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Previous release (v1)
2024-05-01 06:45:38, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_006223 1239 bp mRNA linear PRI 15-MAY-2023
DEFINITION Homo sapiens peptidylprolyl cis/trans isomerase, NIMA-interacting 4
(PIN4), transcript variant 1, mRNA.
ACCESSION NM_006223 XM_001126085
VERSION NM_006223.4
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 1239)
AUTHORS Naito M, Ikeda K, Aoyama S, Kanamoto M, Akasaka Y, Kido Y,
Nakanishi M, Kanna M, Yamamotoya T, Matsubara A, Hinata N, Asano T
and Nakatsu Y.
TITLE Par14 interacts with the androgen receptor, augmenting both its
transcriptional activity and prostate cancer proliferation
JOURNAL Cancer Med 12 (7), 8464-8475 (2023)
PUBMED 36583514
REMARK GeneRIF: Par14 interacts with the androgen receptor, augmenting
both its transcriptional activity and prostate cancer
proliferation.
REFERENCE 2 (bases 1 to 1239)
AUTHORS Fragoza R, Das J, Wierbowski SD, Liang J, Tran TN, Liang S, Beltran
JF, Rivera-Erick CA, Ye K, Wang TY, Yao L, Mort M, Stenson PD,
Cooper DN, Wei X, Keinan A, Schimenti JC, Clark AG and Yu H.
TITLE Extensive disruption of protein interactions by genetic variants
across the allele frequency spectrum in human populations
JOURNAL Nat Commun 10 (1), 4141 (2019)
PUBMED 31515488
REMARK Publication Status: Online-Only
REFERENCE 3 (bases 1 to 1239)
AUTHORS Saeed U, Kim J, Piracha ZZ, Kwon H, Jung J, Chwae YJ, Park S, Shin
HJ and Kim K.
TITLE Parvulin 14 and Parvulin 17 Bind to HBx and cccDNA and Upregulate
Hepatitis B Virus Replication from cccDNA to Virion in an
HBx-Dependent Manner
JOURNAL J Virol 93 (6), e01840-18 (2019)
PUBMED 30567987
REMARK GeneRIF: In the presence of HBx, the Par14 and Par17 proteins bound
to cccDNA.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 1239)
AUTHORS Kessler D, Papatheodorou P, Stratmann T, Dian EA, Hartmann-Fatu C,
Rassow J, Bayer P and Mueller JW.
TITLE The DNA binding parvulin Par17 is targeted to the mitochondrial
matrix by a recently evolved prepeptide uniquely present in
Hominidae
JOURNAL BMC Biol 5, 37 (2007)
PUBMED 17875217
REMARK Publication Status: Online-Only
REFERENCE 5 (bases 1 to 1239)
AUTHORS Mueller JW, Kessler D, Neumann D, Stratmann T, Papatheodorou P,
Hartmann-Fatu C and Bayer P.
TITLE Characterization of novel elongated Parvulin isoforms that are
ubiquitously expressed in human tissues and originate from
alternative transcription initiation
JOURNAL BMC Mol Biol 7, 9 (2006)
PUBMED 16522211
REMARK GeneRIF: Identification of a longer Parvulin isoform (Par17) that
has an extension at the 5' end including a 75 bp extended open
reading frame.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 1239)
AUTHORS Surmacz TA, Bayer E, Rahfeld JU, Fischer G and Bayer P.
TITLE The N-terminal basic domain of human parvulin hPar14 is responsible
for the entry to the nucleus and high-affinity DNA-binding
JOURNAL J Mol Biol 321 (2), 235-247 (2002)
PUBMED 12144781
REMARK GeneRIF: The N-terminal basic domain of human parvulin hPar14 is
responsible for the entry to the nucleus and high-affinity
DNA-binding.
REFERENCE 7 (bases 1 to 1239)
AUTHORS Fujiyama S, Yanagida M, Hayano T, Miura Y, Isobe T, Fujimori F,
Uchida T and Takahashi N.
TITLE Isolation and proteomic characterization of human
Parvulin-associating preribosomal ribonucleoprotein complexes
JOURNAL J Biol Chem 277 (26), 23773-23780 (2002)
PUBMED 11960984
REMARK Erratum:[J Biol Chem. 2002 Nov 1;277(44):42418.]
REFERENCE 8 (bases 1 to 1239)
AUTHORS Terada T, Shirouzu M, Fukumori Y, Fujimori F, Ito Y, Kigawa T,
Yokoyama S and Uchida T.
