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2024-04-20 05:41:28, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001080529 4195 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens WAS/WASL interacting protein family, member 3 (WIPF3),
mRNA.
ACCESSION NM_001080529 XM_929463
VERSION NM_001080529.2 GI:336455071
KEYWORDS RefSeq.
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 4195)
AUTHORS Mishra,A., Yazar,S., Hewitt,A.W., Mountain,J.A., Ang,W.,
Pennell,C.E., Martin,N.G., Montgomery,G.W., Hammond,C.J.,
Young,T.L., Macgregor,S. and Mackey,D.A.
TITLE Genetic variants near PDGFRA are associated with corneal curvature
in Australians
JOURNAL Invest. Ophthalmol. Vis. Sci. 53 (11), 7131-7136 (2012)
PUBMED 22969067
REMARK Publication Status: Online-Only
REFERENCE 2 (bases 1 to 4195)
AUTHORS Wen,Z.N., Pang,W.J. and Xiang,W.P.
TITLE [Expression of CR16 in the testis of patients with idiopathic
azoospermia]
JOURNAL Zhonghua Nan Ke Xue 16 (12), 1101-1104 (2010)
PUBMED 21348202
REMARK GeneRIF: The expressions of the CR16 protein and mRNA decrease
markedly in the testis of patients with idiopathic azoospermia.
REFERENCE 3 (bases 1 to 4195)
AUTHORS Suetsugu,S., Banzai,Y., Kato,M., Fukami,K., Kataoka,Y., Takai,Y.,
Yoshida,N. and Takenawa,T.
TITLE Male-specific sterility caused by the loss of CR16
JOURNAL Genes Cells 12 (6), 721-733 (2007)
PUBMED 17573773
REMARK GeneRIF: CR16 and N-WASP are suggested to play important roles in
spermatogenesis
Erratum:[Genes Cells. 2007 Aug;12(8):981. Banzai, Yoshibumi
[corrected to Banzai, Yoshifumi]]
REFERENCE 4 (bases 1 to 4195)
AUTHORS Zettl,M. and Way,M.
TITLE The WH1 and EVH1 domains of WASP and Ena/VASP family members bind
distinct sequence motifs
JOURNAL Curr. Biol. 12 (18), 1617-1622 (2002)
PUBMED 12372256
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC004912.2, BX107905.1 and AW105171.1.
On Jun 21, 2011 this sequence version replaced gi:122937495.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. There are no full-length human
transcripts supporting this RefSeq; it is predicted based on
partial human transcript alignments and on full-length transcript
alignments from the rat homolog, GeneID:259242.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns ERS025084,
ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-125 AC004912.2 2028-2152
126-272 AC004912.2 30142-30288
273-405 AC004912.2 71304-71436
406-537 AC004912.2 74483-74614
538-1163 AC004912.2 79324-79949
1164-1638 BX107905.1 1-475
1639-3881 AC004912.2 109995-112237
3882-4195 AW105171.1 1-314 c
FEATURES Location/Qualifiers
source 1..4195
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7p14.3"
gene 1..4195
/gene="WIPF3"
/gene_synonym="CR16"
/note="WAS/WASL interacting protein family, member 3"
/db_xref="GeneID:644150"
/db_xref="HGNC:22004"
/db_xref="MIM:612432"
exon 1..125
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 71
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:368175987"
variation 74
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:13233912"
exon 126..272
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
misc_feature 177..179
/gene="WIPF3"
/gene_synonym="CR16"
/note="upstream in-frame stop codon"
CDS 183..1634
/gene="WIPF3"
/gene_synonym="CR16"
/note="corticosteroids and regional expression protein 16
homolog"
/codon_start=1
/product="WAS/WASL-interacting protein family member 3"
/protein_id="NP_001073998.2"
/db_xref="GI:336455072"
/db_xref="CCDS:CCDS56472.1"
/db_xref="GeneID:644150"
/db_xref="HGNC:22004"
/db_xref="MIM:612432"
/translation="
MPVPPPPPPPLPPPPPPLGAPPPPPPSAPPVSTDTSSLRRADPKGRSALLADIQQGTRLRKVTQINDRSAPQIESSKGTNKEGGGSANTRGASTPPTLGDLFAGGFPVLRPAGQRDVAGGKTGQGPGSRAPSPRLPNKTISGPLIPPASPRLGNTSEAHGAARTAPPRPNVPAPPPPTPPPPPPPLPPPLPSSSPIKTPLVSPPGPLTKGNLPVVAPPVPCAPPPPPPPPPPTPPPLPPASVLSDKAVKPQLAPLHLPPIPPPLPLLPPCGYPGLKAEPASPAQDAQEPPAPPPPLPPYASCSPRASLPAPPLPGVNSSSETPPPLPPKSPSFQAPPQKAGAQALPAPPAPPGSQPFLQKKRHGRPGAGGGKLNPPPAPPARSPTTELSSKSQQATAWTPTQQPGGQLRNGSLHIIDDFESKFTFHSVEDFPPPDEYKPCQKIYPSKIPRSRTPGPWLQAEAVGQSSDDIKGRNSQLSLKTLR
"
misc_feature 189..206
/gene="WIPF3"
/gene_synonym="CR16"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (A6NGB9.4);
Region: Profilin-binding motif"
misc_feature 213..230
/gene="WIPF3"
/gene_synonym="CR16"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (A6NGB9.4);
Region: Profilin-binding motif"
misc_feature 240..257
/gene="WIPF3"
/gene_synonym="CR16"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (A6NGB9.4);
Region: Profilin-binding motif"
misc_feature 306..389
/gene="WIPF3"
/gene_synonym="CR16"
/note="WH2 motif; Region: WH2; pfam02205"
/db_xref="CDD:202153"
misc_feature 354..365
/gene="WIPF3"
/gene_synonym="CR16"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (A6NGB9.4);
Region: RLRK"
misc_feature 1452..1526
/gene="WIPF3"
/gene_synonym="CR16"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (A6NGB9.4);
Region: WASP-binding motif"
variation 271
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:374540847"
exon 273..405
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 326
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:374280179"
variation 360
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:368411759"
variation 361
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:145862657"
variation 375
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:375470917"
variation 379
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:367618336"
variation 380
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:189877440"
variation 395
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:376006007"
exon 406..537
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 427
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:377037903"
variation 441
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:369623039"
variation 451
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="g"
/db_xref="dbSNP:368644231"
variation 455
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:374360350"
variation 456
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:200511759"
variation 457
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:201706623"
variation 462
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:370263957"
variation 510
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="g"
/db_xref="dbSNP:200004509"
variation 526
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:372583980"
variation 531
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:377091221"
exon 538..1281
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 548
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:201392764"
variation 644
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:28439342"
variation 650
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="g"
/db_xref="dbSNP:200470921"
variation 674
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:376450346"
variation 676
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:200642657"
variation 842
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:370820026"
variation 872
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:372109072"
variation 938
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:138069702"
variation 1042
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="t"
/db_xref="dbSNP:174965"
variation 1046
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:373625381"
variation 1067
/gene="WIPF3"
/gene_synonym="CR16"
/replace="g"
/replace="t"
/db_xref="dbSNP:367797283"
variation 1074
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:371924598"
variation 1093
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:376892798"
variation 1113
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:200878248"
variation 1144
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:3750092"
variation 1153
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:376589211"
variation 1164
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="g"
/db_xref="dbSNP:145976937"
STS 1189..1680
/gene="WIPF3"
/gene_synonym="CR16"
/standard_name="ha2063"
/db_xref="UniSTS:515480"
variation 1228
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:374006288"
variation 1231
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="g"
/db_xref="dbSNP:200533925"
variation 1278
