Mutagenetix > Incidental Mutation

Incidental Mutation 'R2079:Man2b2'

229331

Institutional Source

Beutler Lab

Gene Symbol

Man2b2

Ensembl Gene

ENSMUSG00000029119

Gene Name

mannosidase 2, alpha B2

Synonyms

135 kDa alpha-D-mannosidase

MMRRC Submission

040084-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2079 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

36964265-36987997 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 36971716 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 667 (V667M)

Ref Sequence

ENSEMBL: ENSMUSP00000031002 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031002]

AlphaFold

O54782

Predicted Effect

possibly damaging
Transcript: ENSMUST00000031002
AA Change: V667M

PolyPhen 2 Score 0.638 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000031002
Gene: ENSMUSG00000029119
AA Change: V667M

Domain	Start	End	E-Value	Type
signal peptide	1	23	N/A	INTRINSIC
Pfam:Glyco_hydro_38	28	351	4e-100	PFAM
Alpha-mann_mid	356	439	3.3e-20	SMART
Pfam:Glyco_hydro_38C	487	1013	2e-98	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000124711
AA Change: V246M

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000115495
Gene: ENSMUSG00000029119
AA Change: V246M

Domain	Start	End	E-Value	Type
Pfam:Glyco_hydro_38C	67	469	2.5e-80	PFAM
low complexity region	483	493	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000147893

