ZNF598 (zinc finger protein 598, E3 ubiquitin ligase) - Rat Genome Database

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Gene: ZNF598 (zinc finger protein 598, E3 ubiquitin ligase) Homo sapiens
Analyze
Symbol: ZNF598
Name: zinc finger protein 598, E3 ubiquitin ligase
RGD ID: 1312605
HGNC Page HGNC:28079
Description: Enables protein-RNA adaptor activity; stalled ribosome sensor activity; and ubiquitin protein ligase activity. Involved in several processes, including protein ubiquitination; rescue of stalled ribosome; and ribosome-associated ubiquitin-dependent protein catabolic process. Located in cytosol. Is active in cytosolic ribosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp762F135; E3 ubiquitin-protein ligase ZNF598; FLJ00086; HEL2; zinc finger protein 598
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC645937  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Annotation category: suggests misassembly
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38161,997,654 - 2,009,821 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl161,997,654 - 2,009,821 (-)EnsemblGRCh38hg38GRCh38
GRCh37162,047,655 - 2,059,822 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36161,987,769 - 1,999,764 (-)NCBINCBI36Build 36hg18NCBI36
Build 34161,987,768 - 1,999,764NCBI
Celera162,259,947 - 2,271,940 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef161,971,653 - 1,983,818 (-)NCBIHuRef
CHM1_1162,047,585 - 2,059,800 (-)NCBICHM1_1
T2T-CHM13v2.0162,017,608 - 2,029,776 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IEA)
cytosol  (IDA,IEA)
cytosolic ribosome  (IDA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:14702039   PMID:15489334   PMID:15592455   PMID:16094384   PMID:16169070   PMID:20531386   PMID:21873635   PMID:22658674   PMID:22681889   PMID:22751931   PMID:22939629   PMID:22944692  
PMID:24332808   PMID:24550385   PMID:25609649   PMID:25921289   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26638075   PMID:27684187   PMID:28065601   PMID:28132843   PMID:28514442  
PMID:28675297   PMID:28685749   PMID:28718761   PMID:28757607   PMID:28786561   PMID:28986522   PMID:29117863   PMID:29395067   PMID:29719242   PMID:30033366   PMID:30293783   PMID:30561431  
PMID:30917308   PMID:30995489   PMID:31073040   PMID:31091453   PMID:31433974   PMID:31527615   PMID:32041737   PMID:32099016   PMID:32322062   PMID:32513696   PMID:32579943   PMID:32657267  
PMID:32726578   PMID:32737199   PMID:32807901   PMID:32877691   PMID:33060197   PMID:33507233   PMID:33581075   PMID:33658012   PMID:33729478   PMID:33731348   PMID:33916271   PMID:33961781  
PMID:34079125   PMID:34551427   PMID:34597346   PMID:34728620   PMID:34729304   PMID:35256949   PMID:35271311   PMID:35321260   PMID:35563538   PMID:35831314   PMID:35944360   PMID:36057605  
PMID:36114006   PMID:36215168   PMID:36232890   PMID:36302773   PMID:36339263   PMID:36379255   PMID:36398662   PMID:36526897   PMID:36929488   PMID:36931259   PMID:37499664   PMID:37827155  
PMID:38113892   PMID:38280479  


Genomics

Comparative Map Data
ZNF598
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38161,997,654 - 2,009,821 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl161,997,654 - 2,009,821 (-)EnsemblGRCh38hg38GRCh38
GRCh37162,047,655 - 2,059,822 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36161,987,769 - 1,999,764 (-)NCBINCBI36Build 36hg18NCBI36
Build 34161,987,768 - 1,999,764NCBI
Celera162,259,947 - 2,271,940 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef161,971,653 - 1,983,818 (-)NCBIHuRef
CHM1_1162,047,585 - 2,059,800 (-)NCBICHM1_1
T2T-CHM13v2.0162,017,608 - 2,029,776 (-)NCBIT2T-CHM13v2.0
Zfp598
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391724,888,661 - 24,900,997 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1724,888,661 - 24,900,990 (+)EnsemblGRCm39 Ensembl
GRCm381724,669,687 - 24,682,023 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1724,669,687 - 24,682,016 (+)EnsemblGRCm38mm10GRCm38
MGSCv371724,806,697 - 24,818,961 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361724,397,352 - 24,409,616 (+)NCBIMGSCv36mm8
Celera1725,191,744 - 25,203,995 (+)NCBICelera
Cytogenetic Map17A3.3NCBI
cM Map1712.46NCBI
Zfp598
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81014,198,763 - 14,210,773 (+)NCBIGRCr8
mRatBN7.21013,694,224 - 13,706,235 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1013,694,286 - 13,706,233 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1018,441,140 - 18,453,063 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01017,929,992 - 17,941,915 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01013,429,195 - 13,441,118 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01014,035,114 - 14,047,100 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1014,035,149 - 14,047,096 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01013,852,103 - 13,864,078 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41013,922,112 - 13,934,058 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11013,922,202 - 13,934,063 (+)NCBI
