Mutagenetix > Incidental Mutation

Incidental Mutation 'R6149:Ifi213'

489052

Institutional Source

Beutler Lab

Gene Symbol

Ifi213

Ensembl Gene

ENSMUSG00000073491

Gene Name

interferon activated gene 213

Synonyms

Pyr-A, Pydc4, E030037K03Rik

MMRRC Submission

044296-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R6149 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

173393849-173426840 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 173421581 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 103 (S103T)

Ref Sequence

ENSEMBL: ENSMUSP00000136238 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000097462] [ENSMUST00000150649] [ENSMUST00000180215]

AlphaFold

D3Z5G0

Predicted Effect

probably benign
Transcript: ENSMUST00000097462
AA Change: S103T

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000095070
Gene: ENSMUSG00000073491
AA Change: S103T

Domain	Start	End	E-Value	Type
PYRIN	10	88	3.71e-20	SMART
low complexity region	101	112	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000150649
AA Change: S103T

PolyPhen 2 Score 0.058 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000117222
Gene: ENSMUSG00000073491
AA Change: S103T

Domain	Start	End	E-Value	Type
PYRIN	10	88	3.71e-20	SMART
low complexity region	101	112	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000180215
AA Change: S103T

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000136238
Gene: ENSMUSG00000073491
AA Change: S103T

Domain	Start	End	E-Value	Type
PYRIN	10	88	3.71e-20	SMART
low complexity region	101	112	N/A	INTRINSIC

