Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Ovarian Neoplasms | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:35442568 | |
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Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Ovarian Neoplasms | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:35442568 | |
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# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
3. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:9817599 | PMID:11331580 | PMID:11919186 | PMID:12477932 | PMID:14702039 | PMID:15302935 | PMID:15489334 | PMID:16079077 | PMID:16169070 | PMID:16344560 | PMID:16575408 | PMID:16636064 |
PMID:18029348 | PMID:19147277 | PMID:20729920 | PMID:21044950 | PMID:21832049 | PMID:22629402 | PMID:22658674 | PMID:22863883 | PMID:23404198 | PMID:23422002 | PMID:25127057 | PMID:25333256 |
PMID:25843803 | PMID:25866896 | PMID:26186194 | PMID:26496610 | PMID:26718507 | PMID:26902425 | PMID:27693506 | PMID:27737724 | PMID:27932448 | PMID:28514442 | PMID:29295721 | PMID:30143514 |
PMID:30488195 | PMID:31521826 | PMID:31812473 | PMID:32694731 | PMID:33046716 | PMID:33111431 | PMID:33391467 | PMID:33845483 | PMID:33961781 | PMID:34135057 | PMID:34265287 | PMID:34452557 |
PMID:34978663 | PMID:35156780 | PMID:35230201 | PMID:35831314 | PMID:35906200 | PMID:36180926 | PMID:36215168 | PMID:36736316 | PMID:36811957 | PMID:37477507 | PMID:38581570 |
TRIM16 (Homo sapiens - human) |
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Trim16 (Mus musculus - house mouse) |
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Trim16 (Rattus norvegicus - Norway rat) |
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Trim16 (Chinchilla lanigera - long-tailed chinchilla) |
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TRIM16 (Pan paniscus - bonobo/pygmy chimpanzee) |
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TRIM16 (Canis lupus familiaris - dog) |
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Trim16 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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TRIM16 (Sus scrofa - pig) |
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TRIM16 (Chlorocebus sabaeus - green monkey) |
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Trim16 (Heterocephalus glaber - naked mole-rat) |
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Variants in TRIM16
25 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 17p12-11.2(chr17:15259164-20925299)x3 | copy number gain | See cases [RCV000051852] | Chr17:15259164..20925299 [GRCh38] Chr17:15162481..20828612 [GRCh37] Chr17:15103206..20769204 [NCBI36] Chr17:17p12-11.2 |
pathogenic |
GRCh38/hg38 17p12(chr17:14126296-15659587)x3 | copy number gain | See cases [RCV000051843] | Chr17:14126296..15659587 [GRCh38] Chr17:14029613..15562901 [GRCh37] Chr17:13970338..15503626 [NCBI36] Chr17:17p12 |
pathogenic |
GRCh38/hg38 17p12-11.2(chr17:15234685-20620700)x3 | copy number gain | See cases [RCV000051849] | Chr17:15234685..20620700 [GRCh38] Chr17:15138002..20524013 [GRCh37] Chr17:15078727..20464605 [NCBI36] Chr17:17p12-11.2 |
pathogenic |
GRCh38/hg38 17p12-11.2(chr17:10892259-17964282)x3 | copy number gain | See cases [RCV000052476] | Chr17:10892259..17964282 [GRCh38] Chr17:10795576..17867596 [GRCh37] Chr17:10736301..17808321 [NCBI36] Chr17:17p12-11.2 |
pathogenic |
NM_006470.3(TRIM16):c.1516C>T (p.Leu506Phe) | single nucleotide variant | Malignant melanoma [RCV000071348] | Chr17:15628794 [GRCh38] Chr17:15532108 [GRCh37] Chr17:15472833 [NCBI36] Chr17:17p12 |
not provided |
GRCh38/hg38 17p12-11.2(chr17:15210400-18280816)x3 | copy number gain | See cases [RCV000137171] | Chr17:15210400..18280816 [GRCh38] Chr17:15113717..18184130 [GRCh37] Chr17:15054442..18124855 [NCBI36] Chr17:17p12-11.2 |
pathogenic|likely pathogenic |
GRCh38/hg38 17p12(chr17:14671118-15952996)x1 | copy number loss | See cases [RCV000137782] | Chr17:14671118..15952996 [GRCh38] Chr17:14574435..15856310 [GRCh37] Chr17:14515160..15797035 [NCBI36] Chr17:17p12 |
pathogenic |
GRCh38/hg38 17p12(chr17:15190283-15952996)x3 | copy number gain | See cases [RCV000139242] | Chr17:15190283..15952996 [GRCh38] Chr17:15093600..15856310 [GRCh37] Chr17:15034325..15797035 [NCBI36] Chr17:17p12 |
pathogenic |
