Mutagenetix > Incidental Mutation

Incidental Mutation 'R2027:A4gnt'

220828

Institutional Source

Beutler Lab

Gene Symbol

A4gnt

Ensembl Gene

ENSMUSG00000037953

Gene Name

alpha-1,4-N-acetylglucosaminyltransferase

Synonyms

alpha4GnT, LOC333424

MMRRC Submission

040035-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.101) question?

Stock #

R2027 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

99494555-99504420 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 99502254 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 138 (V138A)

Ref Sequence

ENSEMBL: ENSMUSP00000045629 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042553]

AlphaFold

Q14BT6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000042553
AA Change: V138A

PolyPhen 2 Score 0.502 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000045629
Gene: ENSMUSG00000037953
AA Change: V138A

Domain	Start	End	E-Value	Type
transmembrane domain	5	24	N/A	INTRINSIC
Pfam:Gly_transf_sug	65	188	4e-26	PFAM
Pfam:Gb3_synth	197	324	2.5e-49	PFAM

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.1%
20x: 94.7%

Validation Efficiency

100% (70/70)

MGI Phenotype

FUNCTION: This gene encodes a protein from the glycosyltransferase 32 family. The encoded enzyme catalyzes the transfer of N-acetylglucosamine to alpha-1,4-linked beta-galactose residues. This enzyme is required for type III mucin synthesis and it is largely associated with the Golgi apparatus membrane. The encoded protein appears to be expressed in adenocarcinoma cells of pancreatic, biliary tract and gastric cancers.[provided by RefSeq, Jan 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit gastric adenocarcinoma with increased cell proliferation, angiogenesis, inflammation and gastric mucosal thickness. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aatk	A	G	11: 119,900,143 (GRCm39)	S1291P	probably damaging	Het
Adgrv1	C	T	13: 81,743,301 (GRCm39)	V67M	probably damaging	Het
Apoa4	G	A	9: 46,154,298 (GRCm39)	V300M	probably damaging	Het
Bcl2a1d	A	T	9: 88,613,438 (GRCm39)	V112E	possibly damaging	Het
Bltp1	T	A	3: 37,102,110 (GRCm39)		probably benign	Het
Cabp2	T	A	19: 4,137,126 (GRCm39)	M166K	probably damaging	Het
Camsap1	A	G	2: 25,828,538 (GRCm39)	V1062A	possibly damaging	Het
Cap1	T	G	4: 122,756,686 (GRCm39)		probably benign	Het
Caprin2	A	G	6: 148,779,385 (GRCm39)	Y141H	probably damaging	Het
Card11	T	C	5: 140,892,522 (GRCm39)	Y181C	probably damaging	Het
Ccdc107	T	C	4: 43,495,874 (GRCm39)	V259A	probably benign	Het
Ccn4	A	G	15: 66,789,258 (GRCm39)	E248G	possibly damaging	Het
Chd9	A	G	8: 91,634,619 (GRCm39)		probably benign	Het
Cibar1	T	A	4: 12,171,216 (GRCm39)	D79V	probably damaging	Het
Col12a1	T	C	9: 79,553,075 (GRCm39)		probably null	Het
Cuzd1	T	C	7: 130,921,820 (GRCm39)	T61A	possibly damaging	Het
Dbp	C	A	7: 45,357,700 (GRCm39)	D89E	probably benign	Het
Dhps	A	T	8: 85,799,240 (GRCm39)	N140Y	probably damaging	Het
Dido1	A	T	2: 180,330,974 (GRCm39)	L158*	probably null	Het
Dnah9	T	G	11: 65,846,164 (GRCm39)	N2958T	probably benign	Het
Dpp8	T	A	9: 64,986,056 (GRCm39)	Y849N	probably damaging	Het
Dsg2	A	G	18: 20,716,061 (GRCm39)		probably benign	Het
Efemp1	A	T	11: 28,864,696 (GRCm39)	Y250F	possibly damaging	Het
Faxc	T	C	4: 21,958,439 (GRCm39)		probably benign	Het
Frem3	G	T	8: 81,421,966 (GRCm39)	C2122F	possibly damaging	Het
Gan	T	C	8: 117,914,238 (GRCm39)		probably null	Het
Gnl1	A	G	17: 36,293,850 (GRCm39)	N274D	probably benign	Het
Hook3	T	C	8: 26,528,126 (GRCm39)	E588G	probably damaging	Het
Itpr1	C	A	6: 108,363,814 (GRCm39)	S812Y	possibly damaging	Het
Kbtbd3	C	T	9: 4,317,075 (GRCm39)		probably benign	Het
Macf1	C	T	4: 123,265,711 (GRCm39)	A4821T	probably damaging	Het
Mepe	T	C	5: 104,474,957 (GRCm39)	S13P	possibly damaging	Het
Msantd5f6	A	G	4: 73,321,295 (GRCm39)	I154T	possibly damaging	Het
Myh11	A	G	16: 14,050,532 (GRCm39)	Y478H	probably damaging	Het
Myo7b	A	G	18: 32,118,013 (GRCm39)	V871A	probably benign	Het
Nckap1	A	T	2: 80,365,862 (GRCm39)	M466K	probably damaging	Het
Nup155	A	T	15: 8,187,244 (GRCm39)	H1391L	probably damaging	Het
Or4k6	A	G	14: 50,475,406 (GRCm39)	I312T	probably benign	Het
Or52r1b	A	T	7: 102,690,731 (GRCm39)	H15L	probably benign	Het
Or5aq1b	T	A	2: 86,901,897 (GRCm39)	N194Y	possibly damaging	Het
Or5m13	A	C	2: 85,749,114 (GRCm39)	S282R	probably damaging	Het
Or9k2	A	G	10: 129,998,604 (GRCm39)	I197T	probably benign	Het
Or9s23	A	T	1: 92,501,489 (GRCm39)	T199S	probably damaging	Het
Otof	T	C	5: 30,578,358 (GRCm39)	T97A	probably benign	Het
Peli2	G	A	14: 48,493,602 (GRCm39)	E275K	probably benign	Het
Pik3c2a	T	C	7: 115,950,057 (GRCm39)	Y1320C	probably damaging	Het
Pkn1	A	G	8: 84,398,007 (GRCm39)	V795A	probably damaging	Het
Pramel5	A	G	4: 143,998,274 (GRCm39)	L323P	probably damaging	Het
Prr5	A	T	15: 84,585,580 (GRCm39)	R183W	probably damaging	Het
Ptch1	T	G	13: 63,672,773 (GRCm39)	E944A	probably benign	Het
Rabgef1	A	G	5: 130,237,620 (GRCm39)	D231G	possibly damaging	Het
Rbp3	C	T	14: 33,677,975 (GRCm39)	T641M	probably damaging	Het
Rc3h1	C	T	1: 160,782,507 (GRCm39)	P662L	probably benign	Het
Rpl7a-ps5	G	T	17: 58,146,090 (GRCm39)	Q47K	probably benign	Het
Sclt1	G	A	3: 41,685,323 (GRCm39)	T45I	probably benign	Het
Slc22a17	A	G	14: 55,145,543 (GRCm39)	I202T	probably damaging	Het
Slc25a13	A	G	6: 6,073,487 (GRCm39)	L457S	probably damaging	Het
Slc44a3	T	C	3: 121,257,059 (GRCm39)		probably benign	Het
Slc7a9	G	A	7: 35,153,562 (GRCm39)	V188M	probably damaging	Het
Spata31d1e	A	G	13: 59,890,401 (GRCm39)	M55T	possibly damaging	Het
Tmem161a	T	A	8: 70,630,170 (GRCm39)	F119I	probably damaging	Het
Tmem240	A	G	4: 155,819,892 (GRCm39)	D32G	possibly damaging	Het
Tmtc4	T	C	14: 123,158,677 (GRCm39)	N682S	probably benign	Het
Uqcrc1	G	A	9: 108,776,083 (GRCm39)	V262M	probably benign	Het
Vmn1r87	G	A	7: 12,865,823 (GRCm39)	R155C	probably damaging	Het
Vmn2r100	A	T	17: 19,742,334 (GRCm39)	Q236L	probably benign	Het
Vmn2r97	T	A	17: 19,149,944 (GRCm39)	I444N	unknown	Het
Yif1a	A	T	19: 5,139,900 (GRCm39)	H115L	probably damaging	Het
Zfp280b	T	C	10: 75,874,328 (GRCm39)	L69S	probably damaging	Het
Zfp579	C	A	7: 4,996,520 (GRCm39)	E464*	probably null	Het

Other mutations in A4gnt

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00979:A4gnt	APN	9	99,502,489 (GRCm39)	nonsense	probably null
IGL01509:A4gnt	APN	9	99,495,819 (GRCm39)	missense	probably benign	0.01
IGL02335:A4gnt	APN	9	99,502,266 (GRCm39)	missense	probably benign
IGL03339:A4gnt	APN	9	99,502,601 (GRCm39)	missense	probably damaging	1.00
PIT4466001:A4gnt	UTSW	9	99,502,613 (GRCm39)	missense	probably damaging	0.99
PIT4472001:A4gnt	UTSW	9	99,502,613 (GRCm39)	missense	probably damaging	0.99
R2061:A4gnt	UTSW	9	99,502,412 (GRCm39)	missense	probably damaging	1.00
R4130:A4gnt	UTSW	9	99,502,671 (GRCm39)	missense	possibly damaging	0.81
R4131:A4gnt	UTSW	9	99,502,671 (GRCm39)	missense	possibly damaging	0.81
R5249:A4gnt	UTSW	9	99,502,284 (GRCm39)	missense	probably damaging	0.99
R5338:A4gnt	UTSW	9	99,502,597 (GRCm39)	missense	probably damaging	1.00
R5672:A4gnt	UTSW	9	99,502,383 (GRCm39)	missense	possibly damaging	0.95
R5785:A4gnt	UTSW	9	99,502,725 (GRCm39)	missense	probably damaging	1.00
R6519:A4gnt	UTSW	9	99,495,723 (GRCm39)	missense	probably damaging	1.00
R6630:A4gnt	UTSW	9	99,495,971 (GRCm39)	missense	probably benign	0.00
R7296:A4gnt	UTSW	9	99,502,335 (GRCm39)	missense	probably damaging	0.97
R7514:A4gnt	UTSW	9	99,502,598 (GRCm39)	missense	probably benign	0.05
R7731:A4gnt	UTSW	9	99,502,470 (GRCm39)	missense	possibly damaging	0.63
R9311:A4gnt	UTSW	9	99,495,816 (GRCm39)	missense	possibly damaging	0.82
R9786:A4gnt	UTSW	9	99,502,536 (GRCm39)	missense	possibly damaging	0.65
Z1088:A4gnt	UTSW	9	99,495,894 (GRCm39)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- GATTGCTACAAACTCTAGACTTCAAGG -3'
(R):5'- ACAAAGTTCTCCATGCAGGC -3'

Sequencing Primer
(F):5'- GGTTGCGGTCAAATAGGT -3'
(R):5'- TTCTCCATGCAGGCCCACAG -3'

Posted On

2014-08-25