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.6%
20x: 96.1%

Validation Efficiency

99% (69/70)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930558K02Rik	T	A	1: 161,777,211 (GRCm39)	R115S	probably benign	Het
Adgre1	A	G	17: 57,752,018 (GRCm39)	K589E	probably benign	Het
Adgrv1	A	T	13: 81,330,893 (GRCm39)	L74Q	probably damaging	Het
Avil	A	G	10: 126,842,451 (GRCm39)	I77V	probably benign	Het
Best2	T	C	8: 85,739,896 (GRCm39)	E57G	probably benign	Het
Cacna1a	T	C	8: 85,296,581 (GRCm39)	C1200R	probably damaging	Het
Catsperb	T	A	12: 101,516,098 (GRCm39)	I578K	probably damaging	Het
Chsy1	A	G	7: 65,775,133 (GRCm39)	Y154C	probably damaging	Het
Chuk	A	G	19: 44,090,270 (GRCm39)	V74A	probably damaging	Het
Ckb	T	C	12: 111,638,248 (GRCm39)	S49G	probably damaging	Het
Crtac1	A	G	19: 42,272,048 (GRCm39)	Y632H	unknown	Het
Ern1	C	A	11: 106,296,641 (GRCm39)	E770*	probably null	Het
Fam114a2	A	C	11: 57,378,415 (GRCm39)	V450G	probably benign	Het
Fgf15	C	T	7: 144,453,506 (GRCm39)	Q125*	probably null	Het
Frem2	A	T	3: 53,458,762 (GRCm39)	S2036T	probably damaging	Het
Fxr2	G	A	11: 69,540,030 (GRCm39)	V296I	probably benign	Het
Gm15264	C	A	3: 94,640,736 (GRCm39)		noncoding transcript	Het
Igkv5-37	T	A	6: 69,940,472 (GRCm39)	Q57H	probably damaging	Het
Il1rap	A	G	16: 26,530,969 (GRCm39)	Y435C	probably damaging	Het
Kl	T	A	5: 150,912,318 (GRCm39)	M689K	possibly damaging	Het
Lcor	T	A	19: 41,573,641 (GRCm39)	W799R	probably damaging	Het
Lnp1	C	T	16: 56,737,735 (GRCm39)	E118K	probably benign	Het
Lrif1	A	C	3: 106,639,643 (GRCm39)	K243Q	possibly damaging	Het
Lrp1b	G	T	2: 40,765,165 (GRCm39)		probably null	Het
Lvrn	G	A	18: 47,017,499 (GRCm39)	V610I	probably benign	Het
Med1	T	C	11: 98,074,679 (GRCm39)	K67R	possibly damaging	Het
Midn	T	C	10: 79,990,291 (GRCm39)	S278P	probably damaging	Het
Nrap	A	G	19: 56,377,885 (GRCm39)	V35A	possibly damaging	Het
Nynrin	A	T	14: 56,091,780 (GRCm39)	Q32L	possibly damaging	Het
Oog1	C	T	12: 87,653,043 (GRCm39)	T113I	possibly damaging	Het
Or10ak7	A	G	4: 118,791,628 (GRCm39)	L139P	probably damaging	Het
Or10j3	G	T	1: 173,031,582 (GRCm39)	V220F	probably benign	Het
Or4x11	C	T	2: 89,867,860 (GRCm39)	A199V	probably benign	Het
Or5b21	A	T	19: 12,839,723 (GRCm39)	I195F	probably benign	Het
Or6a2	T	C	7: 106,600,807 (GRCm39)	I87V	probably benign	Het
Otogl	C	T	10: 107,717,314 (GRCm39)	V386I	probably benign	Het
Patj	A	G	4: 98,312,562 (GRCm39)	N300S	possibly damaging	Het
Pcdhb16	T	A	18: 37,612,208 (GRCm39)	D389E	possibly damaging	Het
Pdcd6ip	T	C	9: 113,488,939 (GRCm39)	I699V	probably benign	Het
Pfas	A	G	11: 68,882,771 (GRCm39)	V790A	probably benign	Het
Plppr4	A	T	3: 117,116,043 (GRCm39)	C605S	probably benign	Het
Ppl	G	A	16: 4,925,460 (GRCm39)	Q60*	probably null	Het
Ppp1r1c	A	G	2: 79,586,810 (GRCm39)	K52R	possibly damaging	Het
Pramel29	A	G	4: 143,933,983 (GRCm39)	S375P	probably damaging	Het
Prpf40a	T	C	2: 53,047,927 (GRCm39)	M197V	probably benign	Het
Rpe65	G	A	3: 159,319,780 (GRCm39)	E217K	probably benign	Het
Rufy4	T	C	1: 74,186,892 (GRCm39)	I560T	probably benign	Het
Ryr2	T	C	13: 11,683,903 (GRCm39)	S3054G	probably benign	Het
Serpinb6a	A	T	13: 34,102,343 (GRCm39)	L273H	probably damaging	Het
Sf3b1	A	T	1: 55,046,666 (GRCm39)	W293R	probably damaging	Het
Sik1	A	T	17: 32,067,771 (GRCm39)	S435T	possibly damaging	Het
Slc2a12	G	T	10: 22,540,401 (GRCm39)	M85I	probably benign	Het
Stk36	T	C	1: 74,673,388 (GRCm39)	S1094P	probably benign	Het
Tctn1	A	T	5: 122,384,649 (GRCm39)	Y393N	probably benign	Het
Tex9	C	T	9: 72,369,282 (GRCm39)		probably null	Het
Thbs2	A	G	17: 14,899,942 (GRCm39)		probably null	Het
Tmprss7	A	T	16: 45,494,268 (GRCm39)	C412*	probably null	Het
Tpp1	T	C	7: 105,396,934 (GRCm39)	T399A	probably benign	Het
Trim25	T	A	11: 88,906,362 (GRCm39)	V387D	probably benign	Het
Usp45	A	C	4: 21,810,797 (GRCm39)	D331A	probably damaging	Het
Vill	T	G	9: 118,887,482 (GRCm39)	V82G	possibly damaging	Het
Vmn1r189	T	C	13: 22,286,054 (GRCm39)	D261G	probably benign	Het
Vmn2r111	T	C	17: 22,778,032 (GRCm39)	N549S	possibly damaging	Het
Vmn2r111	G	A	17: 22,767,796 (GRCm39)	T567I	probably benign	Het
Vmn2r60	A	G	7: 41,786,400 (GRCm39)	Y401C	probably damaging	Het
Zc3h11a	G	A	1: 133,566,613 (GRCm39)	R69*	probably null	Het

