Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
2621 to 2630 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2621
C-type lectin domain family 4 member A
CD367, CLECSF6, DCIR, DDB27, HDCGC13P, LLIR, hDCIR
Color vision deficiency, Hypersensitivity

2622
C-type lectin domain family 4 member C
BDCA-2, BDCA2, CD303, CLECSF11, CLECSF7, DLEC, HECL, PRO34150
Amyotrophic lateral sclerosis

2623
C-type lectin domain family 4 member D
CD368, CLEC-6, CLEC6, CLECSF8, Dectin-3, MCL, MPCL
Lung disease

2624
C-type lectin domain family 4 member E
CLECSF9, MINCLE
Brain injuries, Lung disease

2625
C-type lectin domain family 4 member F
CLECSF13, KCLR, KCR
Seasonal allergic rhinitis

2626
C-type lectin domain family 4 member G
DTTR431, LP2698, LSECtin, UNQ431
Hepatocellular carcinoma

2627
C-type lectin domain family 4 member M
CD209L, CD299, DC-SIGN2, DC-SIGNR, DCSIGNR, HP10347, L-SIGN, LSIGN
Hepatocellular carcinoma, Coronary artery disease, Venous thromboembolism

2628
Clathrin heavy chain linker domain containing 1
C2orf63
Bipolar disorder, Major depressive disorder, Nasal disorder, Respiratory system disease

2629
Chloride intracellular channel 1
CL1C1, CLCNL1, G6, NCC27
Anxiety disorder, Breast neoplasms, Esophageal squamous cell carcinoma, Major depressive disorder, Mastocytosis, Neurotic disorder, Osteoarthritis, Stevens-johnson syndrome, Systemic mastocytosis, Toxic epidermal necrolysis

2630
Chloride intracellular channel 2
CLCNL2, CLIC2b, MRXS32, XAP121
Chromosome xq28 duplication syndrome, Intellectual developmental disorder, x-linked, X-linked complex neurodevelopmental disorder, X-linked intellectual disability