The HUGO Gene Nomenclature Committee (HGNC) is a committee of the Human Genome Organisation (HUGO) that sets the standards for human gene nomenclature.
The HGNC approves a unique and meaningful name for every known human gene, based on a group of experts. In addition, the HGNC also provides the mapping between gene symbols to gene entries in other popular databases or resources: the HGNC complete gene set.
The goal of hgnc is to easily download and import the latest HGNC complete gene data set into R.
This data set provides a useful mapping of HGNC symbols to gene entries in other popular databases or resouces, such as, the Entrez gene identifier or the UCSC gene identifier, among many others. Check the documentation of the function import_hgnc_dataset()
for a description of the several fields available.
Installation
Install hgnc from CRAN:
install.packages("hgnc")
You can install the development version of hgnc like so:
# install.packages("remotes")
remotes::install_github("maialab/hgnc")
Usage
Basic usage
To import the latest HGNC gene data set in tabular format directly into memory as a tibble do as follows:
library(hgnc)
# Date of HGNC last update
last_update()
#> [1] "2023-06-20 12:46:57 UTC"
# Direct URL to the latest archive in TSV format
(url <- latest_archive_url())
#> [1] "https://ftp.ebi.ac.uk/pub/databases/genenames/hgnc/tsv/hgnc_complete_set.txt"
# Import the data set in tidy tabular format
# NB: Multiple-value columns are kept as list-columns
hgnc_dataset <- import_hgnc_dataset(url)
dplyr::glimpse(hgnc_dataset)
#> Rows: 43,700
#> Columns: 55
#> $ hgnc_id <chr> "HGNC:5", "HGNC:37133", "HGNC:24086", "HGNC:7…
#> $ hgnc_id2 <chr> "5", "37133", "24086", "7", "27057", "23336",…
#> $ symbol <chr> "A1BG", "A1BG-AS1", "A1CF", "A2M", "A2M-AS1",…
#> $ name <chr> "alpha-1-B glycoprotein", "A1BG antisense RNA…
#> $ locus_group <chr> "protein-coding gene", "non-coding RNA", "pro…
#> $ locus_type <chr> "gene with protein product", "RNA, long non-c…
#> $ status <chr> "Approved", "Approved", "Approved", "Approved…
#> $ location <chr> "19q13.43", "19q13.43", "10q11.23", "12p13.31…
#> $ location_sortable <chr> "19q13.43", "19q13.43", "10q11.23", "12p13.31…
#> $ alias_symbol <list> NA, "FLJ23569", <"ACF", "ASP", "ACF64", "ACF…
#> $ alias_name <list> NA, NA, NA, NA, NA, NA, NA, NA, NA, <"iGb3 s…
#> $ prev_symbol <list> NA, <"NCRNA00181", "A1BGAS", "A1BG-AS">, NA,…
#> $ prev_name <list> NA, <"non-protein coding RNA 181", "A1BG ant…
#> $ gene_group <list> "Immunoglobulin like domain containing", "An…
#> $ gene_group_id <list> "594", "1987", "725", "2148", "1987", "2148"…
#> $ date_approved_reserved <date> 1989-06-30, 2009-07-20, 2007-11-23, 1986-01-…
#> $ date_symbol_changed <date> NA, 2010-11-25, NA, NA, NA, 2005-09-01, NA, …
#> $ date_name_changed <date> NA, 2012-08-15, NA, NA, 2018-03-21, 2016-03-…
#> $ date_modified <date> 2023-01-20, 2013-06-27, 2023-01-20, 2023-01-…
#> $ entrez_id <int> 1, 503538, 29974, 2, 144571, 144568, 10087410…
#> $ ensembl_gene_id <chr> "ENSG00000121410", "ENSG00000268895", "ENSG00…
#> $ vega_id <chr> "OTTHUMG00000183507", "OTTHUMG00000183508", "…
