Mutagenetix > Incidental Mutation

Incidental Mutation 'R6466:Fut11'

538080

Institutional Source

Beutler Lab

Gene Symbol

Fut11

Ensembl Gene

ENSMUSG00000039357

Gene Name

fucosyltransferase 11

Synonyms

3110009G03Rik

MMRRC Submission

044599-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.124) question?

Stock #

R6466 (G1)

Quality Score

52.0072

Status

Validated

Chromosome

Chromosomal Location

20745036-20750265 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 20745377 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Tryptophan at position 103 (R103W)

Ref Sequence

ENSEMBL: ENSMUSP00000040370 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048016]

AlphaFold

Q8BHC9

Predicted Effect

probably damaging
Transcript: ENSMUST00000048016
AA Change: R103W

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000040370
Gene: ENSMUSG00000039357
AA Change: R103W

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
Pfam:Glyco_tran_10_N	70	178	2.6e-12	PFAM
Pfam:Glyco_transf_10	204	403	2.3e-37	PFAM

Meta Mutation Damage Score

0.1984

Coding Region Coverage

1x: 99.9%
3x: 99.4%
10x: 97.3%
20x: 91.1%

Validation Efficiency

98% (56/57)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1190005I06Rik	A	T	8: 121,335,735 (GRCm39)	D69E	probably damaging	Het
AAdacl4fm3	T	A	4: 144,430,437 (GRCm39)	D184V	probably damaging	Het
Adgrv1	G	T	13: 81,723,220 (GRCm39)		probably null	Het
Ahr	A	T	12: 35,554,031 (GRCm39)	V696E	probably benign	Het
Akap13	A	G	7: 75,376,792 (GRCm39)	T2007A	probably benign	Het
Arid1b	T	C	17: 5,377,953 (GRCm39)	F753S	probably damaging	Het
Bpifb3	G	T	2: 153,764,108 (GRCm39)	K105N	probably damaging	Het
C2cd2	A	G	16: 97,680,822 (GRCm39)	C331R	probably benign	Het
Chrm1	T	A	19: 8,655,542 (GRCm39)	Y82*	probably null	Het
Clcn3	A	C	8: 61,382,595 (GRCm39)	V331G	probably damaging	Het
Dchs1	A	T	7: 105,413,748 (GRCm39)	D1022E	probably benign	Het
Dnah2	T	A	11: 69,430,241 (GRCm39)	T106S	probably benign	Het
Fam171a2	T	A	11: 102,330,711 (GRCm39)	D256V	probably damaging	Het
Firrm	G	T	1: 163,781,734 (GRCm39)	R898S	probably benign	Het
Fmn2	T	A	1: 174,437,149 (GRCm39)		probably benign	Het
Gas2l2	A	C	11: 83,320,179 (GRCm39)	S26A	probably damaging	Het
Gramd1a	A	T	7: 30,843,221 (GRCm39)	I29N	probably benign	Het
Grem2	A	G	1: 174,664,450 (GRCm39)	V133A	probably damaging	Het
Hydin	T	A	8: 111,233,600 (GRCm39)	S1813T	possibly damaging	Het
Igkv3-2	T	C	6: 70,676,023 (GRCm39)	F111L	probably benign	Het
Ints8	T	C	4: 11,252,878 (GRCm39)	Q68R	probably damaging	Het
Irx5	A	G	8: 93,086,354 (GRCm39)	I146V	probably damaging	Het
Kcnh3	T	C	15: 99,136,124 (GRCm39)	L707P	probably damaging	Het
Kcnk4	T	A	19: 6,905,665 (GRCm39)	I101F	probably damaging	Het
Klhl9	A	G	4: 88,639,399 (GRCm39)	Y281H	probably benign	Het
Klra9	G	T	6: 130,155,995 (GRCm39)	Y253*	probably null	Het
Lmbr1	C	T	5: 29,583,166 (GRCm39)	A9T	probably benign	Het
Map10	G	T	8: 126,399,123 (GRCm39)	E839*	probably null	Het
Nectin4	C	A	1: 171,214,321 (GRCm39)	A492D	probably damaging	Het
Nfat5	T	A	8: 108,082,140 (GRCm39)		probably null	Het
Or5p5	A	G	7: 107,413,901 (GRCm39)	T37A	probably benign	Het
Plec	A	G	15: 76,062,084 (GRCm39)	Y2608H	probably benign	Het
Pold3	A	G	7: 99,749,839 (GRCm39)	S42P	probably benign	Het
Ppp2r1a	G	T	17: 21,180,893 (GRCm39)	G432*	probably null	Het
Qki	T	C	17: 10,434,394 (GRCm39)	E315G	probably benign	Het
Rfx2	C	T	17: 57,091,397 (GRCm39)	V354I	probably benign	Het
Rp1	T	C	1: 4,418,109 (GRCm39)	Y1001C	probably benign	Het
Sez6l	A	G	5: 112,609,007 (GRCm39)		probably null	Het
Slc39a14	A	G	14: 70,547,335 (GRCm39)	I337T	probably damaging	Het
Slc3a2	G	T	19: 8,686,683 (GRCm39)	L76M	probably damaging	Het
Slco1a5	T	C	6: 142,183,260 (GRCm39)	T555A	probably benign	Het
Sprr2e	A	T	3: 92,260,341 (GRCm39)	K57N	unknown	Het
Syne2	A	G	12: 75,990,675 (GRCm39)	T1886A	probably damaging	Het
Tenm3	A	T	8: 48,689,098 (GRCm39)	I2147N	probably damaging	Het
Thbs1	G	T	2: 117,950,328 (GRCm39)	G654W	probably damaging	Het
Tigd5	A	G	15: 75,782,352 (GRCm39)	Y238C	possibly damaging	Het
Tmem221	A	G	8: 72,010,493 (GRCm39)	F126S	probably damaging	Het
Trp63	C	A	16: 25,582,108 (GRCm39)	P52Q	probably damaging	Het
Ugp2	A	T	11: 21,278,883 (GRCm39)	S434R	probably benign	Het
Vmn2r69	A	C	7: 85,056,378 (GRCm39)	F587V	probably benign	Het
Vps13d	T	A	4: 144,784,065 (GRCm39)	N3872I	possibly damaging	Het
Wdfy2	A	G	14: 63,186,115 (GRCm39)	Y250C	probably damaging	Het
Zbtb16	T	C	9: 48,576,619 (GRCm39)	D487G	possibly damaging	Het

Other mutations in Fut11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0733:Fut11	UTSW	14	20,745,427 (GRCm39)	nonsense	probably null
R1524:Fut11	UTSW	14	20,746,234 (GRCm39)	missense	possibly damaging	0.89
R5087:Fut11	UTSW	14	20,746,229 (GRCm39)	missense	probably damaging	1.00
R5512:Fut11	UTSW	14	20,746,069 (GRCm39)	missense	probably damaging	1.00
R5773:Fut11	UTSW	14	20,748,383 (GRCm39)	missense	probably damaging	0.99
R7385:Fut11	UTSW	14	20,746,325 (GRCm39)	missense	probably damaging	1.00
R7632:Fut11	UTSW	14	20,745,096 (GRCm39)	missense	probably benign	0.23

Predicted Primers

PCR Primer
(F):5'- TGAGAGGAGTTACGCATGC -3'
(R):5'- GATTGAAGAGACGGATGCCC -3'

Sequencing Primer
(F):5'- ACATGGCTGCTCGCTGTAC -3'
(R):5'- GTGGCTCAGTAGGAAGTTA -3'

Posted On

2018-11-02