GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **3851 - 3875** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
3284	hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2	HSD3B2 SDR11E2 short chain dehydrogenase/reductase family 11E, member 2	Alzheimer's disease Bartter disease Conn's syndrome Sertoli cell-only syndrome Waterhouse-Friderichsen syndrome X-linked spermatogenic failure 1 acne adrenal adenoma adrenal cortex cancer adrenal gland hyperfunction autoimmune hepatitis bipolar disorder bladder carcinoma congenital adrenal hyperplasia cryptorchidism delusional disorder depressive disorder disorder of sexual development endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis essential hypertension gynecomastia hepatitis hepatocellular carcinoma hermaphroditism hyperandrogenism hyperprolactinemia hypertension hypertrichosis hypertrophy of breast hypogonadotropic hypogonadism 23 with or without anosmia hypospadias infant gynecomastia lactic acidosis liver cancer major depressive disorder melancholic depression obsolete Cushing's syndrome obsolete melancholia osteoporosis paranoid schizophrenia polycystic ovary syndrome pre-eclampsia primary hyperaldosteronism prostate cancer prostate carcinoma pseudohermaphroditism urinary bladder cancer uterine corpus cancer
80270	hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7	HSD3B7 C(27)-3BETA-HSD SDR11E3 short chain dehydrogenase/reductase family 11E, member 3	Gilbert syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease bilirubin metabolic disorder blood coagulation disease cancer cholestasis congenital bile acid synthesis defect 1 congenital bile acid synthesis defect congenital stationary night blindness 1A congenital stationary night blindness diarrhea gallbladder disease giant cell glioblastoma glioblastoma high grade glioma intrahepatic cholestasis liver disease neuropathy night blindness obsolete inherited blood coagulation disease obsolete steatorrhea osteomalacia osteoporosis peripheral nervous system disease progressive familial intrahepatic cholestasis 1 progressive familial intrahepatic cholestasis 4 progressive familial intrahepatic cholestasis rickets tropical sprue
3297	heat shock transcription factor 1	HSF1
3299	heat shock transcription factor 4	HSF4
100506164	heat shock transcription factor family, X-linked 1	HSFX1
100130086	heat shock transcription factor family, X-linked 2	HSFX2
3320	heat shock protein 90 alpha family class A member 1	HSP90AA1 FLJ31884 HSP90N Hsp89 Hsp90
3326	heat shock protein 90 alpha family class B member 1	HSP90AB1
7184	heat shock protein 90 beta family member 1	HSP90B1
259217	heat shock protein family A (Hsp70) member 12A	HSPA12A
6782	heat shock protein family A (Hsp70) member 13	HSPA13
51182	heat shock protein family A (Hsp70) member 14	HSPA14
3303	heat shock protein family A (Hsp70) member 1A	HSPA1A
3304	heat shock protein family A (Hsp70) member 1B	HSPA1B
3305	heat shock protein family A (Hsp70) member 1 like	HSPA1L
3306	heat shock protein family A (Hsp70) member 2	HSPA2
3308	heat shock protein family A (Hsp70) member 4	HSPA4
22824	heat shock protein family A (Hsp70) member 4 like	HSPA4L
3309	heat shock protein family A (Hsp70) member 5	HSPA5 BiP glucose-regulated protein, 78kDa
3310	heat shock protein family A (Hsp70) member 6	HSPA6
3312	heat shock protein family A (Hsp70) member 8	HSPA8 HSC70 HSC71 HSP73
3313	heat shock protein family A (Hsp70) member 9	HSPA9
3315	heat shock protein family B (small) member 1	HSPB1
26353	heat shock protein family B (small) member 8	HSPB8
23640	HSPA (Hsp70) binding protein 1	HSPBP1

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