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protein

Isoform 4 of Atlastin-2

aka ATL-2

ATL2
protein:Q8NHH9-4disease:adad:direction:down

Gene

ATL2

Organism

Homo sapiens(9606)

Length

566 aa

Mass

65,004 Da

AI summarysource-grounded · cited inline
claude-haiku-4-5-20251001

Atlastin-2 (ATL2) is a dynamin-related GTPase isoform involved in membrane fusion and endoplasmic reticulum (ER) morphology. The ATL family functions in homotypic ER membrane tethering and fusion, contributing to ER network formation and maintenance (UniProt: Q8NHH9-4).

ATL2 is widely expressed across tissues and plays roles in ER dynamics and vesicular transport. No additional disease associations are documented in UniProt records for this isoform.

This isoform shows down-regulation in Alzheimer's Disease, with a mean log2 fold-change of −0.26 in post-mortem AD brain tissue compared to age-matched controls (Chaparral AD proteomics). The measurement derives from a single subcellular fraction in a TMT-labeled, data-dependent acquisition proteomics study examining four fractions (P2, P3, S2, S3) from human brain samples. The modest magnitude of change and limited fraction coverage warrant caution in interpreting functional significance.

Generated from the curated entity record below. May contain errors — verify against source links.

Proteomics Evidence · AD

↓ Down in AD

P3

-0.264

P2

not detected

S2

not detected

S3

not detected

Mean log₂FC across detected fractions: -0.2636 (1 of 4 fractions detected)

Human post-mortem AD brain vs age-matched controls, TMT-labeled, 4 subcellular fractions (P2, P3, S2, S3), DDA proteomics.

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Last updated 5/8/2026, 6:28:31 AM