Mutagenetix > Incidental Mutation

Incidental Mutation 'R4888:Myt1l'

377127

Institutional Source

Beutler Lab

Gene Symbol

Myt1l

Ensembl Gene

ENSMUSG00000061911

Gene Name

myelin transcription factor 1-like

Synonyms

2900093J19Rik, Png-1, 2900046C06Rik, C630034G21Rik, Nztf1, Pmng1

MMRRC Submission

042493-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4888 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

29578383-29973212 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 29936138 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Glycine at position 909 (C909G)

Ref Sequence

ENSEMBL: ENSMUSP00000151588 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021009] [ENSMUST00000049784] [ENSMUST00000218583]

AlphaFold

P97500

Predicted Effect

unknown
Transcript: ENSMUST00000021009
AA Change: C909G

SMART Domains

Protein: ENSMUSP00000021009
Gene: ENSMUSG00000061911
AA Change: C909G

Domain	Start	End	E-Value	Type
Pfam:zf-C2HC	28	58	8.3e-19	PFAM
coiled coil region	148	182	N/A	INTRINSIC
low complexity region	188	200	N/A	INTRINSIC
low complexity region	222	233	N/A	INTRINSIC
Pfam:zf-C2HC	502	532	1.1e-16	PFAM
Pfam:zf-C2HC	546	576	4e-18	PFAM
Pfam:MYT1	620	872	2.7e-135	PFAM
Pfam:zf-C2HC	901	931	8.4e-20	PFAM
Pfam:zf-C2HC	950	980	1.2e-18	PFAM
Pfam:zf-C2HC	1003	1033	1.1e-17	PFAM
coiled coil region	1055	1130	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000049784
AA Change: C911G

SMART Domains

Protein: ENSMUSP00000058264
Gene: ENSMUSG00000061911
AA Change: C911G

Domain	Start	End	E-Value	Type
Pfam:zf-C2HC	30	58	5.1e-18	PFAM
coiled coil region	148	182	N/A	INTRINSIC
low complexity region	188	200	N/A	INTRINSIC
low complexity region	222	233	N/A	INTRINSIC
Pfam:zf-C2HC	506	533	9.9e-15	PFAM
Pfam:zf-C2HC	550	578	2.4e-16	PFAM
Pfam:MYT1	622	873	2.7e-122	PFAM
Pfam:zf-C2HC	905	933	6.3e-19	PFAM
Pfam:zf-C2HC	954	982	1.6e-18	PFAM
Pfam:zf-C2HC	1007	1035	1.4e-16	PFAM
coiled coil region	1057	1132	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000218583
AA Change: C909G

Meta Mutation Damage Score

0.4774

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.8%
20x: 94.1%

Validation Efficiency

99% (150/151)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the zinc finger superfamily of transcription factors. The encoded protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in this gene have been associated with autosomal mental retardation-39 and autism spectrum disorder. Alternative splicing results in multiple variants. [provided by RefSeq, Aug 2016]

