2,756 articles
ATP2C1
ATP2C1 (SPCA1, hSPCA1, PMR1) is a human gene on chromosome 3q22.1 encoding a Golgi P-type ATPase pump that transports one Ca2+ or Mn2+ ion per ATP; haploinsufficiency causes Hailey–Hailey disease.
ATP5F1A
ATP5F1A (ATP5A1) is a human gene on chromosome 18q21.1 encoding the alpha subunit of mitochondrial ATP synthase F1; dominant de novo missense variants cause developmental delay, dystonia, and complex V deficiency.
ATP6AP2
ATP6AP2, also known as the (pro)renin receptor, is a human X-linked gene on chromosome Xp11.4 encoding a 350-amino-acid membrane protein essential to V-ATPase function and linked to intellectual disability.
ATR-interacting protein
ATRIP (ATR-interacting protein), also called the ATRIP-Ddc2 family, is the 85 kDa obligate partner of the ATR checkpoint kinase; its N-terminal CRD binds RPA-coated ssDNA to recruit ATR–ATRIP to DNA damage, though RPA binding is dispensable for Chk1 phosphorylation.
ATRX
ATRX (XH2, XNP) is an X-linked gene encoding a SWI/SNF-like chromatin remodeler that with DAXX deposits histone H3.3 at telomeres; germline variants cause ATR-X syndrome and somatic loss drives ALT in gliomas and other cancers.
Attractin
Attractin (ATRN, DPPT-L, mahogany) is a human chromosome 20p13 gene encoding membrane and secreted glycoprotein isoforms involved in pigmentation, energy homeostasis, CNS myelination, and immune cell clustering.
ATXN1
ATXN1 (ataxin 1, HGNC:10548) is a human protein-coding gene at 6p22.3 encoding the 815-aa nuclear protein ataxin-1; CAG repeat expansion (pathogenic above ~39 repeats) causes spinocerebellar ataxia type 1 via toxic gain of function.
ATXN2
ATXN2 (ataxin 2), gene at 12q24.12 encoding a 1,312-aa RNA-binding protein; CAG repeat expansion beyond 33 causes SCA2, intermediate 29-34 repeats raise ALS risk.
ATXN7
ATXN7 (ataxin 7) is a chromosome 3 gene encoding a SAGA deubiquitinase-module subunit; CAG repeat expansion in exon 3 causes spinocerebellar ataxia type 7 with ataxia and retinal blindness.
Augmin complex subunit msd1
Msd1 (mitotic spindle density 1, CG13914) is a Drosophila subunit of the eight-subunit augmin complex, homolog of human HAUS2, required for spindle-templated microtubule nucleation; distinct from fission yeast Msd1, a spindle-pole-body anchoring protein.
Augurin
Augurin (ECRG4, C2orf40) is a 148-amino-acid secreted peptide hormone identified in 2007, a tumor suppressor, HPA-axis stimulator, Wnt and PI3K/Akt/mTOR inhibitor, and LOX-1/TLR4 ligand.
Autism susceptibility gene 2 protein
Autism susceptibility gene 2 protein (AUTS2), activator of transcription and developmental regulator on 7q11.22, a nuclear PRC1 and cytoplasmic Rac1 regulator; its haploinsufficiency causes AUTS2 syndrome with intellectual disability and microcephaly.
Autosomal fragile site
Autosomal fragile site: heritable breakage-prone loci on non-sex chromosomes, induced by replication stress (aphidicolin, folate deficiency). Includes rare sites like FRA11B, fra(16)(q22); ICD-11 LD47.4, ICD-10 Q95.5.
Autosome
Autosome: any of the 22 numbered chromosome pairs in human cells, distinct from the X and Y sex chromosomes; numbered roughly by size, chromosome 1 largest with about 2,800 genes, chromosome 22 smallest-numbered with about 750.
AXIN2
AXIN2 (axin 2, conductin/Axil) is a human chromosome 17q24.1 gene encoding a Wnt pathway beta-catenin destruction-complex scaffold; germline variants cause autosomal dominant oligodontia-colorectal cancer syndrome (OMIM 608615).
