| Name |
|---|
TRIQK Genetriple QxxK/R motif containing Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CTHRC1 Genecollagen triple helix repeat containing 1 This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012] |
ZNHIT3 Genezinc finger, HIT-type containing 3 Predicted to enable nuclear thyroid hormone receptor binding activity. Predicted to be involved in box C/D snoRNP assembly; maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA); and snoRNA localization. Located in cytoplasm and nucleus. Implicated in PEHO syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT2 Genezinc finger, HIT-type containing 2 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT1 Genezinc finger, HIT-type containing 1 Enables histone binding activity. Involved in muscle cell differentiation and positive regulation of DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT6 Genezinc finger, HIT-type containing 6 Enables ATPase binding activity; TFIID-class transcription factor complex binding activity; and identical protein binding activity. Involved in box C/D snoRNP assembly; protein complex oligomerization; and snoRNA localization. Located in extracellular exosome. Part of pre-snoRNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT1P1 Genezinc finger, HIT-type containing 1 pseudogene 1 |