| Description |
keratin associated protein 13-2 |
coiled-coil domain containing 24 |
| 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 |
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- Autism spectrum disorder or schizophrenia ( 28540026)
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| Interacting Genes |
80 interacting genes:
ANAPC11
ANXA11
BCL6
C11orf1
C22orf39
CBFA2T2
CCDC125
CCDC24
CCDC57
CCNK
CRYBA1
CSKMT
CYSRT1
ENKD1
EPDR1
ETFDH
FANCL
FBXO17
FCHO1
GATA3
GEMIN4
GNE
GPS2
GRN
HNRNPH1
HOXA1
HR
KCTD9
KLHL38
KPRP
KRT3
KRTAP1-1
KRTAP10-5
KRTAP11-1
KRTAP12-2
KRTAP12-3
KRTAP15-1
KRTAP26-1
KRTAP3-1
KRTAP3-3
KRTAP4-4
KRTAP4-5
KRTAP9-2
MAGOHB
MEOX2
MGAT5B
NBPF19
NEK8
NHLRC4
NOTCH2NLA
OIP5
OTX1
P4HB
PATZ1
PHETA1
PITX1
POU2AF1
PPP1R32
RECK
RHOXF2
SLC25A18
SLIT1
SMUG1
SNRPC
SPEF1
SSC4D
STK16
TCAF1
TEX37
TLE5
TNS2
TRAPPC6A
TRIM68
TSPYL6
TSSK3
UNC5CL
VGLL3
VWC2
YPEL3
ZIC1
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39 interacting genes:
ADRA2C
AKAP8L
ANTKMT
ARMH1
CDC23
DISC1
DYNLT4
FAM166B
FNTB
GATA1
HPDL
HYI
IKZF3
KLF17
KRT33B
KRT34
KRTAP13-2
KRTAP15-1
KRTAP19-1
KRTAP19-6
KRTAP19-7
KRTAP6-1
KRTAP6-3
LRP2BP
MAGEA6
NDUFAB1
NDUFB7
OIP5
REN
RNF31
TCEAL8
TRIM42
TRIP6
TTC23
TTC23L
USHBP1
USP54
WWOX
ZMYND12
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| Entrez ID |
337959 |
149473 |
| HPRD ID |
11201 |
14636 |
| Ensembl ID |
ENSG00000182816
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ENSG00000159214
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| Uniprot IDs |
Q52LG2
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Q8N4L8
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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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