Mutagenetix > Incidental Mutation

Incidental Mutation 'R6748:Agr3'

530656

Institutional Source

Beutler Lab

Gene Symbol

Agr3

Ensembl Gene

ENSMUSG00000036231

Gene Name

anterior gradient 3

Synonyms

E030025L21Rik, LOC380754

MMRRC Submission

044865-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R6748 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

35975620-35999736 bp(+) (GRCm39)

Type of Mutation

splice site (3 bp from exon)

DNA Base Change (assembly)

A to G at 35997594 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000049212 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042101]

AlphaFold

Q8R3W7

Predicted Effect

probably null
Transcript: ENSMUST00000042101

SMART Domains

Protein: ENSMUSP00000049212
Gene: ENSMUSG00000036231

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
Pfam:Thioredox_DsbH	21	115	9.8e-10	PFAM
Pfam:Thioredoxin_7	42	123	3.9e-26	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.8%

Validation Efficiency

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 disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, and a C-terminal ER-retention sequence. This gene is expressed in ciliated airway epithelial cells and, in mouse, plays a role in ciliary beat frequency in multiciliated cells. This gene is also over-expressed in breast, ovarian, and prostrate cancers. [provided by RefSeq, Dec 2016]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aff3	C	A	1: 38,574,327 (GRCm39)	R178I	probably damaging	Het
Aoc1	C	T	6: 48,883,228 (GRCm39)	T368I	possibly damaging	Het
Aph1c	A	G	9: 66,740,577 (GRCm39)	S50P	probably damaging	Het
Arhgap30	A	G	1: 171,232,378 (GRCm39)	E341G	possibly damaging	Het
Atp8b3	A	T	10: 80,361,058 (GRCm39)	M926K	possibly damaging	Het
C1qtnf9	A	G	14: 61,017,276 (GRCm39)	N269D	probably damaging	Het
Cdc42bpb	T	C	12: 111,261,273 (GRCm39)		probably benign	Het
Clec4a1	T	C	6: 122,910,856 (GRCm39)	I237T	possibly damaging	Het
Clpx	A	G	9: 65,217,441 (GRCm39)	N3S	probably benign	Het
Col19a1	A	G	1: 24,573,151 (GRCm39)	I207T	unknown	Het
Cyp2j8	T	A	4: 96,363,782 (GRCm39)	T294S	probably benign	Het
Dnah1	A	G	14: 31,021,945 (GRCm39)	I1186T	probably damaging	Het
Dnhd1	T	G	7: 105,369,844 (GRCm39)	V4423G	probably benign	Het
Dock4	A	T	12: 40,754,465 (GRCm39)	I485F	probably benign	Het
Drd2	T	A	9: 49,314,502 (GRCm39)	C244*	probably null	Het
Frmpd1	T	A	4: 45,274,397 (GRCm39)	I435K	probably benign	Het
Fzd5	A	G	1: 64,774,723 (GRCm39)	M346T	possibly damaging	Het
Gc	T	C	5: 89,583,431 (GRCm39)	T371A	probably benign	Het
Gm12185	T	A	11: 48,807,123 (GRCm39)	T23S	possibly damaging	Het
Hbq1a	A	G	11: 32,250,169 (GRCm39)		probably null	Het
Herc1	TCCC	TCC	9: 66,408,470 (GRCm39)		probably null	Het
Il1rap	A	T	16: 26,541,106 (GRCm39)	N449I	probably benign	Het
Itgb5	T	A	16: 33,719,667 (GRCm39)	D279E	probably damaging	Het
Mat2b	T	A	11: 40,571,021 (GRCm39)	I268F	probably benign	Het
Mtor	T	C	4: 148,634,641 (GRCm39)	F2421L	probably damaging	Het
Myo5b	G	A	18: 74,834,574 (GRCm39)	R878Q	possibly damaging	Het
Nkx2-6	A	G	14: 69,412,555 (GRCm39)	D241G	probably benign	Het
Or4f14	T	A	2: 111,742,702 (GRCm39)	N191I	possibly damaging	Het
Or5h23	T	A	16: 58,906,253 (GRCm39)	M198L	probably benign	Het
Pcdhb22	A	C	18: 37,651,799 (GRCm39)	D89A	probably damaging	Het
Pcnx2	C	T	8: 126,577,074 (GRCm39)	R986Q	probably damaging	Het
Plxna2	A	G	1: 194,476,490 (GRCm39)		probably null	Het
Ppwd1	A	T	13: 104,344,538 (GRCm39)	Y527*	probably null	Het
Pramel35	T	C	5: 94,000,072 (GRCm39)	W38R	probably benign	Het
Rnf126	A	G	10: 79,597,970 (GRCm39)	L131P	probably benign	Het
Rsl1	T	A	13: 67,330,688 (GRCm39)	C379S	probably benign	Het
Sec23b	A	G	2: 144,408,714 (GRCm39)	Y133C	probably damaging	Het
Slc25a24	T	A	3: 109,056,823 (GRCm39)	V112D	possibly damaging	Het
Slc35f3	A	T	8: 127,121,377 (GRCm39)	R413*	probably null	Het
Tas1r2	T	C	4: 139,396,922 (GRCm39)	F754L	probably damaging	Het
Tbc1d14	A	G	5: 36,652,598 (GRCm39)	S615P	probably damaging	Het
Ttc17	T	C	2: 94,216,447 (GRCm39)	K80R	probably benign	Het
Ttn	T	C	2: 76,576,428 (GRCm39)	T24822A	possibly damaging	Het
Vmn1r222	C	A	13: 23,417,117 (GRCm39)	R32L	probably benign	Het
Zfp354b	G	A	11: 50,813,659 (GRCm39)	T422M	probably damaging	Het
Zfp407	G	A	18: 84,226,955 (GRCm39)	T2218M	probably damaging	Het

Other mutations in Agr3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02902:Agr3	APN	12	35,996,915 (GRCm39)	missense	probably damaging	0.99
R0031:Agr3	UTSW	12	35,997,590 (GRCm39)	missense	probably benign	0.00
R0033:Agr3	UTSW	12	35,978,329 (GRCm39)	missense	possibly damaging	0.68
R0033:Agr3	UTSW	12	35,978,329 (GRCm39)	missense	possibly damaging	0.68
R0546:Agr3	UTSW	12	35,978,329 (GRCm39)	missense	probably benign	0.37
R0963:Agr3	UTSW	12	35,984,433 (GRCm39)	missense	probably benign	0.00
R1498:Agr3	UTSW	12	35,984,379 (GRCm39)	critical splice acceptor site	probably null
R1619:Agr3	UTSW	12	35,997,858 (GRCm39)	splice site	probably null
R3945:Agr3	UTSW	12	35,997,512 (GRCm39)	splice site	probably benign
R3946:Agr3	UTSW	12	35,997,512 (GRCm39)	splice site	probably benign
R4678:Agr3	UTSW	12	35,997,832 (GRCm39)	missense	probably damaging	1.00
R5475:Agr3	UTSW	12	35,997,539 (GRCm39)	missense	probably benign	0.00
R5750:Agr3	UTSW	12	35,996,941 (GRCm39)	missense	probably benign	0.00
R8092:Agr3	UTSW	12	35,997,593 (GRCm39)	critical splice donor site	probably null
R9568:Agr3	UTSW	12	35,998,349 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CATTTACACCCATGCCATTGAC -3'
(R):5'- CCCATCAGGTGACAAGTTCTTG -3'

Sequencing Primer
(F):5'- CCCATGCCATTGACACAATTATAG -3'
(R):5'- CGTGGTCTCATGCTAGCAGAAG -3'

Posted On

2018-08-01