Celera1013,374,239 - 13,386,160 (+)NCBICelera
Cytogenetic Map10q12NCBI
Znf598
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544215,252,927 - 15,269,087 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495544215,253,649 - 15,265,420 (+)NCBIChiLan1.0ChiLan1.0
ZNF598
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2182,337,619 - 2,349,758 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1166,119,279 - 6,131,421 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v016694,562 - 706,711 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1162,086,264 - 2,094,749 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl162,086,844 - 2,092,277 (-)Ensemblpanpan1.1panPan2
ZNF598
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1638,928,845 - 38,939,768 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl638,928,839 - 38,957,780 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha640,168,620 - 40,179,508 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0639,250,490 - 39,256,378 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1638,921,642 - 38,933,616 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0638,893,954 - 38,905,926 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0639,373,903 - 39,384,800 (+)NCBIUU_Cfam_GSD_1.0
Znf598
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344104,673,578 - 104,685,651 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366942,023,806 - 2,036,864 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366942,019,714 - 2,035,885 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF598
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl339,962,988 - 39,972,656 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1339,962,896 - 39,972,659 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2342,209,054 - 42,218,784 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ZNF598
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.151,894,662 - 1,906,613 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl51,895,250 - 1,906,539 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606829,161,304 - 29,173,254 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Znf598
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624913237,658 - 252,189 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624913237,668 - 249,786 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZNF598
19 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3 copy number gain 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(chr16:29941-2560460)x3 copy number gain See cases [RCV000052368] Chr16:29941..2560460 [GRCh38]
Chr16:79941..2610461 [GRCh37]
Chr16:19941..2550462 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:46766-3214623)x3 copy number gain See cases [RCV000052370] Chr16:46766..3214623 [GRCh38]
Chr16:96766..3264623 [GRCh37]
Chr16:36766..3204624 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:1221651-2233773)x3 copy number gain See cases [RCV000052373] Chr16:1221651..2233773 [GRCh38]
Chr16:1271651..2283774 [GRCh37]
Chr16:1211652..2223775 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:1816283-2020966)x3 copy number gain See cases [RCV000052377] Chr16:1816283..2020966 [GRCh38]
Chr16:1866284..2070967 [GRCh37]
Chr16:1806285..2010968 [NCBI36]
Chr16:16p13.3
pathogenic
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(chr16:1850978-2116369)x3 copy number gain See cases [RCV000135695] Chr16:1850978..2116369 [GRCh38]
Chr16:1900979..2166370 [GRCh37]
Chr16:1840980..2106371 [NCBI36]
Chr16:16p13.3
uncertain significance
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 16p13.3-13.11(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(chr16:1860861-2070554)x3 copy number gain See cases [RCV000240428] Chr16:1860861..2070554 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.2401G>A (p.Asp801Asn) single nucleotide variant Inborn genetic diseases [RCV003244145] Chr16:1998546 [GRCh38]
Chr16:2048547 [GRCh37]
Chr16:16p13.3
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-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
NM_178167.5(ZNF598):c.1784C>T (p.Ser595Leu) single nucleotide variant Inborn genetic diseases [RCV003282592] Chr16:1999765 [GRCh38]
Chr16:2049766 [GRCh37]
Chr16:16p13.3
uncertain significance
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-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
NM_178167.5(ZNF598):c.1558C>G (p.Pro520Ala) single nucleotide variant Inborn genetic diseases [RCV003260882] Chr16:1999991 [GRCh38]
Chr16:2049992 [GRCh37]
Chr16:16p13.3
uncertain significance
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(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(chr16:1734363-2285561)x1 copy number loss not provided [RCV000683746] Chr16:1734363..2285561 [GRCh37]
Chr16:16p13.3
