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TCF12

TCF12

Protein-coding gene in the species Homo sapiens

Transcription factor 12 is a protein that in humans is encoded by the TCF12 gene. The protein encoded by this gene is a member of the basic helix-loop-helix

TCF12

Low anterior hairline

Medical condition

dysplasia, Bieganski type Spondyloepimetaphyseal dysplasia, Genevieve type TCF12-related craniosynostosis Vertebral anomalies and variable endocrine and

Low anterior hairline

Low_anterior_hairline

Biology and sexual orientation

Field of sexual orientation research

Chromosome 14 14q31 TSHR male only Sanders et al. 2017 Chromosome 15 15q21 TCF12 male only Ganna et al. 2019 1Reported primary studies are not conclusive

Biology and sexual orientation

Biology_and_sexual_orientation

Scaphocephaly

Skull malformation such that the head is long and narrow

type 1 (Chromosome 2q35 Duplication Syndrome) Tatton-Brown–Rahman syndrome TCF12-related craniosynostosis Teebi hypertelorism syndrome 1 Trigonocephaly-short

Scaphocephaly

Nuclear receptor 4A3

Protein-coding gene in the species Homo sapiens

"Fusion of the NH2-terminal domain of the basic helix-loop-helix protein TCF12 to TEC in extraskeletal myxoid chondrosarcoma with translocation t(9;15)(q22;q21)"

Nuclear receptor 4A3

Nuclear_receptor_4A3

Basic helix–loop–helix

Protein structural motif

PTF1A; SCL; SCXB; SIM1; SIM2; SOHLH1; SOHLH2; SREBF1; SREBF2; TAL1; TAL2; TCF12; TCF15; TCF21; TCF3; TCF4; TCFL5; TFAP4; TFE3; TFEB; TFEC; TWIST1; TWIST2;

Basic helix–loop–helix

Basic_helix–loop–helix

Extraskeletal myxoid chondrosarcoma

Type of abnormal growth in the body

RNA-binding protein which is a component of transcription factor II D, TCF12 (15q21) encoding a transcription factor in the basic helix–loop–helix family

Extraskeletal myxoid chondrosarcoma

Extraskeletal_myxoid_chondrosarcoma

List of conditions with craniosynostosis

List of medical conditions involving craniosynostosis

C4551902) - MedGen - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2023-07-03. "TCF12-related craniosynostosis (Concept Id: C3715051)". www.ncbi.nlm.nih.gov.

List of conditions with craniosynostosis

List_of_conditions_with_craniosynostosis

List of human transcription factors

ENSG00000149922 T-box Known motif – High-throughput in vitro [911] TVACACSY TCF12 ENSG00000140262 bHLH Known motif – High-throughput in vitro [912] VCACSTGB

List of human transcription factors

List_of_human_transcription_factors

List of human protein-coding genes 8

P36402 16450 TCF7L1 HGNC:11640; Q9HCS4 16451 TCF7L2 HGNC:11641; Q9NQB0 16452 TCF12 HGNC:11623; Q99081 16453 TCF15 HGNC:11627; Q12870 16454 TCF19 HGNC:11629;

List of human protein-coding genes 8

List_of_human_protein-coding_genes_8

SCARF syndrome

Medical condition

identification of new casual genes related to craniosynostosis including EFNB1 and TCF12 as well as genes involved in rare craniofacial malformations, including

SCARF syndrome

SCARF_syndrome

MiR-155

Non-coding RNA in the species Homo sapiens

SPI1, SOCS, etc.) and known tumor suppressors (e.g. CEBPβ, IL17RB, PCCD4, TCF12, ZNF652, etc.). The validated miR-155-5p binding site harbored in the SPI1

MiR-155

TCF21 (gene)

Protein-coding gene in the species Homo sapiens

patients suffering from metastatic skin melanoma. TCF21, together with E12 and TCF12, bind the KISS1 promoter, sustaining its activity. Without TCF21 to interact

TCF21 (gene)