LP193292-2
TMEM216 gene
Active
Description
The TMEM216 (transmembrane protein 216) gene [HGNC Gene ID: 25018] is located on chromosome 11q13.1. This locus encodes a transmembrane domain-containing protein. Mutations at this locus have been associated with Meckel-Gruber Syndrome Type 2, and Joubert Syndrome 2, also known as Cerebello-oculorenal Syndrome 2. [provided by RefSeq, Aug 2010][NCBI Gene ID: 51259] Source: National Center for Biotechnology Information (NCBI) Gene
Basic Part Properties
- Part Name
- TMEM216 gene
- Part Display Name
- TMEM216 gene
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2015-06-06
- Construct for LOINC Short Name
- TMEM216
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://