As of 2022-03-07, the Wikidata property HGNC ID (P354) is used on 43,518 items as main value on statements (not counting qualifiers) of the Q and P namespaces.

Closest properties: by cardinality of intersection, by Jaccard index.

Display properties of the following types:                                    

Closest properties by cardinality of intersection

IDLabelIntersection cardinalityJaccard index
P351 Entrez Gene ID 43,517
 0.0559
P353 HGNC gene symbol 43,516
 0.9955
P31 instance of 43,513
 0.0005
P703 found in taxon 43,512
 0.0168
P4196 cytogenetic location 42,987
 0.2310
P2888 exact match 42,484
 0.0131
P279 subclass of 40,548
 0.0153
P594 Ensembl gene ID 36,869
 0.2340
P639 RefSeq RNA ID 28,154
 0.0997
P1057 chromosome 24,739
 0.0394
P704 Ensembl transcript ID 24,429
 0.1579
P644 genomic start 24,420
 0.0234
P645 genomic end 24,420
 0.0234
P2548 strand orientation 24,378
 0.0234
P5572 expressed in 23,396
 0.5247
P688 encodes 19,275
 0.0196
P593 HomoloGene ID 18,944
 0.1518
P684 ortholog 17,280
 0.0609
P492 OMIM ID 15,978
 0.3076
P646 Freebase ID 10,857
 0.0024
P692 Gene Atlas Image 7,730
 0.1736
P2671 Google Knowledge Graph ID 6,917
 0.0009
P2293 genetic association 3,527
 0.0738
P18 image 3,487
 0.0008
P6366 Microsoft Academic ID 3,293
 0.0106
P10283 OpenAlex ID 832
 0.0058
P373 Commons category 161
 0.0000
P1417 Encyclopædia Britannica Online ID 106
 0.0005
P1889 different from 62
 0.0001
P3417 Quora topic ID 58
 0.0003
P486 MeSH descriptor ID 45
 0.0006
P2581 BabelNet ID 42
 0.0004
P8408 KBpedia ID 35
 0.0004
P9272 DeCS ID 32
 0.0007
P10376 ScienceDirect topic ID 30
 0.0007
P3519 Pfam ID 29
 0.0007
P682 biological process 26
 0.0001
P244 Library of Congress authority ID 22
 0.0000
P3471 WikiSkripta ID 19
 0.0004
P680 molecular function 19
 0.0000
P3827 JSTOR topic ID 18
 0.0003
P672 MeSH tree code 17
 0.0003
P681 cell component 15
 0.0000
P361 part of 15
 0.0000
P3523 Rfam ID 13
 0.0003
P527 has part or parts 12
 0.0000
P1916 gene substitution association with 11
 0.0003
P1910 decreased expression in 11
 0.0003
P6611 Semantic Scholar topic ID 10
 0.0002
P1911 increased expression in 9
 0.0002

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P353 HGNC gene symbol 43,516
 0.9955
P5572 expressed in 23,396
 0.5247
P492 OMIM ID 15,978
 0.3076
P594 Ensembl gene ID 36,869
 0.2340
P4196 cytogenetic location 42,987
 0.2310
P692 Gene Atlas Image 7,730
 0.1736
P704 Ensembl transcript ID 24,429
 0.1579
P593 HomoloGene ID 18,944
 0.1518
P639 RefSeq RNA ID 28,154
 0.0997
P2293 genetic association 3,527
 0.0738
P684 ortholog 17,280
 0.0609
P351 Entrez Gene ID 43,517
 0.0559
P1057 chromosome 24,739
 0.0394
P644 genomic start 24,420
 0.0234
P645 genomic end 24,420
 0.0234
P2548 strand orientation 24,378
 0.0234
P688 encodes 19,275
 0.0196
P703 found in taxon 43,512
 0.0168
P279 subclass of 40,548
 0.0153
P2888 exact match 42,484
 0.0131
P6366 Microsoft Academic ID 3,293
 0.0106
P10283 OpenAlex ID 832
 0.0058
P646 Freebase ID 10,857
 0.0024
P2671 Google Knowledge Graph ID 6,917
 0.0009
P18 image 3,487
 0.0008
P9272 DeCS ID 32
 0.0007
P10376 ScienceDirect topic ID 30
 0.0007
P3519 Pfam ID 29
 0.0007
P486 MeSH descriptor ID 45
 0.0006
P1417 Encyclopædia Britannica Online ID 106
 0.0005
P31 instance of 43,513
 0.0005
P8408 KBpedia ID 35
 0.0004
P3471 WikiSkripta ID 19
 0.0004
P2581 BabelNet ID 42
 0.0004
P3523 Rfam ID 13
 0.0003
P672 MeSH tree code 17
 0.0003
P3827 JSTOR topic ID 18
 0.0003
P3417 Quora topic ID 58
 0.0003
P1916 gene substitution association with 11
 0.0003
P1910 decreased expression in 11
 0.0003
P6611 Semantic Scholar topic ID 10
 0.0002
P1911 increased expression in 9
 0.0002
P2004 NALT ID 9
 0.0002
P3365 Treccani ID 8
 0.0001
P1918 altered regulation leads to 5
 0.0001
P1912 gene deletion association with 5
 0.0001
P638 PDB structure ID 8
 0.0001
P4317 GARD rare disease ID 5
 0.0001
P1889 different from 62
 0.0001
P3219 Encyclopædia Universalis ID 7
 0.0001