Mutagenetix > Incidental Mutation

Incidental Mutation 'R7466:Zfyve26'

578796

Institutional Source

Beutler Lab

Gene Symbol

Zfyve26

Ensembl Gene

ENSMUSG00000066440

Gene Name

zinc finger, FYVE domain containing 26

Synonyms

A630028O16Rik, LOC380767, 9330197E15Rik

MMRRC Submission

045540-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7466 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

79232346-79296304 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 79287807 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Lysine at position 146 (E146K)

Ref Sequence

ENSEMBL: ENSMUSP00000021547 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021547] [ENSMUST00000218377]

AlphaFold

Q5DU37

Predicted Effect

probably benign
Transcript: ENSMUST00000021547
AA Change: E146K

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000021547
Gene: ENSMUSG00000066440
AA Change: E146K

Domain	Start	End	E-Value	Type
low complexity region	8	24	N/A	INTRINSIC
low complexity region	233	244	N/A	INTRINSIC
low complexity region	752	775	N/A	INTRINSIC
low complexity region	778	796	N/A	INTRINSIC
low complexity region	982	1001	N/A	INTRINSIC
low complexity region	1073	1091	N/A	INTRINSIC
low complexity region	1104	1115	N/A	INTRINSIC
low complexity region	1151	1163	N/A	INTRINSIC
low complexity region	1177	1192	N/A	INTRINSIC
low complexity region	1228	1241	N/A	INTRINSIC
low complexity region	1565	1584	N/A	INTRINSIC
low complexity region	1743	1770	N/A	INTRINSIC
FYVE	1794	1863	1.49e-27	SMART
low complexity region	2486	2498	N/A	INTRINSIC
low complexity region	2517	2528	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000218377
AA Change: E146K

