Pathway candidate — not linked to PFS or PSSD by any record here
Gene summary
A protein-coding gene on chromosome 9 (steroid receptor chaperones). The oncogene BCL2 is a membrane protein that blocks a step in a pathway leading to apoptosis or programmed cell death. The protein encoded by this gene binds to BCL2 and is referred to as BCL2-associated athanogene.
Source: NCBI Gene, accessed 2026-10-07.
Protein reference (UniProt)
- Protein
BAG family molecular chaperone regulator 1
- Function
Co-chaperone for HSP70 and HSC70 chaperone proteins. Acts as a nucleotide-exchange factor (NEF) promoting the release of ADP from the HSP70 and HSC70 proteins thereby triggering client/substrate protein release. Nucleotide release is mediated via its binding to the nucleotide-binding domain (NBD) of HSPA8/HSC70 where as the substrate release is mediated via its binding to the substrate-binding domain (SBD) of HSPA8/HSC70. Inhibits the pro-apoptotic function of PPP1R15A, and has anti-apoptotic activity. Markedly increases the anti-cell death function of BCL2 induced by various stimuli. Involved in the STUB1-mediated proteasomal degradation of ESR1 in response to age-related circulating estradiol (17-beta-estradiol/E2) decline, thereby promotes neuronal apoptosis in response to ischemic reperfusion injury (By similarity).
- Subcellular location
Nucleus; Cytoplasm.
- Tissue specificity
Isoform 4 is the most abundantly expressed isoform. It is ubiquitously expressed throughout most tissues, except the liver, colon, breast and uterine myometrium. Isoform 1 is expressed in the ovary and testis. Isoform 4 is expressed in several types of tumor cell lines, and at consistently high levels in leukemia and lymphoma cell lines. Isoform 1 is expressed in the prostate, breast and leukemia cell lines. Isoform 3 is the least abundant isoform in tumor cell lines (at protein level).
Source: UniProtKB/Swiss-Prot Q99933, release 2026_03, licensed CC BY 4.0. This is the protein’s normal biology, not evidence about post-drug syndromes; associated conditions are inherited disorders of the gene, not PFS, PSSD or PRSD.
Why its pathway is in the library
Chaperone/co-chaperone control of steroid-receptor folding and sensitivity is a regulatory layer above the receptors themselves, tied to stress-axis signaling.
Written for the whole receptor chaperones family, not for BAG1 specifically.
Mentioned in 0 corpus records
No corpus record names BAG1 directly yet. It is in the library because it sits in a pathway the corpus tracks (Receptor chaperones).
Also in steroid receptor chaperones
All 14 genes- BAG3
BAG cochaperone 3
chr 10· Receptor chaperones· Pathway candidate - FKBP4
FKBP prolyl isomerase 4
chr 12· Receptor chaperones· Pathway candidate - FKBP5
FKBP prolyl isomerase 5
chr 6· Receptor chaperones· Pathway candidate - FKBP6
FKBP prolyl isomerase family member 6 (inactive)
chr 7· Receptor chaperones· Pathway candidate - HSP90AA1
heat shock protein 90 alpha family class A member 1
chr 14· Receptor chaperones· Pathway candidate - HSP90AB1
heat shock protein 90 alpha family class B member 1
chr 6· Receptor chaperones· Pathway candidate - HSPD1
heat shock protein family D (Hsp60) member 1
chr 2· Receptor chaperones· Pathway candidate - HSPE1
heat shock protein family E (Hsp10) member 1
chr 2· Receptor chaperones· Pathway candidate
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