ZMP
actn2
Ensembl ID:
ZFIN ID:
Description:
alpha-actinin-2 [Source:RefSeq peptide;Acc:NP_001032662]
Human Orthologue:
ACTN2
Human Description:
actinin, alpha 2 [Source:HGNC Symbol;Acc:164]
Mouse Orthologue:
Actn2
Mouse Description:
actinin alpha 2 Gene [Source:MGI Symbol;Acc:MGI:109192]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa274 | Nonsense, Stop Lost | Confirmed mutation in F2 line | Not yet available |
sa36380 | Nonsense | Available for shipment | Available now |
sa36379 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42906
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104882 | Nonsense | 213 | 895 | 7 | 21 |
ENSDART00000133327 | None | None | 126 | None | 16 |
ENSDART00000138911 | Nonsense | 212 | 894 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 19964856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 20114867 |
GRCz11 | 17 | 20134703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTGTGCCCGTTCCTCTCCTTTCCTGTAGGATGATCCACTGGGTAATT[T/A]AAATCTGGCATTTGACATTGCTGAAAAACATCTGGACATCCCCAAAATGC
Long Flanking Sequence:
ATTCTGCTGTGGCGACACCTGATTAATAAAGGGACTAAGCTGTAAAGAAAATGAATGATTGAATGAATATAATTTATTTCTGTAATGGCAAAACTGTAAACACATACAGTAGATAAAAAATGCAACAGAATAGGATTTAATTTAAGTATAGTAAGTTACATTTTACTAACACTTTTGAACAATGAATCAGTATGAAGGTTTGTTGAATCAAAGTATAATTTCAAACAAAAAATAAATCTATATAAAATCTCACAATCCCCAAACTTTTCAAAACTTTTGTATATTAAAGGCAACTCTTTTTCAGATAACTAATATAAAAAACTTATTTTTATTCTCCCTAATAATTTTAAATGTGAAAGTTTTCTTCTCCAGCTGCTCCATACTGACACTTCCTCATGCATGAAAAAAGACGATAATTTTTGTACAATGTTTATGTGATGACGTTTGGTGACACTGTGCCCGTTCCTCTCCTTTCCTGTAGGATGATCCACTGGGTAATT[T/A]AAATCTGGCATTTGACATTGCTGAAAAACATCTGGACATCCCCAAAATGCTGGATGCAGAGGGTAAACCATAAGCATAAAATATGAGTTTTAAAATACAGCCTTTTTTAGACTCTGTTATTGTAAAACACTAAACCATTATGCCATGTATTCCGATTAAGGTCTACTGAATATGTCATAGTTGATTGTGACAAACAAACCTCTCACATATTTTGTCAAGAAACCTTTATAAGATGAAATTCTAGACCAAGACTTGTTGTTCTTCCAAAGTAGCAAAAATACAATACTGTAAAAGGATTTCAAGCAAGCAAAAATATGCCAGTTTTAACTGTGAAATAGTACAAAATATTGCTTTTGCTTCTCAGTCCTGGTTAGCAGCCAAAGGCCAGATGAGAGGACAGTCATGACATATATTTCCAGTTATTATCACACCTTTGCTGAGGCTCAGAAGGTACAGCTCATCCCTGAGCTTGTTAGAAATTTTAGAAATATAGTTTCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa274
Status:
Confirmed mutation in F2 line
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 > A
Consequence:
Nonsense, Stop Lost
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104882 | Nonsense | 287 | 895 | 9 | 21 |
ENSDART00000133327 | Stop Lost | 127 | 126 | 4 | 16 |
ENSDART00000138911 | Nonsense | 286 | 894 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 19963205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 20113216 |
GRCz11 | 17 | 20133052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAAGGTGCTTGGAGTGAATCAGGAAAATGAGAAGTTGATGGAGGATTA[T/A]GAAAGGCTGGCTAGTGAGGTGAGAAGACACATTGTAGTCTAATACATATC
Long Flanking Sequence:
ATAATTCTGACTTCAGCTGTAGTTGTCTTTCATTCCTCTCCTTCCCATCAGACATCCTGAGCACCCCTAAACCTGATGAGAGGGCTATTATGACATACGTGTCCTGCTTTTACCATGCATTTGCTGGAGCTGAGCAGGTATTGAGTTTTGCATGAGTTAGACTGAGTGATTCTTTTGTCAAGTTTATATTTGGGTTTCACATATGTCATATATGCAACATTTCAAATATGTGCTTTCAAATACAGTATATGGCCATTATATAGTGATTTTTGCAATGTTTAGAAACATGTTTTGCATATAAAATGTATGTGAAATCCAAATATGAACTAGTGTGGCATAAATGTAATTTGCATATATTGCCATGTATCATGTTTACATGTGGGCGCCCATCTCTTCTTCTGTTCTTACTGTATTTTTCCTGCTCAGGCTGAAACTGCTGCGAACAGGATCTGTAAGGTGCTTGGAGTGAATCAGGAAAATGAGAAGTTGATGGAGGATTA[T/A]GAAAGGCTGGCTAGTGAGGTGAGAAGACACATTGTAGTCTAATACATATCAGACGCACATGGATATTTGTTCCACTTCTCCTAAATGTCTCTCTACTTTCCTGTAGCTGTTGGAGTGGATCAGACGTACCATTCCTTGGCTGGAGAATCGTGCAGCTGAGAAGACCATGGTTGAGATGCAGAGGAAGCTGGAAGATTTTCGAGATTACCGCAGGATGCACAAACCACCCAAAGTGCAGGAGAAATGTCAGCTGGAAATCAGCTTCAACACGCTGCAGACCAAACTCCGCATCAGCAACCGGCCTGCGTTTATGCCCTCTGAGGGCAAAATGGTGTCGGTGAGAGTTTATCCCACACAATAAAGTGATGCATGTTTAAGTGGCTACCTAATTGGGCACCCAGTGATTTCATTTATTCATTCCATTCATTCATTGTATGTATTAGTTAGTTTGATCAATAATAACAATAATATACATTGATTTATCTTCATTTACTTATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36380
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 |
---|---|---|---|---|---|
ENSDART00000104882 | Nonsense | 681 | 895 | 17 | 21 |
ENSDART00000133327 | None | None | 126 | 12 | 16 |
ENSDART00000138911 | Nonsense | 680 | 894 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 19957340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 20107351 |
GRCz11 | 17 | 20127187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTATGGCGATGGGCGGAACTCTGGAGGATCAGATGACCCAACTGAAG[C/T]AGTATGAGCATGTGATCGTCAGCTACAAATCCAACATAGACCGACTTGAG
Long Flanking Sequence:
AATATAATTTGCGCAAAGAAATTATGGGTTCTTCTCTAAAGAAGTTGTACTCCTCCCCGTTTAGAGCATCATTATGGGTGTTTTATGCTATAAATGACGTGGTTCAAGTGATGGATCTGCAACAGAGAAAGTAGGGGTCTTGGGAAACACTTGTCACTACATCATTCTTTTCCCAAATGATGCATCGTACTATGATAGTTCAGTAGTGAGTTACGTCATTGTTTGAGAAACGCACCCCTGGTTGTTTAAACTACTCATTTAAAATGAGCAGAATCAACACAATTCTTGAGTTTTTTTTTTGTAATAACAATTGTTTTACGTTTAAGCTAACTTAATCAATTTGTTTTGGGACAACATGAAAGAATTGTGTGGAACCCAGCATTTTTTGCAGTGTGTGTCATGCAAATGACATATAAGTTCATCTATCTCTCTGAAAGGAAATTGGTCATTGTTCTATGGCGATGGGCGGAACTCTGGAGGATCAGATGACCCAACTGAAG[C/T]AGTATGAGCATGTGATCGTCAGCTACAAATCCAACATAGACCGACTTGAGGGAGATCACCAACTCATTCAGGAGTCACTTATCTTTGACAACAAACACACTAACTACACTATGGAGGTAGATATATTAAACATTCATCTTTAATTATAAACTATTTTTCCTAACGTACTGTACTACTGTACATTGAAGATTGGGGTCAATACATGATGCTTTGAATCCAAACAAACAGTTGTAAAGCTTAGAGAATGTATCAAATATACTGAAAAACATTGCTGACACCAATTGTTTTTGACTAGTAATGTACAGTTTCCCAGTAGTGGGTTGCAGCTGGAAGGGAAATCACTGCGTAAAACATATGCCAGGATAGATGCCGGTTCATTCTGGTGTGGCTACCCCTGATAAATAAAGGACTAAGCCGAAGGAAAATGAATGAATAAAATGATAGTGTACATAGAAAGCAAATCTAACATTTGGTTTGATGCTTATTTCTTTCTTCTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36379
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104882 | Nonsense | 682 | 895 | 17 | 21 |
ENSDART00000133327 | None | None | 126 | 12 | 16 |
ENSDART00000138911 | Nonsense | 681 | 894 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 19957335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 20107346 |
GRCz11 | 17 | 20127182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCGATGGGCGGAACTCTGGAGGATCAGATGACCCAACTGAAGCAGTA[T/A]GAGCATGTGATCGTCAGCTACAAATCCAACATAGACCGACTTGAGGGAGA
Long Flanking Sequence:
AATTTGCGCAAAGAAATTATGGGTTCTTCTCTAAAGAAGTTGTACTCCTCCCCGTTTAGAGCATCATTATGGGTGTTTTATGCTATAAATGACGTGGTTCAAGTGATGGATCTGCAACAGAGAAAGTAGGGGTCTTGGGAAACACTTGTCACTACATCATTCTTTTCCCAAATGATGCATCGTACTATGATAGTTCAGTAGTGAGTTACGTCATTGTTTGAGAAACGCACCCCTGGTTGTTTAAACTACTCATTTAAAATGAGCAGAATCAACACAATTCTTGAGTTTTTTTTTTGTAATAACAATTGTTTTACGTTTAAGCTAACTTAATCAATTTGTTTTGGGACAACATGAAAGAATTGTGTGGAACCCAGCATTTTTTGCAGTGTGTGTCATGCAAATGACATATAAGTTCATCTATCTCTCTGAAAGGAAATTGGTCATTGTTCTATGGCGATGGGCGGAACTCTGGAGGATCAGATGACCCAACTGAAGCAGTA[T/A]GAGCATGTGATCGTCAGCTACAAATCCAACATAGACCGACTTGAGGGAGATCACCAACTCATTCAGGAGTCACTTATCTTTGACAACAAACACACTAACTACACTATGGAGGTAGATATATTAAACATTCATCTTTAATTATAAACTATTTTTCCTAACGTACTGTACTACTGTACATTGAAGATTGGGGTCAATACATGATGCTTTGAATCCAAACAAACAGTTGTAAAGCTTAGAGAATGTATCAAATATACTGAAAAACATTGCTGACACCAATTGTTTTTGACTAGTAATGTACAGTTTCCCAGTAGTGGGTTGCAGCTGGAAGGGAAATCACTGCGTAAAACATATGCCAGGATAGATGCCGGTTCATTCTGGTGTGGCTACCCCTGATAAATAAAGGACTAAGCCGAAGGAAAATGAATGAATAAAATGATAGTGTACATAGAAAGCAAATCTAACATTTGGTTTGATGCTTATTTCTTTCTTCTGCAGCATGT
Associated Phenotype:
Not determined