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Cytoskeletal protein
Spectrin is a cytoskeletal protein that lines the intracellular side of the plasma membrane in many eukaryotic cells, including animal cells but not in
Spectrin
Protein-coding gene in the species Homo sapiens
Spectrin alpha chain, erythrocyte is a protein that in humans is encoded by the SPTA1 gene. Spectrin is an actin crosslinking and molecular scaffold protein
Spectrin,_alpha_1
Protein-coding gene in the species Homo sapiens
Alpha II-spectrin, also known as Spectrin alpha chain, brain is a protein that in humans is encoded by the SPTAN1 gene. Alpha II-spectrin is expressed
SPTAN1
Layer on the inner face of a cell membrane
protein spectrin may be present in the cortex. Spectrin helps to create a network by cross-linked actin filaments. The proportions of spectrin and actin
Cell_cortex
Protein family
Spectrin repeats are found in several proteins involved in cytoskeletal structure. These include spectrin, alpha-actinin, dystrophin and more recently
Spectrin_repeat
Protein family
Nesprins (nuclear envelope spectrin repeat proteins) are a family of proteins that are found primarily in the outer nuclear membrane, as well as other
Nesprin
Protein-coding gene in the species Homo sapiens
stability and deformability by stabilizing spectrin-actin interaction. Protein 4.1 (80 kD) interacts with spectrin and short actin filaments to form the erythrocyte
Protein_4.1
Network of filamentous proteins that forms the internal framework of cells
immobilizing the harmful microbes and preventing them from invading other cells. Spectrin is a cytoskeletal protein that lines the intracellular side of the plasma
Cytoskeleton
Protein factor that regulates the length of R-actin
horizontal axis. Alpha-actinin is a part of the spectrin superfamily. This superfamily is made of spectrin, dystrophin, and their homologous and isoforms
Actinin
Protein-coding gene in the species Homo sapiens
Spectrin, beta, non-erythrocytic 5 also known as SPTBN5 is a protein that in humans is encoded by the SPTBN5 gene. SPTBN5 belongs to the spectrin family
SPTBN5
Genetic disorder causing red blood cells to be spherical
Alpha-1 refers the alpha-1 subunit of the spectrin protein. The Beta refers the beta subunit of the spectrin protein. These genetic mutations are acted
Hereditary_spherocytosis
Medical condition
process called calpain-mediated spectrin proteolysis, or CMSP, begins to occur. Calpain breaks down a molecule called spectrin, which holds the membrane onto
Diffuse_axonal_injury
Gaps between myelin sheaths on the axon of a neuron
expression of Na+ channels. Ankyrin has been found to be bounded to βIV spectrin, a spectrin isoform enriched at nodes of Ranvier and axon initial segments. The
Node_of_Ranvier
Protein-coding gene in the species Homo sapiens
Spectrin beta chain, brain 1 is a protein that in humans is encoded by the SPTBN1 gene. Spectrin is an actin crosslinking and molecular scaffold protein
SPTBN1
Protein family
membrane proteins to the spectrin-actin based membrane cytoskeleton. Ankyrins have binding sites for the beta subunit of spectrin and at least 12 families
Ankyrin
Topics referred to by the same term
folk religion. Nezha or Ne Zha may also refer to: Calmodulin-regulated spectrin-associated protein 3, also sometimes known as Nezha Nezha (given name)
Nezha_(disambiguation)
Protein-coding gene in the species Homo sapiens
Spectrin, beta, non-erythrocytic 4, also known as SPTBN4, is a protein that in humans is encoded by the SPTBN4 gene. Spectrin is an actin crosslinking
SPTBN4
Chemical compound
precise mode of action is not known, but it is thought to act by affecting spectrin-like proteins in the cytoskeleton of oomycetes. This mode of action differs
Fluopicolide
Genetic haematological condition
it is generally true that α-spectrin mutations result in an inability of α-spectrin to interact properly with β-spectrin to form a heterodimer. In contrast
Hereditary_elliptocytosis
Protein-coding gene in the species Homo sapiens
Spectrin beta chain, erythrocyte is a protein that in humans is encoded by the SPTB gene. GRCh38: Ensembl release 89: ENSG00000070182 – Ensembl, May 2017
SPTB
Class of proteins
polymers, or both. Many actin-binding proteins, including α-actinin, β-spectrin, dystrophin, utrophin and fimbrin, do this through the actin-binding calponin
