Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
286002
Gene name Gene Name - the full gene name approved by the HGNC.
SLC26A4 antisense RNA 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC26A4-AS1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q22.3
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC 22385 N/A
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Deafness DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT rs267607135, rs387906219, rs387906220, rs387906221, rs387906222, rs606231120, rs267606855, rs121918370, rs137853185, rs137853186, rs137853187, rs137853188, rs587776522, rs587776523, rs200781822
View all (1019 more)
24105851
Pendred syndrome Pendred`s syndrome rs121908360, rs111033308, rs80338848, rs28939086, rs80338849, rs111033244, rs111033303, rs121908364, rs121908362, rs121908363, rs765884316, rs111033307, rs111033348, rs1584344687, rs2129315781
View all (141 more)
23918157, 22285650, 12676893, 23965030, 11317356, 17876604, 16914891, 24224479, 23336812, 29196752, 26969326, 16570074, 19040761, 25394566, 24341454
View all (8 more)
Wolff-parkinson-white syndrome Wolff-Parkinson-White Syndrome rs111033205, rs121908987, rs3218716, rs199472712, rs869312065, rs1554284604, rs1553197939, rs1553624186, rs1553631968, rs1555100687, rs1555418832