|Institutional Source||Beutler Lab|
|Synonyms||alpha albumin, Alf|
|Is this an essential gene?||Probably non essential (E-score: 0.055)|
|Stock #||R0009 (G1)|
|Chromosomal Location||90518932-90553543 bp(+) (GRCm38)|
|Type of Mutation||splice site|
|DNA Base Change (assembly)||C to A at 90545384 bp (GRCm38)|
|Amino Acid Change|
|Ref Sequence||ENSEMBL: ENSMUSP00000117180 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000113179] [ENSMUST00000128740]|
|Coding Region Coverage||
|Validation Efficiency||100% (68/68)|
|MGI Phenotype||FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. The protein encoded by this gene is regulated developmentally, expressed in the liver and secreted into the bloodstream. [provided by RefSeq, Jul 2008]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Afm||
(F):5'- GGGAACAAGAGCCGACATTCTCAC -3'
(R):5'- GTTTATGGGACCTACCACATGGCG -3'
(F):5'- ATGCAGTGCCTATGACACGTC -3'
(R):5'- ACATGGCGGTAACAACCTG -3'