Q7L3V2 (CV029_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 48.
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 protein C22orf29 | ||
| 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 | 364 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Sequence caution | The sequence BAB14998.1 differs from that shown. Reason: Erroneous initiation. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 364 | 364 | Uncharacterized protein C22orf29 | PRO_0000295910 | |||||
Regions | |||||||||
| Compositional bias | 265 – 324 | 60 | Pro-rich | ||||||
Natural variations | |||||||||
| Natural variant | 116 | 1 | R → H. Corresponds to variant rs17745302 [ dbSNP | Ensembl ]. | VAR_034590 | |||||
| Natural variant | 123 | 1 | D → Y. Ref.1 Corresponds to variant rs34027839 [ dbSNP | Ensembl ]. | VAR_034591 | |||||
Experimental info | |||||||||
| Sequence conflict | 206 | 1 | A → V in CAE45984. Ref.1 | ||||||
| Sequence conflict | 206 | 1 | A → V in CAE46001. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | BX640785 mRNA. Translation: CAE45875.1. BX640969 mRNA. Translation: CAE45984.1. BX640998 mRNA. Translation: CAE46001.1. CH471176 Genomic DNA. Translation: EAX03018.1. CH471176 Genomic DNA. Translation: EAX03019.1. BC011679 mRNA. Translation: AAH11679.2. AK024778 mRNA. Translation: BAB14998.1. Different initiation. |
| IPI | IPI00472049. |
| RefSeq | NP_078903.3. NM_024627.5. |
| UniGene | Hs.105642. |
3D structure databases | |
| ProteinModelPortal | Q7L3V2. |
| ModBase | Search... |
Polymorphism databases | |
| DMDM | 74739166. |
Proteomic databases | |
| PRIDE | Q7L3V2. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000328554; ENSP00000330596; ENSG00000215012. ENST00000405640; ENSP00000384924; ENSG00000215012. ENST00000407472; ENSP00000386111; ENSG00000215012. |
| GeneID | 79680. |
| KEGG | hsa:79680. |
| UCSC | uc002zqg.1. human. |
Organism-specific databases | |
| CTD | 79680. |
| GeneCards | GC22M019833. |
| HGNC | HGNC:26112. C22orf29. |
| HPA | HPA000721. HPA001419. |
| neXtProt | NX_Q7L3V2. |
| PharmGKB | PA145149415. |
| GenAtlas | Search... |
Phylogenomic databases | |
| GeneTree | ENSGT00510000050172. |
| HOVERGEN | HBG099854. |
| InParanoid | Q7L3V2. |
| OMA | GRCRQQG. |
| OrthoDB | EOG476K14. |
| PhylomeDB | Q7L3V2. |
Gene expression databases | |
| Bgee | Q7L3V2. |
| Genevestigator | Q7L3V2. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| NextBio | 68930. |
Entry information
| Entry name | CV029_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q7L3V2 Secondary accession number(s): D3DX21 Q9H7A0 | ||||||||
| 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 22 Human chromosome 22: 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