Q9BVV8 (CS024_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 68.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Uncharacterized membrane protein C19orf24 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 132 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Membrane; Single-pass type I membrane protein Potential. |
| Sequence caution | The sequence BAA91305.1 differs from that shown. Reason: |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Domain | Signal Transmembrane Transmembrane helix |
| PTM | Glycoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular component | cytoplasm Inferred from direct assay. Source: HGNC extracellular region partInferred from direct assay. Source: HGNC integral to membraneInferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 26 | 26 | Potential | ||||||
| Chain | 27 – 132 | 106 | Uncharacterized membrane protein C19orf24 | PRO_0000079385 | |||||
Regions | |||||||||
| Transmembrane | 73 – 93 | 21 | Helical; Potential | ||||||
Amino acid modifications | |||||||||
| Glycosylation | 47 | 1 | N-linked (GlcNAc...) Potential | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AC004258 Genomic DNA. No translation available. BC000890 mRNA. Translation: AAH00890.2. AK000647 mRNA. Translation: BAA91305.1. Sequence problems. |
| IPI | IPI00306440. |
| RefSeq | NP_060384.3. NM_017914.3. |
| UniGene | Hs.591383. |
3D structure databases | |
| ProteinModelPortal | Q9BVV8. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q9BVV8. 1 interaction. |
PTM databases | |
| PhosphoSite | Q9BVV8. |
Polymorphism databases | |
| DMDM | 294862428. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000416408; ENSP00000407816; ENSG00000226593. |
| GeneID | 55009. |
| KEGG | hsa:55009. |
| UCSC | uc002lrx.2. human. |
Organism-specific databases | |
| CTD | 55009. |
| GeneCards | GC19P001275. GC19P001276. |
| HGNC | HGNC:26073. C19orf24. |
| HPA | HPA043279. |
| neXtProt | NX_Q9BVV8. |
| PharmGKB | PA134930220. |
| GenAtlas | Search... |
Phylogenomic databases | |
| GeneTree | ENSGT00500000045679. |
| InParanoid | Q9BVV8. |
| OMA | LANTEDP. |
| OrthoDB | EOG49W2GV. EOG4G1MJ3. |
Gene expression databases | |
| CleanEx | HS_C19orf24. |
| Genevestigator | Q9BVV8. |
| GermOnline | ENSG00000118050. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR009565. DUF1180. [Graphical view] |
| Pfam | PF06679. DUF1180. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Entry information
| Entry name | CS024_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9BVV8 Secondary accession number(s): Q9NWS2 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 19 Human chromosome 19: entries, gene names and cross-references to MIM |

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