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Gene: PNMA6E (PNMA family member 6E) Homo sapiens
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Symbol: PNMA6E
Name: PNMA family member 6E
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH aflatoxin B1
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: paraneoplastic antigen Ma6E; paraneoplastic Ma antigen family member 6E; putative paraneoplastic antigen-like protein 6B-like
Orthologs:
Pan paniscus (bonobo/pygmy chimpanzee) : PNMA6E (PNMA family member 6E)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX153,395,639 - 153,401,392 (-)Ensembl
GRCh38X153,395,639 - 153,414,404 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X152,662,364 - 152,666,148 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X152,315,381 - 152,317,501 (-)NCBINCBI36hg18NCBI36
CeleraX152,896,085 - 152,896,990 (-)NCBI
Cytogenetic MapXq28NCBI
CHM1_1X152,529,920 - 152,533,884 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on PNMA6E
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 12790877
Created: 2017-02-21
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.