RBP Type	N.A.
Diseases
Drug
Main interacting RNAs
Moonlighting functions
Localizations
BulkPerturb-seq

Ensembl ID	ENSXCOG00000008158	Gene ID		Accession	-
Symbol		Alias	-	Full Name	fragile X mental retardation, autosomal homolog 1
Status	Confidence	Length	13556 bases	Strand	Plus strand
Position	KQ557224.1 : 27606034 - 27619589	RNA binding domain	FXR_C1 , KH_1 , KH_9 , FXMRP1_C_core
Summary	N.A.

Protein	Domain	Pfam ID	E-value	Domain number
ENSXCOP00000010810	FXR_C1	PF16096	1.3e-34	1
ENSXCOP00000010810	KH_1	PF00013	1.2e-17	2
ENSXCOP00000010810	KH_1	PF00013	1.2e-17	3
ENSXCOP00000010810	KH_9	PF17904	4.8e-24	4
ENSXCOP00000010810	FXMRP1_C_core	PF12235	1.3e-36	5
ENSXCOP00000010810	FXMRP1_C_core	PF12235	1.3e-36	6
ENSXCOP00000010808	FXR_C1	PF16096	2.9e-34	1
ENSXCOP00000010808	KH_1	PF00013	1.9e-17	2
ENSXCOP00000010808	KH_1	PF00013	1.9e-17	3
ENSXCOP00000010808	KH_9	PF17904	6.8e-24	4
ENSXCOP00000010808	FXMRP1_C_core	PF12235	7.2e-54	5

Pubmed ID	Full Name	Cell	Author	Time	Doi

Pubmed ID	Title	Author	Time	Journal

Name	Transcript ID	bp	Protein	Translation ID
-	ENSXCOT00000010933	1791	596aa	ENSXCOP00000010808
-	ENSXCOT00000010935	1470	489aa	ENSXCOP00000010810

Pathway ID	Pathway Name	Source

ensgID	Trait	pValue	Pubmed ID

ensgID	SNP	Chromosome	Position	Trait	PubmedID	Or or BEAT	EFO ID

Ensembl ID	Source				Target
	Species	Protein ID	Perc_pos	Perc_id	Species	Protein ID	Perc_pos	Perc_id
ENSXCOG00000008158

Ensembl ID	Source				Target
	Species	Protein ID	Perc_pos	Perc_id	Species	Protein ID	Perc_pos	Perc_id
ENSXCOG00000008158

Go ID	Go term	No. evidence	Entries	Species	Category