Search results for Literature Guide pages at SGD

Your query, SSC1, returned 2 hits to the following gene names:

Match Gene Name Systematic Name Alias(es) Position Info Description
SSC1 PMR1 YGL167C BSD1, LDB1, SSC1, Ca(2+)/Mn(2+)-transporting P-type ATPase PMR1

ChrVII:190468 to 187616 | ORF Map | GBrowse

Note: this feature is encoded on the Crick strand.

Relative
Coordinates		 Chromosomal
Coordinates
CDS 1..2853 190468..187616

Genetic position: -104 cM

High affinity Ca2+/Mn2+ P-type ATPase required for Ca2+ and Mn2+ transport into Golgi; involved in Ca2+ dependent protein sorting and processing; mutations in human homolog ATP2C1 cause acantholytic skin condition Hailey-Hailey disease
SSC1 SSC1 YJR045C ENS1, mtHSP70, Hsp70 family ATPase SSC1

ChrX:521602 to 519638 | ORF Map | GBrowse

Note: this feature is encoded on the Crick strand.

Relative
Coordinates		 Chromosomal
Coordinates
CDS 1..1965 521602..519638

Hsp70 family ATPase; constituent of the import motor component of the Translocase of the Inner Mitochondrial membrane (TIM23 complex); involved in protein translocation and folding; subunit of SceI endonuclease; SSC1 has a paralog, ECM10, that arose from the whole genome duplication