Mutagenetix > Incidental Mutation

Incidental Mutation 'R0472:AI182371'

46803

Institutional Source

Beutler Lab

Gene Symbol

AI182371

Ensembl Gene

ENSMUSG00000035875

Gene Name

expressed sequence AI182371

Synonyms

MMRRC Submission

038672-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

R0472 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

34971873-34991555 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 34975218 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 337 (N337S)

Ref Sequence

ENSEMBL: ENSMUSP00000154033 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045776] [ENSMUST00000134940] [ENSMUST00000226375] [ENSMUST00000226631] [ENSMUST00000226972]

AlphaFold

A2AS37

Predicted Effect

probably benign
Transcript: ENSMUST00000045776
AA Change: N327S

PolyPhen 2 Score 0.235 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000037754
Gene: ENSMUSG00000035875
AA Change: N327S

Domain	Start	End	E-Value	Type
Pfam:A2M_N	133	227	4.7e-19	PFAM
ANATO	284	318	1.97e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000134940

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151161

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154817

Predicted Effect

probably benign
Transcript: ENSMUST00000226375

Predicted Effect

probably benign
Transcript: ENSMUST00000226631
AA Change: N338S

PolyPhen 2 Score 0.346 (Sensitivity: 0.90; Specificity: 0.89)

Predicted Effect

probably benign
Transcript: ENSMUST00000226972
AA Change: N337S

PolyPhen 2 Score 0.346 (Sensitivity: 0.90; Specificity: 0.89)

Meta Mutation Damage Score

0.0748

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.3%

Validation Efficiency

97% (65/67)

Allele List at MGI

All alleles(1) : Targeted, other(1)

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700128F08Rik	A	G	9: 8,222,123 (GRCm39)		noncoding transcript	Het
Aldh3b1	C	T	19: 3,964,024 (GRCm39)	R426H	probably damaging	Het
Arap2	A	G	5: 62,864,002 (GRCm39)	F541L	probably damaging	Het
Asap2	G	T	12: 21,263,186 (GRCm39)	R267L	possibly damaging	Het
Ass1	A	T	2: 31,404,831 (GRCm39)	N371Y	probably damaging	Het
Bmp8b	T	A	4: 123,015,692 (GRCm39)	D226E	probably benign	Het
C1ra	T	A	6: 124,494,403 (GRCm39)	D283E	possibly damaging	Het
Cacul1	G	T	19: 60,531,464 (GRCm39)	H268Q	probably damaging	Het
Cd9	T	C	6: 125,449,396 (GRCm39)	N49D	probably benign	Het
Cdc42bpa	A	G	1: 179,867,744 (GRCm39)	H193R	probably damaging	Het
Cep290	G	A	10: 100,387,317 (GRCm39)	G1935E	probably benign	Het
Cep350	A	T	1: 155,790,469 (GRCm39)	I1362N	probably damaging	Het
Chchd7	A	T	4: 3,943,416 (GRCm39)	N61I	possibly damaging	Het
Clca3a1	A	T	3: 144,733,106 (GRCm39)	L134Q	probably damaging	Het
Clec2j	T	C	6: 128,633,565 (GRCm39)		noncoding transcript	Het
Clvs1	G	A	4: 9,281,801 (GRCm39)	A82T	probably damaging	Het
Csn1s1	A	T	5: 87,825,486 (GRCm39)	Y231F	possibly damaging	Het
Cyp2c55	A	T	19: 39,019,823 (GRCm39)	T254S	probably benign	Het
Decr1	A	G	4: 15,919,849 (GRCm39)	S290P	probably damaging	Het
Dnai2	T	A	11: 114,636,015 (GRCm39)		probably benign	Het
Dock4	C	A	12: 40,888,437 (GRCm39)		probably benign	Het
Dst	T	C	1: 34,306,041 (GRCm39)		probably null	Het
Elmo2	A	G	2: 165,140,250 (GRCm39)	I315T	probably damaging	Het
Fcho2	A	G	13: 98,884,775 (GRCm39)	F431L	probably benign	Het
Fez2	A	G	17: 78,692,261 (GRCm39)		probably benign	Het
Gas2l3	C	T	10: 89,262,339 (GRCm39)	A128T	probably damaging	Het
Hpse2	T	C	19: 43,001,602 (GRCm39)	I222M	probably damaging	Het
Katnip	A	G	7: 125,472,139 (GRCm39)	N1548S	probably damaging	Het
Kcna2	A	G	3: 107,012,832 (GRCm39)	D471G	probably benign	Het
Kcnj13	T	A	1: 87,314,568 (GRCm39)	Y218F	probably benign	Het
Kif1a	T	C	1: 92,946,719 (GRCm39)	H1763R	probably damaging	Het
Krt1c	C	T	15: 101,721,688 (GRCm39)	R451H	probably damaging	Het
Lama2	A	G	10: 26,866,863 (GRCm39)	V2877A	probably damaging	Het
Lrrc2	A	T	9: 110,791,685 (GRCm39)	M80L	probably benign	Het
Naip6	A	G	13: 100,438,768 (GRCm39)	V343A	probably benign	Het
Nedd4l	T	C	18: 65,341,532 (GRCm39)	Y753H	probably damaging	Het
Nif3l1	A	C	1: 58,486,987 (GRCm39)	S58R	probably damaging	Het
Or51h7	A	T	7: 102,591,258 (GRCm39)	C175*	probably null	Het
Or5w20	T	A	2: 87,726,837 (GRCm39)	V98E	possibly damaging	Het
Or9r3	G	A	10: 129,948,449 (GRCm39)	S70F	probably damaging	Het
Osbpl11	C	A	16: 33,054,814 (GRCm39)	Y632*	probably null	Het
Pask	A	T	1: 93,248,639 (GRCm39)	D920E	probably benign	Het
Pclo	T	C	5: 14,731,608 (GRCm39)	V3370A	unknown	Het
Ptpn21	G	A	12: 98,670,499 (GRCm39)		probably benign	Het
Rph3al	T	C	11: 75,799,795 (GRCm39)	I55V	probably benign	Het
Rsad2	T	G	12: 26,504,167 (GRCm39)	I121L	possibly damaging	Het
Sergef	T	G	7: 46,283,170 (GRCm39)		probably benign	Het
Sp110	C	T	1: 85,516,841 (GRCm39)	E219K	possibly damaging	Het
Tas2r104	T	C	6: 131,662,434 (GRCm39)	I92V	probably benign	Het
Tasor2	A	G	13: 3,638,364 (GRCm39)	S456P	possibly damaging	Het
Tbc1d23	T	A	16: 56,993,469 (GRCm39)	I566F	possibly damaging	Het
Tbc1d9b	A	G	11: 50,059,055 (GRCm39)		probably null	Het
Tie1	T	A	4: 118,333,344 (GRCm39)	I841L	possibly damaging	Het
Tpo	A	G	12: 30,150,485 (GRCm39)	V465A	probably benign	Het
Ttll3	A	T	6: 113,386,300 (GRCm39)	Q711L	probably damaging	Het
Ttn	C	T	2: 76,783,385 (GRCm39)	R869H	probably benign	Het
Uggt2	A	G	14: 119,332,748 (GRCm39)	V62A	probably damaging	Het
Usp34	T	C	11: 23,334,509 (GRCm39)		probably benign	Het
Vmn1r17	C	A	6: 57,338,304 (GRCm39)	M20I	probably benign	Het
Vmn1r71	G	C	7: 10,482,019 (GRCm39)	S223C	possibly damaging	Het
Vmn2r120	C	T	17: 57,831,518 (GRCm39)	V424I	probably benign	Het
Vps13b	T	C	15: 35,417,779 (GRCm39)		probably null	Het
Wdfy3	C	A	5: 102,105,309 (GRCm39)	A173S	probably benign	Het
Wdr59	T	C	8: 112,213,629 (GRCm39)		probably null	Het
Ythdc2	A	T	18: 44,997,424 (GRCm39)	M994L	probably benign	Het
Zfp808	T	A	13: 62,320,120 (GRCm39)	F450I	probably damaging	Het

