![]()
Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | BCL7C | Human | Ependymomas | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:26075792 | |
|
![]()
Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | BCL7C | Human | Ependymomas | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:26075792 | |
|
|
|
|
|
# | Reference Title | Reference Citation |
1. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
2. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:8605326 | PMID:8804307 | PMID:9931421 | PMID:10078207 | PMID:10778858 | PMID:11790558 | PMID:12192000 | PMID:12215535 | PMID:12477932 | PMID:15302935 | PMID:15345747 | PMID:15489334 |
PMID:17081983 | PMID:17207965 | PMID:18809673 | PMID:19279220 | PMID:19336552 | PMID:19573080 | PMID:19759913 | PMID:19773279 | PMID:20467437 | PMID:21555454 | PMID:21832049 | PMID:23275444 |
PMID:23644491 | PMID:24981860 | PMID:25066234 | PMID:26186194 | PMID:26344197 | PMID:26496610 | PMID:27634302 | PMID:28514442 | PMID:29374058 | PMID:30510198 | PMID:30554943 | PMID:30884312 |
PMID:30945288 | PMID:31043422 | PMID:31753913 | PMID:33306126 | PMID:33640491 | PMID:33961781 | PMID:34079125 | PMID:34591612 | PMID:35013218 | PMID:35140242 | PMID:35271311 | PMID:36089195 |
PMID:38297188 |
BCL7C (Homo sapiens - human) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bcl7c (Mus musculus - house mouse) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bcl7c (Rattus norvegicus - Norway rat) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bcl7c (Chinchilla lanigera - long-tailed chinchilla) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
LOC100971944 (Pan paniscus - bonobo/pygmy chimpanzee) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BCL7C (Canis lupus familiaris - dog) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bcl7c (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BCL7C (Sus scrofa - pig) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BCL7C (Chlorocebus sabaeus - green monkey) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bcl7c (Heterocephalus glaber - naked mole-rat) |
|
.
Variants in BCL7C
19 total Variants ![]() |
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_004765.3(BCL7C):c.349G>A (p.Gly117Ser) | single nucleotide variant | Malignant melanoma [RCV000071095] | Chr16:30892679 [GRCh38] Chr16:30904000 [GRCh37] Chr16:30811501 [NCBI36] Chr16:16p11.2 |
not provided |
GRCh38/hg38 16p11.2-11.1(chr16:30691912-36160463)x3 | copy number gain | See cases [RCV000133811] | Chr16:30691912..36160463 [GRCh38] Chr16:30703233..35147508 [GRCh37] Chr16:30610734..35005009 [NCBI36] Chr16:16p11.2-11.1 |
pathogenic |
GRCh38/hg38 16p11.2(chr16:29909613-31438697)x3 | copy number gain | See cases [RCV000135339] | Chr16:29909613..31438697 [GRCh38] Chr16:29920934..31450018 [GRCh37] Chr16:29828435..31357519 [NCBI36] Chr16:16p11.2 |
pathogenic |
GRCh38/hg38 16p12.1-11.2(chr16:27311746-31193406)x3 | copy number gain | See cases [RCV000140341] | Chr16:27311746..31193406 [GRCh38] Chr16:27323067..31204727 [GRCh37] Chr16:27230568..31112228 [NCBI36] Chr16:16p12.1-11.2 |
pathogenic |
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3 | copy number gain | See cases [RCV000141141] | Chr16:23752047..31943755 [GRCh38] Chr16:23763368..31955076 [GRCh37] Chr16:23670869..31862577 [NCBI36] Chr16:16p12.2-11.2 |
pathogenic |
GRCh37/hg19 16p11.2(chr16:30391304-31122666)x3 | copy number gain | Breast ductal adenocarcinoma [RCV000207028] | Chr16:30391304..31122666 [GRCh37] Chr16:16p11.2 |
uncertain significance |
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 | copy number gain | Breast ductal adenocarcinoma [RCV000207053] | Chr16:1279324..31926800 [GRCh37] Chr16:16p13.3-11.2 |
uncertain significance |
Single allele | deletion | Branched-chain keto acid dehydrogenase kinase deficiency [RCV000735205] | Chr16:30554158..31536880 [GRCh37] Chr16:16p11.2 |
uncertain significance |
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 | copy number gain | See cases [RCV000446684] | Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3 |
pathogenic |
GRCh37/hg19 16p11.2(chr16:30830287-31827011)x4 | copy number gain | See cases [RCV000447708] | Chr16:30830287..31827011 [GRCh37] Chr16:16p11.2 |
uncertain significance |
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1 | copy number loss | See cases [RCV000448084] | Chr16:28826162..29043901 [GRCh37] Chr16:16p11.2 |
likely pathogenic |
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 | copy number gain | See cases [RCV000511622] | Chr16:9273328..89548493 [GRCh37] Chr16:16p13.2-q24.3 |
uncertain significance |
GRCh37/hg19 16p11.2(chr16:30607048-31117069)x1 | copy number loss | See cases [RCV000511454] | Chr16:30607048..31117069 [GRCh37] Chr16:16p11.2 |
uncertain significance |
maternal UPD(16p) | complex | Hemimegalencephaly [RCV000494707] | Chr16:1280042..33710558 [GRCh37] Chr16:16p13.3-11.2 |
