ZMP
ace2
Ensembl ID:
ZFIN ID:
Description:
angiotensin-converting enzyme 2 [Source:RefSeq peptide;Acc:NP_001007298]
Human Orthologue:
ACE2
Human Description:
angiotensin I converting enzyme (peptidyl-dipeptidase A) 2 [Source:HGNC Symbol;Acc:13557]
Mouse Orthologue:
Ace2
Mouse Description:
angiotensin I converting enzyme (peptidyl-dipeptidase A) 2 Gene [Source:MGI Symbol;Acc:MGI:1917258]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1003 | Nonsense | Available for shipment | Available now |
sa10138 | Essential Splice Site | Available for shipment | Available now |
sa41865 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1003
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:
Founder:
mrf144
KASP Assay Location:
Project 554.15, Plate 16, Well E07
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003712 | Nonsense | 5 | 785 | 1 | 18 |
ENSDART00000126110 | Nonsense | 5 | 785 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 30871772)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29749134 |
GRCz11 | 11 | 29996318 |
KASP Assay ID:
554-0907.1 (used for ordering genotyping assays)
KASP Sequence:
ACAACAGCGTCAGAATCGGTGGGACAAGGCTGTGGTCATGTGTGCTCGCT[G/A]GCTCCTGCTTTTGGCCTTGGCCTCTGTGGCCTGCTGTCAGACTGTGGAGG
Long Flanking Sequence:
CTCCTCAAACTGAAATTCACAGGTGGTCTCTTCACAAAGAAAATAATTTTAGTGTGTTTTCCTTATTTCCATGTATGCTTTCAGTAGCCATTACAACTTGTTTACCTTCTATAAAACTCAGATTTGTTTCAAATAAACTGTATTAAAAAAAGTACAGTTTAACAACTTTTAACAACATGACTTTACTTTTAACAACATGACTGATTTCATCAACATCTAATTTCTACTCACTTGCAGTGCTCACACAGTGAAAGTCTAAGTTTCATTCATACAGAACTTTTCTATAAATCTGGTCATATAAGCAGAAAATATGTTGCGCAACGTCCATCAAGACTCGTTCCTGGAATCATCCCATCTGCATTCAAATAGATTGTGCACCATTAGGGTTATAGCACTGGTCAAAGGGCAAAGCAAATGAGCTGTCTTCAATAAAAAGCGCACACGGGGAAAACAACAGCGTCAGAATCGGTGGGACAAGGCTGTGGTCATGTGTGCTCGCT[G/A]GCTCCTGCTTTTGGCCTTGGCCTCTGTGGCCTGCTGTCAGACTGTGGAGGACAGAGCAAGGGAATTCCTCAACAAATTTGATGAAGAGGCATCTGACATCATGTACCAGTACACCCTTGCATCCTGGGCCTACAACACAGATATCTCCCAGGAAAATGCAGATAAAGAGGTAAGAGTGGAAAAGTAGAGGAGGGATGTTAAGCATCACAACTGAATCTACTGAAATCTGAAAATATAGGAGAAGTAATATTTGAACAATAGAAATACGATTTTAGTAAAAATACTATTATTTTTAGTATTTAGTAAATACTACATTTTTTTTTATTCTTTCAGCTACTGAAATCACAAAATATGTATTTTAGGGGTAAATAATCTGAATATGACATATCTGAATATGAGTATTTAAGACACATTGAGCAGCCTTTTCTGTCTTCCGCAAGCAATTCTAAGACGTTAAACTATTGAAATATATATAAAATATATTGATAATATATTCGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10138
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:
Founder:
SL4_02_C9
KASP Assay Location:
Unknown
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003712 | Essential Splice Site | 115 | 785 | 3 | 18 |
ENSDART00000126110 | Essential Splice Site | 115 | 785 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 30869304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29746666 |
