HGNC output data

Custom Downloads

Giving unique and meaningful names to every human gene

Main Index

Custom Downloads

Program Documentation

Column Definitions

Pattern Matching

Bookmark Title:

Use HGNC Database Identifier (This prefixes the HGNC ID number with HGNC:)

HGNC ID +

Approved Symbol +

Approved Name +

Status +

Locus Type +

Previous Symbols +

Previous Names +

Aliases +

Name Aliases +

Chromosome +

Date Approved +

Date Modified +

Date Symbol Changed +

Date Name Changed +

Accession Numbers +

Enzyme IDs +

Entrez Gene ID +

Ensembl Gene ID +

MGD ID +

Specialist Database Links +

Specialist Database IDs +

Pubmed IDs +

RefSeq IDs +

Gene Family Name +

Record Type +

Primary IDs +

Secondary IDs +

VEGA IDs +

Locus Specific Databases +

GDB ID (mapped data) +

Entrez Gene ID (mapped data supplied by NCBI) +

OMIM ID (mapped data supplied by NCBI) +

RefSeq (mapped data supplied by NCBI) +

UniProt ID (mapped data supplied by UniProt) +

Ensembl ID (mapped data supplied by Ensembl) +

UCSC ID (mapped data supplied by UCSC) +

Select Status

Approved

Entry and Symbol Withdrawn

Display+

Primary records

Primary and Secondary records

Secondary records

Select all Chromosomes

Select individual Chromosomes
1	2	3	4	5	6	7	8	9	10	11	12
13	14	15	16	17	18	19	20	21	22	X	Y
Both X and Y				mitochondrial				reserved

WHERE
Pattern Matching

ORDER BY

LIMIT

Output format

If you have any problems using this page please feel free to contact up at hgnc@genenames.org

Quick Column Reference

If limiting results using the 'WHERE' field use the Database name rather than the External Name. see the Custom Downloads Documentation for more information.

gd_ stands for HGNC data ie data we curate ourselves
md_ signifies Mapped Data
The _id suffix indicates the field contains a single ID number
_ids indicates a comma delimited list of IDs
LocusLink IDs have gone into the field gd_eg_id and md_eg_id, as sooner or later we will be moving from LocusLink to Entrez Gene.

External name	Database name	External name	Database name
HGNC ID	gd_hgnc_id	Approved Symbol	gd_app_sym
Approved Name	gd_app_name	Status	gd_status
Locus Type	gd_locus_type	Previous Symbols	gd_prev_sym
Previous Names	gd_prev_name	Aliases	gd_aliases
Name Aliases	gd_name_aliases	Chromosome	gd_pub_chrom_map
Date Approved	gd_date2app_or_res	Date Modified	gd_date_mod
Date Symbol Changed	gd_date_sym_change	Date Name Changed	gd_date_name_change
Accession Numbers	gd_pub_acc_ids	Enzyme IDs	gd_enz_ids
Entrez Gene ID	gd_pub_eg_id	Ensembl Gene ID	gd_pub_ensembl_id
MGD ID	gd_mgd_id	Specialist Database Links	gd_other_ids
Specialist Database IDs	gd_other_ids_list	Pubmed IDs	gd_pubmed_ids
RefSeq IDs	gd_pub_refseq_ids	Gene Family Name	gd_gene_fam_name
Record Type	gd_record_type	Primary IDs	gd_primary_ids
Secondary IDs	gd_secondary_ids	VEGA IDs	gd_vega_ids
Locus Specific Databases	gd_lsdb_links	GDB ID (mapped data)	md_gdb_id
Entrez Gene ID (mapped data supplied by NCBI)	md_eg_id	OMIM ID (mapped data supplied by NCBI)	md_mim_id
RefSeq (mapped data supplied by NCBI)	md_refseq_id	UniProt ID (mapped data supplied by UniProt)	md_prot_id
Ensembl ID (mapped data supplied by Ensembl)	md_ensembl_id	UCSC ID (mapped data supplied by UCSC)	md_ucsc_id

NHGRI
	The work of the HGNC is supported by NHGRI grant P41 HG003345, the UK Medical Research Council and the Wellcome Trust.