Search references for GENE POLYMORPHISM. Phrases containing GENE POLYMORPHISM
See searches and references containing GENE POLYMORPHISM!GENE POLYMORPHISM
Occurrence in an interbreeding population of two or more discontinuous genotypes
strand conformation polymorphism analysis. A polymorphism can be any sequence difference. Examples include: Single nucleotide polymorphisms (SNPs) are a single
Gene_polymorphism
Species having two or more distinct forms
(one with random mating). Put simply, polymorphism is when there are two or more possibilities of a trait on a gene. For example, there is more than one
Polymorphism_(biology)
Protein-coding gene in the species Homo sapiens
very small. The meta-analysis of 11 studies did find that another polymorphism in the gene, the -521C/T, showed an association with novelty seeking. While
Dopamine_receptor_D4
Mammalian protein found in humans
sodium:neurotransmitter symporter family. A repeat length polymorphism in the promoter of this gene has been shown to affect the rate of serotonin uptake
Serotonin_transporter
Topics referred to by the same term
Look up polymorphism, polymorph, polymorphic, polymorphous, or polymorphy in Wiktionary, the free dictionary. Polymorphism, polymorphic, polymorph, polymorphous
Polymorphism
Protein-coding gene in the species Homo sapiens
with the polymorphism (MTR): 2756A>G, lung cancer risk is further increased in a dose dependent manner. Correlation between this polymorphism and increased
MTRR_(gene)
Medical condition of a man whose semen contains no sperm
human breast cancer susceptibility gene 2 (BRCA2) is employed in DNA repair. A common single nucleotide polymorphism in BRCA2 is associated with idiopathic
Azoospermia
Receptors that respond to gamma-aminobutyric acid
GABRR3rs832032 polymorphism and the risk for RLS, and a modifier effect of GABRA4 rs2229940 on the age of onset of RLS" - the latter of which is a modifier gene polymorphism
GABA_receptor
Mammalian protein found in humans
occurring in the winter. Gene polymorphism of interleukin-1 family, interleukin 6, and polymorphic GT repeat of the CRP gene do affect the usual CRP concentrations
C-reactive_protein
Single nucleotide in genomic DNA at which different sequence alternatives exist
C1236T polymorphism changes a GGC codon to GGT at amino acid position 412 of the polypeptide (both encode glycine) and the C3435T polymorphism changes
Single-nucleotide polymorphism
Single-nucleotide_polymorphism
polymorphism is the occurrence of two or more clearly different forms or phenotypes in a population of a species. Different types of polymorphism have
List_of_polymorphisms
Genetic polymorphism
code) polymorphic region in SLC6A4, the gene that codes for the serotonin transporter. Since the polymorphism was identified in the middle of the 1990s
5-HTTLPR
Male lions with a gene polymorphism
known for their mane, not all males have one. This might be because of a polymorphism within males. The Asiatic lion is often considered to have a weak mane
Maneless_lion
Type of biological selective process
The polymorphism survives in almost all habitats, though the proportions of morphs varies considerably. The alleles controlling the polymorphism form
Balancing_selection
Mixed-breed dog with socio-environmental typology
knowledge on canine gene polymorphism tends to unfold as dogs from a wider geographic distribution are studied. Studies on gene polymorphisms have been less
Caramelo_(dog)
Disease of the kidney
interstitial scarring, are associated with a poor prognosis. ACE gene polymorphism has recently been shown to have an impact, with the DD genotype associated
IgA_nephropathy
Genetic condition involving iron buildup
(with mutations of other gene locus, such as HAMP, HJV, TFR2), or environmental factors. The H63D variant is just a gene polymorphism, and if there are no
Hereditary_haemochromatosis
Theory of evolution by changes at the molecular level
controversy over the interpretation of patterns of molecular divergence and gene polymorphism, peaking in the 1970s and 1980s. Neutral theory is frequently used
Neutral theory of molecular evolution
Neutral_theory_of_molecular_evolution
Extension of endometrial tissue into the myometrium
G, Nakamura N, Honjo H (January 2001). "Oestrogen receptor-alpha gene polymorphism is associated with endometriosis, adenomyosis and leiomyomata". Hum
Adenomyosis
