Q8NDV7 (TNR6A_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 94.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Trinucleotide repeat-containing gene 6A protein Alternative name(s): CAG repeat protein 26 EMSY interactor protein GW182 autoantigen Short name=Protein GW1 Glycine-tryptophan protein of 182 kDa | ||||
| 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 | 1962 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Plays a role in RNA-mediated gene silencing by both micro-RNAs (miRNAs) and short interfering RNAs (siRNAs). Required for miRNA-dependent repression of translation and for siRNA-dependent endonucleolytic cleavage of complementary mRNAs by argonaute family proteins. Ref.13 Ref.14 Ref.17 Ref.19 Ref.21 Ref.25 |
| Subunit structure | Interacts with EIF2C1/AGO1, EIF2C2/AGO2, EIF2C3/AGO3 and EIF2C4/AGO4. Ref.13 Ref.14 Ref.22 Ref.25 Ref.26 |
| Subcellular location | Cytoplasm › P-body. Note: Mammalian P-bodies are also known as GW bodies (GWBs). Ref.1 Ref.10 Ref.11 Ref.12 Ref.13 Ref.14 Ref.16 Ref.21 Ref.24 Ref.26 |
| Tissue specificity | Ubiquitous. Ref.1 |
| Induction | By exogenous short interfering RNA (siRNA). Ref.24 |
| Miscellaneous | Antibodies against TNRC6A are found in sera from patients with Sjoegren syndrome (SS), ataxia and sensor neuropathy diseases that developed autoantibodies against protein of the GWB structure. Autoantibodies were mapped to the GW-rich mid-part, the non-GW-rich region and the C-terminus of the protein. |
| Sequence similarities | Belongs to the GW182 family. Contains 1 RRM (RNA recognition motif) domain. |
| Sequence caution | The sequence BAA91899.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended. The sequence CAD28525.2 differs from that shown. Reason: Erroneous initiation. Translation N-terminally shortened. |
Ontologies
| Keywords | |
|---|---|
| Biological process | RNA-mediated gene silencing Translation regulation |
| Cellular component | Cytoplasm |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Coiled coil |
| Ligand | RNA-binding |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | negative regulation of translation involved in gene silencing by miRNA Inferred from direct assay Ref.17. Source: UniProtKB |
| Cellular component | cytoplasmic mRNA processing body Inferred from direct assay. Source: MGI micro-ribonucleoprotein complexInferred from direct assay Ref.17. Source: UniProtKB |
| Molecular function | RNA binding Inferred from electronic annotation. Source: UniProtKB-KW nucleotide bindingInferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 6 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q8NDV7-1) Also known as: TNGW1; This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q8NDV7-2) The sequence of this isoform differs from the canonical sequence as follows: 1-253: Missing. | ||||||
| Isoform 3 (identifier: Q8NDV7-3) The sequence of this isoform differs from the canonical sequence as follows: 1-1232: Missing. 1280-1328: Missing. 1611-1962: Missing. | ||||||
| Isoform 4 (identifier: Q8NDV7-4) The sequence of this isoform differs from the canonical sequence as follows: 1-1801: Missing. | ||||||