#> $ ucsc_id <chr> "uc002qsd.5", "uc002qse.3", "uc057tgv.1", "uc…
#> $ ena <list> NA, "BC040926", "AF271790", <"BX647329", "X6…
#> $ refseq_accession <list> "NM_130786", "NR_015380", "NM_014576", "NM_0…
#> $ ccds_id <list> "CCDS12976", NA, <"CCDS7243", "CCDS7242", "C…
#> $ uniprot_ids <list> "P04217", NA, "Q9NQ94", "P01023", NA, "A8K2U…
#> $ pubmed_id <list> "2591067", NA, <"11815617", "11072063">, <"2…
#> $ mgd_id <list> "MGI:2152878", NA, "MGI:1917115", "MGI:24491…
#> $ rgd_id <list> "RGD:69417", NA, "RGD:619834", "RGD:2004", N…
#> $ lsdb <chr> NA, NA, NA, "LRG_591|http://ftp.ebi.ac.uk/pub…
#> $ cosmic <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ omim_id <list> "138670", NA, "618199", "103950", NA, "61062…
#> $ mirbase <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ homeodb <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ snornabase <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ bioparadigms_slc <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ orphanet <chr> NA, NA, NA, NA, NA, "410627", NA, NA, NA, NA,…
#> $ pseudogene.org <chr> NA, NA, NA, NA, NA, NA, NA, NA, "PGOHUM000002…
#> $ horde_id <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ merops <chr> "I43.950", NA, NA, "I39.001", NA, "I39.007", …
#> $ imgt <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ iuphar <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ kznf_gene_catalog <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ `mamit-trnadb` <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ cd <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ lncrnadb <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ enzyme_id <list> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, "2.4…
#> $ intermediate_filament_db <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ rna_central_ids <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ lncipedia <chr> NA, "A1BG-AS1", NA, NA, "A2M-AS1", NA, "A2ML1…
#> $ gtrnadb <chr> NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, NA, N…
#> $ agr <chr> "HGNC:5", "HGNC:37133", "HGNC:24086", "HGNC:7…
#> $ mane_select <list> <"ENST00000263100.8", "NM_130786.4">, NA, <"…
#> $ gencc <chr> NA, NA, NA, "HGNC:7", NA, "HGNC:23336", NA, N…
The original data set does not contain the column hgnc_id2
, which is added as a convenience by hgnc; this is because although the HGNC identifiers should formally contain the prefix "HGNC:"
, it is often found elsewhere that they are stripped of this prefix, so the column hgnc_id2
is also provided whose values only contain the integer part.
hgnc_dataset %>%
dplyr::select(c('hgnc_id', 'hgnc_id2'))
#> # A tibble: 43,700 × 2
#> hgnc_id hgnc_id2
#> <chr> <chr>
#> 1 HGNC:5 5
#> 2 HGNC:37133 37133
#> 3 HGNC:24086 24086
#> 4 HGNC:7 7
#> 5 HGNC:27057 27057
#> 6 HGNC:23336 23336
#> 7 HGNC:41022 41022
#> 8 HGNC:41523 41523
#> 9 HGNC:8 8
#> 10 HGNC:30005 30005
#> # ℹ 43,690 more rows
Locus groups
The HGNC defines a group name (locus_group
) for a set of related locus types. Here’s how you can quickly check how many gene entries there are per locus group.
