Mutagenetix > Incidental Mutation

Incidental Mutation 'R9652:Ces3b'

735385

Institutional Source

Beutler Lab

Gene Symbol

Ces3b

Ensembl Gene

ENSMUSG00000062181

Gene Name

carboxylesterase 3B

Synonyms

ES31L, Gm4738

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

R9652 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

105083753-105093929 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 105085625 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Serine at position 169 (A169S)

Ref Sequence

ENSEMBL: ENSMUSP00000090909 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074403] [ENSMUST00000093221] [ENSMUST00000173088]

AlphaFold

Q8VCU1

Predicted Effect

possibly damaging
Transcript: ENSMUST00000074403
AA Change: A169S

PolyPhen 2 Score 0.947 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000074004
Gene: ENSMUSG00000062181
AA Change: A169S

Domain	Start	End	E-Value	Type
Pfam:COesterase	13	436	1.8e-127	PFAM
Pfam:Abhydrolase_3	147	303	2.8e-13	PFAM
Pfam:COesterase	423	497	5.8e-10	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000093221
AA Change: A169S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000090909
Gene: ENSMUSG00000062181
AA Change: A169S

Domain	Start	End	E-Value	Type
Pfam:COesterase	13	547	9.5e-163	PFAM
Pfam:Abhydrolase_3	147	304	2.1e-12	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000173088

SMART Domains

Protein: ENSMUSP00000134204
Gene: ENSMUSG00000062181

Domain	Start	End	E-Value	Type
Pfam:COesterase	1	114	2e-11	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.8%
10x: 99.6%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Afap1l1	G	A	18: 61,743,361	T395M	probably damaging	Het
Akap8l	T	C	17: 32,338,809	N35D	probably damaging	Het
Atr	T	A	9: 95,874,834	L922Q	probably damaging	Het
B3gnt9	G	T	8: 105,254,497	F86L	probably damaging	Het
Bmp1	T	C	14: 70,477,920	D925G	probably damaging	Het
C77080	T	C	4: 129,224,169	E279G	possibly damaging	Het
Camkmt	A	T	17: 85,452,285	R284S	probably benign	Het
Cavin3	G	T	7: 105,482,097	H21Q	probably damaging	Het
Ccp110	A	G	7: 118,735,330	H180R		Het
Cdh23	A	T	10: 60,331,356	V1837E	probably damaging	Het
Chpt1	T	C	10: 88,489,637	N122S	probably benign	Het
Cramp1l	C	A	17: 24,982,809	K566N	probably damaging	Het
Ctbp2	C	G	7: 133,014,204	R334P	probably damaging	Het
Cwh43	T	C	5: 73,414,997	S193P	probably benign	Het
Dcstamp	A	T	15: 39,760,396	D469V	probably benign	Het
Dst	T	A	1: 34,180,377	I1966N	probably benign	Het
Eif3i	G	T	4: 129,595,301	F121L	probably benign	Het
Erbb2	T	C	11: 98,435,986	S1074P	probably damaging	Het
Fam186b	G	A	15: 99,279,735	A570V	probably damaging	Het
Fbn2	A	G	18: 58,013,650		probably null	Het
Foxo3	C	T	10: 42,197,025	V499M	probably damaging	Het
Gm2a	T	C	11: 55,108,938	V95A	probably benign	Het
Gp5	A	C	16: 30,309,575	F94V	probably damaging	Het
Gramd4	G	A	15: 86,131,959	E504K	probably damaging	Het
Gusb	A	G	5: 129,997,811	S450P	probably damaging	Het
Htr5a	A	G	5: 27,842,840	N131S	possibly damaging	Het
Itga2	G	A	13: 114,884,455	P120L	probably benign	Het
Itpkb	G	T	1: 180,332,491	E61*	probably null	Het
Katnbl1	T	A	2: 112,409,152	V232D	probably damaging	Het
Kifap3	T	C	1: 163,862,088	L547P	probably damaging	Het
Krt6a	C	T	15: 101,690,685	V482M	probably benign	Het
Lrfn5	T	A	12: 61,843,632	V569D	probably damaging	Het
Luzp2	A	G	7: 55,052,832	T48A	probably damaging	Het
Mical2	G	T	7: 112,346,789	R986L	probably damaging	Het
Mroh8	G	A	2: 157,253,050	Q339*	probably null	Het
Msln	A	T	17: 25,749,068	V541E	probably damaging	Het
Muc16	T	A	9: 18,586,882	M6590L	probably benign	Het
Nisch	A	T	14: 31,171,671	V1315E	probably damaging	Het
Nubp2	G	A	17: 24,884,408	T165I	probably damaging	Het
Olfr1089	A	T	2: 86,733,292	F107I	probably damaging	Het
Olfr13	A	G	6: 43,174,057	M24V	probably benign	Het
Olfr57	T	C	10: 79,035,396	I200T	probably benign	Het
Olfr682-ps1	A	T	7: 105,126,778	N164K	probably benign	Het
Olfr820	T	C	10: 130,017,940	I193T	possibly damaging	Het
Oog3	T	G	4: 144,157,919	R482S	probably benign	Het
P3h4	A	T	11: 100,413,673	C247*	probably null	Het
Palm2	G	A	4: 57,710,125	A357T	possibly damaging	Het
Plch2	T	A	4: 154,998,485	M569L	probably benign	Het
Plcl1	A	G	1: 55,696,291	T264A	probably benign	Het
Rad51ap1	G	T	6: 126,927,563	N178K	probably benign	Het
Rasa4	T	C	5: 136,101,640	L340P	probably damaging	Het
Rassf10	A	G	7: 112,955,577	T462A	probably benign	Het
Rlf	G	C	4: 121,150,668	L482V	probably damaging	Het
Robo1	T	G	16: 73,024,442	S1357A	possibly damaging	Het
Rp1l1	T	C	14: 64,032,265	S1767P	probably damaging	Het
Rpl3l	T	A	17: 24,728,354	L14Q	probably damaging	Het
Ryr3	T	A	2: 112,804,702	T2024S	possibly damaging	Het
Sbf2	T	C	7: 110,441,495	Q375R	possibly damaging	Het
Sema6a	T	C	18: 47,249,185	Q765R	probably damaging	Het
Senp6	T	A	9: 80,113,946	Y303N	probably damaging	Het
Sertad4	C	T	1: 192,846,528	D327N	probably damaging	Het
Slc22a15	T	A	3: 101,883,532	Y219F	possibly damaging	Het
Slco1b2	T	G	6: 141,648,632		probably null	Het
Snrnp200	G	T	2: 127,226,039	V819L	probably damaging	Het
Ssb	C	A	2: 69,870,440	A288E	probably damaging	Het
Syne2	A	G	12: 76,054,846	H638R	probably benign	Het
Tm7sf3	A	G	6: 146,626,200	S43P	probably benign	Het
Tmem200c	A	G	17: 68,842,186	H588R	probably benign	Het
Tnpo3	G	A	6: 29,560,174	R657*	probably null	Het
Traf6	T	C	2: 101,688,582	C139R	probably damaging	Het
Txnrd1	C	A	10: 82,884,556	N424K	possibly damaging	Het
Ubqln3	T	C	7: 104,142,755	I43V	probably damaging	Het
Usp32	A	G	11: 85,030,491	V699A	probably damaging	Het
Vmn2r103	T	C	17: 19,793,765	V273A	probably benign	Het
Vmn2r8	A	G	5: 108,803,241	S113P	probably benign	Het
Wdr7	T	A	18: 63,727,755	I161N	probably damaging	Het
Zfp474	A	T	18: 52,638,943	I223F	probably damaging	Het
Zfp583	A	G	7: 6,317,329	L228P	probably damaging	Het
Zfyve27	A	G	19: 42,177,417	T76A	possibly damaging	Het

Other mutations in Ces3b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01069:Ces3b	APN	8	105091574	missense	probably benign	0.00
IGL01324:Ces3b	APN	8	105093252	missense	probably damaging	0.99
IGL02418:Ces3b	APN	8	105085647	missense	probably damaging	1.00
IGL02612:Ces3b	APN	8	105085269	missense	possibly damaging	0.83
IGL03400:Ces3b	APN	8	105092936	missense	probably damaging	1.00
R0244:Ces3b	UTSW	8	105092635	missense	probably damaging	1.00
R0282:Ces3b	UTSW	8	105083851	missense	probably benign	0.00
R0800:Ces3b	UTSW	8	105085269	missense	possibly damaging	0.83
R1833:Ces3b	UTSW	8	105085639	missense	probably damaging	0.98
R2130:Ces3b	UTSW	8	105092975	critical splice donor site	probably null
R3790:Ces3b	UTSW	8	105086888	missense	possibly damaging	0.50
R4827:Ces3b	UTSW	8	105086895	missense	probably benign	0.12
R5411:Ces3b	UTSW	8	105088632	missense	possibly damaging	0.94
R5790:Ces3b	UTSW	8	105092638	missense	probably damaging	1.00
R5798:Ces3b	UTSW	8	105088440	missense	probably damaging	1.00
R5929:Ces3b	UTSW	8	105093165	missense	probably damaging	1.00
R6437:Ces3b	UTSW	8	105092606	missense	probably damaging	1.00
R6470:Ces3b	UTSW	8	105088653	missense	possibly damaging	0.87
R6943:Ces3b	UTSW	8	105093078	missense	probably damaging	1.00
R7828:Ces3b	UTSW	8	105086596	missense	probably damaging	1.00
R7856:Ces3b	UTSW	8	105093262	makesense	probably null
R8162:Ces3b	UTSW	8	105090753	missense	possibly damaging	0.83
R8924:Ces3b	UTSW	8	105084987	missense	probably benign	0.08
R9369:Ces3b	UTSW	8	105086870	missense	probably damaging	1.00
R9381:Ces3b	UTSW	8	105085038	missense	probably benign	0.30
R9651:Ces3b	UTSW	8	105085625	missense	probably damaging	1.00
R9653:Ces3b	UTSW	8	105085625	missense	probably damaging	1.00
Z1177:Ces3b	UTSW	8	105085083	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- CCTGTTTCCTAAACACTCCAGAAG -3'
(R):5'- ATCTGTCGAGTGTGGAGATCAG -3'

Sequencing Primer
(F):5'- CCAGAAGTTCTTATAATACCCTGGGC -3'
(R):5'- GCTTTTACATAAATGTTGGGGACCC -3'

Posted On

2022-11-14