SMART Domains

Protein: ENSMUSP00000114319
Gene: ENSMUSG00000029119

Domain	Start	End	E-Value	Type
Pfam:Glyco_hydro_38C	2	86	4.2e-8	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts6	A	T	13: 104,598,746 (GRCm39)	R862S	probably benign	Het
Aldoa	T	C	7: 126,396,076 (GRCm39)	D164G	probably null	Het
Ankle2	T	C	5: 110,392,371 (GRCm39)	V459A	probably damaging	Het
Atp11a	A	G	8: 12,907,902 (GRCm39)	Y482C	probably damaging	Het
BC035947	A	G	1: 78,488,561 (GRCm39)		probably benign	Het
Cfap65	G	A	1: 74,956,358 (GRCm39)	R1074C	probably benign	Het
Ciart	G	T	3: 95,786,350 (GRCm39)	H242N	probably damaging	Het
Cidec	T	A	6: 113,402,615 (GRCm39)	M220L	probably benign	Het
Clca3a1	A	G	3: 144,713,534 (GRCm39)	I699T	possibly damaging	Het
Csf2rb2	T	C	15: 78,172,207 (GRCm39)	D401G	probably benign	Het
Cyp2j6	C	A	4: 96,419,962 (GRCm39)	L256F	possibly damaging	Het
Ddr2	A	T	1: 169,832,345 (GRCm39)	Y148*	probably null	Het
Depdc5	T	A	5: 33,104,018 (GRCm39)	I373N	possibly damaging	Het
Dpp10	A	T	1: 123,360,721 (GRCm39)	M268K	probably damaging	Het
Fam118b	C	A	9: 35,134,960 (GRCm39)	V216F	possibly damaging	Het
Fancd2	T	C	6: 113,532,148 (GRCm39)	V487A	probably damaging	Het
Fhad1	T	A	4: 141,718,513 (GRCm39)	R147*	probably null	Het
Flt3	A	G	5: 147,291,893 (GRCm39)	S544P	probably damaging	Het
Frem3	C	A	8: 81,341,732 (GRCm39)	Q1342K	probably benign	Het
Garin3	T	G	11: 46,295,934 (GRCm39)	V102G	probably benign	Het
Gimap4	T	C	6: 48,667,881 (GRCm39)	M84T	possibly damaging	Het
Gm20481	T	C	17: 35,189,196 (GRCm39)	K569R	probably benign	Het
Gm4871	A	C	5: 144,966,741 (GRCm39)	D247E	possibly damaging	Het
Gm5141	A	T	13: 62,922,424 (GRCm39)	N248K	probably benign	Het
Gulo	A	G	14: 66,227,832 (GRCm39)	Y367H	probably damaging	Het
Hap1	T	C	11: 100,244,572 (GRCm39)	E120G	probably damaging	Het
Heatr3	T	A	8: 88,868,404 (GRCm39)	N51K	probably damaging	Het
Hipk2	T	C	6: 38,795,720 (GRCm39)	D183G	probably damaging	Het
Hnrnpll	T	A	17: 80,342,806 (GRCm39)	T439S	probably benign	Het
Hoxd3	A	C	2: 74,574,610 (GRCm39)	E85D	probably damaging	Het
Ipo8	A	T	6: 148,690,660 (GRCm39)	M694K	probably damaging	Het
Jag2	A	G	12: 112,883,997 (GRCm39)	I194T	probably damaging	Het
Jrkl	A	T	9: 13,244,864 (GRCm39)	F266I	probably damaging	Het
Kcnt1	A	G	2: 25,790,260 (GRCm39)	I436V	possibly damaging	Het
Kdm3b	A	T	18: 34,936,570 (GRCm39)	D284V	probably damaging	Het
Khdrbs2	A	G	1: 32,506,955 (GRCm39)	T200A	probably benign	Het
Kmt2c	T	C	5: 25,557,278 (GRCm39)	D1143G	possibly damaging	Het
Kremen1	G	GGGGT	11: 5,151,794 (GRCm39)		probably null	Het
Lama2	A	C	10: 27,245,049 (GRCm39)	I244S	probably damaging	Het
Lama5	G	A	2: 179,867,301 (GRCm39)	P99S	possibly damaging	Het
Lrrc30	A	T	17: 67,938,875 (GRCm39)	L235Q	possibly damaging	Het
Mmp2	T	A	8: 93,576,817 (GRCm39)	N77K	probably damaging	Het
Myo1a	A	G	10: 127,556,482 (GRCm39)	E1009G	probably benign	Het
Ndst1	A	G	18: 60,828,581 (GRCm39)	Y658H	probably damaging	Het
Nlrp10	A	G	7: 108,524,835 (GRCm39)	L215P	possibly damaging	Het
Nrbp1	T	C	5: 31,408,417 (GRCm39)	F526L	probably benign	Het
Or10p21	T	C	10: 128,847,898 (GRCm39)	V248A	probably damaging	Het
Or51t4	T	A	7: 102,598,702 (GRCm39)	F333L	probably benign	Het
Padi2	T	C	4: 140,660,507 (GRCm39)	L329P	probably damaging	Het
Pcdhb20	A	G	18: 37,638,224 (GRCm39)	Q250R	probably benign	Het
Pcdhb3	T	A	18: 37,436,362 (GRCm39)	L776Q	possibly damaging	Het
Pik3cb	A	T	9: 98,942,257 (GRCm39)	M700K	probably benign	Het
Pla2g6	C	T	15: 79,197,194 (GRCm39)	V127M	probably damaging	Het
Rabgef1	T	C	5: 130,219,776 (GRCm39)	S80P	probably damaging	Het
Sema3a	C	T	5: 13,501,098 (GRCm39)	T47I	possibly damaging	Het
Sik2	C	T	9: 50,818,706 (GRCm39)		probably null	Het
Sin3a	T	C	9: 56,996,807 (GRCm39)	V112A	probably benign	Het
Slc26a6	G	A	9: 108,736,257 (GRCm39)	A472T	probably damaging	Het
Syne1	A	G	10: 5,311,502 (GRCm39)	V561A	probably benign	Het
Syt16	C	T	12: 74,285,073 (GRCm39)	T422I	probably damaging	Het
Tlr11	A	T	14: 50,598,437 (GRCm39)	H141L	probably damaging	Het
Tmem252	A	T	19: 24,655,017 (GRCm39)	E131D	probably benign	Het
Trim55	T	G	3: 19,698,830 (GRCm39)	L20V	probably damaging	Het
Uqcrfs1	A	T	13: 30,725,291 (GRCm39)	V83D	probably benign	Het
Utf1	C	T	7: 139,524,808 (GRCm39)	R309*	probably null	Het
Uxs1	T	C	1: 43,804,133 (GRCm39)	T261A	probably damaging	Het
Vmn1r24	T	C	6: 57,932,655 (GRCm39)	I288V	probably benign	Het
Vmn1r80	A	T	7: 11,927,121 (GRCm39)	D77V	probably damaging	Het
Vmn2r74	T	G	7: 85,606,383 (GRCm39)	H321P	probably benign	Het
Zfp638	T	C	6: 83,930,371 (GRCm39)		probably null	Het
Zwilch	T	A	9: 64,060,856 (GRCm39)	Q332L	probably damaging	Het
Zwilch	G	T	9: 64,060,857 (GRCm39)	Q332K	probably damaging	Het

