full name
regulatory factor X5

synonyms
RFX5, ENSG00000143390

HGNC
HGNC:9986

Entrez Gene
Gene:5993

ENSEMBL
ENSG00000143390

location
chr: 1
start: 151313116
stop: 151319785
strand: -

OMIM
OMIM:601863: RFX5 (Autosomal dominant inheritance,Autosomal recessive inheritance)
OMIM:209920: Bare lymphocyte syndrome, type II, complementation group C
OMIM:209920: Bare lymphocyte syndrome, type II, complementation group E

transcripts
ENST00000290524.4

pathways
Antigen processing and presentation [NCBI:83074] [KEGG:hsa04612] [PUBMED:12776207] [PUBMED:15653315] [PUBMED:15814328] [PUBMED:20010787] [PUBMED:15224094] [PUBMED:15745856] [PUBMED:11244040] [PUBMED:15304636] [PUBMED:11905820] [PUBMED:16181333] [PUBMED:16200082] [PUBMED:15653312] [PUBMED:15224093] [PUBMED:15771591] [PUBMED:12974477]
Primary immunodeficiency [NCBI:83125] [KEGG:hsa05340] [PUBMED:11941303] [PUBMED:18093537] [PUBMED:11058677] [PUBMED:17952897] [PUBMED:14699405] [PUBMED:15661024] [PUBMED:14647478] [PUBMED:17960151] [PUBMED:16261175]
Tuberculosis [NCBI:213780] [KEGG:hsa05152] [PUBMED:20199890] [PUBMED:21274449] [PUBMED:17359235] [PUBMED:20415982] [PUBMED:18541216] [PUBMED:19369951] [PUBMED:15083155] [PUBMED:11378475] [PUBMED:15228522] [PUBMED:19634703] [PUBMED:21274433] [PUBMED:19563525] [PUBMED:18407066] [PUBMED:18288961] [PUBMED:16200082] [PUBMED:17785780] [PUBMED:11932234]