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C1orf216 and MLPH
Data Source:
BioGRID
(two hybrid)
C1orf216
MLPH
Description
chromosome 1 open reading frame 216
melanophilin
Image
No pdb structure
No pdb structure
GO Annotations
Cellular Component
Dendrite
Cortical Actin Cytoskeleton
Perinuclear Region Of Cytoplasm
Extracellular Exosome
Molecular Function
Protein Binding
Actin Binding
Protein Binding
Myosin Binding
Protein-macromolecule Adaptor Activity
Small GTPase Binding
Metal Ion Binding
Biological Process
Intracellular Protein Transport
Melanosome Transport
Pathways
Drugs
Diseases
Other phagocyte defects, including the following eight diseases: Chediak-Higashi syndrome; Griscelli syndrome, type 1 (GS1); Griscelli syndrome, type 2 (GS2); Griscelli syndrome, type 3 (GS3); beta-actin deficiency; Neutrophil-specific granule deficiency; Myeloperoxidase deficiency; Glucose 6-phosphate dehydrogenase deficiency; Shwachman syndrome
GWAS
Central corneal thickness (
32528159
)
Heel bone mineral density (
30598549
28869591
)
Intraocular pressure (
29617998
)
Prostate cancer (
21743057
)
Interacting Genes
71 interacting genes:
ABI2
AIMP2
AMOT
BORCS6
CCDC136
CCDC158
CCDC197
CDR2
CDR2L
CENPH
CEP170P1
CEP55
CMC2
DES
DMAP1
EIF3F
EXOC5
FSD2
GGA1
HAP1
HAUS8
IFT20
KLHL20
KRT13
KRT15
KRT16
KRT24
KRT27
KRT31
KRT33B
KRT34
KRT36
KRT38
KRT39
KRT40
KRT75
KRT76
LRRC61
MAGEA6
MDFI
MED4
MIS18A
MLPH
MRFAP1L1
MTUS2
MYRIP
NECAB2
NMI
NRBF2
NUP62
ODAD1
PKNOX2
PPP1R16A
PSMC6
RALBP1
SERTAD3
SNW1
SYCE1L
THAP1
TLE5
TMCO5A
TPM1
TPM3
TRAF1
TRIM54
TRIM72
USHBP1
VPS52
WASHC1
ZDHHC17
ZNF620
7 interacting genes:
BLOC1S6
C1orf216
MTDH
MYO5A
RAB27A
RAB27B
RECK
Entrez ID
127703
79083
HPRD ID
08798
09409
Ensembl ID
ENSG00000142686
ENSG00000115648
Uniprot IDs
Q8TAB5
A0A024R4D3
Q9BV36
PDB IDs
Enriched GO Terms of Interacting Partners
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Tagcloud
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Tagcloud (Difference)
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Tagcloud (Intersection)
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