pathogenic |
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 | copy number gain | See cases [RCV000512138] | Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3 |
pathogenic |
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) | copy number gain | See cases [RCV000511296] | Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3 |
pathogenic |
NM_004765.4(BCL7C):c.109A>G (p.Thr37Ala) | single nucleotide variant | not specified [RCV004310782] | Chr16:30893274 [GRCh38] Chr16:30904595 [GRCh37] Chr16:16p11.2 |
uncertain significance |
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 | copy number gain | not provided [RCV000738918] | Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3 |
pathogenic |
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 | copy number gain | not provided [RCV000738915] | Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3 |
pathogenic |
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 | copy number gain | not provided [RCV000738917] | Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3 |
pathogenic |
GRCh37/hg19 16p11.2(chr16:30738551-34194635)x3 | copy number gain | not provided [RCV000739123] | Chr16:30738551..34194635 [GRCh37] Chr16:16p11.2 |
benign |
GRCh37/hg19 16p11.2(chr16:30851860-31156762)x1 | copy number loss | not provided [RCV000848082] | Chr16:30851860..31156762 [GRCh37] Chr16:16p11.2 |
pathogenic |
GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001) | copy number gain | Microcephaly [RCV001252948] | Chr16:5805001..34230001 [GRCh37] Chr16:16p13.3-11.2 |
pathogenic |
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3 | copy number gain | not provided [RCV001258619] | Chr16:30350747..31905898 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NC_000016.9:g.(?_30712146)_(31021717_?)dup | duplication | Generalized epilepsy with febrile seizures plus, type 9 [RCV003122990] | Chr16:30712146..31021717 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.251G>C (p.Gly84Ala) | single nucleotide variant | not specified [RCV004318604] | Chr16:30892869 [GRCh38] Chr16:30904190 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.422C>A (p.Pro141Gln) | single nucleotide variant | not specified [RCV004332185] | Chr16:30892606 [GRCh38] Chr16:30903927 [GRCh37] Chr16:16p11.2 |
uncertain significance |
GRCh37/hg19 16p11.2(chr16:30460206-30906733)x3 | copy number gain | not provided [RCV002475788] | Chr16:30460206..30906733 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.224G>A (p.Arg75Gln) | single nucleotide variant | not specified [RCV004119189] | Chr16:30892896 [GRCh38] Chr16:30904217 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.73A>G (p.Ile25Val) | single nucleotide variant | not specified [RCV004177074] | Chr16:30893872 [GRCh38] Chr16:30905193 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.188G>A (p.Gly63Asp) | single nucleotide variant | not specified [RCV004153592] | Chr16:30892932 [GRCh38] Chr16:30904253 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.528+3G>C | single nucleotide variant | not provided [RCV002510557] | Chr16:30888857 [GRCh38] Chr16:30900178 [GRCh37] Chr16:16p11.2 |
not provided |
NM_004765.4(BCL7C):c.617C>A (p.Pro206Gln) | single nucleotide variant | not specified [RCV004071140] | Chr16:30887902 [GRCh38] Chr16:30899223 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.308C>T (p.Ser103Leu) | single nucleotide variant | not specified [RCV004108134] | Chr16:30892720 [GRCh38] Chr16:30904041 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.425G>A (p.Arg142Gln) | single nucleotide variant | not specified [RCV004086358] | Chr16:30892603 [GRCh38] Chr16:30903924 [GRCh37] Chr16:16p11.2 |
likely benign |
NM_004765.4(BCL7C):c.535G>A (p.Glu179Lys) | single nucleotide variant | not specified [RCV004332811] | Chr16:30887984 [GRCh38] Chr16:30899305 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.602C>T (p.Ser201Leu) | single nucleotide variant | not specified [RCV004300049] | Chr16:30887917 [GRCh38] Chr16:30899238 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.220C>T (p.Arg74Cys) | single nucleotide variant | not specified [RCV004426335] | Chr16:30892900 [GRCh38] Chr16:30904221 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NC_000016.9:g.(?_28889993)_(31202759_?)del | deletion | Dilated Cardiomyopathy, Dominant [RCV004582801] | Chr16:28889993..31202759 [GRCh37] Chr16:16p11.2 |
uncertain significance |
NM_004765.4(BCL7C):c.643C>T (p.Pro215Ser) | single nucleotide variant | not specified [RCV004605855] | Chr16:30887876 [GRCh38] Chr16:30899197 [GRCh37] Chr16:16p11.2 |
uncertain significance |
The detailed report is available here: | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer |
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
The following QTLs overlap with this region. | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer | ![]() | Gviewer |
D16S3338 |
|
adipose tissue
|
alimentary part of gastrointestinal system
|
appendage
|
circulatory system
|
ectoderm
|
endocrine system
|
endoderm
|
entire extraembryonic component
|
exocrine system
|
hemolymphoid system
|
hepatobiliary system
|
integumental system
|
mesenchyme
|
mesoderm
|
musculoskeletal system
|
nervous system
|
pharyngeal arch
|
renal system
|
reproductive system
|
respiratory system
|
sensory system
|
visual system
|
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1204 | 2438 | 2788 | 2251 | 4973 | 1726 | 2351 | 5 | 624 | 1949 | 465 | 2269 | 7302 | 6469 | 53 | 3734 | 1 | 852 | 1744 | 1617 | 175 | 1 |
RefSeq Transcripts | NM_001286526 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_004765 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011545980 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017023885 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017023886 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017023887 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017023888 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047434896 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047434897 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047434898 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047434899 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047434900 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314371 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314372 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314373 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314374 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314375 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314376 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054314377 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AC135048 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC138417 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AJ223980 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC019071 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC058863 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BG055884 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471192 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068262 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
MW804112 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
Ensembl Acc Id: | ENST00000215115 ⟹ ENSP00000215115 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000380317 ⟹ ENSP00000369674 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000572628 ⟹ ENSP00000459007 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000574418 ⟹ ENSP00000461177 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000576194 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001286526 ⟹ NP_001273455 | ||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||
Position: |
|
||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_004765 ⟹ NP_004756 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | XM_011545980 ⟹ XP_011544282 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_047434896 ⟹ XP_047290852 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047434897 ⟹ XP_047290853 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047434898 ⟹ XP_047290854 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047434899 ⟹ XP_047290855 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047434900 ⟹ XP_047290856 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314371 ⟹ XP_054170346 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314372 ⟹ XP_054170347 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314373 ⟹ XP_054170348 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314374 ⟹ XP_054170349 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314375 ⟹ XP_054170350 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314376 ⟹ XP_054170351 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054314377 ⟹ XP_054170352 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Protein RefSeqs | NP_001273455 | (Get FASTA) | NCBI Sequence Viewer |
NP_004756 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011544282 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047290852 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047290853 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047290854 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047290855 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047290856 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170346 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170347 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170348 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170349 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170350 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170351 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054170352 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH19071 | (Get FASTA) | NCBI Sequence Viewer |
