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

Chr.1:228205976 on build GRCh38
Cytoband
1q42.13
Assay ID Hs03343130_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 Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C1orf145 NR_073154.1 4 1383
NR_073155.1
AK056556.1 4 1383 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 GJC2 MRPL55 C1orf35 ARF1 IBA57-AS1 OBSCN C1orf145 IBA57 MIR3620 GUK1
nsv826908 Chr.1:227707685 - 228503399 on Build GRCh38 Gain LOC101060022 GJC2 LOC107985355 IBA57 MIR3620 MIR4666A LOC105373289 TRIM11 SNAP47 MIR6742 WNT3A TRIM17 HIST3H2BB C1orf35 HIST3H3 IBA57-AS1 MIR5008 OBSCN PRSS38 GUK1 MRPL55 ARF1 JMJD4 C1orf145 RNF187 WNT9A LOC101927401 HIST3H2A LOC100506571
esv32853 Chr.1:227692415 - 228670462 on Build GRCh38 Gain GJC2 RNA5S8 RNA5S7 RNA5S12 RNA5S14 RNA5S4 LOC105373289 TRIM11 RNA5S5 LOC105373132 SNAP47 DUSP5P1 HIST3H3 RNA5S6 PRSS38 RNA5S13 RNA5S11 BTNL10 RNA5S16 RNA5S3 MRPL55 ARF1 JMJD4 LOC101927401 RNA5S17 LOC101060022 RNA5S2 LOC107985355 IBA57 MIR3620 MIR4666A MIR6742 RNA5S1 WNT3A TRIM17 HIST3H2BB RNA5S9 C1orf35 IBA57-AS1 MIR5008 OBSCN RHOU GUK1 RNA5S10 C1orf145 RNF187 WNT9A HIST3H2A RNA5S15 LOC100506571
nsv827019 Chr.1:228126466 - 228463319 on Build GRCh38 Loss GJC2 TRIM17 HIST3H2BB HIST3H3 IBA57-AS1 OBSCN IBA57 MIR4666A GUK1 TRIM11 C1orf145 MIR6742 LOC101927401 HIST3H2A
nsv523935 Chr.1:227850423 - 228494048 on Build GRCh38 Loss LOC101060022 GJC2 LOC107985355 IBA57 MIR3620 MIR4666A TRIM11 MIR6742 WNT3A TRIM17 HIST3H2BB C1orf35 HIST3H3 IBA57-AS1 MIR5008 OBSCN GUK1 MRPL55 ARF1 C1orf145 RNF187 WNT9A LOC101927401 HIST3H2A LOC100506571

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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