TITLE Solution structure of the human parvulin-like peptidyl prolyl
cis/trans isomerase, hPar14
JOURNAL J Mol Biol 305 (4), 917-926 (2001)
PUBMED 11162102
REFERENCE 9 (bases 1 to 1239)
AUTHORS Rulten S, Thorpe J and Kay J.
TITLE Identification of eukaryotic parvulin homologues: a new subfamily
of peptidylprolyl cis-trans isomerases
JOURNAL Biochem Biophys Res Commun 259 (3), 557-562 (1999)
PUBMED 10364457
REFERENCE 10 (bases 1 to 1239)
AUTHORS Uchida T, Fujimori F, Tradler T, Fischer G and Rahfeld JU.
TITLE Identification and characterization of a 14 kDa human protein as a
novel parvulin-like peptidyl prolyl cis/trans isomerase
JOURNAL FEBS Lett 446 (2-3), 278-282 (1999)
PUBMED 10100858
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AV709926.2, BC112281.1,
BE504461.1 and AL135749.3.
This sequence is a reference standard in the RefSeqGene project.
On Dec 15, 2018 this sequence version replaced NM_006223.3.
Summary: This gene encodes a member of the parvulin subfamily of
the peptidyl-prolyl cis/trans isomerase protein family. The encoded
protein catalyzes the isomerization of peptidylprolyl bonds, and
may play a role in the cell cycle, chromatin remodeling, and/or
ribosome biogenesis. The encoded protein may play an additional
role in the mitochondria. [provided by RefSeq, Dec 2009].
Transcript Variant: This variant (1) encodes isoform 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: BC111394.1, BC070288.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1965299, SAMEA1966682
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
gene product(s) localized to mito. :: PMID: 10364457, 17875217
MANE Ensembl match :: ENST00000373669.8/
ENSP00000362773.3
RefSeq Select criteria :: based on conservation,
expression
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-8 AV709926.2 31-38
9-507 BC112281.1 87-585
508-554 BE504461.1 437-483 c
555-1239 AL135749.3 11545-12229
FEATURES Location/Qualifiers
source 1..1239
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq13.1"
gene 1..1239
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="peptidylprolyl cis/trans isomerase,
NIMA-interacting 4"
/db_xref="GeneID:5303"
/db_xref="HGNC:HGNC:8992"
/db_xref="MIM:300252"
exon 1..72
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:6525589"
variation 3
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:776253818"
variation 8
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:7058353"
variation 9
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769563285"
variation 14
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:140494564"
variation 16
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1248894800"
variation 17
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:764456398"
variation 18
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1356496363"
variation 22
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198053299"
variation 26
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1161859993"
variation 27
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:774679844"
CDS 30..425
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/EC_number="5.2.1.8"
/note="isoform 1 is encoded by transcript variant 1;
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4;
rotamase PIN4; PPIase PIN4; parvulin-14; parvulin-17;
eukaryotic parvulin homolog; protein (peptidylprolyl
cis/trans isomerase) NIMA-interacting, 4 (parvulin);
peptidyl-prolyl cis-trans isomerase Pin4; peptidyl-prolyl
cis/trans isomerase EPVH"
/codon_start=1
/product="peptidyl-prolyl cis-trans isomerase
NIMA-interacting 4 isoform 1"
/protein_id="NP_006214.3"
/db_xref="CCDS:CCDS14417.2"
/db_xref="GeneID:5303"
/db_xref="HGNC:HGNC:8992"
/db_xref="MIM:300252"
/translation="
MPPKGKSGSGKAGKGGAASGSDSADKKAQGPKGGGNAVKVRHILCEKHGKIMEAMEKLKSGMRFNEVAAQYSEDKARQGGDLGWMTRGSMVGPFQEAAFALPVSGMDKPVFTDPPVKTKFGYHIIMVEGRK"
misc_feature 30..152
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y237.1);
Region: Necessary for association with the pre-rRNP
complexes"
misc_feature 30..146
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y237.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 30..104
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="propagated from UniProtKB/Swiss-Prot (Q9Y237.1);
Region: Necessary for nuclear localization and
DNA-binding"
misc_feature 84..86
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="Phosphoserine, by CK2.
