Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5178
Gene name Gene Name - the full gene name approved by the HGNC.
Paternally expressed 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PEG3
Synonyms (NCBI Gene) Gene synonyms aliases
PW1, ZKSCAN22, ZNF904, ZSCAN24
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.43
Summary Summary of gene provided in NCBI Entrez Gene.
In human, ZIM2 and PEG3 are treated as two distinct genes though they share multiple 5` exons and a common promoter and both genes are paternally expressed (PMID:15203203). Alternative splicing events connect their shared 5` exons either with the remainin
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018787 hsa-miR-335-5p Microarray 18185580
MIRT440005 hsa-miR-412-3p HITS-CLIP 24374217
MIRT440005 hsa-miR-412-3p HITS-CLIP 24374217
MIRT1224680 hsa-miR-1236 CLIP-seq
MIRT1224681 hsa-miR-1262 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
YY1 Unknown 18458536
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IBA 21873635
GO:0000122 Process Negative regulation of transcription by RNA polymerase II ISS
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0001227 Function DNA-binding transcription repressor activity, RNA polymerase II-specific IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601483 8826 ENSG00000198300
Protein
UniProt ID Q9GZU2
Protein name Paternally-expressed gene 3 protein (Zinc finger and SCAN domain-containing protein 24)
Protein function Induces apoptosis in cooperation with SIAH1A. Acts as a mediator between p53/TP53 and BAX in a neuronal death pathway that is activated by DNA damage. Acts synergistically with TRAF2 and inhibits TNF induced apoptosis through activation of NF-ka
PDB 4BHX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02023 SCAN 42 131 SCAN domain Domain
PF00096 zf-C2H2 452 474 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 505 527 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 627 649 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 969 991 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 1107 1129 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 1163 1185 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 1225 1247 Zinc finger, C2H2 type Domain
PF13913 zf-C2HC_2 1280 1303 Domain
PF00096 zf-C2H2 1332 1354 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 1564 1586 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Brain, glial cells, astrocytes, embryo, placenta, testis, ovary and uterus. In the placenta it is found in the layer of villous cytotrophoblast cells while in the ovary it is found in the cells of the ovarian stroma including the theca
Sequence
MLPPKHLSATKPKKSWAPNLYELDSDLTKEPDVIIGEGPTDSEFFHQRFRNLIYVEFVGP
RKTLIKLRNLCLDWLQPETRTKEEIIELLVLEQYLTIIPEKLKPWVRAKKPENCEKLVTL
LENYKEMYQPE
DDNNSDVTSDDDMTRNRRESSPPHSVHSFSDRDWDRRGRSRDMEPRDRW
SHTRNPRSRMPPRDLSLPVVAKTSFEMDREDDRDSRAYESRSQDAESYQNVVDLAEDRKP
HNTIQDNMENYRKLLSLVQLAEDDGHSHMTQGHSSRSKRSAYPSTSRGLKTMPEAKKSTH
RRGICEDESSHGVIMEKFIKDVSRSSKSGRARESSDRSQRFPRMSDDNWKDISLNKRESV
IQQRVYEGNAFRGGFRFNSTLVSRKRVLERKRRYHFDTDGKGSIHDQKGCPRKKPFECGS
EMRKAMSVSSLSSLSSPSFTESQPIDFGAMPYVCDECGRSFSVISEFVEHQIMHTRENLY
EYGESFIHSVAVSEVQKSQVGGKRFECKDCGETFNKSAALAEHRKIHARGYLVECKNQEC
EEAFMPSPTFSELQKIYGKDKFYECRVCKETFLHSSALIEHQKIHFGDDKDNEREHERER
ERERGETFRPSPALNEFQKMYGKEKMYECKVCGETFLHSSSLKEHQKIHTRGNPFENKGK
VCEETFIPGQSLKRRQKTYNKEKLCDFTDGRDAFMQSSELSEHQKIHSRKNLFEGRGYEK
SVIHSGPFTESQKSHTITRPLESDEDEKAFTISSNPYENQKIPTKENVYEAKSYERSVIH
SLASVEAQKSHSVAGPSKPKVMAESTIQSFDAINHQRVRAGGNTSEGREYSRSVIHSLVA
SKPPRSHNGNELVESNEKGESSIYISDLNDKRQKIPARENPCEGGSKNRNYEDSVIQSVF
RAKPQKSVPGEGSGEFKKDGEFSVPSSNVREYQKARAKKKYIEHRSNETSVIHSLPFGEQ
TFRPRGMLYECQECGECFAHSSDLTEHQKIHDREKPSGSRNYEWSVIRSLAPTDPQTSYA
QEQYAKEQARNKCKDFRQFFATSEDLNTNQKIYDQEKSHGEESQGENTDGEETHSEETHG
QETIEDPVIQGSDMEDPQKDDPDDKIYECEDCGLGFVDLTDLTDHQKVHSRKCLVDSREY
THSVIHTHSISEYQRDYTGEQLYECPKCGESFIHSSFLFEHQRIHEQDQLYSMKGCDDGF
IALLPMKPRRNRAAERNPALAGSAIRCLLCGQGFIHSSALNEHMRLHREDDLLEQSQMAE
EAIIPGLALTEFQRSQTEERLFECAVCGESFVNPAELADHVTVHKNEPYEYGSSYTHTSF
LTEPLKGAIPFYECKDCGKSFIHSTVLTKHKELHLEEEEEDEAAAAAAAAAQEVEANVHV
PQVVLRIQGLNVEAAEPEVEAAEPEVEAAEPEVEAAEPNGEAEGPDGEAAEPIGEAGQPN
GEAEQPNGDADEPDGAGIEDPEERAEEPEGKAEEPEGDADEPDGVGIEDPEEGEDQEIQV
EEPYYDCHECTETFTSSTAFSEHLKTHASMIIFEPANAFGECSGYIERASTSTGGANQAD
EKYFKCDVCGQLFNDRLSLARHQNTHTG
Sequence length 1588
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Cholangiocarcinoma Cholangiocarcinoma, Extrahepatic Cholangiocarcinoma 22561520 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Abortion Habitual Associate 37699152
Breast Neoplasms Associate 25560175, 32729618
Carcinogenesis Associate 19367087
Cell Transformation Neoplastic Inhibit 32209654
Diabetes Gestational Associate 40147358
Diabetes Mellitus Type 2 Associate 25201977
Endometrial Neoplasms Associate 32555395
Glioblastoma Inhibit 19367087
Glioma Associate 19367087
Hemangioma Cavernous Central Nervous System Associate 40238631