that factor. In this theory, every evolutionary event, mutation, and gene polymorphism (neutral differences in phenotype or genotype) would have to be positively
The Neutral Theory of Molecular Evolution
The_Neutral_Theory_of_Molecular_Evolution
Protein-coding gene in the species Homo sapiens
that there was no impact of the polymorphism on energy expenditure. This finding of an effect of the rs9939609 polymorphism on food intake or satiety has
FTO_gene
Autoimmune disease
gene polymorphisms may have variable peripheral T3 availability", leading to localised hypothyroidism in some tissues. The Thr92Ala DIO2 polymorphism
Hashimoto's_thyroiditis
Unusually small penis
"Testosterone enanthate therapy is effective and independent of SRD5A2 and AR gene polymorphisms in boys with micropenis". J. Urol. 172 (1): 319–24. doi:10.1097/01
Micropenis
Endogenous enzyme
Sabol SZ, Hu S, Hamer D (September 1998). "A functional polymorphism in the monoamine oxidase A gene promoter". Human Genetics. 103 (3): 273–9. doi:10.1007/s004390050816
Monoamine_oxidase_A
Class of enzymes
so far. The COMT Val158Met polymorphism also has a pleiotropic effect on emotional processing. Furthermore, the polymorphism has been shown to affect ratings
Catechol-O-methyltransferase
Enlargement of the heart muscle
severity and age of onset cannot be predicted. An insertion/deletion polymorphism in the gene encoding for angiotensin converting enzyme (ACE) alters the clinical
Hypertrophic_cardiomyopathy
The C957T gene polymorphism is a synonymous mutation located within the 957th base pair of the DRD2 gene. This base pair is located in exon 7. Most synonymous
C957T
Protein-coding gene in the species Homo sapiens
et al. (2003). "Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease". Dementia and Geriatric
STH_(gene)
Mammalian protein found in humans
the codon 72 polymorphism and cervical cancer risk. Other studies have identified possible associations between the codon 72 polymorphism and various cancers
P53
Molecular biology technique
species in order to pinpoint the locations of genes within a sequence. The term may refer to a polymorphism itself, as detected through the differing locations
Restriction fragment length polymorphism
Restriction_fragment_length_polymorphism
Mammalian protein found in humans
et al. (November 2018). "Polycystic ovarian syndrome: rs1799752 polymorphism of ACE gene". Revista da Associação Médica Brasileira. 64 (11): 1017–1022.
Angiotensin-converting_enzyme
Three key elements of depression
of serotonin) which is primarily associated with the 5HTTLPR gene. This gene polymorphism promotes hyperactivity of the amygdala through decreased pre-frontal
Beck's_cognitive_triad
Abnormal exit of tissues or organs from the cavity they usually reside in
AP, et al. (August 2014). "Association of collagen type I alpha 1 gene polymorphism with inguinal hernia". Hernia. 18 (4): 507–512. doi:10.1007/s10029-013-1147-y
Hernia
Branch of psychology
neurotrophic factor in the brain, whereas the Val66Met polymorphism (rs6265) is a variant of the BDNF gene. Brain derived neurotrophic factor is a protein that
Sport_psychology
Species of fruit-bearing tree
Myrica gale, Alnus incana, and Shepherdia canadensis Determined by rrs Gene Polymorphism". Applied and Environmental Microbiology. 67 (5): 2116–2122. Bibcode:2001ApEnM
Myrica_rubra
Patient with little to no pain or negative affect
heterozygous for a common hypomorphic single nucleotide polymorphism (SNP) in her FAAH gene (rs324420; C385A; C allele frequency 74%, A allele frequency
Jo_Cameron
Autoimmune disease
Albuisson E, Sauvezie B (1998). "IL-1 receptor antagonist (IL-1RA) gene polymorphism in Sjögren's disease and rheumatoid arthritis". Clinical Immunology
Sjögren's_disease
Loss of function in the spine's intervertebral discs
intervertebral disc prolapse and its association of collagen I alpha 1 Spl gene polymorphism: A preliminary case control study of Indian population. Indian J Orthop
Degenerative_disc_disease
Protein-coding gene in the species Homo sapiens
VKORC1 gene encodes a subunit of the enzyme that is responsible for reducing vitamin K 2,3-epoxide to the activated form. A genetic polymorphism on the
VKORC1
Type of autoimmune arthritis
Possible gene polymorphism: STAT4, PTPN2, PSORS1C1 and TRAF3IP2 genes had been correlated with response to TNF inhibitors. The HLA-DRB1 gene is part of
Rheumatoid_arthritis
Human disease-causing mutation
The HFE H63D is a single-nucleotide polymorphism in the HFE gene (c.187C>G, rs1799945), which results in the substitution of a histidine for an aspartic
