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Search references for TRPM1. Phrases containing TRPM1
See searches and references containing TRPM1!TRPM1
Protein-coding gene in humans
channel subfamily M member 1 is a protein that in humans is encoded by the TRPM1 gene. The protein encoded by this gene is a member of the transient receptor
TRPM1
Condition making it difficult or impossible to see in relatively low light
that both CSNB and leopard complex spotting patterns are linked to the TRPM1 gene. The region on horse chromosome 1 to which the Lp gene has now been
Nyctalopia
American horse breed noted for spotted color pattern
when LP is present. LP is an autosomal incomplete dominant mutation in the TRPM1 gene located at horse chromosome 1 (ECA 1). All horses with at least one
Appaloosa
Family of transport proteins
to form tetramers. The TRPM family consists of eight different channels, TRPM1–TRPM8. Unlike the TRPC and TRPV sub-families, TRPM subunits do not contain
TRPM
Coat pattern in horses
team mapped the Lp gene to a transient receptor potential channel gene, TRPM1 or Melastatin 1 (MLSN1). The leopard complex allele contains a 1378 bp long
Leopard_complex
Medical condition
CSNB has been identified in horses and dogs as the result of mutations in TRPM1 (Horse, "LP"), GRM6 (Horse, "CSNB2"), and LRIT3 (Dog, CSNB). Congenital
Congenital stationary night blindness
Congenital_stationary_night_blindness
Chemical compound
sulfate is an agonist of the sigma receptor, as well as an activator of the TRPM1 and TRPM3 channels. It may also interact with potassium channels and voltage-gated
Pregnenolone_sulfate
Archaeological culture of northern Central Asia
through the use of reins or bridles), and horse remains were found with the TRPM1 coat-colour locus, which causes leopard-spotted coats. Horses with two copies
Botai_culture
DNA profile of a horse
indicated that both CSNB and leopard complex spotting patterns are linked to TRPM1. As this disorder also afflicts humans, a researcher and lead author from
Horse_genome
Index of articles on biophysics
TPCN2 TRPA (channel) TRPC TRPC1 TRPC2 TRPC3 TRPC4AP TRPC5 TRPC6 TRPC7 TRPM TRPM1 TRPM2 TRPM3 TRPM4 TRPM5 TRPM6 TRPM7 TRPM8 TRPML TRPN TRPP TRPP3 TRPV TRPV1
Index_of_biophysics_articles
Class of transport proteins
split into two major clades, αTRPM and βTRPM. αTRPMs include vertebrate TRPM1, TRPM3, and the "chanzymes" TRPM6 and TRPM7, as well as the only insect
Transient receptor potential channel
Transient_receptor_potential_channel
Subgroup of TRP cation channels named after the vanilloid receptor
expression of TRP proteins often leads to tumorigenesis, clearly seen in TRPM1. Particularly high levels of TRPV6 in prostate cancer have been noted. Such
TRPV
Genetics behind the equine coat color
since then living homozygous roan horses have been found. n/n: No roan. TRPM1 (Leopard complex) LP n Appaloosa or Leopard spotting gene. Produces coat
Equine_coat_color_genetics
Mammalian protein found in humans
"Transcriptional regulation of the melanoma prognostic marker melastatin (TRPM1) by MITF in melanocytes and melanoma". Cancer Research. 64 (2): 509–16.
Microphthalmia-associated transcription factor
Microphthalmia-associated_transcription_factor
Horse coat color and its genetics
Ernest Bailey; Bruce Grahn (August 2008). "Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting
Dominant_white
Mammalian protein found in humans
for initiating a signaling cascade that ultimately controls gating of the TRPM1 channel. In human patients, mutations in the GRM6 gene are associated with
Metabotropic glutamate receptor 6
Metabotropic_glutamate_receptor_6
Family of ion channel proteins
of voltage gated ion channels. TRPC1; TRPC3; TRPC4; TRPC5; TRPC6; TRPC7 TRPM1; TRPM2; TRPM3; TRPM4; TRPM5; TRPM6; TRPM7; TRPM8 TRPV1; TRPV2; TRPV3; TRPV4;
Cation_channel_superfamily
A6NMA1 17477 TRPC6 HGNC:12338; Q9Y210 17478 TRPC7 HGNC:20754; Q9HCX4 17479 TRPM1 HGNC:7146; Q7Z4N2 17480 TRPM2 HGNC:12339; O94759 17481 TRPM3 HGNC:17992;
List of human protein-coding genes 8
List_of_human_protein-coding_genes_8
610427; CABP4 Night blindness, congenital stationary, type IC; 613216; TRPM1 Night blindness, congenital stationary, X-linked, type 2A; 300071; CACNA1F
List_of_OMIM_disorder_codes
TRPM1
TRPM1
TRPM1
TRPM1
Girl/Female
Australian, Danish, Dutch, French, German, Hebrew, Netherlands, Swiss
Bitterness; Diminutive Form of Marie; Similar to Mary Bitter
Female
French
French form of Latin Victoria, VICTOIRE means "conqueror" or "victory."
Male
Swedish
Medieval Swedish form of Old Norse Lögmaðr, LAGMAN means "lawman."
Girl/Female
Latin
Furies.
Male
Vietnamese
Vietnamese name CUONG means "flourishing, healthy."
Surname or Lastname
English
English : unexplained.
Girl/Female
Indian, Telugu
God of Mather
Boy/Male
Hindu, Indian, Vietnamese
Dawn; Decorated; Honored
Boy/Male
Indian
Allah
Female
Persian/Iranian
(پری) Persian name PARI means "fairy."
TRPM1
TRPM1
TRPM1
TRPM1
TRPM1