Actin-binding_protein
Protein domain
In molecular biology, the calmodulin-regulated spectrin-associated CKK domain (also known as the CKK domain) is a domain which occurs at the C-terminus
Calmodulin-regulated spectrin-associated CKK domain
Calmodulin-regulated_spectrin-associated_CKK_domain
Species of antelope found in Africa
dorsalis) and the klipspringer (Oreotragus oreotragus). An rRNA and β-spectrin nuclear sequence analysis in 2003 also supported an association between
Impala
Protein found in humans
Calmodulin-regulated spectrin-associated protein family member 2 (CAMSAP2) is a protein in humans that is encoded by the CAMSAP2 gene. CAMSAP2 possesses
CAMSAP2
Filament in the cytoplasm of eukaryotic cells
embryonic kidney cells, neurons, and sperm cells. In red blood cells, a spectrin-actin hexagonal lattice is formed by interconnected short actin filaments
Actin_filament
Microtubule minus-end binding human protein
Calmodulin-regulated spectrin-associated protein family member 3 (CAMSAP3) is a human protein encoded by the gene CAMSAP3. The protein is commonly referred
Calmodulin-regulated spectrin-associated protein 3
Calmodulin-regulated_spectrin-associated_protein_3
Protein-coding gene in the species Homo sapiens
Spectrin beta chain, brain 2 is a protein that in humans is encoded by the SPTBN2 gene. Mutations in this gene is associated with Spinocerebellar ataxia
SPTBN2
Medical condition
associated with a defect of the erythrocyte membrane protein spectrin and with spectrin deficiency. It was characterized in 1975. It is considered a severe
Hereditary_pyropoikilocytosis
Microtubule minus-end binding human protein
Calmodulin-regulated spectrin-associated protein 1 (CAMSAP1) is a human protein encoded by the gene CAMSAP1. Like other CAMSAP-family proteins, it is a
CAMSAP1
Protein-coding gene in the species Homo sapiens
the nuclear envelope (NE) spectrin-repeat (nesprin) family. Nesprins are modular proteins with a central extended spectrin-repeat (SR) rod domain and
SYNE2
Protein-coding gene in the species Homo sapiens
Spectrin repeat containing nuclear envelope family member 3, or Nesprin-3, is a Nesprin-family protein that in humans is encoded by the SYNE3 gene. Nesprin-3
Spectrin repeat containing nuclear envelope family member 3
Spectrin_repeat_containing_nuclear_envelope_family_member_3
Extracellular non-fibrous substance
during staining in the preparation process. Link proteins such as vinculin, spectrin and actomyosin stabilize the proteoglycans and organize elastic fibers
Ground_substance
The following is a partial list of the "D" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM)
List_of_MeSH_codes_(D12.776)
Clinical Significance
Caenorhabditis elegans kinesin-like protein unc-104 (see InterPro: IPR001752), spectrin beta-chain, syntrophin (2 PH domains), and S. cerevisiae nuclear migration
Pleckstrin_homology_domain
Structure on the surface of epithelial cells
microvilli. It is composed primarily of actin filaments stabilized by spectrin, which also anchors the terminal web to the apical cell membrane. The presence
Terminal_web
Structure in an embryo which will become the nervous system
6a7022.2006. PMID 16899759. Sadler, T.W. (1986). "A potential role for spectrin during neurulation". J. Embryol. 94 (1): 73–82. Retrieved 27 April 2013
Neural_plate
Protein found in Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Filaggrin
Protein found in humans
the growing ends of actin filaments and promote their association with spectrin, another cytoskeletal protein, to create stable and integrated cytoskeletal
Brain-derived neurotrophic factor
Brain-derived_neurotrophic_factor
germ cell development. Cytoskeleton components, such as alpha and beta spectrins, hu-li tai shao (hts), and ankyrin were the first proteins identified
Fusome
American physician and academic (born 1949)
Department at Johns Hopkins where he studied red cell membranes and identified spectrin deficiency as a common cause of hereditary spherocytosis, a hemolytic anemia
Peter_Agre
Protein-coding gene in the species Homo sapiens
belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins
Alpha-actinin-4
Protein-coding gene in the species Homo sapiens
is conserved across vertebrate species and has low sequence homology to spectrin, a cytoskeletal protein involved in forming the actin cellular cortex.