GRCh38/hg38 17p12(chr17:14179737-15664355)x3 | copy number gain | See cases [RCV000142324] | Chr17:14179737..15664355 [GRCh38] Chr17:14083054..15567669 [GRCh37] Chr17:14023779..15508394 [NCBI36] Chr17:17p12 |
pathogenic |
GRCh38/hg38 17p12(chr17:15140036-15708439)x3 | copy number gain | See cases [RCV000142461] | Chr17:15140036..15708439 [GRCh38] Chr17:15043353..15611753 [GRCh37] Chr17:14984078..15552478 [NCBI36] Chr17:17p12 |
uncertain significance |
GRCh38/hg38 17p12-11.2(chr17:15552362-19014200)x3 | copy number gain | See cases [RCV000142169] | Chr17:15552362..19014200 [GRCh38] Chr17:15455676..18917513 [GRCh37] Chr17:15396401..18858238 [NCBI36] Chr17:17p12-11.2 |
pathogenic |
GRCh38/hg38 17p12-11.2(chr17:15066799-17472457)x1 | copy number loss | See cases [RCV000143046] | Chr17:15066799..17472457 [GRCh38] Chr17:14970116..17375771 [GRCh37] Chr17:14910841..17316496 [NCBI36] Chr17:17p12-11.2 |
pathogenic |
GRCh37/hg19 17p12(chr17:14139857-15707850)x3 | copy number gain | See cases [RCV000239776] | Chr17:14139857..15707850 [GRCh37] Chr17:17p12 |
pathogenic |
Single allele | complex | Breast ductal adenocarcinoma [RCV000207129] | Chr17:9586165..16325968 [GRCh37] Chr17:17p13.1-11.2 |
uncertain significance |
GRCh37/hg19 17p12(chr17:15339667-15592758)x3 | copy number gain | See cases [RCV000447335] | Chr17:15339667..15592758 [GRCh37] Chr17:17p12 |
likely benign |
GRCh37/hg19 17p12-11.2(chr17:10771948-21510992)x1 | copy number loss | See cases [RCV000447345] | Chr17:10771948..21510992 [GRCh37] Chr17:17p12-11.2 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) | copy number gain | See cases [RCV000511439] | Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 | copy number gain | See cases [RCV000512441] | Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 | copy number gain | not provided [RCV000739320] | Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 | copy number gain | not provided [RCV000739325] | Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 | copy number gain | not provided [RCV000739324] | Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
NM_001348119.1(TRIM16):c.1682G>T (p.Gly561Val) | single nucleotide variant | not provided [RCV000949595] | Chr17:15628628 [GRCh38] Chr17:15531942 [GRCh37] Chr17:17p12 |
benign |
GRCh37/hg19 17p12(chr17:14105874-15611546) | copy number gain | Charcot-Marie-Tooth disease, type IA [RCV000767736] | Chr17:14105874..15611546 [GRCh37] Chr17:17p12 |
pathogenic |
GRCh37/hg19 17p12(chr17:14104012-15551814) | copy number loss | Hereditary liability to pressure palsies [RCV000767735] | Chr17:14104012..15551814 [GRCh37] Chr17:17p12 |
pathogenic |
NM_001348119.1(TRIM16):c.802G>A (p.Glu268Lys) | single nucleotide variant | Inborn genetic diseases [RCV003252885] | Chr17:15636083 [GRCh38] Chr17:15539397 [GRCh37] Chr17:17p12 |
uncertain significance |
GRCh37/hg19 17p12(chr17:14195642-15545880)x3 | copy number gain | not provided [RCV001006872] | Chr17:14195642..15545880 [GRCh37] Chr17:17p12 |
pathogenic |
Single allele | complex | PMP22-RAI1 contiguous gene duplication syndrome [RCV002280690] | Chr17:14876984..22124952 [GRCh37] Chr17:17p12-11.2 |
pathogenic |
GRCh37/hg19 17p12-11.2(chr17:12524223-16047567)x1 | copy number loss | Hereditary liability to pressure palsies [RCV001825295] | Chr17:12524223..16047567 [GRCh37] Chr17:17p12-11.2 |
not provided |
Single allele | duplication | not specified [RCV002286369] | Chr17:11915997..17892664 [GRCh38] Chr17:17p12-11.2 |
pathogenic |
NM_001348119.1(TRIM16):c.1196C>A (p.Thr399Lys) | single nucleotide variant | Inborn genetic diseases [RCV002684216] | Chr17:15629114 [GRCh38] Chr17:15532428 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.133G>C (p.Val45Leu) | single nucleotide variant | Inborn genetic diseases [RCV002821649] | Chr17:15651477 [GRCh38] Chr17:15554791 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.569A>T (p.Asn190Ile) | single nucleotide variant | Inborn genetic diseases [RCV002708008] | Chr17:15642767 [GRCh38] Chr17:15546081 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.143C>T (p.Ser48Leu) | single nucleotide variant | Inborn genetic diseases [RCV003000531] | Chr17:15651467 [GRCh38] Chr17:15554781 [GRCh37] Chr17:17p12 |
likely benign |
