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

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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