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Browse our anti-WD Repeat Domain 19 (WDR19) Antibodies

Full name:: anti-WD Repeat Domain 19 Antibodies (WDR19)

On www.antibodies-online.com are 40 WD Repeat Domain 19 (WDR19) Antibodies from 8 different suppliers available. Additionally we are shipping WD Repeat Domain 19 Proteins (3) and and many more products for this protein. A total of 48 WD Repeat Domain 19 products are currently listed.

Synonyms:: ATD5, C330027H04Rik, CED4, D330023L08Rik, DYF-2, DYF2, Ift144, mKIAA1638, NPHP13, ORF26, Oseg6, PWDMP, RGD1306997, WDR19

list all antibodies	Gene Name	GeneID	UniProt
	WDR19	305349
	WDR19	57728	Q8NEZ3
	WDR19	213081	Q3UGF1
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Most Popular Reactivities for anti-WD Repeat Domain 19 (WDR19) Antibodies

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anti-Rat (Rattus) Antibodies:

4 WB Antibodies

anti-Human Antibodies:

anti-Mouse (Murine) Antibodies:

4 WB Antibodies

All available anti-WD Repeat Domain 19 Antibodies

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Relevant Pathways for anti-WD Repeat Domain 19 Antibodies

Hedgehog Signaling

More product categories related to WD Repeat Domain 19 Antibody

Top referenced anti-WD Repeat Domain 19 Antibodies

Human Polyclonal WDR19 Primary Antibody for WB - ABIN528302 : Bredrup, Saunier, Oud, Fiskerstrand, Hoischen, Brackman, Leh, Midtbø, Filhol, Bole-Feysot, Nitschké, Gilissen, Haugen, Sanders, Stolte-Dijkstra, Mans, Steenbergen, Hamel, Matignon, Pfundt, Jeanpierre et al.: Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. ... in American journal of human genetics 2011 (PubMed)
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Human Polyclonal WDR19 Primary Antibody for WB - ABIN528301 : Jiang, Chiou, Wang, Chien, Ho, Tsai, Lin, Tsai, Li: Essential role of nephrocystin in photoreceptor intraflagellar transport in mouse. in Human molecular genetics 2009 (PubMed)

More Antibodies against WD Repeat Domain 19 Interaction Partners

Human WD Repeat Domain 19 (WDR19) interaction partners

Case Reports: that WDR19 mutations can cause dysplastic kidney in addition to nephronophthisis in infants with Sensenbrenner syndrome.
Nephronophthisis 13 (Autosomal Recessive Polycystic Kidney Disease) is associated with mutations in the WDR19 gene.Caroli disease is a major extra-renal phenotype associated with mutations in WDR19 in the Korean population.
WDR19 mutations can cause a broad spectrum of ciliopathies that extends to Jeune and Sensenbrenner syndromes, RP and renal NPHP-like phenotypes
Mutations in WDR19 gene is associated with Caroli disease.
WDR19: an ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndrome.
Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19
Expressed in normal and neoplastic prostate epithelium and is regulated by androgenic hormones.
Overexpression of WDR19 is associated with prostate cancer

Mouse (Murine) WD Repeat Domain 19 (WDR19) interaction partners

Mutations in Ift144, encoding a component of the trafficking machinery of primary cilia assembly, result in a range of embryo patterning defects, affecting the limbs, skeleton and neural system. Here, we show that embryos
study describes a mouse with an N-ethyl-N-nitrosourea -induced hypomorphic mutation in the gene encoding the IFT-A protein WDR19/IFT144; phenotypically, this mutant, twinkle-toes (Ift144twt), displays a number of features reminiscent of skeletal ciliopathies; Ift144 mutant embryos display a generalized ligand-independent expansion of hedgehog signalling
A weak allele of the IFT-A gene, Ift144, caused subtle defects in cilia structure and ectopic activation of the Shh pathway.
Expressed in normal and neoplastic prostate epithelium and is regulated by androgenic hormones.

WD Repeat Domain 19 (WDR19) Antigen Profile

Antigen Summary

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains six WD repeats, a clathrin heavy-chain repeat, and three transmembrane domains. This gene is conserved from C. elegans to human. It may participate in androgen-regulated signaling mechanisms or in the vesicular trafficking of androgen-regulated secretory processes. Alternatively spliced transcript variants encoding distinct isoforms have been reported but the full-length nature of one of these variants has not been defined.

Alternative names and synonyms associated with WD Repeat Domain 19 (WDR19)

WD repeat domain 19 (Wdr19) antibody
WD repeat domain 19 (WDR19) antibody
WD repeat domain 19 (wdr19) antibody
WD repeat-containing protein 19 (LOC100461090) antibody

ATD5 antibody
C330027H04Rik antibody
CED4 antibody
D330023L08Rik antibody
DYF-2 antibody
DYF2 antibody
Ift144 antibody
mKIAA1638 antibody
NPHP13 antibody
ORF26 antibody
Oseg6 antibody
PWDMP antibody
RGD1306997 antibody
WDR19 antibody

Protein level used designations for WDR19

WD repeat-containing protein 19 , WD repeat domain 19 , WD repeat-containing protein 19-like , WD repeat membrane protein PWDMP , intraflagellar transport 144 homolog

GENE ID	SPECIES
305349	Rattus norvegicus
430829	Gallus gallus
461172	Pan troglodytes
479113	Canis lupus familiaris
533633	Bos taurus
698866	Macaca mulatta
100055207	Equus caballus
100144725	Xenopus (Silurana) tropicalis
100352314	Oryctolagus cuniculus
100389252	Callithrix jacchus
100461090	Pongo abelii
100607550	Nomascus leucogenys
57728	Homo sapiens
213081	Mus musculus

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Show all anti-WD Repeat Domain 19 (WDR19) Antibodies with Pubmed References

Human WD Repeat Domain 19 (WDR19) interaction partners

Mouse (Murine) WD Repeat Domain 19 (WDR19) interaction partners

Antigen Summary

Alternative names and synonyms associated with WD Repeat Domain 19 (WDR19)

Protein level used designations for WDR19