NP_998307.1

Ensembl ID:
ENSDARG00000045422
Description:
hypothetical protein LOC406416 [Source:RefSeq peptide;Acc:NP_998307]
Human Orthologue:
C7orf36
Human Description:
chromosome 7 open reading frame 36 [Source:HGNC Symbol;Acc:24857]
Mouse Orthologues:
1600012F09Rik, Gm6505
Mouse Descriptions:
predicted pseudogene 6505 Pseudogene [Source:MGI Symbol;Acc:MGI:3648080]
RIKEN cDNA 1600012F09 gene Gene [Source:MGI Symbol;Acc:MGI:1914258]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa7513 Missense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa7513
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 2017.
Mutation:
A > T
Consequence:
Missense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066794 Missense 146 220 3 3
Genomic Location (Zv9):
Chromosome 24 (position 10110009)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 10168893
KASP Assay ID:
554-4288.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GGTGGATGACATGGRRGACCTAAATGTWGAGCAAACCAACCAGGGTGGAG[A/T]ATCTAAATGYTCAAAYGATGGGGACTGTTGTCGGAGAGATGGASCGAATC
Associated Phenotype:
Not determined

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