Mutagenetix > Incidental Mutation

Incidental Mutation 'R8316:Ugt2b34'

641683

Institutional Source

Beutler Lab

Gene Symbol

Ugt2b34

Ensembl Gene

ENSMUSG00000029260

Gene Name

UDP glucuronosyltransferase 2 family, polypeptide B34

Synonyms

MMRRC Submission

067854-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.147) question?

Stock #

R8316 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

87037626-87054796 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 87039249 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 471 (M471L)

Ref Sequence

ENSEMBL: ENSMUSP00000031181 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031181] [ENSMUST00000113333]

AlphaFold

Q8K154

Predicted Effect

probably damaging
Transcript: ENSMUST00000031181
AA Change: M471L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000031181
Gene: ENSMUSG00000029260
AA Change: M471L

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:UDPGT	26	529	2.4e-253	PFAM
Pfam:Glyco_tran_28_C	331	456	3.2e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000113333

SMART Domains

Protein: ENSMUSP00000108959
Gene: ENSMUSG00000029260

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:UDPGT	26	440	5.7e-190	PFAM
Pfam:Glyco_tran_28_C	344	440	1.1e-8	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

98% (56/57)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610008E11Rik	A	C	10: 78,903,573 (GRCm39)	C248G	probably damaging	Het
4933427D14Rik	A	T	11: 72,059,612 (GRCm39)	V693E	possibly damaging	Het
Abcc10	G	T	17: 46,638,735 (GRCm39)	L42I	probably damaging	Het
Alb	A	G	5: 90,616,449 (GRCm39)	E318G	probably benign	Het
Alkal2	G	T	12: 30,934,850 (GRCm39)	G23V	probably damaging	Het
Aox4	T	A	1: 58,293,470 (GRCm39)	C941S	possibly damaging	Het
Aqp9	A	G	9: 71,045,495 (GRCm39)	V38A	probably benign	Het
AW209491	A	G	13: 14,812,349 (GRCm39)	T401A	probably damaging	Het
Ccdc57	C	T	11: 120,776,742 (GRCm39)	A553T	probably damaging	Het
Celf2	C	T	2: 6,551,914 (GRCm39)	D522N	probably benign	Het
Cfap210	A	G	2: 69,612,287 (GRCm39)		probably null	Het
Cmpk2	A	G	12: 26,524,136 (GRCm39)	N311S	probably damaging	Het
Dcn	T	C	10: 97,330,939 (GRCm39)	I91T	probably damaging	Het
Defa30	G	A	8: 21,624,709 (GRCm39)	V11I	probably benign	Het
Dnmt3a	T	A	12: 3,946,965 (GRCm39)	V397E	probably benign	Het
Ehhadh	G	A	16: 21,585,053 (GRCm39)	A276V	probably benign	Het
Fibcd1	T	C	2: 31,723,791 (GRCm39)		probably benign	Het
Gpr156	A	G	16: 37,818,336 (GRCm39)	D344G	probably null	Het
H2-T5	A	G	17: 36,479,154 (GRCm39)	S32P	unknown	Het
Invs	G	T	4: 48,426,199 (GRCm39)	R995S	possibly damaging	Het
Itpr3	T	C	17: 27,325,199 (GRCm39)	M1264T	possibly damaging	Het
Lzic	C	T	4: 149,572,527 (GRCm39)	A39V	probably benign	Het
Marchf6	A	G	15: 31,482,650 (GRCm39)	L516P	possibly damaging	Het
Mecom	C	T	3: 30,011,529 (GRCm39)	E591K	probably benign	Het
Mical3	T	C	6: 120,911,944 (GRCm39)	D1916G	probably damaging	Het
Mms22l	T	C	4: 24,578,855 (GRCm39)	I738T	probably damaging	Het
Mroh2b	G	A	15: 4,980,746 (GRCm39)	W1438*	probably null	Het
Mroh8	G	T	2: 157,071,879 (GRCm39)	T542K	possibly damaging	Het
Msl1	A	T	11: 98,691,074 (GRCm39)	K416I	probably damaging	Het
Myh15	C	A	16: 48,940,381 (GRCm39)	T777N	probably damaging	Het
Or51a10	A	T	7: 103,698,829 (GRCm39)	V244E	probably damaging	Het
Or5p5	G	T	7: 107,414,030 (GRCm39)	V82F	possibly damaging	Het
Or5p58	A	G	7: 107,694,450 (GRCm39)	F109S	probably benign	Het
Or6c70	A	G	10: 129,709,891 (GRCm39)	V245A	probably damaging	Het
Pdzk1ip1	T	A	4: 114,946,323 (GRCm39)	V61D	probably benign	Het
Plcxd1	A	T	5: 110,250,180 (GRCm39)	M212L	probably benign	Het
Pld1	A	G	3: 28,078,361 (GRCm39)	T7A	probably benign	Het
Ppm1n	T	C	7: 19,012,302 (GRCm39)	D310G	probably damaging	Het
Prpf8	A	G	11: 75,390,641 (GRCm39)	N1264S	possibly damaging	Het
Pum2	T	A	12: 8,763,456 (GRCm39)	N204K	possibly damaging	Het
Recql5	G	A	11: 115,784,861 (GRCm39)	T822I	possibly damaging	Het
Rfc1	T	C	5: 65,436,077 (GRCm39)	T656A	probably benign	Het
Sacs	T	C	14: 61,427,068 (GRCm39)	Y159H	possibly damaging	Het
Septin14	A	G	5: 129,773,194 (GRCm39)	S148P	probably damaging	Het
Slco1c1	T	A	6: 141,492,640 (GRCm39)	M341K	probably benign	Het
Smok2a	T	C	17: 13,445,160 (GRCm39)	S246P	probably damaging	Het
Spata9	C	A	13: 76,125,890 (GRCm39)	S124R	possibly damaging	Het
Sri	A	G	5: 8,113,317 (GRCm39)	N103D	probably damaging	Het
Sspo	G	A	6: 48,459,622 (GRCm39)	C3327Y	probably damaging	Het
Trank1	A	G	9: 111,178,370 (GRCm39)	M353V	probably benign	Het
Trim80	A	T	11: 115,332,006 (GRCm39)	E66V	probably damaging	Het
Txndc16	A	G	14: 45,448,641 (GRCm39)	L73P	probably damaging	Het
Ush2a	G	T	1: 188,178,899 (GRCm39)	V1357L	probably benign	Het
Usp15	G	T	10: 122,959,848 (GRCm39)	P855T		Het
Uspl1	C	T	5: 149,135,491 (GRCm39)	T290I	possibly damaging	Het
Zbtb2	A	C	10: 4,319,084 (GRCm39)	M314R	probably benign	Het
Zcchc2	A	G	1: 105,959,844 (GRCm39)	Y1151C	probably damaging	Het
Zmat3	T	C	3: 32,395,670 (GRCm39)	Y279C	probably damaging	Het

Other mutations in Ugt2b34

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00488:Ugt2b34	APN	5	87,040,818 (GRCm39)	missense	probably damaging	1.00
IGL00498:Ugt2b34	APN	5	87,049,084 (GRCm39)	missense	probably damaging	1.00
IGL00710:Ugt2b34	APN	5	87,054,448 (GRCm39)	missense	probably damaging	1.00
IGL01089:Ugt2b34	APN	5	87,054,185 (GRCm39)	missense	probably benign	0.02
IGL01090:Ugt2b34	APN	5	87,041,679 (GRCm39)	missense	probably damaging	1.00
IGL01152:Ugt2b34	APN	5	87,049,062 (GRCm39)	missense	probably damaging	0.99
IGL01343:Ugt2b34	APN	5	87,052,247 (GRCm39)	missense	possibly damaging	0.93
IGL01410:Ugt2b34	APN	5	87,040,689 (GRCm39)	missense	possibly damaging	0.77
IGL01419:Ugt2b34	APN	5	87,039,264 (GRCm39)	missense	probably damaging	1.00
IGL01986:Ugt2b34	APN	5	87,049,111 (GRCm39)	missense	probably benign	0.01
IGL02702:Ugt2b34	APN	5	87,040,750 (GRCm39)	missense	probably benign	0.21
IGL02725:Ugt2b34	APN	5	87,054,284 (GRCm39)	missense	probably benign
IGL02810:Ugt2b34	APN	5	87,054,383 (GRCm39)	missense	probably benign	0.01
IGL03199:Ugt2b34	APN	5	87,054,739 (GRCm39)	missense	unknown
IGL03335:Ugt2b34	APN	5	87,054,499 (GRCm39)	missense	probably benign	0.29
IGL03355:Ugt2b34	APN	5	87,054,544 (GRCm39)	missense	probably benign	0.01
R0624:Ugt2b34	UTSW	5	87,041,591 (GRCm39)	critical splice donor site	probably null
R0707:Ugt2b34	UTSW	5	87,040,758 (GRCm39)	missense	possibly damaging	0.60
R0825:Ugt2b34	UTSW	5	87,054,560 (GRCm39)	missense	possibly damaging	0.64
R1029:Ugt2b34	UTSW	5	87,052,246 (GRCm39)	nonsense	probably null
R1857:Ugt2b34	UTSW	5	87,052,241 (GRCm39)	missense	possibly damaging	0.90
R1982:Ugt2b34	UTSW	5	87,054,172 (GRCm39)	missense	probably damaging	1.00
R2032:Ugt2b34	UTSW	5	87,039,131 (GRCm39)	missense	probably damaging	1.00
R2133:Ugt2b34	UTSW	5	87,054,416 (GRCm39)	missense	probably benign	0.39
R4439:Ugt2b34	UTSW	5	87,040,726 (GRCm39)	missense	probably damaging	1.00
R4783:Ugt2b34	UTSW	5	87,039,332 (GRCm39)	missense	probably damaging	1.00
R5046:Ugt2b34	UTSW	5	87,052,246 (GRCm39)	missense	probably benign	0.00
R5304:Ugt2b34	UTSW	5	87,040,724 (GRCm39)	missense	probably damaging	1.00
R5543:Ugt2b34	UTSW	5	87,054,560 (GRCm39)	missense	probably damaging	0.99
R6235:Ugt2b34	UTSW	5	87,054,223 (GRCm39)	missense	probably benign	0.09
R6841:Ugt2b34	UTSW	5	87,040,675 (GRCm39)	missense	probably benign	0.01
R7459:Ugt2b34	UTSW	5	87,049,134 (GRCm39)	missense	possibly damaging	0.56
R7624:Ugt2b34	UTSW	5	87,039,141 (GRCm39)	missense	possibly damaging	0.95
R8939:Ugt2b34	UTSW	5	87,039,158 (GRCm39)	missense	probably damaging	1.00
R9602:Ugt2b34	UTSW	5	87,054,163 (GRCm39)	missense	probably damaging	1.00
V8831:Ugt2b34	UTSW	5	87,054,533 (GRCm39)	missense	probably benign	0.39
Z1177:Ugt2b34	UTSW	5	87,054,578 (GRCm39)	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- CATGTGTCAGTCTTCCCCAG -3'
(R):5'- GCTCTACTACTGAATTGATAGAGTCTC -3'

Sequencing Primer
(F):5'- ATGTGTCAGTCTTCCCCAGTTCAG -3'
(R):5'- GAGTCTCATGATACTATCCTTGAAAC -3'

Posted On

2020-07-28