Mutagenetix > Incidental Mutation

Incidental Mutation 'R1794:Prrc2c'

202015

Institutional Source

Beutler Lab

Gene Symbol

Prrc2c

Ensembl Gene

ENSMUSG00000040225

Gene Name

proline-rich coiled-coil 2C

Synonyms

9630039I18Rik, 1810043M20Rik, Bat2d, Bat2l2

MMRRC Submission

039824-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.307) question?

Stock #

R1794 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

162670725-162740556 bp(-) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 162705959 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138698 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028016] [ENSMUST00000182149] [ENSMUST00000182393] [ENSMUST00000182593] [ENSMUST00000182660] [ENSMUST00000183011] [ENSMUST00000183223]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000028016
AA Change: K1027R

SMART Domains

Protein: ENSMUSP00000028016
Gene: ENSMUSG00000040225
AA Change: K1027R

Domain	Start	End	E-Value	Type
Pfam:BAT2_N	1	164	7.7e-56	PFAM
internal_repeat_2	167	349	4.39e-5	PROSPERO
internal_repeat_1	336	391	2.14e-5	PROSPERO
low complexity region	407	414	N/A	INTRINSIC
SCOP:d1eq1a_	447	591	2e-5	SMART
low complexity region	649	669	N/A	INTRINSIC
low complexity region	733	745	N/A	INTRINSIC
coiled coil region	996	1026	N/A	INTRINSIC
low complexity region	1157	1186	N/A	INTRINSIC
low complexity region	1212	1222	N/A	INTRINSIC
internal_repeat_1	1240	1295	2.14e-5	PROSPERO
low complexity region	1308	1335	N/A	INTRINSIC
low complexity region	1388	1409	N/A	INTRINSIC
low complexity region	1715	1746	N/A	INTRINSIC
low complexity region	1765	1803	N/A	INTRINSIC
low complexity region	1815	1832	N/A	INTRINSIC
low complexity region	1844	1909	N/A	INTRINSIC
internal_repeat_2	1962	2148	4.39e-5	PROSPERO
low complexity region	2163	2177	N/A	INTRINSIC
low complexity region	2230	2252	N/A	INTRINSIC
low complexity region	2272	2286	N/A	INTRINSIC
low complexity region	2321	2338	N/A	INTRINSIC
low complexity region	2427	2438	N/A	INTRINSIC
low complexity region	2553	2576	N/A	INTRINSIC
low complexity region	2811	2828	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000182149
AA Change: K1029R

SMART Domains

Protein: ENSMUSP00000138548
Gene: ENSMUSG00000040225
AA Change: K1029R

Domain	Start	End	E-Value	Type
Pfam:BAT2_N	1	167	5.6e-73	PFAM
internal_repeat_1	336	391	1.49e-5	PROSPERO
low complexity region	407	414	N/A	INTRINSIC
SCOP:d1eq1a_	447	591	2e-5	SMART
low complexity region	649	669	N/A	INTRINSIC
low complexity region	733	745	N/A	INTRINSIC
internal_repeat_3	754	925	9.16e-5	PROSPERO
coiled coil region	996	1026	N/A	INTRINSIC
low complexity region	1157	1186	N/A	INTRINSIC
low complexity region	1212	1222	N/A	INTRINSIC
internal_repeat_1	1240	1295	1.49e-5	PROSPERO
low complexity region	1308	1335	N/A	INTRINSIC
low complexity region	1388	1409	N/A	INTRINSIC
low complexity region	1715	1746	N/A	INTRINSIC
low complexity region	1765	1803	N/A	INTRINSIC
low complexity region	1815	1832	N/A	INTRINSIC
low complexity region	1844	1909	N/A	INTRINSIC
internal_repeat_2	1962	2148	3.08e-5	PROSPERO
internal_repeat_3	1983	2153	9.16e-5	PROSPERO
low complexity region	2163	2177	N/A	INTRINSIC
low complexity region	2230	2252	N/A	INTRINSIC
low complexity region	2272	2286	N/A	INTRINSIC
low complexity region	2321	2338	N/A	INTRINSIC
low complexity region	2427	2438	N/A	INTRINSIC
low complexity region	2553	2576	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000182393

SMART Domains

Protein: ENSMUSP00000138451
Gene: ENSMUSG00000040225

Domain	Start	End	E-Value	Type
low complexity region	24	51	N/A	INTRINSIC
low complexity region	104	125	N/A	INTRINSIC
low complexity region	431	462	N/A	INTRINSIC
low complexity region	481	519	N/A	INTRINSIC
low complexity region	531	548	N/A	INTRINSIC
low complexity region	560	625	N/A	INTRINSIC
low complexity region	879	893	N/A	INTRINSIC
low complexity region	946	968	N/A	INTRINSIC
low complexity region	988	1002	N/A	INTRINSIC
low complexity region	1037	1054	N/A	INTRINSIC
low complexity region	1143	1154	N/A	INTRINSIC
low complexity region	1274	1297	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000182593
AA Change: K1027R

SMART Domains

Protein: ENSMUSP00000138674
Gene: ENSMUSG00000040225
AA Change: K1027R

Domain	Start	End	E-Value	Type
Pfam:BAT2_N	1	165	4.1e-70	PFAM
internal_repeat_1	334	389	9.57e-6	PROSPERO
low complexity region	405	412	N/A	INTRINSIC
SCOP:d1eq1a_	445	589	3e-5	SMART
low complexity region	647	667	N/A	INTRINSIC
low complexity region	731	743	N/A	INTRINSIC
internal_repeat_3	752	923	6.11e-5	PROSPERO
coiled coil region	994	1024	N/A	INTRINSIC
low complexity region	1155	1184	N/A	INTRINSIC
low complexity region	1210	1220	N/A	INTRINSIC
internal_repeat_1	1238	1293	9.57e-6	PROSPERO
low complexity region	1306	1333	N/A	INTRINSIC
low complexity region	1386	1407	N/A	INTRINSIC
low complexity region	1713	1744	N/A	INTRINSIC
low complexity region	1763	1801	N/A	INTRINSIC
low complexity region	1813	1830	N/A	INTRINSIC
low complexity region	1842	1907	N/A	INTRINSIC
internal_repeat_2	1960	2146	2.01e-5	PROSPERO
internal_repeat_3	1981	2151	6.11e-5	PROSPERO
low complexity region	2161	2175	N/A	INTRINSIC
low complexity region	2228	2250	N/A	INTRINSIC
low complexity region	2270	2284	N/A	INTRINSIC
low complexity region	2319	2336	N/A	INTRINSIC
low complexity region	2425	2436	N/A	INTRINSIC
low complexity region	2551	2574	N/A	INTRINSIC
low complexity region	2671	2682	N/A	INTRINSIC
low complexity region	2730	2747	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000182660
AA Change: K1029R

SMART Domains

Protein: ENSMUSP00000138433
Gene: ENSMUSG00000040225
AA Change: K1029R

Domain	Start	End	E-Value	Type
Pfam:BAT2_N	1	167	7e-73	PFAM
internal_repeat_1	336	391	2.14e-5	PROSPERO
low complexity region	407	414	N/A	INTRINSIC
SCOP:d1eq1a_	447	591	2e-5	SMART
low complexity region	649	669	N/A	INTRINSIC
low complexity region	733	745	N/A	INTRINSIC
coiled coil region	996	1026	N/A	INTRINSIC
low complexity region	1157	1186	N/A	INTRINSIC
low complexity region	1212	1222	N/A	INTRINSIC
internal_repeat_1	1240	1295	2.14e-5	PROSPERO
low complexity region	1308	1335	N/A	INTRINSIC
low complexity region	1388	1409	N/A	INTRINSIC
low complexity region	1715	1746	N/A	INTRINSIC
low complexity region	1765	1803	N/A	INTRINSIC
low complexity region	1815	1832	N/A	INTRINSIC
low complexity region	1844	1909	N/A	INTRINSIC
internal_repeat_2	1962	2148	4.39e-5	PROSPERO
low complexity region	2163	2177	N/A	INTRINSIC
low complexity region	2230	2252	N/A	INTRINSIC
low complexity region	2272	2286	N/A	INTRINSIC
low complexity region	2321	2338	N/A	INTRINSIC
low complexity region	2427	2438	N/A	INTRINSIC
low complexity region	2553	2576	N/A	INTRINSIC
low complexity region	2811	2828	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000183011

