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RPGRIP1L

Index RPGRIP1L

RPGRIP1L is a human gene. [1]

15 relations: Centrosome, CEP290, Cilium, Copy-number variation, DNA Research, Dominance (genetics), Gene, Joubert syndrome, Meckel syndrome, Microtubule nucleation, Nature Genetics, Nephronophthisis, NPHP4, Schizophrenia, Schizophrenia Research Forum.

Centrosome

In cell biology, the centrosome (Latin centrum 'center' + Greek sōma 'body') is an organelle that serves as the main microtubule organizing center (MTOC) of the animal cell as well as a regulator of cell-cycle progression.

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CEP290

Centrosomal protein of 290 kDa is a protein that in humans is encoded by the CEP290 gene.

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Cilium

A cilium (the plural is cilia) is an organelle found in eukaryotic cells.

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Copy-number variation

Copy number variation (CNV) is a phenomenon in which sections of the genome are repeated and the number of repeats in the genome varies between individuals in the human population.

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DNA Research

DNA Research is an international, peer reviewed journal of genomics and DNA research.

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Dominance (genetics)

Dominance in genetics is a relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus.

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Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

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Joubert syndrome

Joubert syndrome is a rare autosomal recessive genetic disorder that affects the cerebellum, an area of the brain that controls balance and coordination.

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Meckel syndrome

Meckel syndrome (also known as Meckel–Gruber syndrome, Gruber syndrome, dysencephalia splanchnocystica) is a rare, lethal, ciliopathic, genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations (occipital encephalocele), polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios.

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Microtubule nucleation

In cell biology, microtubule nucleation is the event that initiates de novo formation of microtubules (MTs).

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Nature Genetics

Nature Genetics is a scientific journal founded as part of the ''Nature'' family of journals in 1992.

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Nephronophthisis

Nephronophthisis is a genetic disorder of the kidneys which affects children.

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NPHP4

Nephrocystin-4 is a protein that in humans is encoded by the NPHP4 gene.

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Schizophrenia

Schizophrenia is a mental disorder characterized by abnormal social behavior and failure to understand reality.

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Schizophrenia Research Forum

Schizophrenia Research Forum is a web knowledge environment dedicated to news, information resources, and discussion about research on schizophrenia.

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References

[1] https://en.wikipedia.org/wiki/RPGRIP1L

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