Q5T750 (XP32_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 61.
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: Skin-specific protein 32 | ||||
| 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 | 250 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Tissue specificity | Expressed at high levels in normal and psoriatic skin, but not in normal keratinocytes, A-431 cells, or any of the other cell lines or tissues tested. Ref.3 |
| Sequence caution | The sequence AAB83961.1 differs from that shown. Reason: Frameshift at position 241. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | epidermis development Non-traceable author statement Ref.3. Source: UniProtKB |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 250 | 250 | Skin-specific protein 32 | PRO_0000307808 | |||||
Regions | |||||||||
| Compositional bias | 33 – 250 | 218 | Cys-rich | ||||||
Natural variations | |||||||||
| Natural variant | 26 | 1 | S → T. Corresponds to variant rs1332500 [ dbSNP | Ensembl ]. | VAR_059739 | |||||
| Natural variant | 159 | 1 | T → P. Corresponds to variant rs873775 [ dbSNP | Ensembl ]. | VAR_059740 | |||||
| Natural variant | 173 | 1 | L → V. Corresponds to variant rs59194678 [ dbSNP | Ensembl ]. | VAR_061726 | |||||
Experimental info | |||||||||
| Sequence conflict | 235 | 1 | R → K in AAB83961. Ref.3 | ||||||
| Sequence conflict | 238 | 1 | G → S in AAB83961. Ref.3 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AL353779 Genomic DNA. Translation: CAI20975.1. CH471121 Genomic DNA. Translation: EAW53369.1. AF005081 mRNA. Translation: AAB83961.1. Frameshift. |
| IPI | IPI00023078. |
| RefSeq | NP_001019850.1. NM_001024679.2. |
| UniGene | Hs.601077. |
3D structure databases | |
| ProteinModelPortal | Q5T750. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q5T750. 1 interaction. |
| STRING | 9606.ENSP00000354769. |
Polymorphism databases | |
| DMDM | 74745320. |
Proteomic databases | |
| PaxDb | Q5T750. |
| PRIDE | Q5T750. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000362017; ENSP00000354769; ENSG00000198854. ENST00000368775; ENSP00000357764; ENSG00000198854. |
| GeneID | 100129271. |
| KEGG | hsa:100129271. |
| UCSC | uc010pdu.2. human. |
Organism-specific databases | |
| CTD | 100129271. |
| GeneCards | GC01P152691. |
| H-InvDB | HIX0200014. |
| HGNC | HGNC:29468. C1orf68. |
| HPA | HPA040836. |
| neXtProt | NX_Q5T750. |
| PharmGKB | PA142672518. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG123992. |
| HOGENOM | HOG000154874. |
| InParanoid | Q5T750. |
| OMA | VKCPPPC. |
| OrthoDB | EOG4G4GR8. |
Gene expression databases | |
| Bgee | Q5T750. |
| CleanEx | HS_C1orf68. |
| Genevestigator | Q5T750. |
Family and domain databases | |
| InterPro | IPR026078. Skin_specific_32. IPR026075. SPRR/LCE. [Graphical view] |
| PANTHER | PTHR23263. PTHR23263. 1 hit. PTHR23263:SF4. PTHR23263:SF4. 1 hit. |
| ProtoNet | Search... |
Other | |
| NextBio | 20789195. |
Entry information
| Entry name | XP32_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q5T750 Secondary accession number(s): O14634 | ||||||||
| 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 1 Human chromosome 1: 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
