ZMP
ARMC3
Ensembl ID:
Description:
armadillo repeat containing 3 [Source:HGNC Symbol;Acc:30964]
Human Orthologue:
ARMC3
Human Description:
armadillo repeat containing 3 [Source:HGNC Symbol;Acc:30964]
Mouse Orthologue:
Armc3
Mouse Description:
armadillo repeat containing 3 Gene [Source:MGI Symbol;Acc:MGI:1918132]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18404 | Essential Splice Site | Available for shipment | Available now |
sa44113 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18333 | Nonsense | Available for shipment | Available now |
sa32483 | Essential Splice Site | Available for shipment | Available now |
sa45826 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18404
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 |
---|---|---|---|---|---|
ENSDART00000111237 | Essential Splice Site | 98 | 867 | 3 | 18 |
ENSDART00000111237 | Essential Splice Site | 98 | 867 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 17614124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16920600 |
GRCz11 | 24 | 17065019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTGCGCAGGAATGCTGTCATGGCTTTGGGCGTCATGGCTTCTAACAG[T/A]ACGTAGGGTTTAAAAATAGGCACAGTAAGTAAATCAAAAGATTTTTAGCA
Long Flanking Sequence:
AAATAAATACCAGTACTTCACGAAAAACATAAGGTCTAAAAAATAGGTACTAGTTTCATGAAAATATGACTTCATATTCCGTATGCCAACATTTTAATACAATTCACATTTAATCCTTTTAGTTCGACCCTTTATCCATCGAAAGCAAAACTGCAACAACAGCAGTTCTGATGCTCAGCTCCCCTGAAGAAGAAGTGCTGGCCAAAGCTTGCGAGGCCATCCACAAATTTGCAGAAAAAGGTAACAGTGTCATCTAGTCTTACAATCTGAGGTCATTGAGAATTTTGCAGAGGTAAGTGTCCACTGTGTTCCCTCATGTGGTATTACTTCATTGATTTCACTGTGTGTTTTTGCTGTCTGCTGCTATTTTTAGGTGATGAGAATAAGACTTGTTTGATGTGTTTGGGAGCGATTGAACCCCTTTCTCTTCTCATATCTCATGAAGACAAGATTGTGCGCAGGAATGCTGTCATGGCTTTGGGCGTCATGGCTTCTAACAG[T/A]ACGTAGGGTTTAAAAATAGGCACAGTAAGTAAATCAAAAGATTTTTAGCAACATAGTATTCATTTATTTGTCACATTTGAACAGATGAAGTTAAAAAGCACTTGAAGTGTCTGGATGTGATACCTGCAATAATCAGCAAACTGTCTCCAGAAGGTACTGGTAGCTTCTATTTTCATTTTTAAATTGAGTGCGCATTTAACCATTCATGCATTCATCTATAGGCTAAATAAAGATAAAGAATATACTCTGTATATATATACAGTTAGAATTATTAGCCCCCCTGTGAATTTTGTTTTCTTTTTAAATATTTCCCAAATAATGTTCAACAGAGCAAGAAAATGTTCACAGTACGTCTGATAATATTTTTTTCTTCTGGAGAAAGTCATATTTGTTTTTATTTCGACTAGAAAAATAGCAGTTTTAAATTTTTTAAACACCATTTTAAGGACAAAATCATTAGCCCCTTTAAGCAATTTTTTTTTTCGATAGTCTACAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44113
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111237 | Essential Splice Site | 98 | 867 | 3 | 18 |
ENSDART00000111237 | Essential Splice Site | 98 | 867 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 17614124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16920600 |
GRCz11 | 24 | 17065019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTGCGCAGGAATGCTGTCATGGCTTTGGGCGTCATGGCTTCTAACAG[T/C]ACGTAGGGTTTAAAAATAGGCACAGTAAGTAAATCAAAAGATTTTTAGCA
Long Flanking Sequence:
AAATAAATACCAGTACTTCACGAAAAACATAAGGTCTAAAAAATAGGTACTAGTTTCATGAAAATATGACTTCATATTCCGTATGCCAACATTTTAATACAATTCACATTTAATCCTTTTAGTTCGACCCTTTATCCATCGAAAGCAAAACTGCAACAACAGCAGTTCTGATGCTCAGCTCCCCTGAAGAAGAAGTGCTGGCCAAAGCTTGCGAGGCCATCCACAAATTTGCAGAAAAAGGTAACAGTGTCATCTAGTCTTACAATCTGAGGTCATTGAGAATTTTGCAGAGGTAAGTGTCCACTGTGTTCCCTCATGTGGTATTACTTCATTGATTTCACTGTGTGTTTTTGCTGTCTGCTGCTATTTTTAGGTGATGAGAATAAGACTTGTTTGATGTGTTTGGGAGCGATTGAACCCCTTTCTCTTCTCATATCTCATGAAGACAAGATTGTGCGCAGGAATGCTGTCATGGCTTTGGGCGTCATGGCTTCTAACAG[T/C]ACGTAGGGTTTAAAAATAGGCACAGTAAGTAAATCAAAAGATTTTTAGCAACATAGTATTCATTTATTTGTCACATTTGAACAGATGAAGTTAAAAAGCACTTGAAGTGTCTGGATGTGATACCTGCAATAATCAGCAAACTGTCTCCAGAAGGTACTGGTAGCTTCTATTTTCATTTTTAAATTGAGTGCGCATTTAACCATTCATGCATTCATCTATAGGCTAAATAAAGATAAAGAATATACTCTGTATATATATACAGTTAGAATTATTAGCCCCCCTGTGAATTTTGTTTTCTTTTTAAATATTTCCCAAATAATGTTCAACAGAGCAAGAAAATGTTCACAGTACGTCTGATAATATTTTTTTCTTCTGGAGAAAGTCATATTTGTTTTTATTTCGACTAGAAAAATAGCAGTTTTAAATTTTTTAAACACCATTTTAAGGACAAAATCATTAGCCCCTTTAAGCAATTTTTTTTTTCGATAGTCTACAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18333
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111237 | Nonsense | 145 | 867 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 17612031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16918507 |
GRCz11 | 24 | 17062926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCCACATTGTGTTTGGCATCATTGTCAGTGGACTTCTCCTACAAGATC[C/T]AGATATTTGAAAGCAATGGACTTGAACCTCTTATTCAGCTCTTGTCCAGC
Long Flanking Sequence:
AAATAATTAAAGCAGGGTAAATGCAGGGTAAACTACTTAAATAGAGATATTAATATTGCTTATTTTACAGGTAAATTATTATCATGAAATAACAATTCTTGTATTGTTTCATCTAAAAAAGTTGTTTATACTTATAATAATAATAAATACTATTATGATTATACACTGATAGAATAATACAGTATATTATTATATATTTAAAATAAGTTTATTGTTATTGTTTTTATTATTATTTTTCAAACTTTGATTATTATTTAAAGAAGAAAAAAATATATCACACTCTGGAAAAAAGTATTTAATAACATAAATATTTTCTGACAATAAGCCTTGGTGTCTAGAGCAGTTTACCCTGCATTTACCCTGCTTTAATTATTTGTAAATGTTTGATTTCTTGTCCACACATTTAACCTGCCACCATCTGTTCCTCAGAGAATGTTATGGTCCATGAATTTGCCACATTGTGTTTGGCATCATTGTCAGTGGACTTCTCCTACAAGATC[C/T]AGATATTTGAAAGCAATGGACTTGAACCTCTTATTCAGCTCTTGTCCAGCCCAGATCCAGATGTGAAGAAAAACTCAGTGGAGTGCATCTTTAATCTAGTGCAAGTAAGACAACAGATTAGTCAGAGTCAGTCAGAAAGTTTGCTGTGATTTCTGATTAAAAGGTATCTTGCAGGATGGTTTCAAATTGGTTGTGTTTTAAATAACATCAAAGATACTTAATCAGCTTTAAAGGGATATTTACACAAAAATGACAATTCTTTTACTCACCCTCCATTTATTCCAATACGGCTTGAGATTTTTTTTTTCAGTTGATCATAAAAATTTGGACTTTTTTGAAGAATGTTAGAAACTCATAATTTTTCTATAGATGTCAGTGGTTACCAGTTTCTGACATTCTTCAATGTATCCTCTTTTTTGTTCAACAAAAAGGTTTGGAACTGTTTTGGAAATTTTAGGGTGAACTGTTCCTTTAAACGCAGAACTCTTTGTATTCCAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32483
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 |
---|---|---|---|---|---|
ENSDART00000111237 | Essential Splice Site | 179 | 867 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 17611926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16918402 |