| Isoform 5 (identifier: Q8NDV7-5) The sequence of this isoform differs from the canonical sequence as follows: 1-54: MRELEAKATK...QKKATEQKIK → MAYFGGTLYWLIFSTPFLLLGL | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 6 (identifier: Q8NDV7-6) The sequence of this isoform differs from the canonical sequence as follows: 1280-1328: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1962 | 1962 | Trinucleotide repeat-containing gene 6A protein | PRO_0000081980 | |||||
Regions | |||||||||
| Domain | 1781 – 1853 | 73 | RRM | ||||||
| Region | 254 – 503 | 250 | Sufficient for interaction with EIF2C1, EIF2C3 and EIF2C4 | ||||||
| Region | 270 – 346 | 77 | Sufficient for interaction with EIF2C2 | ||||||
| Region | 318 – 399 | 82 | Sufficient for interaction with EIF2C2 | ||||||
| Region | 340 – 439 | 100 | Sufficient for interaction with EIF2C2 | ||||||
| Region | 409 – 495 | 87 | Sufficient for interaction with EIF2C2 | ||||||
| Region | 502 – 751 | 250 | Sufficient for interaction with EIF2C2 | ||||||
| Region | 566 – 1343 | 778 | Sufficient for interaction with EIF2C1 and EIF2C4 | ||||||
| Region | 1074 – 1144 | 71 | Sufficient for interaction with EIF2C2 | ||||||
| Region | 1670 – 1962 | 293 | Sufficient for interaction with EIF2C2 | ||||||
| Coiled coil | 7 – 54 | 48 | Potential | ||||||
| Compositional bias | 93 – 127 | 35 | Gln-rich | ||||||
| Compositional bias | 192 – 365 | 174 | Ser-rich | ||||||
Amino acid modifications | |||||||||
| Modified residue | 991 | 1 | Phosphoserine By similarity | ||||||
| Modified residue | 1470 | 1 | Phosphothreonine Ref.23 | ||||||
| Modified residue | 1585 | 1 | Phosphoserine Ref.27 | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 1801 | 1801 | Missing in isoform 4. | VSP_013292 | |||||
| Alternative sequence | 1 – 1232 | 1232 | Missing in isoform 3. | VSP_037287 | |||||
| Alternative sequence | 1 – 253 | 253 | Missing in isoform 2. | VSP_013294 | |||||
| Alternative sequence | 1 – 54 | 54 | MRELE…EQKIK → MAYFGGTLYWLIFSTPFLLL GL in isoform 5. | VSP_013295 | |||||
| Alternative sequence | 1280 – 1328 | 49 | Missing in isoform 3 and isoform 6. | VSP_037288 | |||||
| Alternative sequence | 1611 – 1962 | 352 | Missing in isoform 3. | VSP_037289 | |||||
| Natural variant | 185 | 1 | N → K. Corresponds to variant rs11639856 [ dbSNP | Ensembl ]. | VAR_057251 | |||||
| Natural variant | 592 | 1 | A → T. Corresponds to variant rs6497759 [ dbSNP | Ensembl ]. | VAR_057252 | |||||
| Natural variant | 788 | 1 | P → S. Corresponds to variant rs3803716 [ dbSNP | Ensembl ]. | VAR_057253 | |||||
| Natural variant | 1268 | 1 | E → K. Corresponds to variant rs2112782 [ dbSNP | Ensembl ]. | VAR_057254 | |||||
Experimental info | |||||||||
| Mutagenesis | 313 | 1 | W → A: Does not impair interaction with EIF2C2; when associated with A-345; A-370; A-420 and A-483. Ref.26 | ||||||
| Mutagenesis | 345 | 1 | W → A: Does not impair interaction with EIF2C2; when associated with A-313; A-370; A-420 and A-483. Ref.26 | ||||||
| Mutagenesis | 370 | 1 | W → A: Does not impair interaction with EIF2C2; when associated with A-313; A-345; A-420 and A-483. Ref.26 | ||||||
| Mutagenesis | 420 | 1 | W → A: Does not impair interaction with EIF2C2; when associated with A-313; A-345; A-370 and A-483. Ref.26 | ||||||
| Mutagenesis | 483 | 1 | W → A: Does not impair interaction with EIF2C2; when associated with A-313; A-345; A-370 and A-420. Ref.26 | ||||||
| Sequence conflict | 31 – 34 | 4 | KKKK → TEKE in CAD37348. Ref.2 | ||||||
| Sequence conflict | 1375 | 1 | V → VV in CAD28525. Ref.3 | ||||||
| Sequence conflict | 1704 | 1 | S → F in BAA91899. Ref.8 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "A phosphorylated cytoplasmic autoantigen, GW182, associates with a unique population of human mRNAs within novel cytoplasmic speckles." Eystathioy T., Chan E.K.L., Tenenbaum S.A., Keene J.D., Griffith K., Fritzler M.J. Mol. Biol. Cell 13:1338-1351(2002) [PubMed: 11950943] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2), RNA-BINDING, TISSUE SPECIFICITY, SUBCELLULAR LOCATION, PHOSPHORYLATION. Tissue: Cervix carcinoma. |
| [2] | "Candidate EMSY interactor protein." Hughes-Davies L. Submitted (JUN-2002) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1). |
| [3] | "The full-ORF clone resource of the German cDNA consortium." Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D., Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., Wiemann S., Schupp I. BMC Genomics 8:399-399(2007) [PubMed: 17974005] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 861-1962 (ISOFORM 6). Tissue: Kidney and Stomach. |
| [4] | "The sequence and analysis of duplication-rich human chromosome 16." Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M., Couronne O., Aerts A., Bajorek E., Black S., Blumer H., Branscomb E., Brown N.C., Bruno W.J. Pennacchio L.A.Nature 432:988-994(2004) [PubMed: 15616553] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 4), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1515-1962. Tissue: Kidney and PNS. |
| [6] | "cDNAs with long CAG trinucleotide repeats from human brain." Margolis R.L., Abraham M.R., Gatchell S.B., Li S.-H., Kidwai A.S., Breschel T.S., Stine O.C., Callahan C., McInnis M.G., Ross C.A. Hum. Genet. 100:114-122(1997) [PubMed: 9225980] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 1-157 (ISOFORM 5). Tissue: Brain. |
| [7] | "Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro." Nagase T., Kikuno R., Ishikawa K., Hirosawa M., Ohara O. DNA Res. 7:143-150(2000) [PubMed: 10819331] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 565-1962. Tissue: Brain. |
| [8] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1522-1962. Tissue: Ovarian carcinoma. |
| [9] | "Clinical and serological associations of autoantibodies to GW bodies and a novel cytoplasmic autoantigen GW182." Eystathioy T., Chan E.K.L., Takeuchi K., Mahler M., Luft L.M., Zochodne D.W., Fritzler M.J. J. Mol. Med. 81:811-818(2003) [PubMed: 14598044] [Abstract] Cited for: AUTOANTIGENIC EPITOPE MAPPING. |
| [10] | "The GW182 protein colocalizes with mRNA degradation associated proteins hDcp1 and hLSm4 in cytoplasmic GW bodies." Eystathioy T., Jakymiw A., Chan E.K.L., Seraphin B., Cougot N., Fritzler M.J. RNA 9:1171-1173(2003) [PubMed: 13130130] [Abstract] Cited for: SUBCELLULAR LOCATION. |
| [11] | "GW182 is critical for the stability of GW bodies expressed during the cell cycle and cell proliferation." Yang Z., Jakymiw A., Wood M.R., Eystathioy T., Rubin R.L., Fritzler M.J., Chan E.K.L. J. Cell Sci. 117:5567-5578(2004) [PubMed: 15494374] [Abstract] Cited for: SUBCELLULAR LOCATION. |
| [12] | "Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies." Sen G.L., Blau H.M. Nat. Cell Biol. 7:633-636(2005) [PubMed: 15908945] [Abstract] Cited for: SUBCELLULAR LOCATION. |