NM_001348119.1(TRIM16):c.797A>T (p.Lys266Met) | single nucleotide variant | Inborn genetic diseases [RCV002659731] | Chr17:15636088 [GRCh38] Chr17:15539402 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.1061A>G (p.Lys354Arg) | single nucleotide variant | Inborn genetic diseases [RCV002949771] | Chr17:15631669 [GRCh38] Chr17:15534983 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.1034C>T (p.Thr345Ile) | single nucleotide variant | Inborn genetic diseases [RCV002759996] | Chr17:15631696 [GRCh38] Chr17:15535010 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.255A>T (p.Arg85Ser) | single nucleotide variant | Inborn genetic diseases [RCV002702039] | Chr17:15651355 [GRCh38] Chr17:15554669 [GRCh37] Chr17:17p12 |
likely benign |
NM_001348119.1(TRIM16):c.1183G>T (p.Val395Phe) | single nucleotide variant | Inborn genetic diseases [RCV002892722] | Chr17:15629127 [GRCh38] Chr17:15532441 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.959A>G (p.His320Arg) | single nucleotide variant | Inborn genetic diseases [RCV002666252] | Chr17:15632565 [GRCh38] Chr17:15535879 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.620C>T (p.Ser207Leu) | single nucleotide variant | Inborn genetic diseases [RCV002708473] | Chr17:15636265 [GRCh38] Chr17:15539579 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.721G>A (p.Glu241Lys) | single nucleotide variant | Inborn genetic diseases [RCV002874490] | Chr17:15636164 [GRCh38] Chr17:15539478 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.1322A>T (p.Tyr441Phe) | single nucleotide variant | Inborn genetic diseases [RCV002831989] | Chr17:15628988 [GRCh38] Chr17:15532302 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.947A>G (p.Glu316Gly) | single nucleotide variant | Inborn genetic diseases [RCV002940956] | Chr17:15632577 [GRCh38] Chr17:15535891 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.126A>T (p.Glu42Asp) | single nucleotide variant | Inborn genetic diseases [RCV002854723] | Chr17:15651484 [GRCh38] Chr17:15554798 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.761A>G (p.His254Arg) | single nucleotide variant | Inborn genetic diseases [RCV002832710] | Chr17:15636124 [GRCh38] Chr17:15539438 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.581T>C (p.Ile194Thr) | single nucleotide variant | Inborn genetic diseases [RCV002718003] | Chr17:15642755 [GRCh38] Chr17:15546069 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.1603T>C (p.Trp535Arg) | single nucleotide variant | Inborn genetic diseases [RCV003174138] | Chr17:15628707 [GRCh38] Chr17:15532021 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.133G>A (p.Val45Met) | single nucleotide variant | Inborn genetic diseases [RCV003344250] | Chr17:15651477 [GRCh38] Chr17:15554791 [GRCh37] Chr17:17p12 |
likely benign |
NM_001348119.1(TRIM16):c.1478G>A (p.Arg493Gln) | single nucleotide variant | Inborn genetic diseases [RCV003373259] | Chr17:15628832 [GRCh38] Chr17:15532146 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.1246C>T (p.Arg416Trp) | single nucleotide variant | Inborn genetic diseases [RCV003368647] | Chr17:15629064 [GRCh38] Chr17:15532378 [GRCh37] Chr17:17p12 |
uncertain significance |
NM_001348119.1(TRIM16):c.812G>C (p.Arg271Thr) | single nucleotide variant | not provided [RCV003428153] | Chr17:15636073 [GRCh38] Chr17:15539387 [GRCh37] Chr17:17p12 |
likely benign |
GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3 | copy number gain | not specified [RCV003987215] | Chr17:525..21510992 [GRCh37] Chr17:17p13.3-11.2 |
pathogenic |
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. |
RH67196 |
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RH74977 |
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D8S2279 |
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G32507 |
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alimentary part of gastrointestinal system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | visual system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | ||||||||||||||||||
Medium | 989 | 237 | 707 | 160 | 74 | 44 | 1925 | 606 | 176 | 88 | 620 | 974 | 129 | 765 | 838 | 1 | ||
Low | 1450 | 2627 | 1003 | 448 | 1744 | 405 | 2431 | 1589 | 3557 | 328 | 839 | 639 | 46 | 1 | 439 | 1950 | 3 | 2 |
Below cutoff | 127 | 16 | 16 | 133 | 16 | 1 | 2 | 1 | 3 | 1 | 1 |
