2024-04-25 03:04:21, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001171654 7189 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens kelch-like family member 5 (KLHL5), transcript variant 4, mRNA. ACCESSION NM_001171654 VERSION NM_001171654.1 GI:284413751 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 7189) AUTHORS Xu,J., Gu,S., Wang,S., Dai,J., Ji,C., Jin,Y., Qian,J., Wang,L., Ye,X., Xie,Y. and Mao,Y. TITLE Characterization of a novel splicing variant of KLHL5, a member of the kelch protein family JOURNAL Mol. Biol. Rep. 30 (4), 239-242 (2003) PUBMED 14672410 REMARK GeneRIF: Data report a novel splicing variant of KLHL5, named KLHL5b, and describe its expression pattern in many tissues. REFERENCE 2 (bases 1 to 7189) AUTHORS Wang,S., Zhou,Z., Ying,K., Tang,R., Huang,Y., Wu,C., Xie,Y. and Mao,Y. TITLE Cloning and characterization of KLHL5, a novel human gene encoding a kelch-related protein with a BTB domain JOURNAL Biochem. Genet. 39 (7-8), 227-238 (2001) PUBMED 11590829 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from DB451501.1, DR006899.1, AB208820.1, AC079921.5 and AA715102.1. Transcript Variant: This variant (4) differs in the 5' UTR, lacks of portion of the 5' coding region, and uses a downstream start codon, compared to variant 1. The resulting isoform (4) is shorter at the N-terminus, compared to 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. ##Evidence-Data-START## Transcript exon combination :: AB208820.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025084 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-199 DB451501.1 1-199 200-265 DR006899.1 91-156 266-2832 AB208820.1 38-2604 2833-7021 AC079921.5 168802-172990 7022-7189 AA715102.1 1-168 c FEATURES Location/Qualifiers source 1..7189 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="4" /map="4p14" gene 1..7189 /gene="KLHL5" /note="kelch-like family member 5" /db_xref="GeneID:51088" /db_xref="HGNC:6356" /db_xref="MIM:608064" exon 1..265 /gene="KLHL5" /inference="alignment:Splign:1.39.8" misc_feature 54..56 /gene="KLHL5" /note="upstream in-frame stop codon" variation 200 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:76308346" exon 266..448 /gene="KLHL5" /inference="alignment:Splign:1.39.8" CDS 306..2012 /gene="KLHL5" /note="isoform 4 is encoded by transcript variant 4; lymphocyte activation-associated protein; kelch-like protein 5" /codon_start=1 /product="kelch-like protein 5 isoform 4" /protein_id="NP_001165125.1" /db_xref="GI:284413752" /db_xref="CCDS:CCDS54756.1" /db_xref="GeneID:51088" /db_xref="HGNC:6356" /db_xref="MIM:608064" /translation="
MEPCTSDEFFQALNHAEQTFKKMENYLRHKQLCDVILVAGDRRIPAHRLVLSSVSDYFAAMFTNDVREARQEEIKMEGVEPNSLWSLIQYAYTGRLELKEDNIECLLSTACLLQLSQVVEACCKFLMKQLHPSNCLGIRSFADAQGCTDLHKVAHNYTMEHFMEVIRNQEFVLLPASEIAKLLASDDMNIPNEETILNALLTWVRHDLEQRRKDLSKLLAYIRLPLLAPQFLADMENNVLFRDDIECQKLIMEAMKYHLLPERRPMLQSPRTKPRKSTVGTLFAVGGMDSTKGATSIEKYDLRTNMWTPVANMNGRRLQFGVAVLDDKLYVVGGRDGLKTLNTVECYNPKTKTWSVMPPMSTHRHGLGVAVLEGPMYAVGGHDGWSYLNTVERWDPQARQWNFVATMSTPRSTVGVAVLSGKLYAVGGRDGSSCLKSVECFDPHTNKWTLCAQMSKRRGGVGVTTWNGLLYAIGGHDAPASNLTSRLSDCVERYDPKTDMWTAVASMSISRDAVGVCLLGDKLYAVGGYDGQAYLNTVEAYDPQTNEWTQVAPLCLGRAGACVVTVKL
" misc_feature 372..683 /gene="KLHL5" /note="BTB/POZ domain; Region: BTB; pfam00651" /db_xref="CDD:201372" misc_feature 402..1970 /gene="KLHL5" /note="kelch-like protein; Provisional; Region: PHA03098" /db_xref="CDD:165380" misc_feature 708..1007 /gene="KLHL5" /note="BTB And C-terminal Kelch; Region: BACK; pfam07707" /db_xref="CDD:149006" misc_feature 1149..1286 /gene="KLHL5" /note="Kelch domain; Region: Kelch; smart00612" /db_xref="CDD:128874" misc_feature 1251..1388 /gene="KLHL5" /note="Kelch motif; Region: Kelch_1; pfam01344" /db_xref="CDD:201739" misc_feature 1434..1568 /gene="KLHL5" /note="Kelch domain; Region: Kelch; smart00612" /db_xref="CDD:128874" misc_feature 1569..1709 /gene="KLHL5" /note="Kelch domain; Region: Kelch; smart00612" /db_xref="CDD:128874" misc_feature 1674..1829 /gene="KLHL5" /note="Kelch motif; Region: Kelch_1; pfam01344" /db_xref="CDD:201739" misc_feature 1836..1967 /gene="KLHL5" /note="Kelch motif; Region: Kelch_1; pfam01344" /db_xref="CDD:201739" variation 306 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:148527638" variation 311 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:374439509" variation 325 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:376271956" variation 353 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:183165327" variation 419 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:151171232" variation 424 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:372888059" variation 425 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:144221606" variation 438 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:146536122" exon 449..585 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 503 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:139982106" variation 540 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:201551895" variation 554 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:143433133" variation 569 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:373996184" exon 586..782 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 589 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:151197814" variation 614 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:368239171" variation 637 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:202114333" variation 660 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:201411197" variation 694 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:199889488" exon 783..995 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 895 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:372986724" variation 930 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:140333738" variation 947 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:202137199" variation 975 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:78910806" variation 989 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:35141484" exon 996..1182 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 1005 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:145251992" variation 1042 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:113528556" variation 1044 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:371160515" variation 1078 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:142054317" exon 1183..1407 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 1212 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:373453320" variation 1213 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:145777465" variation 1248 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:199990970" variation 1255 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:374197598" variation 1265 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:200140121" variation 1266 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:34646863" variation 1292 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:138600627" variation 1354 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:370752573" exon 1408..1570 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 1450 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:201562340" variation 1463 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:144118002" variation 1466 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:200458148" variation 1500 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:199537144" variation 1526 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:372279307" variation 1556 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:201433421" exon 1571..1783 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 1591 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:143375036" variation 1606 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:368928021" variation 1726 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:184995654" variation 1729 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:372952200" variation 1743 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:374867267" exon 1784..1955 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 1803 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:148371989" variation 1821 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:141535229" variation 1822 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:150876209" variation 1851 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:199522363" variation 1856 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:199903092" variation 1865 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:180822198" variation 1870 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:200893739" variation 1880 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:139630969" variation 1898 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:377475503" variation 1916 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:3733276" exon 1956..7179 /gene="KLHL5" /inference="alignment:Splign:1.39.8" variation 1961 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:140007123" variation 1965 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:377127906" variation 1967 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:370840660" variation 2023 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:3733275" variation 2024 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:368299836" variation 2032 /gene="KLHL5" /replace="c" /replace="g" /db_xref="dbSNP:374509623" variation 2076 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:56106731" variation 2122 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:190979670" variation 2166..2167 /gene="KLHL5" /replace="" /replace="g" /db_xref="dbSNP:34907990" variation 2239 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:13182" STS 2337..3220 /gene="KLHL5" /standard_name="KLHL5_2058" /db_xref="UniSTS:280811" variation 2386 /gene="KLHL5" /replace="" /replace="t" /db_xref="dbSNP:147851336" variation 2430..2431 /gene="KLHL5" /replace="" /replace="a" /db_xref="dbSNP:34824099" variation 2494 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:149942433" variation 2732 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:375701203" variation 2743 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:144038048" variation 2850 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:377304343" STS 2853..3121 /gene="KLHL5" /standard_name="SGC44694" /db_xref="UniSTS:61813" STS 2894..2994 /gene="KLHL5" /standard_name="SHGC-44694" /db_xref="UniSTS:64252" variation 2959 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:112659616" variation 2964..2967 /gene="KLHL5" /replace="" /replace="caaa" /db_xref="dbSNP:139075962" variation 2987 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:10020528" variation 3008 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:148646095" variation 3156 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:370069210" variation 3208 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:188258289" STS 3374..3458 /gene="KLHL5" /standard_name="SHGC-67763" /db_xref="UniSTS:83334" variation 3438 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:201423474" variation 3471 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:192782197" variation 3473 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:115235909" variation 3483 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:59690657" STS 3528..3736 /gene="KLHL5" /standard_name="sY3084" /db_xref="UniSTS:515126" STS 3576..3673 /gene="KLHL5" /standard_name="D8S2279" /db_xref="UniSTS:473907" variation 3579 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:376487527" variation 3665 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:368884652" variation 3676 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:187365167" variation 3705 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:192371933" variation 3745 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:34615917" variation 3762 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:184761310" variation 3773..3774 /gene="KLHL5" /replace="" /replace="t" /db_xref="dbSNP:113524846" variation 3774 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:2712014" variation 3817 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:190520712" variation 3827 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:151161244" variation 3833 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:140235155" variation 3983 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:143959707" variation 3987 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:11539757" variation 4076 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:1061377" variation 4199 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:1982009" variation 4261 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:1138494" variation 4485..4486 /gene="KLHL5" /replace="" /replace="g" /db_xref="dbSNP:34339263" variation 4492 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:192639742" STS 4648..4772 /gene="KLHL5" /standard_name="SHGC-59567" /db_xref="UniSTS:6381" STS 4787..4929 /gene="KLHL5" /standard_name="SHGC-50250" /db_xref="UniSTS:13243" variation 4909 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:67579768" variation 4957 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:146646997" variation 5020 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:184530880" variation 5034 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:189693127" variation 5079 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:141422861" variation 5086 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:181290227" variation 5157 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:150252398" variation 5225 