Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene information from NCBI Gene database. Gene miRNA Other IDs Pathways Associated diseases
Entrez ID	100529097
Gene name	RPL36A-HNRNPH2 readthrough
Gene symbol	RPL36A-HNRNPH2
Synonyms (NCBI Gene)	-
Chromosome	X
Chromosome location	Xq22.1
Summary	This locus represents naturally occurring read-through transcription between the neighboring ribosomal protein L36a and heterogeneous nuclear ribonucleoprotein H2 (H`) genes on chromosome X. The read-through transcript produces a protein with similarity t

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Show/Hide all (121)

miRTarBase ID	miRNA	Experiments	Reference
MIRT571707	hsa-miR-1914-5p	PAR-CLIP	20371350
MIRT404344	hsa-miR-26a-1-3p	PAR-CLIP	20371350
MIRT404345	hsa-miR-26a-2-3p	PAR-CLIP	20371350
MIRT404354	hsa-miR-6889-3p	PAR-CLIP	20371350
MIRT404348	hsa-miR-581	PAR-CLIP	20371350
MIRT571705	hsa-miR-302b-5p	PAR-CLIP	20371350
MIRT571704	hsa-miR-302d-5p	PAR-CLIP	20371350
MIRT404351	hsa-miR-3124-3p	PAR-CLIP	20371350
MIRT404346	hsa-miR-18b-3p	PAR-CLIP	20371350
MIRT404347	hsa-miR-502-5p	PAR-CLIP	20371350
MIRT404352	hsa-miR-3157-3p	PAR-CLIP	20371350
MIRT571707	hsa-miR-1914-5p	PAR-CLIP	20371350
MIRT404344	hsa-miR-26a-1-3p	PAR-CLIP	20371350
MIRT404345	hsa-miR-26a-2-3p	PAR-CLIP	20371350
MIRT404354	hsa-miR-6889-3p	PAR-CLIP	20371350
MIRT404348	hsa-miR-581	PAR-CLIP	20371350
MIRT571705	hsa-miR-302b-5p	PAR-CLIP	20371350
MIRT571704	hsa-miR-302d-5p	PAR-CLIP	20371350
MIRT404351	hsa-miR-3124-3p	PAR-CLIP	20371350
MIRT404346	hsa-miR-18b-3p	PAR-CLIP	20371350
MIRT404347	hsa-miR-502-5p	PAR-CLIP	20371350
MIRT404352	hsa-miR-3157-3p	PAR-CLIP	20371350
MIRT1316834	hsa-miR-188-3p	CLIP-seq
MIRT1316835	hsa-miR-217	CLIP-seq
MIRT1316836	hsa-miR-4272	CLIP-seq
MIRT1316837	hsa-miR-4719	CLIP-seq
MIRT1316838	hsa-miR-4738-3p	CLIP-seq
MIRT1316839	hsa-miR-532-3p	CLIP-seq
MIRT1316840	hsa-miR-1224-5p	CLIP-seq
MIRT1316841	hsa-miR-1237	CLIP-seq
MIRT1316842	hsa-miR-1245	CLIP-seq
MIRT1316843	hsa-miR-1248	CLIP-seq
MIRT1316844	hsa-miR-132	CLIP-seq
MIRT1316845	hsa-miR-1323	CLIP-seq
MIRT1316846	hsa-miR-186	CLIP-seq
MIRT1316847	hsa-miR-200b	CLIP-seq
MIRT1316848	hsa-miR-200c	CLIP-seq
MIRT1316849	hsa-miR-212	CLIP-seq
MIRT1316835	hsa-miR-217	CLIP-seq
MIRT1316850	hsa-miR-3129-3p	CLIP-seq
MIRT1316851	hsa-miR-3133	CLIP-seq
MIRT1316852	hsa-miR-3143	CLIP-seq
MIRT1316853	hsa-miR-331-5p	CLIP-seq
MIRT1316854	hsa-miR-3591-5p	CLIP-seq
MIRT1316855	hsa-miR-3915	CLIP-seq
MIRT1316856	hsa-miR-3928	CLIP-seq
MIRT1316857	hsa-miR-4268	CLIP-seq
MIRT1316858	hsa-miR-429	CLIP-seq
MIRT1316859	hsa-miR-4311	CLIP-seq
MIRT1316860	hsa-miR-4428	CLIP-seq
MIRT1316861	hsa-miR-4448	CLIP-seq
MIRT1316862	hsa-miR-4473	CLIP-seq
MIRT1316863	hsa-miR-4539	CLIP-seq
MIRT1316864	hsa-miR-4637	CLIP-seq
MIRT1316865	hsa-miR-4671-3p	CLIP-seq
MIRT1316866	hsa-miR-4684-5p	CLIP-seq
MIRT1316867	hsa-miR-4689	CLIP-seq
MIRT1316868	hsa-miR-4724-5p	CLIP-seq
MIRT1316838	hsa-miR-4738-3p	CLIP-seq
MIRT1316869	hsa-miR-4764-3p	CLIP-seq
MIRT1316870	hsa-miR-4765	CLIP-seq
MIRT1316871	hsa-miR-4795-3p	CLIP-seq
MIRT1316872	hsa-miR-4803	CLIP-seq
MIRT1316873	hsa-miR-483-3p	CLIP-seq
MIRT1316874	hsa-miR-512-3p	CLIP-seq
MIRT1316875	hsa-miR-520f	CLIP-seq
MIRT1316876	hsa-miR-548a-3p	CLIP-seq
MIRT1316877	hsa-miR-548e	CLIP-seq
MIRT1316878	hsa-miR-548f	CLIP-seq
MIRT1316879	hsa-miR-548g	CLIP-seq
MIRT1316880	hsa-miR-548o	CLIP-seq
MIRT1316881	hsa-miR-577	CLIP-seq
MIRT1316882	hsa-miR-584	CLIP-seq
MIRT1316883	hsa-miR-676	CLIP-seq
MIRT1316884	hsa-miR-942	CLIP-seq
MIRT2094097	hsa-miR-1243	CLIP-seq
MIRT1316834	hsa-miR-188-3p	CLIP-seq
MIRT2094098	hsa-miR-3654	CLIP-seq
MIRT1316836	hsa-miR-4272	CLIP-seq
MIRT1316872	hsa-miR-4803	CLIP-seq
MIRT2094099	hsa-miR-487a	CLIP-seq
MIRT1316839	hsa-miR-532-3p	CLIP-seq
MIRT2094099	hsa-miR-487a	CLIP-seq
MIRT1316841	hsa-miR-1237	CLIP-seq
MIRT1316843	hsa-miR-1248	CLIP-seq
MIRT2614337	hsa-miR-1470	CLIP-seq
MIRT1316834	hsa-miR-188-3p	CLIP-seq
MIRT2614338	hsa-miR-3126-3p	CLIP-seq
MIRT1316854	hsa-miR-3591-5p	CLIP-seq
MIRT1316857	hsa-miR-4268	CLIP-seq
MIRT1316836	hsa-miR-4272	CLIP-seq
MIRT1316861	hsa-miR-4448	CLIP-seq
MIRT1316862	hsa-miR-4473	CLIP-seq
MIRT2614339	hsa-miR-4667-3p	CLIP-seq
MIRT1316865	hsa-miR-4671-3p	CLIP-seq
MIRT1316866	hsa-miR-4684-5p	CLIP-seq
MIRT1316837	hsa-miR-4719	CLIP-seq
MIRT1316874	hsa-miR-512-3p	CLIP-seq
MIRT2614340	hsa-miR-516b	CLIP-seq
MIRT1316875	hsa-miR-520f	CLIP-seq
MIRT1316839	hsa-miR-532-3p	CLIP-seq
MIRT1316884	hsa-miR-942	CLIP-seq
MIRT1316841	hsa-miR-1237	CLIP-seq
MIRT1316843	hsa-miR-1248	CLIP-seq
MIRT2614337	hsa-miR-1470	CLIP-seq
MIRT1316834	hsa-miR-188-3p	CLIP-seq
MIRT2614338	hsa-miR-3126-3p	CLIP-seq
MIRT1316854	hsa-miR-3591-5p	CLIP-seq
MIRT1316857	hsa-miR-4268	CLIP-seq
MIRT1316836	hsa-miR-4272	CLIP-seq
MIRT1316861	hsa-miR-4448	CLIP-seq
MIRT1316862	hsa-miR-4473	CLIP-seq
MIRT2614339	hsa-miR-4667-3p	CLIP-seq
MIRT1316865	hsa-miR-4671-3p	CLIP-seq
MIRT1316866	hsa-miR-4684-5p	CLIP-seq
MIRT1316837	hsa-miR-4719	CLIP-seq
MIRT1316874	hsa-miR-512-3p	CLIP-seq
MIRT2614340	hsa-miR-516b	CLIP-seq
MIRT1316875	hsa-miR-520f	CLIP-seq
MIRT1316839	hsa-miR-532-3p	CLIP-seq
MIRT1316884	hsa-miR-942	CLIP-seq

