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A Database of Extreme Multifunctional and Moonlighting Proteins
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About
Protein: Q92734
UniprotKB AC
UniprotKB ID
Gene name
Full name
Species
Curated set
Q92734 (Uniprot)
TFG_HUMAN
TFG
Protein TFG
human
No
Protein Function
Uniprot:
Plays a role in the normal dynamic function of the endoplasmic reticulum (ER) and its associated microtubules (PubMed:23479643, PubMed:27813252).
MoonDB Dissimilar Functions
GO ID 1
Function 1
Module ID 1
GO ID 2
Function 2
Module ID 2
Association Probability
(PrOnto)
Interaction Probability
(PrOnto)
GO:0000377
RNA splicing, via transesterification reactions with bulged adenosine as nucleophile
467
GO:0019538
protein metabolic process
578
1.88e-02
4.66e-37
MoonDB Network Modules
Biological Processes
Module ID
(MoonGO)
GO ID (BP)
GO Name
51
GO:0060255
regulation of macromolecule metabolic process
403
GO:0060255
regulation of macromolecule metabolic process
450
GO:0051252
regulation of RNA metabolic process
450
GO:0010646
regulation of cell communication
450
GO:2000112
regulation of cellular macromolecule biosynthetic process
450
GO:0010468
regulation of gene expression
450
GO:0023051
regulation of signaling
450
GO:0007165
signal transduction
467
GO:0000398
mRNA splicing, via spliceosome
467
GO:0060255
regulation of macromolecule metabolic process
578
GO:0044267
cellular protein metabolic process
578
GO:0031325
positive regulation of cellular metabolic process
578
GO:0010604
positive regulation of macromolecule metabolic process
578
GO:0051173
positive regulation of nitrogen compound metabolic process
578
GO:0048584
positive regulation of response to stimulus
578
GO:0009966
regulation of signal transduction
578
GO:0006355
regulation of transcription, DNA-templated
Cellular Components
Module ID
(MoonGO)
GO ID (CC)
GO Name
51
GO:0005634
nucleus
60
GO:0005634
nucleus
402
GO:0005829
cytosol
403
GO:0005634
nucleus
450
GO:0005634
nucleus
467
GO:0005654
nucleoplasm
578
GO:0005634
nucleus
Protein GO Annotations
Biological Processes
GO ID (BP)
GO Name
Evidence Code
(GO EC)
GO:0006888
ER to Golgi vesicle-mediated transport
IMP
GO:0007165
signal transduction
IEA
GO:0043123
positive regulation of I-kappaB kinase/NF-kappaB signaling
IMP
GO:0048208
COPII vesicle coating
TAS
Cellular Components
GO ID (CC)
GO Name
Evidence Code
(GO EC)
GO:0000139
Golgi membrane
IEA
GO:0005737
cytoplasm
NAS
GO:0005829
cytosol
TAS
GO:0070062
extracellular exosome
IDA
GO:0070971
endoplasmic reticulum exit site
IDA
Dissimilar Cellular Components (PrOnto)
No pairs of PrOnto dissimilar CC GO terms found.
All Protein Interactions
Interactor
Also a MoonDB EMF protein
RBPMS_HUMAN
Yes:
Q93062 (MoonDB)
HNRPF_HUMAN
No
PR20D_HUMAN
No
DAZP2_HUMAN
Yes:
Q15038 (MoonDB)
BOLL_HUMAN
No
CRX_HUMAN
No
NADE_HUMAN
No
VP37C_HUMAN
Yes:
A5D8V6 (MoonDB)
OXER1_HUMAN
No
TEX37_HUMAN
No
BPIA1_HUMAN
No
TMM17_HUMAN
Yes:
Q86X19 (MoonDB)
NEMO_HUMAN
Yes:
Q9Y6K9 (MoonDB)
HGS_HUMAN
No
MED25_HUMAN
No
FOXH1_HUMAN
No
LASP1_HUMAN
No
KR261_HUMAN
No
PPR32_HUMAN
No
F168A_HUMAN
No
GRB2_HUMAN
Yes:
P62993 (MoonDB)
PFD5_HUMAN
No
EYA2_HUMAN
No
PLS1_HUMAN
No
PA2GX_HUMAN
No
OBF1_HUMAN
No
CEP55_HUMAN
No
PKHG4_HUMAN
No
Q6ZP95_HUMAN
No
STH_HUMAN
No
MISSL_HUMAN
No
ANX11_HUMAN
No
ARHGG_HUMAN
No
ARL15_HUMAN
No
CE126_HUMAN
No
CF218_HUMAN
No
CREST_HUMAN
No
CSTF2_HUMAN
No
DPYL1_HUMAN
No
DVL3_HUMAN
Yes:
Q92997 (MoonDB)
ERG28_HUMAN
No
EWS_HUMAN
No
GASP1_HUMAN
No
GBP2_HUMAN
No
INCA1_HUMAN
No
INT11_HUMAN
No
LENG8_HUMAN
No
MAGD1_HUMAN
No
MSS51_HUMAN
No
MYOTI_HUMAN
No
PEF1_HUMAN
No
Q8IV28_HUMAN
No
Q8NBE2_HUMAN
No
RIPP2_HUMAN
No
RNF4_HUMAN
No
RSSA_HUMAN
No
SC24A_HUMAN
No
SF3A2_HUMAN
No
SF3B4_HUMAN
No
SMUG1_HUMAN
No
SPG21_HUMAN
No
STA5B_HUMAN
No
TBX19_HUMAN
No
VOPP1_HUMAN
No
Publications Associated
PMID
Article Title
7565764
The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain.
9169129
Characterization and chromosomal mapping of the human TFG gene involved in thyroid carcinoma.
14702039
Complete sequencing and characterization of 21,243 full-length human cDNAs.
15489334
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
16641997
The DNA sequence, annotation and analysis of human chromosome 3.
16959974
The consensus coding sequences of human breast and colorectal cancers.
18669648
A quantitative atlas of mitotic phosphorylation.
19413330
Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.
19690332
Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
21269460
Initial characterization of the human central proteome.
22223895
Comparative large-scale characterisation of plant vs. mammal proteins reveals similar and idiosyncratic N-alpha acetylation features.
22883144
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.
23186163
Toward a comprehensive characterization of a human cancer cell phosphoproteome.
23479643
Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure.
24129315
Immunoaffinity enrichment and mass spectrometry analysis of protein methylation.
24275569
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
27492651
Novel genetic, clinical, and pathomechanistic insights into TFG-associated hereditary spastic paraplegia.
27813252
The calcium-binding protein ALG-2 promotes endoplasmic reticulum exit site localization and polymerization of Trk-fused gene (TFG) protein.
OMIM Diseases Associated
OMIM ID
Disease Name
604484
Neuropathy, hereditary motor and sensory, Okinawa type
615658
Spastic paraplegia 57, autosomal recessive
Protein Domains Associated
Domain Name
Domain ID
Source
PB1_dom
IPR000270
InterPro
TFG
IPR033512
InterPro
PB1_TFG
IPR034857
InterPro
PB1
PF00564
Pfam
PB1
PS51745
PROSITE
PTHR15335
PTHR15335
PANTHER
PB1
SM00666
SMART
PB1_TFG
cd06401
CDD