Activity-regulated cytoskeleton-associated protein
Activity-regulated_cytoskeleton-associated_protein
Protein-coding gene in the species Homo sapiens
to a family of membrane skeletal proteins involved in the assembly of spectrin-actin network in erythrocytes and at sites of cell-cell contact in epithelial
ADD2
Rod-shaped cytoplasmic protein
"The 'spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families". Journal of Cell Science. 115 (Pt 22): 4215–25. doi:10
Dystrophin
Protein found in humans
further sub divided into a region called the "Plakin domain" made up of six spectrin repeat domains separated by SH3 domain. A crystal structure of part of
Desmoplakin
Eukaryotic motor protein
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Kinesin
Structural fibrous protein
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Keratin
Protein-coding gene in humans
costameres, where it binds to zyxin, integrin linked kinase (ILK) and beta1-spectrin; intercalated discs, where it associates with the nebulin-related anchoring
CSRP3
Biological membrane that separates the interior of a cell from its outside environment
packed lipid bilayer that works closely with the cytoskeleton components spectrin and actin. These cytoskeleton components are able to bind to and interact
Cell_membrane
Type III intermediate filament protein
microtubule-associated proteins 1 and 2 and to the 240-kilodalton subunit of spectrin". The Journal of Biological Chemistry. 262 (3): 1320–1325. doi:10
Vimentin
Protein-coding gene in the species Homo sapiens
expression data Gene ontology Molecular function enzyme inhibitor activity spectrin binding cGMP binding protein binding 3',5'-cyclic-GMP phosphodiesterase
PDE6G
Protein-coding gene
that in humans that is encoded by the SYNE1 gene. This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and
Enaptin
Microscopic protrusion of a cell membrane that increases surface area substantially
in the terminal web composed of a complicated set of proteins including spectrin and myosin II. The space between microvilli at a cell's surface is called
Microvillus
Family of proteins that form microfilaments
rings is found in axons. In this structure, the actin rings, together with spectrin tetramers that link the neighboring actin rings, form a cohesive cytoskeleton
Actin
Protein found in humans
SB, Zhang Z, Morrow JS (1997). "Site-directed mutagenesis of alpha II spectrin at codon 1175 modulates its mu-calpain susceptibility". Biochemistry. 36
Calpain-1_catalytic_subunit
Membrane proteins that adhere temporarily to membranes with which they are associated
Archived from the original on 2007-09-29. Retrieved 2007-01-25. "Pfam entry Spectrin". Archived from the original on 2007-09-26. Retrieved 2007-01-25. Rochat
Peripheral_membrane_protein
Mammalian protein found in Homo sapiens
(April 1991). "Interaction domains of neurofilament light chain and brain spectrin". Biochem. J. 275 (Pt 2): 521–7. doi:10.1042/bj2750521. PMC 1150082. PMID 1902666
Microtubule-associated protein 2
Microtubule-associated_protein_2
Type III intermediate filament protein
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Glial fibrillary acidic protein
Glial_fibrillary_acidic_protein
Keratin protein
three components, have been probed to associate also with the ankyrin and spectrin complex protein network that underlies the cell membrane.[citation needed]
Cytokeratin
Protein-coding gene in the species Homo sapiens
(April 1991). "Interaction domains of neurofilament light chain and brain spectrin". The Biochemical Journal. 275 (2): 521–527. doi:10.1042/bj2750521. PMC 1150082
Neurofilament light polypeptide
Neurofilament_light_polypeptide
Chemical compound
in the erythrocyte membrane by the cytoskeletal network: dependence on spectrin association state". Biochemistry. 25 (20): 6133–6139. doi:10.1021/bi00368a045
Fluorescein_isothiocyanate
Nuclear membrane surrounding the nucleus in eukaryotic cells
the endoplasmic reticulum. All four nesprin proteins (nuclear envelope spectrin repeat proteins) present in mammals are expressed in the outer nuclear
Nuclear_envelope
Polymer of tubulin that forms part of the cytoskeleton
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Microtubule
Microtubule element of the tubulin family
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Tubulin_beta-3_chain
Medical condition
{{cite book}}: |work= ignored (help), update 2011 "OMIM Entry – * 608441 – SPECTRIN REPEAT-CONTAINING NUCLEAR ENVELOPE PROTEIN 1; SYNE1". www.omim.org. Archived
Emery–Dreifuss muscular dystrophy
Emery–Dreifuss_muscular_dystrophy
Protein-coding gene in the species Homo sapiens
lymphoid cells where it negatively influence and delay the aggregation of spectrin in an early phase of apoptosis. PKC-θ has a role in the transduction of
PRKCQ
Protein-coding gene in the species Homo sapiens
are believed to link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility
Ankyrin-1
amyloid A1 Solute carrier family 35 (CMP-sialic acid transporter), member A1 Spectrin, alpha 1 Sperm protein associated with the nucleus, X-linked, family member
List of A1 genes, proteins or receptors
List_of_A1_genes,_proteins_or_receptors
Equation used for physiological interfaces, polymer science, and semiconductors
bilayer of an erythrocyte. This takes into account both the glycocalyx and spectrin layers of the erythrocyte membrane. This information is useful for many
