|Institutional Source||Beutler Lab|
|Gene Name||ChaC, cation transport regulator 1|
|Is this an essential gene?||Probably non essential (E-score: 0.182)|
|Stock #||R5609 (G1)|
|Chromosomal Location||119351229-119354381 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to G at 119351406 bp|
|Amino Acid Change||Lysine to Glutamic Acid at position 2 (K2E)|
|Ref Sequence||ENSEMBL: ENSMUSP00000028780 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000028780]|
AA Change: K2E
AA Change: K2E
|Coding Region Coverage||
|MGI Phenotype||FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the gamma-glutamylcyclotransferase family of proteins. The encoded protein has been shown to promote neuronal differentiation by deglycination of the Notch receptor, which prevents receptor maturation and inhibits Notch signaling. This protein may also play a role in the unfolded protein response, and in regulation of glutathione levels and oxidative balance in the cell. Elevated expression of this gene may indicate increased risk of cancer recurrence among breast and ovarian cancer patients. [provided by RefSeq, Sep 2016]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Chac1||
(F):5'- ATTGGCCAGAAAGAGATTTGCCC -3'
(R):5'- GCTATAGCCACGAACGAAGC -3'
(F):5'- CCCAATCATAGGGACAGCTGG -3'
(R):5'- CCCACACGGCTGTCACTATAGG -3'