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ZN415_HUMAN
ID   ZN415_HUMAN             Reviewed;         603 AA.
AC   Q09FC8; F5H287; Q09FC7; Q09FC9; Q09FD0; Q6NSZ2; Q6P3S0; Q9NUR2;
DT   15-MAY-2007, integrated into UniProtKB/Swiss-Prot.
DT   15-MAY-2007, sequence version 2.
DT   03-AUG-2022, entry version 139.
DE   RecName: Full=Zinc finger protein 415;
GN   Name=ZNF415;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1; 2; 3; 4 AND 5), FUNCTION,
RP   SUBCELLULAR LOCATION, ALTERNATIVE SPLICING, TISSUE SPECIFICITY, AND
RP   VARIANTS LEU-229 AND VAL-233.
RC   TISSUE=Fetal heart;
RX   PubMed=17055453; DOI=10.1016/j.bbrc.2006.09.161;
RA   Cheng Y., Wang Y., Li Y., Deng Y., Hu J., Mo X., Li N., Li Y., Luo N.,
RA   Yuan W., Xiao J., Zhu C., Wu X., Liu M.;
RT   "A novel human gene ZNF415 with five isoforms inhibits AP-1- and p53-
RT   mediated transcriptional activity.";
RL   Biochem. Biophys. Res. Commun. 351:33-39(2006).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 5), NUCLEOTIDE SEQUENCE
RP   [LARGE SCALE MRNA] OF 1-72 (ISOFORM 6), AND VARIANTS LEU-229 AND VAL-233.
RC   TISSUE=Brain, Placenta, and Testis;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=15057824; DOI=10.1038/nature02399;
RA   Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E.,
RA   Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M., Aerts A.,
RA   Altherr M., Ashworth L., Bajorek E., Black S., Branscomb E., Caenepeel S.,
RA   Carrano A.V., Caoile C., Chan Y.M., Christensen M., Cleland C.A.,
RA   Copeland A., Dalin E., Dehal P., Denys M., Detter J.C., Escobar J.,
RA   Flowers D., Fotopulos D., Garcia C., Georgescu A.M., Glavina T., Gomez M.,
RA   Gonzales E., Groza M., Hammon N., Hawkins T., Haydu L., Ho I., Huang W.,
RA   Israni S., Jett J., Kadner K., Kimball H., Kobayashi A., Larionov V.,
RA   Leem S.-H., Lopez F., Lou Y., Lowry S., Malfatti S., Martinez D.,
RA   McCready P.M., Medina C., Morgan J., Nelson K., Nolan M., Ovcharenko I.,
RA   Pitluck S., Pollard M., Popkie A.P., Predki P., Quan G., Ramirez L.,
RA   Rash S., Retterer J., Rodriguez A., Rogers S., Salamov A., Salazar A.,
RA   She X., Smith D., Slezak T., Solovyev V., Thayer N., Tice H., Tsai M.,
RA   Ustaszewska A., Vo N., Wagner M., Wheeler J., Wu K., Xie G., Yang J.,
RA   Dubchak I., Furey T.S., DeJong P., Dickson M., Gordon D., Eichler E.E.,
RA   Pennacchio L.A., Richardson P., Stubbs L., Rokhsar D.S., Myers R.M.,
RA   Rubin E.M., Lucas S.M.;
RT   "The DNA sequence and biology of human chromosome 19.";
RL   Nature 428:529-535(2004).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 4), AND VARIANT ASP-463.
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
CC   -!- FUNCTION: Involved in transcriptional regulation. Transcriptional
CC       activity differed among the various isoforms. All isoforms except
CC       isoform 3 seem to suppresses the transcriptional activities of AP-1 and
CC       p53/TP53. {ECO:0000269|PubMed:17055453}.
CC   -!- INTERACTION:
CC       Q09FC8; Q9BQ66: KRTAP4-12; NbExp=3; IntAct=EBI-10226171, EBI-739863;
CC       Q09FC8; Q5JR59: MTUS2; NbExp=3; IntAct=EBI-10226171, EBI-742948;
CC       Q09FC8-4; Q9BWT7: CARD10; NbExp=3; IntAct=EBI-12273744, EBI-3866279;
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000269|PubMed:17055453}. Cytoplasm
CC       {ECO:0000269|PubMed:17055453}. Note=Isoforms 1, isoform 2, isoform 4
CC       and isoform 5 showed both nuclear and cytoplasm localization. Isoform 3
CC       localized only to nucleus.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=6;
CC       Name=1; Synonyms=ZNF415-3;
CC         IsoId=Q09FC8-1; Sequence=Displayed;
CC       Name=2; Synonyms=ZNF415-2;
CC         IsoId=Q09FC8-2; Sequence=VSP_025178;
CC       Name=3; Synonyms=ZNF415-1;
CC         IsoId=Q09FC8-3; Sequence=VSP_025175;
CC       Name=4; Synonyms=ZNF415-4;
CC         IsoId=Q09FC8-4; Sequence=VSP_025177;
CC       Name=5; Synonyms=ZNF415-5;
CC         IsoId=Q09FC8-5; Sequence=VSP_025176;
CC       Name=6;
CC         IsoId=Q09FC8-6; Sequence=VSP_044807;
CC   -!- TISSUE SPECIFICITY: Expressed in all tissues examined. Isoforms are
CC       differentially expressed. Isoform 3 and isoform 5 were highly
CC       expressed, isoform 4 moderately expressed, isoform 2 lower expression,
CC       the lowest expression level was seem with isoform 1.
CC       {ECO:0000269|PubMed:17055453}.
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DR   EMBL; DQ925697; ABI51311.1; -; mRNA.
DR   EMBL; DQ925696; ABI51310.1; -; mRNA.
DR   EMBL; DQ925698; ABI51312.1; -; mRNA.
DR   EMBL; DQ925695; ABI51309.1; -; mRNA.
DR   EMBL; AY283600; AAP35086.1; -; mRNA.
DR   EMBL; AK002053; BAA92059.1; -; mRNA.
DR   EMBL; DA518713; -; NOT_ANNOTATED_CDS; mRNA.
DR   EMBL; AC010328; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; BC069668; AAH69668.1; -; mRNA.
DR   EMBL; BC063880; AAH63880.1; -; mRNA.
DR   CCDS; CCDS12860.1; -. [Q09FC8-5]
DR   CCDS; CCDS54313.1; -. [Q09FC8-6]
DR   CCDS; CCDS82393.1; -. [Q09FC8-3]
DR   RefSeq; NP_001129510.2; NM_001136038.2. [Q09FC8-6]
DR   RefSeq; NP_001157781.1; NM_001164309.1. [Q09FC8-5]
DR   RefSeq; NP_001317688.1; NM_001330759.1. [Q09FC8-3]
DR   RefSeq; NP_001317695.1; NM_001330766.1.
DR   RefSeq; NP_060825.2; NM_018355.3. [Q09FC8-5]
DR   RefSeq; XP_006723335.1; XM_006723272.2.
DR   RefSeq; XP_006723336.1; XM_006723273.2.
DR   RefSeq; XP_006723337.1; XM_006723274.2.
DR   RefSeq; XP_006723340.1; XM_006723277.2.
DR   RefSeq; XP_006723342.1; XM_006723279.1. [Q09FC8-4]
DR   RefSeq; XP_006723343.1; XM_006723280.2. [Q09FC8-3]
DR   RefSeq; XP_006723344.1; XM_006723281.2.
DR   RefSeq; XP_011525405.1; XM_011527103.1.
DR   RefSeq; XP_011525406.1; XM_011527104.1.
DR   RefSeq; XP_016882453.1; XM_017026964.1. [Q09FC8-5]
DR   RefSeq; XP_016882454.1; XM_017026965.1.
DR   RefSeq; XP_016882455.1; XM_017026966.1.
DR   RefSeq; XP_016882456.1; XM_017026967.1.
DR   RefSeq; XP_016882457.1; XM_017026968.1. [Q09FC8-4]
DR   RefSeq; XP_016882459.1; XM_017026970.1. [Q09FC8-2]
DR   RefSeq; XP_016882461.1; XM_017026972.1.
DR   RefSeq; XP_016882462.1; XM_017026973.1.
DR   AlphaFoldDB; Q09FC8; -.
DR   SMR; Q09FC8; -.
DR   BioGRID; 120900; 7.
DR   IntAct; Q09FC8; 4.
DR   STRING; 9606.ENSP00000439435; -.
DR   iPTMnet; Q09FC8; -.
DR   PhosphoSitePlus; Q09FC8; -.
DR   BioMuta; ZNF415; -.
DR   DMDM; 147742905; -.
DR   jPOST; Q09FC8; -.
DR   MassIVE; Q09FC8; -.
DR   MaxQB; Q09FC8; -.
DR   PaxDb; Q09FC8; -.
DR   PeptideAtlas; Q09FC8; -.
DR   PRIDE; Q09FC8; -.
DR   ProteomicsDB; 25895; -.
DR   ProteomicsDB; 58725; -. [Q09FC8-1]
DR   ProteomicsDB; 58726; -. [Q09FC8-2]
DR   ProteomicsDB; 58727; -. [Q09FC8-3]
DR   ProteomicsDB; 58728; -. [Q09FC8-4]
DR   ProteomicsDB; 58729; -. [Q09FC8-5]
DR   Antibodypedia; 820; 140 antibodies from 21 providers.
DR   DNASU; 55786; -.
DR   Ensembl; ENST00000243643.9; ENSP00000243643.3; ENSG00000170954.12. [Q09FC8-5]
DR   Ensembl; ENST00000421033.5; ENSP00000395055.2; ENSG00000170954.12. [Q09FC8-5]
DR   Ensembl; ENST00000500065.8; ENSP00000439435.1; ENSG00000170954.12. [Q09FC8-6]
DR   Ensembl; ENST00000601493.5; ENSP00000472911.1; ENSG00000170954.12. [Q09FC8-3]
DR   GeneID; 55786; -.
DR   KEGG; hsa:55786; -.
DR   MANE-Select; ENST00000243643.9; ENSP00000243643.3; NM_018355.4; NP_060825.2. [Q09FC8-5]
DR   UCSC; uc002qaw.4; human. [Q09FC8-1]
DR   CTD; 55786; -.
DR   DisGeNET; 55786; -.
DR   GeneCards; ZNF415; -.
DR   HGNC; HGNC:20636; ZNF415.
DR   HPA; ENSG00000170954; Low tissue specificity.
DR   MIM; 619506; gene.
DR   neXtProt; NX_Q09FC8; -.
DR   OpenTargets; ENSG00000170954; -.
DR   PharmGKB; PA134984602; -.
DR   VEuPathDB; HostDB:ENSG00000170954; -.
DR   eggNOG; KOG1721; Eukaryota.
DR   GeneTree; ENSGT00940000164638; -.
DR   HOGENOM; CLU_002678_44_0_1; -.
DR   InParanoid; Q09FC8; -.
DR   OMA; HCSNFNR; -.
DR   OrthoDB; 1318335at2759; -.
DR   PhylomeDB; Q09FC8; -.
DR   TreeFam; TF341892; -.
DR   PathwayCommons; Q09FC8; -.
DR   Reactome; R-HSA-212436; Generic Transcription Pathway.
DR   SignaLink; Q09FC8; -.
DR   BioGRID-ORCS; 55786; 11 hits in 1092 CRISPR screens.
DR   ChiTaRS; ZNF415; human.
DR   GenomeRNAi; 55786; -.
DR   Pharos; Q09FC8; Tdark.
DR   PRO; PR:Q09FC8; -.
DR   Proteomes; UP000005640; Chromosome 19.
DR   RNAct; Q09FC8; protein.
DR   Bgee; ENSG00000170954; Expressed in sperm and 175 other tissues.
DR   ExpressionAtlas; Q09FC8; baseline and differential.
DR   Genevisible; Q09FC8; HS.
DR   GO; GO:0005737; C:cytoplasm; IEA:UniProtKB-SubCell.
DR   GO; GO:0001650; C:fibrillar center; IDA:HPA.
DR   GO; GO:0015630; C:microtubule cytoskeleton; IDA:HPA.
DR   GO; GO:0005634; C:nucleus; IBA:GO_Central.
DR   GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; IBA:GO_Central.
DR   GO; GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
DR   GO; GO:0000978; F:RNA polymerase II cis-regulatory region sequence-specific DNA binding; IBA:GO_Central.
DR   GO; GO:0006357; P:regulation of transcription by RNA polymerase II; IBA:GO_Central.
DR   InterPro; IPR036236; Znf_C2H2_sf.
DR   InterPro; IPR013087; Znf_C2H2_type.
DR   Pfam; PF00096; zf-C2H2; 11.
DR   SMART; SM00355; ZnF_C2H2; 11.
DR   SUPFAM; SSF57667; SSF57667; 6.
DR   PROSITE; PS00028; ZINC_FINGER_C2H2_1; 11.
DR   PROSITE; PS50157; ZINC_FINGER_C2H2_2; 11.
PE   1: Evidence at protein level;
KW   Alternative splicing; Cytoplasm; DNA-binding; Metal-binding; Nucleus;
KW   Reference proteome; Repeat; Transcription; Transcription regulation; Zinc;
KW   Zinc-finger.