SMART Domains

Protein: ENSMUSP00000138609
Gene: ENSMUSG00000040225

Domain	Start	End	E-Value	Type
Pfam:BAT2_N	1	160	3.2e-64	PFAM
low complexity region	400	407	N/A	INTRINSIC
coiled coil region	443	560	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000183223

SMART Domains

Protein: ENSMUSP00000138698
Gene: ENSMUSG00000040225

Domain	Start	End	E-Value	Type
low complexity region	289	320	N/A	INTRINSIC
low complexity region	339	377	N/A	INTRINSIC
low complexity region	389	406	N/A	INTRINSIC
low complexity region	418	483	N/A	INTRINSIC
low complexity region	739	761	N/A	INTRINSIC
low complexity region	781	795	N/A	INTRINSIC
low complexity region	830	847	N/A	INTRINSIC
low complexity region	936	947	N/A	INTRINSIC
low complexity region	1062	1085	N/A	INTRINSIC
low complexity region	1182	1193	N/A	INTRINSIC
low complexity region	1241	1258	N/A	INTRINSIC

Coding Region Coverage

1x: 97.4%
3x: 96.7%
10x: 94.8%
20x: 91.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700014D04Rik	T	C	13: 59,742,620	E44G	probably benign	Het
Anxa7	A	G	14: 20,471,467	Y54H	unknown	Het
Arhgef3	A	G	14: 27,397,605	T331A	probably benign	Het
Arhgef40	G	T	14: 51,989,930	C477F	possibly damaging	Het
Arsi	G	A	18: 60,916,651	G202E	probably benign	Het
Atp13a5	C	A	16: 29,321,709	R343L	probably damaging	Het
Brdt	ACAGCAGCAGCAGCAGC	ACAGCAGCAGCAGC	5: 107,359,853		probably benign	Het
Btbd2	G	T	10: 80,643,913	D426E	probably damaging	Het
Cabin1	A	C	10: 75,725,745	I974R	possibly damaging	Het
Cacna1i	G	A	15: 80,389,122	V1670M	probably damaging	Het
Cc2d2a	C	A	5: 43,688,252	Q288K	probably damaging	Het
Ccl20	T	A	1: 83,117,829	I37K	possibly damaging	Het
Cdcp1	A	G	9: 123,190,094	V40A	probably benign	Het
Cdcp1	T	C	9: 123,215,831	T27A	probably benign	Het
Cdh4	C	T	2: 179,886,842	T581I	probably damaging	Het
Cgn	A	G	3: 94,762,557		probably null	Het
Col7a1	G	A	9: 108,965,928	G1493D	unknown	Het
Creb3	A	G	4: 43,563,302	E133G	probably benign	Het
Dchs1	T	C	7: 105,771,720	T498A	probably benign	Het
Dis3l	A	C	9: 64,317,776	V413G	possibly damaging	Het
Dnah6	T	C	6: 73,024,958	E3865G	probably damaging	Het
Fam219b	A	G	9: 57,539,281	Y139C	probably damaging	Het
Fat3	A	T	9: 15,997,136	Y2523*	probably null	Het
Fat3	A	T	9: 15,997,138	Y2523N	probably benign	Het
Fmnl1	T	C	11: 103,197,147	S40P	probably benign	Het
Gm17727	T	A	9: 35,777,122	I56F	probably benign	Het
