Mutagenetix > Incidental Mutation

Incidental Mutation 'R3125:Ifi27l2b'

264256

Institutional Source

Beutler Lab

Gene Symbol

Ifi27l2b

Ensembl Gene

ENSMUSG00000021208

Gene Name

interferon, alpha-inducible protein 27 like 2B

Synonyms

1810023F06Rik

MMRRC Submission

040598-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R3125 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

103417157-103423482 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 103417594 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 198 (T198A)

Ref Sequence

ENSEMBL: ENSMUSP00000041712 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044687]

AlphaFold

Q8VC49

Predicted Effect

unknown
Transcript: ENSMUST00000044687
AA Change: T198A

SMART Domains

Protein: ENSMUSP00000041712
Gene: ENSMUSG00000021208
AA Change: T198A

Domain	Start	End	E-Value	Type
Pfam:Ifi-6-16	10	88	7.6e-30	PFAM
low complexity region	104	118	N/A	INTRINSIC
Pfam:Ifi-6-16	135	213	2.2e-30	PFAM
low complexity region	232	279	N/A	INTRINSIC

Meta Mutation Damage Score

0.0869

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.2%

Validation Efficiency

100% (48/48)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alox5	A	T	6: 116,404,098 (GRCm39)		probably null	Het
Aoc1l1	A	T	6: 48,952,305 (GRCm39)	I77F	probably damaging	Het
Atp4a	G	A	7: 30,419,650 (GRCm39)	R671Q	probably benign	Het
Bag4	C	T	8: 26,259,516 (GRCm39)	A228T	probably benign	Het
Cep135	T	C	5: 76,769,210 (GRCm39)		probably null	Het
Cfap206	T	A	4: 34,716,310 (GRCm39)	H385L	possibly damaging	Het
Dach2	T	C	X: 112,729,664 (GRCm39)	I417T	possibly damaging	Het
Dcaf8l	A	T	X: 88,448,327 (GRCm39)	Y601N	probably benign	Het
Dhx32	T	C	7: 133,327,085 (GRCm39)	Y332C	probably damaging	Het
Dlx1	T	A	2: 71,362,740 (GRCm39)	W216R	probably damaging	Het
Dna2	G	A	10: 62,784,981 (GRCm39)	A33T	possibly damaging	Het
Dyrk1a	G	A	16: 94,469,660 (GRCm39)		probably benign	Het
Fam227b	T	C	2: 125,966,006 (GRCm39)	T140A	probably benign	Het
Fem1b	T	C	9: 62,703,836 (GRCm39)	I475V	probably benign	Het
Fign	T	A	2: 63,809,044 (GRCm39)	Q742L	possibly damaging	Het
Hip1r	A	G	5: 124,138,204 (GRCm39)	D766G	probably benign	Het
Hsd17b12	C	T	2: 93,864,303 (GRCm39)	R268Q	probably benign	Het
Htt	T	C	5: 34,961,875 (GRCm39)	S287P	probably benign	Het
Icam5	A	G	9: 20,947,954 (GRCm39)	I617M	probably benign	Het
Ip6k3	T	C	17: 27,376,516 (GRCm39)	Y65C	probably damaging	Het
Kif15	A	C	9: 122,817,026 (GRCm39)	Q542P	probably damaging	Het
Kit	G	T	5: 75,808,487 (GRCm39)	A744S	probably benign	Het
Kit	C	T	5: 75,808,488 (GRCm39)	A744V	probably null	Het
Lonp1	A	G	17: 56,933,488 (GRCm39)	I129T	possibly damaging	Het
Ltbp4	C	T	7: 27,027,203 (GRCm39)	R389Q	possibly damaging	Het
Map3k21	A	T	8: 126,668,593 (GRCm39)	K726N	probably benign	Het
Mcpt8	A	T	14: 56,321,398 (GRCm39)	I22K	probably damaging	Het
Npb	G	A	11: 120,499,728 (GRCm39)	V103I	possibly damaging	Het
Or13a22	T	C	7: 140,072,764 (GRCm39)	M71T	probably benign	Het
Or2y3	G	A	17: 38,392,903 (GRCm39)		probably null	Het
Plin2	G	T	4: 86,575,381 (GRCm39)	Y389*	probably null	Het
Pnpla6	G	T	8: 3,584,670 (GRCm39)	G763C	probably null	Het
Pnpla7	A	G	2: 24,932,150 (GRCm39)	D935G	probably damaging	Het
Prr29	A	G	11: 106,265,711 (GRCm39)	S10G	probably benign	Het
Pthlh	A	T	6: 147,164,789 (GRCm39)	V27E	probably damaging	Het
Robo4	CGG	CG	9: 37,322,786 (GRCm39)		probably null	Het
Serpina12	G	A	12: 104,004,242 (GRCm39)	T130I	probably benign	Het
Slc6a18	A	G	13: 73,825,921 (GRCm39)	F43S	probably damaging	Het
Stx6	C	T	1: 155,034,654 (GRCm39)	P6S	probably damaging	Het
Togaram1	G	T	12: 65,013,118 (GRCm39)	R123L	probably damaging	Het
Trappc9	G	A	15: 72,897,816 (GRCm39)	R377W	probably damaging	Het
Trim9	C	T	12: 70,295,167 (GRCm39)	G648R	probably damaging	Het
Trpm2	T	A	10: 77,747,208 (GRCm39)	N1430I	probably damaging	Het
Trpm6	C	G	19: 18,831,795 (GRCm39)	H1553Q	probably benign	Het
Vav3	G	A	3: 109,535,484 (GRCm39)		probably null	Het
Zfp574	G	T	7: 24,781,026 (GRCm39)	A683S	possibly damaging	Het

