Form № V·D·J / rev. 01 the dna dance that makes antibodies
⌖ Receptor locus
LOT/230815-A
V variable
50+ alleles
D diversity
12 alleles
J joining
6 alleles
⏷ pull
CDR3 readout junctional · 5′ → 3′ · single-letter aa — aa
Pull the lever. A real human gene segment lands on each reel, a little random "junctional diversity" gets sprinkled in, and out comes a CDR3 that has probably never existed before.
▷ outcome
awaiting pull…
spin 000
score 0000
best 0000
germline source IMGT/GENE-DB · human IGH
recombinase RAG1 / RAG2 · in silico
tdt activity simulated · 0–4 nt

What is this thing ?

Every B cell and T cell in your body is born with a unique receptor. Not picked from a catalogue — built fresh by randomly stitching together gene fragments labeled V, D, and J, then sprinkling in random nucleotides at the seams. Trillions of possible outcomes per person. It's how your immune system is ready for pathogens it has never met.

This page picks one combination at random, like a slot machine. The colored letters are the resulting CDR3 — the part of the receptor that actually touches the antigen.

How do I "win" ?

You don't, really. But longer CDR3s, exotic amino acids, and rare gene families score higher — same things that interest real immunologists, more or less. Pull the lever, see what falls out.

⌖ The IGH side uses ~50 human V genes, 12 D genes, 6 J genes.
⌖ The TRB side uses ~30 V genes, 2 D genes, 14 J genes.
⌖ Allele names follow IMGT nomenclature. The CDR3 fragments are illustrative, not bit-for-bit faithful to the germline.
⌖ N additions mimic terminal deoxynucleotidyl transferase. Junction trimming is, for now, the slot machine's secret.