MIM	HGNC	e!Ensembl
HGNC	N/A	HGNC

Interactions View interactions

	KEGG
	Ribosome Coronavirus disease - COVID-19

Evidence Score: ★☆☆☆☆ Gene-disease association found in Text Mining only ★★☆☆☆ Found in Text Mining and Unknown/Other Associations ★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)

Show/Hide Unknown Diseases (10)

Phenotype Name	Clinical Significance	Source	Evidence Score
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
CARDIOMYOPATHIES	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
FABRY DISEASE	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
FABRY DISEASE, CARDIAC VARIANT	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
HYPERTROPHIC CARDIOMYOPATHY	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
NEPHROTIC SYNDROME	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
NEURODEVELOPMENTAL DISORDERS	—	Disgenet	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
RPL36A-HNRNPH2-related disorder	Likely benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Show/Hide Text Mining Associations (5)

Disease Name	Disease (Merged)	Source	PMID	Evidence Score
Associations from Text Mining Disease associations identified through text mining
Cardiomyopathies	Cardiomyopathy	CLINVAR_DG		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cardiomyopathy, Hypertrophic, Familial	Cardiomyopathy	CLINVAR_DG		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Fabry Disease	Fabry disease	CLINVAR_DG	10090526, 10208848, 10649504, 10666480, 10838196, 10916280, 11322659, 11531969, 11668641, 11688386, 11804208, 11828341, 11889412, 11914245, 12175777 View all (147 more)	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Fabry Disease, Cardiac Variant	Fabry Disease, Cardiac Variant	CLINVAR_DG		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Hypertrophic Cardiomyopathy	Hypertrophic cardiomyopathy	CLINVAR_DG	10666480, 11828341, 11914245, 15702404, 17555407, 19621417, 19823873, 20031620, 20821055, 21598360, 21972175, 22437327, 23109060, 23568732, 27532257 View all (11 more)	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

RPL36A-HNRNPH2 (RPL36A-HNRNPH2 readthrough)