| Name |
|---|
MUPP Genemajor urinary protein, pseudogene |
UAE1 GeneUrinary albumin excretion QTL 1 |
UAE2 GeneUrinary albumin excretion QTL 2 |
SFPQP1 Genesplicing factor proline/glutamine-rich (polypyrimidine tract binding protein associated) pseudogene 1 |
PTBP3 Genepolypyrimidine tract binding protein 3 The protein encoded by this gene binds RNA and is a regulator of cell differentiation. The encoded protein preferentially binds to poly(G) and poly(U) sequences in vitro. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
PTBP2 Genepolypyrimidine tract binding protein 2 The protein encoded by this gene binds to intronic polypyrimidine clusters in pre-mRNA molecules and is implicated in controlling the assembly of other splicing-regulatory proteins. This protein is very similar to the polypyrimidine tract binding protein (PTB) but most of its isoforms are expressed primarily in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
PTBP1 Genepolypyrimidine tract binding protein 1 This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA-binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has four repeats of quasi-RNA recognition motif (RRM) domains that bind RNAs. This protein binds to the intronic polypyrimidine tracts that requires pre-mRNA splicing and acts via the protein degradation ubiquitin-proteasome pathway. It may also promote the binding of U2 snRNP to pre-mRNAs. This protein is localized in the nucleoplasm and it is also detected in the perinucleolar structure. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008] |
PTBP1P Genepolypyrimidine tract binding protein 1 pseudogene |
COPD14 GeneChronic obstructive pulmonary disease QTL 14 |
COPD3 GeneChronic obstructive pulmonary disease QTL 3 |
COPD2 GeneChronic obstructive pulmonary disease QTL 2 |
COPD1 GeneChronic obstructive pulmonary disease QTL 1 |
COPD6 GeneChronic obstructive pulmonary disease QTL 6 |
COPD5 GeneChronic obstructive pulmonary disease QTL 5 |
COPD4 GeneChronic obstructive pulmonary disease QTL 4 |
COPD8 GeneChronic obstructive pulmonary disease QTL 8 |
CLLS1 GeneLeukemia, chronic lymphocytic, susceptibility to, 1 |
CLLS5 GeneLeukemia, chronic lymphocytic susceptiblity to, 5 |
CLLS3 GeneLeukemia, chronic lymphocytic, susceptibility to, 3 |
CLLU1OS Genechronic lymphocytic leukemia up-regulated 1 opposite strand |
COPD17 GeneChronic obstructive pulmonary disease QTL 17 |
CTEPH1 GenePulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to |
COPD7 GeneChronic obstructive pulmonary disease QTL 7 |
COPD9 GeneChronic obstructive pulmonary disease QTL 9 |
CLLU1 Genechronic lymphocytic leukemia up-regulated 1 Expression of this gene has been shown to be upregulated in some individuals with chronic lymphocytic leukemia (CLL), and has been used for prognostic and diagnostic purposes. This gene was originally identified as a human-specific putative protein-coding gene due to the presence of a peptide (PAp00140670, HIIYSTFLSK) that could have supported translation at this locus. This peptide is not present in more recent builds of PeptideAtlas, and the presence of a protein product at this locus has not been independently verified. For this reason, this gene is being represented as non-coding. Sequence comparisons to other primates indicates that no other primate is predicted to contain an open reading frame. [provided by RefSeq, Feb 2017] |
CLLS4 GeneLeukemia, chronic lymphocytic susceptibility to, 4 |
SMAR GeneSpinal muscular atrophy, chronic distal, autosomal recessive |
COPD13 GeneChronic obstructive pulmonary disease QTL 13 |
COPD12 GeneChronic obstructive pulmonary disease QTL 12 |
COPD11 GeneChronic obstructive pulmonary disease QTL 11 |
COPD10 GeneChronic obstructive pulmonary disease QTL 10 |
COPD16 GeneChronic obstructive pulmonary disease QTL 16 |
COPD15 GeneChronic obstructive pulmonary disease QTL 15 |
COPD19 GeneChronic obstructive pulmonary disease QTL 19 |
COPD18 GeneChronic obstructive pulmonary disease QTL 18 |
COPD GenePulmonary disease, chronic obstructive, severe early-onset |
CMTS GeneChronic mountain sickness, susceptibility to |
COPD28 GeneChronic obstructive pulmonary disease QTL 28 |
COPD29 GeneChronic obstructive pulmonary disease QTL 29 |
COPD22 GeneChronic obstructive pulmonary disease QTL 22 |
COPD23 GeneChronic obstructive pulmonary disease QTL 23 |
COPD20 GeneChronic obstructive pulmonary disease QTL 20 |
COPD21 GeneChronic obstructive pulmonary disease QTL 21 |
COPD26 GeneChronic obstructive pulmonary disease QTL 26 |
COPD27 GeneChronic obstructive pulmonary disease QTL 27 |
COPD24 GeneChronic obstructive pulmonary disease QTL 24 |
COPD25 GeneChronic obstructive pulmonary disease QTL 25 |