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:376122326"
exon 1282..1431
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 1286
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:61750796"
variation 1287
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:61750795"
variation 1338
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:201336980"
variation 1344
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:375567050"
variation 1381
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:184114982"
variation 1384
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:367607022"
variation 1412
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:201819942"
variation 1415
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:371649277"
variation 1422
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:375082324"
exon 1432..1533
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 1439
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:367957588"
variation 1453
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:76617740"
variation 1460
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="t"
/db_xref="dbSNP:2893360"
variation 1470
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:375486622"
variation 1485
/gene="WIPF3"
/gene_synonym="CR16"
/replace="g"
/replace="t"
/db_xref="dbSNP:62457635"
variation 1491
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:369891048"
exon 1534..1610
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 1537
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:375804779"
variation 1561
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:140535643"
variation 1565
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:144392113"
variation 1571
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:61756680"
exon 1611..4184
/gene="WIPF3"
/gene_synonym="CR16"
/inference="alignment:Splign:1.39.8"
variation 1614
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:191126276"
variation 1629
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:79136170"
variation 1639
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056061"
variation 1690
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:183712445"
variation 1777
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="g"
/db_xref="dbSNP:35346638"
variation 1963
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:371927317"
variation 2077
/gene="WIPF3"
/gene_synonym="CR16"
/replace="g"
/replace="t"
/db_xref="dbSNP:139121080"
variation 2113
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:2057902"
variation 2140
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:368472950"
variation 2167..2168
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="t"
/db_xref="dbSNP:36068231"
variation 2172
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:188035881"
variation 2196..2197
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="tt"
/db_xref="dbSNP:149325811"
variation 2196
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="tt"
/replace="ttttt"
/db_xref="dbSNP:10534578"
variation 2213
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="tt"
/db_xref="dbSNP:72265605"
variation 2220..2224
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="tt"
/replace="ttttt"
/db_xref="dbSNP:67914039"
variation 2242
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:73305123"
variation 2258
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:146639420"
variation 2267..2269
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="ctt"
/db_xref="dbSNP:200307226"
variation 2278
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:192076285"
STS 2288..2389
/gene="WIPF3"
/gene_synonym="CR16"
/standard_name="RH36247"
/db_xref="UniSTS:8021"
variation 2336..2337
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="actgtttacagtgtccct"
/db_xref="dbSNP:373174889"
variation 2392
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:76905570"
variation 2429
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:138941989"
variation 2450
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:139954899"
variation 2507
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:183198699"
variation 2529
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:187125354"
STS 2564..2713
/gene="WIPF3"
/gene_synonym="CR16"
/standard_name="D7S2044E"
/db_xref="UniSTS:5163"
variation 2570
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:73077921"
variation 2571
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:10215602"
variation 2619
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:59731594"
variation 2650
/gene="WIPF3"
/gene_synonym="CR16"
/replace="g"
/replace="t"
/db_xref="dbSNP:115626593"
variation 2727
/gene="WIPF3"
/gene_synonym="CR16"
/replace="g"
/replace="t"
/db_xref="dbSNP:76231213"
variation 2789
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:192535807"
variation 2911
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:184969767"
variation 2977
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:149825920"
variation 3060
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:10225667"
variation 3173
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:145792294"
variation 3231..3232
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="g"
/db_xref="dbSNP:36124831"
variation 3362..3363
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="ac"
/db_xref="dbSNP:373949563"
variation 3388
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:148978425"
variation 3407
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:10255756"
variation 3499
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:147074183"
variation 3512
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:200272952"
variation 3577
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/db_xref="dbSNP:1971648"
variation 3692
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:1971647"
variation 3723..3724
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="g"
/db_xref="dbSNP:35681705"
variation 3768
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="t"
/db_xref="dbSNP:189032234"
variation 3770
/gene="WIPF3"
/gene_synonym="CR16"
/replace="g"
/replace="t"
/db_xref="dbSNP:376348578"
variation 3796
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:192781466"
variation 3840..3843
/gene="WIPF3"
/gene_synonym="CR16"
/replace=""
/replace="aaag"
/db_xref="dbSNP:201118923"
variation 3881
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1063694"
variation 3894
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:373492630"
variation 3906
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:184617090"
STS 3909..4050
/gene="WIPF3"
/gene_synonym="CR16"
/standard_name="RH92582"
/db_xref="UniSTS:89090"
variation 3927
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:78366128"
STS 3938..4147
/gene="WIPF3"
/gene_synonym="CR16"
/standard_name="RH41875"
/db_xref="UniSTS:6489"
variation 3984
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:142350663"
variation 4049
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:146318458"
variation 4105
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/db_xref="dbSNP:189500285"
variation 4113
/gene="WIPF3"
/gene_synonym="CR16"
/replace="c"
/replace="t"
/db_xref="dbSNP:181499075"
variation 4136
/gene="WIPF3"
/gene_synonym="CR16"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:185716689"
ORIGIN
tcggcggtagcggcgccgcttggagcacgggcgctgcgggacggagcccggagccggaggcggcggcggcggagacgtcggccggagctcgagtccagtccagcccccggctccgccacctgcagagcagaagccactctcttgggaccattcataagcaggagacatcaacaccgtgacacatgccagtgccaccgccacccccacctcctctgcctccacctcccccgcctctgggggctcctccccctcccccaccatcagcacccccggtaagcacagacacctccagcttgcgaagggcagatccgaaaggccggagtgcgctgttggctgatatccagcaaggaactcgcctgcgcaaagtcacgcagatcaacgaccgcagtgccccgcagatcgagagttctaaaggaaccaacaaagaaggaggaggttctgcaaacacacgaggcgcgagcacacctcccaccctgggagatctgtttgctggtggctttcctgtattgcgaccagcaggccagcgggatgtagcaggtggcaagacagggcagggccctggctcccgcgcgccctctcccaggcttcccaacaaaaccatcagcggcccgcttatcccgcctgcctctcccaggctaggcaatacctccgaggcgcatggcgctgccaggacagccccgcctcgccccaacgtgcctgccccgccccctcccaccccaccccctccgcctccacccttacccccgccccttccctcttcctcccccatcaaaactccgcttgtgtccccacccggcccactgaccaaagggaacctcccggtggttgcaccccccgtcccctgtgcgccaccacctccacctccgccacctcccccaacgccacccccgctgcccccggcctcggttcttagtgacaaggcagtgaagcctcagctggctcccttgcacctcccgcccatcccgcccccgctccctctgctcccaccttgtgggtatccggggctcaaagcggagcccgccagccctgcgcaagatgcgcaggagcctcccgccccgccgcccccgctccccccttatgcttcttgctccccgagggcttctttgcccgcgccccctttgccaggagttaatagcagcagtgaaactccacccccgctaccccctaaatcccccagcttccaggccccaccgcagaaggccggtgcgcaggccttgcccgccccgcctgcccctccgggctcccagccgttcctgcagaagaagaggcatggccgaccaggggccggtgggggaaagctaaatccacctccagcaccccctgcgagatcacctaccacagagctttcaagcaagagccagcaggccacagcctggaccccgacgcagcagcctggaggtcaactgcgaaatggaagcctgcacatcattgatgacttcgagtctaaattcacgttccattctgtggaagactttccccctccggatgaatataaaccatgccagaagatttaccccagcaagatccccagaagccgtacacctggtccctggctccaagcggaagcagtcgggcagagctctgatgacatcaaaggcagaaattctcagttatctctaaagactcttcggtgagaagacagatgaagcgaaggtcctggggttccaggttgcagaacaacatgtcagaccccacccaccccatgctcaagctgtaattcagttggcatacaggcttggaattgagaatttatttattgtaaatatgtgatttgcacgggctttaaagcagtattttaattgacttttatttcggtaatattttttaaaacacccctcatttttccattttttgcattgcatcttggcatttgtcagcacagatagagccctgtccctccacctagtgcccactccatgactgtgaatctgcttgcaggctggcccttcctagattctgaaccgtttgtagagagtccttagtttgcaggtagccccaaagttataaatatccacaacggcttcttattggcataatttcatattctcatcacactaactgcaaaatcaaaccaaataatgccttatcaatgatgcagctcagaggaagtagcgtgtcccccacacccagacagtgccgcgcagcctccagggaacgaggtgccatgtctcgcttccattttgcagtacagggaatttttttttttttttttttttttttttttgctgcctaatgtaatacatcacaaagtaaaggcaagagtgggcttggccctccgatgccaaccacagggccccttttgtaactgaataatcctccaagtagccagtgctcctactgtttacagtgtccctcgtgcccaagtctctgtcactttcatcctgttccctccaagttcccagtcccatcccagtagccagctttatgagattttggtatttcttccctacagattaaaaacatacacaactcatcattatgctaaactaccagttgtatctcagaggtctccccttctgcccttgcttcgagtgtggacttccatggaaaatatgacatgaaaaagtgtagaacgaaacatcgtgtgaaatacctgccacaaatacctagtgcctcactgcccccatcttaggatccttggagccacccgtcaggcaaaacctagctcccttctgagctaaaggagaaccttgcctgacaactccacattcattcccttgtggtgggcacctgtctgtggggagatgtgtgcaagctcagccactctgaatatggaaaaggtcaggccgggctggtcctgctcttcactccctcttcttgatcctgtagggagtggaaatgtgtttttgcttgctgcctgacccctgatgttccccatctttggtcggggaagactgtgacagaggaaggagaaaaaatagaaggaaacagactgatccctgggctgtgctcaaaatagctgccctttaaaggaaatcaggcagggaggggagggaaaccagcgaaaaagaaatttgctttgcaacaacccacgcacacattcacccctgaagtatatcatgaacagaccaagccatccagaaaggcagccggtcaggagggtgtgggcaaacatgactgcatctgcctcactgttgtctggagtaacgactcaggtggtgtcctgcagcagtgctgtgctttctcattccagatggaagcaagtgagccagggtcaaattcccttctccaggggaatgaatcaagcccaaactgtaacagctaaataagtagaagtttttgcaggtcatcagctctgggcataactaatttgttttattggttctggaagatttccaaaaagccagaatttattattataacagtgtccactccactgccctcacagttgtgtaaaataattatagaagttttaatgatcctgattaagaagaccctagacaaaggcaattccaccttcagagtagactgcctgccctaatgaggtgtttagacattcgtgtctcctatggctgggatggaaattaaaataacactatttaaggacagagcgggccaggagcagtggctcatgcaggtaatcccagcatgggaggctgaggtgggtggattacttgaggttaggagttcaagaccagcctggccaacatggtgaaaccctgtctactcaaatacaaaaaattagccaggcatggtggctcacacctgtaatcccagcaacttgggaggttcaggcacaagaattgcttgaaccctggaggtggaggttgcagtgagctgagatggcaccactgcactctagcctgggcaacagagcgagaccctaactcaaaaaaaaaaaaggacagaggggaggaaggagcagaaaccaaaaatggcaattagggagaaatctcaggaatgtggcatcccatctccccttgagacctatcactgaattcacaacccttcgagctcatgctggtgcactgagtcccttgggcgctgtaaaggtttaaccccttgactgtaaactcagacttagagacatctgagtcacacagtccccgccattgtcacatattctcactgacactgcagtctgtgactcctccaatgtttcacgtgtattttatatttattgatgtctccttccgcagattcatttctttgtacttaataaactttagtaagtggaaatgcttaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:644150 -> Molecular function: GO:0003779 [actin binding] evidence: IEA
GeneID:644150 -> Biological process: GO:0007275 [multicellular organismal development] evidence: IEA
GeneID:644150 -> Biological process: GO:0007283 [spermatogenesis] evidence: IEA
GeneID:644150 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA
GeneID:644150 -> Biological process: GO:0038096 [Fc-gamma receptor signaling pathway involved in phagocytosis] evidence: TAS
GeneID:644150 -> Biological process: GO:0045087 [innate immune response] evidence: TAS
GeneID:644150 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
GeneID:644150 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:644150 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
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