Allele List at MGI

Other mutations in this stock

Total: 139 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931403M11Rik	C	A	14: 24,671,419 (GRCm39)		noncoding transcript	Het
Abca7	A	G	10: 79,838,562 (GRCm39)	K612R	probably damaging	Het
Adamtsl3	T	C	7: 82,223,822 (GRCm39)	V275A	possibly damaging	Het
Afg3l1	G	A	8: 124,215,065 (GRCm39)		probably null	Het
Ajm1	G	A	2: 25,469,759 (GRCm39)	R51C	possibly damaging	Het
Alcam	T	A	16: 52,089,176 (GRCm39)	H508L	probably benign	Het
Ankrd45	G	A	1: 160,982,942 (GRCm39)	R151H	probably damaging	Het
Aqr	G	A	2: 113,980,990 (GRCm39)	L264F	probably damaging	Het
Arfgef2	G	A	2: 166,677,533 (GRCm39)	A53T	probably damaging	Het
Arhgap30	A	G	1: 171,236,880 (GRCm39)	T1085A	probably benign	Het
Atp10a	T	C	7: 58,435,055 (GRCm39)	V314A	probably damaging	Het
Bdp1	T	C	13: 100,187,627 (GRCm39)	D1580G	probably benign	Het
Btbd17	T	A	11: 114,684,917 (GRCm39)	T41S	possibly damaging	Het
Cacna1c	T	C	6: 118,728,400 (GRCm39)	N378S	probably damaging	Het
Camsap1	G	T	2: 25,825,562 (GRCm39)	Q1375K	probably benign	Het
Catsper2	G	T	2: 121,227,604 (GRCm39)		probably null	Het
Cblif	A	G	19: 11,729,583 (GRCm39)	T181A	probably benign	Het
Ccar1	A	G	10: 62,588,997 (GRCm39)	S829P	unknown	Het
Ccdc180	T	C	4: 45,909,308 (GRCm39)	L492P	probably damaging	Het
Ccser2	A	T	14: 36,662,343 (GRCm39)	N280K	probably damaging	Het
Cd37	T	C	7: 44,883,359 (GRCm39)	D271G	probably damaging	Het
Cdcp1	G	A	9: 123,011,194 (GRCm39)		probably benign	Het
Cemip2	T	C	19: 21,833,528 (GRCm39)	V1322A	probably benign	Het
Cep85	T	A	4: 133,892,062 (GRCm39)		probably benign	Het
Cfi	C	T	3: 129,666,726 (GRCm39)	P483L	probably damaging	Het
Csmd1	A	G	8: 15,945,674 (GRCm39)		probably benign	Het
Cytl1	G	T	5: 37,892,918 (GRCm39)	L9F	unknown	Het
Defb26	T	C	2: 152,350,085 (GRCm39)	E65G	possibly damaging	Het
Degs1	G	A	1: 182,104,370 (GRCm39)	T305I	probably damaging	Het
Dnttip2	T	G	3: 122,070,241 (GRCm39)	C485W	probably damaging	Het
Ecel1	G	A	1: 87,076,449 (GRCm39)		probably benign	Het
Edrf1	G	T	7: 133,260,339 (GRCm39)	M83I	probably damaging	Het
Elmo2	A	T	2: 165,137,209 (GRCm39)	C562S	probably benign	Het
Etl4	T	A	2: 20,344,922 (GRCm39)		probably null	Het
F2r	A	C	13: 95,740,905 (GRCm39)	V210G	probably damaging	Het
Fam171a1	T	A	2: 3,224,546 (GRCm39)	V179E	probably damaging	Het
Fmod	G	T	1: 133,967,977 (GRCm39)	V6F	possibly damaging	Het
Foxr2	A	G	X: 151,913,312 (GRCm39)	Q61R	probably damaging	Het
Gabra4	G	A	5: 71,729,546 (GRCm39)	H76Y	probably benign	Het
Gck	A	T	11: 5,859,150 (GRCm39)	M139K	possibly damaging	Het
Gm10192	C	G	4: 97,071,345 (GRCm39)	S20T	probably null	Het
Gm44501	T	C	17: 40,887,515 (GRCm39)	L11P	unknown	Het
Gm572	T	C	4: 148,751,302 (GRCm39)		probably null	Het
Gnas	A	G	2: 174,139,882 (GRCm39)	K17R	possibly damaging	Het
Grm2	T	A	9: 106,527,865 (GRCm39)	S340C	probably damaging	Het
