ZMP
EDEM3
Ensembl ID:
Description:
ER degradation enhancer, mannosidase alpha-like 3 [Source:HGNC Symbol;Acc:16787]
Human Orthologue:
EDEM3
Human Description:
ER degradation enhancer, mannosidase alpha-like 3 [Source:HGNC Symbol;Acc:16787]
Mouse Orthologue:
Edem3
Mouse Description:
ER degradation enhancer, mannosidase alpha-like 3 Gene [Source:MGI Symbol;Acc:MGI:1914217]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41175 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12132 | Nonsense | Available for shipment | Available now |
sa21258 | Nonsense | Available for shipment | Available now |
sa41174 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10752 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41175
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 |
---|---|---|---|---|---|
ENSDART00000111710 | Essential Splice Site | 72 | 889 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 20024743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19454640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTTCAGGTTTTCCCTCACGCTCATCGATACTCTTGACACCCTTGCA[G/A]TGAGTAACATCTCAAACAAAACTTGAAACCTTGTGTATACAGTATGTACA
Long Flanking Sequence:
AAAAGAAAGTGCTATAGATTCACGATGACACCAAGTAGTGAAATGATCCAATAGTTATTATTTATGGGTGAGCTATCTCTTAAACTTAGCTAGTTTGCAACTTAATGATTCTGACAAGTGTAAAATATTTCCCAGAAACACCTGGTATTCCCAAAAGTGTCTCTAGGCAGGCTGGAAGTGATATATGAGAAAAAAAATGGGGATAGGGCATGCATATCAATGTTTGAGAAAAATCTGCATTTTCATTTAATCTCTGTTCTTCTCATTTGCACAGGACCATGCTTACCCTGCAGACGAACTGATGCCTTTGACTTGCCGTGGGCGAGTACGTGGACTAGAGCCCAGTCGAGGGGACGTAGATGATGCCCTGGGGAAGTACGTTAATTGGAGAAAAAAGTAAAATGGAGACTTGTTGATTTTTTTTTTTTAATATTGAAAATATGTTCCTTTGTTCCTTCAGGTTTTCCCTCACGCTCATCGATACTCTTGACACCCTTGCA[G/A]TGAGTAACATCTCAAACAAAACTTGAAACCTTGTGTATACAGTATGTACAGTCAAACCCGAGGTTGTTTGCTCATAATCTTTTCTGATATCTCACAGCTGTTAAATAAGACGGTGGAATTTGAAGAGGCGGTGAGGCGAGTGGTGAAGGATGTACGCTTGGATAATGACATCGTGGTGTCTGTATTTGAAACCAACATCCGGGTTCTGGGGTAAGTTGATATGTTTATCACTGATATCTATGTATTGAAATATCCACAAATGACTGATTTATGCTTGTCCATTTTCTGTACTTTTTATTTTCCAAGTTACAAACATGTTATTGTACTTTTTTAAGATAAGATGTTTAAGATAAAGTTGCTGATATCTATTATTTCTCTATGGAAATGCTGCTTAGTTCAGTGTCACTCTTTGTGGACAAATGAAAATGCATATGTGAGTTGTGTGTCTGTGAGTTCGGCTAGAGATGTAATTAATTCAGAGAAGCAGTTTAATTAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12132
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 |
---|---|---|---|---|---|
ENSDART00000111710 | Nonsense | 235 | 889 | 8 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 20020690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19450587 |
GRCz11 | 8 | 19481307 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGACAGAGGAACAGTAATCTAGTGGGAACAACCATCAACATCCACTCT[G/T]GAGAATGGGTCCGCAGGGGTGAGCCTGAAACGTACCTAACAACCCAGCCA
Long Flanking Sequence:
ACTTGCATAATACATATTTATTTCTTAGAATCTTCATTTCACTTTCAGAGAAGTGTAATTACATTTATTATAATTCATGTTGATTAGAGCATTTGAGGTCACAAGGCTCGTAGAAACACTGTTGTGGTTGTTTTAACAAACAAAAGAATGCTGAGGTTATTTCAACCCAAAGTGTTGAATCCTGGAATCTTAGTTCTCATTCAATCTTCACAATTGTAACACAAATCTCTTCTGACATAACTGTGGCGTCTGTAAAACAGAAAACATTGGCTTGACCCGCTGTGCACTTTGAAAAGTATTATGAGGTTAGGAATGTTCTGATTGTGTGTGTGTGGCGAAAGAGACTTACAATGCTTTAATCATTTTAAGTAGGCCAGTATTTAGGTGTTGGTGTTTTGTTTGATTGTTTACAGGCTCATGCAAGAAGGGCTCTTGATTTCCTTTGGGAAAAGAGACAGAGGAACAGTAATCTAGTGGGAACAACCATCAACATCCACTCT[G/T]GAGAATGGGTCCGCAGGGGTGAGCCTGAAACGTACCTAACAACCCAGCCACAACATAAACGACTTTCAAAATCAGTCAAGTCTGAGTCTTGTTTGTGTGTGTCATTGTTTCTTTGCCAGACAGTGGAGTTGGGGCAGGCATCGATTCTTATTATGAGTACTTGATGAAGGCATATATATTATTGGGCGATGACCAACTTTTACTACGCTTTAACACTGTGAGTATTACCATACTGTTGTTAAAGTTGTCATAATCCTGTAATAGCTTGTTGTTGTACTGTAACAAGTCTCTTCTCTTTACGTCACCAATCTGGGTTTTTTTTCATCCCAAACATGATATATTTTGAGAAAACTTTGATTAAAATTAGGTCAAATTTCAGTTGCACAAGAGTTTCAGACACCATTTCATGCTGAAGAGGCTGACTTTGCTAATTTCATATGCATGATTGCTCAAGTGGATACACAAACGCACTGTGTAGGAGTAAAATTTAAATTTGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21258
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 |
---|---|---|---|---|---|
ENSDART00000111710 | Nonsense | 332 | 889 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 20019014)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19448911 |
GRCz11 | 8 | 19479539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTAAAGGGAGATATCCGGCCAGCCATAGAGACTCATGAAATGCTTTA[T/A]CAGGTTACCAAGAAACACAACTTTCTCCCTGAGGTACCTTTTTCTACCTT
Long Flanking Sequence:
ATTGATTTTTCTTGTAATGTTTTTTCTTGAGTTGTTTTGATTTCTCTTGTTTGTTGTCTTGCCTTGATTTGTCTTAATTTTTTAGATTTGGCTTGTTTTGTTTTGTTTTGTTTTGTCTTGTCTTGTTTTTTCTTGATTTGTTTTATTTTCCAGACTCTTTTTTTATACGTTATCTTTTGCAACTTAATTTTTATTGTTGTTTTATGTGTATTTTTAAGTTGTGACTGCTTGACATATTTTCCAGCACTATGCATCCATTATGAAGTATATCAGCCAACCTCCTCTACTACTGGATGTCCACATCCACAAACCCCTGCTTCCAGCACGCACATGGATGGACTCCTTGCTTGCCTTTTTCCCTGGACTGCAGGTGAGAAATGAGTATATTCGTGGTCTTTTTTTATTGACTAAATCTCTAAACACAATCATACATCTTTTTGGTCTCTGCAGGTGTTAAAGGGAGATATCCGGCCAGCCATAGAGACTCATGAAATGCTTTA[T/A]CAGGTTACCAAGAAACACAACTTTCTCCCTGAGGTACCTTTTTCTACCTTTTAATACCTTGTACATATCATCACTGCCTGTTGTTTACAAAATCTTCTTGACTCAGAGTCTCGTACTGTCTTGCCAGGCATTCACCACTGATTTCAGGGTTCACTGGGCTCAGCACCCCCTGCGGCCAGAGTTTGCAGAAAGCACTTACTTCCTTTACAAGGTAAAAAGTTATCACTTGTTTCTCAGATAAATATCAATGCAACATTTTCATCTTTTCATCTGTTAAGACCCTCAAATGTAACTGCTTTCAGGCTGAATTGCAAAGTTTGTTTCAGGGCACTAATAACACTGATGTTATCTGGATAAAAGGCCAAAACGAAATTAAACTTGTGTTGATTGACCAAAATCTATTGCCATGTTGATAGGGCTTGAGAATCATTAATATTGTTATTGATGAAATCATAATTTTTCTGCCTATTTTAGGAAAAAAATAATAATTTGAAGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41174
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111710 | Nonsense | 391 | 889 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 20017664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19447561 |