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

99% (83/84)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein which contains a FYVE zinc finger binding domain. The presence of this domain is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane. Mutations in this gene are associated with autosomal recessive spastic paraplegia-15. [provided by RefSeq, Oct 2008]
PHENOTYPE: Mice homozygoys for a null allele display a late-onset spastic gait disorder with cerebellar ataxia, axon degeneration, and progressive loss of cortical motoneurons and Purkinje cells preceded by accumulation of autofluorescent, electron-dense, membrane-enclosed material in lysosomal structures. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AI182371	T	A	2: 35,088,741 (GRCm38)	K203*	probably null	Het
Akr1c13	T	C	13: 4,192,437 (GRCm38)		probably benign	Het
Amer3	A	G	1: 34,587,993 (GRCm38)	S438G	probably damaging	Het
Aqp9	T	A	9: 71,163,261 (GRCm38)		probably null	Het
Art4	G	T	6: 136,854,850 (GRCm38)	H98N	probably damaging	Het
Bdh1	T	C	16: 31,447,604 (GRCm38)	S70P	probably benign	Het
Ccdc61	A	C	7: 18,891,105 (GRCm38)	Y503D	probably damaging	Het
Cd163l1	T	C	7: 140,220,706 (GRCm38)		probably null	Het
Cd180	A	T	13: 102,704,995 (GRCm38)	N183I	probably damaging	Het
Cd200r2	C	T	16: 44,909,174 (GRCm38)	A64V	probably damaging	Het
Ceacam9	A	C	7: 16,723,855 (GRCm38)	K98Q	probably benign	Het
Cep44	AACGC	A	8: 56,540,983 (GRCm38)		probably null	Het
Cfap77	G	T	2: 28,955,613 (GRCm38)	D247E	probably benign	Het
Cftr	T	C	6: 18,227,973 (GRCm38)	M388T	probably benign	Het
Chrnb1	G	A	11: 69,784,650 (GRCm38)	H493Y	probably damaging	Het
Ckap2	A	C	8: 22,177,386 (GRCm38)	M153R	probably benign	Het
Cnot6l	A	G	5: 96,131,128 (GRCm38)	V77A	probably benign	Het
Col12a1	C	T	9: 79,655,407 (GRCm38)	E1798K	possibly damaging	Het
Cth	T	A	3: 157,924,885 (GRCm38)	D49V	probably benign	Het
Ctnnb1	T	C	9: 120,955,416 (GRCm38)	S425P	probably damaging	Het
Ctnnd1	T	C	2: 84,610,785 (GRCm38)	N690S	probably benign	Het
Cyhr1	C	T	15: 76,648,186 (GRCm38)	D241N	probably benign	Het
Dennd4c	A	G	4: 86,774,331 (GRCm38)	D26G	probably damaging	Het
Dlg5	G	A	14: 24,245,212 (GRCm38)	P80L	probably damaging	Het
Eef2k	A	G	7: 120,903,484 (GRCm38)		probably null	Het
Ephb2	C	T	4: 136,659,065 (GRCm38)	R791H	probably damaging	Het
Erh	T	C	12: 80,640,983 (GRCm38)	Y22C	probably benign	Het
F5	C	T	1: 164,193,328 (GRCm38)	T1124I	possibly damaging	Het
Fam220a	T	A	5: 143,563,471 (GRCm38)	C213S	possibly damaging	Het
Fat2	G	T	11: 55,310,432 (GRCm38)	N605K	probably damaging	Het
Ganab	C	A	19: 8,914,569 (GRCm38)	S780*	probably null	Het
Gbgt1	C	T	2: 28,502,207 (GRCm38)	P67S	probably damaging	Het
Gm17190	G	T	13: 96,082,779 (GRCm38)	G208*	probably null	Het
Grhl2	A	G	15: 37,291,616 (GRCm38)	Y316C	probably damaging	Het
H2-T10	T	C	17: 36,120,849 (GRCm38)	T38A	probably benign	Het
Ins1	A	G	19: 52,264,420 (GRCm38)		probably benign	Het
Ippk	T	C	13: 49,432,467 (GRCm38)		probably null	Het
Klc4	T	A	17: 46,639,910 (GRCm38)	I258F	probably benign	Het
Manba	C	A	3: 135,542,393 (GRCm38)	L348I	probably benign	Het
Mgam	A	G	6: 40,744,789 (GRCm38)	N347S	probably benign	Het
Myo18b	T	C	5: 112,723,892 (GRCm38)	T2108A	probably benign	Het
Naip5	A	T	13: 100,221,986 (GRCm38)	L914*	probably null	Het
Nsa2	C	T	13: 97,131,220 (GRCm38)	A242T	probably benign	Het
Nsd2	G	A	5: 33,882,147 (GRCm38)	W834*	probably null	Het
Olfr1134	T	C	2: 87,656,396 (GRCm38)	N175S	possibly damaging	Het
Olfr1419	T	A	19: 11,870,316 (GRCm38)	D300V	possibly damaging	Het
Olfr285	T	C	15: 98,313,380 (GRCm38)	M57V	probably damaging	Het
Olfr469	A	T	7: 107,822,922 (GRCm38)	C182*	probably null	Het
Pam	A	T	1: 97,842,247 (GRCm38)	D599E	probably damaging	Het
Phf20l1	A	G	15: 66,636,884 (GRCm38)	K864R	probably damaging	Het
Plcl2	A	G	17: 50,608,468 (GRCm38)	D835G	probably damaging	Het
Ppm1m	C	A	9: 106,196,157 (GRCm38)	A329S	probably damaging	Het
Prep	T	C	10: 45,150,438 (GRCm38)	V486A	probably benign	Het
Prkcb	A	T	7: 122,516,844 (GRCm38)	N182I	probably damaging	Het
Prkcz	A	G	4: 155,271,602 (GRCm38)	F355S	probably damaging	Het
Psg20	C	T	7: 18,684,467 (GRCm38)	S125N	probably benign	Het
Psmd12	A	G	11: 107,492,057 (GRCm38)	D234G	probably benign	Het
Pvrig	A	T	5: 138,342,008 (GRCm38)	M14L	probably benign	Het
Rabgap1l	C	T	1: 160,226,484 (GRCm38)		probably null	Het
Rfc1	A	T	5: 65,275,426 (GRCm38)	C764S	probably damaging	Het
Ryr3	T	C	2: 112,926,957 (GRCm38)	D351G	probably benign	Het
Serpinb9g	T	C	13: 33,495,167 (GRCm38)	F340S	probably benign	Het
Sirpb1c	C	A	3: 15,832,266 (GRCm38)	L315F	probably damaging	Het
Slc24a1	C	G	9: 64,928,404 (GRCm38)	E814Q	unknown	Het
Slc26a11	A	T	11: 119,374,502 (GRCm38)	Q355L	probably damaging	Het
Sp100	C	T	1: 85,707,239 (GRCm38)	L483F	possibly damaging	Het
St5	A	G	7: 109,525,346 (GRCm38)	L1096P	probably damaging	Het
Ston1	T	A	17: 88,635,901 (GRCm38)	M245K	probably benign	Het
Swap70	T	A	7: 110,274,772 (GRCm38)	D442E	probably benign	Het
Syne2	T	A	12: 76,046,186 (GRCm38)	V450D	possibly damaging	Het
Tbck	T	A	3: 132,752,563 (GRCm38)	N651K	probably damaging	Het
Timd4	A	T	11: 46,817,758 (GRCm38)	T204S	probably benign	Het
Tmem102	A	G	11: 69,804,885 (GRCm38)	L87P	probably damaging	Het
Tmem55a	T	A	4: 14,912,477 (GRCm38)	Y195*	probably null	Het
Tmprss11e	T	A	5: 86,709,480 (GRCm38)	T325S	probably benign	Het
Trpm1	G	A	7: 64,240,582 (GRCm38)	V978M	probably damaging	Het
Wdr12	A	T	1: 60,094,511 (GRCm38)	D19E	probably benign	Het
Wdr35	G	A	12: 9,005,773 (GRCm38)	V482I	probably benign	Het
Wdr63	T	C	3: 146,055,618 (GRCm38)	D661G	probably benign	Het
Zer1	T	C	2: 30,101,484 (GRCm38)		probably null	Het
Zfp503	T	C	14: 21,986,011 (GRCm38)	D279G	probably benign	Het
Zfp870	A	T	17: 32,883,762 (GRCm38)	C198S	possibly damaging	Het
Zkscan6	T	C	11: 65,828,531 (GRCm38)	V459A	probably damaging	Het

