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Analyze GeneStrainQTL List |
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Gene Annotator (Annotation Comparison) |
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MOET (Multi-Ontology Enrichement) |
GOLF (Gene-Ortholog Location Finder) |
Imported Annotations - CTD | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Frontotemporal Lobar Degeneration | EXP | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:20154673 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Gene-Chemical Interaction AnnotationsGene Ontology AnnotationsPhenotype AnnotationsDisease Annotations
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Gene-Chemical Interaction Annotations
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Gene Ontology Annotations
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Phenotype Annotations
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References - curatedReferences - uncurated| PubMed | 8125298 9847074 12477932 12690205 12853948 14702039 15489334 16344560 17081983 17207965 20154673 20383883 21104415 21220649 21354975 21873635 22511793 22855871 22889924 22895706 22952603 23006423 23136129 23376485 23648065 23742080 24166182 24252750 24343233 24357581 24385136 24442578 24731779 24872421 24899141 25066864 25085782 25096617 25114081 25470345 25653292 26186194 26651479 27543298 27563066 28126008 28330615 28441426 28446602 28460069 28477711 28514442 28888721 29056226 29180619 29186371 29568061 29970152 30013069 30332472 30390709 |
Comparative Map Data| TMEM106B (Homo sapiens - human) |
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| Tmem106b (Mus musculus - house mouse) |
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| Tmem106b (Rattus norvegicus - Norway rat) |
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| Tmem106b (Chinchilla lanigera - long-tailed chinchilla) |
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| TMEM106B (Pan paniscus - bonobo/pygmy chimpanzee) |
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| TMEM106B (Canis lupus familiaris - dog) |
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| Tmem106b (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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| TMEM106B (Sus scrofa - pig) |
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Position Markers| RH45871 |
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| RH77854 |
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| RH93650 |
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| SHGC-64764 |
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| SHGC-106068 |
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| STS-N51331 |
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| RH48003 |
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| SHGC-31421 |
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| GDB:1318094 |
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miRNA Target Status
| 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. |
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Nucleotide Sequences| RefSeq Transcripts | NM_001134232 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| NM_018374 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| XM_005249789 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| GenBank Nucleotide | AC007321 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| AK001834 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK002135 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK090805 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK223263 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK311651 