Poisson–Boltzmann_equation
The following is a partial list of the "D" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM)
List of MeSH codes (D12.776.543)
List_of_MeSH_codes_(D12.776.543)
Largest known protein in human muscles
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Titin
Protein-coding gene in the species Homo sapiens
Tokito M, Stankewich MC, Morrow JS, Holzbaur EL (Sep 2001). "beta III spectrin binds to the Arp1 subunit of dynactin". The Journal of Biological Chemistry
Beta-actin
Protein
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Tropomyosin
Family of motor proteins
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Myosin
Protein-coding gene in the species Homo sapiens
number of different molecules, including PKC, PIP2, actin, calmodulin, spectrin, palmitate, synaptophysin, amyloid and tau protein, it may be useful to
Gap-43_protein
Ability of red blood cells to deform under stress without rupturing
supports that aid resilience, which include the cytoskeleton: actin and spectrin that are held together by ankyrin. Shape change of erythrocytes under applied
Erythrocyte_deformability
Protein-coding gene in the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
MYH1
Gene of the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
KRIT1
Protein cytoskeletal component
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Tonofibril
Protein found in humans
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Keratin_12
Abnormal presence of spherical red blood cells in the blood
or more of the proteins of the red blood cell cytoskeleton, including spectrin, ankyrin, Band 3, or Protein 4.2. Because the cell skeleton has a defect
Spherocytosis
Protein-coding gene in the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
TUBA8
Protein-coding gene in the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
MYL2
Mammalian protein found in Homo sapiens
"Interaction of the C-terminal domain of delta glutamate receptor with spectrin in the dendritic spines of cultured Purkinje cells". Neuroscience Research
GRIA2
Protein-coding gene in the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
PLEKHA7
Macromolecular complex
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Arp2/3_complex
Oxygen-delivering blood cell and the most common type of blood cell
interactions with skeletal proteins such as spectrin and protein 4.1R. Recent studies have shown that binding of spectrin to PS promotes membrane mechanical stability
Red_blood_cell
Biological gene-regulation phenomenon
infarction. and erectile dysfunction (ED). saRNA-mediated activation of βII spectrin alleviated ischemia/reperfusion (I/R)-induced cardiac contractile dysfunction
RNA_activation
Primary protein link between cadherins and the actin cytoskeleton
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Α-Catenin
Cell membrane of an axon
of this structure is formed by hexagonal or pentagonal arrangement of spectrin on the inside of the cell membrane, as well as actin connected to the transmembrane
Axolemma
filaments (through dynein and kinesin motors), intermediate filaments (through spectrin), centrosomes and cytoplasmic organelles. The number of SUN-domain and
LINC_complex
Motor protein
vesicles (such as Golgi or late endosome) through its association with β-spectrin. The pointed end complex (PEC) has been shown to be involved in selective
Dynactin
Protein-coding gene in the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
MYO9B
Protein found in humans
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Keratin_20
Protein-coding gene in the species Homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
ACTA2
Protein-coding gene in the species Homo sapiens
belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins
Alpha-actinin-1
Mammalian protein found in homo sapiens
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
KIF18B
Type of protein
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Catenin
Fibrous proteins
catenin GAN Membrane Dystrophin Dystroglycan Utrophin Ankyrin ANK1 ANK2 ANK3 Spectrin SPTA1 SPTAN1 SPTB SPTBN1 SPTBN2 SPTBN4 SPTBN5 Other Plakins Corneodesmosin
Lamin
Protein-coding gene in the species Homo sapiens
Maksimova E, Stabach P, Hermel JM, et al. (November 2000). "betaIV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the
PTPRN
SPECTRIN
SPECTRIN
SPECTRIN
SPECTRIN
Boy/Male
Indian
Poor, Needy
Girl/Female
Biblical
Gatherings.
Surname or Lastname
English, Welsh, and Scottish
English, Welsh, and Scottish : variant of Morris.Dutch and North German : variant of Moritz.French : variant of Maurice.Latvian : nickname for a dark person, from Moris ‘Moor’, ‘Negro’. Compare Moore 2.Lithuanian : possibly a nickname from morỹs ‘lazy person’.
Girl/Female
Hebrew
Fourth born.
Surname or Lastname
English and French (Channel Islands)
English and French (Channel Islands) : nickname for a sluggish person, from Middle English, Old French tardif ‘slow’ (Late Latin tardivus, for classical Latin tardus).A Tardif from the Brittany region of France is documented in Quebec City in 1637.
Girl/Female
English American
Modern feminine of John and Jon.
Girl/Female
Indian
Goddess Parvati, Durga, A noble lady
Boy/Male
Australian, Greek, Romanian
Follower of Demeter
Boy/Male
Hindu, Indian, Malayalam, Marathi, Tamil
Truth Seeking
Surname or Lastname
English
English : possibly a variant of Warman.
SPECTRIN
SPECTRIN
SPECTRIN
SPECTRIN
SPECTRIN