ZMP
ide
Ensembl ID:
ZFIN ID:
Description:
insulin-degrading enzyme [Source:RefSeq peptide;Acc:NP_001082994]
Human Orthologue:
IDE
Human Description:
insulin-degrading enzyme [Source:HGNC Symbol;Acc:5381]
Mouse Orthologue:
Ide
Mouse Description:
insulin degrading enzyme Gene [Source:MGI Symbol;Acc:MGI:96412]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42283 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35572 | Essential Splice Site | Available for shipment | Available now |
sa28188 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15036 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42283
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113215 | Nonsense | 43 | 998 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 42965062)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42186021 |
GRCz11 | 13 | 42312081 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGGGTGGTGAGTGATATCATTCGCTCTCCAGAAGACAAACGGGAGTA[T/G]CGAGGACTCGAGTTTACAAATGGTCTGAAAGCCATTCTCATCAGTGACCC
Long Flanking Sequence:
TATGCACATATTACTGGTTTTGTGGATAATGGTCACTAATGAAATTTTGAGTTTCTAAAATAACAATAGACAATAAAATAAACACACTTTGGTTTCTGATGATGCACTGAGGACGGTCTAACGTTGCAGTCTTAAGTGTCTGGAATTTTGTGTTTTAGACTGTCACGAACATGCTCAAGACTATTTAAAGCGGTTGTTAATTAAACATAATTGTTTTTTTTTCATCAAACTTTTTATTGTCAGGACTGGAGCCATGTGTATTAATTTTTAGTTAGCCTGTATATTGTTTTTGTTACTTTCAAAGTGACTGTAGCATCTGTCTTGCATTTTAAAAATCACCATTTACTAGAGTTTGTTTGATAGTAGCTGACCTGAATGAATTCTGAATGAATCTTTTGTTTGTCCAGACGTGTGTCGACTCTGTCCATCAGAATGAGTGATCCGGCTGTCAAGAGGGTGGTGAGTGATATCATTCGCTCTCCAGAAGACAAACGGGAGTA[T/G]CGAGGACTCGAGTTTACAAATGGTCTGAAAGCCATTCTCATCAGTGACCCCACCACTGACAAATCATCAGCTGCCCTGGACGTCCACATGGGTAAACCGGAATAGTCCATCTGTTGTAGACCTATGTCGATATTCAATATTAATTATATTCAAATATAAGTTTATTTGTATAGCACTTTTCACAATAATTATTGTTTCAAAAAAGCTTTATGAAATGTGCATGTTATTGCATTACAGTCAAAATCAGAAAAGTTAAGATTATTAGTTTCATAATTTTAGTATTTACTAATAACTTTAACTAGTAACTAATAGCTTTCAACAGTTAATGTTATTATAAATAAACATGGTTGACCTGCAGAAGTATAGTATAAAAGTGACGTTTATGTCTACATGTTTAATGAAGTGTATTTGTGCATGTCTATTATGTTGCTCAATGTTGATATTATGGCCACTTCAAAATACAGTGAATAGTTATTGAATATTTAATCTTTTAGAGTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35572
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 |
---|---|---|---|---|---|
ENSDART00000113215 | Essential Splice Site | 490 | 998 | 12 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 42982210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42203169 |
GRCz11 | 13 | 42329229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACGGCACACAGTATAAACAAGAAGCCATTACTGATGAAGCTATTAAGG[T/C]GAAGCGCGTTTGATTTTAGCAAATCTCTCTCTCTAGTATGTCATGGTACA
Long Flanking Sequence:
GTGATGTGGTCTAAATCTGGAAGGAGTGATCTGGATTTTAAAGTGAACCTATTCTGGGCTCTCTTATGCAATTGATTAATTGCAGGAGAGTCCAGAATAGCACGTCATTGTCCCAAAAGTTCTCTATTGATCAGTAGAGTCTAAATTGTGCAGAAATAGTGCATTGATCCACAGCCCCGCACAGCAGATTGAGCAGCTTCGGGAAACTTGAACCTTTGATGTAATGACCATAATTCCAAATCTATTTACTGGGCCAGAGAGATCTGATAAAGGCAAAATTGCACAGCCCATTTTTTCCCCCAAGGGACTTGTGAGAAATGGATGGTGTCATGCTGTGTCTGGTGAATTGATCTTTACAATTCTTTTCTTTTTTTCCCCCTCACTCACTTCTTTTAGGGTTGCAGTTGTCTCCAAATCATTTGAAGGACAGACTGATCGGACTGAGGAGTGGTACGGCACACAGTATAAACAAGAAGCCATTACTGATGAAGCTATTAAGG[T/C]GAAGCGCGTTTGATTTTAGCAAATCTCTCTCTCTAGTATGTCATGGTACATAAACCTTATCTTTGACATTTGTCGTTGTGTAGATCACGGGTATCAAACTCAGTTCCTGGAGGGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTGAACACGCCTGATCAAGCTAATTGAGTCCTTCAGGCTTGTTTGATACCTACAGGTAGGCGAGTTGAAGTGCAACTAAACTCTGGAACTAAACTCTGCGGCCCTCTATGAACTGAGTTTAACAGCCCTGGTGTATTTATATATTTATAGAGAAGAGAAACATATAGTTGTGACGAAAGAATATTTTTATTTCAAAAACATGTTAATAGAACAGGGGTGGGCAATCTCGGTCCTGCAGGACCGGTGTCCTGCACAGTTTAGCTCCAACCCTAATCAAACACACCTGCTTATAGATTTCTTGTGATCTTAAAGACACTGATTAGCATGTTCAGGTGTGTTAGACTAGTGTTGGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28188
