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Cellular Component
Molecular Function

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![]() Biological Process Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | post-translational protein modification | | TAS | | 2290271 | | Reactome | Reactome:R-HSA-597592 | protein ubiquitination | | IEA | UniPathway:UPA00143 | 2290271 | | UniProtKB | GO_REF:0000041 | protein ubiquitination | | TAS | | 2290271 | | Reactome | Reactome:R-HSA-8956106 | protein-containing complex assembly | | TAS | | 2290271 | (PMID:7660129) | PINC | PMID:7660129 | regulation of transcription from RNA polymerase II promoter in response to hypoxia | | TAS | | 2290271 | | Reactome | Reactome:R-HSA-1234174 | transcription by RNA polymerase II | | TAS | | 2290271 | | Reactome | Reactome:R-HSA-73857 | transcription elongation from RNA polymerase II promoter | | TAS | | 2290271 | | Reactome | Reactome:R-HSA-112382, Reactome:R-HSA-75955 | transcription elongation from RNA polymerase II promoter | | IEA | InterPro:IPR039049 | 2290271 | | InterPro | GO_REF:0000002 | translational elongation | | IEA | UniProtKB-KW:KW-0251 | 2290271 | | UniProtKB | GO_REF:0000038 | |
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1. | Pipeline to import KEGG annotations from KEGG into RGD |
2. | Pipeline to import Pathway Interaction Database annotations from NCI into RGD |
3. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
4. | RGD automated import pipeline for gene-chemical interactions |
5. | Semenza GL Physiology (Bethesda). 2009 Apr;24:97-106. |
PubMed | 7638163 7660122 7660129 7660130 8244996 8889548 9122164 9751722 9765201 10051596 10205047 10224134 10449727 10535940 10587522 10692460 10823831 10973499 11006129 11384984 11739384 11994304 12004076 12048197 12050673 12052866 12149480 12477932 12559969 12604794 12676794 12943681 14564014 14636579 14960280 15060148 15489334 15574592 15574593 15590664 15590694 15601820 15616553 15781449 15935760 15965468 15966899 16007195 16189514 16303161 16503656 16530799 16675548 16961462 17069461 17110338 17135358 17213182 17244529 17285170 17304241 17339318 17351129 17353931 17611602 17636018 17690245 17786314 17869271 17898068 17922844 17986458 18173839 18187417 18323857 18508766 18541215 18562529 18775313 18789977 19008196 19030229 19038776 19159283 19218568 19295130 19300455 19327355 19385048 19615732 19622774 19706539 19940151 20049704 20096141 20174454 20211142 20302626 20450485 20463065 20532212 20728451 20871634 21030588 21119685 21130766 21145461 21386990 21447700 21516116 21822215 21873635 21942715 21980433 22174154 22190034 22190036 22190037 22234250 22284679 22286099 22402277 22402281 22479405 22863883 22912744 22939629 23098073 23275444 23333304 23376485 23401859 23438482 23455922 23460923 23621690 23806657 23837592 23988114 23990909 24012004 24044920 24076655 24225024 24337577 24352440 24390320 24390335 24402281 24422669 24438103 24469044 24586532 24810617 25124760 25408426 25416956 25499913 25500545 25505247 25661653 25878247 25901786 25912140 25963833 25981045 26121586 26344197 26472337 26496610 26531153 26618866 26735018 26743088 26751167 26846855 26885983 26906416 26972000 27173435 27375898 27517496 27565346 27609421 27634302 27684187 27705803 27875637 28514442 28515276 28581483 28775317 28786561 28883622 28931592 29053956 29229926 29258557 29401731 29507755 29568061 29653302 29656893 29735542 29991678 30166453 30196744 30209976 30293565 30463901 |
ELOB (Homo sapiens - human) |
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Elob (Mus musculus - house mouse) |
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Elob (Rattus norvegicus - Norway rat) |
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Elob (Chinchilla lanigera - long-tailed chinchilla) |
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ELOB (Pan paniscus - bonobo/pygmy chimpanzee) |
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ELOB (Canis lupus familiaris - dog) |
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Elob (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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ELOB (Sus scrofa - pig) |
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RH92618 |
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RH122227 |
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D16S2549E |
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D16S2844 |
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SHGC-32846 |
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SHGC-61065 |
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D9S2087 |
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RH44069 |
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SHGC-61169 |
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TCEB2_3482 |
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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. |
RefSeq Transcripts | NM_007108 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_207013 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AC004493 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC092117 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AC093517 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AI191983 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC013306 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC065000 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BF967495 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BG329435 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BM553320 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BM700019 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BM921799 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BU533433 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471112 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DT217333 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GQ891330 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
L42856 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_007108 ⟹ NP_009039 | |||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | |||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||
Position: |
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Sequence: |
GGGAACGGGGCGGAGCGCGGCTGCGCCGGCGCGTCGAGGGGAGAGGCAGCAGCCGCGATGGACGhide sequence |
RefSeq Acc Id: | NM_207013 ⟹ NP_996896 | |||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | |||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||
Position: |
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Sequence: |
GGGAACGGGGCGGAGCGCGGCTGCGCCGGCGCGTCGAGGGGAGAGGCAGCAGCCGCGATGGACGhide sequence |
Protein RefSeqs | NP_009039 | (Get FASTA) | NCBI Sequence Viewer |
NP_996896 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAA75522 | (Get FASTA) | NCBI Sequence Viewer |
AAC08452 | (Get FASTA) | NCBI Sequence Viewer | |
AAH13306 | (Get FASTA) | NCBI Sequence Viewer | |
AAH65000 | (Get FASTA) | NCBI Sequence Viewer | |
ADO22192 | (Get FASTA) | NCBI Sequence Viewer | |
EAW85472 | (Get FASTA) | NCBI Sequence Viewer | |
EAW85473 | (Get FASTA) | NCBI Sequence Viewer | |
EAW85474 | (Get FASTA) | NCBI Sequence Viewer | |
EAW85475 | (Get FASTA) | NCBI Sequence Viewer | |
EAW85476 | (Get FASTA) | NCBI Sequence Viewer | |
Q15370 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_996896 ⟸ NM_207013 |
- Peptide Label: | isoform b |
- UniProtKB: | Q15370 (UniProtKB/Swiss-Prot) |
- Sequence: |
MDVFLMIRRHKTTIFTDAKESSTVFELKRIVEGILKRPPDEQRLYKDDQLLDDGKTLGECGFTShide sequence |
RefSeq Acc Id: | NP_009039 ⟸ NM_007108 |
- Peptide Label: | isoform a |
- UniProtKB: | Q15370 (UniProtKB/Swiss-Prot) |
- Sequence: |
MDVFLMIRRHKTTIFTDAKESSTVFELKRIVEGILKRPPDEQRLYKDDQLLDDGKTLGECGFTShide sequence |
RGD ID: | 6816086 | |||||||||
Promoter ID: | HG_SPT:22696 | |||||||||
Type: | Non-CpG | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | K562 | |||||||||
Transcripts: | AA146867, AA420847, AA469013, AA523187, AA557625, AA568145, AA576811, AA584218, AA609680, AA632059, AA683534, AA703497, AA707532, AA707599, AA724959, AA744890, AA758576, AA855009, AA889941, AA937134, AA961393, AA968838, AI033767, AI037998, AI051789, AI078626, AI095756, AI131360, AI138721, AI161393, AI188746, AI191983, AI204128, AI264687, AI298244, AI300706, AI300848, AI312889, AI336135, AI338594, AI342092, AI343816, AI344424, AI376062, AI392941, AI573264, AI720892, AI748804, AI749424, AI749529, AI751883, AI827092, AI857469, AI857538, AI884918, AI990681, AL518708, AL522090, AL547349, AW008966, AW026532, AW327625, BE073352, BF000526, BF447322, BF954574, BG231394, BG940700, BI032322, BI493851, BM663171, BM669977, BM975891, BM989154, BQ004377, BQ008180, BU626921, BU628563, BU752143, BX366619, BX371977, BX414592, CA423427, CD368761, CD623674, CK300834, D59501, DB362537, N29939, N74191, R00293, T67995, W35155, W47378 | |||||||||
Position: |
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RGD ID: | 6793501 | |||||||||
Promoter ID: | HG_KWN:22830 | |||||||||
Type: | CpG-Island | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4 | |||||||||