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AX191597 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC028108 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC033901 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC039741 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| CH236948 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| CH471073 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| DA452299 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| RefSeq Acc Id: | NM_001134232 ⟹ NP_001127704 | ||||||||||||||||||||||||||||||||||
| RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||||
| Type: | CODING | ||||||||||||||||||||||||||||||||||
| Position: |
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| Sequence: |
AGGCGCGGACGCAGGTTACAGCAGCGCTTGGCCTCTGCTGATGCCGTCGTTATCCTACCCCTCChide sequence |
| RefSeq Acc Id: | NM_018374 ⟹ NP_060844 | |||||||||||||||||||||||||||||||||||||||
| RefSeq Status: | VALIDATED | |||||||||||||||||||||||||||||||||||||||
| Type: | CODING | |||||||||||||||||||||||||||||||||||||||
| Position: |
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| Sequence: |
AGGCGCGGACGCAGGTTACAGCAGCGCTTGGCCTCTGCTGATGCCGTCGTTATCCTACCCCTCChide sequence |
| RefSeq Acc Id: | XM_005249789 ⟹ XP_005249846 | |||||||||
| RefSeq Status: | ||||||||||
| Type: | CODING | |||||||||
| Position: |
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| Sequence: |
AGCTCTACGGCGGCCGCGCGCTCCAGGCCGGTCGCTCCACCCCCCGGCTCCCGGGACTGTGGAChide sequence |
Protein Sequences| Protein RefSeqs | NP_001127704 | (Get FASTA) | NCBI Sequence Viewer |
| NP_060844 | (Get FASTA) | NCBI Sequence Viewer | |
| XP_005249846 | (Get FASTA) | NCBI Sequence Viewer | |
| GenBank Protein | AAH28108 | (Get FASTA) | NCBI Sequence Viewer |
| AAH33901 | (Get FASTA) | NCBI Sequence Viewer | |
| AAH39741 | (Get FASTA) | NCBI Sequence Viewer | |
| AAQ96840 | (Get FASTA) | NCBI Sequence Viewer | |
| BAA92099 | (Get FASTA) | NCBI Sequence Viewer | |
| BAD96983 | (Get FASTA) | NCBI Sequence Viewer | |
| CAC51183 | (Get FASTA) | NCBI Sequence Viewer | |
| EAL24296 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW93638 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW93639 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW93640 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW93641 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW93642 | (Get FASTA) | NCBI Sequence Viewer | |
| Q9NUM4 | (Get FASTA) | NCBI Sequence Viewer |
| RefSeq Acc Id: | NP_060844 ⟸ NM_018374 |
| - UniProtKB: | Q9NUM4 (UniProtKB/Swiss-Prot), A0A024R9Z1 (UniProtKB/TrEMBL) |
| - Sequence: |
MGKSLSHLPLHSSKEDAYDGVTSENMRNGLVNSEVHNEDGRNGDVSQFPYVEFTGRDSVTCPTChide sequence |
| RefSeq Acc Id: | NP_001127704 ⟸ NM_001134232 |
| - UniProtKB: | Q9NUM4 (UniProtKB/Swiss-Prot), A0A024R9Z1 (UniProtKB/TrEMBL) |
| - Sequence: |
MGKSLSHLPLHSSKEDAYDGVTSENMRNGLVNSEVHNEDGRNGDVSQFPYVEFTGRDSVTCPTChide sequence |
| RefSeq Acc Id: | XP_005249846 ⟸ XM_005249789 |
| - Peptide Label: | isoform X1 |
| - UniProtKB: | Q9NUM4 (UniProtKB/Swiss-Prot), A0A024R9Z1 (UniProtKB/TrEMBL) |
| - Sequence: |
MGKSLSHLPLHSSKEDAYDGVTSENMRNGLVNSEVHNEDGRNGDVSQFPYVEFTGRDSVTCPTChide sequence |
Promoters| RGD ID: | 7209951 | |||||||||
| Promoter ID: | EPDNEW_H10719 | |||||||||
| Type: | initiation region | |||||||||
| Name: | TMEM106B_1 | |||||||||
| Description: | transmembrane protein 106B | |||||||||
| SO ACC ID: | SO:0000170 | |||||||||
| Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
| Experiment Methods: | Single-end sequencing. | |||||||||
| Position: |
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| RGD ID: | 6806284 | |||||||||
| Promoter ID: | HG_KWN:56340 | |||||||||
| Type: | CpG-Island | |||||||||