Other mutations in Ifi213

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00678:Ifi213	APN	1	173,421,619 (GRCm39)	splice site	probably benign
IGL00908:Ifi213	APN	1	173,422,649 (GRCm39)	missense	probably damaging	1.00
IGL00964:Ifi213	APN	1	173,421,518 (GRCm39)	missense	possibly damaging	0.91
IGL02217:Ifi213	APN	1	173,422,598 (GRCm39)	missense	possibly damaging	0.91
R0709:Ifi213	UTSW	1	173,417,366 (GRCm39)	missense	possibly damaging	0.70
R1518:Ifi213	UTSW	1	173,417,229 (GRCm39)	missense	probably damaging	0.99
R1559:Ifi213	UTSW	1	173,394,784 (GRCm39)	missense	probably benign	0.18
R1822:Ifi213	UTSW	1	173,417,408 (GRCm39)	missense	probably damaging	0.99
R1839:Ifi213	UTSW	1	173,417,166 (GRCm39)	missense	probably damaging	0.98
R1989:Ifi213	UTSW	1	173,396,374 (GRCm39)	critical splice donor site	probably null
R2108:Ifi213	UTSW	1	173,396,668 (GRCm39)	critical splice acceptor site	probably null
R2696:Ifi213	UTSW	1	173,417,590 (GRCm39)	missense	probably benign
R3890:Ifi213	UTSW	1	173,394,822 (GRCm39)	missense	probably benign	0.33
R4544:Ifi213	UTSW	1	173,409,693 (GRCm39)	splice site	probably null
R4611:Ifi213	UTSW	1	173,417,480 (GRCm39)	missense	possibly damaging	0.91
R4689:Ifi213	UTSW	1	173,417,986 (GRCm39)	missense	possibly damaging	0.92
R4710:Ifi213	UTSW	1	173,394,738 (GRCm39)	utr 3 prime	probably benign
R5126:Ifi213	UTSW	1	173,417,581 (GRCm39)	missense	possibly damaging	0.85
R5472:Ifi213	UTSW	1	173,394,838 (GRCm39)	splice site	probably null
R5625:Ifi213	UTSW	1	173,396,629 (GRCm39)	missense	possibly damaging	0.73
R5789:Ifi213	UTSW	1	173,396,360 (GRCm39)	splice site	probably benign
R5898:Ifi213	UTSW	1	173,396,545 (GRCm39)	missense	probably benign	0.01
R6025:Ifi213	UTSW	1	173,422,800 (GRCm39)	missense	probably damaging	0.99
R6348:Ifi213	UTSW	1	173,417,848 (GRCm39)	missense	possibly damaging	0.46
R6564:Ifi213	UTSW	1	173,422,862 (GRCm39)	start codon destroyed	probably null	0.06
R7254:Ifi213	UTSW	1	173,421,529 (GRCm39)	missense	probably damaging	0.98
R7292:Ifi213	UTSW	1	173,422,691 (GRCm39)	missense	probably damaging	0.99
R7752:Ifi213	UTSW	1	173,394,784 (GRCm39)	missense	probably benign	0.18
R7901:Ifi213	UTSW	1	173,394,784 (GRCm39)	missense	probably benign	0.18
R8100:Ifi213	UTSW	1	173,422,748 (GRCm39)	missense	probably damaging	1.00
R8352:Ifi213	UTSW	1	173,422,835 (GRCm39)	missense	possibly damaging	0.92
R8425:Ifi213	UTSW	1	173,417,426 (GRCm39)	missense	probably benign
R8452:Ifi213	UTSW	1	173,422,835 (GRCm39)	missense	possibly damaging	0.92
R9357:Ifi213	UTSW	1	173,396,392 (GRCm39)	missense	probably benign	0.01
RF010:Ifi213	UTSW	1	173,409,719 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- TTTCAGCTAGGTCCTTGGCAC -3'
(R):5'- CATGCCACTTGTACCTGAGAAGAG -3'

Sequencing Primer
(F):5'- TAGGTCCTTGGCACACATGAG -3'
(R):5'- AGGAAACCCAGGAGCATTTC -3'

Posted On

2017-10-10