Q96KR6 (F210B_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 75.
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: Protein FAM210B | ||||||
| Gene names |
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| 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 | 192 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Subcellular location | Membrane; Multi-pass membrane protein Potential. |
| Sequence similarities | Belongs to the FAM210 family. Contains 1 DUF1279 domain. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 192 | 192 | Protein FAM210B | PRO_0000079451 | |||||
Regions | |||||||||
| Transmembrane | 22 – 42 | 21 | Helical; Potential | ||||||
| Transmembrane | 99 – 119 | 21 | Helical; Potential | ||||||
| Transmembrane | 150 – 170 | 21 | Helical; Potential | ||||||
| Domain | 80 – 191 | 112 | DUF1279 | ||||||
Natural variations | |||||||||
| Natural variant | 126 | 1 | P → S. Corresponds to variant rs6099115 [ dbSNP | Ensembl ]. | VAR_033763 | |||||
Experimental info | |||||||||
| Sequence conflict | 36 | 1 | P → L in CAC67490. Ref.1 | ||||||
| Sequence conflict | 161 | 1 | A → V in AAH17725. Ref.6 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AJ311123 mRNA. Translation: CAC67490.1. AK075565 mRNA. Translation: BAC11704.1. AK314768 mRNA. Translation: BAG37306.1. AL121914 Genomic DNA. Translation: CAC12716.1. CH471077 Genomic DNA. Translation: EAW75564.1. CH471077 Genomic DNA. Translation: EAW75565.1. BC017725 mRNA. Translation: AAH17725.1. |
| IPI | IPI00096986. |
| RefSeq | NP_543011.2. NM_080821.2. |
| UniGene | Hs.143736. Hs.593629. |
3D structure databases | |
| ProteinModelPortal | Q96KR6. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q96KR6. |
Polymorphism databases | |
| DMDM | 41688811. |
Proteomic databases | |
| PeptideAtlas | Q96KR6. |
| PRIDE | Q96KR6. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000371384; ENSP00000360437; ENSG00000124098. |
| GeneID | 116151. |
| KEGG | hsa:116151. |
| UCSC | uc002xxc.1. human. |
Organism-specific databases | |
| CTD | 116151. |
| GeneCards | GC20P054933. |
| HGNC | HGNC:16102. FAM210B. |
| neXtProt | NX_Q96KR6. |
| PharmGKB | PA25647. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG20582. |
| GeneTree | ENSGT00530000063556. |
| HOGENOM | HBG319178. |
| HOVERGEN | HBG051187. |
| InParanoid | Q96KR6. |
| OMA | IFQEYGT. |
| OrthoDB | EOG4CVG8F. |
| PhylomeDB | Q96KR6. |
Gene expression databases | |
| ArrayExpress | Q96KR6. |
| Bgee | Q96KR6. |
| CleanEx | HS_C20orf108. |
| Genevestigator | Q96KR6. |
| GermOnline | ENSG00000124098. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR009688. DUF1279. [Graphical view] |
| Pfam | PF06916. DUF1279. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 79798. |
Entry information
| Entry name | F210B_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96KR6 Secondary accession number(s): B2RBQ9 Q9H418 | ||||||||
| 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 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 |
| SIMILARITY comments Index of protein domains and families |

Clusters with