HFE_H63D_gene_mutation
Protein and coding gene in humans
-786T>C polymorphism than in TT carriers. Hypertensive patients carrying the TC/CC genotypes and the C allele for the g.-786T>C polymorphism showed better
Endothelial_NOS
Form of albinism
albinism type 1B associated with a functionally significant tyrosinase gene polymorphism detected with Whole Exome Sequencing". Ophthalmic Genetics. 42 (3):
Oculocutaneous_albinism
Vision loss due to damage to the macula of the eye
inhibitor of this inflammatory cascade, and a disease-associated polymorphism in the CFH gene strongly associates with AMD. Thus an AMD pathophysiological
Macular_degeneration
Injury to the intervertebral disc
intervertebral disc prolapse and its association of collagen I alpha 1 Spl gene polymorphism: A preliminary case control study of Indian population. Indian J Orthop
Disc_herniation
Protein found in humans
DA, Sidorenko BA (2006). "[Apolipoprotein B: structure, function, gene polymorphism, and relation to atherosclerosis]". Kardiologiia. 45 (6): 43–55. PMID 16007035
Apolipoprotein_B
Medical condition
adult-onset Still's disease and interleukin-18 gene polymorphisms". Genes and Immunity. 3 (7): 394–9. doi:10.1038/sj.gene.6363922. PMID 12424620. S2CID 10549641
Adult-onset_Still's_disease
Protein-coding gene in the species Homo sapiens
Certain polymorphisms in the ABCC1 gene have been shown to be connected with an increased susceptibility to certain types of cancer. A G2168A polymorphism and
ABCC1
Nasal inflammation due to allergens in the air
Wang XQ, Shen Y, Hong SL, Ke, X. "Association between PTPN22/CTLA-4 Gene Polymorphism and Allergic Rhinitis with Asthma in Children". Iranian Journal of
Allergic_rhinitis
Protrusion of abdominal contents through the inguinal canal in the pelvis
Düzgün AP, et al. (2014). "Association of Collagen Type I Alpha 1 Gene Polymorphism With Inguinal Hernia - PubMed". Hernia: The Journal of Hernias and
Inguinal_hernia
Fibrosis of lungs due to unknown causes
that IPF patients who have a specific genotype in the mucin MUC5B gene polymorphism (see above) experience slower decline in FVC and significantly improved
Idiopathic_pulmonary_fibrosis
Mammalian protein found in humans
Lillevang ST (December 2003). "Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes". Tissue Antigens. 62
Programmed cell death protein 1
Programmed_cell_death_protein_1
Cell surface receptor found in humans
insertion/deletion polymorphism as a prognosis factor in HIV-1 disease progression. The authors showed a correlation of the polymorphism with a faster progression
Toll-like_receptor_2
Post-streptococcal inflammatory disease
Kalil J, Guilherme L (2008). "Association of Mannose-Binding Lectin Gene Polymorphism but Not of Mannose-Binding Serine Protease 2 with Chronic Severe Aortic
Rheumatic_fever
Complication of pregnancy associated with severe pre-eclampsia
Normand N, Halmos A, Papp Z, Witkin SS (March 2009). "Fas (TNFRSF6) gene polymorphism in pregnant women with hemolysis, elevated liver enzymes, and low
HELLP_syndrome
Mental disorder involving eccentricity and social isolation in afflicted individuals
flexibility, and altered perceptual experiences. The rs1006737 polymorphism of the CACNA1C gene is also believed to have a part in schizotypal symptoms. It
Schizotypal personality disorder
Schizotypal_personality_disorder
Rate-limiting enzyme in the methyl cycle
disease and between MTHFR polymorphism status and risk for venous thromboembolism. There is growing evidence that MTHFR polymorphism testing has minimal clinical
Methylenetetrahydrofolate reductase
Methylenetetrahydrofolate_reductase
Variety of white blood cells
functional heterogeneity of eosinophil cationic protein is determined by a gene polymorphism and post-translational modifications". Clinical and Experimental Allergy
Eosinophil
Many types of polymorphism can be seen in the insect order Lepidoptera. Polymorphism is the appearance of forms or "morphs" differing in color and number
Polymorphism_in_Lepidoptera
Protein-coding gene in the species Homo sapiens
and adrenomedullary functional effects of alpha2C-adrenoreceptor gene polymorphism in healthy humans". Pharmacogenet. Genomics. 15 (3): 143–9. doi:10
Alpha-2C_adrenergic_receptor
and -521C/T) is a single nucleotide polymorphism (SNP) located in the promoter region of the DRD4 gene. This gene codes for the dopamine receptor D4.
