Mutagenetix > Incidental Mutation

Incidental Mutation 'R4631:Pgm2'

349180

Institutional Source

Beutler Lab

Gene Symbol

Pgm2

Ensembl Gene

ENSMUSG00000029171

Gene Name

phosphoglucomutase 2

Synonyms

Pgm-1, 3230402E02Rik, Pgm1

MMRRC Submission

041896-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4631 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

64250293-64285694 bp(+) (GRCm39)

Type of Mutation

splice site (3 bp from exon)

DNA Base Change (assembly)

A to G at 64263290 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000084582 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087324]

AlphaFold

Q7TSV4

Predicted Effect

probably null
Transcript: ENSMUST00000087324

SMART Domains

Protein: ENSMUSP00000084582
Gene: ENSMUSG00000029171

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
Pfam:PGM_PMM_I	62	211	7.8e-37	PFAM
Pfam:PGM_PMM_II	235	344	1.9e-25	PFAM
Pfam:PGM_PMM_III	351	480	4.6e-15	PFAM
Pfam:PGM_PMM_IV	523	603	5.5e-8	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129152

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175062

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000177427

Predicted Effect

probably benign
Transcript: ENSMUST00000199093

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.0%

Validation Efficiency

100% (84/84)

MGI Phenotype

PHENOTYPE: Four electrophoretic variants are known, each with a 5-band pattern: the a allele in C57BL/6, BALB/c and AKR; b allele in DBA/2 and SJL; c allele in C3H/He; and d allele in 129/Re. Heterozygotes show a mixture of bands. Mice homozygous for a spontaneous null allele or ENU induced alleles are viable. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017B05Rik	A	T	9: 57,165,270 (GRCm39)	L368Q	probably damaging	Het
Abcc2	C	T	19: 43,803,146 (GRCm39)	P661S	possibly damaging	Het
Adgre4	T	G	17: 56,121,305 (GRCm39)	M457R	probably null	Het
Ank	C	A	15: 27,467,176 (GRCm39)	F29L	probably benign	Het
Arhgap20	T	C	9: 51,751,653 (GRCm39)		probably benign	Het
Atf6	T	C	1: 170,574,766 (GRCm39)		probably null	Het
Bhmt1b	G	A	18: 87,774,525 (GRCm39)	R16H	probably damaging	Het
Bod1l	A	G	5: 41,975,078 (GRCm39)	F2079L	probably damaging	Het
Cd163	T	C	6: 124,306,045 (GRCm39)	*1122Q	probably null	Het
Ces2g	T	C	8: 105,694,094 (GRCm39)		probably null	Het
Cntnap3	A	G	13: 64,926,697 (GRCm39)	Y558H	probably benign	Het
Ctsm	T	A	13: 61,685,510 (GRCm39)	S301C	probably null	Het
Dlc1	A	C	8: 37,404,712 (GRCm39)		probably null	Het
Dlg2	A	T	7: 91,737,822 (GRCm39)	I435F	probably damaging	Het
Dnah5	T	C	15: 28,402,099 (GRCm39)	V3420A	probably damaging	Het
Dnah5	T	A	15: 28,420,140 (GRCm39)	Y3813N	probably damaging	Het
Dnajc13	A	G	9: 104,067,616 (GRCm39)	M1181T	probably damaging	Het
Drc3	C	A	11: 60,255,734 (GRCm39)	T107N	probably benign	Het
Dydc2	T	C	14: 40,771,286 (GRCm39)	E131G	probably benign	Het
Eif5b	T	C	1: 38,080,828 (GRCm39)	V723A	probably damaging	Het
Fndc9	C	A	11: 46,128,675 (GRCm39)	H65N	possibly damaging	Het
Fzd1	A	T	5: 4,805,865 (GRCm39)	Y572*	probably null	Het
Gps1	T	A	11: 120,679,065 (GRCm39)		probably null	Het
Gvin3	A	G	7: 106,198,730 (GRCm39)		noncoding transcript	Het
Kazn	G	A	4: 141,845,471 (GRCm39)		probably benign	Het
