Mutagenetix > Incidental Mutation

Incidental Mutation 'R5294:Ranbp2'

405317

Institutional Source

Beutler Lab

Gene Symbol

Ranbp2

Ensembl Gene

ENSMUSG00000003226

Gene Name

RAN binding protein 2

Synonyms

A430087B05Rik

MMRRC Submission

042877-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R5294 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

58282674-58329977 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 58314490 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 1737 (F1737L)

Ref Sequence

ENSEMBL: ENSMUSP00000003310 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000003310]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000003310
AA Change: F1737L

PolyPhen 2 Score 0.235 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000003310
Gene: ENSMUSG00000003226
AA Change: F1737L

Domain	Start	End	E-Value	Type
Pfam:TPR_1	60	93	1.8e-7	PFAM
Pfam:TPR_8	60	93	8.9e-6	PFAM
low complexity region	235	247	N/A	INTRINSIC
low complexity region	778	801	N/A	INTRINSIC
coiled coil region	808	832	N/A	INTRINSIC
RanBD	1166	1295	6.47e-64	SMART
ZnF_RBZ	1348	1372	5.49e-2	SMART
ZnF_RBZ	1412	1436	3.06e-6	SMART
ZnF_RBZ	1471	1495	4.16e-8	SMART
ZnF_RBZ	1500	1524	4.57e-5	SMART
ZnF_RBZ	1560	1584	3.52e-6	SMART
ZnF_RBZ	1619	1643	1.35e-7	SMART
RanBD	1850	1979	2.84e-60	SMART
low complexity region	2034	2048	N/A	INTRINSIC
low complexity region	2069	2090	N/A	INTRINSIC
low complexity region	2106	2121	N/A	INTRINSIC
RanBD	2147	2276	4.96e-83	SMART
low complexity region	2310	2317	N/A	INTRINSIC
low complexity region	2328	2342	N/A	INTRINSIC
Pfam:IR1-M	2468	2530	2.5e-27	PFAM
Pfam:IR1-M	2544	2604	7e-30	PFAM
low complexity region	2673	2684	N/A	INTRINSIC
low complexity region	2722	2732	N/A	INTRINSIC
RanBD	2741	2869	5e-79	SMART
Pfam:Pro_isomerase	2896	3052	4.5e-45	PFAM

Meta Mutation Damage Score

0.1715

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 96.0%

Validation Efficiency

97% (70/72)

