Mutagenetix > Incidental Mutation

Incidental Mutation 'R9096:Abhd12b'

691374

Institutional Source

Beutler Lab

Gene Symbol

Abhd12b

Ensembl Gene

ENSMUSG00000090121

Gene Name

abhydrolase domain containing 12B

Synonyms

LOC328121

MMRRC Submission

068911-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.102) question?

Stock #

R9096 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

70200916-70230661 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 70210207 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 128 (Y128N)

Ref Sequence

ENSEMBL: ENSMUSP00000134568 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000169156] [ENSMUST00000182512] [ENSMUST00000182782] [ENSMUST00000182927]

AlphaFold

G3UZN6

Predicted Effect

probably damaging
Transcript: ENSMUST00000169156
AA Change: Y128N

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

SMART Domains

Protein: ENSMUSP00000134568
Gene: ENSMUSG00000090121
AA Change: Y128N

Domain	Start	End	E-Value	Type
Pfam:Hydrolase_4	136	289	1e-16	PFAM
Pfam:Abhydrolase_1	137	278	2.6e-10	PFAM
Pfam:Abhydrolase_5	138	337	3.5e-22	PFAM
Pfam:Abhydrolase_6	139	347	2.1e-12	PFAM
Pfam:Peptidase_S9	154	357	2e-7	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000182512

Predicted Effect

probably benign
Transcript: ENSMUST00000182782

Predicted Effect

probably damaging
Transcript: ENSMUST00000182927
AA Change: Y51N

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

SMART Domains

Protein: ENSMUSP00000138681
Gene: ENSMUSG00000090121
AA Change: Y51N

Domain	Start	End	E-Value	Type
Pfam:Abhydrolase_5	61	260	1.5e-22	PFAM
Pfam:Abhydrolase_6	62	266	1.8e-19	PFAM
Pfam:Peptidase_S9	77	280	5.1e-8	PFAM
Pfam:Abhydrolase_1	89	279	1.8e-8	PFAM

Coding Region Coverage

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

Validation Efficiency

98% (57/58)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2900026A02Rik	A	T	5: 113,339,793 (GRCm39)	V73E		Het
Arhgap40	A	T	2: 158,389,584 (GRCm39)	M586L	probably benign	Het
Armt1	T	C	10: 4,384,829 (GRCm39)	S15P	probably damaging	Het
Arnt	G	T	3: 95,397,588 (GRCm39)	S535I	probably benign	Het
Bmper	T	C	9: 23,134,988 (GRCm39)	S18P	possibly damaging	Het
Catsperg1	G	C	7: 28,884,152 (GRCm39)	T987R	probably damaging	Het
Col9a1	A	T	1: 24,224,207 (GRCm39)	I130F	unknown	Het
Dennd1a	G	T	2: 37,690,077 (GRCm39)	L1008I	probably damaging	Het
Depdc1a	T	A	3: 159,204,117 (GRCm39)	D55E	probably benign	Het
Dlc1	A	T	8: 37,080,721 (GRCm39)	I10N	probably benign	Het
Dnah1	T	A	14: 30,983,027 (GRCm39)	I4203F	probably damaging	Het
Dzank1	G	T	2: 144,316,882 (GRCm39)	L767I	possibly damaging	Het
Eprs1	C	A	1: 185,139,303 (GRCm39)	A896E	probably benign	Het
Fryl	T	C	5: 73,265,920 (GRCm39)	D467G	probably benign	Het
Gab3	TTC	TTCCTC	X: 74,043,610 (GRCm39)		probably benign	Het
Gimd1	T	A	3: 132,340,661 (GRCm39)	M59K	probably benign	Het
Gm3667	T	C	14: 18,270,388 (GRCm39)	Y139C	probably damaging	Het
Gng2	T	A	14: 19,941,471 (GRCm39)		probably null	Het
Gpr162	A	G	6: 124,836,570 (GRCm39)	I367T	probably benign	Het
Hacd4	A	G	4: 88,355,695 (GRCm39)		probably null	Het
Hmcn1	C	T	1: 150,532,869 (GRCm39)	V3105M	probably benign	Het
Iws1	T	C	18: 32,216,373 (GRCm39)	V371A	probably benign	Het
Kctd10	C	T	5: 114,508,232 (GRCm39)	R92Q	probably damaging	Het
Lepr	T	C	4: 101,631,418 (GRCm39)	F643L	possibly damaging	Het
Lpgat1	T	C	1: 191,451,569 (GRCm39)	V65A	possibly damaging	Het
Lrrk2	C	T	15: 91,557,459 (GRCm39)		probably benign	Het
Magel2	A	G	7: 62,030,297 (GRCm39)	D1067G	unknown	Het
Mrc2	A	G	11: 105,231,398 (GRCm39)	D777G	probably damaging	Het
Nol10	T	A	12: 17,466,199 (GRCm39)	D531E	probably benign	Het
Odf2	T	A	2: 29,783,508 (GRCm39)	V103D	probably damaging	Het
Or4f7	T	A	2: 111,644,196 (GRCm39)	K292*	probably null	Het
Pcdhb21	A	G	18: 37,648,071 (GRCm39)	Y400C	probably damaging	Het
Pkn2	C	T	3: 142,515,249 (GRCm39)	R695Q	probably benign	Het
Pld3	A	G	7: 27,232,089 (GRCm39)	V397A	probably benign	Het
Ppp1r9a	A	G	6: 4,906,012 (GRCm39)	D189G	probably damaging	Het
Ppp2r1b	A	G	9: 50,777,856 (GRCm39)	K267R	probably benign	Het
Prkca	A	G	11: 107,905,061 (GRCm39)	S226P	probably benign	Het
Ptpru	T	C	4: 131,499,843 (GRCm39)	N1267S	probably damaging	Het
Pxn	T	A	5: 115,686,680 (GRCm39)	C391S	probably benign	Het
Rars1	T	C	11: 35,718,256 (GRCm39)	E136G	probably benign	Het
Rrp12	A	T	19: 41,878,577 (GRCm39)	D189E	probably benign	Het
Rsf1	GCG	GCGACGGCGCCG	7: 97,229,114 (GRCm39)		probably benign	Het
Sdc1	T	C	12: 8,841,665 (GRCm39)	L265P	probably damaging	Het
Sycp2l	A	T	13: 41,300,070 (GRCm39)	D428V	possibly damaging	Het
Tasp1	A	T	2: 139,725,690 (GRCm39)		probably null	Het
Telo2	T	C	17: 25,324,066 (GRCm39)	T550A	probably benign	Het
Tmem131l	A	T	3: 83,850,122 (GRCm39)	N225K	probably damaging	Het
Tmem260	T	A	14: 48,757,803 (GRCm39)	V706D	unknown	Het
Tnr	T	A	1: 159,677,804 (GRCm39)	M63K	probably benign	Het
Ttn	A	G	2: 76,572,413 (GRCm39)	I26160T	probably damaging	Het
Ubap1	T	C	4: 41,379,872 (GRCm39)		probably null	Het
Ush2a	C	T	1: 188,198,333 (GRCm39)	P1466S	probably benign	Het
Usp24	T	G	4: 106,254,508 (GRCm39)	M1495R	probably benign	Het
Utp20	T	C	10: 88,611,180 (GRCm39)	N1379S	probably damaging	Het
Vmn1r16	A	T	6: 57,300,250 (GRCm39)	I124N	probably benign	Het
Vmn1r181	A	G	7: 23,684,444 (GRCm39)	N303S	probably benign	Het
Vmn1r50	G	A	6: 90,085,022 (GRCm39)	V256I	probably benign	Het
Vps54	A	G	11: 21,227,913 (GRCm39)	N288S	possibly damaging	Het
Zfp266	A	T	9: 20,416,440 (GRCm39)	F50Y	probably damaging	Het