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:373521183" variation 5295 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:370981326" variation 5342 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:13109200" STS 5383..5508 /gene="KLHL5" /standard_name="SHGC-67904" /db_xref="UniSTS:28765" variation 5474 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:138883952" variation 5593 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:28749292" variation 5595 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:78257954" variation 5607 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:185986150" STS 5622..5698 /gene="KLHL5" /standard_name="SW919" /db_xref="UniSTS:252117" variation 5713 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:34554601" variation 5735 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:111780757" variation 5748..5749 /gene="KLHL5" /replace="" /replace="aaaa" /db_xref="dbSNP:71643268" variation 5773 /gene="KLHL5" /replace="a" /replace="t" /db_xref="dbSNP:376087232" variation 5774 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:370709415" variation 5891 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:189134201" variation 5989 /gene="KLHL5" /replace="g" /replace="t" /db_xref="dbSNP:60334933" variation 6017 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:148972266" variation 6018 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:143722234" variation 6019 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:370181483" variation 6110..6111 /gene="KLHL5" /replace="" /replace="a" /db_xref="dbSNP:36042316" variation 6125 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:138350647" variation 6133 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:116841485" variation 6161 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:181719351" variation 6177 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:187289187" variation 6236..6238 /gene="KLHL5" /replace="" /replace="aat" /db_xref="dbSNP:150669970" variation 6236 /gene="KLHL5" /replace="" /replace="att" /db_xref="dbSNP:3043408" variation 6238..6240 /gene="KLHL5" /replace="" /replace="taa" /db_xref="dbSNP:371320013" variation 6240 /gene="KLHL5" /replace="" /replace="taa" /db_xref="dbSNP:75541411" variation 6347 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:2890659" variation 6429 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:368034503" variation 6459 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:370624027" variation 6460 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:192130722" variation 6480 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:372552382" variation 6588 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:182817556" variation 6724 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:377037310" variation 6746 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:185985388" variation 6767 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:189913938" variation 6907 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:1063102" variation 6910 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:115698969" variation 6974 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:73238538" STS 6991..7074 /gene="KLHL5" /standard_name="RH93229" /db_xref="UniSTS:90744" variation 7020 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:372626737" variation 7036 /gene="KLHL5" /replace="c" /replace="t" /db_xref="dbSNP:201670996" variation 7073 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:1046655" variation 7135 /gene="KLHL5" /replace="a" /replace="c" /db_xref="dbSNP:78479575" variation 7152 /gene="KLHL5" /replace="a" /replace="g" /db_xref="dbSNP:182595545" ORIGIN
ggtcccctacccccacctactcgcccgccccctccggggccacccggggactctgaccccccggcctggcgccgcctgacggagcgggagtggctcgctccgggccggccggcgccggggatgaggctgcccggacgggtctaggggcgcgcgaggggccgagcatcccactcagctcgccggccccggcccccgcctcccccgctcctcccgcctggccgccccggcccgccgtgacccacggccgcctccggagcccgacgcggacttccaatagtagtcagacattatcatcctgtcatactatggagccatgtacatcagatgaatttttccaagcccttaatcatgccgagcaaacatttaaaaaaatggaaaactatttgagacataaacagttgtgtgatgtaattttagtcgctggtgatcgcagaattccagctcacagattggtgctctcctctgtctcagactattttgctgccatgtttactaatgatgtcagagaggcaagacaagaagaaataaaaatggaaggtgtagaaccaaattcgttgtggtccttgatccagtatgcttatacaggccgccttgaattaaaagaagataatattgagtgcctgttatctacagcttgccttcttcagctttcacaggttgtagaagcatgctgtaagtttttaatgaaacagcttcatccatccaactgtcttggaattcgttcttttgctgatgcccaaggttgtacagatttgcataaagtggctcacaattatactatggagcatttcatggaagtaatcagaaaccaggaatttgtattattaccagccagcgaaattgcaaagctcttggctagtgatgacatgaacattcctaatgaggagacaatattgaatgcacttcttacttgggtccgtcatgatttggaacagagacggaaagatctaagtaaacttttggcttatattaggctacctcttcttgcaccacagttcctggcagacatggaaaataatgtactttttcgggatgatatagaatgtcagaaactcattatggaagcaatgaagtaccatttattaccagagagacgacccatgttacaaagtcctcggacaaaacctaggaagtcaactgttggtacattatttgcagttgggggaatggattcaacaaaaggagcaacaagcattgaaaagtatgatctccgtacaaatatgtggactccagtagcaaatatgaatgggaggaggctacagttcggtgttgcagtgctagatgacaaactgtatgtggttggaggaagagatggactgaagactttgaatactgtagagtgctacaaccccaaaacaaaaacttggagtgtgatgccacctatgtccacacatagacatggccttggtgtggctgtactggaaggtcccatgtatgccgtaggaggacatgatggctggagctatctgaacacagtggaaagatgggaccctcaggctcgccagtggaattttgttgccactatgtctacccctaggagtacagtaggtgtggcagtactaagtggaaaactttatgcagttggtggtcgtgatggaagttcttgtctcaaatcagtagaatgttttgatcctcatactaataagtggacactgtgtgcacagatgtcaaaaaggagaggtggcgtaggagtgacgacctggaatggactgctgtatgctataggggggcacgatgctcccgcatccaacttgacttccagactctcagactgtgtggaaagatatgatcccaaaacagacatgtggactgcagtagcatccatgagcatcagcagagatgcagtgggggtctgtttacttggtgataagttatatgctgttggggggtatgatggacaggcataccttaatactgtggaggcttatgatccccagacaaatgagtggacccaggttgctccactgtgcctaggaagagctggagcttgtgttgtgactgtaaaattataatttagtgccccgttttctacatgaagacaccgtcttcctttattaatttagtataattattctatcaatggatacatttttagtaaatgtgcattgtcacaatcctgggcacaaagtgcctgatgtcaaaatgaagatagtaaaacaagggaggaagcagtggatggaccaggattaattcctttcatttcttagtaaattaaaacctgcagctggtggattgtgatcacacattcccgaagtaataagtgaggacgaatgcactgctctggaacataacccagtgctaactgggggtttcatttattcagtcaagcacatcttactcacatccagatttattttcctacagtgcaaacacaccagatgaaactttaaaatgttactttttgtaagcttatcataaatgagttgcagtaatttgtttgcttgtttgtttaaccacaaccactattttaatgatatactaaagataacactatttagttttttcagaaacatctgcattatatgtgtgttggttgtggattttgtttctaaaattggcttagtccaataaataaagaaaagcattaaggacttaaagcaacaataaccaaataaaaacttgataggatctttgaagtctatttaaatattcattccattacatctagactcaccaagaactacatgttatgatgttaagttgaagttgaaacatgatgttttgcattaaatttaagatatgcaaatttatgtagagaaaataaatgttatataccctataatctttcacctaattagtatttaattatatggatttgttttatattataaaagatgttttgattttgtcttttgatattgacaaaattgtttggatatccttatgttctcaagtctgtatctgcctcccctgccttatttcttatgttttgccacagttaacccattgtgcttctttgtaatcaaacagtttgtgggagaatgggcttattgaatgtctaaaaaataagtttaaagtgtttgttaccctaagttttttacatttttaaactctaattacatatgtgaatgttattactctcagtgaattgttattgtttgcaaaaatgcactgggcagtaacattttgtgataaatcctataagatataagtcattgagatgtctaagatgctttttattttaaccccagttaataaccaccttacggaaaataatatttgctaatattgtttattgtgaactaggaatcaaagtttttgtatgcatcaatgcacttaatccttataacaaccttatgaggtagttctattccctttttatagctaaggaaattggggtacagagaagttagccccaaggttatatattgcaagtaagtggcagagcagggattcatacaaagaccttctcactcagcagtcttcactcttactattcctgccactaggtagaaaaagaaagatttcggccgggcacagtggctcacgcctataattcccagcactttgggaggctgaggtgggcggatcacgaggtcaggagatggagaccatcctggctaacacagtgaaaccccgtctctactaaaaataaaaaataaaaaaaaattagccaggcgtggtggcgggtgcctgtacgcccagctactcgggaggctgaggcgggagaatggcgtgaacccaggaggaggagcttgcagtgtgccaagatcgcaccactgcactccagcctgggtgacagagcgagactccatcaaaaaaaaataaataaaaaaaaaataaaagatttcattttatgtgaggaattattttaataaaaaaaagagggtttatgctctatagtaataaaatttaccagtaacacccaatcagaaaattttggttccttagtatttagggaagacttttgtttaaatctcttatggaattttacatgttttgatttagaaaagtagatgcaatataatatatttcaagttttatacatattagatgaattgcatggtattttaggcaacttaactataaacaaatttattcatagaagcattgttgccaacaatttagatgacctcgatgaaaaaacacaccaattgacaaaactggctcaaaaggaaataaaaaatccaaacagacctgtaacaagtaaagagattgaaccagtaatcaaaaatctcccaacaaagaaagtccaggactaaatgagtttactggcaaactatgccaaacatataaagaagaattaacactaatccttctcgaactctcccaaaaaatggaagagaaaggagcaccctgtgacattctataaggcggacattaccttaacaccaaagccagacaaagacctcacagggaagctacagaccaatatcccttatgaatatagatgcaaaaaaacttcaaaatactagcaggccaaatccagcagcttattaaaatgatcacacagcatgaccaagtgagatttatcaaagaaatgcagggatggttctacatacaaatgtcaatcgatgtaataatataccatattaatagaatgaaggggaaaaaacagcatgatcacctcaattgataagaaaaagcatttgacaaaaatccaacaccctttcatggtaaaaacactctgcaaactaggaagaaaagggaactttcttaacctgataaagacatccataaaaacccacagctaacaacataatagcaaaacattgaaaatttttcccctaatatcatgaaaattcctgatttccccactgctattcaacattatactagaaggtctagccagagcaattaggcaagaaaaagaaataaaatgaatcccaaataggaagaagtaaaactacatttgcagaaaacatggtcctatatattaaaaatcctaaagaatccacaaaatgattccggctgattttaaaaattcagcaatgttgcaggttgcaagatcaacacacaaaagtctaagaaaaacctgaggggaaattaaaacaatttca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//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:51088 -> Molecular function: GO:0003674 [molecular_function] evidence: ND GeneID:51088 -> Molecular function: GO:0003779 [actin binding] evidence: IEA GeneID:51088 -> Biological process: GO:0008150 [biological_process] evidence: ND GeneID:51088 -> Cellular component: GO:0005737 [cytoplasm] evidence: NAS GeneID:51088 -> Cellular component: GO:0005856 [cytoskeleton] evidence: IEA
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