Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "I"

131 to 140 of 359 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
131	3500	IGHG1	Immunoglobulin heavy constant gamma 1 (G1m marker)	-	Lymphocytic leukemia, Inflammatory myopathy, Myositis, Sclerocystic ovaries, Polycystic ovary syndrome
132	3501	IGHG2	Immunoglobulin heavy constant gamma 2 (G2m marker)	-	Igg deficiency disorder, Inflammatory myopathy, Kappa-chain deficiency, Myositis
133	3505	IGHGP	Immunoglobulin heavy constant gamma P (non-functional)	IGHGP1	Hypothyroidism
134	3507	IGHM	Immunoglobulin heavy constant mu	AGM1, MU, VH	Agammaglobulinemia, Arthritis, Bronchiectasis, Congenital epicanthus, Conjunctivitis, Crohn disease, High palate, Hypogammaglobulinemia, Immunologic deficiency syndromes, Malabsorption syndrome, Neutropenia, Osteomyelitis, Otitis media, Sinusitis
135	3508	IGHMBP2	Immunoglobulin mu DNA binding protein 2	CATF1, CMT2S, HCSA, HMN6, HMNR1, SMARD1, SMUBP2, ZFAND7	Anterior horn cell disease, Charcot-marie-tooth disease, Congenital clubfoot, Diaphragmatic eventration, Distal amyotrophy, Distal spinal muscular atrophy, Migraine with aura, Hypotonia, Ptosis, Respiratory failure, Sensorimotor neuropathy, Spinal muscular atrophy, Spinal muscular atrophy with respiratory distress, Vitamin d deficiency
136	3514	IGKC	Immunoglobulin kappa constant	HCAK1, IGKCD, Km	Dysgammaglobulinemia, Igg deficiency disorder, Inflammatory myopathy, Kappa-chain deficiency, Myositis
137	3543	IGLL1	Immunoglobulin lambda like polypeptide 1	14.1, AGM2, CD179b, IGL1, IGL5, IGLJ14.1, IGLL, IGO, IGVPB, VPREB2	Agammaglobulinemia, Arthritis, Bronchiectasis, Congenital epicanthus, Conjunctivitis, High palate, Hypogammaglobulinemia, Immunologic deficiency syndromes, Malabsorption syndrome, Neutropenia, Osteomyelitis, Otitis media, Sinusitis
138	3547	IGSF1	Immunoglobulin superfamily member 1	CHTE, IGCD1, IGDC1, INHBP, PGSF2, p120	Central congenital hypothyroidism with testicular enlargement, x-linked, Central hypothyroidism, Congenital hypothyroidism, Congenital myxedema, Endemic cretinism, Hypothyroidism, Hypothyroidism, central, and testicular enlargement, Isolated somatotropin deficiency, Testicular diseases
139	3549	IHH	Indian hedgehog signaling molecule	BDA1, HHG2	Acrocapitofemoral dysplasia, Acropectorovertebral dysplasia, Brachydactyly, Camptodactyly of fingers, Congenital clubfoot, Short femur, Congenital hypoplasia of radius, Congenital pectus carinatum, Congenital pectus excavatum, Corpus luteum cyst, Dwarfism, Endometrioma, Endometriosis, Gastrointestinal stromal tumor, Hypoplasia of thumb View all (8 more)
140	3550	IK	IK cytokine	CSA2, RED, RER	Prostate cancer

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