RefSeq Transcripts | NM_001348119 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001348120 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001348121 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001348122 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001348124 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001348125 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001348126 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_006470 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AC005324 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AF096870 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK002035 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK056026 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK314557 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC001564 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC015674 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC053514 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC067096 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH878675 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068261 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CR457136 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA709639 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GN344137 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000336708 ⟹ ENSP00000338989 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000416464 ⟹ ENSP00000399918 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000460728 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000473368 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000473540 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000473659 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000494759 ⟹ ENSP00000465169 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000577326 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000577372 ⟹ ENSP00000463293 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000577446 ⟹ ENSP00000467031 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000577886 ⟹ ENSP00000462903 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000578237 ⟹ ENSP00000463188 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000578744 ⟹ ENSP00000465907 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000579219 ⟹ ENSP00000463639 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000579272 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000579535 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000579630 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000579843 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000580110 ⟹ ENSP00000464072 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000580388 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000581200 ⟹ ENSP00000463360 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000581224 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000582182 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000582708 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000584142 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000649191 ⟹ ENSP00000497185 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001348119 ⟹ NP_001335048 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001348120 ⟹ NP_001335049 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001348121 ⟹ NP_001335050 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001348122 ⟹ NP_001335051 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001348124 ⟹ NP_001335053 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001348125 ⟹ NP_001335054 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001348126 ⟹ NP_001335055 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_006470 ⟹ NP_006461 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
Protein RefSeqs | NP_001335048 | (Get FASTA) | NCBI Sequence Viewer |
NP_001335049 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001335050 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001335051 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001335053 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001335054 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001335055 | (Get FASTA) | NCBI Sequence Viewer | |
NP_006461 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAC79080 | (Get FASTA) | NCBI Sequence Viewer |
AAH01564 | (Get FASTA) | NCBI Sequence Viewer | |
AAH53514 | (Get FASTA) | NCBI Sequence Viewer | |
