| Name |
|---|
DISC1 Genedisrupted in schizophrenia 1 This gene encodes a protein with multiple coiled coil motifs which is located in the nucleus, cytoplasm and mitochondria. The protein is involved in neurite outgrowth and cortical development through its interaction with other proteins. This gene is disrupted in a t(1;11)(q42.1;q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
DISC2 Genedisrupted in schizophrenia 2 (non-protein coding) DISC2 is thought to specify a noncoding RNA molecule antisense to DISC1 (MIM 605210). Both genes were found to be disrupted by a translocation in a large schizophrenia (MIM 181500) kindred.[supplied by OMIM, Jul 2002] |
CLLS2 GeneDisrupted in B-cell neoplasia |
DIRC1 Genedisrupted in renal carcinoma 1 Disruption of DIRC1 by translocation is associated with familial clear cell renal cancer. Overexpression of DIRC1 is associated with tumor progression and poor prognosis in gastric cancer. [provided by RefSeq, Mar 2019] |
DIRC3 Genedisrupted in renal carcinoma 3 |
DIRC2 Genedisrupted in renal carcinoma 2 This gene encodes a membrane-bound protein from the major facilitator superfamily of transporters. Disruption of this gene by translocation has been associated with haplo-insufficiency and renal cell carcinomas. Alternatively spliced transcript variants have been described, but their biological validity has not yet been determined. [provided by RefSeq, Jul 2008] |
MN1 Genemeningioma (disrupted in balanced translocation) 1 Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by RefSeq, Jul 2008] |
SCZD12 Geneschizophrenia 12 |
SCZD8 Geneschizophrenia disorder 8 |
SCZD7 Geneschizophrenia disorder 7 |
SCZD6 Geneschizophrenia disorder 6 |
SCZD1 Geneschizophrenia disorder 1 |
SCZD3 Geneschizophrenia disorder 3 |
SCZD10 Geneschizophrenia disorder 10 (periodic catatonia) |
SCZD2 Geneschizophrenia disorder 2 |
SCZD14 Geneschizophrenia, susceptibility to, 14 |
SCZD11 GeneSchizophrenia susceptibility locus, chromosome 10q-related |
SCZD13 Geneschizophrenia 13 |