MNX1 wt Allele

Human MNX1 wild-type allele is located in the vicinity of 7q36 and is approximately 17 kb in length. This allele, which encodes motor neuron and pancreas homeobox protein 1, is involved in transcriptional regulation. Mutation of the gene is associated with Currarino syndrome. (NCI Thesaurus)

YOU MAY ALSO LIKE

MNX1 Gene

This gene plays a role in both the regulation of transcription and DNA binding.

MNSI Questionnaire Question

A question associated with the MNSI questionnaire.

MNSI - Symptoms Worse at Night

Michigan Neuropathy Screening Instrument (MNSI) History; are your symptoms worse at night?

MNSI - Skin So Dry That Feet Crack Open

Michigan Neuropathy Screening Instrument (MNSI) History; is the skin on your feet so dry that it cracks open?

MNSI - Right Foot Vibration Great Toe

Michigan Neuropathy Screening Instrument (MNSI) Physical assessment; right foot - vibration perception at great toe.

MNSI - Right Foot Ulceration

Michigan Neuropathy Screening Instrument (MNSI) Physical assessment; right foot - ulceration.