AI & ChatGPT searches , social queriess for STX16
Search references for STX16. Phrases containing STX16
See searches and references containing STX16!
Search references for STX16. Phrases containing STX16
See searches and references containing STX16!STX16
Protein-coding gene in the species Homo sapiens
Syntaxin-16 (STX16) is a part of a protein family group called SNARE proteins (soluble N-ethylmaleimide-sensitive factor attachment proteins). SNARE proteins
STX16
Endocrine disease
(GNAS1) Type 1B Normal High Low Low High Gene defect from mother (GNAS1 and STX16) Type 2 Normal High Low Low High ? Pseudopseudohypoparathyroidism Skeletal
Hypoparathyroidism
Rare genetic condition
associated with a methylation defect in the A/B exon of GNAS1, caused by STX16 disruption. Type 2 (OMIM 203330) Also lacks the physical appearance of type
Pseudohypoparathyroidism
Rare genetic disorder in the human body
(GNAS1) Type 1B Normal High Low Low High Gene defect from mother (GNAS1 and STX16) Type 2 Normal High Low Low High ? Pseudopseudohypoparathyroidism Skeletal
Pseudopseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Protein family
Syntaxin STX1A STX1B STX2 STX3 STX4 STX5 STX6 STX7 STX8 STX10 STX11 STX12 STX16 STX17 STX18 STX19 Munc-18: STXBP1 STXBP2 STXBP3 STXBP4 STXBP5 STXBP6 R-SNARE
SNARE_protein
Group of proteins
STX1B, STX2, STX3, STX4, STX5, STX6, STX7, STX8, STX10, STX11, STX12, STX16, STX17, STX18, STX19 Tomosyn, a syntaxin binding protein Fernandez I, Ubach
Syntaxin
Protein-coding gene in the species Homo sapiens
interact with the t-SNAREs VTI1A and STX16 and with the v-SNAREs VAMP3 and VAMP4. The SNARE complex of STX10, STX16, VTI1A, and VAMP3 are required for late
STX10
Protein-coding gene in the species Homo sapiens
network-to-endosome transport. VAMP4 has been shown to interact with AP1M1, STX6 and STX16. GRCh38: Ensembl release 89: ENSG00000117533 – Ensembl, May 2017 GRCm38:
VAMP4
O60499 16047 STX11 HGNC:11429; O75558 16048 STX12 HGNC:11430; Q86Y82 16049 STX16 HGNC:11431; O14662 16050 STX17 HGNC:11432; P56962 16051 STX18 HGNC:15942;
List of human protein-coding genes 8
List_of_human_protein-coding_genes_8
Gene locus
uses a downstream start codon to have a shortened amino terminal region. STX16 deletion causes loss of methylation at the A/B exon, leading to PHP1B. XLαs
GNAS_complex_locus
Protein-coding gene in the species Homo sapiens
1999). "Two frequent tetra-nucleotide repeat polymorphisms between VAPB and STX16 on chromosome 20q13". Molecular and Cellular Probes. 13 (6): 449–51. doi:10
VAPB
type IB; 603233; GNASAS Pseudohypoparathyroidism, type IB; 603233; STX16 Pseudovaginal perineoscrotal hypospadias; 264600; SRD5A2 Pseudoxanthoma
List_of_OMIM_disorder_codes
STX16
STX16
STX16
STX16
Girl/Female
English
Blend of Cherie and Cerise: dear one; darling.
Surname or Lastname
English
English : variant spelling of Frain.
Surname or Lastname
English (of Norman origin)
English (of Norman origin) : habitational name from Saint-Léger in La Manche or Saint-Léger-aux-Bois in Seine-Maritime, both so called from the dedication of their churches to St. Leger (see Ledger), the martyred 7th-century bishop of Autun.German and Jewish (Ashkenazic) : from a Germanized form of the personal name Salomon.
Boy/Male
Muslim
Another name of Ali, The generous, The giving
Girl/Female
English
Caprice.
Girl/Female
English
Abbreviation of Carol and Caroline from the masculine Charles meaning manly.
Girl/Female
Indian
Free from impurity, Moonlight
Boy/Male
French, German
Unhappy; Unlucky
Boy/Male
Muslim
Slave of the originator, Servant of the incomparable
Girl/Female
Indian
Prosperous
STX16
STX16
STX16
STX16
STX16