Rs1800955
Human protein and coding gene
humans, a polymorphism in Clock, rs6832769, may be related to the personality trait agreeableness. Another single nucleotide polymorphism (SNP) in Clock
CLOCK
Protein-coding gene in the species Homo sapiens
S2CID 30661322. Zhuo CS, Zhuo XF, Guo YJ, Wang CQ (Apr 2008). "[RHD gene polymorphism of RhD negative individuals in population of Fujian province]". Zhongguo
RHD_(gene)
Nonspecific long-lasting anxiety
example, the Asp54Gly polymorphism of the pituitary adenylate cyclase-activating peptide, which is the product of the ADCYAP1 gene, has been associated
Generalized_anxiety_disorder
Protein and coding gene in humans
86-base pair repeat polymorphism in the interleukin-1--receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene". Journal of Bone
Interleukin-1 receptor antagonist
Interleukin-1_receptor_antagonist
DNA repair mechanism
states. Two important genes in the NER pathway for which polymorphism has shown functional and phenotypic impact are the XPD and XPC genes. XPD, also known
Nucleotide_excision_repair
Difference in coloration, usually of the iris but also of hair or skin
East Asian and South Asian ancestry and association with candidate gene polymorphisms". Pigment Cell & Melanoma Research. 29 (2): 156. doi:10.1111/pcmr
Heterochromia
Birth defect of the palate and upper lip
Ueland PM, et al. (February 2008). "Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts". American Journal
Cleft_lip_and_cleft_palate
Breakdown in empathy
empathic responses may also be influenced by an oxytocin receptor gene polymorphism, such that certain individuals may differ in the extent to which oxytocin
Empathy_gap
Chronic pain syndrome of the vulvar area
Marie; Ledger, William J.; Witkin, Steven S. (2003). "Interleukin-1β gene polymorphism in women with vulvar vestibulitis syndrome". European Journal of Obstetrics
Vulvodynia
Accumulation of collagen in the skin and internal organs
tissue growth factor (CTGF) has a possible role. Indeed, a common CTGF gene polymorphism is present at an increased level in systemic sclerosis. Damage to
Systemic_scleroderma
Hypothesis about ADHD
1016/S1090-5138(99)00015-X. S2CID 12754148. Kiaris, Hippokratis. (1 April 2012). Genes, polymorphisms, and the making of societies : how genetic behavioral traits influence
Hunter versus farmer hypothesis
Hunter_versus_farmer_hypothesis
Dog breed
Cynologique Internationale. Retrieved 24 January 2021. "DRD4 and TH gene polymorphisms are associated with activity, impulsivity and inattention in Siberian
Siberian_Husky
Mammalian protein found in Homo sapiens
overproduction can result in hyperpigmentation. A specific genetic polymorphism in the POMC gene is associated with elevated fasting insulin levels, but only
Proopiomelanocortin
Human blood group classification
Plasmodium knowlesi and simian malarial parasite Plasmodium cynomolgi. Polymorphisms in this gene are the basis of the Duffy blood group system. It was noted in
Duffy_antigen_system
Antibody against interleukin 6
kidney disease (CKD), elevated interleukin-6 (≥4 pg/mL), and a TMPRSS6 gene polymorphism (rs855791) associated with IL-6–mediated inflammation. Patients received
Ziltivekimab
Mammalian protein found in humans
more brittle and prone to fracturing. A particular variation (polymorphism) in the COL1A1 gene appears to increase the risk of developing osteoporosis. A
Collagen,_type_I,_alpha_1
Gene or DNA sequence with a known location on a chromosome
Restriction fragment length polymorphism) SSLP (or Simple sequence length polymorphism) AFLP (or Amplified fragment length polymorphism) AAD (or Arbitrarily
Genetic_marker
Skin condition where patches lose pigment
sequencing studies have demonstrated that vitiligo is associated with polymorphisms in genes involved in the response to oxidative stress, such as CAT, SOD1
Vitiligo
Subtype of serotonin receptor
2A receptor (5-HTR2A) gene polymorphisms with an increased risk of suicidal behavior. One study revealed that T102C polymorphism is associated with suicidal
5-HT2A_receptor
Disease of the tissues surrounding the teeth (periodontium)
exaggerated immune response. Interleukin 1 (IL-1) gene polymorphism: People with this polymorphism produce more IL-1, and subsequently are more at risk
Periodontal_disease
Monoamine neurotransmitter
1996). "Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region". Science. 274 (5292): 1527–1531.
