Category:Low-importance Genetics articles
This category contains articles that have been rated as "Low-importance" by WikiProject Genetics. Articles are automatically placed in this category when the corresponding priority is given; please see the assessment department for more information.
 | This is a maintenance category, used for maintenance of the Wikipedia project. It is not part of the encyclopedia and contains non-article pages, or groups articles by status rather than subject. Do not include this category in content categories. |
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| 73 | 260 | 871 | 3,663 | 752 | 631 |
Pages in category "Low-importance Genetics articles"
The following 200 pages are in this category, out of approximately 3,663 total. This list may not reflect recent changes.
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- Talk:Nablus mask-like facial syndrome
- Talk:NADH-Q
- Talk:Nakajo syndrome
- Talk:Naked cuticle 1
- Talk:Nanopore sequencing
- Talk:Nanos 3′ UTR translation control element
- Talk:NANOS1
- Talk:Nasodigitoacoustic syndrome
- Talk:NASU Institute of Molecular Biology and Genetics
- Talk:National Centers for Biomedical Computing
- Talk:National Society of Genetic Counselors
- Talk:Natural antisense short interfering RNA
- Talk:Natural genetic engineering
- Talk:Nature Reviews Genetics
- Talk:Navigenics
- Talk:NBPF
- Talk:NBPF1
- Talk:NBPF15
- Talk:NCI-60
- Talk:NCOA4
- Talk:NCOA6
- Talk:NCOA7
- Talk:NDUFA3
- Talk:NDUFA4
- Talk:NDUFA4L2
- Talk:NDUFA7
- Talk:NDUFA11
- Talk:NDUFAB1
- Talk:NDUFB4
- Talk:NDUFB5
- Talk:Michael Neale
- Talk:Nearly neutral theory of molecular evolution
- Talk:Daniel W. Nebert
- Talk:NEFH
- Talk:Negative regulatory element
- Talk:Negative selection (natural selection)
- Talk:Neocentromere
- Talk:Neochromosome
- Talk:Neofunctionalization
- Talk:Neotenic complex syndrome
- Talk:Neuroepigenetics
- Talk:Neuropathy, ataxia, and retinitis pigmentosa
- Talk:Neuroscience and intelligence
- Talk:Neutral network (evolution)
- Talk:Neutral theory of molecular evolution
- Talk:New York Genome Center
- Talk:NeXML format
- Talk:NgAgo
- Talk:Niche microdifferentiation
- Talk:Nick translation
- Talk:Nicking enzyme
- Talk:Nicotinic acid adenine dinucleotide phosphate
- Talk:Nif gene
- Talk:Nik operon
- Talk:NIPAL4
- Talk:Nirenberg and Leder experiment
- Talk:Nirenberg and Matthaei experiment
- Talk:Nix (gene)
- Talk:NKG2D
- Talk:NKX3-3
- Talk:NlaIII
- Talk:NMNAT3
- Talk:NOD mice
- Talk:Eva Nogales
- Talk:Non-allelic homologous recombination
- Talk:Non-canonical base pairing
- Talk:Non-Darwinian Evolution (paper)
- Talk:Non-paternity event
- Talk:Non-random segregation of chromosomes
- Talk:Noncompaction cardiomyopathy
- Talk:Noninvasive genotyping
- Talk:Nonsense suppressor
- Talk:Nonsyndromic deafness
- Talk:NRIP1
- Talk:NSG mouse
- Talk:NSP1 (rotavirus)
- Talk:NT5M