AAH67096 | (Get FASTA) | NCBI Sequence Viewer | |
BAG37142 | (Get FASTA) | NCBI Sequence Viewer | |
BAG51004 | (Get FASTA) | NCBI Sequence Viewer | |
BAG51608 | (Get FASTA) | NCBI Sequence Viewer | |
CAG33417 | (Get FASTA) | NCBI Sequence Viewer | |
CAY56004 | (Get FASTA) | NCBI Sequence Viewer | |
EAW50853 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000338989 | ||
ENSP00000338989.7 | |||
ENSP00000399918 | |||
ENSP00000399918.2 | |||
ENSP00000462903 | |||
ENSP00000462903.1 | |||
ENSP00000463188.1 | |||
ENSP00000463293.1 | |||
ENSP00000463360.1 | |||
ENSP00000463639.1 | |||
ENSP00000464072.1 | |||
ENSP00000465169.1 | |||
ENSP00000465907.1 | |||
ENSP00000467031.1 | |||
ENSP00000497185 | |||
ENSP00000497185.2 | |||
GenBank Protein | O95361 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_006461 ⟸ NM_006470 |
- Peptide Label: | isoform a |
- UniProtKB: | Q96BE8 (UniProtKB/Swiss-Prot), Q7Z6I2 (UniProtKB/Swiss-Prot), Q6IAL8 (UniProtKB/Swiss-Prot), Q96J43 (UniProtKB/Swiss-Prot), O95361 (UniProtKB/Swiss-Prot), B2RB95 (UniProtKB/TrEMBL), B3KMJ2 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001335050 ⟸ NM_001348121 |
- Peptide Label: | isoform b |
- UniProtKB: | B3KP96 (UniProtKB/TrEMBL), B4DE22 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001335051 ⟸ NM_001348122 |
- Peptide Label: | isoform b |
- UniProtKB: | B3KP96 (UniProtKB/TrEMBL), B4DE22 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001335049 ⟸ NM_001348120 |
- Peptide Label: | isoform a |
- UniProtKB: | Q96BE8 (UniProtKB/Swiss-Prot), Q7Z6I2 (UniProtKB/Swiss-Prot), Q6IAL8 (UniProtKB/Swiss-Prot), Q96J43 (UniProtKB/Swiss-Prot), O95361 (UniProtKB/Swiss-Prot), B2RB95 (UniProtKB/TrEMBL), B3KMJ2 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001335055 ⟸ NM_001348126 |
- Peptide Label: | isoform d |
- UniProtKB: | B4DE22 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001335053 ⟸ NM_001348124 |
- Peptide Label: | isoform c |
- UniProtKB: | Q309B1 (UniProtKB/Swiss-Prot), B4DWQ8 (UniProtKB/Swiss-Prot), B4DQK2 (UniProtKB/Swiss-Prot), B2RUW6 (UniProtKB/Swiss-Prot), A0PK10 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001335048 ⟸ NM_001348119 |
- Peptide Label: | isoform a |
- UniProtKB: | Q96BE8 (UniProtKB/Swiss-Prot), Q7Z6I2 (UniProtKB/Swiss-Prot), Q6IAL8 (UniProtKB/Swiss-Prot), Q96J43 (UniProtKB/Swiss-Prot), O95361 (UniProtKB/Swiss-Prot), B2RB95 (UniProtKB/TrEMBL), B3KMJ2 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001335054 ⟸ NM_001348125 |
- Peptide Label: | isoform c |
- UniProtKB: | Q309B1 (UniProtKB/Swiss-Prot), B4DWQ8 (UniProtKB/Swiss-Prot), B4DQK2 (UniProtKB/Swiss-Prot), B2RUW6 (UniProtKB/Swiss-Prot), A0PK10 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | ENSP00000464072 ⟸ ENST00000580110 |
RefSeq Acc Id: | ENSP00000497185 ⟸ ENST00000649191 |
RefSeq Acc Id: | ENSP00000463360 ⟸ ENST00000581200 |
RefSeq Acc Id: | ENSP00000338989 ⟸ ENST00000336708 |
RefSeq Acc Id: | ENSP00000465169 ⟸ ENST00000494759 |
RefSeq Acc Id: | ENSP00000399918 ⟸ ENST00000416464 |
RefSeq Acc Id: | ENSP00000463293 ⟸ ENST00000577372 |
RefSeq Acc Id: | ENSP00000467031 ⟸ ENST00000577446 |
RefSeq Acc Id: | ENSP00000462903 ⟸ ENST00000577886 |
RefSeq Acc Id: | ENSP00000465907 ⟸ ENST00000578744 |
RefSeq Acc Id: | ENSP00000463188 ⟸ ENST00000578237 |
RefSeq Acc Id: | ENSP00000463639 ⟸ ENST00000579219 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-O95361-F1-model_v2 | AlphaFold | O95361 | 1-564 | view protein structure |
RGD ID: | 6793980 | ||||||||
Promoter ID: | HG_KWN:25092 | ||||||||
Type: | Non-CpG | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | HeLa_S3, K562, NB4 | ||||||||
Transcripts: | UC002GOR.1 | ||||||||
Position: |
|
RGD ID: | 6794646 | ||||||||
Promoter ID: | HG_KWN:25094 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | HeLa_S3, Lymphoblastoid, NB4 | ||||||||
Transcripts: | ENST00000336708, ENST00000395902, OTTHUMT00000131016, OTTHUMT00000131017, OTTHUMT00000131018 | ||||||||
Position: |
|
RGD ID: | 7234087 | ||||||||
Promoter ID: | EPDNEW_H22789 | ||||||||
Type: | initiation region | ||||||||
Name: | TRIM16_2 | ||||||||
Description: | tripartite motif containing 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H22790 EPDNEW_H22791 | ||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7234089 | ||||||||
Promoter ID: | EPDNEW_H22790 | ||||||||
