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

Ensembl ID	ENSXCOG00000005798	Gene ID		Accession	-
Symbol		Alias	-	Full Name	fragile X mental retardation, autosomal homolog 2
Status	Confidence	Length	16690 bases	Strand	Plus strand
Position	KQ557206.1 : 3892977 - 3909666	RNA binding domain	Agenet , FXR_C1 , KH_1 , KH_9 , FXMRP1_C_core
Summary	N.A.

Protein	Domain	Pfam ID	E-value	Domain number
ENSXCOP00000007802	Agenet	PF05641	6.3e-14	1
ENSXCOP00000007802	FXR_C1	PF16096	1.7e-18	2
ENSXCOP00000007802	KH_1	PF00013	3.2e-17	3
ENSXCOP00000007802	KH_1	PF00013	3.2e-17	4
ENSXCOP00000007802	KH_9	PF17904	5.4e-33	5
ENSXCOP00000007802	FXMRP1_C_core	PF12235	3.6e-35	6
ENSXCOP00000007803	Agenet	PF05641	2.6e-11	1
ENSXCOP00000007803	KH_1	PF00013	5.4e-07	2
ENSXCOP00000007803	KH_9	PF17904	1.3e-33	3

Pubmed ID	Full Name	Cell	Author	Time	Doi

Pubmed ID	Title	Author	Time	Journal

Name	Transcript ID	bp	Protein	Translation ID
-	ENSXCOT00000007900	1965	654aa	ENSXCOP00000007802
-	ENSXCOT00000007901	906	301aa	ENSXCOP00000007803

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
ENSXCOG00000005798

Ensembl ID	Source				Target
	Species	Protein ID	Perc_pos	Perc_id	Species	Protein ID	Perc_pos	Perc_id
ENSXCOG00000005798

Go ID	Go term	No. evidence	Entries	Species	Category