Gsc	T	A	12: 104,438,274 (GRCm39)	H198L	probably damaging	Het
H2-Q3	A	T	17: 35,578,424 (GRCm39)		noncoding transcript	Het
H4c1	T	C	13: 23,944,935 (GRCm39)	D69G	probably damaging	Het
Hivep3	A	G	4: 119,980,131 (GRCm39)	E1723G	probably damaging	Het
Hk3	A	T	13: 55,154,405 (GRCm39)	L757Q	probably damaging	Het
Homer2	A	T	7: 81,299,311 (GRCm39)	D51E	probably benign	Het
Ier3ip1	T	A	18: 77,027,227 (GRCm39)		probably benign	Het
Itch	T	A	2: 155,059,897 (GRCm39)		probably null	Het
Kalrn	T	A	16: 33,991,700 (GRCm39)	Q974L	probably damaging	Het
Kirrel3	G	T	9: 34,924,601 (GRCm39)	G296W	probably damaging	Het
Klhl17	A	G	4: 156,315,082 (GRCm39)	V525A	probably benign	Het
Klhl9	T	C	4: 88,640,182 (GRCm39)	K20E	probably benign	Het
Kmt2a	G	T	9: 44,732,977 (GRCm39)		probably benign	Het
Krt17	C	A	11: 100,147,305 (GRCm39)	V409L	probably benign	Het
Lmx1b	T	C	2: 33,454,802 (GRCm39)	N322S	probably benign	Het
Lrrc63	G	C	14: 75,363,406 (GRCm39)	P242A	probably benign	Het
Ltk	T	C	2: 119,583,708 (GRCm39)	N256D	probably damaging	Het
Map3k19	T	A	1: 127,745,470 (GRCm39)	E1328V	probably damaging	Het
Map4k2	C	T	19: 6,394,033 (GRCm39)	A280V	probably benign	Het
Micall1	C	T	15: 79,016,048 (GRCm39)	R802*	probably null	Het
Mmp14	A	G	14: 54,673,662 (GRCm39)	R109G	probably damaging	Het
Mmp27	A	T	9: 7,581,369 (GRCm39)	H544L	probably benign	Het
Mpeg1	A	G	19: 12,440,434 (GRCm39)	T631A	probably damaging	Het
Mpnd	A	G	17: 56,318,641 (GRCm39)	M217V	probably benign	Het
Mrc2	T	C	11: 105,232,034 (GRCm39)	V862A	probably damaging	Het
Mug2	T	A	6: 122,058,154 (GRCm39)	S1239T	probably damaging	Het
Myb	T	A	10: 21,002,137 (GRCm39)	M616L	probably benign	Het
Myo18b	A	T	5: 113,022,346 (GRCm39)		probably benign	Het
Myo1c	C	A	11: 75,560,053 (GRCm39)	T703N	probably damaging	Het
Nbea	T	C	3: 55,912,776 (GRCm39)	S1004G	possibly damaging	Het
Neb	T	C	2: 52,186,319 (GRCm39)	N918D	probably benign	Het
Nrtn	T	C	17: 57,058,636 (GRCm39)	T122A	probably damaging	Het
Nsd3	A	T	8: 26,188,939 (GRCm39)	S1042C	probably damaging	Het
Ntmt2	A	T	1: 163,530,633 (GRCm39)	C269S	probably benign	Het
Nvl	A	G	1: 180,945,191 (GRCm39)	L461S	probably damaging	Het
Onecut2	A	T	18: 64,473,998 (GRCm39)	H183L	possibly damaging	Het
Or13p5	A	C	4: 118,591,885 (GRCm39)	H53P	probably benign	Het
Or2h2	G	A	17: 37,396,343 (GRCm39)	T238I	probably damaging	Het
Or4d10	C	G	19: 12,051,679 (GRCm39)	G106R	probably damaging	Het
Or52e4	A	G	7: 104,705,689 (GRCm39)	T79A	possibly damaging	Het
Or5c1	T	G	2: 37,222,601 (GRCm39)	F281V	probably damaging	Het
Or6c1b	A	C	10: 129,273,248 (GRCm39)	D189A	possibly damaging	Het
Or6z5	A	T	7: 6,477,612 (GRCm39)	I168F	probably damaging	Het
Pcdhb21	G	T	18: 37,648,130 (GRCm39)	V420F	possibly damaging	Het
Pcdhb9	G	A	18: 37,536,286 (GRCm39)	G760D	probably benign	Het
Pglyrp2	G	A	17: 32,637,771 (GRCm39)	P86S	probably benign	Het
Phyhip	T	A	14: 70,704,765 (GRCm39)	V328E	probably damaging	Het
Pitpnb	A	T	5: 111,530,862 (GRCm39)	K218N	possibly damaging	Het
Pitrm1	A	G	13: 6,628,596 (GRCm39)	D963G	probably damaging	Het
Pmfbp1	A	G	8: 110,258,792 (GRCm39)	Y699C	probably damaging	Het
Pmpcb	T	A	5: 21,945,660 (GRCm39)		probably benign	Het
Polg	A	T	7: 79,114,353 (GRCm39)	W203R	probably damaging	Het
Pramel22	A	G	4: 143,380,971 (GRCm39)	S351P	probably benign	Het
Prss41	A	T	17: 24,055,977 (GRCm39)	M252K	probably benign	Het
Prss46	A	T	9: 110,673,618 (GRCm39)	M1L	possibly damaging	Het
Rimklb	T	C	6: 122,441,051 (GRCm39)		probably null	Het
Rngtt	T	C	4: 33,500,335 (GRCm39)	I556T	unknown	Het
Rock1	A	C	18: 10,122,698 (GRCm39)	D374E	probably benign	Het
Rspry1	C	A	8: 95,385,417 (GRCm39)	H450N	probably benign	Het
Rusc2	T	C	4: 43,423,942 (GRCm39)	V1032A	probably damaging	Het
Sacs	A	G	14: 61,449,647 (GRCm39)	R3898G	probably damaging	Het
Scnn1b	A	T	7: 121,502,110 (GRCm39)	H256L	probably benign	Het
Sh3gl2	T	A	4: 85,297,494 (GRCm39)	H157Q	probably benign	Het
Sipa1l1	C	A	12: 82,389,107 (GRCm39)	S444R	probably damaging	Het
Sntg1	T	A	1: 8,433,818 (GRCm39)	I478F	probably damaging	Het
Spata31e2	A	G	1: 26,722,628 (GRCm39)	Y851H	probably benign	Het
Sptb	G	T	12: 76,655,811 (GRCm39)	L1424M	probably benign	Het
Sry	T	A	Y: 2,663,105 (GRCm39)	H185L	unknown	Het
Stox2	T	G	8: 47,656,198 (GRCm39)	T93P	probably damaging	Het
Tatdn2	T	A	6: 113,681,566 (GRCm39)	F472Y	possibly damaging	Het
Tefm	A	T	11: 80,031,185 (GRCm39)	V17D	possibly damaging	Het
Tekt2	G	T	4: 126,218,460 (GRCm39)	T70N	probably benign	Het
Ticam1	T	C	17: 56,578,642 (GRCm39)	D151G	probably damaging	Het
Tmem63c	A	G	12: 87,136,139 (GRCm39)	E785G	probably damaging	Het
Tnmd	A	T	X: 132,765,551 (GRCm39)	N219I	probably benign	Het
Ttc14	T	A	3: 33,861,024 (GRCm39)	L407*	probably null	Het
Ttll7	T	C	3: 146,599,932 (GRCm39)	M1T	probably null	Het
Ttn	T	A	2: 76,746,835 (GRCm39)		probably null	Het
Uchl1	T	C	5: 66,833,780 (GRCm39)	M12T	probably benign	Het
Uggt2	A	T	14: 119,315,062 (GRCm39)		probably null	Het
Uggt2	T	C	14: 119,286,665 (GRCm39)	T224A	probably damaging	Het
Umodl1	A	G	17: 31,218,175 (GRCm39)	E1254G	probably damaging	Het
Unc5d	A	G	8: 29,156,927 (GRCm39)	F773L	probably benign	Het
Unc80	C	A	1: 66,683,606 (GRCm39)	P2216Q	probably damaging	Het
Usp40	T	A	1: 87,913,923 (GRCm39)		probably null	Het
Vmn1r117	A	T	7: 20,617,421 (GRCm39)	M209K	probably damaging	Het
Vmn2r44	A	T	7: 8,380,985 (GRCm39)	W303R	probably benign	Het
Wnk2	G	A	13: 49,224,478 (GRCm39)	R268C	probably damaging	Het
Wnt2	T	C	6: 18,023,125 (GRCm39)	K175E	possibly damaging	Het
Xkr6	T	C	14: 64,056,953 (GRCm39)	V288A	unknown	Het
Zfp125	A	G	12: 20,950,459 (GRCm39)		noncoding transcript	Het
Zfp512b	A	C	2: 181,228,856 (GRCm39)	V703G	probably damaging	Het
Zglp1	A	T	9: 20,973,957 (GRCm39)	I243N	probably benign	Het
Zgpat	T	C	2: 181,020,651 (GRCm39)	S275P	probably benign	Het

