DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 62726 - 62743 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0080174 Spina Bifida Occulta COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0005744 Blepharophimosis COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0008924 Cleft upper lip COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0026764 Multiple Myeloma COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0036439 Scoliosis, unspecified COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C1378511 Undifferentiated leukemia COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0005745 Blepharoptosis COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0006826 Malignant Neoplasms COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C1306503 Congenital exomphalos COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0206710 Basal Cell Neoplasm COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0158761 Radioulnar Synostosis COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0023434 Chronic Lymphocytic Leukemia COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0023449 Acute lymphocytic leukemia COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C3463824 MYELODYSPLASTIC SYNDROME COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0280141 Acute Undifferentiated Leukemia COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C3714756 Intellectual Disability COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C1384666 hearing impairment COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C0751676 Basal Cell Cancer COLEC10 10584 collectin subfamily member 10 Q9Y6Z7

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024