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See other C1ORF145 CNV Assays ›
Gene Symbol
C1orf145
Assay Reference Genome
Location

Chr.1:228206898 on build GRCh38
Cytoband
1q42.13
Assay ID Hs03352198_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 574407

Gene Name:

 chromosome 1 open reading frame 145

Gene Aliases:

 -

Location:

 Chr.1:228203506-228213664 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C1orf145 NR_073154.1
NR_073155.1
AK056556.1 BAB71215.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1160102 Chr.1:228081212 - 228239280 on Build GRCh38 Deletion IBA57-AS1 C1orf145 ARF1 MRPL55 OBSCN GJC2 MIR3620 IBA57 C1orf35 GUK1
nsv826908 Chr.1:227707685 - 228503399 on Build GRCh38 Gain PRSS38 C1orf145 HIST3H3 MIR6742 LOC107985355 GUK1 MIR5008 IBA57-AS1 WNT9A WNT3A RNF187 GJC2 MIR3620 HIST3H2A MIR4666A LOC100506571 HIST3H2BB TRIM11 LOC101927401 JMJD4 SNAP47 IBA57 LOC101060022 C1orf35 TRIM17 ARF1 MRPL55 LOC105373289 OBSCN
esv32853 Chr.1:227692415 - 228670462 on Build GRCh38 Gain PRSS38 C1orf145 HIST3H3 RNA5S1 MIR6742 LOC107985355 GUK1 IBA57-AS1 LOC105373132 WNT3A RNA5S10 RHOU RNA5S4 GJC2 RNA5S3 BTNL10 HIST3H2A MIR4666A LOC100506571 HIST3H2BB TRIM11 JMJD4 SNAP47 RNA5S13 IBA57 RNA5S5 LOC101060022 C1orf35 RNA5S17 RNA5S11 RNA5S8 RNA5S12 OBSCN RNA5S14 RNA5S6 MIR5008 WNT9A RNF187 MIR3620 RNA5S7 RNA5S9 LOC101927401 RNA5S16 RNA5S2 TRIM17 ARF1 MRPL55 LOC105373289 DUSP5P1 RNA5S15
nsv827019 Chr.1:228126466 - 228463319 on Build GRCh38 Loss LOC101927401 C1orf145 HIST3H3 MIR6742 IBA57 GUK1 IBA57-AS1 TRIM17 OBSCN GJC2 HIST3H2A MIR4666A HIST3H2BB TRIM11
nsv523935 Chr.1:227850423 - 228494048 on Build GRCh38 Loss C1orf145 HIST3H3 MIR6742 LOC107985355 GUK1 MIR5008 IBA57-AS1 WNT9A WNT3A RNF187 GJC2 MIR3620 HIST3H2A MIR4666A LOC100506571 HIST3H2BB TRIM11 LOC101927401 IBA57 LOC101060022 C1orf35 TRIM17 ARF1 MRPL55 OBSCN

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

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