Q96MM6 (HS12B_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 80.
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: Heat shock 70 kDa protein 12B | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference 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 | 686 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Tissue specificity | Highest expression in muscle and heart. Lower levels in liver and kidney. Ref.5 |
| Sequence similarities | Belongs to the heat shock protein 70 family. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Ligand | ATP-binding Nucleotide-binding |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Molecular_function | ATP binding 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 – 686 | 686 | Heat shock 70 kDa protein 12B | PRO_0000078294 | |||||
Amino acid modifications | |||||||||
| Modified residue | 42 | 1 | Phosphothreonine By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 23 | 1 | V → L. Corresponds to variant rs34414870 [ dbSNP | Ensembl ]. | VAR_049621 | |||||
| Natural variant | 270 | 1 | R → H. Corresponds to variant rs6139194 [ dbSNP | Ensembl ]. | VAR_059362 | |||||
Experimental info | |||||||||
| Sequence conflict | 300 | 1 | E → D in BAB71261. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK056712 mRNA. Translation: BAB71261.1. AL109804 Genomic DNA. Translation: CAC17544.3. CH471133 Genomic DNA. Translation: EAX10516.1. BC110881 mRNA. Translation: AAI10882.1. BC117284 mRNA. Translation: AAI17285.1. BC126263 mRNA. Translation: AAI26264.1. |
| IPI | IPI00307820. |
| RefSeq | NP_001184256.1. NM_001197327.1. NP_443202.3. NM_052970.4. |
| UniGene | Hs.516854. |
3D structure databases | |
| ProteinModelPortal | Q96MM6. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000254963. |
PTM databases | |
| PhosphoSite | Q96MM6. |
Polymorphism databases | |
| DMDM | 27734244. |
Proteomic databases | |
| PaxDb | Q96MM6. |
| PRIDE | Q96MM6. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000254963; ENSP00000254963; ENSG00000132622. |
| GeneID | 116835. |
| KEGG | hsa:116835. |
| UCSC | uc002wjd.3. human. |
Organism-specific databases | |
| CTD | 116835. |
| GeneCards | GC20P003708. |
| HGNC | HGNC:16193. HSPA12B. |
| HPA | HPA013659. HPA015639. |
| MIM | 610702. gene. |
| neXtProt | NX_Q96MM6. |
| PharmGKB | PA25771. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG132277. |
| HOGENOM | HOG000231707. |
| HOVERGEN | HBG051928. |
| OMA | QKTPTCL. |
| OrthoDB | EOG4HX50H. |
| PhylomeDB | Q96MM6. |
Gene expression databases | |
| ArrayExpress | Q96MM6. |
| Bgee | Q96MM6. |
| CleanEx | HS_HSPA12B. |
| Genevestigator | Q96MM6. |
| GermOnline | ENSG00000132622. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR026685. HSPA12. [Graphical view] |
| PANTHER | PTHR14187:SF5. PTHR14187:SF5. 1 hit. |
| PROSITE | PS00297. HSP70_1. False negative. PS00329. HSP70_2. False negative. PS01036. HSP70_3. False negative. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 116835. |
| NextBio | 79998. |
| SOURCE | Search... |
Entry information
| Entry name | HS12B_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96MM6 Secondary accession number(s): D3DVX7, Q2TAK3, Q9BR52 | ||||||||
| 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 |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with
