Mutagenetix > Incidental Mutation

Incidental Mutation 'R7745:Mgll'

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Institutional Source

Beutler Lab

Gene Symbol

Mgll

Ensembl Gene

ENSMUSG00000033174

Gene Name

monoglyceride lipase

Synonyms

Magl

MMRRC Submission

045801-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.098) question?

Stock #

R7745 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

88701397-88805342 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 88702770 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 23 (V23A)

Ref Sequence

ENSEMBL: ENSMUSP00000109215 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000089449] [ENSMUST00000113581] [ENSMUST00000113582] [ENSMUST00000113585] [ENSMUST00000150180] [ENSMUST00000163271] [ENSMUST00000203608] [ENSMUST00000203824]

AlphaFold

O35678

Predicted Effect

possibly damaging
Transcript: ENSMUST00000089449
AA Change: V23A

PolyPhen 2 Score 0.769 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000086872
Gene: ENSMUSG00000033174
AA Change: V23A

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	27	105	6e-29	PFAM
Pfam:Abhydrolase_5	43	270	1e-21	PFAM
Pfam:Abhydrolase_6	44	282	4.4e-26	PFAM
Pfam:DUF2305	55	186	1.7e-7	PFAM
Pfam:Lipase_3	56	163	1.6e-9	PFAM
Pfam:Abhydrolase_1	71	284	4.2e-14	PFAM
Pfam:Esterase	82	195	8.6e-8	PFAM
Pfam:Abhydrolase_3	88	273	8.8e-7	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000113581
AA Change: V23A

PolyPhen 2 Score 0.894 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000109211
Gene: ENSMUSG00000033174
AA Change: V23A

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	39	304	6.8e-70	PFAM
Pfam:Abhydrolase_5	43	298	1.1e-20	PFAM
Pfam:Abhydrolase_1	44	186	8.1e-13	PFAM
Pfam:Abhydrolase_6	44	310	4.4e-15	PFAM
Pfam:DUF2305	55	224	2.2e-8	PFAM
Pfam:Lipase_3	58	146	1.4e-8	PFAM
Pfam:Esterase	82	195	1.7e-7	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000113582
AA Change: V23A

PolyPhen 2 Score 0.545 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000109212
Gene: ENSMUSG00000033174
AA Change: V23A

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	27	105	4.4e-29	PFAM
Pfam:Abhydrolase_5	43	225	3.2e-18	PFAM
Pfam:Abhydrolase_6	44	184	1.3e-18	PFAM
Pfam:Lipase_3	55	163	1.2e-9	PFAM
Pfam:DUF2305	55	249	4.9e-8	PFAM
Pfam:Abhydrolase_1	71	220	1.1e-13	PFAM
Pfam:Esterase	81	222	4.8e-8	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000113585
AA Change: V23A

PolyPhen 2 Score 0.769 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000109215
Gene: ENSMUSG00000033174
AA Change: V23A

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	27	105	6e-29	PFAM
Pfam:Abhydrolase_5	43	270	1e-21	PFAM
Pfam:Abhydrolase_6	44	282	4.4e-26	PFAM
Pfam:DUF2305	55	186	1.7e-7	PFAM
Pfam:Lipase_3	56	163	1.6e-9	PFAM
Pfam:Abhydrolase_1	71	284	4.2e-14	PFAM
Pfam:Esterase	82	195	8.6e-8	PFAM
Pfam:Abhydrolase_3	88	273	8.8e-7	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000150180
AA Change: V23A

PolyPhen 2 Score 0.951 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000145068
Gene: ENSMUSG00000033174
AA Change: V23A

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	39	78	3.1e-10	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000163271
AA Change: V39A

PolyPhen 2 Score 0.736 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000127374
Gene: ENSMUSG00000033174
AA Change: V39A

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	43	121	3e-28	PFAM
Pfam:Abhydrolase_5	59	286	3.9e-21	PFAM
Pfam:Abhydrolase_6	60	298	1.1e-25	PFAM
Pfam:DUF2305	71	202	1.3e-7	PFAM
Pfam:Lipase_3	72	179	2.6e-9	PFAM
Pfam:Abhydrolase_1	87	300	1.1e-13	PFAM
Pfam:Esterase	98	211	2e-7	PFAM
Pfam:Abhydrolase_3	104	289	8.7e-7	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000203608
AA Change: V23A

