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

Ensembl ID	ENSGAFG00000010906	Gene ID		Accession	-
Symbol		Alias	-	Full Name	fragile X mental retardation, autosomal homolog 1
Status	Confidence	Length	16690 bases	Strand	Minus strand
Position	NHOQ01001911.1 : 5324762 - 5341451	RNA binding domain	Agenet , FXR_C1 , KH_1 , KH_9 , FXMRP1_C_core
Summary	N.A.

Protein	Domain	Pfam ID	E-value	Domain number
ENSGAFP00000016165	Agenet	PF05641	8.7e-17	1
ENSGAFP00000016165	Agenet	PF05641	8.7e-17	2
ENSGAFP00000016165	FXR_C1	PF16096	2.1e-33	3
ENSGAFP00000016165	KH_1	PF00013	6.5e-16	4
ENSGAFP00000016165	KH_1	PF00013	6.5e-16	5
ENSGAFP00000016165	KH_9	PF17904	4e-33	6
ENSGAFP00000016165	FXMRP1_C_core	PF12235	6.9e-49	7
ENSGAFP00000016184	Agenet	PF05641	1.5e-16	1
ENSGAFP00000016184	Agenet	PF05641	1.5e-16	2
ENSGAFP00000016184	KH_1	PF00013	1.9e-17	3
ENSGAFP00000016184	KH_1	PF00013	1.9e-17	4
ENSGAFP00000016184	KH_9	PF17904	4.3e-33	5
ENSGAFP00000016157	Agenet	PF05641	2.6e-16	1
ENSGAFP00000016157	Agenet	PF05641	2.6e-16	2
ENSGAFP00000016157	FXR_C1	PF16096	2.2e-33	3
ENSGAFP00000016157	KH_1	PF00013	3e-17	4
ENSGAFP00000016157	KH_1	PF00013	3e-17	5
ENSGAFP00000016157	KH_9	PF17904	4.3e-33	6
ENSGAFP00000016157	FXMRP1_C_core	PF12235	5.1e-54	7

Pubmed ID	Full Name	Cell	Author	Time	Doi

Pubmed ID	Title	Author	Time	Journal

Name	Transcript ID	bp	Protein	Translation ID
-	ENSGAFT00000016313	2426	677aa	ENSGAFP00000016157
-	ENSGAFT00000016321	2339	648aa	ENSGAFP00000016165
-	ENSGAFT00000016340	2374	615aa	ENSGAFP00000016184

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
ENSGAFG00000010906

Ensembl ID	Source				Target
	Species	Protein ID	Perc_pos	Perc_id	Species	Protein ID	Perc_pos	Perc_id
ENSGAFG00000010906

Go ID	Go term	No. evidence	Entries	Species	Category