ZMP
wu:fb81h03
Ensembl ID:
ZFIN ID:
Human Orthologue:
ACE
Human Description:
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1 [Source:HGNC Symbol;Acc:2707]
Mouse Orthologue:
Ace
Mouse Description:
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1 Gene [Source:MGI Symbol;Acc:MGI:87874]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12049 | Essential Splice Site | Available for shipment | Available now |
sa19024 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17717 | Essential Splice Site | Available for shipment | Available now |
sa41956 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9141 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12049
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 |
---|---|---|---|---|---|
ENSDART00000114637 | Essential Splice Site | 310 | 1324 | 5 | 25 |
ENSDART00000114637 | Essential Splice Site | 310 | 1324 | 5 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 6234847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5516478 |
GRCz11 | 12 | 5551435 |
KASP Assay ID:
2261-7169.1 (used for ordering genotyping assays)
KASP Sequence:
TGGTCCRAAATACATCAACCTTAAAGGTCCCATCCCTGCTCATCTATTGG[G/A]TAAGTCTTTTAATATTRTGAAAATATTATGCATATTSTTCRTGTTATGAC
Long Flanking Sequence:
TGCTAAAAAAGAGTTATAGATGCAAAAGTAATGAGAAAGAAACATTGTACTGTGTTAAAAAAATGTTATATACAACAAACTTGTCTAGGTCTTGTCTAGGAAAAGACCAAAAAGCTTTCTGTGACTGTTTCTGTGTTGTCCTCTCCCTCATCATCAGTGGCACTTTCTCAAAAATGACCTTCCCAAACTAAAACAGAAGCAGTTGCTGAATATTTTGGTCTGCATTTGCCGTTTAAGCATCTTTGGAAAGAAGACACTTTGATTTGAGAGAGAAAGAACTGAAAACACTTCTTCTTGGTTCTCCTCAGGCTTTAAAGACACAGGCGAGTACTGGCGCTCTTGGTACGAGTCTCCTACCTTCAAGCAAGACCTTGAGAACCTGTTTAAACAGCTGGAACCTCTCTACCAAAACCTGCACGCTTTTGTCCGCCGAAAGCTCTACGACTACTATGGTCCGAAATACATCAACCTTAAAGGTCCCATCCCTGCTCATCTATTGG[G/A]TAAGTCTTTTAATATTGTGAAAATATTATGCATATTGTTCGTGTTATGACAAACAACGGCTTATCATAAACATCTTATCGATAATTATTTACACAGTTGTCATTAAGAAGGAGCAATGAAATGTTATCTGACTAACATTTAGCAGGTAAATGTGTTTGGAAAAATATTCAAAGGCTTTTATTTTCATAAACCGCGCGGAAGTGACTGGTCTGACTGGCTAAAATAGACGTCTCACGTCAGCACGCTCTAGACAGGCACGCACTCTTTCCGGCAATCTTCCTTCTGCGTTCACACAGTGCAGCATTCCAGCAAATTACTAGTAATGTTACAACTTCTCTTCCCGGAAAATAGCCAGAACAAATTTACCAGTAATTTTCCAGAAAGGTCTGTATGTGTGACAGGGGCTACTGTTTGCAACCACTTACCTTAAAAAAATTTAGTAAATCCAAAAAATTTATTTCAGTATACTAACAGTGTTGTGTTTGGCTTTCATTAGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19024
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 |
---|---|---|---|---|---|
ENSDART00000114637 | Essential Splice Site | 310 | 1324 | 5 | 25 |
ENSDART00000114637 | Essential Splice Site | 310 | 1324 | 5 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 6234847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5516478 |
GRCz11 | 12 | 5551435 |
KASP Assay ID:
2261-7169.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCCGAAATACATCAACCTTAAAGGTCCCATCCCTGCTCATCTATTGG[G/A]TAAGTCTTTTAATATTGTGAAAATATTATGCATATTGTTCGTGTTATGAC
