TAF6 gene related symptoms and diseases
All the information presented here about the TAF6 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TAF6 gene
Symptoms // Phenotype | % Cases |
---|---|
Intellectual disability | Very Common - Between 80% and 100% cases |
Narrow chest | Very Common - Between 80% and 100% cases |
Unilateral cryptorchidism | Very Common - Between 80% and 100% cases |
Short columella | Very Common - Between 80% and 100% cases |
Broad hallux | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TAF6 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Low anterior hairline
- Long eyelashes
- Dental crowding
- Wide intermamillary distance
- Underdeveloped nasal alae
- Prominent nose
- Single transverse palmar crease
- Highly arched eyebrow
And 21 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to TAF6 gene
Here you will find a list of rare diseases related to the TAF6. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ALAZAMI-YUAN SYNDROME; ALYUS
Most common symptoms of ALAZAMI-YUAN SYNDROME; ALYUS
- Intellectual disability
- Global developmental delay
- Short stature
- Generalized hypotonia
- Microcephaly
More info about ALAZAMI-YUAN SYNDROME; ALYUS
SOURCES: OMIM
Search interest in TAF6
Potential gene panels for TAF6 gene
Cornelia de Lange Syndrome and Cornelia de Lange Syndrome-Related Disorders Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Cornelia de Lange Syndrome and Cornelia de Lange Syndrome-Related Disorders Sequencing Panel with CNV Detection that also includes the following genes: SMARCA4 SMARCB1 SMARCE1 ARID1A SMC1A SOX11 TAF1 TAF6 MED12 HDAC8
More info about this panelCornelia de Lange Syndrome Panel
By Asper Biogene Asper Biogene LLC Cornelia de Lange Syndrome that also includes the following genes: SMC1A TAF6 HDAC8 AFF4 ANKRD11 SMC3 NIPBL RAD21
More info about this panelTAF6 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TAF6 gene.
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SON ADA2 PNKD UNC13A WFS1 TMEM43 PCYT1A