Other mutations in Ifi27l2b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00336:Ifi27l2b	APN	12	103,417,476 (GRCm39)	missense	unknown
IGL02746:Ifi27l2b	APN	12	103,417,493 (GRCm39)	missense	unknown
R1562:Ifi27l2b	UTSW	12	103,422,780 (GRCm39)	critical splice acceptor site	probably null
R1780:Ifi27l2b	UTSW	12	103,417,578 (GRCm39)	missense	probably damaging	0.99
R2518:Ifi27l2b	UTSW	12	103,422,083 (GRCm39)	missense	unknown
R3123:Ifi27l2b	UTSW	12	103,417,594 (GRCm39)	missense	unknown
R5591:Ifi27l2b	UTSW	12	103,417,566 (GRCm39)	missense	probably damaging	0.99
R5719:Ifi27l2b	UTSW	12	103,422,046 (GRCm39)	missense	unknown
R7124:Ifi27l2b	UTSW	12	103,417,579 (GRCm39)	missense	probably damaging	0.99
R7753:Ifi27l2b	UTSW	12	103,417,519 (GRCm39)	nonsense	probably null
R7788:Ifi27l2b	UTSW	12	103,423,268 (GRCm39)	splice site	probably null
R8801:Ifi27l2b	UTSW	12	103,423,298 (GRCm39)	missense	unknown
R9099:Ifi27l2b	UTSW	12	103,418,114 (GRCm39)	missense	unknown
R9617:Ifi27l2b	UTSW	12	103,422,683 (GRCm39)	missense	probably damaging	0.99
R9780:Ifi27l2b	UTSW	12	103,417,461 (GRCm39)	missense	unknown
X0026:Ifi27l2b	UTSW	12	103,422,074 (GRCm39)	missense	unknown
Z1176:Ifi27l2b	UTSW	12	103,423,292 (GRCm39)	missense	unknown
Z1177:Ifi27l2b	UTSW	12	103,422,119 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AACTTGGAGGCTCCTGTGTC -3'
(R):5'- AAAGCTCTGTCCTGCATCTC -3'

Sequencing Primer
(F):5'- TTCTGCAGCTCCTGAGGC -3'
(R):5'- AAGCTCTGTCCTGCATCTCACTTATC -3'

Posted On

2015-02-05