Other mutations in AI182371

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02338:AI182371	APN	2	34,975,728 (GRCm39)	missense	probably benign	0.02
IGL02344:AI182371	APN	2	34,979,198 (GRCm39)	missense	probably benign	0.01
IGL02817:AI182371	APN	2	34,990,661 (GRCm39)	missense	probably damaging	0.99
IGL02961:AI182371	APN	2	34,976,124 (GRCm39)	missense	possibly damaging	0.53
3-1:AI182371	UTSW	2	34,990,619 (GRCm39)	missense	probably damaging	0.99
R0041:AI182371	UTSW	2	34,975,733 (GRCm39)	missense	possibly damaging	0.79
R0084:AI182371	UTSW	2	34,975,714 (GRCm39)	critical splice donor site	probably null
R1539:AI182371	UTSW	2	34,978,815 (GRCm39)	missense	probably damaging	0.98
R1634:AI182371	UTSW	2	34,976,497 (GRCm39)	missense	probably damaging	1.00
R1635:AI182371	UTSW	2	34,978,749 (GRCm39)	splice site	probably null
R1898:AI182371	UTSW	2	34,990,661 (GRCm39)	missense	probably damaging	0.99
R2065:AI182371	UTSW	2	34,976,441 (GRCm39)	critical splice donor site	probably null
R2155:AI182371	UTSW	2	34,975,366 (GRCm39)	missense	probably benign	0.00
R3694:AI182371	UTSW	2	34,975,764 (GRCm39)	missense	probably benign	0.00
R3900:AI182371	UTSW	2	34,975,228 (GRCm39)	missense	probably benign	0.01
R4766:AI182371	UTSW	2	34,985,829 (GRCm39)	missense	possibly damaging	0.78
R5071:AI182371	UTSW	2	34,975,227 (GRCm39)	missense	probably benign	0.17
R5500:AI182371	UTSW	2	34,990,650 (GRCm39)	missense	probably damaging	0.99
R5907:AI182371	UTSW	2	34,976,134 (GRCm39)	missense	possibly damaging	0.66
R6146:AI182371	UTSW	2	34,987,983 (GRCm39)	missense	probably damaging	1.00
R6333:AI182371	UTSW	2	34,975,281 (GRCm39)	missense	probably damaging	0.99
R6729:AI182371	UTSW	2	34,974,717 (GRCm39)	intron	probably benign
R6732:AI182371	UTSW	2	34,974,717 (GRCm39)	intron	probably benign
R6742:AI182371	UTSW	2	34,974,717 (GRCm39)	intron	probably benign
R6781:AI182371	UTSW	2	34,974,717 (GRCm39)	intron	probably benign
R7196:AI182371	UTSW	2	34,976,441 (GRCm39)	critical splice donor site	probably null
R7381:AI182371	UTSW	2	34,975,371 (GRCm39)	missense	probably damaging	1.00
R7458:AI182371	UTSW	2	34,976,516 (GRCm39)	missense	possibly damaging	0.95
R7466:AI182371	UTSW	2	34,978,753 (GRCm39)	nonsense	probably null
R8832:AI182371	UTSW	2	34,985,909 (GRCm39)	missense	unknown
R8933:AI182371	UTSW	2	34,975,714 (GRCm39)	critical splice donor site	probably null
R8942:AI182371	UTSW	2	34,990,622 (GRCm39)	missense	probably damaging	1.00
R8944:AI182371	UTSW	2	34,990,622 (GRCm39)	missense	probably damaging	1.00
R9690:AI182371	UTSW	2	34,990,600 (GRCm39)	missense	probably benign	0.19
RF009:AI182371	UTSW	2	34,979,209 (GRCm39)	missense	possibly damaging	0.90
Z1177:AI182371	UTSW	2	34,985,771 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- ACAAGTCGTCTGCCTTCCAACTC -3'
(R):5'- AAGTCGCTGTAAGATTCTCAAGCCTG -3'

Sequencing Primer
(F):5'- ggagtgggtgggtggag -3'
(R):5'- TCAAGCCTGAGATGTCATGC -3'

Posted On

2013-06-11