Type: | initiation region | ||||||||
Name: | TRIM16_1 | ||||||||
Description: | tripartite motif containing 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H22789 EPDNEW_H22791 | ||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7234091 | ||||||||
Promoter ID: | EPDNEW_H22791 | ||||||||
Type: | initiation region | ||||||||
Name: | TRIM16_3 | ||||||||
Description: | tripartite motif containing 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H22789 EPDNEW_H22790 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:17241 | AgrOrtholog |
COSMIC | TRIM16 | COSMIC |
Ensembl Genes | ENSG00000221926 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000336708 | ENTREZGENE |
ENST00000336708.11 | UniProtKB/Swiss-Prot | |
ENST00000416464 | ENTREZGENE | |
ENST00000416464.6 | UniProtKB/TrEMBL | |
ENST00000494759.1 | UniProtKB/TrEMBL | |
ENST00000577372.5 | UniProtKB/TrEMBL | |
ENST00000577446.5 | UniProtKB/TrEMBL | |
ENST00000577886 | ENTREZGENE | |
ENST00000577886.5 | UniProtKB/Swiss-Prot | |
ENST00000578237.5 | UniProtKB/Swiss-Prot | |
ENST00000578744.5 | UniProtKB/TrEMBL | |
ENST00000579219.5 | UniProtKB/TrEMBL | |
ENST00000580110.5 | UniProtKB/TrEMBL | |
ENST00000581200.1 | UniProtKB/TrEMBL | |
ENST00000649191 | ENTREZGENE | |
ENST00000649191.2 | UniProtKB/Swiss-Prot | |
Gene3D-CATH | 2.60.120.920 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
4.10.830.40 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Classic Zinc Finger | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
GTEx | ENSG00000221926 | GTEx |
HGNC ID | HGNC:17241 | ENTREZGENE |
Human Proteome Map | TRIM16 | Human Proteome Map |
InterPro | B30.2/SPRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
B30.2/SPRY_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Butyrophylin_SPRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
ConA-like_dom_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KRAB_dom_sf | UniProtKB/TrEMBL | |
PRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
SPRY_dom | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Znf_B-box | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:10626 | UniProtKB/Swiss-Prot |
NCBI Gene | 10626 | ENTREZGENE |
OMIM | 609505 | OMIM |
PANTHER | B-BOX DOMAIN CONTAINING | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
F-BOX AND WD REPEAT DOMAIN CONTAINING PROTEIN 10B-RELATED | UniProtKB/TrEMBL | |
TRIPARTITE MOTIF-CONTAINING PROTEIN 16-RELATED | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
UBIQUITIN LIGASE SPECIFICITY FACTOR/HREP PROTEIN | UniProtKB/TrEMBL | |
Pfam | PRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SPRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
zf-B_box | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PharmGKB | PA38215 | PharmGKB |
PRINTS | BUTYPHLNCDUF | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PROSITE | B302_SPRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
ZF_BBOX | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
SMART | BBOX | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
SPRY | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Superfamily-SCOP | B-box zinc-binding domain | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SSF109640 | UniProtKB/TrEMBL | |
SSF49899 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
UniProt | A0PK10 | ENTREZGENE |
B2RB95 | ENTREZGENE, UniProtKB/TrEMBL | |
B2RUW6 | ENTREZGENE | |
B3KMJ2 | ENTREZGENE, UniProtKB/TrEMBL | |
B3KP96 | ENTREZGENE, UniProtKB/TrEMBL | |
B4DE22 | ENTREZGENE, UniProtKB/TrEMBL | |
B4DQK2 | ENTREZGENE | |
B4DWQ8 | ENTREZGENE | |
J3QKY5_HUMAN | UniProtKB/TrEMBL | |
J3QL38_HUMAN | UniProtKB/TrEMBL | |
J3QLP0_HUMAN | UniProtKB/TrEMBL | |
J3QR69_HUMAN | UniProtKB/TrEMBL | |
K7EJH2_HUMAN | UniProtKB/TrEMBL | |
K7EL43_HUMAN | UniProtKB/TrEMBL | |
K7ENN8_HUMAN | UniProtKB/TrEMBL | |
O95361 | ENTREZGENE | |
Q309B1 | ENTREZGENE | |
Q6IAL8 | ENTREZGENE | |
Q7Z6I2 | ENTREZGENE | |
Q96BE8 | ENTREZGENE | |
Q96J43 | ENTREZGENE | |
TRI16_HUMAN | UniProtKB/Swiss-Prot | |
UniProt Secondary | Q6IAL8 | UniProtKB/Swiss-Prot |
Q7Z6I2 | UniProtKB/Swiss-Prot | |
Q96BE8 | UniProtKB/Swiss-Prot | |
Q96J43 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2011-07-27 | TRIM16 | tripartite motif containing 16 | TRIM16 | tripartite motif-containing 16 | Symbol and/or name change | 5135510 | APPROVED |