Busch Lab

ZMP

LOC797483

Ensembl ID:
ENSDARG00000075956
Human Orthologue:
C6orf168
Human Description:
chromosome 6 open reading frame 168 [Source:HGNC Symbol;Acc:20742]
Mouse Orthologue:
6230409E13Rik
Mouse Description:
RIKEN cDNA 6230409E13 gene Gene [Source:MGI Symbol;Acc:MGI:1923382]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa18658 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa18658
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113864 Nonsense 401 404 6 6
Genomic Location (Zv9):
Chromosome 4 (position 5624859)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 5743040
GRCz11 4 5751610
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTCTGTGTGACTCTGATATGGACACCGAATGCTCAGTCTCAGAGGCG[G/T]AGCTACTGAAGTGATGGCCACACCTCATTTGAWGATGTGTCTGCACGGGC
Long Flanking Sequence:
AAACTTTCATTCATCCTCTCAGCTGTAAAGTTTTTACATTTAGGGTAGAATTTGGATCTTAATGTGCTTTTGTGTATTATGTGTGACATGCTGCAACTAAATTACCTTCGGGAAGTGAATAAAGACTGACTGACTGACTGAATATGAAGTGTGCTGTGCATGTATGAATTCAATTTTATAAATCTGTTATTTCTAAAACTGTTGTGGCTCCATACTTCCTCCATGCAGGTGAGTTCATAAATCTAGCCATGTACTGCGAGCGAATCCGTCGCAAATTCTGGCCTGAGTGGTTCGTGGATGTAGATGACCTTTACTACGATGGGCTGAGCGAAGAGCCGGATTCCCCCTCCCAGCTCCAGGATTTGGGTCTGCACTCATGCAGTTTCCAGGAGCAGGAGAGCAGCGTTTCTCATCAGGACACCCCTTCACCGGACAGTGACATCACCGGACGCTCTCTGTGTGACTCTGATATGGACACCGAATGCTCAGTCTCAGAGGCG[G/T]AGCTACTGAAGTGATGGCCACACCTCATTTGATGATGTGTCTGCACGGGCCCCGCCCCCCATTTATTGTCCCAAACCCTTTATCAGGGAAAGGGCTGGTCAGGAACAGTAGCGTTTTTTTTCCTGCAAGGAATTCTGATGATAATATTGAGGATTTTTACTGATTGAAGGAAAAGCCAGACCAGAGGGAAGTCAGGAAGATGTGTTGAATATTGGAGTGAATGACGCGTCGGCTGAATCACTCCTCCTGTGGATGTGACATCATCACAGCCCTAGAAATGACATCATCACCTGTGACCACTTCCCAATCACTGCGTGTGTTTGTAGCTAGACTGCATTTTTCTTGCATTCTCCCGGGATTTGGTAATGTATGGGTTGCCTAAAATGACTAAAGTGTGTAGATACTGTATGAAGTGAAGCGGCACAATATTTTCTGTGGTCAAATTGCAGTTCATGTCCTGTTTTATTCGGTCAAACCCATAACTAGTGATCAGCTGATAC
Associated Phenotype:
Not determined