|
ECB-GENEPAGE-23157853
???displayGene.symbol??? tti2
![]() Symbol Status
![]() ???displayGene.name??? TELO2 interacting protein 2
![]() Name Status
![]() ???displayGene.synonyms???
human chromosome 8 open reading frame 41-like
,
LOC110984536
,
LOC591081
,
Sp-C8orf41L
,
SPU_023074
,
TELO2-interacting protein 2
[+]
(
???displayGene.geneFunction??? Protein Function
![]() ???displayGene.geneInteractants???
Loading ...
Diseases: Disease Ontology: autosomal recessive non-syndromic intellectual disability
MIM:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39
External Links:
|
|
Symbol legend:
![](img/icons/rocket.gif)
![](img/icons/magnifying_glass.png)
![](img/icons/images.gif)
![](img/icons/info1_blue.png)