Mutagenetix > Incidental Mutation

Incidental Mutation 'R5422:Agmat'

426623

Institutional Source

Beutler Lab

Gene Symbol

Agmat

Ensembl Gene

ENSMUSG00000040706

Gene Name

agmatinase

Synonyms

5033405N08Rik

MMRRC Submission

042846-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.088) question?

Stock #

R5422 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

141473986-141486574 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 141483144 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Asparagine at position 193 (H193N)

Ref Sequence

ENSEMBL: ENSMUSP00000040853 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038014] [ENSMUST00000038161]

AlphaFold

A2AS89

Predicted Effect

probably benign
Transcript: ENSMUST00000038014

SMART Domains

Protein: ENSMUSP00000048714
Gene: ENSMUSG00000040697

Domain	Start	End	E-Value	Type
DnaJ	28	85	4.5e-30	SMART
Pfam:Thioredoxin	142	243	4.4e-8	PFAM
low complexity region	537	549	N/A	INTRINSIC
low complexity region	730	750	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000038161
AA Change: H193N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000040853
Gene: ENSMUSG00000040706
AA Change: H193N

Domain	Start	End	E-Value	Type
low complexity region	44	62	N/A	INTRINSIC
Pfam:Arginase	77	351	9.8e-85	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.9%

Validation Efficiency

Allele List at MGI

All alleles(2) : Targeted, other(2)

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts18	T	C	8: 114,425,606 (GRCm39)	S1219G	probably benign	Het
Adgrg5	T	A	8: 95,660,580 (GRCm39)	I73N	probably damaging	Het
Ambn	T	C	5: 88,612,370 (GRCm39)		probably null	Het
Atp8b5	T	A	4: 43,366,644 (GRCm39)	C803S	probably benign	Het
Btaf1	A	T	19: 36,928,507 (GRCm39)	R109S	probably benign	Het
Btnl6	C	T	17: 34,733,081 (GRCm39)	G261R	possibly damaging	Het
Clk3	A	G	9: 57,672,721 (GRCm39)	V27A	probably benign	Het
Clu	A	G	14: 66,213,051 (GRCm39)	S146G	probably damaging	Het
Cyp2w1	T	C	5: 139,338,528 (GRCm39)	F43L	probably benign	Het
Elf3	C	T	1: 135,182,778 (GRCm39)	E316K	probably damaging	Het
Epha5	A	T	5: 84,479,349 (GRCm39)	D218E	probably damaging	Het
Ereg	T	C	5: 91,222,666 (GRCm39)		probably null	Het
Ewsr1	A	G	11: 5,030,668 (GRCm39)		probably benign	Het
Fat4	A	G	3: 38,941,394 (GRCm39)	I96V	possibly damaging	Het
Fgl2	T	G	5: 21,580,808 (GRCm39)	N383K	probably damaging	Het
Fkbp11	A	T	15: 98,625,989 (GRCm39)		probably null	Het
Fn3k	C	A	11: 121,340,948 (GRCm39)	P201Q	probably damaging	Het
Fsip2	A	G	2: 82,812,572 (GRCm39)	I2964V	probably benign	Het
Gbx1	C	T	5: 24,709,667 (GRCm39)	V393I	possibly damaging	Het
Gch1	C	T	14: 47,394,906 (GRCm39)	A187T	probably damaging	Het
Ghdc	C	A	11: 100,660,020 (GRCm39)	K242N	probably benign	Het
Ghrhr	A	G	6: 55,365,188 (GRCm39)	H394R	probably benign	Het
Gje1	G	A	10: 14,592,428 (GRCm39)	S118L	probably damaging	Het
Hnrnpa2b1	A	T	6: 51,442,208 (GRCm39)	S236R	probably benign	Het
Kcnj5	A	G	9: 32,229,001 (GRCm39)	Y66H	probably benign	Het
Kif15	T	A	9: 122,813,954 (GRCm39)		probably null	Het
Magi3	C	T	3: 103,958,684 (GRCm39)	C467Y	probably damaging	Het
Map7	G	T	10: 20,142,512 (GRCm39)	V303F	probably damaging	Het
Mapk11	A	G	15: 89,030,488 (GRCm39)	L135P	probably damaging	Het
Mapkapk5	T	A	5: 121,669,785 (GRCm39)		probably null	Het
Myh7b	A	C	2: 155,472,954 (GRCm39)	Q1405P	probably damaging	Het
Nalcn	A	T	14: 123,752,777 (GRCm39)	I328N	probably damaging	Het
Nprl2	C	A	9: 107,420,796 (GRCm39)	R144S	probably benign	Het
Ogfr	G	T	2: 180,237,067 (GRCm39)	D551Y	possibly damaging	Het
Ogfr	A	T	2: 180,237,068 (GRCm39)	D551V	probably benign	Het
Or6b13	A	T	7: 139,782,305 (GRCm39)	V126E	probably damaging	Het
Or8c10	A	T	9: 38,279,270 (GRCm39)	T143S	probably benign	Het
Parp14	T	C	16: 35,686,545 (GRCm39)	K101E	probably benign	Het
Pcdhb16	A	T	18: 37,612,920 (GRCm39)	T627S	probably damaging	Het
Pdzrn4	G	A	15: 92,575,502 (GRCm39)	G303S	probably benign	Het
Plcl1	A	T	1: 55,736,543 (GRCm39)	Y628F	probably benign	Het
Ptpn9	T	A	9: 56,940,441 (GRCm39)	W194R	probably damaging	Het
Ranbp9	A	T	13: 43,573,102 (GRCm39)	M474K	probably benign	Het
Rasgef1a	T	A	6: 118,065,095 (GRCm39)	F370Y	probably damaging	Het
Rassf5	C	A	1: 131,108,911 (GRCm39)	R218L	possibly damaging	Het
Scart1	A	T	7: 139,804,068 (GRCm39)	H422L	probably benign	Het
Serpine2	C	A	1: 79,794,592 (GRCm39)	V114L	probably benign	Het
Serpine2	T	C	1: 79,799,206 (GRCm39)	Y16C	probably benign	Het
Sgms1	G	T	19: 32,137,232 (GRCm39)	N111K	probably damaging	Het
Sh3bp5	C	A	14: 31,099,452 (GRCm39)	R265L	probably benign	Het
Slc45a2	C	T	15: 11,027,871 (GRCm39)	T480I	probably damaging	Het
Tbc1d17	A	T	7: 44,498,292 (GRCm39)	M1K	probably null	Het
Tcf12	A	T	9: 71,776,320 (GRCm39)	H403Q	probably damaging	Het
Thoc2l	T	C	5: 104,667,512 (GRCm39)	I678T	probably damaging	Het
Thsd7b	T	C	1: 129,849,071 (GRCm39)	S928P	probably benign	Het
Tjp1	A	T	7: 64,952,715 (GRCm39)	F1540I	probably damaging	Het
Tph2	T	A	10: 114,915,669 (GRCm39)	D457V	possibly damaging	Het
Usp9y	T	C	Y: 1,314,676 (GRCm39)	I2112V	probably benign	Het
Vps51	T	G	19: 6,121,063 (GRCm39)	E283D	probably benign	Het
Zfp335	T	C	2: 164,749,650 (GRCm39)	K249R	probably damaging	Het
Zfp54	C	A	17: 21,654,788 (GRCm39)	S427R	probably benign	Het
Zfp607b	A	G	7: 27,401,813 (GRCm39)	T90A	probably benign	Het

Other mutations in Agmat

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02870:Agmat	APN	4	141,474,253 (GRCm39)	missense	probably benign	0.02
3-1:Agmat	UTSW	4	141,476,921 (GRCm39)	missense	possibly damaging	0.49
3-1:Agmat	UTSW	4	141,476,893 (GRCm39)	missense	probably damaging	1.00
R1635:Agmat	UTSW	4	141,474,380 (GRCm39)	missense	probably damaging	1.00
R2103:Agmat	UTSW	4	141,483,214 (GRCm39)	missense	probably damaging	0.97
R2215:Agmat	UTSW	4	141,476,899 (GRCm39)	missense	probably benign	0.01
R3767:Agmat	UTSW	4	141,483,273 (GRCm39)	missense	probably benign	0.00
R4379:Agmat	UTSW	4	141,484,802 (GRCm39)	missense	probably benign	0.10
R5640:Agmat	UTSW	4	141,483,134 (GRCm39)	missense	probably damaging	1.00
R5750:Agmat	UTSW	4	141,476,998 (GRCm39)	missense	probably benign	0.03
R6728:Agmat	UTSW	4	141,476,897 (GRCm39)	missense	probably benign	0.00
R6891:Agmat	UTSW	4	141,483,192 (GRCm39)	missense	probably benign	0.01
R7293:Agmat	UTSW	4	141,483,246 (GRCm39)	nonsense	probably null
R7298:Agmat	UTSW	4	141,474,275 (GRCm39)	missense	possibly damaging	0.90
R7361:Agmat	UTSW	4	141,474,163 (GRCm39)	missense	probably benign	0.23
R7585:Agmat	UTSW	4	141,477,056 (GRCm39)	missense	probably benign	0.09
R8832:Agmat	UTSW	4	141,474,320 (GRCm39)	missense	probably benign	0.08
R9288:Agmat	UTSW	4	141,474,391 (GRCm39)	missense	probably damaging	1.00
R9400:Agmat	UTSW	4	141,476,981 (GRCm39)	missense	probably damaging	1.00
Z1177:Agmat	UTSW	4	141,474,290 (GRCm39)	missense	possibly damaging	0.72

Predicted Primers

PCR Primer
(F):5'- TTAGCCTTTACAGAGCTCCGTC -3'
(R):5'- CACTCTGCGGGGATAAAGAG -3'

Sequencing Primer
(F):5'- ACAGAGCTCCGTCATTGC -3'
(R):5'- TAAAGAGAGGTGTGCGTCTGTCAC -3'

Posted On

2016-09-01