Reviewed,
UniProtKB/Swiss-Prot Q8NCL9 (APCDL_HUMAN)
Last modified
November 24, 2009.
Version 44.
History...
Clusters with 100%,
90%,
50% identity |
Documents (3) |
Third-party data |
Customize display | text xml rdf/xml gff fasta |
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
Names and origin
| Protein names | Recommended name: Protein APCDD1-like Alternative name(s): Adenomatosis polyposis coli down-regulated 1 protein-like | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Complete proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 501 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 membrane protein Potential. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Signal Transmembrane |
| PTM | Glycoprotein |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Cellular component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 24 | 24 | Potential | ||||||
| Chain | 25 – 501 | 477 | Protein APCDD1-like | PRO_0000264234 | |||||
Regions | |||||||||
| Transmembrane | 481 – 501 | 21 | Potential | ||||||
Amino acid modifications | |||||||||
| Glycosylation | 150 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 30 | 1 | C → R: dbSNP rs3946003. | VAR_029625 | |||||
| Natural variant | 80 | 1 | Y → H: dbSNP rs7265854. | VAR_029626 | |||||
| Natural variant | 83 | 1 | R → Q: dbSNP rs7265902. | VAR_050668 | |||||
| Natural variant | 261 | 1 | R → C: dbSNP rs16981999. | VAR_029627 | |||||
Sequences
| ||||||||||||||||||
References
Cross-references
Sequence databases | |
|---|---|
| AK074647 mRNA. Translation: BAC11111.1. AL118513 Genomic DNA. Translation: CAI22411.1. BC101760 mRNA. Translation: AAI01761.1. BC101758 mRNA. Translation: AAI01759.1. | |
| IPI | IPI00414128. |
| RefSeq | NP_699191.1. |
| UniGene | Hs.119286 |
3D structure databases | |
| ModBase | Search... |
Proteomic databases | |
| PRIDE | Q8NCL9. |
Genome annotation databases | |
| Ensembl | ENST00000371149; ENSP00000360191; ENSG00000198768; Homo sapiens. [Genome view] |
| GeneID | 164284. |
| KEGG | hsa:164284. |
| UCSC | uc002xze.1. human. |
Organism-specific databases | |
| CTD | 164284. |
| GeneCards | GC20M056468. |
| HGNC | HGNC:26892. APCDD1L. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | Q8NCL9. |
| OMA | ERRHYRP |
| OrthoDB | EOG92VC29 |
Gene expression databases | |
| ArrayExpress | Q8NCL9. |
| Bgee | Q8NCL9. |
| CleanEx | HS_APCDD1L. |
| Genevestigator | Q8NCL9. |
| GermOnline | ENSG00000198768. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 88455. |
Entry information
| Entry name | APCDL_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8NCL9 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| 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 20 Human chromosome 20: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |

Clusters with