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113215 | Nonsense | 774 | 998 | 20 | 25 |
ENSDART00000113215 | Nonsense | 774 | 998 | 20 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 42994103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42215062 |
GRCz11 | 13 | 42341122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCAGCAGAGGAACGAGGTTCATAATAACTGTGGGATCGAGATTTACTA[T/G]CAGACTGACATGCAGAACACCCATGAGAACATGCTGCTGGAGCTCTTCTG
Long Flanking Sequence:
GCATGCTCACACTAAACCCCTTCTACCGAGTCAGCTGATTCGCTACAGAGAGGTGCAGGTTCCTGATGGTAAGTGCCTGACACCATAAATGTTTATGCAGTTTTTCATTTTTCAACTTAAGTTTCTTATGTGTGAGATTGGTAAGATTTTTGGAAAAGGGTCTGCTCACCAGGGCTGCATTTATTTGATCAAAACACAAATGCTATTTTATTTAAGAATTTTAGATTTTTATTTTATTTGTTTATATTTTTATGGGAAGGCATTTAACACTATGTAAGCTCCTTTTGGACATTTCACAAGACATTTTTATTAAATTGAGGAACTTGAGGAAAATGAGACTGGTGTTAAACCTAAATCACTGTTGTGTAATTTTGGGTGATTGTTGTGTGTTTGTCATGGTTCTTGTGTTTTAAGTCCAGTTCTCTGTGGTTATCAGGTGGTTGGTATGTATACCAGCAGAGGAACGAGGTTCATAATAACTGTGGGATCGAGATTTACTA[T/G]CAGACTGACATGCAGAACACCCATGAGAACATGCTGCTGGAGCTCTTCTGTCAGATCATCTCTGAGCCATGCTTCAACACGCTACGCACCAAAGAACAGCTGGGTAAATCAAAACTGTCATGAGCCAATGTTTCATTTGTGTGTGTGTGTGTTCGCTAAAACTATATGGTTTTTGTTTGTCAGTAATATAATTGGACCAGTGGAGAAAAAAAACAAATCATTACTGTTTATTTTAAGGACAAAATATAAATTTAACATTACGGTATGCAATGTATAAATGCATTTATGAGTTATTAATTTTTATTATATCTTTATATTTACTAATAAACAGTTATTTTCAAAGATACCATTCTTTAAAGATGACATCTCAGCTGGCAAAGTGTTTCTCAAACAATGTGTGTAATCCAGTTAATATGCATGCAAATGCAGATTTTCTTCTATCGATTTACATGAACACACACCTGCACATGTGGAAGCAAAAACAGCCACACACAGTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15036
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 |
---|---|---|---|---|---|
ENSDART00000113215 | Nonsense | 774 | 998 | 20 | 25 |
ENSDART00000113215 | Nonsense | 774 | 998 | 20 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 42994103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42215062 |
GRCz11 | 13 | 42341122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCAGCAGAGRAACGAGGTTCATAATAACTGTGGGATCGAGATTTACTA[T/A]CAGACTGACATGCAGAACACCCATGAGAACATGCTGCTGGAGCTCTTCTG
Long Flanking Sequence:
GCATGCTCACACTAAACCCCTTCTACCGAGTCAGCTGATTCGCTACAGAGAGGTGCAGGTTCCTGATGGTAAGTGCCTGACACCATAAATGTTTATGCAGTTTTTCATTTTTCAACTTAAGTTTCTTATGTGTGAGATTGGTAAGATTTTTGGAAAAGGGTCTGCTCACCAGGGCTGCATTTATTTGATCAAAACACAAATGCTATTTTATTTAAGAATTTTAGATTTTTATTTTATTTGTTTATATTTTTATGGGAAGGCATTTAACACTATGTAAGCTCCTTTTGGACATTTCACAAGACATTTTTATTAAATTGAGGAACTTGAGGAAAATGAGACTGGTGTTAAACCTAAATCACTGTTGTGTAATTTTGGGTGATTGTTGTGTGTTTGTCATGGTTCTTGTGTTTTAAGTCCAGTTCTCTGTGGTTATCAGGTGGTTGGTATGTATACCAGCAGAGGAACGAGGTTCATAATAACTGTGGGATCGAGATTTACTA[T/A]CAGACTGACATGCAGAACACCCATGAGAACATGCTGCTGGAGCTCTTCTGTCAGATCATCTCTGAGCCATGCTTCAACACGCTACGCACCAAAGAACAGCTGGGTAAATCAAAACTGTCATGAGCCAATGTTTCATTTGTGTGTGTGTGTGTTCGCTAAAACTATATGGTTTTTGTTTGTCAGTAATATAATTGGACCAGTGGAGAAAAAAAACAAATCATTACTGTTTATTTTAAGGACAAAATATAAATTTAACATTACGGTATGCAATGTATAAATGCATTTATGAGTTATTAATTTTTATTATATCTTTATATTTACTAATAAACAGTTATTTTCAAAGATACCATTCTTTAAAGATGACATCTCAGCTGGCAAAGTGTTTCTCAAACAATGTGTGTAATCCAGTTAATATGCATGCAAATGCAGATTTTCTTCTATCGATTTACATGAACACACACCTGCACATGTGGAAGCAAAAACAGCCACACACAGTCTAA
Associated Phenotype:
Not determined