Gm4792	T	C	10: 94,298,490	D6G	unknown	Het
Hhat	G	T	1: 192,693,906	Y306*	probably null	Het
Hmcn1	A	G	1: 150,598,285	I4802T	probably benign	Het
Hmcn1	G	A	1: 150,627,152	T3908I	probably damaging	Het
Hsph1	A	T	5: 149,630,773	N79K	probably damaging	Het
Ikbke	T	A	1: 131,259,218	Y579F	probably damaging	Het
Jak2	A	G	19: 29,299,557	D838G	probably benign	Het
Klhdc7b	T	C	15: 89,387,020	S702P	probably benign	Het
Lingo3	C	A	10: 80,835,598	R166L	probably benign	Het
Lins1	T	C	7: 66,711,909	F436S	probably damaging	Het
Lman1	T	C	18: 65,991,684	D328G	probably benign	Het
Lox	A	G	18: 52,528,307	C232R	probably damaging	Het
Lrrc59	T	C	11: 94,638,595	V165A	probably benign	Het
Map9	A	G	3: 82,380,221	D50G	probably damaging	Het
March1	T	A	8: 66,386,942	Y126N	possibly damaging	Het
Mcf2l	T	C	8: 12,915,982	F3L	probably benign	Het
Mslnl	G	A	17: 25,742,934	V128M	probably damaging	Het
Nin	G	A	12: 70,043,795	Q949*	probably null	Het
Nlgn3	A	G	X: 101,320,033	H636R	probably benign	Het
Notch2	A	G	3: 98,099,547	D411G	possibly damaging	Het
Olfr1263	A	G	2: 90,015,020	Y30C	probably damaging	Het
Olfr1449	G	C	19: 12,934,968	A77P	probably damaging	Het
Plekha7	A	G	7: 116,140,681	V579A	probably damaging	Het
Rab7b	T	C	1: 131,697,068		probably null	Het
Reg3b	G	T	6: 78,372,214		probably null	Het
Rgs20	A	G	1: 4,910,572	Y177H	probably damaging	Het
Ripk3	G	T	14: 55,785,329	N379K	probably benign	Het
Rnf220	G	T	4: 117,307,568	Q7K	probably benign	Het
Ros1	T	A	10: 52,124,103	K1109*	probably null	Het
Slc22a7	T	G	17: 46,433,153	R460S	probably damaging	Het
Slc4a2	A	G	5: 24,439,328	M975V	probably damaging	Het
Slc4a3	A	T	1: 75,557,308	I1100F	probably damaging	Het
Smco1	A	G	16: 32,274,132	E207G	probably benign	Het
Snrnp200	A	G	2: 127,216,736	E369G	probably benign	Het
Tcf4	T	A	18: 69,657,853	M178K	probably benign	Het
Tex2	T	C	11: 106,567,902		probably benign	Het
Tjp1	A	T	7: 65,323,129	I521N	probably damaging	Het
Tmem203	A	G	2: 25,255,994	T109A	probably benign	Het
Tmem50b	T	C	16: 91,578,029	I126V	probably benign	Het
Ugcg	C	T	4: 59,207,798	P46S	probably benign	Het
Ush2a	T	C	1: 188,862,809	F3813L	probably benign	Het
Vmn1r203	C	T	13: 22,524,351	R101W	probably damaging	Het
Vmn2r79	G	A	7: 87,001,413	V136I	probably benign	Het
Wdr38	A	G	2: 39,000,729	Y205C	probably damaging	Het
Zfp248	A	G	6: 118,429,303	F442L	probably damaging	Het
Znrf4	A	G	17: 56,511,599	I236T	probably damaging	Het