Other mutations in Zfyve26

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Zfyve26	APN	12	79,249,460 (GRCm38)	unclassified	probably benign
IGL00940:Zfyve26	APN	12	79,280,900 (GRCm38)	missense	probably benign
IGL01148:Zfyve26	APN	12	79,260,870 (GRCm38)	missense	probably benign	0.01
IGL01347:Zfyve26	APN	12	79,252,183 (GRCm38)	splice site	probably null
IGL01472:Zfyve26	APN	12	79,276,343 (GRCm38)	missense	probably benign	0.01
IGL01490:Zfyve26	APN	12	79,244,373 (GRCm38)	missense	probably damaging	1.00
IGL01516:Zfyve26	APN	12	79,287,851 (GRCm38)	missense	probably benign	0.37
IGL01642:Zfyve26	APN	12	79,261,574 (GRCm38)	splice site	probably null
IGL01689:Zfyve26	APN	12	79,284,053 (GRCm38)	missense	possibly damaging	0.71
IGL01877:Zfyve26	APN	12	79,287,444 (GRCm38)	missense	probably damaging	1.00
IGL01997:Zfyve26	APN	12	79,244,400 (GRCm38)	missense	probably benign	0.00
IGL02077:Zfyve26	APN	12	79,276,395 (GRCm38)	missense	possibly damaging	0.54
IGL02437:Zfyve26	APN	12	79,268,847 (GRCm38)	missense	probably benign	0.01
IGL02933:Zfyve26	APN	12	79,280,080 (GRCm38)	missense	possibly damaging	0.94
IGL02937:Zfyve26	APN	12	79,239,020 (GRCm38)	missense	probably benign	0.08
IGL02982:Zfyve26	APN	12	79,263,870 (GRCm38)	missense	probably damaging	0.99
IGL03064:Zfyve26	APN	12	79,261,791 (GRCm38)	missense	probably damaging	1.00
IGL03086:Zfyve26	APN	12	79,295,564 (GRCm38)	missense	probably damaging	0.96
IGL03146:Zfyve26	APN	12	79,284,072 (GRCm38)	nonsense	probably null
challenge	UTSW	12	79,270,836 (GRCm38)	critical splice donor site	probably null
fourteener	UTSW	12	79,255,263 (GRCm38)	missense	probably damaging	1.00
IGL02799:Zfyve26	UTSW	12	79,273,310 (GRCm38)	missense	probably benign	0.28
R0318:Zfyve26	UTSW	12	79,276,281 (GRCm38)	missense	probably damaging	1.00
R0513:Zfyve26	UTSW	12	79,244,484 (GRCm38)	missense	probably damaging	1.00
R0582:Zfyve26	UTSW	12	79,246,222 (GRCm38)	missense	probably damaging	1.00
R0586:Zfyve26	UTSW	12	79,268,728 (GRCm38)	missense	possibly damaging	0.96
R0718:Zfyve26	UTSW	12	79,265,802 (GRCm38)	splice site	probably benign
R0738:Zfyve26	UTSW	12	79,295,534 (GRCm38)	missense	probably damaging	1.00
R0781:Zfyve26	UTSW	12	79,280,067 (GRCm38)	missense	probably damaging	0.99
R0894:Zfyve26	UTSW	12	79,273,598 (GRCm38)	missense	possibly damaging	0.80
R1109:Zfyve26	UTSW	12	79,272,127 (GRCm38)	missense	probably damaging	1.00
R1110:Zfyve26	UTSW	12	79,280,067 (GRCm38)	missense	probably damaging	0.99
R1186:Zfyve26	UTSW	12	79,263,949 (GRCm38)	missense	probably damaging	1.00
R1295:Zfyve26	UTSW	12	79,274,920 (GRCm38)	missense	probably damaging	1.00
R1430:Zfyve26	UTSW	12	79,282,817 (GRCm38)	missense	probably benign	0.07
R1439:Zfyve26	UTSW	12	79,252,163 (GRCm38)	missense	probably benign	0.03
R1517:Zfyve26	UTSW	12	79,252,151 (GRCm38)	missense	probably damaging	0.98
R1553:Zfyve26	UTSW	12	79,287,761 (GRCm38)	missense	probably benign	0.00
R1721:Zfyve26	UTSW	12	79,261,799 (GRCm38)	missense	possibly damaging	0.94
R1758:Zfyve26	UTSW	12	79,238,944 (GRCm38)	missense	probably damaging	1.00
R1779:Zfyve26	UTSW	12	79,278,463 (GRCm38)	missense	probably damaging	1.00
