Busch Lab

ZMP

LOC557783

Ensembl ID:
ENSDARG00000017579
Human Orthologue:
RIC8A
Human Description:
resistance to inhibitors of cholinesterase 8 homolog A (C. elegans) [Source:HGNC Symbol;Acc:29550]
Mouse Orthologue:
Ric8
Mouse Description:
resistance to inhibitors of cholinesterase 8 homolog (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:21

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa33215 Nonsense Available for shipment Available now
sa44564 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33215
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022660 Nonsense 262 692 5 13
Genomic Location (Zv9):
Chromosome 3 (position 32606118)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32337428
GRCz11 3 32469142
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGGATGAGGAGGGTGAGGAAGGACATGATGATGGTGAGATCTGGAGG[A/T]AAGAGGCGATGAAAACCCTGTGCAATGTCATCTACAACAGCCCGAAAGCA
Long Flanking Sequence:
TGCGCCTGCAGCCGGGCGTTTTGAGAGTGTGTCTGCGAACTCTGAGGATCATCTCACGGGACCGAAAGGCTCTGGCACCCCTGATTACAGACTATGCCATCATAACTCTCGCTCGGCTCGGGGGCATCTCTGCCCTGCCAACCTGGCCTGAGGAAGAGGATGATCAGTGGGGCTCCTCACACAACGACGTCGCTCCTGAGAACGAGACTGACACACTTCCAGATAATGACACCAACACCCAATGTCCAGCATGTTGCAGTGAGACAGATGATTCATGTTGTGGCTCTACAGTCTGCGCTGCGTCTTCGGTCAGAGAAGGAGGTCTGCACTTCAGCCCTATGAATAATACATCTAATCCCAGAGAAACACAAAACGACCACTGTGAAGAAAGTGTAAGGAAAGATGGAGTGTGTGGGCTGTTGACAAGAGGAAAGAGGGAGACCAGAGGAGAGAGGGATGAGGAGGGTGAGGAAGGACATGATGATGGTGAGATCTGGAGG[A/T]AAGAGGCGATGAAAACCCTGTGCAATGTCATCTACAACAGCCCGAAAGCACAAGAGAGAGCCAGCACACTGAGGTGAGACTCACAGTTTGAAACATTTGCCAGATATGGTTTTGTTGAGTAGGTCAGAATAGTTGTGAAAACTCACTGTCATGTGCTTTGTTTTTTTCTCGACCAGGTTACTTCATGGCCTATCAGTGAGAATTAAAGATGGGATACATTCCTCATCACCTCCAAGCGGTCAATTTTATGAACTGCGGCTTCTGTTTTTGTTGACTGCTTTACGGCCTGAGCTCAGGATTGAACTCTGCCAGGTAATTATAGATCATGCAAACATGTGCCCATTAAGCAGAGGGACTTCACGGGCGCAGTAGCTGACCCATTGGTTGACTGAACGATGCAGCTGCGCCCATGGTCCGAATTATGCATTGACAGTCGGGGTGGTCAACTTTTTTGGTTAATTTCATTTGTCTAATACATGCTTCAGTTAATTAAATTTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44564
Status:
Mutation detected in F1 DNA
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
ENSDART00000022660 Nonsense 321 692 6 13
Genomic Location (Zv9):
Chromosome 3 (position 32605837)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32337147
GRCz11 3 32468861
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAAGCGGTCAATTTTATGAACTGCGGCTTCTGTTTTTGTTGACTGCTT[T/A]ACGGCCTGAGCTCAGGATTGAACTCTGCCAGGTAATTATAGATCATGCAA
Long Flanking Sequence:
GGCTCTACAGTCTGCGCTGCGTCTTCGGTCAGAGAAGGAGGTCTGCACTTCAGCCCTATGAATAATACATCTAATCCCAGAGAAACACAAAACGACCACTGTGAAGAAAGTGTAAGGAAAGATGGAGTGTGTGGGCTGTTGACAAGAGGAAAGAGGGAGACCAGAGGAGAGAGGGATGAGGAGGGTGAGGAAGGACATGATGATGGTGAGATCTGGAGGAAAGAGGCGATGAAAACCCTGTGCAATGTCATCTACAACAGCCCGAAAGCACAAGAGAGAGCCAGCACACTGAGGTGAGACTCACAGTTTGAAACATTTGCCAGATATGGTTTTGTTGAGTAGGTCAGAATAGTTGTGAAAACTCACTGTCATGTGCTTTGTTTTTTTCTCGACCAGGTTACTTCATGGCCTATCAGTGAGAATTAAAGATGGGATACATTCCTCATCACCTCCAAGCGGTCAATTTTATGAACTGCGGCTTCTGTTTTTGTTGACTGCTT[T/A]ACGGCCTGAGCTCAGGATTGAACTCTGCCAGGTAATTATAGATCATGCAAACATGTGCCCATTAAGCAGAGGGACTTCACGGGCGCAGTAGCTGACCCATTGGTTGACTGAACGATGCAGCTGCGCCCATGGTCCGAATTATGCATTGACAGTCGGGGTGGTCAACTTTTTTGGTTAATTTCATTTGTCTAATACATGCTTCAGTTAATTAAATTTATGCATTTCAGTTTGGTGAGGGATATTTAGTGTACTCTACCCTACAGTATACTCTGATTAGCTAATTTAGAAGTTAATGTAGTTCAAATTATACAAACTATACATCTAATTTGACTTTACTTGTAGGCTGTATGTAGAAACAAACTTATATTTTTTGAGAAAACAGTCTTTTGTAGGGGTCTACATCTGCAGTTTCAGACTATTGAATAAATCATGTCCACAGTGTTACAAACCGTTATAGGGGTGTGATCAAATGTATATTTTTATTATCTATTATTGTAATT
Associated Phenotype:
Not determined