hgnc_dataset %>%
dplyr::count(locus_group, sort = TRUE)
#> # A tibble: 4 × 2
#> locus_group n
#> <chr> <int>
#> 1 protein-coding gene 19270
#> 2 pseudogene 14364
#> 3 non-coding RNA 9075
#> 4 other 991
locus_type
provides a finer classification:
hgnc_dataset %>%
dplyr::group_by(locus_group) %>%
dplyr::count(locus_type, sort = TRUE) %>%
dplyr::arrange(locus_group) %>%
print(n = Inf)
#> # A tibble: 23 × 3
#> # Groups: locus_group [4]
#> locus_group locus_type n
#> <chr> <chr> <int>
#> 1 non-coding RNA RNA, long non-coding 5738
#> 2 non-coding RNA RNA, micro 1912
#> 3 non-coding RNA RNA, transfer 591
#> 4 non-coding RNA RNA, small nucleolar 568
#> 5 non-coding RNA RNA, cluster 119
#> 6 non-coding RNA RNA, ribosomal 60
#> 7 non-coding RNA RNA, small nuclear 50
#> 8 non-coding RNA RNA, misc 29
#> 9 non-coding RNA RNA, Y 4
#> 10 non-coding RNA RNA, vault 4
#> 11 other immunoglobulin gene 230
#> 12 other T cell receptor gene 206
#> 13 other readthrough 147
#> 14 other fragile site 116
#> 15 other endogenous retrovirus 109
#> 16 other complex locus constituent 69
#> 17 other unknown 68
#> 18 other region 38
#> 19 other virus integration site 8
#> 20 protein-coding gene gene with protein product 19270
#> 21 pseudogene pseudogene 14124
#> 22 pseudogene immunoglobulin pseudogene 203
#> 23 pseudogene T cell receptor pseudogene 37
Downloading to disk
If you prefer to download the data set as a file to disk first, you can use download_archive()
. Then, you can use import_hgnc_dataset()
to import the downloaded file into R.
Downloading other archives
Besides the latest archive, the HUGO Gene Nomenclature Committee (HGNC) website also provides monthly and quarterly updates. Use list_archives()
to list the currently available for download archives. The column url
contains the direct download link that you can pass to import_hgnc_dataset()
to import the data into R.
list_archives()
#> # A tibble: 97 × 6
#> series dataset file date size url
#> <chr> <chr> <chr> <date> <chr> <chr>
#> 1 monthly hgnc_complete_set hgnc_complete_set_2021-03-0… 2023-05-01 14M http…
#> 2 monthly hgnc_complete_set hgnc_complete_set_2021-04-0… 2023-05-01 15M http…
#> 3 monthly hgnc_complete_set hgnc_complete_set_2021-05-0… 2023-05-01 15M http…
#> 4 monthly hgnc_complete_set hgnc_complete_set_2021-06-0… 2023-05-01 15M http…
#> 5 monthly hgnc_complete_set hgnc_complete_set_2021-07-0… 2023-05-01 15M http…
#> 6 monthly hgnc_complete_set hgnc_complete_set_2021-08-0… 2023-05-01 15M http…
#> 7 monthly hgnc_complete_set hgnc_complete_set_2021-09-0… 2023-05-01 15M http…
#> 8 monthly hgnc_complete_set hgnc_complete_set_2021-10-0… 2023-05-01 15M http…
#> 9 monthly hgnc_complete_set hgnc_complete_set_2021-11-0… 2023-05-01 15M http…
#> 10 monthly hgnc_complete_set hgnc_complete_set_2021-12-0… 2023-05-01 15M http…
#> # ℹ 87 more rows
Motivation
You could go to www.genenames.org and download the files yourself. So why the need for this R package?
hgnc really is just a convenience package. The main advantage is that the function import_hgnc_dataset()
reads in the data in tabular format with all the columns with the appropriate type (so you don’t have to specify it yourself). As an extra step, those variables that contain multiple values are encoded as list-columns.
Remember that list-columns can be expanded with tidyr::unnest()
. E.g., alias_symbol
is a list-column containing multiple alternative aliases to the standard symbol
:
hgnc_dataset %>%
dplyr::filter(symbol == 'TP53') %>%
dplyr::select(c('symbol', 'alias_symbol'))
#> # A tibble: 1 × 2
#> symbol alias_symbol
#> <chr> <list>
#> 1 TP53 <chr [2]>
hgnc_dataset %>%
dplyr::filter(symbol == 'TP53') %>%
dplyr::select(c('symbol', 'alias_symbol')) %>%
tidyr::unnest(cols = 'alias_symbol')
#> # A tibble: 2 × 2
#> symbol alias_symbol
#> <chr> <chr>
#> 1 TP53 p53
#> 2 TP53 LFS1
In addition, we also provide the function filter_by_keyword()
that allows filtering the data set based on a keyword or regular expression. By default this function will look into all columns that contain gene symbols or names (symbol
, name
, alias_symbol
, alias_name
, prev_symbol
and prev_name
). It works automatically with list-columns too.