| [13] | "A role for the P-body component GW182 in microRNA function." Liu J., Rivas F.V., Wohlschlegel J., Yates J.R. III, Parker R., Hannon G.J. Nat. Cell Biol. 7:1261-1266(2005) [PubMed: 16284623] [Abstract] Cited for: FUNCTION, INTERACTION WITH EIF2C2, SUBCELLULAR LOCATION. |
| [14] | "Disruption of GW bodies impairs mammalian RNA interference." Jakymiw A., Lian S.L., Eystathioy T., Li S., Satoh M., Hamel J.C., Fritzler M.J., Chan E.K.L. Nat. Cell Biol. 7:1267-1274(2005) [PubMed: 16284622] [Abstract] Cited for: FUNCTION, INTERACTION WITH EIF2C2, ASSOCIATION WITH SIRNA, SUBCELLULAR LOCATION. |
| [15] | Erratum Jakymiw A., Lian S.L., Eystathioy T., Li S., Satoh M., Hamel J.C., Fritzler M.J., Chan E.K.L. Nat. Cell Biol. 8:100-100(2006) |
| [16] | "Formation of GW bodies is a consequence of microRNA genesis." Pauley K.M., Eystathioy T., Jakymiw A., Hamel J.C., Fritzler M.J., Chan E.K.L. EMBO Rep. 7:904-910(2006) [PubMed: 16906129] [Abstract] Cited for: SUBCELLULAR LOCATION, ASSOCIATION WITH MICRORNA. |
| [17] | "Let-7 microRNA-mediated mRNA deadenylation and translational repression in a mammalian cell-free system." Wakiyama M., Takimoto K., Ohara O., Yokoyama S. Genes Dev. 21:1857-1862(2007) [PubMed: 17671087] [Abstract] Cited for: FUNCTION. |
| [18] | Erratum Wakiyama M., Takimoto K., Ohara O., Yokoyama S. Genes Dev. 21:2509-2509(2007) |
| [19] | "Small interfering RNA-mediated silencing induces target-dependent assembly of GW/P bodies." Lian S.L., Fritzler M.J., Katz J., Hamazaki T., Terada N., Satoh M., Chan E.K.L. Mol. Biol. Cell 18:3375-3387(2007) [PubMed: 17596515] [Abstract] Cited for: FUNCTION. |
| [20] | Erratum Lian S.L., Fritzler M.J., Katz J., Hamazaki T., Terada N., Satoh M., Chan E.K.L. Mol. Biol. Cell 18:4200-4200(2007) |
| [21] | "Identification of GW182 and its novel isoform TNGW1 as translational repressors in Ago2-mediated silencing." Li S., Lian S.L., Moser J.J., Fritzler M.L., Fritzler M.J., Satoh M., Chan E.K.L. J. Cell Sci. 121:4134-4144(2008) [PubMed: 19056672] [Abstract] Cited for: FUNCTION, SUBCELLULAR LOCATION. |
| [22] | "Prolyl 4-hydroxylation regulates Argonaute 2 stability." Qi H.H., Ongusaha P.P., Myllyharju J., Cheng D., Pakkanen O., Shi Y., Lee S.W., Peng J., Shi Y. Nature 455:421-424(2008) [PubMed: 18690212] [Abstract] Cited for: IDENTIFICATION BY MASS SPECTROMETRY, INTERACTION WITH EIF2C2. |
| [23] | "A quantitative atlas of mitotic phosphorylation." Dephoure N., Zhou C., Villen J., Beausoleil S.A., Bakalarski C.E., Elledge S.J., Gygi S.P. Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed: 18669648] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-1470, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [24] | "Localization of double-stranded small interfering RNA to cytoplasmic processing bodies is Ago2 dependent and results in up-regulation of GW182 and Argonaute-2." Jagannath A., Wood M.J.A. Mol. Biol. Cell 20:521-529(2009) [PubMed: 18946079] [Abstract] Cited for: SUBCELLULAR LOCATION, INDUCTION. |
| [25] | "Importance of the C-terminal domain of the human GW182 protein TNRC6C for translational repression." Zipprich J.T., Bhattacharyya S., Mathys H., Filipowicz W. RNA 15:781-793(2009) [PubMed: 19304925] [Abstract] Cited for: FUNCTION, INTERACTION WITH EIF2C2. |