GRCz11 | 8 | 19478187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACCCATATTACCTGGAAGTGGGCCGTACTGTACTGGAGAACCTGAAT[C/T]GATTCGCTCGAGTTCCCTGTGGCTTTGCTGCTATGAAGGATGTGAGAACG
Long Flanking Sequence:
AGAAACAGTGACACTTCGTGATTCAAAACACAAAACTGAAATGGTTTCTTAAATATACATACATGTTAGCTTCTCTCTCTGCGTCAGCAGCAGCACAGATAGGACCTTTCCAAGTGATTGTATTAGTAAAGGTTTAATAGACAGCCAAATCATTCTTATTTAGTAATAACATTGTCATAAAGATCCCACCCCATTAAAAATTAGCTCTAATATGCACTTTAATACAGAAATCCATTGAGAAGATTAAAGCAAGGCAAGTATTTATACAGCACATTTCATACACAATGATAATTCAAAGTGCTTTCCATAAACAAGAATAAAAGTAACAAGTAAAAATAAATAAATAAAAATTATTAAAAGCATATTAAAATGTGTTAAAAGAGGTTTTAAAGAAATAAAAAAAGAAAAGAAAGACCAAATTTAACTGTGAATTTCCATTAAAGGCAACCAGAGACCCATATTACCTGGAAGTGGGCCGTACTGTACTGGAGAACCTGAAT[C/T]GATTCGCTCGAGTTCCCTGTGGCTTTGCTGCTATGAAGGATGTGAGAACGGGGAGCCACGAGGATCGGTAAGATTTGTGGGTAGTGAGAGAGTAAATTGGTTTATGTGAATTTTTCAACTACAAATAGATTTTTGGTAAAGAGATGGTTCATGAGTGGGCAACAGGCTGTCTCACGGCATATTTATTTCCCTTCACCGCCGCCCACCTTGTTTAAGCATGGACTCGTTTTTCCTGGCGGAGATGTTTAAGTACCTGTTCCTGCTGTTTGCTGAAGAGGAGGATTTGCCTTTCAACGTGGAGGACTACGTCTTTACCACTGAAGCTCATCTCCTGCCTCTGTCCCTCTCCACTGCTTCAAACTCACCGGCGCCCCCTGTCATTAACAGCGTGGTACTGCACATTATTACAATAACAGATCTTATTGTGGAAACTGGACACAAGTTGATTTAATTCACTCAGTACTCTCAATTTAATCGCCTTTAGGTGGTTCCAAACACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10752
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111710 | Essential Splice Site | 632 | 889 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 20014365)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19444262 |
GRCz11 | 8 | 19474034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCAGGCCCCGCRCAGTTTGGAATGGACCTTTCCAAAAGCAGCTCTGGAG[T/C]GAGAATGATTAACRSWGACCTTTTATGATAAAACTTTCTCACCGGCTATT
Long Flanking Sequence:
AACATATATAAATAAACATTTTCTTTAATATATGCATGTCTGTGTGTATTTATATGCATAACAAATATACACAGTACACACACTTAAATCATATCAAAACACTTTAATTTTGGATGCTATTCATTTTTGCCCAGCACCAATCAATACAAAAGCATAAACCAGCCAATGTGCTAGTACAAAACACACTTCTTGACAAAATGTAATTATCATTATCTGAAAAACATTTAATTTATTAAGATAATTTACATGAGACAATGCAGTTAGTATTTTGAATCTGCAACTCAAGTCCTGTTCTTCCTCTCTCCAGGCGGTGAGTGCAGTTGCTGCAGAGGACGGCATGCGCTTTATGCAGGAAATGATGGAGCTTTCTAGCCAGCAGCAGAAAGAACAGCTTCCTCCACGTGCTGTTCAGATCGTCTCACACCCCTTTTTCGGCAGAGTGGTTCTGACCGCAGGCCCCGCGCAGTTTGGAATGGACCTTTCCAAAAGCAGCTCTGGAG[T/C]GAGAATGATTAACGCTGACCTTTTATGATAAAACTTTCTCACCGGCTATTTCTGTGTCATTCTTGGTCTTTTCTAGCTAAAGGGAGTCCATTTATTAGTCATACTGTTCTCTTTTTTCCCCTCTACCTCAGGTGCGTGGGTTTGTGACTGTAGCAGAGCCCTATAATGGCTGTTCTGAGTTGAGTAATGGTGAGATTGTGGCAGGTCGTATCGCTCTGCTGCAGAGAGGCCAGTGCATGTTTGCAGAAAAGGCAAGGCATGTGCAGAAAGCTGGAGCCATCGGAGGAATTGTCATTGGTGAGAAATACTTTAGGGTTCACTAAATGTAATGGTCCTCTTTTAAAAAGCTGTTCAAGCTCAATTGTTAAAATATCATCTAAGAAATATTTACTGTTTATTAAATTGCTAAAAGTCTTGTAGGACTAGAATTTGGTGTTTAACGCTCTTTTTTTTTCCAAATCTTTTTATTAACATTTTGGTACATAAAACATCAATTTCAA
Associated Phenotype:
Not determined