AAH58863 | (Get FASTA) | NCBI Sequence Viewer | |
CAA11754 | (Get FASTA) | NCBI Sequence Viewer | |
EAW52193 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000215115 | ||
ENSP00000215115.4 | |||
ENSP00000369674 | |||
ENSP00000369674.4 | |||
ENSP00000459007 | |||
ENSP00000459007.1 | |||
ENSP00000461177 | |||
ENSP00000461177.1 | |||
GenBank Protein | Q8WUZ0 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_004756 ⟸ NM_004765 |
- Peptide Label: | isoform 2 |
- UniProtKB: | Q8WUZ0 (UniProtKB/Swiss-Prot), O43770 (UniProtKB/Swiss-Prot), Q6PD89 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001273455 ⟸ NM_001286526 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q8WUZ0 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | XP_011544282 ⟸ XM_011545980 |
- Peptide Label: | isoform X2 |
- UniProtKB: | I3L1Q2 (UniProtKB/TrEMBL) |
- Sequence: |
Ensembl Acc Id: | ENSP00000215115 ⟸ ENST00000215115 |
Ensembl Acc Id: | ENSP00000459007 ⟸ ENST00000572628 |
Ensembl Acc Id: | ENSP00000461177 ⟸ ENST00000574418 |
Ensembl Acc Id: | ENSP00000369674 ⟸ ENST00000380317 |
RefSeq Acc Id: | XP_047290854 ⟸ XM_047434898 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_047290853 ⟸ XM_047434897 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_047290852 ⟸ XM_047434896 |
- Peptide Label: | isoform X1 |
- UniProtKB: | I3L1Q2 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047290855 ⟸ XM_047434899 |
- Peptide Label: | isoform X5 |
RefSeq Acc Id: | XP_047290856 ⟸ XM_047434900 |
- Peptide Label: | isoform X6 |
- UniProtKB: | I3L4D5 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054170347 ⟸ XM_054314372 |
- Peptide Label: | isoform X2 |
- UniProtKB: | I3L1Q2 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054170349 ⟸ XM_054314374 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054170348 ⟸ XM_054314373 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_054170346 ⟸ XM_054314371 |
- Peptide Label: | isoform X1 |
- UniProtKB: | I3L1Q2 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054170350 ⟸ XM_054314375 |
- Peptide Label: | isoform X7 |
RefSeq Acc Id: | XP_054170351 ⟸ XM_054314376 |
- Peptide Label: | isoform X5 |
RefSeq Acc Id: | XP_054170352 ⟸ XM_054314377 |
- Peptide Label: | isoform X6 |
- UniProtKB: | I3L4D5 (UniProtKB/TrEMBL) |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q8WUZ0-F1-model_v2 | AlphaFold | Q8WUZ0 | 1-217 | view protein structure |
RGD ID: | 6792999 | ||||||||
Promoter ID: | HG_KWN:23576 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell, HeLa_S3, K562, Lymphoblastoid | ||||||||
Transcripts: | ENST00000358950, OTTHUMT00000255547, OTTHUMT00000255548 | ||||||||
Position: |
|
RGD ID: | 7232029 | ||||||||
Promoter ID: | EPDNEW_H21760 | ||||||||
Type: | initiation region | ||||||||
Name: | BCL7C_1 | ||||||||
Description: | BCL tumor suppressor 7C | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:1006 | AgrOrtholog |
COSMIC | BCL7C | COSMIC |
Ensembl Genes | ENSG00000099385 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000215115 | ENTREZGENE |
ENST00000215115.5 | UniProtKB/Swiss-Prot | |
ENST00000380317 | ENTREZGENE | |
ENST00000380317.8 | UniProtKB/Swiss-Prot | |
ENST00000572628 | ENTREZGENE | |
ENST00000572628.5 | UniProtKB/TrEMBL | |
ENST00000574418 | ENTREZGENE | |
ENST00000574418.5 | UniProtKB/TrEMBL | |
Gene3D-CATH | 1.10.10.1450 | UniProtKB/TrEMBL |
GTEx | ENSG00000099385 | GTEx |
HGNC ID | HGNC:1006 | ENTREZGENE |
Human Proteome Map | BCL7C | Human Proteome Map |
InterPro | BCL7 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Mos1_HTH | UniProtKB/TrEMBL | |
KEGG Report | hsa:9274 | UniProtKB/Swiss-Prot |
NCBI Gene | 9274 | ENTREZGENE |
OMIM | 605847 | OMIM |
PANTHER | B-CELL CLL/LYMPHOMA 7 PROTEIN FAMILY MEMBER C | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
BAF CHROMATIN REMODELING COMPLEX SUBUNIT BCL7C | UniProtKB/TrEMBL | |
PTHR12767 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | BCL_N | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
HTH_48 | UniProtKB/TrEMBL | |
PharmGKB | PA25316 | PharmGKB |
UniProt | BCL7C_HUMAN | UniProtKB/Swiss-Prot |
I3L1Q2 | ENTREZGENE, UniProtKB/TrEMBL | |
I3L4D5 | ENTREZGENE, UniProtKB/TrEMBL | |
O43770 | ENTREZGENE | |
Q6PD89 | ENTREZGENE | |
Q8WUZ0 | ENTREZGENE | |
UniProt Secondary | O43770 | UniProtKB/Swiss-Prot |
Q6PD89 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2019-01-29 | BCL7C | BAF chromatin remodeling complex subunit BCL7C | BCL7C | BCL7C, BAF complex component | Symbol and/or name change | 5135510 | APPROVED |
2018-11-06 | BCL7C | BCL7C, BAF complex component | BCL7C | BCL tumor suppressor 7C | Symbol and/or name change | 5135510 | APPROVED |
2016-07-12 | BCL7C | BCL tumor suppressor 7C | BCL7C | B-cell CLL/lymphoma 7C | Symbol and/or name change | 5135510 | APPROVED |