FT   CHAIN           1..603
FT                   /note="Zinc finger protein 415"
FT                   /id="PRO_0000286808"
FT   ZN_FING         264..286
FT                   /note="C2H2-type 1; degenerate"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         292..314
FT                   /note="C2H2-type 2"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         320..342
FT                   /note="C2H2-type 3"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         348..370
FT                   /note="C2H2-type 4"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         376..398
FT                   /note="C2H2-type 5"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         404..426
FT                   /note="C2H2-type 6"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         432..454
FT                   /note="C2H2-type 7"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         460..482
FT                   /note="C2H2-type 8"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         488..510
FT                   /note="C2H2-type 9"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         516..538
FT                   /note="C2H2-type 10"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         544..566
FT                   /note="C2H2-type 11"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         572..594
FT                   /note="C2H2-type 12"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   VAR_SEQ         1..278
FT                   /note="Missing (in isoform 3)"
FT                   /evidence="ECO:0000303|PubMed:17055453"
FT                   /id="VSP_025175"
FT   VAR_SEQ         1..93
FT                   /note="MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRV
FT                   EIDQRCENRLECNGAISAHCNLRLPDSNDSPASASRVAGIT -> MAFTQLTFRDVAIE
FT                   FSQDEWKCLNSTQRTLYRDVMLENYRNLVSL (in isoform 5)"
FT                   /evidence="ECO:0000303|PubMed:14702039,
FT                   ECO:0000303|PubMed:17055453"
FT                   /id="VSP_025176"
FT   VAR_SEQ         1..93
FT                   /note="MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRV
FT                   EIDQRCENRLECNGAISAHCNLRLPDSNDSPASASRVAGIT -> MDGDGLTFRDVAIE
FT                   FSQDEWKCLNSTQRTLYRDVMLENYRNLVSL (in isoform 6)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_044807"
FT   VAR_SEQ         1..92
FT                   /note="MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRV
FT                   EIDQRCENRLECNGAISAHCNLRLPDSNDSPASASRVAGI -> MWEHRKEPWTIESQV
FT                   RVARKPKGWEWIKGVK (in isoform 4)"
FT                   /evidence="ECO:0000303|PubMed:15489334,
FT                   ECO:0000303|PubMed:17055453"
FT                   /id="VSP_025177"
FT   VAR_SEQ         26..61
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:17055453"
FT                   /id="VSP_025178"
FT   VARIANT         196
FT                   /note="H -> P (in dbSNP:rs16984466)"
FT                   /id="VAR_032166"
FT   VARIANT         229
FT                   /note="I -> L (in dbSNP:rs1054485)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:17055453"
FT                   /id="VAR_032167"
FT   VARIANT         233
FT                   /note="I -> V (in dbSNP:rs1133327)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:17055453"
FT                   /id="VAR_032168"
FT   VARIANT         241
FT                   /note="Y -> C (in dbSNP:rs1560099)"
FT                   /id="VAR_032169"
FT   VARIANT         463
FT                   /note="N -> D (in dbSNP:rs10410030)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_032170"
SQ   SEQUENCE   603 AA;  68798 MW;  6B62D29A4E6E9300 CRC64;
     MPELYTEDFI QGCDVGELQE PGLPGVLSYV GAQERALDHR KPSTSSKKTK RVEIDQRCEN
     RLECNGAISA HCNLRLPDSN DSPASASRVA GITDLSRNCV IKELAPQQEG NPGEVFHTVT
     LEQHEKHDIE EFCFREIKKK IHDFDCQWRD DERNCNKVTT APKENLTCRR DQRDRRGIGN
     KSIKHQLGLS FLPHPHELQQ FQAEGKIYEC NHVEKSVNHG SSVSPPQIIS STIKTHVSNK
     YGTDFICSSL LTQEQKSCIR EKPYRYIECD KALNHGSHMT VRQVSHSGEK GYKCDLCGKV
     FSQKSNLARH WRVHTGEKPY KCNECDRSFS RNSCLALHRR VHTGEKPYKC YECDKVFSRN
     SCLALHQKTH IGEKPYTCKE CGKAFSVRST LTNHQVIHSG KKPYKCNECG KVFSQTSSLA
     THQRIHTGEK PYKCNECGKV FSQTSSLARH WRIHTGEKPY KCNECGKVFS YNSHLASHRR
     VHTGEKPYKC NECGKAFSVH SNLTTHQVIH TGEKPYKCNQ CGKGFSVHSS LTTHQVIHTG
     EKPYKCNECG KSFSVRPNLT RHQIIHTGKK PYKCSDCGKS FSVRPNLFRH QIIHTKEKPY
     KRN
 
 
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