GRCz11 | 11 | 29993850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATATGACAAACATAGAAACTAAAATKGTGTGAATGACTTRTGTATCACA[G/A]CTGAGAAATATCATGTCAGAGATGAGCACTATTTACAACACGGCRACTGT
Long Flanking Sequence:
CATACCATACAATGTATTTTTGGCTGTTTCAATATATGGGGAAAGTATGAGAACAACACCATTAGTAACTGTAAATTGGTGTTCAACACAAGGCGATCAACTTCAACCCTTTTACGCAACAGTTTTAACTAACTAAATTATTGAAATTACAAATATCTAATGTTTATTGAAATGATTGATAGGAGAACACCAATAATCCCTGCACCACTAGTGATCATGGGTTCTCTTCAACTCTCTCTTCAGGCAGAGGCATATGCAATCTGGAGCGAGTACTACAACAAGATGTCAGAAGAGTCTAATGCCTACCCCATAGACCAAATATCGGATCCAATCATTAAAATGCAGCTCCAGAAGCTTCAAGATAAAGGATCTGGGGCCCTTTCACCTGACAAAGCTAGTGAAGTAAGTATGACATTGCAATTTCATGTGCTGTATCACTTCTCCTGTAGTAATATGACAAACATAGAAACTAAAATTGTGTGAATGACTTATGTATCACA[G/A]CTGAGAAATATCATGTCAGAGATGAGCACTATTTACAACACGGCGACTGTGTGCAAAATAGACGACCCCACCGATTGTCAGACTTTGGAGCCAGGTAATATCAACTTTGCATACCATTCTAATGATAAAGCGAAATCTCAGGATCATAAATAGATGGCTTGTTTAATAATAAAAGAGTGTGTGTAAGAGGTTTCTGTTATCTGCTTTACTTATTCACGTGTAAAAAAAAAAAAACAATAGGGAACCATCAGTTTTCATTCTCAGGTTCATTGTTGAATGTGGTGAGATGTGAAAAAAAGAGGATATGAAATATGAAACATAGTGTGAAGCAAAGGTAAAAAGAGCCAGAAAGGGTTTGCATTCAAAATGCTTCAATATTCAACAATAAATTAATACAATCAAACAACGAAGTGGGATACTGTGAGTTTAAAGAGCCAGATGTATTTTATTCATTTACCATTTTAGCTAATTTAATTATTTTTCAGTTCTCAGTTAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41865
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
Founder:
SL7_03_A10
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003712 | Nonsense | 529 | 785 | 12 | 18 |
ENSDART00000126110 | Nonsense | 529 | 785 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 30860853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29738215 |
GRCz11 | 11 | 29985399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTACTTCACTAGAACCATATATCAGTTCCAGTTTCAAGAGGCATTATG[T/A]AAGGCAGCTGGCCACACCGGTCCCCTTTACAAATGTGACATTACAAACTC
Long Flanking Sequence:
CAACAACAGAGATAATCCAAAGCATAATCCTAAAAAAGGCAAAGGGTCAAGACAGGGAGCAAATAATCAGAACAGATAAACAGTCCAAGGGTCAAAAAAACAAGGAAACGTTTTGTAATGAATGCAACAGCTAGACAAGATTAATTGTTTAAATAGTCTAGGTAATTAGTGATAATTTCCTTCAGCTGTGAGTAATCAGAGTGAACTTGAGACAGGTGTGTGGATGCAGGGTATGATGAGACATGTAGTCCGGAAAGATGATACTTGGTGAAGTGTTCTACAGCGGCCCATTAGGGTAACCCCCTGCCAATCATAACAGTTTAATTGACAAAATTAGCTGAAAGAAAATGTTTTTTTTTTCAGAATTAAACTACTACAAATTATACATTCAGCAGAATATAAAACTCGAGCTATATAGCCAAATAAATAACCATATCTTGTTTCATAAATAGGTACTTCACTAGAACCATATATCAGTTCCAGTTTCAAGAGGCATTATG[T/A]AAGGCAGCTGGCCACACCGGTCCCCTTTACAAATGTGACATTACAAACTCAACCAAAGCTGGTGACAAACTCAGGTATGGCTTCATTCCTTTGATGTTGTTTATTAATATACTTTTTTTGTAATAACTCCCCTAGAGACCTGACTTGTTTAAAACCAGAATGACCTGTAAATCCCTTTAGAGACCTGTATAGAATAAACAGAATAGCTAATAACTATTTTGTGATTTATATTTGCAGGCATATGCTTGAGTTAGGCCGATCCATGTCTTGGACTCGTGCTTTGGAAGAAGTTGCAGGAACCACAAAGATGGACTCACAGCCACTGCTACATTACTTCAGTACTCTCATGGAGTGGTTGAAGGAGGAAAACCAGAAGAACAACAGAGTTCCTGGCTGGAACGTCAATGTTAACCCTGGTTAGTTTTCTATTTGAATATACATAACATTATTAATGTGTACATTGTCTCCTACACTGTAAAACCCAACAGTCAACTTTATCA
Associated Phenotype:
Not determined