Prps1 | ENSMUSG00000031432 | NCBI 19139

Details for: Prps1

Gene ID: 19139

Symbol: Prps1

Ensembl ID: ENSMUSG00000031432

Description: phosphoribosyl pyrophosphate synthetase 1

Associated with

5-phosphoribose 1-diphosphate biosynthesis
(R-MMU-73843)
Metabolism
(R-MMU-1430728)
Metabolism of carbohydrates
(R-MMU-71387)
Pentose phosphate pathway
(R-MMU-71336)
5-phosphoribose 1-diphosphate biosynthetic process
(GO:0006015)
Adp binding
(GO:0043531)
Amp binding
(GO:0016208)
Atp binding
(GO:0005524)
Carbohydrate binding
(GO:0030246)
Cellular biosynthetic process
(GO:0044249)
Cytoplasm
(GO:0005737)
Cytosol
(GO:0005829)
Gdp binding
(GO:0019003)
Hypoxanthine biosynthetic process
(GO:0046101)
Identical protein binding
(GO:0042802)
Kinase activity
(GO:0016301)
Magnesium ion binding
(GO:0000287)
Metal ion binding
(GO:0046872)
Nervous system development
(GO:0007399)
Nucleotide binding
(GO:0000166)
Nucleotide biosynthetic process
(GO:0009165)
Pentose-phosphate shunt
(GO:0006098)
Phosphorylation
(GO:0016310)
Protein-containing complex
(GO:0032991)
Protein homodimerization activity
(GO:0042803)
Purine nucleobase metabolic process
(GO:0006144)
Purine nucleotide biosynthetic process
(GO:0006164)
Ribonucleoside monophosphate biosynthetic process
(GO:0009156)
Ribose phosphate diphosphokinase activity
(GO:0004749)
Ribose phosphate diphosphokinase complex
(GO:0002189)
Transferase activity
(GO:0016740)
Urate biosynthetic process
(GO:0034418)

Other Information

Proteins

Ribose-phosphate pyrophosphokinase 1

Genular Protein ID: 2135161846

Symbol: PRPS1_MOUSE

Name: Ribose-phosphate pyrophosphokinase 1

UniProtKB Accession Codes:

Q9D7G0 Q76MX9

Database IDs:

Citations:

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 19468303

Title: Lineage-specific biology revealed by a finished genome assembly of the mouse.

PubMed ID: 19468303

DOI: 10.1371/journal.pbio.1000112

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 20021999

Title: Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2.

PubMed ID: 20021999

DOI: 10.1016/j.ajhg.2009.11.015

Sequence Information:

Length: 318
Mass: 34834
Checksum: 46D017E969908BA0
Sequence:

MPNIKIFSGS SHQDLSQKIA DRLGLELGKV VTKKFSNQET CVEIGESVRG EDVYIVQSGC 
GEINDNLMEL LIMINACKIA SASRVTAVIP CFPYARQDKK DKSRAPISAK LVANMLSVAG 
ADHIITMDLH ASQIQGFFDI PVDNLYAEPA VLKWIRENIS EWRNCTIVSP DAGGAKRVTS 
IADRLNVDFA LIHKERKKAN EVDRMVLVGD VKDRVAILVD DMADTCGTIC HAADKLLSAG 
ATRVYAILTH GIFSGPAISR INNACFEAVV VTNTIPQEDK MKHCSKIQVI DISMILAEAI 
RRTHNGESVS YLFSHVPL

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: Prps1

Associated with

Other Information

The transcriptional landscape of the mammalian genome. PubMed ID: 16141072

Lineage-specific biology revealed by a finished genome assembly of the mouse. PubMed ID: 19468303

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2. PubMed ID: 20021999

Database document:

PubMed ID: 16141072

PubMed ID: 19468303

PubMed ID: 15489334

PubMed ID: 20021999