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PCNT

PCNT

Protein-coding gene in humans

Pericentrin (kendrin), also known as PCNT and pericentrin-B (PCNTB), is a protein which in humans is encoded by the PCNT gene on chromosome 21. This protein

PCNT

Primordial dwarfism

Form of dwarfism that results in a smaller body size in all stages of life

In January 2008, it was published that mutations in the pericentrin gene (PCNT) were found to cause primordial dwarfism. Pericentrin has a role in cell

Primordial dwarfism

Primordial_dwarfism

Microcephalic osteodysplastic primordial dwarfism type II

Medical condition

people in the US population. It is associated with the protein pericentrin (PCNT). Intelligence is reported by usually within low-normal or mild intellectual

Microcephalic osteodysplastic primordial dwarfism type II

Microcephalic_osteodysplastic_primordial_dwarfism_type_II

Red panda

Species of mammal in Asia

pandas show modifications to certain limb development genes (DYNC2H1 and PCNT), which may play roles in the development of the thumbs. In switching from

Red panda

Red_panda

Sesamoid bone

Bone embedded within a tendon or muscle

used in grasping the bamboo. In these two panda species, DYNC2H1 gene and PCNT gene have been identified as possible causes for the pseudo-thumb development

Sesamoid bone

Sesamoid_bone

Chromosome 21

Human chromosome

sequence DNA-binding factor homolog PCBP3: encoding poly(rC)-binding protein 3 PCNT: encoding protein centrosomal pericentrin PCP4: encoding calmodulin regulator

Chromosome 21

Chromosome_21

Pericentriolar material

protein TNKS, Tankyrase-1 TNKS2, Tankyrase-2 TUBE1, Tubulin epsilon chain PCNT, pericentrin, a matrix scaffold protein CDK5RAP2, cyclin dependant kinase

Pericentriolar material

Pericentriolar_material

EFM32

Family of integrated circuits

triggers block of the MCU includes a CRYOTIMER, low energy pulse counter (PCNT), and backup real-time-counter (RTC). Analog modules: ADCs, DACs, operational

EFM32

CENPJ

Centromere- and microtubule-associated protein

complex of Cnn, Asl, CP-190, tubulin and D-PLP (similar to the human proteins PCNT and AKAP9). These complexes are then anchored at the centriole to begin formation

CENPJ

PROSER3

the Golgi apparatus as well as co-localized with γ-tubulin or pericentrin (PCNT) in the centrosome, suggesting Proline and Serine-rich 3 is a centrosome

PROSER3

List of human protein-coding genes 6

Q9NV79 11813 PCNA HGNC:8729; P12004 11814 PCNP HGNC:30023; Q8WW12 11815 PCNT HGNC:16068; O95613 11816 PCNX1 HGNC:19740; Q96RV3 11817 PCNX2 HGNC:8736;

List of human protein-coding genes 6

List_of_human_protein-coding_genes_6

PCM1

Protein-coding gene in the species Homo sapiens

with the pathology of schizophrenia. PCM1 has been shown to interact with PCNT. GRCm38: Ensembl release 89: ENSMUSG00000031592 – Ensembl, May 2017 "Human

PCM1

BTRC (gene)

Protein-coding gene in the species Homo sapiens

biology. 2015;17(1):31-43. doi:10.1038/ncb3076. Degradation of Cep68 and PCNT cleavage mediate Cep215 removal from the PCM to allow centriole separation

BTRC (gene)

BTRC_(gene)

C21orf58

Protein-coding gene in the species Homo sapiens

promoter sequence overlaps with the 5'UTR and coding sequence of Pericentrin (PCNT) on the plus strand of Chromosome 21. Predicted transcription factors are

C21orf58

List of OMIM disorder codes

SLC25A3 Microcephalic osteodysplastic primordial dwarfism type II; 210720; PCNT Microcephaly and digital abnormalities with normal intelligence; 602585;

List of OMIM disorder codes

List_of_OMIM_disorder_codes