Other mutations in Prrc2c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00425:Prrc2c	APN	1	162720613	splice site	probably null
IGL00577:Prrc2c	APN	1	162698116	missense	unknown
IGL00580:Prrc2c	APN	1	162698116	missense	unknown
IGL01295:Prrc2c	APN	1	162682492	missense	probably damaging	1.00
IGL01554:Prrc2c	APN	1	162710786	missense	probably damaging	0.99
IGL01684:Prrc2c	APN	1	162706462	unclassified	probably benign
IGL01745:Prrc2c	APN	1	162724728	missense	probably damaging	1.00
IGL01770:Prrc2c	APN	1	162704499	missense	probably benign	0.23
IGL01905:Prrc2c	APN	1	162705329	unclassified	probably benign
IGL02304:Prrc2c	APN	1	162684136	missense	probably benign	0.05
IGL02389:Prrc2c	APN	1	162692870	missense	probably damaging	1.00
IGL02540:Prrc2c	APN	1	162723137	missense	probably damaging	1.00
IGL02681:Prrc2c	APN	1	162705612	unclassified	probably benign
IGL02686:Prrc2c	APN	1	162707947	unclassified	probably benign
IGL02795:Prrc2c	APN	1	162714299	missense	probably benign
IGL02894:Prrc2c	APN	1	162678057	missense	probably damaging	1.00
IGL02957:Prrc2c	APN	1	162706535	unclassified	probably benign
IGL02981:Prrc2c	APN	1	162705179	unclassified	probably benign
IGL03070:Prrc2c	APN	1	162677409	missense	probably damaging	1.00
IGL03096:Prrc2c	APN	1	162702359	missense	unknown
R0058:Prrc2c	UTSW	1	162698884	missense	unknown
R0058:Prrc2c	UTSW	1	162698884	missense	unknown
R0135:Prrc2c	UTSW	1	162715483	splice site	probably benign
R0279:Prrc2c	UTSW	1	162715464	missense	probably damaging	1.00
R0363:Prrc2c	UTSW	1	162697811	missense	unknown
R0436:Prrc2c	UTSW	1	162705314	unclassified	probably benign
R0605:Prrc2c	UTSW	1	162682426	missense	probably damaging	1.00
R0696:Prrc2c	UTSW	1	162708852	critical splice donor site	probably null
R0981:Prrc2c	UTSW	1	162705981	unclassified	probably benign
R1693:Prrc2c	UTSW	1	162718713	missense	probably damaging	0.98
R1714:Prrc2c	UTSW	1	162677376	missense	probably damaging	1.00
R1791:Prrc2c	UTSW	1	162704982	unclassified	probably benign
R1998:Prrc2c	UTSW	1	162704918	unclassified	probably benign
R2040:Prrc2c	UTSW	1	162697557	missense	probably damaging	1.00
R2168:Prrc2c	UTSW	1	162710334	unclassified	probably benign
R2246:Prrc2c	UTSW	1	162707791	unclassified	probably benign
R2830:Prrc2c	UTSW	1	162708916	unclassified	probably benign
R2926:Prrc2c	UTSW	1	162706127	unclassified	probably benign
R3703:Prrc2c	UTSW	1	162710691	missense	probably damaging	1.00
R3745:Prrc2c	UTSW	1	162698185	missense	unknown
R3760:Prrc2c	UTSW	1	162692851	missense	probably damaging	1.00
R3784:Prrc2c	UTSW	1	162709669	unclassified	probably benign
R3959:Prrc2c	UTSW	1	162708892	unclassified	probably benign
R4255:Prrc2c	UTSW	1	162706326	unclassified	probably benign
R4276:Prrc2c	UTSW	1	162673591	missense	probably damaging	1.00
R4421:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R4593:Prrc2c	UTSW	1	162697532	missense	probably damaging	1.00
R4651:Prrc2c	UTSW	1	162723274	missense	probably damaging	1.00
R4652:Prrc2c	UTSW	1	162723274	missense	probably damaging	1.00
R4660:Prrc2c	UTSW	1	162680895	missense	probably damaging	1.00
R4677:Prrc2c	UTSW	1	162705179	unclassified	probably benign
R4688:Prrc2c	UTSW	1	162697687	missense	unknown
R4753:Prrc2c	UTSW	1	162691230	missense	probably damaging	1.00
R4790:Prrc2c	UTSW	1	162710481	missense	unknown