Serotonin
Mammalian protein found in humans
Wudarski M, Łacki JK, Jagodziński PP (June 2010). "CD24 Ala57Val gene polymorphism and the risk of systemic lupus erythematosus". Tissue Antigens. 75
CD24
One gene variant masking the effect of another in the other copy of the gene
genes exist in a large number of allelic versions in the population as a whole. This is called polymorphism, and is caused by mutations. Polymorphism
Dominance_(genetics)
Dog breed
nature of the breed. A Japanese study found that the CAG repeat polymorphism in the AR gene in the Akita Inu was correlated with increased reports of aggression
Akita_(dog_breed)
Organic compound involved in immune responses
ulcerative colitis is associated with a polymorphism at diamine oxidase gene but not at histamine N-methyltransferase gene". World Journal of Gastroenterology
Histamine
Mammalian protein found in Homo sapiens
055 and 2,190 nucleotide pairs. Gene polymorphism between species is much more diverse than the intraspecific polymorphism of lactoferrin. There are differences
Lactoferrin
Human enzyme
(March 2010). "A potential regulatory single nucleotide polymorphism in the promoter of the Klotho gene may be associated with essential hypertension in the
Klotho_(biology)
Protein-coding gene in the species Homo sapiens
5 times between birth and age seven. An association between PON1 gene polymorphism and susceptibility to Parkinson's disease was not found in a Chinese
PON1
Penetrative sexual activity for reproduction or sexual pleasure
hypothesizing common mesolimbic activation as a function of reward gene polymorphisms". Journal of Psychoactive Drugs. 44 (1): 38–55. doi:10.1080/02791072
Sexual_intercourse
Protein found in humans
nucleotide polymorphism (SNP) in this gene is responsible for determination of human earwax type and presence of underarm odour. This gene and family
ABCC11
Variant of DNA sequence at a locus
alleles (polymorphism) present, or the proportion of heterozygotes in the population. A null allele is a gene variant that lacks the gene's normal function
Allele
C(-1019)G, is a gene variation—a single nucleotide polymorphism (SNP)—in the HTR1A gene. It is one of the most investigated SNPs of its gene. The C-allele
Rs6295
Human protein
plasminogen activators. The PAI-1 gene is SERPINE1, located on chromosome 7 (7q21.3-q22). There is a common polymorphism known as 4G/5G in the promoter region
Plasminogen activator inhibitor-1
Plasminogen_activator_inhibitor-1
Emotional state
Yamasue, Hidenori (2018-12-21). "Culture and cannabinoid receptor gene polymorphism interact to influence the perception of happiness". PLOS ONE. 13 (12)
Contentment
Protein-coding gene in humans
mutations in the granulin (GRN) gene, a known cause of familial FTLD-GRN identified a single nucleotide polymorphism (SNP), rs1990622, located 6.9 kilobases
TMEM106B
Non-clinical mental health condition
(July–August 2007). "Effects of chronic stress and interleukin-10 gene polymorphism on antibody response to tetanus vaccine in family caregivers of patients
Caregiver_stress
Mental disorder
2007). "Meta-analysis of the association of serotonin transporter gene polymorphism with obsessive-compulsive disorder". Progress in Neuro-Psychopharmacology
Obsessive–compulsive_disorder
Protein-coding gene in mammals
et al. (May 2001). "Association between an agouti-related protein gene polymorphism and anorexia nervosa". Molecular Psychiatry. 6 (3): 325–8. doi:10
Agouti-signaling_protein
Enzyme protein
Snalina NE, Sozaeva ZA, Grabuzdov AM, Matsneva IA (2017). "SLCO1B1 gene-polymorphism frequency in Russian and Nanai populations". Pharmacogenomics and
CYP2C9
GENE POLYMORPHISM
GENE POLYMORPHISM
Male
English
Variant spelling of English Dean, DENE means "dean, ecclesiastical supervisor."
