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Gene referenceSep 23, 2026

AOC1

Encodes diamine oxidase, an enzyme involved in breaking down histamine and other amines. DAO is used here as an enzyme nickname; it is also the official symbol of a different gene.

Gene referenceSep 23, 2026

ATG16L1

ATG16L1 is involved in autophagy, a process that helps cells recycle parts.

Gene referenceSep 23, 2026

BHMT

BHMT helps recycle homocysteine into methionine using betaine. It is a different route from the folate and B12 pathway.

Gene referenceSep 23, 2026

CHDH

CHDH helps convert choline toward betaine, a nutrient involved in the homocysteine pathway.

Gene referenceSep 23, 2026

FOLH1

FOLH1 helps break down folate from food so it can be absorbed. This is different from the MTHFR step.

Gene referenceSep 23, 2026

FUT2

FUT2 affects substances on the surfaces of the gut and other moist tissues and is studied in relation to the microbiome.

Gene referenceSep 23, 2026

HLA-DQA1

HLA-DQA1 contributes to an HLA-DQ protein that presents antigen fragments to CD4 T cells. HLA-DQ function depends on pairing with an HLA-DQB chain, so an isolated marker is not a complete HLA type.

Gene referenceSep 23, 2026

IL23R

IL23R encodes part of the receptor that receives IL-23 signals. This connects the gene to the maintenance of Th17-related immune responses, which differ from the Th2 patterns discussed in allergy.

Gene referenceSep 23, 2026

PEMT

Makes an enzyme involved in producing phosphatidylcholine, a component of cell membranes. Genetic findings alone do not establish a choline deficiency.

Gene referenceSep 23, 2026

IL18R1

IL18R1 encodes a component of the receptor for IL-18. It works with an accessory component, IL18RAP, to support IL-18 signaling.

FacebookSep 17, 2026

Good questions deserve a deeper conversation.

Good questions deserve a deeper conversation. Purser Wellness Explore is a new space to follow yours - videos, articles, and guided journeys with me. Start with MTHFR, cytokines, homocysteine, gut health… or whatever thread you’re holding

Report teachingSep 16, 2026

Hirschsprung’s disease & genetics

Explore enteric nerve development, aganglionosis, bowel function, RET, EDNRB, EDN3, SOX10, PHOX2B, and genetic syndromes discussed alongside Hirschsprung’s disease.

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