SLC27A3

Chr 1

solute carrier family 27 member 3

Also known as: ACSVL3, FATP3, VLCS-3

This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]

GeneReviewsResearchGenerating clinical summary…
0
Active trials
9
Pubs (1 yr)
P/LP submissions
P/LP missense
1.48
LOEUF
GOF
Mechanism· predicted
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GeneReview available — SLC27A3
Authoritative clinical overview · Recommended first read
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Some data sources returned errors (1)

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint?
1.48LOEUF
pLI 0.000
Z-score -0.48
OE 1.10 (0.821.48)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint?
-1.35Z-score
OE missense 1.19 (1.101.28)
485 obs / 408.0 exp
Tolerant

Tolerant to missense variation

Observed / Expected Ratios?
LoF OE?1.10 (0.821.48)
00.351.4
Missense OE?1.19 (1.101.28)
00.61.4
Synonymous OE?1.21
01.21.6
LoF obs/exp: 31 / 28.3Missense obs/exp: 485 / 408.0Syn Z: -2.19

ClinVar Variant Classifications

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

SLC27A3 · 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.

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