/evidence=ECO:0000269|PubMed:12860119; propagated from
UniProtKB/Swiss-Prot (Q9Y237.1); phosphorylation site"
misc_feature 105..422
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="PPIC-type PPIASE domain; Region: Rotamase_2;
cl29122"
/db_xref="CDD:421736"
variation 32
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:928957074"
variation 33
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761901303"
variation 34
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:767947505"
variation 35
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042674116"
variation 36
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396116235"
variation 37
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:750693487"
variation 38
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:972910933"
variation 41
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:756647963"
variation 42
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:766793709"
variation 43
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042674272"
variation 44
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282237271"
variation 45
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042674317"
variation 48
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:752263746"
variation 50
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1602423545"
variation 51
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042674403"
variation 54
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1406000209"
variation 55
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:919695845"
variation 58
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:757882457"
variation 62
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042674505"
variation 63
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274971838"
variation 64
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:376742840"
variation 65
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042674568"
variation 66
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389483169"
variation 67
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042674636"
variation 71
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042674656"
exon 73..146
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 73
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:889080355"
variation 77
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:771318018"
variation 78
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000835180"
variation 79
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:371226434"
variation 80
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:760052937"
variation 83
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354887405"
variation 86
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209742577"
variation 87
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266101192"
variation 91
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042704083"
variation 98
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042704119"
variation 99
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:914083195"
variation 100
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042704179"
variation 104
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184254268"
variation 105..110
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aag"
/replace="aagaag"
/db_xref="dbSNP:1473857391"
variation 106
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:754347273"
variation 112
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213489459"
variation 115
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:946447218"
variation 117
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286399946"
variation 118
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042704295"
variation 120..122
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2147567048"
variation 123
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043439923"
variation 127
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042704348"
variation 130
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2147567063"
variation 132
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1032364083"
variation 136
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:145654350"
variation 137
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:761204353"
variation 141
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042704489"
variation 142
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042704520"
variation 145
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:956775117"
exon 147..266
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 149
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:2042768419"
variation 151
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212456427"
variation 152
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489194758"
variation 155
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:758379340"
variation 161
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186725109"
variation 167
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208971104"
variation 173
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1263638121"
variation 175
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042768627"
variation 176
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356830897"
variation 182
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:777869803"
variation 184
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:747218626"
variation 192
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418507010"
variation 197
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1602431274"
variation 199..203
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="agtta"
/replace="agttagtta"
/db_xref="dbSNP:1462890104"
variation 199
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771087340"
variation 200
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:776986443"
variation 203
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:367799837"
variation 210
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042768901"
variation 213
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1454539015"
variation 218
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371560354"
variation 221
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042768952"
variation 223
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042768987"
variation 224
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042769012"
variation 227
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:775826431"
variation 233
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:11415"
variation 234
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144390339"
variation 237
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:772719143"
variation 238
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227047935"
variation 249
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:760407590"
variation 251
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327836879"
variation 252
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:761536707"
variation 255
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:376285927"
variation 257
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178733216"
variation 258
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1010056637"
exon 267..1239
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/inference="alignment:Splign:2.1.0"
variation 267
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:987800721"
variation 268
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354853451"
variation 270
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:769139448"
variation 273
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486526891"
variation 276
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327148409"
variation 278
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:772664721"
variation 283
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311831095"
variation 287
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042772300"
variation 288
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250999628"
variation 297
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:760247738"
variation 300
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042772395"
variation 302
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:766182674"
variation 307
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1423088655"
variation 308
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042772482"
variation 312
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354538511"
variation 315
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285035008"
variation 321
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:776392747"
variation 338..339
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1174467156"
variation 353
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:143295755"
variation 362
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:148339434"
variation 364
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042772692"
variation 370
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:752479921"
variation 371
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1044552"
variation 372
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:945815294"
variation 373
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1373543056"
variation 374
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201381459"
variation 375
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299431242"
variation 379
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042772823"
variation 384
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:751700739"
variation 397
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439793400"
variation 398..406
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="tattat"
/replace="tattattat"
/db_xref="dbSNP:1291112739"
variation 398
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:35470967"
variation 399
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2147576297"
variation 400
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:781205028"
variation 405
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:750663705"
variation 406
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042773029"
variation 407
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:959476923"
variation 408
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1667663132"
variation 410
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:937788922"
variation 411
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:756299765"
variation 414
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272123247"
regulatory 421..426
/regulatory_class="polyA_signal_sequence"
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="hexamer: AATAAA"
variation 421
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488868680"
variation 430..433
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="at"
/replace="atat"
/db_xref="dbSNP:754858466"
variation 430
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773189"
variation 432
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376487600"
polyA_site 444
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="major polyA site"
variation 444
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:369019391"
variation 445
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194570777"
variation 447
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769101076"
variation 457
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569488931"
variation 458..461
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="tt"
/replace="tttt"
/db_xref="dbSNP:756508072"
variation 468
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:779452784"
variation 474
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773393"
variation 477
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773420"
variation 482
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042773447"
variation 501
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1321537358"
variation 504
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290831636"
variation 507
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569488932"
variation 508
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230302948"
variation 512
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409325654"
variation 517
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773565"
variation 518
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1056320924"
variation 525..529
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:2147576386"
variation 525
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778253319"
variation 529
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1012235097"
variation 532
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773665"
variation 533
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042773689"
variation 539
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159890837"
variation 542
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569488935"
variation 546
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1602431789"
variation 548
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042773775"
variation 550
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:749719040"
variation 554
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773821"
variation 556
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:187578610"
variation 559
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773873"
variation 565
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042773899"
variation 567
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1418653034"
variation 568
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042773940"
variation 569
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1303364642"
variation 574
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774004"
variation 586
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:191822305"
variation 597
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774048"
variation 603
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:878886192"
variation 612
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1349141102"
variation 613
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774131"
variation 619
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017383723"
variation 620
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:962765281"
variation 622
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:747010973"
variation 623
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1421037070"
variation 628
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:887097938"
variation 632..641
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="tcagtc"
/replace="tcagtcagtc"
/db_xref="dbSNP:201724035"
variation 641
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774327"
variation 648..650
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:1190029718"
variation 649
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774353"
variation 650..654
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aga"
/replace="agaga"
/db_xref="dbSNP:2042774383"
variation 656
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1373902318"
variation 664
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:994214495"
variation 673
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025731243"
variation 678
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774449"
variation 680
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569488943"
variation 681
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042774491"
variation 684
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2147576493"
variation 685
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576498"
variation 691
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:183989280"
variation 695
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:187600228"
variation 700
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576509"
variation 702
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219288448"
variation 706
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042774575"
variation 710..714
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:1320151265"
variation 724
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1602431880"
variation 725
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:192028442"
variation 727
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1602431894"
variation 728
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1385071582"
variation 734
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2041668432"
variation 736
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:964676337"
variation 745
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:768901954"
variation 753
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042774729"
variation 764
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576549"
variation 768
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774752"
variation 771
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2042774786"
variation 777
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303755683"
variation 778
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042774832"
variation 781
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353065086"
variation 788
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438369222"
variation 796
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042774897"
variation 799
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:772969634"
variation 807
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042774945"
variation 811
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247081390"
variation 825
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="t"
/db_xref="dbSNP:2042775012"
variation 836
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1602431914"
variation 839
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:184474327"
variation 840
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:914281688"
variation 841
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:945741790"
variation 844..849
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aca"
/replace="acaaca"
/db_xref="dbSNP:1221234465"
variation 845
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1041495818"
variation 852