| SO ACC ID: | SO:0000170 | |||||||||
| Source: | MPROMDB | |||||||||
| Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4 | |||||||||
| Transcripts: | NM_001134232, NM_018374, OTTHUMT00000325799, OTTHUMT00000325865, OTTHUMT00000325866, OTTHUMT00000325867, UC003SSI.1 | |||||||||
| Position: |
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Clinical Variants| Name | Type | Condition(s) | Position(s) | Clinical significance |
| GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3 | copy number gain | Global developmental delay [RCV000051159]|See cases [RCV000051159] | Chr7:54185..41875885 [GRCh38] Chr7:54185..41915483 [GRCh37] Chr7:149268..41882008 [NCBI36] Chr7:7p22.3-14.1 |
pathogenic |
| GRCh38/hg38 7p21.3-15.3(chr7:8274775-21988311)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052280]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052280]|See cases [RCV000052280] | Chr7:8274775..21988311 [GRCh38] Chr7:8314405..22027929 [GRCh37] Chr7:8280930..21994454 [NCBI36] Chr7:7p21.3-15.3 |
pathogenic |
| GRCh38/hg38 7p21.3-21.1(chr7:9975653-19356878)x1 | copy number loss | Plagiocephaly [RCV000052281]|See cases [RCV000052281] | Chr7:9975653..19356878 [GRCh38] Chr7:10015280..19396501 [GRCh37] Chr7:9981805..19363026 [NCBI36] Chr7:7p21.3-21.1 |
pathogenic |
| GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 | copy number loss | Ambiguous genitalia [RCV000052250]|See cases [RCV000052250] | Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh38/hg38 7p22.3-15.3(chr7:53985-24361531)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053528]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053528]|See cases [RCV000053528] | Chr7:53985..24361531 [GRCh38] Chr7:53985..24401150 [GRCh37] Chr7:149068..24367675 [NCBI36] Chr7:7p22.3-15.3 |
pathogenic |
| GRCh38/hg38 7p22.3-14.2(chr7:54185-37089712)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053530]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053530]|See cases [RCV000053530] | Chr7:54185..37089712 [GRCh38] Chr7:54185..37129317 [GRCh37] Chr7:149268..37095842 [NCBI36] Chr7:7p22.3-14.2 |
pathogenic |
| GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 | copy number loss | See cases [RCV000135401] | Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh38/hg38 7p22.3-15.2(chr7:54185-26827634)x3 | copy number gain | See cases [RCV000136557] | Chr7:54185..26827634 [GRCh38] Chr7:54185..26867253 [GRCh37] Chr7:149268..26833778 [NCBI36] Chr7:7p22.3-15.2 |
pathogenic |
| GRCh38/hg38 7p21.3(chr7:12109334-12653407)x3 | copy number gain | See cases [RCV000137033] | Chr7:12109334..12653407 [GRCh38] Chr7:12148960..12693032 [GRCh37] Chr7:12115485..12659557 [NCBI36] Chr7:7p21.3 |
benign |
| GRCh38/hg38 7p22.1-15.2(chr7:5682209-27230311)x3 | copy number gain | See cases [RCV000136649] | Chr7:5682209..27230311 [GRCh38] Chr7:5721840..27269930 [GRCh37] Chr7:5688366..27236455 [NCBI36] Chr7:7p22.1-15.2 |
pathogenic |
| GRCh38/hg38 7p22.3-15.3(chr7:45130-25221165)x3 | copy number gain | See cases [RCV000137824] | Chr7:45130..25221165 [GRCh38] Chr7:45130..25260784 [GRCh37] Chr7:140213..25227309 [NCBI36] Chr7:7p22.3-15.3 |
pathogenic |
| GRCh38/hg38 7p21.3(chr7:11181583-12423003)x3 | copy number gain | See cases [RCV000141626] | Chr7:11181583..12423003 [GRCh38] Chr7:11221210..12462629 [GRCh37] Chr7:11187735..12429154 [NCBI36] Chr7:7p21.3 |
uncertain significance |
| GRCh38/hg38 7p22.3-15.2(chr7:1698124-27207295)x3 | copy number gain | See cases [RCV000143060] | Chr7:1698124..27207295 [GRCh38] Chr7:1737760..27246914 [GRCh37] Chr7:1704286..27213439 [NCBI36] Chr7:7p22.3-15.2 |
pathogenic |
