Retinitis pigmentosa 9 protein

AltitudeomicsDB
Protein Official symbol RP9
Aliases RP9
Chromosomal Location  7
Length 221
Uniprot ID Q8TA86
EC number None
Protein family Information(Pfam) None
PDB id None
InterPro ID IPR034585;
dbSNP rs104894037 rs104894039 rs150987618

Protein Protein Interaction

0%
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AltitudeomicsDB
Protein 1 Protein 2 Combine Score
PRPF4 PRPF3 0.996
PRPF31 PRPF6 0.995
PRPF31 PRPF3 0.994
PRPF8 PRPF31 0.993
PRPF8 PRPF3 0.992
PRPF8 PRPF6 0.992
PRPF3 PRPF6 0.991
PRPF8 PRPF4 0.988
PRPF4 PRPF6 0.986
PRPF4 PRPF31 0.986
PRPF3 RP9 0.877
PRPF31 RP9 0.814
PRPF8 RP9 0.809
PRPF4 RP9 0.797
IMPDH1 PRPF31 0.777
RP9 BBS9 0.744
FSCN2 RP9 0.735
FKBP9 RP9 0.731
FKBP9 KBTBD2 0.725
RP9 PRPF6 0.724
KBTBD2 RP9 0.721
FSCN2 PRPF31 0.721
IMPDH1 PRPF3 0.712
FSCN2 PRPF3 0.701
IMPDH1 RP9 0.7
Gene Ontology Semantic Similarity
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# 9129 (PRPF3) 24148 (PRPF6) 26121 (PRPF31) 9128 (PRPF4) 6100 (RP9) 27241 (BBS9) 10594 (PRPF8) 3614 (IMPDH1) 25794 (FSCN2) 11328 (FKBP9)
9129 (PRPF3) 1.00 0.75 0.81 0.86 0.96 0.73 0.80 0.57 0.54 0.36
24148 (PRPF6) 0.75 1.00 0.83 0.69 0.74 0.59 0.71 0.47 0.43 0.36
26121 (PRPF31) 0.81 0.83 1.00 0.80 0.81 0.54 0.75 0.57 0.41 0.36
9128 (PRPF4) 0.86 0.69 0.80 1.00 0.87 0.62 0.77 0.54 0.46 0.36
6100 (RP9) 0.96 0.74 0.81 0.87 1.00 0.71 0.79 0.61 0.53 0.36
27241 (BBS9) 0.73 0.59 0.54 0.62 0.71 1.00 0.49 0.36 0.55 0.36
10594 (PRPF8) 0.80 0.71 0.75 0.77 0.79 0.49 1.00 0.61 0.33 0.36
3614 (IMPDH1) 0.57 0.47 0.57 0.54 0.61 0.36 0.61 1.00 0.23 0.25
25794 (FSCN2) 0.54 0.43 0.41 0.46 0.53 0.55 0.33 0.23 1.00 0.24
11328 (FKBP9) 0.36 0.36 0.36 0.36 0.36 0.36 0.36 0.25 0.24 1.00
Association with High Altitude
Protein Official symbol Source Organism Tissue of Expression Level of hypoxia Altitude Duration of experiment Level of expression Fold change Experiment details geographical location ethnicity of the patients Control group Control (Fold change) Reference (PMID)
RP9 Bird Lungs - 4000 m Native downregulated -2.25 Sequencing Central Asia L. dichrous (Bird) 1 L. dichrous vs. Po. Palustris 31127049
Association with TF
TF TF Entrez Gene Gene Entrez Type PMID Database
CTCF 10664 RP9 6100 proximal_filtered 22955619 TRANSFAC
Association with miRNA
miRTarBase ID miRNA Species (miRNA) Protein Official Symbol Human Entrez ID Species (Target Gene) Experiments Support Type References (PMID)
Gene Ontology
ID GO ID GO Term GO Type
6100 GO:0005737 cytoplasm GOTERM_CC_DIRECT
6100 GO:0005785 signal recognition particle receptor complex GOTERM_CC_DIRECT
6100 GO:0044822 poly GOTERM_MF_DIRECT
6100 GO:0046872 metal ion binding GOTERM_MF_DIRECT
6100 GO:0005634 nucleus GOTERM_CC_DIRECT
6100 GO:0005515 protein binding GOTERM_MF_DIRECT
6100 GO:0008380 RNA splicing GOTERM_BP_DIRECT
6100 GO:0050890 cognition GOTERM_BP_DIRECT
Pathways
Human Entrez ID KEGG ID KEGG Term
Association with Disease
Protein Official Symbol Human Entrez ID Disease Name Disease Id Disease Semantic Type Semantic score DSI DPI Disease Type
RP9 6100 RETINITIS PIGMENTOSA 9 C1867300 Disease or Syndrome 0.62 0.672 0.414 disease
RP9 6100 Retinitis Pigmentosa C0035334 Disease or Syndrome 0.41 0.672 0.414 disease
Association with Drug
Protein Official Symbol Human Entrez ID drug_claim_primary_name drug_name drug_chembl_id interaction_types