Description |
proline rich 20B |
PHD finger protein 1 |
Image |
No pdb structure |
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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 |
- Mosaic loss of chromosome Y (Y chromosome dosage) ( 31624269)
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- Autism spectrum disorder or schizophrenia ( 28540026)
- Body mass index ( 26426971)
- Chronic obstructive pulmonary disease or resting heart rate (pleiotropy) ( 30940143)
- Refractive error ( 32231278)
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Interacting Genes |
90 interacting genes:
ABI2
ANKHD1
ARID5A
ATXN1
BANP
BEND2
BHLHE40
BICRAL
C10orf55
C1orf94
C3orf36
CABP2
CCNK
CDC37
CELF4
DAZAP2
DMRT3
DVL3
EIF4ENIF1
ESRP1
FAM168A
FAM222B
FAM9A
FOXH1
FOXP3
GLIS2
GTF2A1
HIVEP1
HLX
HYPK
KRTAP19-1
KRTAP19-5
LASP1
MAGED1
MBNL3
NCK2
NFYC
NOTCH3
NTAQ1
OLFM4
OXER1
PATZ1
PHF1
PITX1
POGZ
POU2F1
POU6F2
PRR20A
PRR20C
PRR20D
PRR20E
PRR34
PRR35
PTTG2
RBM23
RBM42
RBPMS
RBPMS2
RHOXF2
RIPPLY1
RNF4
ROR2
SAMD11
SH3RF1
SIAH1
SMAP1
SNRPB
SNRPC
SP4
SRPK2
TBX3
TBX6
TCF7L2
TFG
THAP1
TIAL1
TLX3
TOLLIP
TPRX1
TRIM35
VAC14
VENTX
VEZF1
VPS37C
YPEL3
ZBTB32
ZC3H10
ZCCHC14
ZNF385C
ZNF683
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78 interacting genes:
ABI2
ARID5A
ARRDC3
ATXN7L1
AVPI1
BHLHB9
BHLHE40
BIRC7
BOLL
BRD2
C11orf49
CALCOCO2
DISC1
DPF1
DYSF
EFHC2
EZH2
FHL2
FOSB
GOLGA6L9
GPKOW
H3C1
H3C10
H3C11
H3C12
H3C2
H3C3
H3C6
H3C7
H3C8
H4C1
HOMEZ
HSD17B14
INCA1
IRAK1BP1
KIAA0408
KRT40
LBX1
LZTS2
MAGED1
MDFI
MEOX2
MORN3
NAB2
NEK6
PATZ1
PDLIM7
PFDN5
PIBF1
PRR20A
PRR20B
PRR20C
PRR20D
PRR20E
RBBP8NL
RBPMS
SMG9
SORBS3
SPAG8
TFCP2
TFIP11
THAP1
TLE5
TNS2
TOX2
TP53BP2
TRIM23
USP54
VAC14
ZBTB10
ZBTB16
ZIM2
ZNF500
ZNF526
ZNF688
ZNF71
ZRANB1
ZSCAN32
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Entrez ID |
729233 |
5252 |
HPRD ID |
19668 |
04195 |
Ensembl ID |
ENSG00000204918
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ENSG00000112511
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Uniprot IDs |
P86478
P86479
P86480
P86481
P86496
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A0A140VJR4
A0A1U9X8A3
O43189
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PDB IDs |
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2E5P
2M0O
4HCZ
5XFN
5XFO
5XFP
6WAT
6WAV
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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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