FCRL3

Chr 1

Fc receptor like 3

Also known as: CD307c, FCRH3, IFGP3, IRTA3, MAIA, SPAP2

This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein contains immunoreceptor-tyrosine activation motifs and immunoreceptor-tyrosine inhibitory motifs in its cytoplasmic domain and may play a role in regulation of the immune system. Mutations in this gene have been associated with rheumatoid arthritis, autoimmune thyroid disease, and systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

OMIMResearchGenerating clinical summary…

Primary Disease Associations & Inheritance

UniProtRheumatoid arthritis
0
Active trials
32
Pubs (1 yr)
P/LP submissions
P/LP missense
1.28
LOEUF
Multiple*
Mechanism· predicted

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint?
1.28LOEUF
pLI 0.000
Z-score 0.25
OE 0.95 (0.721.28)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint?
-1.17Z-score
OE missense 1.17 (1.081.26)
453 obs / 387.9 exp
Tolerant

Tolerant to missense variation

Observed / Expected Ratios?
LoF OE?0.95 (0.721.28)
00.351.4
Missense OE?1.17 (1.081.26)
00.61.4
Synonymous OE?1.11
01.21.6
LoF obs/exp: 32 / 33.6Missense obs/exp: 453 / 387.9Syn Z: -1.14

ClinVar Variant Classifications

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

FCRL3 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →