ZMP
acta2
Ensembl ID:
ZFIN ID:
Description:
actin, aortic smooth muscle [Source:RefSeq peptide;Acc:NP_997785]
Human Orthologue:
ACTG2
Human Description:
actin, gamma 2, smooth muscle, enteric [Source:HGNC Symbol;Acc:145]
Mouse Orthologue:
Actg2
Mouse Description:
actin, gamma 2, smooth muscle, enteric Gene [Source:MGI Symbol;Acc:MGI:104589]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35248 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16546 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35248
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066430 | Essential Splice Site | None | 377 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 18167952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16978650 |
GRCz11 | 12 | 17100524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACCATCACCAAGTGGCTAAATACCCCCCCGGCCCAGCACTGTCAGGG[T/A]AAGTGCCACCTAGCTTCTCTCACCTCCTTCTCTTTCTATTTTGCAAGCTT
Long Flanking Sequence:
TTTTCTGTTCCAAACGTATGCATAAGATTTTATTTTATTTACTTTTTGCTTTGTTTTTACAGTACAGCTTGGGAGTTTAAACTTTTAAACTCGTGTGACCTATGTACTTAAGTGACCAAATGTCTTTGCCATTCCTTCTCAGGTGTGGGCCGTGGTGAGCGTCTGTGTAGCAGATCAGGCCCAGCCCTGTGTTTATTCTCGTGCATAGTGAAGTCCCCACAATTTCTGAGGAGAAAAAAGGAAAAGGTCCATTGGAATGCCCAGAGTAAGGAGGCAAGAGGCCGCCCTGGTGCTGCCCGGATTGGAGTGTTTTCTCCCAGTCATCCCTATAAGGCTTTAGTGGAGTGAGGCTACCGATCCGAGTGCAGCCCAGGCTCCTTGTTTGGGATGTTAGAGGGTGTGGTGAGCAGAGATGGAAACTACATAAGTACACCACAAACCAGTGAGGTGTACACCATCACCAAGTGGCTAAATACCCCCCCGGCCCAGCACTGTCAGGG[T/A]AAGTGCCACCTAGCTTCTCTCACCTCCTTCTCTTTCTATTTTGCAAGCTTTATCTGATTACTCTTGAAACTCGCTGTGTAAAGGGTCAAAGAAGTGCTGTTGTTGTTGTTGTTGTTTTTTGCACAGGTGTAAGCTGGCTTTAAATATTTTGGCTGGTTAGAGTGTTTTCTGAGAAAGATTTGATCTACATTTCTGTAAATGTGATTGTGAGGATTGATTTTCCTAGAGACGTGCCTTCTGAAAGATACATTTTCTACCTATCTTCCTTTTCTTTAAAGAAGCACTTAAAGTTTTAAAGAACAATTCTGCATGGTTGTGTCTAAAGCATCCATATTTTAGTATCTTTATTGTGATTTTATAGTAAAATCTCTGTGGGTGTGAGTGTTTTTTAAAGAGAGGTTCTGAATGGCTGTTGAAGCCTGTCTGATTTGTTAGGTTTTTGACTAAATATGGTTCTTCTGGACCGCTGACCAGTCCCCTCTTTTCCTCACCCACTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16546
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 |
---|---|---|---|---|---|
ENSDART00000066430 | Essential Splice Site | 123 | 377 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 18174374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16984951 |
GRCz11 | 12 | 17106825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAGAAGCCCCACTTAATCCTAAAGCCAACAGGGAGAAGATGACCCAGG[T/C]TAGAGGTGTCACTGAGAAACCYAATRATGGGTACACATTTANTTTTTATGG
Long Flanking Sequence:
TCCACTAAAAATATCTTCTTTTGGTAAACACGGCTTATCTTGTTTTAGGCTCAAATTTATTTTCACAGTATTCCCATATTACATACAATAGGCAGCATGTGATATAACTTTTTACATCTACATTACTCAAGAGCACTTTTCCAAATAACTCTGACTCACACGTTGAAAATATTCCAGCGTCATTCATTTCACACCACATGGTGTCATATTTTAACACATGCACACATCAGAGGGTATTATTTGGAAAATGAATGTGATGTTTGTCATTCTGTAATAATGGGAATCAGCTTTCAATTTCCACACAAAATGGTTCATTAGCCCGTTTATTTTCTTAATAGTGAATTTGATCATTGTTTGTTCATTGTTGCCCATTGTTTATGTTCACCAGATCTGGCATCACTCTTTCTACAACGAGCTCCGTGTGGCTCCAGAGGAACACCCCACTCTGTTGACAGAAGCCCCACTTAATCCTAAAGCCAACAGGGAGAAGATGACCCAGG[T/C]TAGAGGTGTCACTGAGAAACCCAATAATGGGTACACATTTATTTTTATGGTCCCTTTTACACATTTTGTTACCTTGCAACTACATGTTAACAAATTTTTTAAGTAGTATTAACAGTAGGGCTGGGCAATATAGCCACAATGTAAGTCTGATAATGATATATATTATGTATATCCGTATCATTCTAGTACCATTTTTTTTTCATTTCAATCCATTACTAGTTCATTTAATGACCAAATGTAAAGGACTATTGCTTTTTATATCTTAAATTATGTACTTAGAGGTGTATTTGTTCATATGTGATCTCTTTTCTCACTTTATTTAGAGCTTAAATGTTTGATGAAAATTTAAATGAATGTATAGGTTCCAAAATTAATGATTACAGGTCAAACATAAAAATAACAAACATTGCTAAATAAAATGTAAACATCACCATGTAATATGGTAACATTGCACCATGAAATAAACAATAGAGTATAATATGAAACGATAGAGTATTTAT
Associated Phenotype:
Not determined