| Description |
chromosome 19 open reading frame 54 |
tektin 5 |
| Image |
No pdb structure |
No pdb structure |
| GO Annotations |
Cellular Component |
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| Molecular Function |
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| Biological Process |
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| Pathways |
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| Drugs |
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| Diseases |
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| GWAS |
- Blood protein levels ( 28240269)
- Carotid intima media thickness (mean) ( 31801372)
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- Cerebrospinal AB1-42 levels in normal cognition ( 29274321)
- Chronic obstructive pulmonary disease ( 30804561)
- Eating disorders ( 23568457)
- Lung adenocarcinoma ( 28604730)
- Lung function (FEV1/FVC) ( 26635082 30804560)
- Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) ( 32047095)
- Nickel levels ( 26025379)
- Normal facial asymmetry (angle of surface orientation score) ( 30631343)
- Peak expiratory flow ( 30804560)
- Resting heart rate ( 27798624)
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| Interacting Genes |
67 interacting genes:
A1CF
ABI2
AGXT
ANKS1A
ARID5A
COL8A1
CYSRT1
DTX2
ENKD1
FAM222B
FANCL
FBLIM1
FNDC3B
FOXH1
FRS3
GLIS2
GLYCTK
GPS2
HOXC8
HR
HSF4
IGFN1
INCA1
KCTD9
KPRP
KRTAP23-1
KRTAP26-1
LASP1
LMO3
MISP
NEDD9
NOXA1
PATZ1
PITX1
PLAC8
PLSCR3
POGZ
PRKAB2
PROP1
PRR35
QRICH1
RBPMS
RBPMS2
ROR2
SAXO1
SMARCD1
SNRPC
SPAG8
TBX6
TCAP
TCF7L2
TEKT5
TFG
TLE5
TLX3
TOLLIP
TRAF4
TRIP13
TROAP
VAC14
VENTX
WDR25
WWOX
YPEL3
ZC2HC1C
ZC3H10
ZMYND19
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47 interacting genes:
AKAP8L
BAG4
C19orf54
C7orf31
CABP2
CSKMT
DTX2
EPHB6
EYA2
FNDC3B
FOXH1
FOXI1
GSK3B
HGS
HOXA1
HOXB6
KLHL38
KRTAP12-4
KRTAP15-1
KRTAP19-6
KRTAP19-7
KRTAP6-2
LASP1
MAPKBP1
MGAT5B
NFKBID
NHLRC2
PITX1
PLSCR4
PROP1
PSMB4
QRICH1
RBPMS
RORB
RUNX1
SMARCB1
SMUG1
SPAG8
SSC4D
TBX15
TLX3
TNS2
TOX2
USP54
VENTX
ZMYND12
ZNF76
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| Entrez ID |
284325 |
146279 |
| HPRD ID |
13449 |
08736 |
| Ensembl ID |
ENSG00000188493
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ENSG00000153060
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| Uniprot IDs |
Q5BKX5
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Q96M29
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| PDB IDs |
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| 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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