GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4151 - 4175** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
9779	TBC1 domain family member 5	TBC1D5
9780	piezo type mechanosensitive ion channel component 1 (Er blood group)	PIEZO1
9782	matrin 3	MATR3
9784	sorting nexin 17	SNX17
9785	DEAH-box helicase 38	DHX38
9787	DLG associated protein 5	DLGAP5
9788	MTSS I-BAR domain containing 1	MTSS1
9789	signal peptidase complex subunit 2	SPCS2
9790	BMS1 ribosome biogenesis factor	BMS1
9791	phosphatidylserine synthase 1	PTDSS1 KIAA0024 PSS1 PSSA	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bell's palsy Hailey-Hailey disease Laron syndrome Lenz-Majewski hyperostotic dwarfism Pick's disease Reye syndrome Rothmund-Thomson syndrome achondroplasia aortic disease aortic valve disease 2 aortic valve stenosis autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant osteopetrosis 2 autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 7 cerebral degeneration choanal atresia communicating hydrocephalus cryptorchidism cutis laxa dental enamel hypoplasia facial nerve disease facial paralysis humeroradial synostosis hydrocephalus hypogonadism hypospadias inguinal hernia intellectual disability lateral meningocele syndrome learning disability mal de Meleda obstructive hydrocephalus osteopetrosis osteosclerosis placental insufficiency priapism restrictive dermopathy scoliosis senile degeneration of brain sensorineural hearing loss syndactyly tongue disease
9792	SERTA domain containing 2	SERTAD2
9793	cytoskeleton associated protein 5	CKAP5
9794	mastermind like transcriptional coactivator 1	MAML1
9796	phytanoyl-CoA 2-hydroxylase interacting protein	PHYHIP
9797	TatD DNase domain containing 2	TATDN2
9801	mitochondrial ribosomal protein L19	MRPL19
9806	SPARC (osteonectin), cwcv and kazal like domains proteoglycan 2	SPOCK2
9810	ring finger protein 40	RNF40
9811	cap binding complex dependent translation initiation factor	CTIF
9812	DAP3 binding cell death enhancer 1	DELE1
9813	EF-hand calcium binding domain 14	EFCAB14
9815	GIT ArfGAP 2	GIT2
9817	kelch like ECH associated protein 1	KEAP1
9818	nucleoporin 58	NUP58
9819	TSC22 domain family member 2	TSC22D2

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