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)

Predicted Effect

probably damaging
Transcript: ENSMUST00000203824
AA Change: V23A

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

96% (55/57)

MGI Phenotype

FUNCTION: This gene encodes a monoglyceride lipase, which catalyzes the hydrolysis of monoglycerides into fatty acids and glycerol. This enzyme is also thought to hydrolyze the endocannabinoid 2-arachidonoylglycerol. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit hypoalgesia, increased body temperature, and decreased fatty acid levels. Mice homozygous for a targeted allele exhibit impaired lipolysis and improved glucose homeostasis on a high-fat diet. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadac	A	C	3: 59,945,893 (GRCm39)	S188R	probably damaging	Het
Aars1	T	A	8: 111,768,289 (GRCm39)	I220N	probably damaging	Het
Abca15	A	G	7: 119,931,440 (GRCm39)	N16S	probably damaging	Het
Adck1	A	T	12: 88,423,570 (GRCm39)	M358L	probably benign	Het
Adck5	A	T	15: 76,478,748 (GRCm39)	Q345L	probably benign	Het
Adgrl2	A	G	3: 148,542,094 (GRCm39)	F876S	probably damaging	Het
Aebp2	T	A	6: 140,569,584 (GRCm39)	L55Q	unknown	Het
Ampd2	C	A	3: 107,987,432 (GRCm39)	V134L	probably benign	Het
Aox3	T	C	1: 58,215,676 (GRCm39)	V1036A	possibly damaging	Het
Aox4	A	G	1: 58,279,866 (GRCm39)	D494G	probably benign	Het
Cacna1a	C	A	8: 85,286,023 (GRCm39)	H889Q	probably benign	Het
Cacna1c	T	C	6: 119,029,587 (GRCm39)	D151G		Het
Car8	A	G	4: 8,237,939 (GRCm39)	V92A	possibly damaging	Het
Ccdc8	G	T	7: 16,729,614 (GRCm39)	A368S	unknown	Het
Ccng2	C	G	5: 93,421,202 (GRCm39)	S237R	probably benign	Het
Cfap57	C	T	4: 118,472,128 (GRCm39)	V84I	probably benign	Het
Cntnap5a	A	G	1: 116,370,013 (GRCm39)	I877V	probably benign	Het
Copa	A	T	1: 171,939,509 (GRCm39)	D582V	probably damaging	Het
Cpne2	T	G	8: 95,295,312 (GRCm39)	S466A	probably damaging	Het
Crybg2	A	G	4: 133,816,156 (GRCm39)	K1311R	possibly damaging	Het
Csmd1	A	G	8: 15,982,461 (GRCm39)		probably null	Het
Dnah2	A	T	11: 69,342,144 (GRCm39)	C2947*	probably null	Het
Exoc1	A	T	5: 76,709,359 (GRCm39)	K656*	probably null	Het
Exoc8	T	C	8: 125,622,558 (GRCm39)	N603S	probably benign	Het
Fam171a1	T	A	2: 3,226,483 (GRCm39)	C539S	possibly damaging	Het
Fastkd5	A	T	2: 130,456,988 (GRCm39)	I534K	probably damaging	Het
Fbn1	T	C	2: 125,145,115 (GRCm39)	D2708G	probably benign	Het
Fhad1	A	G	4: 141,618,250 (GRCm39)	L1392P	probably benign	Het
Fras1	A	T	5: 96,874,754 (GRCm39)	T2306S	probably benign	Het
Gdf7	G	T	12: 8,351,854 (GRCm39)	A27E	unknown	Het
Hnrnph1	A	T	11: 50,270,324 (GRCm39)	I43F	probably damaging	Het
Igkv8-27	T	A	6: 70,148,999 (GRCm39)	S52C	probably benign	Het
Jmjd1c	T	C	10: 67,052,824 (GRCm39)	F24L	probably damaging	Het
Knl1	T	G	2: 118,902,037 (GRCm39)	L1246R	probably benign	Het
Limk2	C	T	11: 3,305,896 (GRCm39)	S191N	probably damaging	Het
Mdga2	C	A	12: 66,736,125 (GRCm39)	A368S	possibly damaging	Het
Mdga2	G	A	12: 66,736,124 (GRCm39)	A368V	probably damaging	Het
Med24	A	T	11: 98,595,793 (GRCm39)	L966Q	probably damaging	Het
Nedd1	C	T	10: 92,550,034 (GRCm39)	D84N	probably benign	Het
Obscn	A	C	11: 58,951,681 (GRCm39)	L4024R	probably damaging	Het
Or5k1b	A	T	16: 58,580,782 (GRCm39)	Y252*	probably null	Het
Pcnx2	T	C	8: 126,577,846 (GRCm39)	I944V	probably benign	Het
Pecr	T	C	1: 72,306,157 (GRCm39)		probably null	Het
Phf3	A	T	1: 30,843,305 (GRCm39)	W1885R	probably damaging	Het
Pitpnm2	C	G	5: 124,266,768 (GRCm39)	A697P	probably benign	Het
Piwil2	T	A	14: 70,631,638 (GRCm39)	H602L	probably benign	Het
Pprc1	T	C	19: 46,053,781 (GRCm39)	S1104P	unknown	Het
Prkar1a	T	A	11: 109,544,673 (GRCm39)	Y21*	probably null	Het
Prl2c3	A	T	13: 12,813,186 (GRCm39)	Y9*	probably null	Het
Rhbdl3	T	A	11: 80,214,405 (GRCm39)	L172Q	possibly damaging	Het
Rsph3a	T	G	17: 8,198,075 (GRCm39)	L484W	probably damaging	Het
Sbno1	A	T	5: 124,530,962 (GRCm39)	S809T	probably benign	Het
Stmnd1	T	A	13: 46,453,077 (GRCm39)	V251E	possibly damaging	Het
Stt3a	A	T	9: 36,662,535 (GRCm39)	C241*	probably null	Het
Tas2r114	A	T	6: 131,666,401 (GRCm39)	M209K	probably damaging	Het
Tchh	G	T	3: 93,352,084 (GRCm39)	R508L	unknown	Het
Tgfbr3l	T	C	8: 4,300,622 (GRCm39)	S267P	possibly damaging	Het
Ttn	T	A	2: 76,598,144 (GRCm39)	I19590F	probably damaging	Het
Vmn1r171	A	G	7: 23,332,035 (GRCm39)	T87A	probably benign	Het

