Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03372:Fut2'

420334

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fut2

Ensembl Gene

ENSMUSG00000055978

Gene Name

fucosyltransferase 2

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03372

Quality Score

Status

Chromosome

Chromosomal Location

45298015-45315818 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 45300193 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Glutamic Acid at position 193 (G193E)

Ref Sequence

ENSEMBL: ENSMUSP00000063719 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069800] [ENSMUST00000210620]

AlphaFold

Q9JL27

Predicted Effect

possibly damaging
Transcript: ENSMUST00000069800
AA Change: G193E

PolyPhen 2 Score 0.939 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000063719
Gene: ENSMUSG00000055978
AA Change: G193E

Domain	Start	End	E-Value	Type
Pfam:Glyco_transf_11	21	338	2.1e-139	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000210620

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210988

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211324

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: This gene is one of three genes in mouse which encode a galactoside 2-L-fucosyltransferase. These genes differ in their developmental- and tissue-specific expression. The encoded type II membrane protein is anchored in the Golgi apparatus and controls the final step in the creation of alpha (1,2) fucosylated carbhohydrates by the addition of a terminal fucose in an alpha (1,2) linkage. This enzyme is involved in the synthesis of the Lewis antigen as well as the H-antigen, a precursor of the A and B antigens of the ABH histo-blood group. The biological function of the fucosylated carbhohydrate products is thought to involve cell-adhesion and interactions with microorganisms. Disruption of this gene results in altered glycosylation of gastric mucosa and uterine epithelia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
PHENOTYPE: Mice homozygous for disruptions in this gene display an essentially normal phenotype. Females are somewhate more susceptible to infections withCandida albicans. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrb2	C	T	4: 129,911,362 (GRCm39)	A1161V	probably benign	Het
Alpi	A	G	1: 87,028,350 (GRCm39)		probably benign	Het
Asxl1	A	T	2: 153,242,333 (GRCm39)	N961I	probably damaging	Het
Bcl2l10	A	G	9: 75,255,329 (GRCm39)	I49V	probably benign	Het
Bod1l	T	C	5: 41,962,578 (GRCm39)		probably benign	Het
Ccl20	A	G	1: 83,095,597 (GRCm39)	M54V	probably benign	Het
Cep72	A	C	13: 74,191,637 (GRCm39)	L200V	possibly damaging	Het
Clic4	T	C	4: 134,945,925 (GRCm39)	D164G	probably damaging	Het
Col5a3	G	A	9: 20,686,624 (GRCm39)	P1334S	unknown	Het
Dab2	T	C	15: 6,459,030 (GRCm39)	L293P	probably damaging	Het
Ddx50	A	T	10: 62,479,109 (GRCm39)	S140T	probably benign	Het
Dnah6	A	T	6: 73,052,833 (GRCm39)	M2897K	probably benign	Het
Dnmt3a	A	G	12: 3,952,666 (GRCm39)	E721G	probably damaging	Het
Esyt3	A	T	9: 99,218,109 (GRCm39)		probably benign	Het
Fat4	G	T	3: 38,943,283 (GRCm39)	K725N	possibly damaging	Het
Fezf1	T	C	6: 23,246,909 (GRCm39)	I308V	probably damaging	Het
Gapdhs	T	C	7: 30,432,674 (GRCm39)		probably benign	Het
Gm10109	A	T	7: 43,871,126 (GRCm39)		probably benign	Het
Gpd2	G	A	2: 57,245,519 (GRCm39)	V405I	probably damaging	Het
Gtf2e1	T	C	16: 37,356,077 (GRCm39)		probably benign	Het
Iqca1	A	G	1: 90,072,691 (GRCm39)	I63T	possibly damaging	Het
Kcmf1	A	C	6: 72,826,546 (GRCm39)	L161R	probably damaging	Het
Kif19a	G	T	11: 114,670,044 (GRCm39)	V80L	probably damaging	Het
Kif21a	A	T	15: 90,840,579 (GRCm39)	M1179K	probably benign	Het
Krtap19-2	A	G	16: 88,670,774 (GRCm39)		probably benign	Het
Ksr2	T	A	5: 117,840,783 (GRCm39)	I575N	possibly damaging	Het
L3mbtl1	A	T	2: 162,813,077 (GRCm39)		probably benign	Het
Larp1b	A	T	3: 40,978,962 (GRCm39)	H6L	possibly damaging	Het
Map4k2	T	A	19: 6,392,279 (GRCm39)		probably benign	Het
Mdh1b	T	C	1: 63,759,154 (GRCm39)	H146R	possibly damaging	Het
Morc2a	T	C	11: 3,631,813 (GRCm39)		probably benign	Het
Mvd	A	G	8: 123,170,113 (GRCm39)		probably benign	Het
Myo7b	C	T	18: 32,131,654 (GRCm39)	S514N	probably damaging	Het
Nav1	A	T	1: 135,378,641 (GRCm39)	I1610K	probably damaging	Het
Nbas	T	C	12: 13,584,473 (GRCm39)	L2095P	probably damaging	Het
Nrros	T	C	16: 31,963,588 (GRCm39)	N115S	probably damaging	Het
Or5p52	T	C	7: 107,502,577 (GRCm39)	Y218H	probably damaging	Het
Otud6b	A	C	4: 14,812,519 (GRCm39)	I276R	possibly damaging	Het
P2rx6	G	A	16: 17,385,356 (GRCm39)	E150K	probably damaging	Het
Pan2	T	A	10: 128,150,996 (GRCm39)	L771Q	probably benign	Het
Pbrm1	T	A	14: 30,806,976 (GRCm39)	N1087K	probably benign	Het
Pcdhb5	G	T	18: 37,453,713 (GRCm39)	R31L	probably benign	Het
Proser3	A	C	7: 30,242,993 (GRCm39)	S195A	probably damaging	Het
Rad50	T	C	11: 53,586,121 (GRCm39)	K292E	probably benign	Het
Rbm27	G	A	18: 42,438,781 (GRCm39)	R394H	probably damaging	Het
Samd9l	A	G	6: 3,375,314 (GRCm39)	I649T	probably damaging	Het
Skint3	G	A	4: 112,113,103 (GRCm39)		probably benign	Het
Slc4a4	T	A	5: 89,304,285 (GRCm39)	L576Q	probably damaging	Het
Snx2	A	G	18: 53,349,463 (GRCm39)	D408G	probably damaging	Het
Taar2	T	C	10: 23,817,069 (GRCm39)	V203A	probably benign	Het
Tdrd6	C	T	17: 43,936,459 (GRCm39)	V1530M	probably damaging	Het
Tsc2	A	C	17: 24,838,444 (GRCm39)	L515R	probably damaging	Het
Unc13a	A	T	8: 72,108,353 (GRCm39)	M500K	probably damaging	Het
Vmn1r75	A	G	7: 11,614,496 (GRCm39)	D76G	probably benign	Het
Whrn	T	C	4: 63,336,855 (GRCm39)	D127G	probably damaging	Het

Other mutations in Fut2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02814:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL02831:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL02982:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03071:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03090:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03126:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03146:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03151:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03179:Fut2	APN	7	45,300,073 (GRCm39)	missense	probably benign	0.02
IGL03212:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03213:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03234:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03271:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03381:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03385:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
IGL03392:Fut2	APN	7	45,300,193 (GRCm39)	missense	possibly damaging	0.94
PIT4515001:Fut2	UTSW	7	45,299,890 (GRCm39)	missense	probably damaging	1.00
R0553:Fut2	UTSW	7	45,300,698 (GRCm39)	missense	probably damaging	1.00
R1895:Fut2	UTSW	7	45,300,748 (GRCm39)	missense	probably damaging	1.00
R1946:Fut2	UTSW	7	45,300,748 (GRCm39)	missense	probably damaging	1.00
R2347:Fut2	UTSW	7	45,299,752 (GRCm39)	missense	probably damaging	0.99
R3155:Fut2	UTSW	7	45,300,091 (GRCm39)	missense	probably damaging	1.00
R3156:Fut2	UTSW	7	45,300,091 (GRCm39)	missense	probably damaging	1.00
R4590:Fut2	UTSW	7	45,300,370 (GRCm39)	missense	possibly damaging	0.64
R6311:Fut2	UTSW	7	45,299,804 (GRCm39)	missense	possibly damaging	0.46
R6810:Fut2	UTSW	7	45,299,929 (GRCm39)	missense	probably damaging	1.00
R6965:Fut2	UTSW	7	45,300,305 (GRCm39)	missense	probably damaging	1.00
R8135:Fut2	UTSW	7	45,300,566 (GRCm39)	missense	probably damaging	1.00
R9087:Fut2	UTSW	7	45,300,493 (GRCm39)	missense	probably damaging	1.00
R9097:Fut2	UTSW	7	45,300,375 (GRCm39)	missense	probably benign	0.01
R9462:Fut2	UTSW	7	45,300,492 (GRCm39)	missense	probably damaging	1.00
X0066:Fut2	UTSW	7	45,299,798 (GRCm39)	missense	probably damaging	0.99

Posted On

2016-08-02