Other mutations in Man2b2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00970:Man2b2	APN	5	36,973,487 (GRCm39)	nonsense	probably null
IGL01098:Man2b2	APN	5	36,972,900 (GRCm39)	missense	probably damaging	1.00
IGL01367:Man2b2	APN	5	36,971,681 (GRCm39)	nonsense	probably null
IGL01781:Man2b2	APN	5	36,971,089 (GRCm39)	missense	possibly damaging	0.80
IGL01809:Man2b2	APN	5	36,971,860 (GRCm39)	missense	probably benign	0.01
IGL02824:Man2b2	APN	5	36,979,195 (GRCm39)	missense	probably benign	0.09
IGL03323:Man2b2	APN	5	36,975,858 (GRCm39)	missense	probably benign	0.07
IGL03333:Man2b2	APN	5	36,973,483 (GRCm39)	missense	probably damaging	0.96
R0505:Man2b2	UTSW	5	36,973,542 (GRCm39)	missense	probably benign	0.00
R0715:Man2b2	UTSW	5	36,983,402 (GRCm39)	missense	probably benign	0.00
R1435:Man2b2	UTSW	5	36,970,411 (GRCm39)	missense	probably damaging	0.98
R1536:Man2b2	UTSW	5	36,978,271 (GRCm39)	missense	probably benign	0.10
R1944:Man2b2	UTSW	5	36,973,524 (GRCm39)	missense	probably benign
R2475:Man2b2	UTSW	5	36,965,219 (GRCm39)	missense	probably benign	0.01
R2924:Man2b2	UTSW	5	36,981,446 (GRCm39)	missense	probably benign	0.01
R2925:Man2b2	UTSW	5	36,981,446 (GRCm39)	missense	probably benign	0.01
R2938:Man2b2	UTSW	5	36,978,330 (GRCm39)	missense	probably benign	0.27
R3777:Man2b2	UTSW	5	36,972,871 (GRCm39)	missense	probably benign	0.00
R3778:Man2b2	UTSW	5	36,972,871 (GRCm39)	missense	probably benign	0.00
R3982:Man2b2	UTSW	5	36,971,164 (GRCm39)	missense	probably benign	0.10
R4618:Man2b2	UTSW	5	36,974,983 (GRCm39)	missense	probably benign	0.06
R4822:Man2b2	UTSW	5	36,972,865 (GRCm39)	missense	probably damaging	1.00
R5320:Man2b2	UTSW	5	36,967,677 (GRCm39)	missense	probably damaging	1.00
R5394:Man2b2	UTSW	5	36,971,862 (GRCm39)	missense	probably benign	0.03
R5468:Man2b2	UTSW	5	36,964,519 (GRCm39)	missense	probably benign	0.00
R5993:Man2b2	UTSW	5	36,978,324 (GRCm39)	missense	probably benign	0.12
R6053:Man2b2	UTSW	5	36,970,382 (GRCm39)	missense	probably benign	0.00
R6083:Man2b2	UTSW	5	36,966,385 (GRCm39)	missense	probably damaging	1.00
R6376:Man2b2	UTSW	5	36,978,378 (GRCm39)	missense	probably damaging	1.00
R6669:Man2b2	UTSW	5	36,967,702 (GRCm39)	missense	probably benign	0.00
R7000:Man2b2	UTSW	5	36,979,213 (GRCm39)	missense	probably damaging	1.00
R7108:Man2b2	UTSW	5	36,972,829 (GRCm39)	missense	probably benign	0.04
R7376:Man2b2	UTSW	5	36,970,722 (GRCm39)	missense	probably damaging	1.00
R7478:Man2b2	UTSW	5	36,967,657 (GRCm39)	missense	probably damaging	1.00
R7712:Man2b2	UTSW	5	36,967,658 (GRCm39)	missense	probably benign	0.00
R8059:Man2b2	UTSW	5	36,973,504 (GRCm39)	missense	probably damaging	1.00
R8471:Man2b2	UTSW	5	36,979,183 (GRCm39)	missense	probably damaging	1.00
R8729:Man2b2	UTSW	5	36,973,462 (GRCm39)	missense	probably benign	0.25
R9341:Man2b2	UTSW	5	36,975,951 (GRCm39)	missense	probably damaging	1.00
R9343:Man2b2	UTSW	5	36,975,951 (GRCm39)	missense	probably damaging	1.00
R9421:Man2b2	UTSW	5	36,978,271 (GRCm39)	missense	probably benign	0.10
X0022:Man2b2	UTSW	5	36,971,236 (GRCm39)	missense	probably damaging	0.99
Z1088:Man2b2	UTSW	5	36,972,700 (GRCm39)	missense	possibly damaging	0.46
Z1177:Man2b2	UTSW	5	36,971,141 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATAATGGCTCAGGCGTATGC -3'
(R):5'- CTGCAGGTGAGTGATCTTGC -3'

Sequencing Primer
(F):5'- CTCAGGCGTATGCAAAAAGC -3'
(R):5'- TGATCTTGCTGAGGGCGACAC -3'

Posted On

2014-09-17