R1785:Zfyve26	UTSW	12	79,268,434 (GRCm38)	missense	possibly damaging	0.48
R1786:Zfyve26	UTSW	12	79,268,434 (GRCm38)	missense	possibly damaging	0.48
R1826:Zfyve26	UTSW	12	79,269,049 (GRCm38)	missense	probably damaging	1.00
R1833:Zfyve26	UTSW	12	79,286,258 (GRCm38)	missense	probably benign	0.36
R1868:Zfyve26	UTSW	12	79,261,799 (GRCm38)	missense	possibly damaging	0.94
R1900:Zfyve26	UTSW	12	79,264,351 (GRCm38)	missense	probably damaging	1.00
R1928:Zfyve26	UTSW	12	79,239,970 (GRCm38)	nonsense	probably null
R1982:Zfyve26	UTSW	12	79,255,243 (GRCm38)	missense	possibly damaging	0.55
R2062:Zfyve26	UTSW	12	79,284,032 (GRCm38)	splice site	probably null
R2071:Zfyve26	UTSW	12	79,287,446 (GRCm38)	missense	possibly damaging	0.95
R2130:Zfyve26	UTSW	12	79,268,434 (GRCm38)	missense	possibly damaging	0.48
R2132:Zfyve26	UTSW	12	79,268,434 (GRCm38)	missense	possibly damaging	0.48
R2133:Zfyve26	UTSW	12	79,268,434 (GRCm38)	missense	possibly damaging	0.48
R2135:Zfyve26	UTSW	12	79,246,052 (GRCm38)	missense	possibly damaging	0.80
R2207:Zfyve26	UTSW	12	79,246,087 (GRCm38)	missense	probably damaging	0.99
R2280:Zfyve26	UTSW	12	79,275,040 (GRCm38)	missense	probably damaging	1.00
R2352:Zfyve26	UTSW	12	79,284,116 (GRCm38)	missense	probably damaging	1.00
R2398:Zfyve26	UTSW	12	79,282,799 (GRCm38)	splice site	probably null
R3084:Zfyve26	UTSW	12	79,265,683 (GRCm38)	splice site	probably benign
R3086:Zfyve26	UTSW	12	79,265,683 (GRCm38)	splice site	probably benign
R4626:Zfyve26	UTSW	12	79,269,070 (GRCm38)	missense	possibly damaging	0.95
R4727:Zfyve26	UTSW	12	79,244,396 (GRCm38)	missense	probably benign	0.16
R4908:Zfyve26	UTSW	12	79,249,695 (GRCm38)	splice site	probably null
R4926:Zfyve26	UTSW	12	79,275,011 (GRCm38)	missense	probably benign
R4990:Zfyve26	UTSW	12	79,287,833 (GRCm38)	missense	probably damaging	1.00
R4999:Zfyve26	UTSW	12	79,280,385 (GRCm38)	nonsense	probably null
R5029:Zfyve26	UTSW	12	79,286,323 (GRCm38)	missense	probably damaging	0.99
R5070:Zfyve26	UTSW	12	79,255,361 (GRCm38)	missense	probably damaging	1.00
R5100:Zfyve26	UTSW	12	79,280,058 (GRCm38)	nonsense	probably null
R5252:Zfyve26	UTSW	12	79,268,982 (GRCm38)	missense	probably damaging	1.00
R5318:Zfyve26	UTSW	12	79,270,850 (GRCm38)	missense	probably benign	0.35
R5509:Zfyve26	UTSW	12	79,246,521 (GRCm38)	missense	probably damaging	1.00
R5574:Zfyve26	UTSW	12	79,239,924 (GRCm38)	missense	possibly damaging	0.63
R5735:Zfyve26	UTSW	12	79,273,373 (GRCm38)	missense	probably damaging	0.96
R5756:Zfyve26	UTSW	12	79,264,357 (GRCm38)	missense	probably damaging	1.00
R5773:Zfyve26	UTSW	12	79,287,737 (GRCm38)	missense	probably damaging	1.00
R5834:Zfyve26	UTSW	12	79,266,537 (GRCm38)	missense	probably benign	0.30
R6075:Zfyve26	UTSW	12	79,293,854 (GRCm38)	missense	possibly damaging	0.74
R6184:Zfyve26	UTSW	12	79,268,727 (GRCm38)	missense	probably damaging	0.98
R6235:Zfyve26	UTSW	12	79,249,599 (GRCm38)	missense	probably damaging	1.00
R6247:Zfyve26	UTSW	12	79,282,984 (GRCm38)	missense	probably benign	0.04
R6320:Zfyve26	UTSW	12	79,240,002 (GRCm38)	missense	probably damaging	0.97
R6548:Zfyve26	UTSW	12	79,238,335 (GRCm38)	missense	probably damaging	1.00