MGI Phenotype

PHENOTYPE: Mice homozygous for a gene trap allele display embryonic lethality. Heterozygous mice on some backgrounds display reduced ATP levels in the CNS, decreased glucose clearance, decreased weight gain on a high fat diet, and reduced scotopic responses. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579C12Rik	T	C	9: 89,034,056 (GRCm39)		noncoding transcript	Het
Acaca	A	G	11: 84,282,345 (GRCm39)	E2154G	probably benign	Het
Acacb	T	C	5: 114,380,013 (GRCm39)	F2056L	probably damaging	Het
Aff1	A	G	5: 103,959,023 (GRCm39)		probably benign	Het
Amn1	T	A	6: 149,086,622 (GRCm39)		probably benign	Het
Arid1a	C	A	4: 133,418,366 (GRCm39)		probably benign	Het
Aste1	T	A	9: 105,279,904 (GRCm39)		probably null	Het
Asxl3	T	A	18: 22,649,496 (GRCm39)	V495D	possibly damaging	Het
Atp1a3	T	A	7: 24,687,473 (GRCm39)	H688L	probably damaging	Het
B3gnt8	T	C	7: 25,328,191 (GRCm39)	L207P	probably damaging	Het
Baz2b	T	C	2: 59,808,946 (GRCm39)	H101R	probably benign	Het
Bicc1	G	A	10: 70,783,730 (GRCm39)	T387M	possibly damaging	Het
Champ1	A	C	8: 13,928,981 (GRCm39)	K380Q	probably damaging	Het
Cnst	A	G	1: 179,438,005 (GRCm39)	E523G	probably benign	Het
Cops6	G	C	5: 138,159,378 (GRCm39)		probably benign	Het
Cp	G	C	3: 20,020,480 (GRCm39)	V158L	probably benign	Het
Cyfip1	T	A	7: 55,523,231 (GRCm39)	M52K	possibly damaging	Het
Dars1	A	T	1: 128,292,039 (GRCm39)	F480I	probably benign	Het
Diaph1	C	A	18: 38,030,603 (GRCm39)	E284*	probably null	Het
Diaph1	T	C	18: 38,030,633 (GRCm39)	M274V	unknown	Het
Dock8	G	A	19: 25,038,517 (GRCm39)	V68M	probably benign	Het
Elavl4	A	G	4: 110,068,627 (GRCm39)	F247L	possibly damaging	Het
Emc10	C	T	7: 44,145,863 (GRCm39)		probably benign	Het
Fbxw16	T	C	9: 109,265,712 (GRCm39)	D369G	probably benign	Het
Fgr	A	T	4: 132,724,811 (GRCm39)	D304V	probably benign	Het
Filip1l	G	A	16: 57,390,399 (GRCm39)	S91N	possibly damaging	Het
Haus8	A	G	8: 71,708,354 (GRCm39)	S103P	unknown	Het
Hscb	A	G	5: 110,982,658 (GRCm39)	L143P	probably damaging	Het
Hsd11b2	A	T	8: 106,249,929 (GRCm39)	M347L	probably benign	Het
Jrk	C	A	15: 74,579,185 (GRCm39)	E33D	possibly damaging	Het
Kbtbd8	T	A	6: 95,098,813 (GRCm39)	Y123*	probably null	Het
Lrrc37	A	G	11: 103,507,057 (GRCm39)		probably benign	Het
Mis18bp1	A	C	12: 65,203,817 (GRCm39)	M59R	probably damaging	Het
Mrps27	T	C	13: 99,546,381 (GRCm39)	V260A	probably damaging	Het
Ncapg2	G	T	12: 116,391,414 (GRCm39)	V488L	possibly damaging	Het
Nepn	A	T	10: 52,276,896 (GRCm39)	N211Y	probably benign	Het
Ntrk3	A	T	7: 78,167,254 (GRCm39)		probably null	Het
Or10x4	A	T	1: 174,218,791 (GRCm39)	Y52F	probably benign	Het
Or11h23	A	G	14: 50,947,900 (GRCm39)	T38A	possibly damaging	Het
Or11h23	A	G	14: 50,948,236 (GRCm39)	I150V	probably benign	Het
Or52w1	C	T	7: 105,017,620 (GRCm39)	T20I	probably benign	Het
Otud4	A	T	8: 80,399,521 (GRCm39)	Q744L	possibly damaging	Het
P2ry14	A	T	3: 59,022,989 (GRCm39)	I166N	possibly damaging	Het
Pak2	T	A	16: 31,840,648 (GRCm39)	N478Y	probably damaging	Het
Papss2	A	G	19: 32,616,400 (GRCm39)	D202G	probably benign	Het
Pcdh7	C	A	5: 57,885,453 (GRCm39)		probably null	Het
Peg3	C	A	7: 6,720,848 (GRCm39)	S19I	possibly damaging	Het
Prim2	G	T	1: 33,707,974 (GRCm39)	T40K	probably benign	Het
Rex2	A	C	4: 147,142,442 (GRCm39)	N310T	probably benign	Het
Rnf123	AT	ATT	9: 107,941,202 (GRCm39)		probably null	Het
Rnf39	C	T	17: 37,258,092 (GRCm39)	A86V	probably damaging	Het
Ror1	A	T	4: 100,283,135 (GRCm39)	N400I	probably benign	Het
Slc38a8	C	T	8: 120,221,028 (GRCm39)	G177D	probably damaging	Het
Slc43a3	T	C	2: 84,786,654 (GRCm39)	V445A	probably benign	Het
Sptbn2	A	G	19: 4,768,936 (GRCm39)	N23S	possibly damaging	Het
Taf5l	A	G	8: 124,734,957 (GRCm39)	F74L	probably benign	Het
Trappc11	G	C	8: 47,983,766 (GRCm39)	A42G	possibly damaging	Het
Trim30d	T	C	7: 104,121,695 (GRCm39)	K350R	probably damaging	Het
Trnt1	T	C	6: 106,750,375 (GRCm39)	F93S	probably damaging	Het
Ube2c	T	C	2: 164,619,110 (GRCm39)	V161A	probably benign	Het
Usp24	A	G	4: 106,219,554 (GRCm39)	E555G	possibly damaging	Het
Vmn2r55	T	G	7: 12,385,791 (GRCm39)	S730R	probably damaging	Het
Vmn2r89	T	A	14: 51,692,570 (GRCm39)	N124K	probably benign	Het
Vmn2r98	T	A	17: 19,290,016 (GRCm39)	C517*	probably null	Het
Vps13a	A	T	19: 16,619,031 (GRCm39)	I2845N	probably damaging	Het
Vps51	T	G	19: 6,121,063 (GRCm39)	E283D	probably benign	Het
Xpo5	T	C	17: 46,547,848 (GRCm39)	V896A	probably benign	Het
Zfp2	T	C	11: 50,792,068 (GRCm39)		probably benign	Het
Zgrf1	G	A	3: 127,394,629 (GRCm39)	M1328I	probably benign	Het
Zswim5	A	G	4: 116,836,774 (GRCm39)	D686G	possibly damaging	Het

Other mutations in Ranbp2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00229:Ranbp2	APN	10	58,313,078 (GRCm39)	missense	probably damaging	1.00
IGL00336:Ranbp2	APN	10	58,287,806 (GRCm39)	missense	probably damaging	1.00
IGL00486:Ranbp2	APN	10	58,313,434 (GRCm39)	missense	probably benign	0.06
IGL00800:Ranbp2	APN	10	58,326,526 (GRCm39)	missense	probably benign
IGL00834:Ranbp2	APN	10	58,289,145 (GRCm39)	missense	possibly damaging	0.94
IGL00852:Ranbp2	APN	10	58,313,723 (GRCm39)	missense	probably benign
IGL00984:Ranbp2	APN	10	58,297,786 (GRCm39)	nonsense	probably null
IGL01299:Ranbp2	APN	10	58,328,639 (GRCm39)	missense	probably damaging	1.00
IGL01325:Ranbp2	APN	10	58,312,120 (GRCm39)	missense	probably damaging	0.99
IGL01444:Ranbp2	APN	10	58,311,122 (GRCm39)	missense	possibly damaging	0.79
IGL01545:Ranbp2	APN	10	58,314,703 (GRCm39)	missense	possibly damaging	0.48
IGL01619:Ranbp2	APN	10	58,299,900 (GRCm39)	splice site	probably null
IGL01782:Ranbp2	APN	10	58,314,131 (GRCm39)	missense	probably damaging	0.97
IGL02020:Ranbp2	APN	10	58,315,769 (GRCm39)	missense	probably damaging	1.00
IGL02096:Ranbp2	APN	10	58,297,789 (GRCm39)	missense	probably damaging	1.00
IGL02182:Ranbp2	APN	10	58,321,582 (GRCm39)	nonsense	probably null
IGL02211:Ranbp2	APN	10	58,314,064 (GRCm39)	missense	probably benign
IGL02249:Ranbp2	APN	10	58,315,900 (GRCm39)	missense	possibly damaging	0.89
IGL02268:Ranbp2	APN	10	58,329,475 (GRCm39)	unclassified	probably benign
IGL02421:Ranbp2	APN	10	58,316,376 (GRCm39)	missense	probably damaging	1.00
IGL03080:Ranbp2	APN	10	58,312,613 (GRCm39)	missense	probably benign	0.01
IGL03119:Ranbp2	APN	10	58,287,825 (GRCm39)	missense	probably damaging	1.00
IGL03206:Ranbp2	APN	10	58,301,369 (GRCm39)	missense	probably damaging	1.00
IGL03237:Ranbp2	APN	10	58,328,783 (GRCm39)	missense	probably damaging	0.98
En_passant	UTSW	10	58,287,839 (GRCm39)	missense	probably damaging	1.00
red_river	UTSW	10	58,301,489 (GRCm39)	missense	probably damaging	1.00
IGL02799:Ranbp2	UTSW	10	58,316,086 (GRCm39)	missense	probably damaging	1.00
R0058:Ranbp2	UTSW	10	58,316,353 (GRCm39)	missense	probably damaging	0.98
R0058:Ranbp2	UTSW	10	58,316,353 (GRCm39)	missense	probably damaging	0.98
R0145:Ranbp2	UTSW	10	58,315,868 (GRCm39)	missense	probably damaging	1.00
R0309:Ranbp2	UTSW	10	58,315,690 (GRCm39)	missense	probably benign	0.04
R0375:Ranbp2	UTSW	10	58,313,105 (GRCm39)	missense	probably damaging	1.00
R0441:Ranbp2	UTSW	10	58,321,590 (GRCm39)	missense	probably benign	0.40
R0494:Ranbp2	UTSW	10	58,303,254 (GRCm39)	missense	possibly damaging	0.53
R0542:Ranbp2	UTSW	10	58,314,236 (GRCm39)	missense	probably benign	0.02
R0565:Ranbp2	UTSW	10	58,312,158 (GRCm39)	missense	probably benign	0.41
R0608:Ranbp2	UTSW	10	58,329,720 (GRCm39)	missense	probably damaging	1.00
R0661:Ranbp2	UTSW	10	58,314,555 (GRCm39)	missense	probably benign
R0670:Ranbp2	UTSW	10	58,316,520 (GRCm39)	missense	probably benign	0.01
R0760:Ranbp2	UTSW	10	58,312,613 (GRCm39)	missense	possibly damaging	0.70
R0811:Ranbp2	UTSW	10	58,301,351 (GRCm39)	missense	probably benign	0.01
R0812:Ranbp2	UTSW	10	58,301,351 (GRCm39)	missense	probably benign	0.01
R1180:Ranbp2	UTSW	10	58,301,285 (GRCm39)	missense	probably damaging	1.00
R1196:Ranbp2	UTSW	10	58,312,875 (GRCm39)	missense	probably damaging	1.00
R1216:Ranbp2	UTSW	10	58,319,034 (GRCm39)	splice site	probably benign
R1374:Ranbp2	UTSW	10	58,321,715 (GRCm39)	splice site	probably benign
R1541:Ranbp2	UTSW	10	58,318,916 (GRCm39)	missense	possibly damaging	0.90
R1589:Ranbp2	UTSW	10	58,299,808 (GRCm39)	missense	probably benign	0.01
R1711:Ranbp2	UTSW	10	58,296,341 (GRCm39)	missense	probably benign	0.11
R1761:Ranbp2	UTSW	10	58,321,563 (GRCm39)	missense	probably benign	0.02
R1831:Ranbp2	UTSW	10	58,315,044 (GRCm39)	nonsense	probably null
R1840:Ranbp2	UTSW	10	58,314,588 (GRCm39)	missense	probably benign	0.41
R1869:Ranbp2	UTSW	10	58,328,383 (GRCm39)	missense	probably damaging	1.00
R1871:Ranbp2	UTSW	10	58,328,383 (GRCm39)	missense	probably damaging	1.00
R1892:Ranbp2	UTSW	10	58,299,921 (GRCm39)	missense	probably benign	0.36
R2270:Ranbp2	UTSW	10	58,291,749 (GRCm39)	missense	probably benign	0.06
R2363:Ranbp2	UTSW	10	58,314,758 (GRCm39)	missense	possibly damaging	0.79
R3844:Ranbp2	UTSW	10	58,313,717 (GRCm39)	missense	possibly damaging	0.87
R3937:Ranbp2	UTSW	10	58,312,294 (GRCm39)	missense	probably benign	0.00
R3938:Ranbp2	UTSW	10	58,312,294 (GRCm39)	missense	probably benign	0.00
R4025:Ranbp2	UTSW	10	58,316,378 (GRCm39)	missense	probably benign	0.23
R4183:Ranbp2	UTSW	10	58,301,488 (GRCm39)	missense	possibly damaging	0.53
R4247:Ranbp2	UTSW	10	58,314,686 (GRCm39)	missense	possibly damaging	0.79
R4334:Ranbp2	UTSW	10	58,299,816 (GRCm39)	missense	probably damaging	1.00
R4656:Ranbp2	UTSW	10	58,289,244 (GRCm39)	missense	possibly damaging	0.82
R4746:Ranbp2	UTSW	10	58,328,492 (GRCm39)	missense	probably damaging	1.00
R4852:Ranbp2	UTSW	10	58,312,878 (GRCm39)	missense	possibly damaging	0.94
R4863:Ranbp2	UTSW	10	58,328,243 (GRCm39)	missense	probably damaging	0.99
R5011:Ranbp2	UTSW	10	58,297,717 (GRCm39)	missense	probably benign	0.36
R5014:Ranbp2	UTSW	10	58,299,942 (GRCm39)	missense	probably benign	0.40
R5145:Ranbp2	UTSW	10	58,315,860 (GRCm39)	missense	probably damaging	1.00
R5178:Ranbp2	UTSW	10	58,312,607 (GRCm39)	missense	probably benign	0.01
R5199:Ranbp2	UTSW	10	58,300,265 (GRCm39)	missense	probably benign
R5508:Ranbp2	UTSW	10	58,315,827 (GRCm39)	missense	probably damaging	0.97
R5511:Ranbp2	UTSW	10	58,329,561 (GRCm39)	missense	probably benign	0.29
R5575:Ranbp2	UTSW	10	58,328,405 (GRCm39)	missense	probably damaging	1.00
R5617:Ranbp2	UTSW	10	58,301,489 (GRCm39)	missense	probably damaging	1.00
R5630:Ranbp2	UTSW	10	58,314,898 (GRCm39)	missense	probably damaging	1.00
R5733:Ranbp2	UTSW	10	58,321,658 (GRCm39)	missense	probably damaging	1.00
R5751:Ranbp2	UTSW	10	58,300,086 (GRCm39)	splice site	probably null
R5767:Ranbp2	UTSW	10	58,312,647 (GRCm39)	missense	probably benign	0.02
R6122:Ranbp2	UTSW	10	58,301,351 (GRCm39)	missense	probably benign	0.02
R6147:Ranbp2	UTSW	10	58,315,250 (GRCm39)	missense	probably damaging	1.00
R6286:Ranbp2	UTSW	10	58,315,394 (GRCm39)	missense	probably benign	0.02
R6344:Ranbp2	UTSW	10	58,319,708 (GRCm39)	splice site	probably null
R6452:Ranbp2	UTSW	10	58,313,979 (GRCm39)	missense	probably benign	0.00
R6487:Ranbp2	UTSW	10	58,321,563 (GRCm39)	missense	probably benign	0.02
R6620:Ranbp2	UTSW	10	58,291,629 (GRCm39)	critical splice acceptor site	probably null
R6759:Ranbp2	UTSW	10	58,293,559 (GRCm39)	nonsense	probably null
R7010:Ranbp2	UTSW	10	58,290,393 (GRCm39)	critical splice acceptor site	probably null
