Homo sapiens SH2B adaptor protein 1 (SH2B1), transcript variant 4, mRN - Nucleotide

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Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease. [Cell Rep Med. 2023]
Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease.
Hanssen R, Auwerx C, Jõeloo M, Sadler MC, Estonian Biobank Research Team, Henning E, Keogh J, Bounds R, Smith M, Firth HV, et al. Cell Rep Med. 2023 Aug 15; 4(8):101155.
SH2B1 variants as potential causes of non-syndromic monogenic obesity in a Brazilian cohort. [Eat Weight Disord. 2022]
SH2B1 variants as potential causes of non-syndromic monogenic obesity in a Brazilian cohort.
da Fonseca ACP, Assis ISS, Salum KCR, Palhinha L, Abreu GM, Zembrzuski VM, Campos Junior M, Nogueira Neto JF, Mattos FCC, Cambraia A, et al. Eat Weight Disord. 2022 Dec; 27(8):3665-3674. Epub 2022 Nov 27.
ALS-linked loss of Cyclin-F function affects HSP90. [Life Sci Alliance. 2022]
ALS-linked loss of Cyclin-F function affects HSP90.
Siebert A, Gattringer V, Weishaupt JH, Behrends C. Life Sci Alliance. 2022 Sep 16; 5(12). Epub 2022 Sep 16.

RefSeq protein product
See the reference protein sequence for SH2B adapter protein 1 isoform 2 (NP_001139268.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide