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Gene: RAB40AL (RAB40A like) Homo sapiens
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Symbol: RAB40AL
Name: RAB40A like
Description: Predicted to have GTPase activity. Predicted to be involved in Rab protein signal transduction; intracellular protein transport; and protein localization to plasma membrane. Localizes to the mitochondrion. Implicated in deafness-intellectual disability, Martin-Probst type syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: MGC119958; MGC119959; MGC119960; MGC119961; MRXSMP; RAB40A, member RAS oncogene family-like; RAR2; Ras like GTPase; ras-like GTPase; Ras-like GTPase-like; ras-related protein Rab-40A-like; RLGP; SOCS box containing protein RAR2
Orthologs:
Pan paniscus (bonobo/pygmy chimpanzee) : RAB40AL (RAB40A like)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX102,937,272 - 102,938,300 (+)Ensembl
GRCh38X102,937,272 - 102,938,300 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X102,192,200 - 102,193,228 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X102,078,856 - 102,079,884 (+)NCBINCBI36hg18NCBI36
CeleraX102,631,242 - 102,632,270 (+)NCBI
Cytogenetic MapXq22.1NCBI
HuRefX91,857,158 - 91,858,186 (+)NCBIHuRef
CHM1_1X102,084,918 - 102,085,946 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on RAB40AL
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 2291808
Created: 2008-03-28
Species: Homo sapiens
Last Modified: 2019-12-25
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.