ArcPathVisio
Brace
Octagon
Ellipse
EndoplasmicReticulum
HexagonPathVisio
GolgiApparatus
MimDegradation
Mitochondria
Octagon
PentagonPathVisio
Rectangle
RoundedRectangle
SarcoplasmicReticulum
TrianglePathVisio
none
increased Ca2+ flux
upon stimulation
recruitment and
stimulation of
leukocytes and NKs
Regulation of
photosensitiviy
of retina
unspecific
cation channel
unclear
function
Schizophrenia risk gene
light
Chromosome 15:32,500,000
RNA gene
exact function unclear
possibly involved in golgi
apparatus organization
stacking of cristae
Chromosome 15:30,500,00
tumor growth
neocortex
development
dendritic growth
neuronal
development
ASD risk gene
ubiquitinated protein
Function unclear
Inactive phosphatidyl-
inositol 3-phosphatase 10
Source: https://www.uniprot.org/uniprot/Q9NXD2
RN7SL796P
DNM1P50
ULK4P2
RN7SL628P
GOLGA8UP
RN7SL82P
HERC2P10
RNU6-466P
LINC02352
UBE2CP4
RNU6-18P
RNU6-17P
RN7SL196P
KLF13
Fanconi Anemia Pathway
CHRNA7
MTMR10
GPR75
DNA
GOLGA8R
Acetylcholine
CREBBP
TRPM1
FANCD2
OTUD7A
glutamate
GOLGA8Q
hsa-mir-211
CHRFAM7A
ARHGAP11B
CCL5
FAN1
ADP/ATP translocases
Alpha-Bungarotoxin
GOLGA8H
FYN
GRM6
pseudo gene
exact function unclear
possibly involved in golgi
apparatus organization
stacking of cristae
U
FANCD2
U
CCL5
SERPINH1
KAT2B
Name: 15q13.3 copy number variation syndrome
Last Modified: 20210312083718
Organism: Homo sapiens