FAM162B

Chr 6

family with sequence similarity 162 member B

Also known as: C6orf189, bA86F4.2

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

ResearchGenerating clinical summary…
0
Active trials
0
Pubs (1 yr)
P/LP submissions
P/LP missense
1.88
LOEUF
Multiple*
Mechanism· predicted
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?
1.88LOEUF
pLI 0.000
Z-score -0.76
OE 1.30 (0.781.88)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint?
0.12Z-score
OE missense 0.96 (0.801.17)
74 obs / 77.0 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios?
LoF OE?1.30 (0.781.88)
00.351.4
Missense OE?0.96 (0.801.17)
00.61.4
Synonymous OE?0.81
01.21.6
LoF obs/exp: 10 / 7.7Missense obs/exp: 74 / 77.0Syn Z: 0.80

ClinVar Variant Classifications

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

FAM162B · 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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