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

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

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