Look for entries in the data set that contain the keyword "TP53"
:
hgnc_dataset %>%
filter_by_keyword('TP53') %>%
dplyr::select(1:4)
#> # A tibble: 66 × 4
#> hgnc_id hgnc_id2 symbol name
#> <chr> <chr> <chr> <chr>
#> 1 HGNC:49685 49685 ABHD15-AS1 ABHD15 antisense RNA 1
#> 2 HGNC:20679 20679 ANO9 anoctamin 9
#> 3 HGNC:40093 40093 BCAR3-AS1 BCAR3 antisense RNA 1
#> 4 HGNC:13276 13276 EI24 EI24 autophagy associated transmembrane prot…
#> 5 HGNC:3345 3345 ENC1 ectodermal-neural cortex 1
#> 6 HGNC:27919 27919 ERVMER61-1 endogenous retrovirus group MER61 member 1
#> 7 HGNC:56226 56226 FAM169A-AS1 FAM169A antisense RNA 1
#> 8 HGNC:4136 4136 GAMT guanidinoacetate N-methyltransferase
#> 9 HGNC:54868 54868 KLRK1-AS1 KLRK1 antisense RNA 1
#> 10 HGNC:6568 6568 LGALS7 galectin 7
#> # ℹ 56 more rows
Restrict the search to the symbol
column:
hgnc_dataset %>%
filter_by_keyword('TP53', cols = 'symbol') %>%
dplyr::select(1:4)
#> # A tibble: 23 × 4
#> hgnc_id hgnc_id2 symbol name
#> <chr> <chr> <chr> <chr>
#> 1 HGNC:11998 11998 TP53 tumor protein p53
#> 2 HGNC:29984 29984 TP53AIP1 tumor protein p53 regulated apoptosis inducing…
#> 3 HGNC:11999 11999 TP53BP1 tumor protein p53 binding protein 1
#> 4 HGNC:12000 12000 TP53BP2 tumor protein p53 binding protein 2
#> 5 HGNC:16328 16328 TP53BP2P1 tumor protein p53 binding protein 2 pseudogene…
#> 6 HGNC:43652 43652 TP53COR1 tumor protein p53 pathway corepressor 1
#> 7 HGNC:19373 19373 TP53I3 tumor protein p53 inducible protein 3
#> 8 HGNC:16842 16842 TP53I11 tumor protein p53 inducible protein 11
#> 9 HGNC:25102 25102 TP53I13 tumor protein p53 inducible protein 13
#> 10 HGNC:18022 18022 TP53INP1 tumor protein p53 inducible nuclear protein 1
#> # ℹ 13 more rows
Search for the whole word "TP53"
exactly by taking advantage of regular expressions:
hgnc_dataset %>%
filter_by_keyword('^TP53$', cols = 'symbol') %>%
dplyr::select(1:4)
#> # A tibble: 1 × 4
#> hgnc_id hgnc_id2 symbol name
#> <chr> <chr> <chr> <chr>
#> 1 HGNC:11998 11998 TP53 tumor protein p53
Citing the HGNC
To cite HGNC nomenclature resources use:
- Tweedie S, Braschi B, Gray KA, Jones TEM, Seal RL, Yates B, Bruford EA. Genenames.org: the HGNC and VGNC resources in 2021. Nucleic Acids Res. 49, D939–D946 (2021). doi: 10.1093/nar/gkaa980
To cite data within the database use the following format:
- HGNC Database, HUGO Gene Nomenclature Committee (HGNC), European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom www.genenames.org.
Please include the month and year you retrieved the data cited.