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Protein-coding gene in the species Homo sapiens
protein subunit delta is a protein that in humans is encoded by the SSR4 gene. SSR4, also called TRAPD, is assumed to be involved in protein secretion
SSR4
Condition in which the jaw is small
dysplasia-short limb-abnormal calcification syndrome Squalene synthase deficiency SSR4-congenital disorder of glycosylation Stickler syndrome types 1 and 2 Stromme
Micrognathism
Sex chromosome present in both sexes in the XY and X0 sex-determination systems
encoding protein Spastic paraplegia 16 (complicated, X-linked recessive) SSR4: encoding protein Translocon-associated protein subunit delta TAF7L: encoding
X_chromosome
Medical condition
obtained, cerebellar hypoplasia is a common finding. Some CDG subtypes, like SSR4-CDG 1y, have been classified as connective tissue disorders. Ocular abnormalities
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
Family of proteins
SSR2) Somatostatin receptor 3 (SSTR3, SSR3) Somatostatin receptor 4 (SSTR4, SSR4) Somatostatin receptor 5 (SSTR5, SSR5) GPCR neuropeptide receptor InterPro: IPR009150
Rhodopsin-like_receptors
P43307 15874 SSR2 HGNC:11324; P43308 15875 SSR3 HGNC:11325; Q9UNL2 15876 SSR4 HGNC:11326; P51571 15877 SSRP1 HGNC:11327; Q08945 15878 SST HGNC:11329; P61278
List of human protein-coding genes 8
List_of_human_protein-coding_genes_8
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