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-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(chr16:1807896-2311160)x3 copy number gain not provided [RCV000738986] Chr16:1807896..2311160 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:1813658-2319717)x3 copy number gain not provided [RCV000738989] Chr16:1813658..2319717 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2018777-2087562)x3 copy number gain not provided [RCV000751513] Chr16:2018777..2087562 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2022074-2081503)x3 copy number gain not provided [RCV000751514] Chr16:2022074..2081503 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2024204-2087562)x3 copy number gain not provided [RCV000751515] Chr16:2024204..2087562 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2024205-2070582)x3 copy number gain not provided [RCV000751516] Chr16:2024205..2070582 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2024205-2087547)x3 copy number gain not provided [RCV000751517] Chr16:2024205..2087547 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2026891-2048437)x3 copy number gain not provided [RCV000751519] Chr16:2026891..2048437 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2026891-2081503)x3 copy number gain not provided [RCV000751520] Chr16:2026891..2081503 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2027115-2087562)x3 copy number gain not provided [RCV000751521] Chr16:2027115..2087562 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2036937-2093576)x1 copy number loss not provided [RCV000751522] Chr16:2036937..2093576 [GRCh37]
Chr16:16p13.3
benign
NC_000016.9:g.(?_624055)_(2148005_?)del deletion Tuberous sclerosis 2 [RCV001033183] Chr16:624055..2148005 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2550979_?)dup duplication Idiopathic generalized epilepsy [RCV001033790] Chr16:624055..2550979 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.122_123= (p.Leu41=) variation not provided [RCV000947661] Chr16:2009624..2009625 [GRCh38]
Chr16:2059625..2059626 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:109978-4316797) copy number gain Chromosome 16p13.3 duplication syndrome [RCV000767731] Chr16:109978..4316797 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2115656_?)del deletion Tuberous sclerosis 2 [RCV000811345] Chr16:624055..2115656 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:85880-2053328)x1 copy number loss not provided [RCV000849039] Chr16:85880..2053328 [GRCh37]
Chr16:16p13.3
pathogenic
Single allele inversion Hereditary cancer-predisposing syndrome [RCV000850149] Chr16:1566500..2119769 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.2131C>T (p.Pro711Ser) single nucleotide variant Inborn genetic diseases [RCV003272386] Chr16:1999044 [GRCh38]
Chr16:2049045 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.9:g.(?_2034220)_(2152787_?)del deletion Tuberous sclerosis 2 [RCV003105244] Chr16:2034220..2152787 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:2021144-2146432)x1 copy number loss not provided [RCV002472911] Chr16:2021144..2146432 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.10:g.(?_1523498)_(2064447_?)del deletion Tuberous sclerosis 2 [RCV001032344] Chr16:1573499..2114448 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:84485-5251013)x3 copy number gain not provided [RCV001537890] Chr16:84485..5251013 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_1203718)_(2185710_?)del deletion Tuberous sclerosis 2 [RCV001033886] Chr16:1203718..2185710 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:2011148-2161281)x3 copy number gain not provided [RCV001259758] Chr16:2011148..2161281 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-5249457)x3 copy number gain not provided [RCV001259749] Chr16:85880..5249457 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2153916_?)dup duplication Epilepsy [RCV001344085]|Idiopathic generalized epilepsy [RCV001316565] Chr16:624055..2153916 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.10:g.1851807_2093151del deletion Tuberous sclerosis 2 [RCV001257345] Chr16:1851807..2093151 [GRCh38]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_2003468)_(2126543_?)del deletion Tuberous sclerosis 2 [RCV001949704] Chr16:2003468..2126543 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1847662-2653144) copy number gain not specified [RCV002052502] Chr16:1847662..2653144 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:1830141-2592737)x3 copy number gain not provided [RCV001827737] Chr16:1830141..2592737 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.9:g.(?_2029297)_(2096295_?)del deletion not provided [RCV001958665] Chr16:2029297..2096295 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_2034220)_(2136892_?)del deletion Tuberous sclerosis 2 [RCV001939677] Chr16:2034220..2136892 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_256302)_(5971108_?)dup duplication Familial Mediterranean fever [RCV001877532]|Fanconi anemia [RCV001877533]|not provided [RCV001877531] Chr16:256302..5971108 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.9:g.(?_256302)_(4852572_?)dup duplication Epilepsy [RCV003113403]|Idiopathic generalized epilepsy [RCV003109446]|Saldino-Mainzer syndrome [RCV003113404] Chr16:256302..4852572 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:111043-6627459)x3 copy number gain See cases [RCV002292215] Chr16:111043..6627459 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.10:g.1903155_2093402del deletion Tuberous sclerosis 2 [RCV002267197] Chr16:1903155..2093402 [GRCh38]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:2021144-2266791)x1 copy number loss not provided [RCV002472534] Chr16:2021144..2266791 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1942430-2653144)x3 copy number gain not provided [RCV002473837] Chr16:1942430..2653144 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1819C>T (p.Pro607Ser) single nucleotide variant Inborn genetic diseases [RCV002972772] Chr16:1999730 [GRCh38]
Chr16:2049731 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.197C>T (p.Ala66Val) single nucleotide variant Inborn genetic diseases [RCV002793900] Chr16:2009549 [GRCh38]
Chr16:2059550 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1993C>T (p.Pro665Ser) single nucleotide variant Inborn genetic diseases [RCV002977172] Chr16:1999556 [GRCh38]
Chr16:2049557 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1388G>A (p.Gly463Asp) single nucleotide variant Inborn genetic diseases [RCV002951832] Chr16:2000161 [GRCh38]
Chr16:2050162 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.2338A>G (p.Ser780Gly) single nucleotide variant Inborn genetic diseases [RCV003001790] Chr16:1998725 [GRCh38]
Chr16:2048726 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1438G>A (p.Ala480Thr) single nucleotide variant Inborn genetic diseases [RCV002869308] Chr16:2000111 [GRCh38]
Chr16:2050112 [GRCh37]
Chr16:16p13.3
likely benign
NM_178167.5(ZNF598):c.2375C>T (p.Ala792Val) single nucleotide variant Inborn genetic diseases [RCV002788995] Chr16:1998572 [GRCh38]
Chr16:2048573 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1776A>C (p.Lys592Asn) single nucleotide variant Inborn genetic diseases [RCV002939784] Chr16:1999773 [GRCh38]
Chr16:2049774 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1715C>G (p.Ser572Cys) single nucleotide variant Inborn genetic diseases [RCV002669205] Chr16:1999834 [GRCh38]
Chr16:2049835 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.2189C>T (p.Ala730Val) single nucleotide variant Inborn genetic diseases [RCV002678041] Chr16:1998986 [GRCh38]
Chr16:2048987 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.2014C>T (p.Leu672Phe) single nucleotide variant Inborn genetic diseases [RCV003204120] Chr16:1999535 [GRCh38]
Chr16:2049536 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1397G>T (p.Gly466Val) single nucleotide variant Inborn genetic diseases [RCV003215183] Chr16:2000152 [GRCh38]
Chr16:2050153 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1697G>C (p.Ser566Thr) single nucleotide variant Inborn genetic diseases [RCV003218097] Chr16:1999852 [GRCh38]
Chr16:2049853 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:811896-2130379)x1 copy number loss not provided [RCV003222891] Chr16:811896..2130379 [GRCh37]
Chr16:16p13.3
pathogenic
NM_178167.5(ZNF598):c.1640C>T (p.Pro547Leu) single nucleotide variant Inborn genetic diseases [RCV003189672] Chr16:1999909 [GRCh38]
Chr16:2049910 [GRCh37]
Chr16:16p13.3
likely benign
NM_178167.5(ZNF598):c.2153T>C (p.Leu718Pro) single nucleotide variant Inborn genetic diseases [RCV003304077] Chr16:1999022 [GRCh38]
Chr16:2049023 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1205C>A (p.Pro402His) single nucleotide variant Inborn genetic diseases [RCV003357078] Chr16:2000478 [GRCh38]
Chr16:2050479 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.884G>A (p.Arg295His) single nucleotide variant Inborn genetic diseases [RCV003356864] Chr16:2002217 [GRCh38]
Chr16:2052218 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_178167.5(ZNF598):c.1919C>T (p.Pro640Leu) single nucleotide variant not provided [RCV003395223] Chr16:1999630 [GRCh38]
Chr16:2049631 [GRCh37]
Chr16:16p13.3
likely benign
GRCh37/hg19 16p13.3(chr16:1054247-2592737)x3 copy number gain not provided [RCV003485080] Chr16:1054247..2592737 [GRCh37]
Chr16:16p13.3
likely pathogenic
NM_178167.5(ZNF598):c.1140G>A (p.Ala380=) single nucleotide variant not provided [RCV003395225] Chr16:2001065 [GRCh38]
Chr16:2051066 [GRCh37]
Chr16:16p13.3
likely benign
NM_178167.5(ZNF598):c.1890C>T (p.Ala630=) single nucleotide variant not provided [RCV003395224] Chr16:1999659 [GRCh38]
Chr16:2049660 [GRCh37]
Chr16:16p13.3
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3009
Count of miRNA genes:942
Interacting mature miRNAs:1146
Transcripts:ENST00000431526, ENST00000561787, ENST00000562103, ENST00000562988, ENST00000563630, ENST00000564556, ENST00000564824, ENST00000565396, ENST00000567008, ENST00000567625
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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.

Markers in Region
G43500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37162,047,690 - 2,047,814UniSTSGRCh37
GRCh37990,558,640 - 90,558,764UniSTSGRCh37
Build 36989,748,460 - 89,748,584RGDNCBI36
Celera162,259,869 - 2,259,993UniSTS
Celera961,124,359 - 61,124,483RGD
Cytogenetic Map9q22.1UniSTS
Cytogenetic Map16p13.3UniSTS
HuRef161,971,690 - 1,971,814UniSTS
HuRef960,381,511 - 60,381,635UniSTS
G44316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37162,047,790 - 2,047,940UniSTSGRCh37
GRCh37990,558,740 - 90,558,893UniSTSGRCh37
Build 36989,748,560 - 89,748,713RGDNCBI36
Celera162,259,969 - 2,260,119UniSTS
Celera961,124,459 - 61,124,612RGD
Cytogenetic Map9q22.1UniSTS
Cytogenetic Map16p13.3UniSTS
HuRef161,971,790 - 1,971,940UniSTS
HuRef960,381,611 - 60,381,764UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

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 2425 2304 1642 556 1658 398 4218 1760 2456 285 1441 1594 171 1204 2654 3
Low 14 687 84 68 290 67 139 437 1277 134 19 19 4 1 134 3 2
Below cutoff 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_032989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001405664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001405665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_178167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide ABBA01030283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL834428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC010990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC029270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC050477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA309611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000561787
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,999,894 - 2,001,744 (-)Ensembl
RefSeq Acc Id: ENST00000562103   ⟹   ENSP00000455308
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,997,655 - 2,009,821 (-)Ensembl
RefSeq Acc Id: ENST00000562988
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,997,654 - 2,009,764 (-)Ensembl
RefSeq Acc Id: ENST00000563630   ⟹   ENSP00000455882
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,997,655 - 2,009,821 (-)Ensembl
RefSeq Acc Id: ENST00000564556   ⟹   ENSP00000456128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,998,424 - 2,000,071 (-)Ensembl
RefSeq Acc Id: ENST00000564824
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,999,500 - 2,009,764 (-)Ensembl
RefSeq Acc Id: ENST00000565396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,997,655 - 2,009,795 (-)Ensembl
RefSeq Acc Id: ENST00000567008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,998,153 - 1,999,195 (-)Ensembl
RefSeq Acc Id: ENST00000567625   ⟹   ENSP00000455292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl162,000,010 - 2,002,345 (-)Ensembl
RefSeq Acc Id: ENST00000652647
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl161,997,654 - 2,009,814 (-)Ensembl
RefSeq Acc Id: NM_001405664   ⟹   NP_001392593
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38161,997,654 - 2,009,821 (-)NCBI
T2T-CHM13v2.0162,017,608 - 2,029,776 (-)NCBI
RefSeq Acc Id: NM_001405665   ⟹   NP_001392594
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38161,997,654 - 2,009,821 (-)NCBI
T2T-CHM13v2.0162,017,608 - 2,029,776 (-)NCBI
RefSeq Acc Id: NM_178167   ⟹   NP_835461
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38161,997,654 - 2,009,821 (-)NCBI
GRCh37162,047,653 - 2,059,822 (-)NCBI
Build 36161,987,769 - 1,999,764 (-)NCBI Archive
Celera162,259,947 - 2,271,940 (-)RGD
HuRef161,971,653 - 1,983,818 (-)NCBI
CHM1_1162,047,585 - 2,059,800 (-)NCBI
T2T-CHM13v2.0162,017,608 - 2,029,776 (-)NCBI
Sequence:
RefSeq Acc Id: NP_835461   ⟸   NM_178167
- Peptide Label: isoform 1
- UniProtKB: Q9H7J3 (UniProtKB/Swiss-Prot),   Q96FG3 (UniProtKB/Swiss-Prot),   Q8N3D9 (UniProtKB/Swiss-Prot),   Q8IW49 (UniProtKB/Swiss-Prot),   Q86UK7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000455308   ⟸   ENST00000562103
RefSeq Acc Id: ENSP00000455882   ⟸   ENST00000563630
RefSeq Acc Id: ENSP00000456128   ⟸   ENST00000564556
RefSeq Acc Id: ENSP00000455292   ⟸   ENST00000567625
RefSeq Acc Id: NP_001392594   ⟸   NM_001405665
- Peptide Label: isoform 3
- UniProtKB: Q9H7J3 (UniProtKB/Swiss-Prot),   Q96FG3 (UniProtKB/Swiss-Prot),   Q8N3D9 (UniProtKB/Swiss-Prot),   Q8IW49 (UniProtKB/Swiss-Prot),   Q86UK7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001392593   ⟸   NM_001405664
- Peptide Label: isoform 2
- UniProtKB: Q9H7J3 (UniProtKB/Swiss-Prot),   Q96FG3 (UniProtKB/Swiss-Prot),   Q8N3D9 (UniProtKB/Swiss-Prot),   Q8IW49 (UniProtKB/Swiss-Prot),   Q86UK7 (UniProtKB/Swiss-Prot)
Protein Domains
RING-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q86UK7-F1-model_v2 AlphaFold Q86UK7 1-904 view protein structure

Promoters
RGD ID:6811112
Promoter ID:HG_ACW:28638
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562,   Lymphoblastoid
Transcripts:ZNF598.GAPR07,   ZNF598.IAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 36161,989,136 - 1,989,636 (-)MPROMDB
RGD ID:6793638
Promoter ID:HG_KWN:22753
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:UC002COE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36161,992,036 - 1,993,252 (-)MPROMDB
RGD ID:6793637
Promoter ID:HG_KWN:22754
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:ENST00000248125,   NM_178167,   UC002COF.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36161,999,666 - 2,000,166 (-)MPROMDB
RGD ID:7230979
Promoter ID:EPDNEW_H21235
Type:initiation region
Name:ZNF598_1
Description:zinc finger protein 598
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38162,009,814 - 2,009,874EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28079 AgrOrtholog
COSMIC ZNF598 COSMIC
Ensembl Genes ENSG00000167962 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000562103.2 UniProtKB/TrEMBL
  ENST00000562988 ENTREZGENE
  ENST00000564556.1 UniProtKB/TrEMBL
  ENST00000567625.1 UniProtKB/TrEMBL
  ENST00000652647 ENTREZGENE
Gene3D-CATH 3.30.40.10 UniProtKB/TrEMBL
GTEx ENSG00000167962 GTEx
HGNC ID HGNC:28079 ENTREZGENE
Human Proteome Map ZNF598 Human Proteome Map
InterPro RING-HC_ZNF598/Hel2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZNF598/Hel2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_RING/FYVE/PHD UniProtKB/TrEMBL
KEGG Report hsa:90850 UniProtKB/Swiss-Prot
NCBI Gene 90850 ENTREZGENE
OMIM 617508 OMIM
PANTHER E3 UBIQUITIN-PROTEIN LIGASE ZNF598 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR22938 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134944505 PharmGKB
PROSITE ZF_RING_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt H3BPF3_HUMAN UniProtKB/TrEMBL
  H3BPG6_HUMAN UniProtKB/TrEMBL
  H3BR87_HUMAN UniProtKB/TrEMBL
  L8E9B0_HUMAN UniProtKB/TrEMBL
  Q86UK7 ENTREZGENE
  Q8IW49 ENTREZGENE
  Q8N3D9 ENTREZGENE
  Q96FG3 ENTREZGENE
  Q9H7J3 ENTREZGENE
  ZN598_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q8IW49 UniProtKB/Swiss-Prot
  Q8N3D9 UniProtKB/Swiss-Prot
  Q96FG3 UniProtKB/Swiss-Prot
  Q9H7J3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2020-04-20 ZNF598  zinc finger protein 598, E3 ubiquitin ligase  ZNF598  zinc finger protein 598  Symbol and/or name change 19259463 PROVISIONAL