WNT1
Wnt family member 1 | INT1

The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region. [provided by RefSeq, Jul 2008]

Biological processes 76 terms
Golgi lumen (GO:0005796)Spemann organizer formation (GO:0060061)Spemann organizer formation (GO:0060061)Wnt signaling pathway (GO:0016055)Wnt signaling pathway (GO:0016055)astrocyte-dopaminergic neuron signaling (GO:0036520)bone development (GO:0060348)canonical Wnt signaling pathway (GO:0060070)canonical Wnt signaling pathway (GO:0060070)canonical Wnt signaling pathway (GO:0060070)canonical Wnt signaling pathway (GO:0060070)canonical Wnt signaling pathway (GO:0060070)cell fate commitment (GO:0045165)cell proliferation in midbrain (GO:0033278)cell surface (GO:0009986)cell-cell signaling (GO:0007267)cell-cell signaling (GO:0007267)central nervous system morphogenesis (GO:0021551)central nervous system morphogenesis (GO:0021551)cerebellum development (GO:0021549)cerebellum formation (GO:0021588)cerebellum formation (GO:0021588)cytokine activity (GO:0005125)cytokine activity (GO:0005125)cytokine activity (GO:0005125)cytokine activity (GO:0005125)cytoplasm (GO:0005737)dopaminergic neuron differentiation (GO:0071542)embryonic axis specification (GO:0000578)embryonic axis specification (GO:0000578)embryonic brain development (GO:1990403)endocytic vesicle membrane (GO:0030666)endoplasmic reticulum lumen (GO:0005788)extracellular exosome (GO:0070062)extracellular region (GO:0005576)extracellular region (GO:0005576)extracellular region (GO:0005576)frizzled binding (GO:0005109)frizzled binding (GO:0005109)frizzled binding (GO:0005109)midbrain development (GO:0030901)midbrain development (GO:0030901)midbrain dopaminergic neuron differentiation (GO:1904948)midbrain dopaminergic neuron differentiation (GO:1904948)midbrain dopaminergic neuron differentiation (GO:1904948)morphogen activity (GO:0016015)negative regulation of BMP signaling pathway (GO:0030514)negative regulation of apoptotic process (GO:0043066)negative regulation of cell differentiation (GO:0045596)negative regulation of cell-cell adhesion (GO:0022408)negative regulation of cell-substrate adhesion (GO:0010812)negative regulation of cellular senescence (GO:2000773)negative regulation of fat cell differentiation (GO:0045599)negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway (GO:1903377)neurogenesis (GO:0022008)neuron differentiation (GO:0030182)plasma membrane (GO:0005886)positive regulation of DNA-templated transcription (GO:0045893)positive regulation of DNA-templated transcription (GO:0045893)positive regulation of DNA-templated transcription (GO:0045893)positive regulation of DNA-templated transcription (GO:0045893)positive regulation of Notch signaling pathway (GO:0045747)positive regulation of cell population proliferation (GO:0008284)positive regulation of cell population proliferation (GO:0008284)positive regulation of dermatome development (GO:0061184)positive regulation of fibroblast proliferation (GO:0048146)positive regulation of insulin-like growth factor receptor signaling pathway (GO:0043568)positive regulation of lamellipodium assembly (GO:0010592)protein domain specific binding (GO:0019904)receptor ligand activity (GO:0048018)receptor ligand activity (GO:0048018)receptor ligand activity (GO:0048018)receptor ligand activity (GO:0048018)response to wounding (GO:0009611)signal transduction in response to DNA damage (GO:0042770)signaling receptor binding (GO:0005102)
Expression (TPM)
WNT1 — as a Regulated Gene

TFs regulating WNT1 0 TFs

Transcription factors with Perturb-seq knockdown data for WNT1. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = WNT1 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to WNT1

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of WNT1, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chr12:48,969,884–48,970,343 8.0 kb Proximal (<10kb) 254
chr12:48,971,536–48,971,866 6.5 kb Proximal (<10kb) 258
chr12:48,974,156–48,974,361 4.0 kb Proximal (<10kb) 158
chr12:48,978,055–48,978,819 at TSS At TSS 360
chr12:48,980,647–48,981,153 2.3 kb Proximal (<10kb) 259
chr12:48,986,693–48,987,241 8.4 kb Proximal (<10kb) 65
chr12:48,988,160–48,988,373 9.8 kb Proximal (<10kb) 177

Genome Browser

Genomic view of the WNT1 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chr12:48,959,884 – 48,998,373
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq