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

Gene Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	127795
Gene name Gene Name - the full gene name approved by the HGNC.	Chromosome 1 open reading frame 87
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	C1orf87
Synonyms (NCBI Gene) Gene synonyms aliases	CREF
Chromosome Chromosome number	1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	1p32.1

Show/Hide all(94)

miRTarBase ID	miRNA	Experiments	Reference
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT616392	hsa-miR-4714-5p	HITS-CLIP	23824327
MIRT616391	hsa-miR-22-3p	HITS-CLIP	23824327
MIRT616390	hsa-miR-6777-3p	HITS-CLIP	23824327
MIRT616388	hsa-miR-1234-3p	HITS-CLIP	23824327
MIRT616389	hsa-miR-7107-5p	HITS-CLIP	23824327
MIRT616387	hsa-miR-301a-5p	HITS-CLIP	23824327
MIRT616386	hsa-miR-301b-5p	HITS-CLIP	23824327
MIRT616385	hsa-miR-6730-3p	HITS-CLIP	23824327
MIRT616384	hsa-miR-3660	HITS-CLIP	23824327
MIRT616383	hsa-miR-4526	HITS-CLIP	23824327
MIRT616382	hsa-miR-6719-3p	HITS-CLIP	23824327
MIRT841677	hsa-miR-1234	CLIP-seq
MIRT841678	hsa-miR-22	CLIP-seq
MIRT1949510	hsa-miR-338-5p	CLIP-seq
MIRT2676761	hsa-miR-1283	CLIP-seq
MIRT1949510	hsa-miR-338-5p	CLIP-seq
MIRT2676762	hsa-miR-4422	CLIP-seq

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GO ID	Ontology	Definition	Evidence	Reference
GO:0005929	Component	Cilium	IDA	28282151
GO:0005930	Component	Axoneme	IDA	28282151

MIM	HGNC	e!Ensembl
618860	28547	ENSG00000162598

Protein

UniProt ID

Q8N0U7

Protein name

Uncharacterized protein C1orf87

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF17743	DUF5580	1 → 546	Family of unknown function (DUF5580)	Family

Sequence

MSSAWKTPRGSDAMPEIMVKIIGSKHFQYLVEKPKIKENDSLKTETQTMHQKPMTDNARQ
MSRDTPVPINFTDQQTTDNPDDVKEKKHPENNQKSENNQKLLTGANSSRFLDGNIPSQAN
VHCSSVPTGDQSLSYVHGIPRRKLRDWSLEQMVRGSSDQPEDIGQSPSGTTNEDAFLLAL
VRRELKSRPLSSNLLEKLQKELKILDPISSGFLLQSQLSRLFLKHEVPLQLPTVKILCQR
FSKRGSPEMVNYEKLLWFLNSAASDYPQQNKAAADLRKTESHGTHSQSTPPQHSSSQPEV
NRSLLEILKMALRTTNGRLNIDNLNLSFRKEDRSFSGCLPLPKVRAICGKHGLYLTLSLL
ETLLNHQDLGYQNEIKWQNFVEMLTRASSDLLSDLPTGKNEKKAPAPPMEPEVPEMSQSK
TEHMKTPEEELQPESSPAETSACKDPLKPLKIRPVSQPFVNPAVKNKAEECETWIDRFRK
LENALYLCDLSNTGVLEKERARRLIHNYNLIYNLSLSPQKIDQALRRFRSGENMLLEPAL
RYLKEL

Sequence length

546

Interactions

View interactions

Show/Hide Unknown Diseases (1)

Disease merge term	Disease name	Evidence	References	Source
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Dyslexia	Dyslexia	N/A	N/A	GWAS

C1orf87 (chromosome 1 open reading frame 87)