Other mutations in Mgll

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03182:Mgll	APN	6	88,800,173 (GRCm39)	missense	probably damaging	1.00
PIT4677001:Mgll	UTSW	6	88,802,663 (GRCm39)	missense	possibly damaging	0.96
R0624:Mgll	UTSW	6	88,702,799 (GRCm39)	missense	probably damaging	0.98
R1550:Mgll	UTSW	6	88,790,871 (GRCm39)	missense	probably benign	0.00
R1779:Mgll	UTSW	6	88,790,930 (GRCm39)	nonsense	probably null
R2230:Mgll	UTSW	6	88,802,714 (GRCm39)	missense	possibly damaging	0.65
R3712:Mgll	UTSW	6	88,741,570 (GRCm39)	intron	probably benign
R4751:Mgll	UTSW	6	88,702,093 (GRCm39)	utr 5 prime	probably benign
R5030:Mgll	UTSW	6	88,795,647 (GRCm39)	critical splice donor site	probably null
R5216:Mgll	UTSW	6	88,743,311 (GRCm39)	nonsense	probably null
R5523:Mgll	UTSW	6	88,702,743 (GRCm39)	missense	probably benign	0.04
R6545:Mgll	UTSW	6	88,802,685 (GRCm39)	missense	probably benign
R7251:Mgll	UTSW	6	88,800,357 (GRCm39)	missense	probably benign	0.17
R7307:Mgll	UTSW	6	88,791,103 (GRCm39)	splice site	probably null
R8269:Mgll	UTSW	6	88,790,930 (GRCm39)	nonsense	probably null
R8892:Mgll	UTSW	6	88,743,306 (GRCm39)	missense	unknown
R9063:Mgll	UTSW	6	88,802,690 (GRCm39)	missense	possibly damaging	0.62

Predicted Primers

PCR Primer
(F):5'- TTGCCTAGAAAAGAAGCCACAG -3'
(R):5'- GAACTCTTGAGCCGTCATTTTAAAG -3'

Sequencing Primer
(F):5'- GCCACAGCCACAGTCCTG -3'
(R):5'- TGCTAACACCGCTGTGC -3'

Posted On

2019-11-26