| [26] | "The C-terminal half of human Ago2 binds to multiple GW-rich regions of GW182 and requires GW182 to mediate silencing." Lian S.L., Li S., Abadal G.X., Pauley B.A., Fritzler M.J., Chan E.K.L. RNA 15:804-813(2009) [PubMed: 19324964] [Abstract] Cited for: INTERACTION WITH EIF2C1; EIF2C2; EIF2C3 AND EIF2C4, SUBCELLULAR LOCATION, MUTAGENESIS OF TRP-313; TRP-345; TRP-370; TRP-420 AND TRP-483. |
| [27] | "Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions." Mayya V., Lundgren D.H., Hwang S.-I., Rezaul K., Wu L., Eng J.K., Rodionov V., Han D.K. Sci. Signal. 2:RA46-RA46(2009) [PubMed: 19690332] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1585, MASS SPECTROMETRY. Tissue: Leukemic T-cell. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AY035864 mRNA. Translation: AAK62026.1. AJ492221 mRNA. Translation: CAD37348.1. AL713750 mRNA. Translation: CAD28525.2. Different initiation. AL833757 mRNA. Translation: CAH56236.1. AC002565 Genomic DNA. No translation available. AC008731 Genomic DNA. No translation available. BC024324 mRNA. Translation: AAH24324.2. BC068209 mRNA. No translation available. U80739 mRNA. Translation: AAB91438.1. AB040893 mRNA. Translation: BAA95984.1. AK001773 mRNA. Translation: BAA91899.1. Different initiation. |
| IPI | IPI00160265. IPI00382618. IPI00395878. IPI00554606. IPI00554721. IPI00853634. |
| RefSeq | NP_055309.2. NM_014494.2. |
| UniGene | Hs.655057. |
3D structure databases | |
| ProteinModelPortal | Q8NDV7. |
| SMR | Q8NDV7. Positions 1186-1258, 1774-1862. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q8NDV7. 31 interactions. |
| STRING | Q8NDV7. |
PTM databases | |
| PhosphoSite | Q8NDV7. |
Polymorphism databases | |
| DMDM | 296452846. |
Proteomic databases | |
| PRIDE | Q8NDV7. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000395799; ENSP00000379144; ENSG00000090905. |
| GeneID | 27327. |
| KEGG | hsa:27327. |
| UCSC | uc002dmm.1. human. uc002dmn.1. human. uc002dmr.1. human. |
Organism-specific databases | |
| CTD | 27327. |
| GeneCards | GC16P024741. |
| H-InvDB | HIX0012904. |
| HGNC | HGNC:11969. TNRC6A. |
| HPA | HPA015305. HPA017869. |
| MIM | 610739. gene. |
| neXtProt | NX_Q8NDV7. |
| PharmGKB | PA36656. |
| HUGE | Search... |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG05635. |
| GeneTree | ENSGT00410000025966. |
| HOVERGEN | HBG062594. |
| InParanoid | Q8NDV7. |
| OMA | WGDSKGS. |
Gene expression databases | |
| ArrayExpress | Q8NDV7. |
| Bgee | Q8NDV7. |
| Genevestigator | Q8NDV7. |
| GermOnline | ENSG00000090905. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR019486. Argonaute_hook_dom. IPR012677. Nucleotide-bd_a/b_plait. IPR000504. RRM_dom. IPR009060. UBA-like. [Graphical view] |
| Gene3D | G3DSA:3.30.70.330. a_b_plait_nuc_bd. 1 hit. |
| Pfam | PF10427. Ago_hook. 1 hit. [Graphical view] |
| SMART | SM00360. RRM. 1 hit. [Graphical view] |
| SUPFAM | SSF46934. UBA_like. 1 hit. |
| PROSITE | PS50102. RRM. False negative. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 50354. |
| SOURCE | Search... |
Entry information
| Entry name | TNR6A_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8NDV7 Secondary accession number(s): C9JAR8 Q9P268 | ||||||||
| Entry history |
| ||||||||
| 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 16 Human chromosome 16: 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