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- Gene Symbol
- BAHCC1
- Assay Reference Genome
Location
Chr.17:81414644 on build GRCh38- Cytoband
- 17q25.3
Genomic Map
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Target Gene Details
Entrez Gene ID: | 57597 |
Gene Name: | BAH domain and coiled-coil containing 1 |
Gene Aliases: |
BAHD2 |
Location: |
Chr.17:81395431-81466332 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BAHCC1 | NM_001291324.1 | NP_001278253.1 | ||
| XM_011525063.2 | XP_011523365.1 | |||
| XM_017024898.1 | XP_016880387.1 | |||
| XM_017024899.1 | XP_016880388.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv828128 | Chr.17:80659041 - 81736487 on Build GRCh38 | Loss |
 MIR338
PDE6G
MIR6786
CEP131
TMEM105
TEPSIN
MIR4740
LOC101928855
NPLOC4
RPTOR
LOC107985022
BAHCC1
CCDC137
BAIAP2-AS1
AATK-AS1
SLC38A10
LOC100130370
LOC107985021
C17orf89
LOC400627
FSCN2
LOC105371921
MIR3065
MIR3186
LINC00482
ACTG1
LOC105371925
HGS
AATK
LOC100129503
MIR657
TSPAN10
SLC25A10
MRPL12
ARL16
BAIAP2
FAAP100
MIR1250
OXLD1
CHMP6
|
| nsv428351 | Chr.17:81152631 - 83064073 on Build GRCh38 | Gain |
ARHGDIA
RFNG
MIR6786
NOTUM
MIR4740
ALYREF
NPLOC4
STRA13
GCGR
LRRC45
SNORD134
RAB40B
CCDC137
MAFG-AS1
SLC38A10
LOC100130370
TBCD
C17orf89
FASN
OGFOD3
LOC105376791
CSNK1D
FOXK2
CD7
FN3KRP
LINC00482
C17orf62
HGS
LOC105371944
AATK
ZNF750
DCXR
TSPAN10
SLC25A10
PPP1R27
MRPL12
ARL16
MIR6787
FN3K
P4HB
HEXDC
NARF
PDE6G
UTS2R
CEP131
TMEM105
TEPSIN
SLC16A3
B3GNTL1
MYADML2
MAFG
LOC105376790
GPS1
MCRIP1
CCDC57
RAC3
BAHCC1
ASPSCR1
AATK-AS1
FSCN2
WDR45B
NPB
PYCR1
MIR4525
MIR3186
SIRT7
ACTG1
TEX19
DUS1L
LOC105371925
ANAPC11
SECTM1
LOC101929511
PCYT2
LOC101929552
FAAP100
OXLD1
|
| nsv576175 | Chr.17:81349843 - 81509075 on Build GRCh38 | Loss |
BAHCC1
MIR3186
LOC100130370
MIR4740
|
| nsv2163 | Chr.17:81412129 - 81446240 on Build GRCh38 | Insertion |
BAHCC1
|
| nsv1160500 | Chr.17:81402211 - 81421889 on Build GRCh38 | Duplication |
BAHCC1
|
| nsv576176 | Chr.17:81406747 - 81526679 on Build GRCh38 | Loss |
BAHCC1
MIR3186
ACTG1
FSCN2
|
| nsv576174 | Chr.17:81328349 - 81446410 on Build GRCh38 | Loss |
BAHCC1
TMEM105
LOC100130370
MIR4740
|
| nsv165 | Chr.17:81412148 - 81437932 on Build GRCh38 | Insertion |
BAHCC1
|
| nsv1057744 | Chr.17:81402199 - 81462332 on Build GRCh38 | Gain |
BAHCC1
MIR3186
|
| esv1007420 | Chr.17:81411536 - 81433376 on Build GRCh38 | Insertion |
BAHCC1
|
| nsv952389 | Chr.17:81137501 - 81593774 on Build GRCh38 | Deletion |
CEP131
TMEM105
TEPSIN
MIR3186
LINC00482
ACTG1
MIR4740
LOC105371925
AATK
NPLOC4
BAHCC1
AATK-AS1
SLC38A10
LOC100130370
C17orf89
FSCN2
FAAP100
|
Back To Top추가 정보
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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