Normal function · from ai-gene-review (P21580, commit 79fe13b38970) · AI-generated, not KB evidence

ai-gene-review has this gene at status DRAFT; the description is shown only once the review is complete. Read the draft upstream.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
A20 Haploinsufficiency causative germline
mechanism: TNFAIP3 Loss of Function
Celiac Disease susceptibility
Classic Hodgkin Lymphoma somatic driver somatic
mechanism: Mutation-Driven NF-kappaB Activation
Neuropsychiatric Systemic Lupus Erythematosus susceptibility germline
Splenic Marginal Zone Lymphoma cooperating somatic
Type I Diabetes susceptibility germline
Ankylosing Spondylitis untyped
GWAS
Asthma untyped
GWAS
Atopic Dermatitis untyped
GWAS
Crohn Disease untyped
GWAS
Hodgkin Lymphoma untyped
Somatic Loss-of-Function Mutation
somatic
mechanism: Mutation-Driven NF-kappaB Activation (Classic HL)
subtype: Classic HL
Multiple Sclerosis untyped
GWAS
Psoriasis untyped
Risk Factor
Rheumatoid Arthritis untyped
GWAS
mechanism: NF-κB Activation
Systemic Lupus Erythematosus untyped
GWAS
Ulcerative Colitis untyped
GWAS
mechanism: Mucosal Inflammation
Marginal Zone Lymphoma no genetic record
mechanism: Histologic Transformation to Diffuse Large B-Cell Lymphoma

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.