ZMP
atxn7l2a
Ensembl ID:
ZFIN ID:
Description:
ataxin 7-like 2 [Source:RefSeq peptide;Acc:NP_001038750]
Human Orthologue:
ATXN7L2
Human Description:
ataxin 7-like 2 [Source:HGNC Symbol;Acc:28713]
Mouse Orthologue:
Atxn7l2
Mouse Description:
ataxin 7-like 2 Gene [Source:MGI Symbol;Acc:MGI:1919772]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45436 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35137 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45436
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 |
---|---|---|---|---|---|
ENSDART00000090520 | Essential Splice Site | 249 | 624 | 5 | 11 |
ENSDART00000127742 | Essential Splice Site | 260 | 723 | 5 | 10 |
ENSDART00000135360 | Essential Splice Site | 259 | 722 | 5 | 10 |
The following transcripts of ENSDARG00000055300 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 37230746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36127974 |
GRCz11 | 11 | 36389957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAATGCATTAAATCCTGAATTTGATCATAAAATTTGTTGTGCTCCACA[G/A]AAAAAGAATGTGACCTTGACAAACACTGTGGTGTTTTGGACACTGAGAGA
Long Flanking Sequence:
TCGCTGATCCACTGCCATGTCCTGATATATCCACCTGCAACCGACCCGCAATTAATCATAATGTATTTTTTTATTACCGGACCCTTAGATTATCCGCAGCACCCGCGCATATAACCGCCATCCGCGCATCACTACACAGCGCTGTTACCTAGCTGGGGACTATTTTCAGGCACTGTGTAACAGAATTTTGCAATGCGCTACTTTTAATGTAATGAGACATTTATAATCGGGAGAGAATTTTTATTAAATGTGTATCCTTACAATGTATAACTATTTATTTTATGTATTATTCATTGTTGAGCACAGGCAATTTTCTAAAATCGCCCATGCTGTTAACATTTGTATTGTTAAAATCTTGTTTAGTATAGAAAAGGGTTATTTATCTTGTTTGTTTTTGCCATGTTAGCTGATATGGCAGTAAACAACTCTTTCTCCATCCAAACAAGGTGTTGTAATGCATTAAATCCTGAATTTGATCATAAAATTTGTTGTGCTCCACA[G/A]AAAAAGAATGTGACCTTGACAAACACTGTGGTGTTTTGGACACTGAGAGAAAGAAAGTGTGTACTCGACTTCTGACCTGCAATGTGAGTTGAGCACCACTTCCACATCATCTCACAATGACATGTTACCAGTGTTTCTAGCTCAGAGTGAACATGTATGCTGGTCTTCAGAGTTCAGATGGAATATTCTGGAAAGCAGAATTGTTGTTTGATGCATTTTGCTGTCCTGTATTTAAATGGTAAATGTACAGTAGAAGTCAGTTATTAGCCCCCTGTATATTTTTTTCAACACATTTCTAATCATAATAGTTTTAATAACTAATTTTTTAATAATTTCTTTTACTTTTGCCATGATGACTACATAATATTTTACAAGATGTTTTTCAACATACTAGTATTCAGCTTACAGTGACATTTAAAAGCTTAACTAGGATAACTTGGCAGGTTAGGTTAATTAGTCGAGTCATTGTGTAACAGGGGTTTATTCTGTAGACACTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35137
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 |
---|---|---|---|---|---|
ENSDART00000090520 | Essential Splice Site | None | 624 | None | 11 |
ENSDART00000127742 | Essential Splice Site | 718 | 723 | None | 10 |
ENSDART00000135360 | Essential Splice Site | 717 | 722 | None | 10 |
The following transcripts of ENSDARG00000055300 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 37239646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36136874 |
GRCz11 | 11 | 36398857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGTCGGGACTCTCTGTAGGAGGAGAGAAGAAACTCAGCACACAAAAGG[T/C]GAGGGAGTGTTTAGGGCTGGATCTGACTTGTTCTCTGTTCTCATCACAGT
Long Flanking Sequence:
AGTCGGGCGACCCAGCAAACAGCAGATGCGTCTCAGGGAATCAGATCGGACGCCCACACCGGACGCCGCTGCACTGCGCAAGCGAAAAGCCTCTTTCGAAGACTCTGACTCAGCCGTCAGCCCGGACAAGAACTGCGTGCCCCAGAACAAGAGTCGTCCTCTCATTAGCAAAACACCACCGTCAGCCTCTCACGGACAAACTAACGGCTCGCTTTCGCCCGGAAGCAAAGCAAGGCCCTCGGACTCTCACTCCCCTTCCTCGTGGGCCTTTAAGAGGACACATCAGTCGGCCCCGGACAGCCGAGGACTGGACTCGGGACTCAGGGTGTCCAGCTTTGACCATAAGAGTTTGGGGAAGAAACGCAAGAGCAGCGGGTCGTCTCCGCCCTCCAAACCCCACCGGCTGCCCACGTCCCCTCACTCCGGCTTTTACACCTGGAAGGAAAGCAAAGGGTCGGGACTCTCTGTAGGAGGAGAGAAGAAACTCAGCACACAAAAGG[T/C]GAGGGAGTGTTTAGGGCTGGATCTGACTTGTTCTCTGTTCTCATCACAGTGAAGTGACTGTGCAGCCAGTTTTTGCAGATGTGAGGTGGTTGTTCAACACCGAGTTCAATAGGTGGTACTGTCTATGCTGATCTACAGTTCAATGTATTTTAATAGCTACACCAACATTATTGTAGTAGTAGTACTATTATTAATGGGGTTTGCCTTAGGCAAAGTCCATTCTTACAATTGTGCTGGTTTATTATTATTCTTCTTCCATCTTCCGTGCGCTTTTTCGGCGCGTAACTAGTCCCGCAGCTTTTGTCCCACACCCTTGAAAGTGGTGTCAAATCGTCCGGTTTAATCGGGAATGGTGTGCTATGACTTTTGTAAGGGGTCGGGGGTTTTTTGGCCCCGCAGGGGCCAAAAAACCCCCCCAAAAATCCCATAGACTTAACATTGAGCCAAACTTTGACGACTCACAGCGCCGCGTGTGAATTTCATAGAAATATGGGATTCAC
Associated Phenotype:
Not determined