LOC571902

Ensembl ID:
ENSDARG00000088171
Human Orthologue:
C1orf51
Human Description:
chromosome 1 open reading frame 51 [Source:HGNC Symbol;Acc:25200]
Mouse Orthologue:
Gm129
Mouse Description:
predicted gene 129 Gene [Source:MGI Symbol;Acc:MGI:2684975]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa24689 Nonsense Mutation detected in F1 DNA During 2016
sa44313 Essential Splice Site Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa24689
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129337 Nonsense 103 379 1 5
Genomic Location (Zv9):
Chromosome 25 (position 27537112)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 26227206
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATCAAGGATGGTGGCTATTTTCACCTGGGACAAGAGAAACAAACAAATTA[C/A]AGATGGTGCCCTGAGAGCTCTATAGACAAAAATAGACAGGCACAGAAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44313
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129337 Essential Splice Site 174 379 2 5
Genomic Location (Zv9):
Chromosome 25 (position 27536383)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 26226477
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CCTCTGTCCTCAATCCTTAATGGTCTCCGATCAGGCAGATACAGAGAACG[T/A]GAGTAATCTTTATATTTGTTCCTATTAGTCTTATATTTTACTGAATCTGA
Associated Phenotype:
Not determined

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