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PRDM12, the Glossary

Index PRDM12

PR domain zinc finger protein 12 is a protein that in humans is encoded by the PRDM12 gene.[1]

Table of Contents

  1. 23 relations: Bone morphogenetic protein 4, C-terminus, Chronic myelogenous leukemia, Congenital insensitivity to pain, DBX1, EHMT2, FOXD3, Gene, Homeobox protein SIX1, Hypohidrosis, NKX6-1, NKX6-2, Osteomyelitis, PAX3, PAX6, Protein, SET domain, SIX3, Sodium voltage-gated channel alpha subunit 9, Tropomyosin receptor kinase A, Wnt signaling pathway, Xenopus, Zinc finger.

Bone morphogenetic protein 4

Bone morphogenetic protein 4 is a protein that in humans is encoded by BMP4 gene.

See PRDM12 and Bone morphogenetic protein 4

C-terminus

The C-terminus (also known as the carboxyl-terminus, carboxy-terminus, C-terminal tail, carboxy tail, C-terminal end, or COOH-terminus) is the end of an amino acid chain (protein or polypeptide), terminated by a free carboxyl group (-COOH).

See PRDM12 and C-terminus

Chronic myelogenous leukemia

Chronic myelogenous leukemia (CML), also known as chronic myeloid leukemia, is a cancer of the white blood cells.

See PRDM12 and Chronic myelogenous leukemia

Congenital insensitivity to pain

Congenital insensitivity to pain (CIP), also known as congenital analgesia, is one or more extraordinarily rare conditions in which a person cannot feel (and has never felt) physical pain.

See PRDM12 and Congenital insensitivity to pain

DBX1

Homeobox protein DBX1, also known as developing brain homeobox protein 1, is a protein that in humans is encoded by the DBX1 gene.

See PRDM12 and DBX1

EHMT2

Euchromatic histone-lysine N-methyltransferase 2 (EHMT2), also known as G9a, is a histone methyltransferase enzyme that in humans is encoded by the EHMT2 gene.

See PRDM12 and EHMT2

FOXD3

Forkhead box D3 also known as FOXD3 is a forkhead protein that in humans is encoded by the FOXD3 gene.

See PRDM12 and FOXD3

Gene

In biology, the word gene has two meanings. PRDM12 and gene are genes.

See PRDM12 and Gene

Homeobox protein SIX1

Homeobox protein SIX1 (Sine oculis homeobox homolog 1) is a protein that in humans is encoded by the SIX1 gene.

See PRDM12 and Homeobox protein SIX1

Hypohidrosis

Hypohidrosis is a medical condition in which a person exhibits diminished sweating in response to appropriate stimuli.

See PRDM12 and Hypohidrosis

NKX6-1

Homeobox protein Nkx-6.1 is a protein that in humans is encoded by the NKX6-1 gene.

See PRDM12 and NKX6-1

NKX6-2

Homeobox protein Nkx-6.2 is a protein that in humans is encoded by the NKX6-2 gene.

See PRDM12 and NKX6-2

Osteomyelitis

Osteomyelitis (OM) is an infection of bone.

See PRDM12 and Osteomyelitis

PAX3

The PAX3 (paired box gene 3) gene encodes a member of the paired box or PAX family of transcription factors.

See PRDM12 and PAX3

PAX6

Paired box protein Pax-6, also known as aniridia type II protein (AN2) or oculorhombin, is a protein that in humans is encoded by the PAX6 gene.

See PRDM12 and PAX6

Protein

Proteins are large biomolecules and macromolecules that comprise one or more long chains of amino acid residues.

See PRDM12 and Protein

SET domain

The SET domain is a protein domain that typically has methyltransferase activity.

See PRDM12 and SET domain

SIX3

Homeobox protein SIX3 is a protein that in humans is encoded by the SIX3 gene.

See PRDM12 and SIX3

Sodium voltage-gated channel alpha subunit 9

Sodium voltage-gated channel alpha subunit 9 (also Nav1.7) is a sodium ion channel that in humans is encoded by the SCN9A gene.

See PRDM12 and Sodium voltage-gated channel alpha subunit 9

Tropomyosin receptor kinase A

Tropomyosin receptor kinase A (TrkA), also known as high affinity nerve growth factor receptor, neurotrophic tyrosine kinase receptor type 1, or TRK1-transforming tyrosine kinase protein is a protein that in humans is encoded by the NTRK1 gene.

See PRDM12 and Tropomyosin receptor kinase A

Wnt signaling pathway

The Wnt signaling pathways are a group of signal transduction pathways which begin with proteins that pass signals into a cell through cell surface receptors. PRDM12 and Wnt signaling pathway are genes.

See PRDM12 and Wnt signaling pathway

Xenopus

Xenopus (Gk., ξενος, xenos.

See PRDM12 and Xenopus

Zinc finger

A zinc finger is a small protein structural motif that is characterized by the coordination of one or more zinc ions (Zn2+) which stabilizes the fold.

See PRDM12 and Zinc finger

References

[1] https://en.wikipedia.org/wiki/PRDM12