Mutagenetix > Incidental Mutation

Incidental Mutation 'R3890:Ifi213'

310316

Institutional Source

Beutler Lab

Gene Symbol

Ifi213

Ensembl Gene

ENSMUSG00000073491

Gene Name

interferon activated gene 213

Synonyms

Pyr-A, Pydc4, E030037K03Rik

MMRRC Submission

040802-MU

Accession Numbers

Essential gene?

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

Stock #

R3890 (G1)

Quality Score

222

Status

Validated

Chromosome

Chromosomal Location

173393849-173426840 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 173394822 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 571 (I571T)

Ref Sequence

ENSEMBL: ENSMUSP00000117222 (fasta)

Gene Model

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

AlphaFold

D3Z5G0

Predicted Effect

probably benign
Transcript: ENSMUST00000150649
AA Change: I571T

PolyPhen 2 Score 0.332 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000117222
Gene: ENSMUSG00000073491
AA Change: I571T

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000178186

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000179648

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.9%

Validation Efficiency

98% (60/61)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700029H14Rik	T	C	8: 13,604,700 (GRCm39)	Y201C	probably damaging	Het
Adam10	A	G	9: 70,676,136 (GRCm39)	T624A	probably benign	Het
Atf2	T	C	2: 73,693,557 (GRCm39)	S2G	probably damaging	Het
Atf7ip	T	C	6: 136,564,043 (GRCm39)	V762A	possibly damaging	Het
Cacna1e	C	T	1: 154,359,299 (GRCm39)	R265Q	probably damaging	Het
Cckbr	A	C	7: 105,075,376 (GRCm39)	T49P	probably benign	Het
Clip2	T	C	5: 134,551,847 (GRCm39)	K92E	probably damaging	Het
Clrn3	T	C	7: 135,120,194 (GRCm39)	T131A	possibly damaging	Het
Cntrl	T	G	2: 35,060,492 (GRCm39)	C1342G	probably benign	Het
Def8	T	C	8: 124,185,083 (GRCm39)		probably benign	Het
Dennd4a	T	C	9: 64,779,310 (GRCm39)	S598P	probably damaging	Het
Deup1	A	G	9: 15,511,009 (GRCm39)	Y257H	probably damaging	Het
Dnajc28	G	A	16: 91,413,755 (GRCm39)	T187M	probably damaging	Het
Ect2	T	C	3: 27,192,689 (GRCm39)	D387G	probably damaging	Het
Fat3	G	A	9: 15,909,567 (GRCm39)	S2145F	probably damaging	Het
Fmo4	A	T	1: 162,621,624 (GRCm39)	I529N	probably benign	Het
Frs3	A	G	17: 48,014,360 (GRCm39)	D351G	probably damaging	Het
Gcat	T	A	15: 78,921,376 (GRCm39)	V378D	probably damaging	Het
Hmcn1	A	T	1: 150,510,946 (GRCm39)	D3592E	probably damaging	Het
Hspa4l	A	T	3: 40,736,026 (GRCm39)	Q570L	possibly damaging	Het
Lsamp	T	C	16: 39,805,054 (GRCm39)	V11A	probably benign	Het
Mettl1	T	C	10: 126,880,998 (GRCm39)		probably null	Het
Mettl15	A	G	2: 109,021,924 (GRCm39)	I127T	probably benign	Het
Mipep	T	C	14: 61,046,444 (GRCm39)	L322P	probably damaging	Het
Mob1b	T	A	5: 88,901,061 (GRCm39)	I156K	probably damaging	Het
Mobp	G	A	9: 119,997,022 (GRCm39)	C51Y	probably damaging	Het
Ms4a3	T	C	19: 11,610,271 (GRCm39)	N97S	probably benign	Het
Myrip	A	G	9: 120,251,324 (GRCm39)	E210G	probably damaging	Het
Nos1ap	T	C	1: 170,177,025 (GRCm39)	Y126C	probably damaging	Het
Nuak2	G	T	1: 132,259,223 (GRCm39)	A342S	possibly damaging	Het
Obscn	T	C	11: 59,022,472 (GRCm39)	R758G	possibly damaging	Het
Or10ah1-ps1	G	T	5: 143,123,152 (GRCm39)	S290R	probably benign	Het
Or2aj5	A	G	16: 19,425,205 (GRCm39)	I71T	probably damaging	Het
Or7e165	T	G	9: 19,695,011 (GRCm39)	I194S	probably benign	Het
Pdgfra	A	G	5: 75,328,588 (GRCm39)	N240S	probably null	Het
Pdxdc1	T	C	16: 13,654,312 (GRCm39)	T759A	probably benign	Het
Pex2	C	T	3: 5,626,008 (GRCm39)	C267Y	probably damaging	Het
Pgghg	T	C	7: 140,525,616 (GRCm39)	I473T	probably damaging	Het
Prdm15	T	C	16: 97,600,771 (GRCm39)	H829R	probably damaging	Het
Pum1	T	C	4: 130,491,393 (GRCm39)	L774P	probably damaging	Het
Rcbtb1	T	A	14: 59,465,804 (GRCm39)	H382Q	possibly damaging	Het
Rprd2	A	T	3: 95,672,536 (GRCm39)	F956I	probably damaging	Het
Samd1	G	A	8: 84,724,361 (GRCm39)		probably benign	Het
Slc4a11	A	T	2: 130,527,705 (GRCm39)	S592T	probably damaging	Het
Slc5a4b	A	G	10: 75,898,094 (GRCm39)	V540A	probably benign	Het
Slfn8	G	A	11: 82,895,270 (GRCm39)	T512I	possibly damaging	Het
Slx4	A	T	16: 3,797,773 (GRCm39)	I1537N	probably damaging	Het
Sorl1	G	A	9: 41,915,401 (GRCm39)	T1276M	probably damaging	Het
Specc1	C	T	11: 62,042,739 (GRCm39)	T872M	probably benign	Het
Speer4f1	T	C	5: 17,684,500 (GRCm39)	I176T	probably damaging	Het
Spint1	T	C	2: 119,079,283 (GRCm39)	I455T	probably benign	Het
Srp54a	A	G	12: 55,135,978 (GRCm39)		probably null	Het
Stoml3	T	A	3: 53,414,875 (GRCm39)	N222K	probably damaging	Het
Syce1	C	A	7: 140,359,809 (GRCm39)	L83F	probably damaging	Het
Tanc2	A	T	11: 105,689,504 (GRCm39)	D222V	probably damaging	Het
Tasor2	T	C	13: 3,646,785 (GRCm39)	E80G	probably damaging	Het
Thsd7a	G	A	6: 12,418,336 (GRCm39)	S631L	probably benign	Het
Vmn2r73	G	A	7: 85,507,144 (GRCm39)	H723Y	probably benign	Het
Wdfy4	T	C	14: 32,769,237 (GRCm39)	E2076G	probably damaging	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
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
R6149:Ifi213	UTSW	1	173,421,581 (GRCm39)	missense	probably benign	0.18
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'- TATGAAATTCCAAGCCCAGGG -3'
(R):5'- TCATGCCATTACCTTATAATGCAACC -3'

Sequencing Primer
(F):5'- CTCCAGGACTGCCTAGGATATTG -3'
(R):5'- CTGGAACGGTTAAAGACAGAAATTTC -3'

Posted On

2015-04-17