| GRCh38/hg38 7p21.3-21.2(chr7:11122492-16479303)x1 | copy number loss | See cases [RCV000142652] | Chr7:11122492..16479303 [GRCh38] Chr7:11162119..16518928 [GRCh37] Chr7:11128644..16485453 [NCBI36] Chr7:7p21.3-21.2 |
pathogenic |
| GRCh38/hg38 7p21.3-15.2(chr7:10610069-25760560)x1 | copy number loss | See cases [RCV000142708] | Chr7:10610069..25760560 [GRCh38] Chr7:10649696..25800180 [GRCh37] Chr7:10616221..25766705 [NCBI36] Chr7:7p21.3-15.2 |
pathogenic |
| GRCh38/hg38 7p22.3-15.2(chr7:43360-27196404)x3 | copy number gain | See cases [RCV000143586] | Chr7:43360..27196404 [GRCh38] Chr7:43360..27236023 [GRCh37] Chr7:138443..27202548 [NCBI36] Chr7:7p22.3-15.2 |
pathogenic |
| TMEM106B-BRAF fusion | deletion | Pleomorphic xanthoastrocytoma [RCV000454357] | Chr7:12258147..140494267 [GRCh37] Chr7:7p21.3-q34 |
pathogenic |
| GRCh37/hg19 7p22.3-21.3(chr7:183556-12746636)x3 | copy number gain | See cases [RCV000449446] | Chr7:183556..12746636 [GRCh37] Chr7:7p22.3-21.3 |
pathogenic |
| GRCh37/hg19 7p22.3-21.1(chr7:43360-17656861)x3 | copy number gain | See cases [RCV000449347] | Chr7:43360..17656861 [GRCh37] Chr7:7p22.3-21.1 |
pathogenic |
| GRCh37/hg19 7p21.3-14.2(chr7:11562624-36395416)x3 | copy number gain | See cases [RCV000446478] | Chr7:11562624..36395416 [GRCh37] Chr7:7p21.3-14.2 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 | copy number loss | See cases [RCV000446044] | Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p21.3-12.1(chr7:11048840-52863626)x3 | copy number gain | See cases [RCV000512091] | Chr7:11048840..52863626 [GRCh37] Chr7:7p21.3-12.1 |
pathogenic |
| GRCh37/hg19 7p22.3-15.3(chr7:43360-23674928)x3 | copy number gain | See cases [RCV000510652] | Chr7:43360..23674928 [GRCh37] Chr7:7p22.3-15.3 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) | copy number gain | See cases [RCV000510686] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p22.3-14.3(chr7:704573-29257946)x3 | copy number gain | See cases [RCV000510275] | Chr7:704573..29257946 [GRCh37] Chr7:7p22.3-14.3 |
pathogenic |
| GRCh37/hg19 7p21.3(chr7:9645570-12393614)x3 | copy number gain | See cases [RCV000510670] | Chr7:9645570..12393614 [GRCh37] Chr7:7p21.3 |
uncertain significance |
| GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 | copy number gain | See cases [RCV000511549] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p21.3(chr7:12217852-12522283)x1 | copy number loss | See cases [RCV000511517] | Chr7:12217852..12522283 [GRCh37] Chr7:7p21.3 |
uncertain significance |
| GRCh37/hg19 7p21.3-21.1(chr7:7660104-18400293)x3 | copy number gain | See cases [RCV000511575] | Chr7:7660104..18400293 [GRCh37] Chr7:7p21.3-21.1 |
uncertain significance |
| GRCh37/hg19 7p22.3-21.2(chr7:43360-14664158)x3 | copy number gain | See cases [RCV000511772] | Chr7:43360..14664158 [GRCh37] Chr7:7p22.3-21.2 |
pathogenic |
| NM_001134232.2(TMEM106B):c.754G>A (p.Asp252Asn) | single nucleotide variant | LEUKODYSTROPHY, HYPOMYELINATING, 16 [RCV000626490] | Chr7:12231904 [GRCh38] Chr7:12271530 [GRCh37] Chr7:7p21.3 |
pathogenic|likely pathogenic |
| GRCh37/hg19 7p21.3(chr7:12229501-12303848)x1 | copy number loss | not provided [RCV000682774] | Chr7:12229501..12303848 [GRCh37] Chr7:7p21.3 |
uncertain significance |
| GRCh37/hg19 7p21.3(chr7:11970873-12259649)x1 | copy number loss | not provided [RCV000682816] | Chr7:11970873..12259649 [GRCh37] Chr7:7p21.3 |
uncertain significance |
| GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 | copy number gain | not provided [RCV000746280] | Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 | copy number gain | not provided [RCV000746278] | Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p21.3(chr7:12253880-12300751)x1 | copy number loss | not provided [RCV000746476] | Chr7:12253880..12300751 [GRCh37] Chr7:7p21.3 |