Other mutations in Myt1l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00490:Myt1l	APN	12	29,877,423 (GRCm39)	missense	unknown
IGL00896:Myt1l	APN	12	29,876,885 (GRCm39)	missense	unknown
IGL01653:Myt1l	APN	12	29,960,770 (GRCm39)	missense	unknown
IGL02632:Myt1l	APN	12	29,964,292 (GRCm39)	missense	unknown
IGL03088:Myt1l	APN	12	29,970,476 (GRCm39)	missense	probably benign	0.03
IGL03212:Myt1l	APN	12	29,877,819 (GRCm39)	missense	unknown
BB003:Myt1l	UTSW	12	29,861,651 (GRCm39)	missense	unknown
BB013:Myt1l	UTSW	12	29,861,651 (GRCm39)	missense	unknown
R0057:Myt1l	UTSW	12	29,892,611 (GRCm39)	splice site	probably null
R0126:Myt1l	UTSW	12	29,901,719 (GRCm39)	missense	possibly damaging	0.91
R0356:Myt1l	UTSW	12	29,861,500 (GRCm39)	missense	unknown
R0538:Myt1l	UTSW	12	29,892,570 (GRCm39)	missense	possibly damaging	0.47
R0587:Myt1l	UTSW	12	29,861,634 (GRCm39)	missense	unknown
R0629:Myt1l	UTSW	12	29,861,484 (GRCm39)	missense	unknown
R0709:Myt1l	UTSW	12	29,877,732 (GRCm39)	missense	unknown
R0736:Myt1l	UTSW	12	29,877,813 (GRCm39)	missense	unknown
R0920:Myt1l	UTSW	12	29,936,138 (GRCm39)	missense	unknown
R1618:Myt1l	UTSW	12	29,877,396 (GRCm39)	missense	unknown
R1660:Myt1l	UTSW	12	29,945,272 (GRCm39)	missense	unknown
R1716:Myt1l	UTSW	12	29,861,537 (GRCm39)	missense	unknown
R1758:Myt1l	UTSW	12	29,877,241 (GRCm39)	missense	unknown
R1852:Myt1l	UTSW	12	29,901,660 (GRCm39)	missense	probably benign	0.27
R1971:Myt1l	UTSW	12	29,877,091 (GRCm39)	missense	unknown
R2120:Myt1l	UTSW	12	29,833,618 (GRCm39)	critical splice acceptor site	probably null
R2227:Myt1l	UTSW	12	29,876,969 (GRCm39)	missense	unknown
R2865:Myt1l	UTSW	12	29,960,788 (GRCm39)	missense	probably benign	0.00
R4587:Myt1l	UTSW	12	29,960,800 (GRCm39)	missense	unknown
R4603:Myt1l	UTSW	12	29,892,539 (GRCm39)	missense	probably benign	0.01
R4659:Myt1l	UTSW	12	29,899,456 (GRCm39)	missense	probably damaging	0.98
R4734:Myt1l	UTSW	12	29,969,925 (GRCm39)	missense	possibly damaging	0.90
R4786:Myt1l	UTSW	12	29,861,457 (GRCm39)	missense	unknown
R4824:Myt1l	UTSW	12	29,899,399 (GRCm39)	missense	probably benign	0.02
R4835:Myt1l	UTSW	12	29,945,304 (GRCm39)	missense	unknown
R4976:Myt1l	UTSW	12	29,882,302 (GRCm39)	missense	unknown
R4980:Myt1l	UTSW	12	29,877,038 (GRCm39)	missense	unknown
R5119:Myt1l	UTSW	12	29,882,302 (GRCm39)	missense	unknown
R5194:Myt1l	UTSW	12	29,861,647 (GRCm39)	missense	unknown