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433045777"
variation 860
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233998408"
variation 861
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1602431935"
variation 873
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:2042775238"
variation 874
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042775263"
variation 878
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193237409"
variation 885
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029803076"
variation 887
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:928424044"
variation 888
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:2042775364"
variation 893
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:938547889"
variation 900
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1056059235"
variation 901
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:894384309"
variation 904
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:988282416"
variation 921
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006591018"
variation 922
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038293724"
variation 926
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163523336"
variation 928
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:143233900"
variation 929
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403413347"
variation 934
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220707153"
variation 942
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163755801"
variation 947
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:774348069"
variation 948
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775628"
variation 952
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2147576701"
variation 953
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448983565"
variation 954
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447149646"
variation 960
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329225580"
regulatory 963..968
/regulatory_class="polyA_signal_sequence"
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="hexamer: AATAAA"
variation 965
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042775714"
variation 967
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775737"
variation 969
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300508199"
variation 976
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042775765"
variation 977
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775784"
variation 978
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465129571"
variation 979
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:190749180"
variation 980
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="g"
/db_xref="dbSNP:1378680798"
variation 981
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042775861"
variation 982..987
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:979124188"
variation 983
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775887"
polyA_site 990
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
variation 1011
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438202695"
variation 1013
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380140557"
variation 1014
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042775957"
variation 1017
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179654206"
variation 1022
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="a"
/db_xref="dbSNP:926492764"
variation 1022
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042775995"
variation 1023
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776037"
variation 1026
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:767086808"
variation 1028
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025700115"
variation 1029
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776093"
variation 1036
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:752296762"
variation 1037
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776147"
variation 1054
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:955477282"
variation 1057
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199899582"
variation 1066
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776212"
variation 1076
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:937926043"
variation 1079
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776260"
variation 1085
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256492081"
variation 1091
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776306"
variation 1092
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776322"
variation 1095
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1056288083"
variation 1098
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776375"
variation 1104
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008381055"
variation 1106
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:745343572"
variation 1109
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1602432032"
variation 1113
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213007704"
variation 1114
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776473"
variation 1125..1126
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="tt"
/db_xref="dbSNP:917740392"
variation 1129
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042776521"
variation 1130
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776538"
variation 1131
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776555"
variation 1132
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569488983"
variation 1134
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:929186001"
variation 1135
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:769356424"
variation 1145
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="t"
/db_xref="dbSNP:1337113038"
variation 1150
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310182148"
variation 1152
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:1394918103"
variation 1159..1174
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="catat"
/replace="catatttatgacatat"
/db_xref="dbSNP:760382674"
variation 1160
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/db_xref="dbSNP:2147576898"
variation 1168
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305101967"
variation 1169
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:763902424"
variation 1170
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:990813025"
variation 1171..1175
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1274084941"
variation 1174
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="t"
/db_xref="dbSNP:2042776852"
variation 1174
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042776825"
variation 1182
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042776878"
variation 1185
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754254826"
variation 1191
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242348603"
variation 1202..1211
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="atact"
/replace="atactatact"
/db_xref="dbSNP:2042776958"
variation 1208..1212
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace=""
/replace="tactg"
/db_xref="dbSNP:2042776989"
regulatory 1220..1225
/regulatory_class="polyA_signal_sequence"
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/note="hexamer: AATAAA"
variation 1228
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="g"
/replace="t"
/db_xref="dbSNP:2042777007"
variation 1231
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="a"
/replace="g"
/db_xref="dbSNP:2042777020"
variation 1232
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:2042777044"
variation 1236
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441961302"
polyA_site 1239
/gene="PIN4"
/gene_synonym="EPVH; hEPVH; hPar14; hPar17; PAR14; PAR17"
ORIGIN
ggttcagcgttcaacaacaagcttccaagatgccgcccaaaggaaaaagtggttctggaaaagcggggaaagggggagcagcctctgggagtgacagtgctgacaagaaggctcaaggtcccaaaggtggtggcaatgcagtaaaggtcagacacattctatgtgaaaaacatggcaaaatcatggaagccatggaaaagttaaagtctgggatgagattcaatgaagtggccgcacagtatagtgaagataaagccaggcaagggggtgacttgggttggatgaccagagggtccatggtgggaccatttcaagaagcagcatttgccttgcctgtaagtgggatggataagcctgtgtttacagacccaccggttaagacaaaatttggatatcatattattatggtcgaaggaagaaaataaaatcatatgaaagactgaataagttttatacattttgtttctttaaaaggtattacatattcttttgagctggagctgcaaggaaatacaaaaatttttaaaaagaaaagatattggatgctccttgtattctgtgaaagctctaagtatgggtttgtaggtgtaagagagggtggggctaagtgaatgtcaactgtagtaggtattcagtcagtctttctcaaagagaagtcaagcagactccctttaacctgtattctctttcctcccagaactatatctgactctcagtctgtcccataaattaattcagaaaccatcttcaggggaagcagatatcaactcacactattcacacaactgaaaatattgggcatcaaatagattagtgtgtgagaatcataaaataagttcctagacaacatttgttttacatgttagtcaactctgatcttccaggacaggtggtattagctccactgtcttaacatagtacgtggcacgttatgcctttcagtgttaactcctttctttttaaataaatgtttattggaggaaaaaagcactcagttgttccatgagttgttttgtactagactaaccgagtgctggttaaagggagggatgtcagcataaaaatgtcattccctcatcttcagtgtatgggttacattaagactgtcctttccagggccaatgttctgtgcatctaaatttttaaaatttaaaatgccatatttatgacatataaaaaagtataaagattactaatataaatactatactgcttcaaaaataaaactttgccaacaca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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