CACrown ArchivesThe cinema collection
Menu
Research dossier · Science & Nature

MINDY2

protein-coding gene in the species Homo sapiens

Specimen drawers, botanical folios and brass scientific instruments under study light
Science and natureInterpretive dossier study · Crown Archives visual atlas
Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionAug 18, 2026
Entity authorityQ18041142
Source-derived summary

Ubiquitin carboxyl-terminal hydrolase MINDY-2 is an enzyme which in humans is encoded by the gene MINDY2 (previously FAM63B). MINDY-2 functions to remove ubiquitin from proteins (specifically 'Lys-48'-linked conjugated ubiquitin), and may be involved in regulating the turnover of proteins in cells.

Gene

Locus

FAM63B is located at 15q21.3-q22.1, spanning 90,707 base pairs on chromosome 15.

Alternative Names

The full name of FAM63B is family with sequence similarity 63, member B. FAM63B is also listed by its alias, KIAA1164, in some publications.

mRNA

Isoforms

The FAM63B gene encodes a primary transcript that can be alternatively spliced into 9 protein variants. FAM63B variant a is the most common isoform found in humans.

Protein

Structure

Primary Structure

FAM63B is a member of the Pfam super family, and contains a domain of unknown function (DUF544) that is homologous within the protein family. FAM63B protein variant an also contains a bipartite tryptophan binding motif from W476 to W533. Variant a of the protein also contains a hydrophobic stretch of alanine from 567 to 574 and a mixed charge sequence from residue 598 to 617. FAM63B protein may contain a signal sequence specifying return to the endoplasmic reticulum (KDEL) from residue 607 to 621 in variant a.

Editorial summary

“MINDY2” enters the record as protein-coding gene in the species Homo sapiens. Crown Archives preserves that source wording while asking what MINDY2, protein-coding and gene can confirm, complicate or overturn.

Editorial reviewUseful for establishing the present vocabulary of the subject while preserving a route back to the evidence on which that vocabulary rests. The current 201-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its strongest next move is a source search built around MINDY2, protein-coding and gene.
Editorial analysis

Why this record matters

“MINDY2” is worth following because a concise public description often conceals a longer documentary argument. Here, MINDY2, protein-coding and gene provides the most credible route into that argument.

Evidence profile

Datasets, specimens, observations and peer-reviewed methods provide the appropriate test for the technical claims summarized here. The source revision retrieved here is dated Aug 18, 2026. The linked authority identifier is Q18041142. None of the 0 selected statements returned an explicit reference.

Critical limits

A general summary may omit uncertainty, sample limits or methodological disagreement that is explicit in the technical record. The source lead contains qualifying language; that uncertainty should survive quotation, summary and reuse. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

How to read it

Check terminology, classification and the date of the cited evidence. Scientific names and technical consensus can change while older records retain historical value.

Best used for
  • Current terminology
  • Classification context
  • Finding cited technical literature
Verify next

Primary datasets, specimen catalogues, standards bodies and the most recent peer-reviewed literature.

Three-step research path

  1. Establish the record: confirm the title “MINDY2”, its source revision and the description used here.
  2. Expand the search: follow MINDY2 primary sources, MINDY2 archive and MINDY2 research across catalogues and specialist indexes.
  3. Test the account: compare the strongest cited source with the responsible institution’s current record and note any disagreement.

Questions for further research

  1. Which source most directly establishes the central claim about “MINDY2”?
  2. Is the terminology current, historical or disputed?
  3. Has classification or technical consensus changed since the cited source?
Subject index

Search terms from this dossier

Source & attribution

This entry incorporates text from MINDY2” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.