Other mutations in Abhd12b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01306:Abhd12b	APN	12	70,215,822 (GRCm39)	missense	probably damaging	0.99
IGL02886:Abhd12b	APN	12	70,229,740 (GRCm39)	missense	possibly damaging	0.70
ANU23:Abhd12b	UTSW	12	70,215,822 (GRCm39)	missense	probably damaging	0.99
R0112:Abhd12b	UTSW	12	70,227,791 (GRCm39)	missense	probably benign	0.16
R0542:Abhd12b	UTSW	12	70,210,269 (GRCm39)	missense	possibly damaging	0.82
R1427:Abhd12b	UTSW	12	70,229,193 (GRCm39)	missense	probably damaging	1.00
R4782:Abhd12b	UTSW	12	70,215,838 (GRCm39)	missense	probably damaging	1.00
R4799:Abhd12b	UTSW	12	70,215,838 (GRCm39)	missense	probably damaging	1.00
R5238:Abhd12b	UTSW	12	70,210,142 (GRCm39)	splice site	probably null
R5372:Abhd12b	UTSW	12	70,227,800 (GRCm39)	missense	probably damaging	0.98
R6974:Abhd12b	UTSW	12	70,206,221 (GRCm39)	missense	probably benign	0.03
R8773:Abhd12b	UTSW	12	70,213,708 (GRCm39)	critical splice acceptor site	probably null
R9498:Abhd12b	UTSW	12	70,210,237 (GRCm39)	missense	probably benign	0.09
R9554:Abhd12b	UTSW	12	70,215,988 (GRCm39)	missense	probably benign	0.04
R9738:Abhd12b	UTSW	12	70,216,039 (GRCm39)	missense	probably benign	0.00
Z1176:Abhd12b	UTSW	12	70,210,225 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTCGCAGTAGCAATTTTCCTCTG -3'
(R):5'- GGCATGTCTATGATTGAAAACTGC -3'

Sequencing Primer
(F):5'- CATCATTAGCTTATGCACCAGTTG -3'
(R):5'- TGATTGAAAACTGCCTTCACTC -3'

Posted On

2021-12-30