Description |
CDGSH iron sulfur domain 2 |
immediate early response 3 |
Image |
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No pdb structure |
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 |
- Asthma and attention deficit hyperactivity disorder ( 31619474)
- Estimated glomerular filtration rate ( 31152163)
- Primary biliary cholangitis ( 26394269)
- Schizophrenia ( 28991256)
- Type 2 diabetes ( 28869590)
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- Age-related macular degeneration ( 23455636)
- Autism spectrum disorder or schizophrenia ( 28540026)
- Blood protein levels ( 28240269)
- Chronic obstructive pulmonary disease ( 30804561)
- Decreased fine motor function in Charcot-Marie-Tooth disease 1A (eating with utensils) ( 30958311)
- Rosacea symptom severity ( 29771307)
- Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) ( 26651848)
- Sleep duration ( 25469926)
- Small cell lung carcinoma ( 28604730)
- Type 1 diabetes and autoimmune thyroid diseases ( 25936594)
- Ulcerative colitis ( 20848476)
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Interacting Genes |
58 interacting genes:
AIG1
APOL2
APP
AQP10
BCL2L2
BET1
BMP10
BTN2A2
C14orf180
C2CD2L
C4orf3
CDIPT
CFHR5
CLDN10
CLN6
CYBC1
EHHADH
EMD
FAM241B
GALNT15
GAST
GPR37L1
HHATL
IER3
KIR2DL3
LEPROTL1
LRP10
MAN2B2
MIP
NAPB
NRG4
NSG1
PGAP2
PLPP4
PLPPR2
PNKP
POMGNT1
RTP2
RUSF1
SEC22A
SERP2
SLC13A3
SLC35B4
SMIM1
SNORC
SPP1
STX12
STX7
THSD7B
TMEM187
TMEM243
TMEM43
TMEM86A
TSPAN33
TTPA
VAMP4
VKORC1L1
YIPF6
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17 interacting genes:
APP
AQP2
CD79A
CISD2
FHL2
FKBP7
GLP1R
MAPK1
MAPK3
MDM2
PPP2R5B
PPP2R5C
PRNP
SGTA
SLC13A4
TMBIM6
TMX2
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Entrez ID |
493856 |
8870 |
HPRD ID |
17413 |
04295 |
Ensembl ID |
ENSG00000145354
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ENSG00000137331
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Uniprot IDs |
Q8N5K1
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A0A1U9X7X2
P46695
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PDB IDs |
3FNV
4OO7
4OOA
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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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