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

Chr.1:228205210 on build GRCh38
Cytoband
1q42.13
Assay ID Hs03331954_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 2149
NR_073155.1
AK056556.1 4 2149 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 C1orf35 MIR3620 IBA57 C1orf145 MRPL55 GUK1 OBSCN GJC2 ARF1
nsv826908 Chr.1:227707685 - 228503399 on Build GRCh38 Gain IBA57-AS1 LOC105373289 LOC100506571 C1orf35 IBA57 JMJD4 C1orf145 HIST3H2A TRIM11 WNT9A OBSCN LOC107985355 LOC101060022 HIST3H3 GUK1 ARF1 WNT3A HIST3H2BB MIR4666A MIR5008 MIR3620 RNF187 PRSS38 TRIM17 LOC101927401 MIR6742 SNAP47 MRPL55 GJC2
esv32853 Chr.1:227692415 - 228670462 on Build GRCh38 Gain RNA5S12 LOC105373289 RNA5S8 C1orf35 IBA57 JMJD4 C1orf145 HIST3H2A OBSCN RNA5S16 RNA5S11 LOC101060022 HIST3H3 ARF1 RNA5S4 MIR5008 RNA5S7 TRIM17 LOC101927401 MRPL55 RNA5S1 RNA5S3 IBA57-AS1 LOC105373132 LOC100506571 RHOU TRIM11 WNT9A RNA5S9 LOC107985355 RNA5S17 BTNL10 GUK1 WNT3A RNA5S2 HIST3H2BB MIR4666A RNA5S15 RNA5S10 MIR3620 RNA5S5 RNF187 PRSS38 DUSP5P1 RNA5S14 RNA5S13 MIR6742 SNAP47 GJC2 RNA5S6
nsv827019 Chr.1:228126466 - 228463319 on Build GRCh38 Loss IBA57-AS1 HIST3H2BB MIR4666A IBA57 C1orf145 HIST3H2A TRIM11 OBSCN TRIM17 LOC101927401 MIR6742 HIST3H3 GUK1 GJC2
nsv523935 Chr.1:227850423 - 228494048 on Build GRCh38 Loss IBA57-AS1 LOC100506571 C1orf35 IBA57 C1orf145 HIST3H2A TRIM11 WNT9A OBSCN LOC107985355 LOC101060022 HIST3H3 GUK1 ARF1 WNT3A HIST3H2BB MIR4666A MIR5008 MIR3620 RNF187 TRIM17 LOC101927401 MIR6742 MRPL55 GJC2

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

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