Long Flanking Sequence:
TGCTAAAAAAGAGTTATAGATGCAAAAGTAATGAGAAAGAAACATTGTACTGTGTTAAAAAAATGTTATATACAACAAACTTGTCTAGGTCTTGTCTAGGAAAAGACCAAAAAGCTTTCTGTGACTGTTTCTGTGTTGTCCTCTCCCTCATCATCAGTGGCACTTTCTCAAAAATGACCTTCCCAAACTAAAACAGAAGCAGTTGCTGAATATTTTGGTCTGCATTTGCCGTTTAAGCATCTTTGGAAAGAAGACACTTTGATTTGAGAGAGAAAGAACTGAAAACACTTCTTCTTGGTTCTCCTCAGGCTTTAAAGACACAGGCGAGTACTGGCGCTCTTGGTACGAGTCTCCTACCTTCAAGCAAGACCTTGAGAACCTGTTTAAACAGCTGGAACCTCTCTACCAAAACCTGCACGCTTTTGTCCGCCGAAAGCTCTACGACTACTATGGTCCGAAATACATCAACCTTAAAGGTCCCATCCCTGCTCATCTATTGG[G/A]TAAGTCTTTTAATATTGTGAAAATATTATGCATATTGTTCGTGTTATGACAAACAACGGCTTATCATAAACATCTTATCGATAATTATTTACACAGTTGTCATTAAGAAGGAGCAATGAAATGTTATCTGACTAACATTTAGCAGGTAAATGTGTTTGGAAAAATATTCAAAGGCTTTTATTTTCATAAACCGCGCGGAAGTGACTGGTCTGACTGGCTAAAATAGACGTCTCACGTCAGCACGCTCTAGACAGGCACGCACTCTTTCCGGCAATCTTCCTTCTGCGTTCACACAGTGCAGCATTCCAGCAAATTACTAGTAATGTTACAACTTCTCTTCCCGGAAAATAGCCAGAACAAATTTACCAGTAATTTTCCAGAAAGGTCTGTATGTGTGACAGGGGCTACTGTTTGCAACCACTTACCTTAAAAAAATTTAGTAAATCCAAAAAATTTATTTCAGTATACTAACAGTGTTGTGTTTGGCTTTCATTAGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17717
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114637 | Essential Splice Site | 524 | 1324 | 9 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 6231981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5519344 |
GRCz11 | 12 | 5554301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGAGAGACACCGCCTGMCCGCTACAATGCAGATTGGTGGTACCTCAGG[T/A]AAAAAAATAAACATATACAGTTGAAGTCAGAATTATTAGCCCTCCTGTAA
Long Flanking Sequence:
ACTCTCATGCTTATAATCGCAACCAGTAACTACGCATTTTTTTTTCTTTGACAGAATCAAGCAGTGCACGACTGTGACCATGGAACAGCTGTTCACAGTGCATCATGAGATGGGGCATGTGGAATATTACCTCCAGTACAAAGATCAGCCAGTGAGCTTCAGAAGAGGAGCCAATCCTGGCTTCCATGAGGCCATCGGGGACGTTCTCTCTCTTTCTGTGTCCACTCCCAAACATCTCCACAGCATTGACCTCCTGGACCAACTAACCGATGACGCTGGTGAGTGAGAGACATGTCAAATTATACTGCCAGTGTAAACTTCTGATAAGCTGAAGAAGTTTATGAAATTCCACAGAGAGTGACATCAATTACCTGTTGAAGATGGCCTTGGAAAAGATCGCCTTCCTTCCTTTTGGGTACCTTATTGACCAGTGGCGATGGAGTGTGTTCAGTGGAGAGACACCGCCTGACCGCTACAATGCAGATTGGTGGTACCTCAGG[T/A]AAAAAAATAAACATATACAGTTGAAGTCAGAATTATTAGCCCTCCTGTAAATATTTTTTTTCTTTTTTAAGTATTTCCTAAATGATGCTTAACAGAGCAAGGACTTTTTCACAGTATTTCCTATAATATTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCAGCTAGGGAACTTTTTATTAACCATTTCTAAGTCAATAATATTAGCCCCCTCAAGCAAATCCTTTTTTTCCAATAGTCTACAAAACAAGCCATCACTATACAGCAATTGCCTAATTACCCTAACTAACCTAGATAAAACTTGAATACTAGTATCTTGAATAATGATGTACTCTCATTATGGCAAATTTAAAAGAAATGTGTTATTAAAACTATTATGTTTAGAAAGGTGTTGATAAAAATCTTCTTTCCGTTAAACATAAATTTGGAAAAATATATAGGGGGGCTAATAATTCAGTGGGGCTAATAATAATAATTAATAATAATTTTATGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41956
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 |
---|---|---|---|---|---|
ENSDART00000114637 | Essential Splice Site | 668 | 1324 | 12 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 6228160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5523165 |