GRCz11 | 24 | 17062821 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCAGATGTGAAGAAAAACTCAGTGGAGTGCATCTTTAATCTAGTGCAA[G/A]TAAGACAACAGATTAGTCAGAGTCAGTCAGAAAGTTTGCTGTGATTTCTG
Long Flanking Sequence:
GTTTCATCTAAAAAAGTTGTTTATACTTATAATAATAATAAATACTATTATGATTATACACTGATAGAATAATACAGTATATTATTATATATTTAAAATAAGTTTATTGTTATTGTTTTTATTATTATTTTTCAAACTTTGATTATTATTTAAAGAAGAAAAAAATATATCACACTCTGGAAAAAAGTATTTAATAACATAAATATTTTCTGACAATAAGCCTTGGTGTCTAGAGCAGTTTACCCTGCATTTACCCTGCTTTAATTATTTGTAAATGTTTGATTTCTTGTCCACACATTTAACCTGCCACCATCTGTTCCTCAGAGAATGTTATGGTCCATGAATTTGCCACATTGTGTTTGGCATCATTGTCAGTGGACTTCTCCTACAAGATCCAGATATTTGAAAGCAATGGACTTGAACCTCTTATTCAGCTCTTGTCCAGCCCAGATCCAGATGTGAAGAAAAACTCAGTGGAGTGCATCTTTAATCTAGTGCAA[G/A]TAAGACAACAGATTAGTCAGAGTCAGTCAGAAAGTTTGCTGTGATTTCTGATTAAAAGGTATCTTGCAGGATGGTTTCAAATTGGTTGTGTTTTAAATAACATCAAAGATACTTAATCAGCTTTAAAGGGATATTTACACAAAAATGACAATTCTTTTACTCACCCTCCATTTATTCCAATACGGCTTGAGATTTTTTTTTTCAGTTGATCATAAAAATTTGGACTTTTTTGAAGAATGTTAGAAACTCATAATTTTTCTATAGATGTCAGTGGTTACCAGTTTCTGACATTCTTCAATGTATCCTCTTTTTTGTTCAACAAAAAGGTTTGGAACTGTTTTGGAAATTTTAGGGTGAACTGTTCCTTTAAACGCAGAACTCTTTGTATTCCAGAAGGACACATTTCAGATCAATTATTTGTGCTCTCTGCTGCTCTGTGTAAACTCAGGACGTCCAGAATAGAGCGGCTGTGCAACGTCTGAATGGACTCCCTCCACTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45826
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 |
---|---|---|---|---|---|
ENSDART00000111237 | Nonsense | 412 | 867 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 17605127)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16911603 |
GRCz11 | 24 | 17056022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGATGCAGAAGGAGACAGGCTGTTGGTGCGACAGCTGCAAGACAGCTG[C/A]ACTGGAGCAGCTGTGTATGCGGCAATGGCCTTGACAAACATGGCATCACA
Long Flanking Sequence:
AAATGTGTATAAATATATATTTATTCAGTTTTTATATTGAATTTAGTACTGCTTTTTAAAAAAAAATGGAAATGTTTTATGTACAATTCAGTTTAAAAAGTCAAATTTTCTGTCTTTTAGTAGATATATTTTATGAGAGACTCCTATAGCTTCCTATAGCTTTGTTTACCATAATTGGGTCCGCTGCTTAAAACATATGCTGGAATAGTTGGCGGTTCATTTCGCTGTGATGACCCCTGATAAATAAGAGACTAAGCTGAAGGAAAATGAATGAATGAAAGTTTTTAGTCACGATACTCCTAAAATCATTCTGCATTAACCTGTAGAGTTTTTACAAAATTATGCACAAAAATGACAAACAAGTTTGCAGATTCGGTCTGGCCCTGGTCAAGATTATCTACTCCAGAATGACATTTTTAACCTTTCTTTGTCCCCATTTTTAGTGCTATATATGATGCAGAAGGAGACAGGCTGTTGGTGCGACAGCTGCAAGACAGCTG[C/A]ACTGGAGCAGCTGTGTATGCGGCAATGGCCTTGACAAACATGGCATCACAGGAGGAGCTGCGGAAAAGCATTCTGGCCCATGAAGCCATGCCAGCATTGGTGGAGCTGCTTCACTCCACTGATAATAACATTCTCATCAGTGCAGTGCAGGCTGTGGCTTCACTGACCTGTGATGCAGAGGCCAGGCAGGAGGTAACAAGCAGTGCACTGCACAAAAGAGTCCATTTCAAAGGTCTACACAATCACCACAGCTTATCAGCTAACTGAGCGCCGGACAAACAAACTTTTTTTCTGGGTCAGGGGTGTGAAGGGCGTAAATGGATATTGTTGTGCAGTGCATTATGTGTCATTTCTGGTGATTGTTTTGCTGTTTTCTTTACTTGCAGCTGAGAAATGTTGGAGGGCTATCAGCTTTAGTTCAGCTGCTCAAATCGATCAATGCTGAAATTCGCAGAAATGCTTCCTGGGCAATTAGTGTGTGCGCAAACGACGAAATAACA
Associated Phenotype:
Not determined