AZU1
AZU1 (azurocidin 1), also called HBP or CAP37, is a human chromosome 19p13.3 gene encoding a neutrophil azurophil granule protein with antimicrobial and monocyte chemotactic activity, used as an early serum biomarker for sepsis and infection.
B-cell differentiation antigen CD72
CD72 (CD72 molecule, formerly Lyb-2) is a human 9p13.3 gene encoding a type II transmembrane B-cell co-receptor with a C-type lectin-like domain and ITIM that recruits SHP-1 to inhibit BCR signaling, binds Sm/RNP self-antigen, and serves as the ligand for CD5.
BAALC
BAALC (brain and acute leukemia, cytoplasmic) is a human gene at 8q22.3 encoding a 145-aa cytoplasmic protein; overexpressed in 50-60% of cytogenetically normal AML, marking poor prognosis and MRD.
BACE1
BACE1 (β-site APP cleaving enzyme 1, β-secretase) is a transmembrane aspartic protease identified in 1999 that performs the rate-limiting cleavage of APP to generate amyloid-β; its inhibitors all failed in Alzheimer's clinical trials.
BACE2
BACE2 (beta-secretase 2, DRAP) is a chromosome 21q22.3 gene encoding a transmembrane aspartyl protease homologous to BACE1; it cleaves APP non-amyloidogenically and acts in pigmentation and pancreatic beta-cell function.
Backcrossing
Backcrossing: breeding method, described by Harlan and Pope (1922), repeatedly crossing hybrids to a recurrent parent to introgress a donor trait; donor genome halves each generation, with marker-assisted and speed-breeding variants.
Baculoviral IAP repeat-containing protein 1
Baculoviral IAP repeat-containing protein 1, better known as neuronal apoptosis inhibitory protein (NAIP), is a human protein that inhibits apoptosis and senses bacterial type III secretion system components.
Baculovirus p35, apoptosis preventing protein
Baculovirus p35 is a gene of the baculovirus AcMNPV encoding P35, a 299 amino acid protein that blocks apoptosis in infected insect cells by inhibiting caspases.
BAG1
BAG1 (BAG cochaperone 1, BAG-1, RAP46, HAP) is a human chromosome 9 gene encoding a multifunctional Hsp70/Hsc70 nucleotide exchange factor and Bcl-2-binding co-chaperone with four isoforms, studied as a cancer biomarker.
BAG3
BAG3 (BAG cochaperone 3, Bcl-2-associated athanogene 3) is a human 575-aa HSP70 co-chaperone and nucleotide-exchange factor scaffolding CASA autophagy; mutations cause myofibrillar myopathy and dilated cardiomyopathy.
BAK1
BAK1 (BCL2 antagonist/killer 1, BAK) is a human gene at 6p21.31 encoding a pro-apoptotic BCL-2 family protein that oligomerizes in the mitochondrial outer membrane to release cytochrome c; redundant with BAX, linked to CLL and germ cell tumor risk loci.
BARD1
BARD1 (BRCA1 associated RING domain 1), gene ID 580 at 2q35, encodes the BRCA1 partner protein forming a ubiquitin ligase heterodimer in DNA repair; a low-penetrance breast cancer susceptibility gene on multigene panels.
Bardet-Biedl syndrome 2 protein
Bardet-Biedl syndrome 2 protein (BBS2), also called BBSome complex member BBS2, is encoded by BBS2 on chromosome 16 and forms the BBS2-BBS7-BBS9 core of the BBSome ciliary trafficking complex; mutations cause Bardet-Biedl syndrome and nonsyndromic retinitis pigmentosa.
Barr body
Barr body (sex chromatin): the condensed, mostly silent inactive X chromosome seen near the nuclear membrane in female mammal somatic cells, discovered by Barr and Bertram in 1949, formed via XIST RNA, count one fewer than X chromosomes, with some genes escaping silencing.
Barttin
Barttin (BSND, Q8WZ55) is a 320-aa two-transmembrane-helix accessory beta subunit of ClC-Ka/ClC-Kb chloride channels in kidney and inner ear; BSND mutations cause Bartter syndrome type 4A with sensorineural deafness, while hypomorphic alleles cause nonsyndromic deafness DFNB73.