GRCz11 | 12 | 5558122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTTAACTGGGTGCCACCAATACCAGAGGGCTACCCTGAAGACATTG[G/A]TAGGAACTTGAGTGAATGCTATTTTTATTAGGGTTCAACAAAACTGTGCA
Long Flanking Sequence:
CCACAATCTATTCTCTCCACTGACTTTTTACTCAACTACATTTAGAAAATAAATAGAGTAAAAAGTGAAGTAAAAAGTGCAATATATTGTTTTAAATTGTAGTGAAGTAGAATTAAAAGTTTGCTGAAAAAGATATAGCCTGATGAAGTACAGATCCTTAAATTTTGTACTTAAGCACAGTAGTGAAACCCACTTAGTTACTGTCAGCAACTGGTAAAGATAGACTGAGACCACAGTTTCATCATAATGTCTGTACGCTGAGTGTTGTTTATATATTGTGTTTGAAAGGAAAGTCTTGAAGGCTGGCTCTTCAGAACCTTGGACTCAGGTGCTACAAGAGGCGCTGGGCACTGACAAAATGGACGCCACCCCCCTGATGAGCTATTTTCTGCCAGTTACCACCTGGCTGAGGGAACAGAATGAGAAAACCGGCGAGACGCTTGGCTGGCCTGATTTTAACTGGGTGCCACCAATACCAGAGGGCTACCCTGAAGACATTG[G/A]TAGGAACTTGAGTGAATGCTATTTTTATTAGGGTTCAACAAAACTGTGCAGAGCTGCAGCCCTCCAGGTATCGAGTTTAAGACCTATGCCATAGAAAAACATACAGTTGAAGTCAGAATTATTAGTCCCCCTGTTTTTTTTTTTCTCCCAAATTATGCTTAACGGAGAGAAGACTTTTTCAGCACATTTTTAAACATAATAGTTTTAAAAACTCATCTCTAATAATTGATTTATTTTATCTTTGCCACGATGACAGTAAATAATATTTGAGTAGAAATTTTTCAAGGCTCTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAATTAATGTATAACGATGGTTTGTTCTGTACACTATTAAAAAAAAAAAAAAAAACTTAAAGGGGCTAATAACTTTGTACTAAAATGGTGTTTAAAACTAAAAACAGCTTTTATTCTAGCCGAAATAAAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9141
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 |
---|---|---|---|---|---|
ENSDART00000114637 | Essential Splice Site | 999 | 1324 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 6217432)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5533893 |
GRCz11 | 12 | 5568850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTGTGCCATGCCTCTGCCTGGGACTTCTACAACCGCAAAGACTTTAG[G/A]TRTSRCAATCGTATCACTTTAAACTCCCTGTTATACAACAACACACTGGT
Long Flanking Sequence:
GTTCTTTCACCATACTGACACTGACACCTCTAATAGAAATAGAAAGGTTGAGCAATCAACTAAAGGTTACTAATGGTTTTATGTATGGGCGATATATATTACATCACCAAAACTGATTAAGGTCATGTCCATACTTTGTGCAATAAAGTCGATATGTTGATTATTGTGACAGGCCTAACTAAAGCATTTATAGTAACTAAAAACTTTAGCTTTTCTGATTTTGATTGTAACGCAAATATGTGCAACTTCTGTAAAGCTGCTTTGAAACAATAACTATTGTTAAAAGCGCTATACAAAAAAACTTCAATTGAACTGAATATTCTTTAGGGCTGGACCCCCAAGCGTATGTTTGAGGAATCTGACAGGTTTTTCACATCTCTGGGTCTCCTGCCCATGCCTCCTGAGTTCTGGAACAAGTCCATGCTGGAAAAGCCAACAGATGGCCGTGAAGTGGTGTGCCATGCCTCTGCCTGGGACTTCTACAACCGCAAAGACTTTAG[G/A]TATCGCAATCGTATCACTTTAAACTCCCTGTTATACAACAACACACTGGTGTGATTACATTTCAAACAAAAATCAGGGCATAATAAAATCCAACTGAGAAAAAAGTTAACTTTTCAGAAAATGTTTCCGATTCAGTTGCCTGTGGGCGAAATGACTAGGCCAGATAACAGTCAAACTACTAACAACTAACACTACTACTAGTACTTGTACTAACTCTACTAACGAGTGTGTTCATGACTATAGAGACAAAGCAGAATAATATAATACGAAAATATCAGTTTGCAACATCAAGCAGCACAACTGAGCTGTTTTTAATGTCTAAAAATGAATGGAAGTGAACGAGACCGAAAGCAAAAAAGATTCAAATGGCTGCACCCGCTCGTACGCAAAGAATAAGGTCAATAATGTTATCTGATATTCCAGTTAAATCAGTATATTTTAAATACACTAAATCATCGCTTCATCAATACAAATATTTAAATAAATGATATATAAGCTGT
Associated Phenotype:
Not determined