- Talk:Nuage (cell biology)
- Talk:NUBPL
- Talk:Nuclear export signal
- Talk:Nuclear localization sequence
- Talk:Nuclear RNase P
- Talk:Nuclear run-on
- Talk:Nuclear transfer
- Talk:Nuclease protection assay
- Talk:Nucleasome
- Talk:Nucleic acid analogue
- Talk:Nucleofection
- Talk:Nucleosome repeat length
- Talk:Nucleotide diversity
- Talk:Nucleotide salvage
- Talk:Nucleotide universal IDentifier
- Talk:Nullisomic
- Talk:Nussinov plots
- Talk:Nutritional genomics
O
- Talk:Obsolete models of DNA structure
- Talk:Oct-2
- Talk:Ogden syndrome
- Talk:Ohno's law
- Talk:Tomoko Ohta
- Talk:Oligogenic inheritance
- Talk:Oligomer
- Talk:Oligomer restriction
- Talk:OMA1
- Talk:OmcS oxidoreductase
- Talk:OMICS (journal)
- Talk:Omnigenic model
- Talk:OmniPop
- Talk:OmrA-B RNA
- Talk:Oncomouse
- Talk:Oncotecture
- Talk:Onion Test
- Talk:Opaline budgerigar mutation
- Talk:Opitz G/BBB syndrome
- Talk:Stephen Oppenheimer
- Talk:Opsismodysplasia
- Talk:Optical transfection
- Talk:OR4F5
- Talk:Or83b odorant receptor
- Talk:Orange petunia
- Talk:ORFeome
- Talk:Organellar DNA
- Talk:Origin and function of meiosis
- Talk:Origin of SARS-CoV-2
- Talk:Orphan gene
- Talk:Orphon
- Talk:Yasuji Oshima
- Talk:OST Family
- Talk:Elaine Ostrander
- Talk:Otodental syndrome
- Talk:Outbreeding depression
- Talk:Outron
- Talk:Overdominance
- Talk:Överkalix study
- Talk:Overlap extension polymerase chain reaction
- Talk:Overlapping gene
- Talk:Overlapping generations
- Talk:OxyS RNA
P
- Talk:P-Aminobenzoyl-glutamate transporter
- Talk:P14arf
- Talk:P16
- Talk:P21
- Talk:P27 cis-regulatory element
- Talk:P53 p63 p73 family
- Talk:P73
- Talk:P300-CBP coactivator family
- Talk:Svante Pääbo
- Talk:PABPI
- Talk:PABPII
- Talk:PAFAH1B1
- Talk:Paleogenomics
- Talk:Paleopolyploidy
- Talk:Palladin
- Talk:Abraham Palmer
- Talk:Pier Paolo Pandolfi
- Talk:Pangenesis
- Talk:PAQR5
- Talk:PAQR6
- Talk:PAR-CLIP
- Talk:ParABS system
- Talk:Paragroup
- Talk:Parahaplogroup
- Talk:ParaHox
- Talk:Paralytic (gene)
- Talk:Parasitic chromosome
- Talk:Paratransgenesis
- Talk:Parkin (protein)
- Talk:ParMRC system
- Talk:Partial dominance hypothesis
- Talk:Particulate inheritance
- Talk:Patau syndrome
- Talk:Paternal mtDNA transmission
- Talk:Paucimorphism
- Talk:PAX3
- Talk:PBAD promoter
- Talk:PBR322
- Talk:PCAF
- Talk:PCK2
- Talk:PComb3H
- Talk:PDPR
- Talk:Pdr1p
- Talk:Pearson syndrome
- Talk:Pedigree collapse
- Talk:PelB leader sequence
- Talk:PELP-1
- Talk:Pentasomy X
- Talk:Peopling of China
- Talk:PEPCK-Cmus mouse
- Talk:Peptide YY
- Talk:Peptides (journal)
- Talk:Peptidoglycan recognition protein 3
- Talk:Peptidoglycan recognition protein 4
- Talk:Perilipin-4
- Talk:Period circadian protein homolog 1
- Talk:Peritrich nuclear code
- Talk:Peroxisomal targeting signal
- Talk:Margaret M. Perry
- Talk:Persistent truncus arteriosus
- Talk:Personal Genetics Education Project
- Talk:Personal Genome Project