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See other TMC4 CNV Assays ›
Gene Symbol
TMC4
Assay Reference Genome
Location

Chr.19:54162717 on build GRCh38
Cytoband
19q13.42
Assay ID Hs02313573_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 147798

Gene Name:

 transmembrane channel like 4

Gene Aliases:

 -

Location:

 Chr.19:54160095-54173250 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 10 - Exon 10
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TMC4 NM_001145303.2 NP_001138775.2
NM_144686.3 NP_653287.2
XM_011526486.2 XP_011524788.1
AK124406.1 2 501
AK314973.1
AY236492.1 AAP69870.1
AY263166.1 AAP78781.1
BC025323.1 AAH25323.1
BC032477.1 AAH32477.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv9751 Chr.19:54158885 - 54193528 on Build GRCh38 Gain TMC4 LENG1 MBOAT7 TSEN34
nsv515623 Chr.19:54102901 - 54179150 on Build GRCh38 Loss TMC4 LENG1 MBOAT7 TFPT PRPF31 CNOT3 NDUFA3
nsv953613 Chr.19:54097214 - 54198733 on Build GRCh38 Deletion TMC4 LENG1 MBOAT7 TFPT OSCAR TSEN34 PRPF31 CNOT3 NDUFA3
esv2718812 Chr.19:53184636 - 54322450 on Build GRCh38 Deletion MIR524 MIR515-1 CACNG6 MIR519A1 MIR520B MIR512-1 LILRB5 LILRB3 MIR520H VSTM1 MIR521-2 ZNF665 MIR516A2 ZNF677 LOC105372457 TMC4 MIR527 BIRC8 MIR512-2 TFPT MIR519A2 NLRP12 MIR4752 CACNG8 LILRA6 DPRX LILRB2 VN1R4 PRPF31 MIR522 MYADM MIR521-1 RPS9 MIR516B2 MIR517B MIR518C MIR519D CACNG7 MIR372 MIR518A2 MBOAT7 VN1R2 MIR1283-2 MIR526A1 MIR520G MIR518B MIR520A MIR516B1 MIR523 MIR520C ZNF765 ZNF525 MIR518A1 MIR519E MIR935 MIR520E MIR1283-1 MIR371A LILRA5 ZNF813 MIR519B MIR373 ZNF331 MIR517C MIR517A OSCAR ZNF845 MIR526A2 FAM90A27P MIR526B NDUFA3 LENG1 ZNF761 MIR525 TARM1 LOC284379 MIR516A1 TSEN34 MIR518D TPM3P9 MIR1323 MIR518E MIR520D MIR520F PRKCG MIR371B MIR518F MIR515-2 ZNF818P MIR519C CNOT3 MIR498
nsv510774 Chr.19:54158011 - 54269511 on Build GRCh38 Deletion TMC4 LENG1 LILRA6 MBOAT7 LILRB5 LILRB3 TSEN34 RPS9

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s)


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