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PRDM12

PRDM12

Protein-coding gene in the species Homo sapiens

the PRDM12 gene. This gene is normally switched on during the development of pain-sensing nerve cells. People with homozygous mutations of the PRDM12 gene

PRDM12

Congenital insensitivity to pain

Medical condition for inability to feel pain

propagation. The PRDM12 gene is normally switched on during the development of pain-sensing nerve cells. People with homozygous mutations of the PRDM12 gene experience

Congenital insensitivity to pain

Congenital_insensitivity_to_pain

Hereditary sensory and autonomic neuropathy

Medical condition

an autosomal recessive genetic disorder caused by a mutation in the gene PRDM12, with signs and symptoms usually appearing at birth or during infancy. Subject

Hereditary sensory and autonomic neuropathy

Hereditary_sensory_and_autonomic_neuropathy

List of human transcription factors

specific TF according to literature or domain structure – No motif [730] PRDM12 ENSG00000130711 C2H2 ZF Known motif – In vivo/Misc source [731] GACAGNTKACC

List of human transcription factors

List_of_human_transcription_factors

List of human protein-coding genes 6

Q9NQV7 12772 PRDM10 HGNC:13995; Q9NQV6 12773 PRDM11 HGNC:13996; Q9NQV5 12774 PRDM12 HGNC:13997; Q9H4Q4 12775 PRDM13 HGNC:13998; Q9H4Q3 12776 PRDM14 HGNC:14001;

List of human protein-coding genes 6

List_of_human_protein-coding_genes_6