R7071:Ranbp2	UTSW	10	58,328,659 (GRCm39)	missense	probably damaging	1.00
R7083:Ranbp2	UTSW	10	58,315,052 (GRCm39)	missense	probably damaging	1.00
R7088:Ranbp2	UTSW	10	58,299,728 (GRCm39)	missense	probably damaging	1.00
R7102:Ranbp2	UTSW	10	58,299,772 (GRCm39)	missense	probably damaging	1.00
R7194:Ranbp2	UTSW	10	58,312,591 (GRCm39)	missense	probably benign	0.05
R7217:Ranbp2	UTSW	10	58,287,839 (GRCm39)	missense	probably damaging	1.00
R7318:Ranbp2	UTSW	10	58,318,909 (GRCm39)	nonsense	probably null
R7341:Ranbp2	UTSW	10	58,321,619 (GRCm39)	missense	possibly damaging	0.72
R7398:Ranbp2	UTSW	10	58,303,099 (GRCm39)	missense	probably damaging	1.00
R7424:Ranbp2	UTSW	10	58,315,016 (GRCm39)	missense	probably damaging	0.98
R7727:Ranbp2	UTSW	10	58,291,260 (GRCm39)	missense	probably benign	0.09
R7795:Ranbp2	UTSW	10	58,319,729 (GRCm39)	nonsense	probably null
R7812:Ranbp2	UTSW	10	58,303,224 (GRCm39)	missense	probably benign
R7845:Ranbp2	UTSW	10	58,282,844 (GRCm39)	missense	probably damaging	1.00
R7875:Ranbp2	UTSW	10	58,314,277 (GRCm39)	nonsense	probably null
R7934:Ranbp2	UTSW	10	58,312,297 (GRCm39)	missense	probably damaging	0.98
R8022:Ranbp2	UTSW	10	58,321,683 (GRCm39)	missense	possibly damaging	0.53
R8050:Ranbp2	UTSW	10	58,315,441 (GRCm39)	missense	probably damaging	0.99
R8100:Ranbp2	UTSW	10	58,326,470 (GRCm39)	missense	possibly damaging	0.58
R8194:Ranbp2	UTSW	10	58,291,747 (GRCm39)	missense	possibly damaging	0.84
R8258:Ranbp2	UTSW	10	58,291,755 (GRCm39)	missense	probably benign	0.04
R8259:Ranbp2	UTSW	10	58,291,755 (GRCm39)	missense	probably benign	0.04
R8461:Ranbp2	UTSW	10	58,312,216 (GRCm39)	missense	probably damaging	0.97
R8722:Ranbp2	UTSW	10	58,312,049 (GRCm39)	missense	probably damaging	1.00
R8755:Ranbp2	UTSW	10	58,300,969 (GRCm39)	nonsense	probably null
R8794:Ranbp2	UTSW	10	58,328,414 (GRCm39)	missense	probably damaging	1.00
R8879:Ranbp2	UTSW	10	58,313,711 (GRCm39)	missense	probably benign	0.10
R8994:Ranbp2	UTSW	10	58,315,891 (GRCm39)	missense	possibly damaging	0.89
R9023:Ranbp2	UTSW	10	58,315,343 (GRCm39)	nonsense	probably null
R9124:Ranbp2	UTSW	10	58,328,719 (GRCm39)	missense	probably benign	0.01
R9133:Ranbp2	UTSW	10	58,313,050 (GRCm39)	missense	probably damaging	1.00
R9145:Ranbp2	UTSW	10	58,291,736 (GRCm39)	missense	probably benign	0.03
R9190:Ranbp2	UTSW	10	58,313,117 (GRCm39)	missense	probably damaging	1.00
R9369:Ranbp2	UTSW	10	58,316,486 (GRCm39)	missense	probably benign	0.04
R9394:Ranbp2	UTSW	10	58,291,698 (GRCm39)	missense	probably damaging	0.97
R9642:Ranbp2	UTSW	10	58,318,907 (GRCm39)	missense	probably damaging	0.99
R9673:Ranbp2	UTSW	10	58,300,963 (GRCm39)	missense	probably damaging	1.00
X0018:Ranbp2	UTSW	10	58,314,406 (GRCm39)	missense	probably benign	0.13
X0022:Ranbp2	UTSW	10	58,300,977 (GRCm39)	missense	probably benign	0.33
Z1088:Ranbp2	UTSW	10	58,328,715 (GRCm39)	missense	probably benign	0.35
Z1088:Ranbp2	UTSW	10	58,313,805 (GRCm39)	frame shift	probably null
Z1088:Ranbp2	UTSW	10	58,313,794 (GRCm39)	frame shift	probably null
Z1176:Ranbp2	UTSW	10	58,297,708 (GRCm39)	missense	probably damaging	1.00
Z1177:Ranbp2	UTSW	10	58,329,713 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TCTGCAGGAAGTCAAGTGGG -3'
(R):5'- GTCTTTCTTGCCAAATTGAAACCC -3'

Sequencing Primer
(F):5'- GGAACAGAATTCAAAAGTAACTTTCC -3'
(R):5'- GCCAAATTGAAACCCTTCTCTTGATG -3'

Posted On

2016-07-22