R6887:Zfyve26	UTSW	12	79,266,449 (GRCm38)	missense	probably damaging	1.00
R7133:Zfyve26	UTSW	12	79,284,152 (GRCm38)	missense	probably benign	0.06
R7152:Zfyve26	UTSW	12	79,279,114 (GRCm38)	missense	probably benign	0.42
R7165:Zfyve26	UTSW	12	79,280,405 (GRCm38)	missense	probably damaging	1.00
R7181:Zfyve26	UTSW	12	79,268,408 (GRCm38)	missense	probably benign	0.00
R7223:Zfyve26	UTSW	12	79,246,171 (GRCm38)	missense	probably damaging	0.99
R7296:Zfyve26	UTSW	12	79,278,372 (GRCm38)	splice site	probably null
R7299:Zfyve26	UTSW	12	79,282,984 (GRCm38)	missense	probably benign	0.01
R7301:Zfyve26	UTSW	12	79,282,984 (GRCm38)	missense	probably benign	0.01
R7302:Zfyve26	UTSW	12	79,251,168 (GRCm38)	missense	probably damaging	1.00
R7355:Zfyve26	UTSW	12	79,240,054 (GRCm38)	missense	probably damaging	1.00
R7540:Zfyve26	UTSW	12	79,268,676 (GRCm38)	missense	probably damaging	0.99
R7552:Zfyve26	UTSW	12	79,290,957 (GRCm38)	missense	probably damaging	0.97
R7762:Zfyve26	UTSW	12	79,268,635 (GRCm38)	missense	probably benign	0.02
R7806:Zfyve26	UTSW	12	79,280,355 (GRCm38)	critical splice donor site	probably null
R7821:Zfyve26	UTSW	12	79,255,324 (GRCm38)	missense	probably damaging	1.00
R8141:Zfyve26	UTSW	12	79,268,557 (GRCm38)	missense	possibly damaging	0.79
R8190:Zfyve26	UTSW	12	79,280,836 (GRCm38)	missense	probably benign	0.00
R8207:Zfyve26	UTSW	12	79,260,831 (GRCm38)	missense	probably damaging	1.00
R8210:Zfyve26	UTSW	12	79,255,263 (GRCm38)	missense	probably damaging	1.00
R8500:Zfyve26	UTSW	12	79,287,680 (GRCm38)	missense	probably damaging	0.99
R8686:Zfyve26	UTSW	12	79,287,453 (GRCm38)	missense	probably benign
R8758:Zfyve26	UTSW	12	79,264,309 (GRCm38)	critical splice donor site	probably benign
R8826:Zfyve26	UTSW	12	79,238,968 (GRCm38)	missense	probably benign	0.05
R8877:Zfyve26	UTSW	12	79,287,378 (GRCm38)	missense	probably benign	0.05
R9067:Zfyve26	UTSW	12	79,272,141 (GRCm38)	missense	probably damaging	0.99
R9195:Zfyve26	UTSW	12	79,264,394 (GRCm38)	missense	probably benign	0.12
R9269:Zfyve26	UTSW	12	79,276,302 (GRCm38)	missense	possibly damaging	0.73
R9273:Zfyve26	UTSW	12	79,270,836 (GRCm38)	critical splice donor site	probably null
R9340:Zfyve26	UTSW	12	79,274,906 (GRCm38)	nonsense	probably null
R9348:Zfyve26	UTSW	12	79,268,457 (GRCm38)	missense	possibly damaging	0.81
R9482:Zfyve26	UTSW	12	79,244,465 (GRCm38)	missense	probably damaging	1.00
R9536:Zfyve26	UTSW	12	79,251,272 (GRCm38)	missense	probably benign	0.32
R9653:Zfyve26	UTSW	12	79,287,644 (GRCm38)	missense	probably benign
R9676:Zfyve26	UTSW	12	79,284,185 (GRCm38)	missense	probably benign	0.01
R9797:Zfyve26	UTSW	12	79,246,232 (GRCm38)	missense	probably damaging	0.98
RF010:Zfyve26	UTSW	12	79,255,338 (GRCm38)	missense	probably damaging	1.00
X0020:Zfyve26	UTSW	12	79,239,005 (GRCm38)	missense	probably damaging	1.00
Z1176:Zfyve26	UTSW	12	79,268,533 (GRCm38)	missense	probably benign	0.07
Z1177:Zfyve26	UTSW	12	79,287,375 (GRCm38)	missense	probably null	1.00

Predicted Primers

PCR Primer
(F):5'- GCTTTGCAGCATAGAGCCTG -3'
(R):5'- GCATACATTTTGGGGAAAGTGG -3'

Sequencing Primer
(F):5'- CTGAAGGGCTCCACAGACAG -3'
(R):5'- ACTTGGGTAACTGGGCTAATCAC -3'

Posted On

2019-10-07