Homo sapiens alpha 2-HS glycoprotein (AHSG), transcript variant 4, mRN - Nucleotide

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Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
EVALUATION OF FETUIN-A LEVEL IN POLYCYSTIC OVARY SYNDROME AND ITS ASSOCIATION WITH ASPROSIN AND SOME BIOCHEMICAL PARAMETERS. [Georgian Med News. 2023]
EVALUATION OF FETUIN-A LEVEL IN POLYCYSTIC OVARY SYNDROME AND ITS ASSOCIATION WITH ASPROSIN AND SOME BIOCHEMICAL PARAMETERS.
Mahmmoed B, Hilal N, Sarhat E. Georgian Med News. 2023 Oct; (343):63-66.
Fetuin-A and its genetic association with cardiometabolic disease. [Sci Rep. 2023]
Fetuin-A and its genetic association with cardiometabolic disease.
Al Ali L, van de Vegte YJ, Said MA, Groot HE, Hendriks T, Yeung MW, Lipsic E, van der Harst P. Sci Rep. 2023 Dec 6; 13(1):21469. Epub 2023 Dec 6.

RefSeq protein product
See the reference protein sequence for alpha-2-HS-glycoprotein isoform 4 preproprotein (NP_001341502.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens molybdenum cofactor synthesis 3 (MOCS3), mRNA
Homo sapiens molybdenum cofactor synthesis 3 (MOCS3), mRNA
gi|414144885|ref|NM_014484.4|

Nucleotide
Homo sapiens
Homo sapiens
RefSeq annotation of the human reference genome assembly

BioProject
Alopecia-intellectual disability syndrome 1
Alopecia-intellectual disability syndrome 1

MedGen
C1859878[conceptid] (1)
MedGen
BioProject Links for Nucleotide (Select 2217331030) (1)
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Nucleotide