Homo sapiens (human): 5993
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Entry
5993 CDS
T01001
Symbol
RFX5, MHC2D3, MHC2D5
Name
(RefSeq) regulatory factor X5
KO
K08061
regulatory factor X 5
Organism
hsa
Homo sapiens (human)
Pathway
hsa04612
Antigen processing and presentation
hsa05152
Tuberculosis
hsa05340
Primary immunodeficiency
Disease
H00985
MHC class II deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04612 Antigen processing and presentation
5993 (RFX5)
09160 Human Diseases
09171 Infectious disease: bacterial
05152 Tuberculosis
5993 (RFX5)
09163 Immune disease
05340 Primary immunodeficiency
5993 (RFX5)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
5993 (RFX5)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Other basic domains
RF-X
5993 (RFX5)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RFX5_DNA_bdg
RFX5_N
RFX_DNA_binding
Pox_D5
Motif
Other DBs
NCBI-GeneID:
5993
NCBI-ProteinID:
NP_000440
OMIM:
601863
HGNC:
9986
Ensembl:
ENSG00000143390
UniProt:
P48382
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(151340640..151347252)
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AA seq
616 aa
AA seq
DB search
MAEDEPDAKSPKTGGRAPPGGAEAGEPTTLLQRLRGTISKAVQNKVEGILQDVQKFSDND
KLYLYLQLPSGPTTGDKSSEPSTLSNEEYMYAYRWIRNHLEEHTDTCLPKQSVYDAYRKY
CESLACCRPLSTANFGKIIREIFPDIKARRLGGRGQSKYCYSGIRRKTLVSMPPLPGLDL
KGSESPEMGPEVTPAPRDELVEAACALTCDWAERILKRSFSSIVEVARFLLQQHLISARS
AHAHVLKAMGLAEEDEHAPRERSSKPKNGLENPEGGAHKKPERLAQPPKDLEARTGAGPL
ARGERKKSVVESSAPGANNLQVNALVARLPLLLPRAPRSLIPPIPVSPPILAPRLSSGAL
KVATLPLSSRAGAPPAAVPIINMILPTVPALPGPGPGPGRAPPGGLTQPRGTENREVGIG
GDQGPHDKGVKRTAEVPVSEASGQAPPAKAAKQDIEDTASDAKRKRGRPRKKSGGSGERN
STPLKSAAAMESAQSSRLPWETWGSGGEGNSAGGAERPGPMGEAEKGAVLAQGQGDGTVS
KGGRGPGSQHTKEAEDKIPLVPSKVSVIKGSRSQKEAFPLAKGEVDTAPQGNKDLKEHVL
QSSLSQEHKDPKATPP
NT seq
1851 nt
NT seq
+upstream
nt +downstream
nt
atggcagaagatgagcctgatgctaagagccccaagactgggggaagggcccccccaggt
ggtgctgaggctggggaacctaccacccttcttcagaggctccgaggtaccatttccaag
gccgtgcagaacaaagtagaggggatcctgcaagatgtacagaaattttctgacaatgac
aagctgtatctctaccttcagctcccctcaggacccaccactggagacaaaagctcagag
ccaagtacactgagcaatgaggagtacatgtatgcctataggtggatccgcaaccacctg
gaagagcacactgacacctgtctgccaaagcaaagtgtttatgatgcctatcggaagtac
tgtgagagtcttgcctgttgccgcccactcagcacagccaactttggcaagatcatcaga
gagatcttccctgacatcaaagctcgaaggcttggtggccggggccagtccaaatattgc
tacagtggcataaggaggaagaccttggtgtctatgccacccctgcctggacttgaccta
aagggttctgagagtccagaaatgggcccagaagtaaccccagcacctcgagatgaactg
gtggaggcagcgtgtgccctgacctgtgactgggcagagcggatcctgaaacggtccttc
agttccatcgttgaggtcgcccgcttcctgctacagcagcatctcatctctgcccgatct
gcacatgcccatgtgcttaaggccatggggctcgctgaagaggacgaacatgcacctcgg
gaacggtcatctaaaccaaagaatggtttagagaacccagagggtggagcccacaagaag
ccagagagactggcccagcctcctaaggatctggaagcccgaactggggccggtcctctc
gcacgtggagagcggaagaagagtgtagttgagagctcggccccaggagccaataacctg
caggttaatgccctagtggctcggctgcctctgctccttccccgggcccctcgctcacta
attccgccaatcccagtctctccacctattctggcccccaggctttcttcaggtgccctg
aaagtggctacactgcctctgtctagtagggccggggcacccccagcagctgtgcccatc
attaacatgatcttaccaactgttcctgctttgcctggacctggacctgggcctgggcga
gctccacctgggggactcactcagccccggggcacagagaacagagaggtaggcataggt
ggtgaccaaggaccacatgacaagggtgtcaagaggacagctgaagtacctgtgagtgag
gccagtgggcaggctccaccagctaaagcagcaaagcaggatatagaggatacagcaagt
gatgccaaaaggaaacgggggcgccctcgaaaaaagtcaggtggaagtggggaaaggaat
tctacccctctcaagtcagcagctgccatggaatctgcccagtcctcaaggttaccatgg
gagacatggggctcaggaggggaaggcaactcagctggaggggcagagaggccagggcca
atgggagaggctgaaaagggggcagtacttgcccagggtcagggagatggtactgtttcc
aaaggaggaaggggccccggttcccagcataccaaagaagcagaagataaaattcccttg
gtcccctcaaaagtgagtgtcatcaagggcagcagaagccaaaaggaggcttttcctttg
gcaaagggagaggtagacactgcaccacagggtaataaagacttaaaggagcatgtgctt
caaagttccttatcccaggagcataaagacccaaaagcaacacccccatga
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