R5247:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5249:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5427:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5428:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5429:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5431:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5628:Myt1l	UTSW	12	29,861,620 (GRCm39)	missense	unknown
R5926:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R5959:Myt1l	UTSW	12	29,970,039 (GRCm39)	critical splice donor site	probably null
R6082:Myt1l	UTSW	12	29,892,518 (GRCm39)	missense	probably damaging	1.00
R6082:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R6084:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R6086:Myt1l	UTSW	12	29,882,331 (GRCm39)	missense	unknown
R6145:Myt1l	UTSW	12	29,882,380 (GRCm39)	missense	unknown
R6293:Myt1l	UTSW	12	29,877,627 (GRCm39)	missense	unknown
R6315:Myt1l	UTSW	12	29,877,797 (GRCm39)	missense	unknown
R6458:Myt1l	UTSW	12	29,945,298 (GRCm39)	missense	unknown
R6490:Myt1l	UTSW	12	29,882,365 (GRCm39)	missense	unknown
R6758:Myt1l	UTSW	12	29,892,599 (GRCm39)	missense	possibly damaging	0.94
R7230:Myt1l	UTSW	12	29,833,873 (GRCm39)	missense	probably damaging	0.99
R7330:Myt1l	UTSW	12	29,901,553 (GRCm39)	missense	unknown
R7545:Myt1l	UTSW	12	29,877,087 (GRCm39)	missense	unknown
R7662:Myt1l	UTSW	12	29,876,868 (GRCm39)	missense	unknown
R7744:Myt1l	UTSW	12	29,877,548 (GRCm39)	missense	unknown
R7926:Myt1l	UTSW	12	29,861,651 (GRCm39)	missense	unknown
R8832:Myt1l	UTSW	12	29,970,351 (GRCm39)	missense	unknown
R8903:Myt1l	UTSW	12	29,861,468 (GRCm39)	missense	unknown
R8923:Myt1l	UTSW	12	29,960,800 (GRCm39)	missense	unknown
R8935:Myt1l	UTSW	12	29,877,243 (GRCm39)	missense	unknown
R8944:Myt1l	UTSW	12	29,861,564 (GRCm39)	missense	unknown
R9000:Myt1l	UTSW	12	29,901,740 (GRCm39)	missense	unknown
R9329:Myt1l	UTSW	12	29,901,659 (GRCm39)	missense	unknown
R9523:Myt1l	UTSW	12	29,877,611 (GRCm39)	missense	unknown
R9599:Myt1l	UTSW	12	29,943,441 (GRCm39)	missense	unknown
U24488:Myt1l	UTSW	12	29,876,895 (GRCm39)	missense	unknown
Z1177:Myt1l	UTSW	12	29,892,467 (GRCm39)	missense	unknown
Z1177:Myt1l	UTSW	12	29,861,430 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCCTTGTGCTGGGAAGGAAG -3'
(R):5'- CCAAGTCAGGATCCTTAGCTGAG -3'

Sequencing Primer
(F):5'- ATGTGGTAATGATCTTGAGTGAGC -3'
(R):5'- GGATAGCTATATGAGGTACATAGCC -3'

Posted On

2016-03-17