R4981:Prrc2c	UTSW	1	162692547	missense	probably damaging	1.00
R4995:Prrc2c	UTSW	1	162705310	unclassified	probably benign
R5119:Prrc2c	UTSW	1	162705440	unclassified	probably benign
R5127:Prrc2c	UTSW	1	162697846	missense	unknown
R5291:Prrc2c	UTSW	1	162705582	unclassified	probably benign
R5474:Prrc2c	UTSW	1	162709644	unclassified	probably benign
R5543:Prrc2c	UTSW	1	162673511	missense	probably damaging	0.99
R5579:Prrc2c	UTSW	1	162680758	critical splice donor site	probably null
R5594:Prrc2c	UTSW	1	162699031	missense	unknown
R5620:Prrc2c	UTSW	1	162673529	missense	probably damaging	1.00
R5994:Prrc2c	UTSW	1	162674156	splice site	probably null
R6142:Prrc2c	UTSW	1	162710387	missense	unknown
R6199:Prrc2c	UTSW	1	162682516	missense	probably damaging	1.00
R6277:Prrc2c	UTSW	1	162714314	missense	probably benign
R6504:Prrc2c	UTSW	1	162697795	missense	unknown
R6671:Prrc2c	UTSW	1	162697585	missense	probably damaging	1.00
R6785:Prrc2c	UTSW	1	162709101	unclassified	probably benign
R6799:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6801:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6850:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6851:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6856:Prrc2c	UTSW	1	162682371	missense	probably damaging	1.00
R6869:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6882:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6884:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R6897:Prrc2c	UTSW	1	162705506	unclassified	probably benign
R6934:Prrc2c	UTSW	1	162720505	missense	probably benign	0.10
R6976:Prrc2c	UTSW	1	162692844	missense	probably damaging	1.00
R7132:Prrc2c	UTSW	1	162681281	missense	possibly damaging	0.77
R7165:Prrc2c	UTSW	1	162673517	missense	possibly damaging	0.94
R7282:Prrc2c	UTSW	1	162679974	missense	possibly damaging	0.59
R7467:Prrc2c	UTSW	1	162677363	missense	possibly damaging	0.84
R7915:Prrc2c	UTSW	1	162692408	missense	probably benign	0.39
R8068:Prrc2c	UTSW	1	162709061	unclassified	probably benign
R8529:Prrc2c	UTSW	1	162709094	unclassified	probably benign
R8734:Prrc2c	UTSW	1	162679512	missense	possibly damaging	0.92
R8735:Prrc2c	UTSW	1	162709558	missense	unknown
R8813:Prrc2c	UTSW	1	162705243	missense	unknown
R8946:Prrc2c	UTSW	1	162708909	unclassified	probably benign
R8975:Prrc2c	UTSW	1	162706061	missense	unknown
R9035:Prrc2c	UTSW	1	162675726	missense	possibly damaging	0.96
R9185:Prrc2c	UTSW	1	162704643	missense	unknown
R9261:Prrc2c	UTSW	1	162678053	missense	possibly damaging	0.48
R9287:Prrc2c	UTSW	1	162714274	missense	probably benign	0.34
R9289:Prrc2c	UTSW	1	162679561	missense	probably benign	0.33
R9466:Prrc2c	UTSW	1	162675689	missense	possibly damaging	0.53
R9523:Prrc2c	UTSW	1	162697729	missense	unknown
R9542:Prrc2c	UTSW	1	162680790	missense	possibly damaging	0.88
R9629:Prrc2c	UTSW	1	162692390	missense	possibly damaging	0.95
R9744:Prrc2c	UTSW	1	162678164	missense	possibly damaging	0.96
R9748:Prrc2c	UTSW	1	162707866	missense	unknown
X0020:Prrc2c	UTSW	1	162707847	unclassified	probably benign
X0039:Prrc2c	UTSW	1	162704793	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- TGGACACTACCAACAGGTTCC -3'
(R):5'- TCTGAAGGGCCTAAACCAGAG -3'

Sequencing Primer
(F):5'- CAACAGGTTCCAAAGGTTTCTC -3'
(R):5'- TCTAAATCAGAAACTCGGTGGGGTC -3'

Posted On

2014-06-23