Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6041 to 6050 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6041
Heat shock protein family B (small) member 6
HEL55, Hsp20, PPP1R91
Heart disease

6042
Heat shock protein family B (small) member 7
cvHSP
Breast cancer, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Ovarian cancer, Prostate cancer

6043
Heat shock protein family B (small) member 8
CMT2L, DHMN2, E2IG1, H11, HMN2, HMN2A, HMND2, HSP22, HSPB8-N1, HSPB8-N2, MFM13
Charcot-marie-tooth disease, Distal axonal motor neuropathy-myofibrillar myopathy syndrome, Distal hereditary motor neuropathy, Dejerine-sottas disease, Distal muscular dystrophy, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Osteosarcoma, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Spinal muscular atrophy, Vacuolar myopathy

6044
Heat shock protein family B (small) member 9
CT51
Developmental disability

6045
HSPB1 associated protein 1
PASS1
Atrial septal defect, Congenital heart septal defect

6046
Heat shock protein family D (Hsp60) member 1
CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13
Arteriosclerosis, Autism, Spastic paraplegia, Renal cell carcinoma, Cardiomyopathy, Ischemic heart disease, Coronary artery disease, Hypertrophic cardiomyopathy, Hypomyelinating leukodystrophy, Leukodystrophy, Major depressive disorder, Myocardial ischemia, Pelizaeus-merzbacher disease, Schizophrenia, Hereditary spastic paraplegia
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6047
Heat shock protein family E (Hsp10) member 1
CPN10, EPF, GROES, HSP10
Cardiomyopathy

6048
HSPE1-MOB4 readthrough
HSPE1-PHOCN
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Insomnia, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

6049
Heparan sulfate proteoglycan 2
HSPG, PLC, PRCAN, SJA, SJS, SJS1
1p36 deletion syndrome, Alzheimer disease, Atrial fibrillation, Chromosome 1p36 deletion syndrome, Congenital cartilage disorder, Connective tissue disease, Craniofacial abnormalities, Desbuquois syndrome, Dyssegmental dysplasia, Metabolic syndrome, Osteochondrodysplasias, Schizophrenia, Schwartz-jampel syndrome, Spondyloepiphyseal dysplasia, Stuve-wiedemann syndrome
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6050
Heat shock protein family H (Hsp110) member 1
HSP105, HSP105A, HSP105B, NY-CO-25
Colorectal cancer