Kcnd3	C	T	3: 105,566,082 (GRCm39)	A421V	probably damaging	Het
Kcnip1	T	A	11: 33,942,821 (GRCm39)		noncoding transcript	Het
Kif19a	A	G	11: 114,675,673 (GRCm39)	I382V	possibly damaging	Het
Krt1	C	T	15: 101,754,622 (GRCm39)	G543S	unknown	Het
Malsu1	A	T	6: 49,061,467 (GRCm39)	E177V	probably damaging	Het
Man2a2	A	G	7: 80,012,211 (GRCm39)	F649L	probably benign	Het
Map3k11	A	G	19: 5,740,941 (GRCm39)	I223V	probably benign	Het
Mroh2a	A	G	1: 88,186,386 (GRCm39)	S64G	probably benign	Het
Myh9	T	G	15: 77,681,228 (GRCm39)	D164A	probably damaging	Het
Myo16	T	C	8: 10,556,984 (GRCm39)	I1040T	probably damaging	Het
Myo18b	C	T	5: 112,994,266 (GRCm39)	A896T	probably damaging	Het
Myocd	G	T	11: 65,069,685 (GRCm39)	N798K	probably benign	Het
Or13c7b	T	C	4: 43,820,563 (GRCm39)	D266G	probably benign	Het
Or1n1b	T	G	2: 36,780,630 (GRCm39)	T77P	probably benign	Het
Or2l13b	G	A	16: 19,348,891 (GRCm39)	R260*	probably null	Het
Or4c11	C	T	2: 88,695,174 (GRCm39)	T75I	probably benign	Het
Or4g7	T	A	2: 111,309,908 (GRCm39)	W260R	probably damaging	Het
Or52a5	A	T	7: 103,426,682 (GRCm39)	L290Q	probably damaging	Het
Or5b105	T	A	19: 13,080,636 (GRCm39)	I11F	probably benign	Het
Pcdh18	T	A	3: 49,710,890 (GRCm39)	I142F	probably damaging	Het
Pcyox1	T	C	6: 86,366,212 (GRCm39)	E334G	possibly damaging	Het
Pcyox1	T	C	6: 86,366,125 (GRCm39)	D363G	probably benign	Het
Plagl1	T	G	10: 13,003,743 (GRCm39)		probably benign	Het
Ppp1r9a	A	G	6: 4,906,537 (GRCm39)	D364G	possibly damaging	Het
Rab2b	T	A	14: 52,503,699 (GRCm39)	H141L	possibly damaging	Het
Rev3l	A	G	10: 39,704,412 (GRCm39)	K279E	probably benign	Het
Rnf111	G	T	9: 70,357,678 (GRCm39)	T607N	probably benign	Het
Scn8a	C	A	15: 100,914,384 (GRCm39)	S1130*	probably null	Het
Selenbp1	A	G	3: 94,851,879 (GRCm39)	*473W	probably null	Het
Sh3bp4	A	C	1: 89,071,995 (GRCm39)	D281A	probably damaging	Het
Skint5	T	A	4: 113,486,314 (GRCm39)		probably null	Het
Slc1a4	A	G	11: 20,258,452 (GRCm39)	L249P	probably damaging	Het
Slc45a2	T	A	15: 11,012,662 (GRCm39)	S222T	probably benign	Het
Slc7a4	A	G	16: 17,392,255 (GRCm39)	F393S	probably damaging	Het
Slc9a2	A	T	1: 40,801,078 (GRCm39)	D536V	possibly damaging	Het
Stra6	T	A	9: 58,048,115 (GRCm39)		probably benign	Het
Tmem145	A	G	7: 25,007,250 (GRCm39)	D156G	probably benign	Het
Tns3	A	C	11: 8,401,119 (GRCm39)	F1060V	probably benign	Het
Trak1	G	A	9: 121,283,491 (GRCm39)	R419Q	probably benign	Het
Trappc8	A	G	18: 21,000,865 (GRCm39)	S273P	probably benign	Het
Trmt11	A	G	10: 30,435,200 (GRCm39)	S320P	probably benign	Het
Ugt1a6a	A	T	1: 88,066,980 (GRCm39)	Y262F	probably benign	Het
Vmn1r73	G	A	7: 11,490,758 (GRCm39)	C192Y	probably benign	Het
Vmn2r103	T	C	17: 20,013,958 (GRCm39)	I250T	probably benign	Het
Vmn2r25	T	A	6: 123,829,962 (GRCm39)	D63V	possibly damaging	Het
Vps13b	C	T	15: 35,646,278 (GRCm39)	H1461Y	possibly damaging	Het
Ythdc2	A	T	18: 45,020,698 (GRCm39)	E1427D	probably benign	Het
Zbed6	A	T	1: 133,586,482 (GRCm39)	V285E	probably damaging	Het
Zbtb26	A	G	2: 37,326,968 (GRCm39)	F23L	probably benign	Het
Zfp62	T	A	11: 49,108,632 (GRCm39)	*908R	probably null	Het
Zfp975	A	T	7: 42,312,369 (GRCm39)	N81K	probably benign	Het
Zkscan16	G	A	4: 58,951,918 (GRCm39)	V198M	probably damaging	Het

