regulated autophagy modulator 2 [Source:HGNC Symbol;Acc:28769]
Mouse Orthologue:
Dram2
Mouse Description:
VDNA-damage regulated autophagy modulator 2 Gene [Source:MGI Symbol;Acc:MGI:1914421]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24049 | Essential Splice Site | Available for shipment | Available now |
sa37394 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43737 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24049
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105897 | Essential Splice Site | None | 272 | 1 | 8 |
ENSDART00000146619 | Essential Splice Site | None | 273 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 846195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 849107 |
GRCz11 | 22 | 866005 |
KASP Assay ID:
2261-6197.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAAAGGGATTTAAAATGTTTCCGTTCGGACTGAGGGATGATTGACAG[G/A]TAAAGCTGTTCCTCATTGATGTACAGTAACTGTTGACATCTGACACAGAT
Long Flanking Sequence:
TATAACTATGTATTATAGCTACCGCCATTTTTAGTAGTATAAATATCCAACTATTCGTTAATTATAACTAACAGTAAACTAACACTTTACACAACGCAAGTATGTCTATTTATTATACTTCTACTTATTTAACACTATATTTCGATCATTAAACGAGAATAGGAATGATTTTCTTACGAATTTCAATATGAGTGCGTTAAATTGCCCGAAAATTACAATATTTTGCTCCCTGAGGTGGATTTTTCCCGCGCTGGCGACCCGCCGAAAGACTCCACATCCGGGTTTTTTTTACCGCGGGTCTCGTGATTTAGAGCGGAAGAAAACGCTGATAGTTGATGTGTGACAATAACGGAAGAAAAAACAGCGATAAATTTGAGCAATAAACGAATAAAAGGAATATATAAAGCATTTAAGCATGCAACAGAACCCTTAACGAGAGATGCAAAGTCATTCAAAAGGGATTTAAAATGTTTCCGTTCGGACTGAGGGATGATTGACAG[G/A]TAAAGCTGTTCCTCATTGATGTACAGTAACTGTTGACATCTGACACAGATTTAATGACAGATTTAATAACTATTAAACAATAACACAGCTACTGCAATTGAGCCTCCGCTTCTTAATAAGTCATAGAAAGTTAAACTAAAGAAATCTACAGTGAAACATTGCTTACATTTGATTTGTTTCGTTTTTATGACATCTCTAACAATAACTCGACATATTTTTAGCCGCTTAATTATTTAAATGTAATTATTCAGCTCATTATTATAGCAGCAACCAGCAAACATGTTAGTTTTACTTGTGTTTATGTATTTTGTCATGAAAAGGTTGTTAAAATGTTCCGTTTTCTCAATGTTTTCTTATTTATTAGAGTTTTTTTCTGATTGCTTTAGCACAATTTTGAAATTAATTTGTCAAAACACTACGCATAATTTCCACGTCCACACACACACACACACACACAAACAGCAGAACACATCAGTTCTGTTGCAAAATGAAACACTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37394
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 |
---|---|---|---|---|---|
ENSDART00000105897 | Essential Splice Site | 114 | 272 | 4 | 8 |
ENSDART00000146619 | Essential Splice Site | 115 | 273 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 841272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 844184 |
GRCz11 | 22 | 861082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGGCTGCTGCAGCTCATTCGGCATGTGCGTCGTTGCTAACTTCCAG[G/A]TACGTATTTAAATTTTGGCCCCTGTATTGTTTTTTTGACTACATGAATGT
Long Flanking Sequence:
TGAACGCAAAATTTTGTTCTCGTTTTTAGCTTGTTGTTGAGTCAATTTGTATTCACTAGCTTTATGCATCTAGCTATATGTTTATGCTAACTTGCAAACATATACACTAAATTATAAAAAATCTGCAATGGGACCACATATAAAAATTGGTGTAGAAACAACTTTCTTCCAGAAATTGCTATTATAACTCATCGTTTAGAGAAACGACTAACGGAGTTAAGTAAACATGACATTTTGGTGTATAAAACAGACAGAACTTCCTTGTAAAATGAACATCAACAGTGTGTGAAGTTAGGGGGTGTAGCCTGTGGCTCCGCCCCCTGTGTTTGAGTTGTAATGTTGCGTGTTTTCCTGCAGGTGTCGCCACTATGTATGTGCGCTATAAGCAGCTCCAGGCTCTGGCGGATGTGGAAGACACTCGTTTAAACCGGCTCAATGTGGTCGGATTTGTTTTTGGCTGCTGCAGCTCATTCGGCATGTGCGTCGTTGCTAACTTCCAG[G/A]TACGTATTTAAATTTTGGCCCCTGTATTGTTTTTTTGACTACATGAATGTTTGGTTAAAAAAAAAAAAAACGTCTACATTTTTAGTAATTTAAAAGTAAATTTAAACTTAAATCATAACATTTTCAAGAGTGTGCGTATGACCAAGATTGTGCGTCTTATTGGTTGGCAAGTTTTTCACGCGCTAAATCTGGCACAATGATGAAACAAGAAATTTTGAAAATTAACAGTCATCTATTTAAATTTAAAACAATTGTCACAAATTTCCACACTAAATATTTGAATAGAGAAAAAAACGCAAAAAATTTGCTCGTAGTTTCGCATACTTGTGTATTAACATGAATGCATGATGAAACAATTATAGTAGTTCAGTTTGTTGTTAATAAACATGAAATACAAAAAAGGACCATTTTCAGATTCTGTTGATTATTATTGTCAAATTGACAAATTAATCCACATGTCAAATGTTATTGGTCCGCTAGTTTCTTCGCAGTGTAATCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43737
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105897 | Nonsense | 144 | 272 | 5 | 8 |
ENSDART00000146619 | Nonsense | 145 | 273 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 840388)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 843300 |
GRCz11 | 22 | 860198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGACGTTCGGCATCGGCGCGCTCTACGTTTTCATCCAGACGGCTCTGT[C/A]GTACCTCATGCAGCCTCACATCCACAGCAAAACCATGTTCTGGACGCGGC
Long Flanking Sequence:
AACATGAAATACAAAAAAGGACCATTTTCAGATTCTGTTGATTATTATTGTCAAATTGACAAATTAATCCACATGTCAAATGTTATTGGTCCGCTAGTTTCTTCGCAGTGTAATCGTCAAACTAATGATATGCTATTCATGTCCTAAAAGACGATTCAGAAGCAGCTTGTTTAAATTAAAATGTTTATTGCACTAAATTTTCACCATAAACACAATTGTTCGTCATCTGAGAAATGCTTTCGACCACAGTGTCCTAAAACACACCTGCAGGCAATCAGCAGTAAGGGGCGTGTCTAGTAACTAAAGTGGTGATATCAAAATAAGGTGGAGTCTTGTTTGTTTAGATGTATTATTTGGCGTCAAAGTTTTGCCAATTTTCACAATCCCATTTTGTGTGTTGCATCTTTCGCAGAAAACCACTCTGTTCTCGATGCACCTGGTGGGCGCCATTTTGACGTTCGGCATCGGCGCGCTCTACGTTTTCATCCAGACGGCTCTGT[C/A]GTACCTCATGCAGCCTCACATCCACAGCAAAACCATGTTCTGGACGCGGCTGAGTGTTGGTATCTGGACCCTCAGCAGCATCATCAGCAGTATCCTTTACCCCCAGTGCATGCTGGGAAAATTAGCATTTAGCTACTTCTAAGGAATTTCCCTCTATATCACTTAAAATGTAAAATAGTCACATTTAAAAAGACACACGGGTCCATAGAGGTCTAAATATCCATCTAAAAATGTAATGTAAAAATGTAAACGTATTGTATTCTAATACGTCTATTGGTCTCAAATATTTTAAACCTTTAAGTATCACTTCAATATTTCTATTATACTTCCATTTACTTGTATCGATAAAAACCAACATTATATTCAATGTTCAGAAACAACATCTACTGCATTTTCCATGGCCTGCACAAAAAAATGGGAGGGAAACGTTTATTATTAGCAATTAGCATTTAGCATTCAAACTGAGTATTTTCCTTGACGGGCTAAAGTGTTTGTGTCGT
Associated Phenotype:
Not determined