|List |< first << previous [record 15 of 58] next >> last >||
|Institutional Source||Beutler Lab|
|Gene Name||chromogranin A|
|Is this an essential gene?||Probably non essential (E-score: 0.098)|
|Stock #||RF006 (G1)|
|Chromosomal Location||102554969-102565028 bp(+) (GRCm38)|
|Type of Mutation||small insertion (1 aa in frame mutation)|
|DNA Base Change (assembly)||GCA to GCATCA at 102561412 bp|
|Amino Acid Change|
|Ref Sequence||ENSEMBL: ENSMUSP00000021610 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000021610]|
|Predicted Effect||probably benign
|Coding Region Coverage||
|Validation Efficiency||97% (36/37)|
FUNCTION: This gene encodes a member of the granin family of acidic secretory glycoproteins that are expressed in endocrine cells and neurons. The encoded preproprotein undergoes proteolytic processing to generate multiple functions peptides including pancreastatin, catestatin and serpinin. The encoded protein plays important roles in the neuroendocrine system including regulated secretion of peptide hormones and neurotransmitters. Mice lacking the encoded protein exhibit elevated blood pressure which can be rescued by transgenic expression of the human ortholog. [provided by RefSeq, Nov 2015]
PHENOTYPE: Homozygotes and heterozygotes for one allele display hypertension, abnormal plasma and adrenal adrenaline and noradrenaline levels and, in homozygotes, partial embryonic lethality. Homozygotes for a second allele only have elevated urinary adrenaline, noradrenaline and dopamine levels. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Chga||
(F):5'- AGTAGAACTTTCTCACATTTCCCAC -3'
(R):5'- AGCTGACTTCCTGCTGTGAAG -3'
(F):5'- CACTGAGTCAGAGGGGTGGTG -3'
(R):5'- CTTCCTGCTGTGAAGAAGCAG -3'