benign |
| GRCh37/hg19 7p21.3(chr7:12269417-12277081)x4 | copy number gain | not provided [RCV000746477] | Chr7:12269417..12277081 [GRCh37] Chr7:7p21.3 |
benign |
| GRCh37/hg19 7p21.3(chr7:12269417-12286409)x4 | copy number gain | not provided [RCV000746478] | Chr7:12269417..12286409 [GRCh37] Chr7:7p21.3 |
benign |
| GRCh37/hg19 7p21.3(chr7:12271666-12286409)x3 | copy number gain | not provided [RCV000746479] | Chr7:12271666..12286409 [GRCh37] Chr7:7p21.3 |
benign |
| GRCh37/hg19 7p21.3(chr7:12272026-12276522)x4 | copy number gain | not provided [RCV000746480] | Chr7:12272026..12276522 [GRCh37] Chr7:7p21.3 |
benign |
| GRCh37/hg19 7p22.3-21.3(chr7:10239-13116278)x3 | copy number gain | not provided [RCV000746277] | Chr7:10239..13116278 [GRCh37] Chr7:7p22.3-21.3 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 | copy number gain | not provided [RCV000848126] | Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p21.3(chr7:12272341-12311788)x1 | copy number loss | not provided [RCV000848761] | Chr7:12272341..12311788 [GRCh37] Chr7:7p21.3 |
uncertain significance |
| GRCh37/hg19 7p22.3-21.1(chr7:43376-19520619)x3 | copy number gain | not provided [RCV000848100] | Chr7:43376..19520619 [GRCh37] Chr7:7p22.3-21.1 |
pathogenic |
| GRCh37/hg19 7p21.3(chr7:12109939-13730434)x3 | copy number gain | not provided [RCV000846616] | Chr7:12109939..13730434 [GRCh37] Chr7:7p21.3 |
uncertain significance |
External Database Links| Database | Acc Id | Source(s) |
| AGR Gene | HGNC:22407 | AgrOrtholog |
| COSMIC | TMEM106B | COSMIC |
| Ensembl Genes | ENSG00000106460 | ENTREZGENE, UniProtKB/Swiss-Prot |
| Ensembl Protein | ENSP00000379901 | ENTREZGENE, UniProtKB/Swiss-Prot |
| ENSP00000379902 | ENTREZGENE, UniProtKB/Swiss-Prot | |
| ENSP00000391016 | UniProtKB/TrEMBL | |
| ENSP00000391985 | UniProtKB/TrEMBL | |
| ENSP00000401302 | UniProtKB/TrEMBL | |
| Ensembl Transcript | ENST00000396667 | ENTREZGENE, UniProtKB/Swiss-Prot |
| ENST00000396668 | ENTREZGENE, UniProtKB/Swiss-Prot | |
| ENST00000420833 | UniProtKB/TrEMBL | |
| ENST00000442107 | UniProtKB/TrEMBL | |
| ENST00000444443 | UniProtKB/TrEMBL | |
| GTEx | ENSG00000106460 | GTEx |
| HGNC ID | HGNC:22407 | ENTREZGENE |
| Human Proteome Map | TMEM106B | Human Proteome Map |
| InterPro | DUF1356_TMEM106 | UniProtKB/Swiss-Prot |
| KEGG Report | hsa:54664 | UniProtKB/Swiss-Prot |
| NCBI Gene | 54664 | ENTREZGENE |
| OMIM | 613413 | OMIM |
| 617964 | OMIM | |
| PANTHER | PTHR28556 | UniProtKB/Swiss-Prot |
| Pfam | DUF1356 | UniProtKB/Swiss-Prot |
| PharmGKB | PA142670756 | PharmGKB |
| UniGene | Hs.396358 | ENTREZGENE |
| UniProt | A0A024R9Z1 | ENTREZGENE, UniProtKB/TrEMBL |
| C9J998_HUMAN | UniProtKB/TrEMBL | |
| C9JZ87_HUMAN | UniProtKB/TrEMBL | |
| F2Z3N7_HUMAN | UniProtKB/TrEMBL | |
| Q8N353_HUMAN | UniProtKB/TrEMBL | |
| Q9NUM4 | ENTREZGENE, UniProtKB/Swiss-Prot | |
| UniProt Secondary | A4D108 | UniProtKB/Swiss-Prot |
| Q53FL9 | UniProtKB/Swiss-Prot | |
| Q8N4L0 | UniProtKB/Swiss-Prot |
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| More on TMEM106B | |
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Alliance Gene |
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NCBI Gene |
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Ensembl Gene |
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JBrowse: hg19 hg38 |
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HGNC Report |
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NCBI Genome Data Viewer |
| CRRD Object Information | |
| CRRD ID: | 1603394 |
| Created: | 2007-04-28 |
| Species: | Homo sapiens |
| Last Modified: | 2019-11-26 |
| Status: | ACTIVE |
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.