Other mutations in Pgm2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00435:Pgm2	APN	5	64,265,612 (GRCm39)	splice site	probably benign
IGL01068:Pgm2	APN	5	64,265,139 (GRCm39)	missense	probably damaging	0.99
IGL01112:Pgm2	APN	5	64,260,225 (GRCm39)	missense	possibly damaging	0.86
IGL01634:Pgm2	APN	5	64,258,317 (GRCm39)	missense	probably benign	0.01
IGL02513:Pgm2	APN	5	64,260,289 (GRCm39)	unclassified	probably benign
R0255:Pgm2	UTSW	5	64,269,386 (GRCm39)	missense	possibly damaging	0.93
R0268:Pgm2	UTSW	5	64,263,151 (GRCm39)	missense	probably damaging	1.00
R0511:Pgm2	UTSW	5	64,267,898 (GRCm39)	missense	probably damaging	1.00
R0722:Pgm2	UTSW	5	64,265,022 (GRCm39)	nonsense	probably null
R0881:Pgm2	UTSW	5	64,250,351 (GRCm39)	missense	unknown
R0924:Pgm2	UTSW	5	64,269,490 (GRCm39)	missense	possibly damaging	0.90
R0930:Pgm2	UTSW	5	64,269,490 (GRCm39)	missense	possibly damaging	0.90
R1773:Pgm2	UTSW	5	64,265,194 (GRCm39)	critical splice donor site	probably null
R1777:Pgm2	UTSW	5	64,285,125 (GRCm39)	missense	probably benign
R2137:Pgm2	UTSW	5	64,273,709 (GRCm39)	missense	probably benign
R2244:Pgm2	UTSW	5	64,264,045 (GRCm39)	missense	probably benign	0.00
R3946:Pgm2	UTSW	5	64,269,404 (GRCm39)	missense	probably benign
R4301:Pgm2	UTSW	5	64,261,140 (GRCm39)	nonsense	probably null
R4601:Pgm2	UTSW	5	64,265,070 (GRCm39)	missense	probably benign	0.02
R4795:Pgm2	UTSW	5	64,261,217 (GRCm39)	missense	probably damaging	1.00
R4871:Pgm2	UTSW	5	64,261,237 (GRCm39)	missense	probably benign
R4893:Pgm2	UTSW	5	64,263,283 (GRCm39)	missense	probably benign
R4907:Pgm2	UTSW	5	64,261,221 (GRCm39)	missense	probably benign	0.00
R4915:Pgm2	UTSW	5	64,258,291 (GRCm39)	missense	probably damaging	1.00
R5092:Pgm2	UTSW	5	64,265,092 (GRCm39)	missense	possibly damaging	0.49
R5197:Pgm2	UTSW	5	64,263,175 (GRCm39)	missense	possibly damaging	0.87
R5621:Pgm2	UTSW	5	64,269,381 (GRCm39)	nonsense	probably null
R6311:Pgm2	UTSW	5	64,273,758 (GRCm39)	missense	probably benign	0.05
R6651:Pgm2	UTSW	5	64,269,437 (GRCm39)	missense	probably benign	0.07
R6731:Pgm2	UTSW	5	64,258,318 (GRCm39)	missense	probably benign	0.27
R6885:Pgm2	UTSW	5	64,261,221 (GRCm39)	missense	probably benign	0.00
R6919:Pgm2	UTSW	5	64,254,368 (GRCm39)	missense	probably benign	0.11
R7211:Pgm2	UTSW	5	64,263,193 (GRCm39)	missense	probably damaging	0.99
R7631:Pgm2	UTSW	5	64,265,522 (GRCm39)	missense	possibly damaging	0.90
R7982:Pgm2	UTSW	5	64,258,302 (GRCm39)	missense	probably damaging	1.00
R8070:Pgm2	UTSW	5	64,269,425 (GRCm39)	missense	probably benign	0.00
R8161:Pgm2	UTSW	5	64,269,503 (GRCm39)	missense	probably damaging	1.00
R8181:Pgm2	UTSW	5	64,269,467 (GRCm39)	missense	possibly damaging	0.83
R9110:Pgm2	UTSW	5	64,261,159 (GRCm39)	missense	probably benign	0.01
R9333:Pgm2	UTSW	5	64,263,100 (GRCm39)	missense	probably benign
R9580:Pgm2	UTSW	5	64,265,092 (GRCm39)	missense	possibly damaging	0.49
R9673:Pgm2	UTSW	5	64,273,671 (GRCm39)	missense	probably damaging	1.00
R9681:Pgm2	UTSW	5	64,254,391 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AAGTTCGTGCACACCTCTGTC -3'
(R):5'- TTTGGCAATAGAGAAACTGTCAACG -3'

Sequencing Primer
(F):5'- ACACCTCTGTCCATGGTGTG -3'
(R):5'- CTTATTTCCTCACGAAAGATGCCAAG -3'

Posted On

2015-10-08