Transcripts: | ENST00000409477, NM_007108, NM_207013, OTTHUMT00000333978 | |||||||||
Position: |
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RGD ID: | 7231069 | |||||||||
Promoter ID: | EPDNEW_H21281 | |||||||||
Type: | initiation region | |||||||||
Name: | ELOB_1 | |||||||||
Description: | elongin B | |||||||||
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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Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 16p13.3(chr16:2326840-3487106)x3 | copy number gain | Global developmental delay [RCV000052394]|See cases [RCV000052394] | Chr16:2326840..3487106 [GRCh38] Chr16:2376841..3537106 [GRCh37] Chr16:2316842..3477107 [NCBI36] Chr16:16p13.3 |
pathogenic |
GRCh38/hg38 16p13.3(chr16:2717952-4041020)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052395]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052395]|See cases [RCV000052395] | Chr16:2717952..4041020 [GRCh38] Chr16:2767953..4091021 [GRCh37] Chr16:2707954..4031022 [NCBI36] Chr16:16p13.3 |
pathogenic |
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3 | copy number gain | Global developmental delay [RCV000052367]|See cases [RCV000052367] | Chr16:23141..11296695 [GRCh38] Chr16:73141..11390552 [GRCh37] Chr16:13141..11298053 [NCBI36] Chr16:16p13.3-13.13 |
pathogenic |
GRCh38/hg38 16p13.3(chr16:46766-3214623)x3 | copy number gain | Nonsyndromic microcephaly [RCV000052370]|See cases [RCV000052370] | Chr16:46766..3214623 [GRCh38] Chr16:96766..3264623 [GRCh37] Chr16:36766..3204624 [NCBI36] Chr16:16p13.3 |
pathogenic |
GRCh38/hg38 16p13.3(chr16:2494804-3246579)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053269]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053269]|See cases [RCV000053269] | Chr16:2494804..3246579 [GRCh38] Chr16:2544805..3296579 [GRCh37] Chr16:2484806..3236580 [NCBI36] Chr16:16p13.3 |
pathogenic |
NM_016333.3(SRRM2):c.6150C>T (p.Ile2050=) | single nucleotide variant | Malignant melanoma [RCV000071067] | Chr16:2766678 [GRCh38] Chr16:2816679 [GRCh37] Chr16:2756680 [NCBI36] Chr16:16p13.3 |
not provided |
GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3 | copy number gain | See cases [RCV000133780] | Chr16:46766..11525516 [GRCh38] Chr16:96766..11619372 [GRCh37] Chr16:36766..11526873 [NCBI36] Chr16:16p13.3-13.13 |
pathogenic |
GRCh38/hg38 16p13.3(chr16:46766-4247185)x3 | copy number gain | See cases [RCV000136687] | Chr16:46766..4247185 [GRCh38] Chr16:96766..4297186 [GRCh37] Chr16:36766..4237187 [NCBI36] Chr16:16p13.3 |
pathogenic |
GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3 | copy number gain | See cases [RCV000139166] | Chr16:43732..13326806 [GRCh38] Chr16:93732..13420663 [GRCh37] Chr16:33732..13328164 [NCBI36] Chr16:16p13.3-13.12 |
pathogenic |
GRCh38/hg38 16p13.3(chr16:2406643-2782411)x1 | copy number loss | See cases [RCV000141237] | Chr16:2406643..2782411 [GRCh38] Chr16:2456644..2832412 [GRCh37] Chr16:2396645..2772413 [NCBI36] Chr16:16p13.3 |
likely pathogenic |
GRCh38/hg38 16p13.3(chr16:2586110-2804741)x1 | copy number loss | See cases [RCV000142770] | Chr16:2586110..2804741 [GRCh38] Chr16:2636111..2854742 [GRCh37] Chr16:2576112..2794743 [NCBI36] Chr16:16p13.3 |
uncertain significance |
GRCh38/hg38 16p13.3-13.11(chr16:666662-15743104)x3 | copy number gain | See cases [RCV000143710] | Chr16:666662..15743104 [GRCh38] Chr16:716662..15836961 [GRCh37] Chr16:656663..15744462 [NCBI36] Chr16:16p13.3-13.11 |
pathogenic |
GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3 | copy number gain | See cases [RCV000203445] | Chr16:102839..28327676 [GRCh37] Chr16:16p13.3-11.2 |
pathogenic |
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 | copy number gain | Ductal breast carcinoma [RCV000207053] | Chr16:1279324..31926800 [GRCh37] Chr16:16p13.3-11.2 |
uncertain significance |
GRCh37/hg19 16p13.3-12.3(chr16:1274615-19073133)x3 | copy number gain | Ductal breast carcinoma [RCV000207326] | Chr16:1274615..19073133 [GRCh37] Chr16:16p13.3-12.3 |
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 16p13.3-13.2(chr16:78801-9169448) | copy number gain | See cases [RCV000446555] | Chr16:78801..9169448 [GRCh37] Chr16:16p13.3-13.2 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:97133-5122974)x3 | copy number gain | See cases [RCV000445663] | Chr16:97133..5122974 [GRCh37] Chr16:16p13.3 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:643377-3125125)x3 | copy number gain | See cases [RCV000510815] | Chr16:643377..3125125 [GRCh37] Chr16:16p13.3 |
uncertain significance |