Girl/Female
Biblical
Who reckons or is counted.
Boy/Male
Greek American English
Well born.
Female
Greek
(ΞÎνη) Feminine form of Greek Xenon, XENE means "foreigner; stranger."
Female
English
Pet form of English Eugenia, GENA means "well born."
Surname or Lastname
Americanized form of German Gehr.English
Americanized form of German Gehr.English : perhaps a variant of Geary 3.Hungarian : from a reduced form of the personal name Gergely, Latin Gregorius (see Gregory).
Surname or Lastname
English and French
English and French : nickname, possibly sometimes applied ironically, from Middle English gente, Old French gent(il) ‘well born’, ‘noble’, ‘courteous’. Compare Gentle.German and English : habitational name for someone from Ghent in Flanders, French name Gand.
Surname or Lastname
English
English : variant spelling of Gain.
Female
German
 Short form of German Helene, possibly LENE means "torch." Compare with another form of Lene.
Female
Yiddish
Variant spelling of Yiddish Heneh, HENE means "favor; grace."
Girl/Female
American, Australian, Greek, Hebrew, Scottish
Well Born; The Lord is Gracious; Noble; Similar to Jane
Female
French
French form of Latin Regina, RÉGINE means "queen."
Female
English
Pet form of English Eugenia, GENIE means "well born." This is also a pet form of English Genevieve, probably meaning "race of women."
Girl/Female
French American Greek
Reborn.
Boy/Male
American, Australian, British, Christian, English, French, German, Greek
Well-born; Noble; Form of Eugene; Born Lucky
Surname or Lastname
English (Cornish)
English (Cornish) : from a short form of the female personal name Jennifer, from Welsh Gwenhwyfar (see Gaynor). Until the 19th century Jennifer was a characteristically Cornish name.German : of uncertain origin; possibly from a Celtic root or from a short form of Heinrich (see Henry) or Johannes (see John).
Girl/Female
English
Combination of Deana (divine) and Dina (from the valley; avenged).
Female
English
English short form of Latin Penelope, PENE means "weaver of cunning."
Male
English
Short form of English Eugene, GENE means "well born."
Girl/Female
Norse
Distinguished.
GENE POLYMORPHISM
GENE POLYMORPHISM
Boy/Male
Bengali, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
Lord Shiva
Girl/Female
Tamil
Boy/Male
Indian
Kind friend, Noble, Eminent
Male
Hebrew
(×וּרְיָן) Hebrew name of Aramaic origin, URYAN means "light."
Boy/Male
Tamil
Peethambar | பீதாஂபர
Vishnu
Girl/Female
Muslim
The cloud that carries the rain
Boy/Male
Hindu
Deliverer of ramas ring
Boy/Male
Gaelic
Brave chieftain.
Boy/Male
Hebrew
Change.
Girl/Female
Bengali, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit, Tamil, Telugu
Happiness; Smile; Faith; Night; Name of a River
GENE POLYMORPHISM
GENE POLYMORPHISM
GENE POLYMORPHISM
GENE POLYMORPHISM
GENE POLYMORPHISM
imp. & p. p.
of Gee
a.
Already past or gone; bygone.
a. & adv.
Past; gone by; since; as, ten years ago; gone long ago.
a.
Past; gone by.
v. t. & i.
See Gee.
a.
Smooth; as, the lene breathing.
pl.
of Gens
p. p.
Gone.
a.
Past; gone by.
a.
Already spent; gone by; past.
pl.
of Genu
n.
Any one of the lene consonants, as p, k, or t (or Gr. /, /, /).
p. p.
Gone.
p. p.
Stepped; gone; advanced.
p. pr. & vb. n.
of Gee
n.
See Genet, a horse.
a.
Passed away; dead; gone.
n.
An African genet (Genetta pardina). See Genet.