maternal UPD(16p) | complex | Hemimegalencephaly [RCV000494707] | Chr16:1280042..33710558 [GRCh37] Chr16:16p13.3-11.2 |
pathogenic |
GRCh37/hg19 16p13.3-12.3(chr16:85880-19806921)x3 | copy number gain | See cases [RCV000512194] | Chr16:85880..19806921 [GRCh37] Chr16:16p13.3-12.3 |
pathogenic |
GRCh37/hg19 16p13.3-12.2(chr16:85880-22442007)x3 | copy number gain | See cases [RCV000511360] | Chr16:85880..22442007 [GRCh37] Chr16:16p13.3-12.2 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:2606710-3382546)x3 | copy number gain | See cases [RCV000512346] | Chr16:2606710..3382546 [GRCh37] Chr16:16p13.3 |
uncertain significance |
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 |
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 16p13.3-13.2(chr16:85880-9883129)x3 | copy number gain | See cases [RCV000510698] | Chr16:85880..9883129 [GRCh37] Chr16:16p13.3-13.2 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:85880-3216551)x3 | copy number gain | not provided [RCV000683742] | Chr16:85880..3216551 [GRCh37] Chr16:16p13.3 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:1505184-4415346)x3 | copy number gain | not provided [RCV000683745] | Chr16:1505184..4415346 [GRCh37] Chr16:16p13.3 |
pathogenic |
GRCh37/hg19 16p13.3-13.13(chr16:85880-11209288)x3 | copy number gain | not provided [RCV000683743] | Chr16:85880..11209288 [GRCh37] Chr16:16p13.3-13.13 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:2651354-4460114)x3 | copy number gain | not provided [RCV000683747] | Chr16:2651354..4460114 [GRCh37] Chr16:16p13.3 |
pathogenic |
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 16p13.3(chr16:109978-4316797) | copy number gain | Chromosome 16p13.3 duplication syndrome [RCV000767731] | Chr16:109978..4316797 [GRCh37] Chr16:16p13.3 |
pathogenic |
GRCh37/hg19 16p13.3(chr16:2817166-3056563)x3 | copy number gain | not provided [RCV000846256] | Chr16:2817166..3056563 [GRCh37] Chr16:16p13.3 |
uncertain significance |
GRCh37/hg19 16p13.3(chr16:2716924-3055626)x3 | copy number gain | not provided [RCV000849054] | Chr16:2716924..3055626 [GRCh37] Chr16:16p13.3 |
uncertain significance |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:11619 | AgrOrtholog |
COSMIC | ELOB | COSMIC |
Ensembl Genes | ENSG00000103363 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000262306 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSP00000386652 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000387189 | UniProtKB/TrEMBL | |
ENSP00000458213 | UniProtKB/TrEMBL | |
ENSP00000458443 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000262306 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENST00000409477 | UniProtKB/TrEMBL | |
ENST00000409906 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000494946 | UniProtKB/TrEMBL | |
ENST00000572954 | UniProtKB/TrEMBL | |
GTEx | ENSG00000103363 | GTEx |
HGNC ID | HGNC:11619 | ENTREZGENE |
Human Proteome Map | ELOB | Human Proteome Map |
InterPro | ELOB | UniProtKB/Swiss-Prot |
Ubiquitin-like_domsf | UniProtKB/Swiss-Prot | |
Ubiquitin_dom | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:6923 | UniProtKB/Swiss-Prot |
NCBI Gene | 6923 | ENTREZGENE |
OMIM | 600787 | OMIM |
PANTHER | PTHR13248 | UniProtKB/Swiss-Prot |
Pfam | ubiquitin | UniProtKB/Swiss-Prot |
PharmGKB | PA36378 | PharmGKB |
PROSITE | UBIQUITIN_2 | UniProtKB/Swiss-Prot |
SMART | UBQ | UniProtKB/Swiss-Prot |
Superfamily-SCOP | SSF54236 | UniProtKB/Swiss-Prot |
UniGene | Hs.172772 | ENTREZGENE |
UniProt | A0A0B4J296_HUMAN | UniProtKB/TrEMBL |
A0A384MDL3_HUMAN | UniProtKB/TrEMBL | |
B8ZZU8_HUMAN | UniProtKB/TrEMBL | |
ELOB_HUMAN | UniProtKB/Swiss-Prot | |
I3L0M9_HUMAN | UniProtKB/TrEMBL | |
Q15370 | ENTREZGENE | |
UniProt Secondary | B7WPD3 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-11-08 | ELOB | elongin B | TCEB2 | transcription elongation factor B subunit 2 | Symbol and/or name change | 5135510 | APPROVED |
2016-03-14 | TCEB2 | transcription elongation factor B subunit 2 | transcription elongation factor B (SIII), polypeptide 2 (18kDa, elongin B) | Symbol and/or name change | 5135510 | APPROVED | |
2011-08-16 | TCEB2 | transcription elongation factor B (SIII), polypeptide 2 (18kDa, elongin B) | TCEB2 | transcription elongation factor B (SIII), polypeptide 2 (18kDa, elongin B) | Symbol and/or name change | 5135510 | APPROVED |
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More on ELOB | |
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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: | 734149 |
Created: | 2004-01-12 |
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.