Mutagenetix > Incidental Mutations

Incidental Mutation 'R4952:Birc2'

382066

Institutional Source

Beutler Lab

Gene Symbol

Birc2

Ensembl Gene

ENSMUSG00000057367

Gene Name

baculoviral IAP repeat-containing 2

Synonyms

cIAP-1, Api1, HIAP1, IAP1, MIAP1, mcIAP1, MIHB, cIAP1

MMRRC Submission

042549-MU

Accession Numbers

Genbank: NM_007465.2; Ensembl: ENSMUST00000074246

Is this an essential gene?

Probably essential (E-score: 0.841) question?

Stock #

R4952 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

7818227-7837064 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 7836740 bp

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 109 (I109V)

Ref Sequence

ENSEMBL: ENSMUSP00000062610 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054878] [ENSMUST00000074246] [ENSMUST00000190341]

Predicted Effect

probably damaging
Transcript: ENSMUST00000054878
AA Change: I109V

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000062610
Gene: ENSMUSG00000057367
AA Change: I109V

Domain	Start	End	E-Value	Type
transmembrane domain	67	86	N/A	INTRINSIC
transmembrane domain	93	115	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000074246

SMART Domains

Protein: ENSMUSP00000091422
Gene: ENSMUSG00000057367

Domain	Start	End	E-Value	Type
BIR	44	115	4.06e-33	SMART
BIR	175	245	4.25e-36	SMART
BIR	260	331	2.24e-35	SMART
low complexity region	432	446	N/A	INTRINSIC
CARD	447	535	1.64e-20	SMART
low complexity region	552	563	N/A	INTRINSIC
RING	565	599	1.65e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000189935

Predicted Effect

probably benign
Transcript: ENSMUST00000190341

SMART Domains

Protein: ENSMUSP00000140049
Gene: ENSMUSG00000057367

Domain	Start	End	E-Value	Type
BIR	44	115	4.06e-33	SMART
BIR	175	245	4.25e-36	SMART
BIR	260	331	2.24e-35	SMART
low complexity region	432	446	N/A	INTRINSIC
CARD	447	535	1.64e-20	SMART
low complexity region	552	563	N/A	INTRINSIC
RING	565	599	1.65e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191248

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.0%
3x: 98.3%
10x: 96.5%
20x: 93.0%

Validation Efficiency

99% (93/94)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of a family of proteins that inhibits apoptosis by binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2, probably by interfering with activation of ICE-like proteases. This encoded protein inhibits apoptosis induced by serum deprivation and menadione, a potent inducer of free radicals. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
PHENOTYPE: Homozygous null mice showed a modest reduction in the number of lymphocytes. Mice homozygous for a knock-in allele exhibit increased T cell poliferation and IFNG secretion in response to anti-CD3 stimulation. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted, knock-out(2) Gene trapped(2)

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930522L14Rik	A	G	5: 109,739,197		probably null	Het
4933421I07Rik	T	C	7: 42,447,659	Y76C	possibly damaging	Het
Adcy4	C	T	14: 55,779,029	D322N	probably damaging	Het
Ak9	A	G	10: 41,420,589	M1444V	probably benign	Het
Amfr	A	G	8: 93,973,159		probably benign	Het
Ankef1	A	G	2: 136,550,529	E546G	probably damaging	Het
Ankrd24	A	G	10: 81,647,148	M977V	probably benign	Het
Ap3m1	A	T	14: 21,040,066	S5T	probably benign	Het
Aqr	C	A	2: 114,109,937	D1243Y	probably damaging	Het
Arhgef2	T	C	3: 88,642,462	L591P	probably damaging	Het
Arid4a	C	A	12: 71,023,525	T70K	possibly damaging	Het
Asphd1	C	T	7: 126,948,685	A149T	probably benign	Het
Avpr1a	T	A	10: 122,449,754	M317K	probably damaging	Het
Catsperd	A	G	17: 56,632,303	Y44C	probably damaging	Het
Ccdc114	A	C	7: 45,942,191	E293A	probably damaging	Het
Crygb	T	G	1: 65,082,109	S20R	probably benign	Het
Cyp3a25	T	C	5: 145,991,524	N237S	probably benign	Het
Dkk3	C	T	7: 112,118,351	A304T	probably benign	Het
Dst	T	C	1: 34,271,422	L4101S	probably damaging	Het
Dysf	A	G	6: 84,149,986	N1407S	possibly damaging	Het
Epb41	A	G	4: 132,000,270	V265A	probably damaging	Het
Faim2	C	T	15: 99,521,228	E75K	possibly damaging	Het
Fbn1	T	A	2: 125,317,534	D2208V	probably damaging	Het
Fbxo28	A	G	1: 182,326,385	S129P	probably damaging	Het
Fbxw14	T	A	9: 109,276,201	I299L	probably benign	Het
Fras1	C	T	5: 96,647,498	A1050V	probably benign	Het
Fyb	C	A	15: 6,638,811	T495K	probably damaging	Het
Ghdc	A	T	11: 100,769,151	W257R	probably damaging	Het
Gm10719	T	C	9: 3,018,962	L69S	probably benign	Het
Gm11492	A	G	11: 87,567,772	N324S	probably benign	Het
Gm12250	G	T	11: 58,188,384		noncoding transcript	Het
Gm4846	A	T	1: 166,483,934	F452Y	probably damaging	Het
Gm8773	T	A	5: 5,575,387	F28I	probably benign	Het
Gm884	T	C	11: 103,614,207	T2312A	possibly damaging	Het
Gpbp1	T	C	13: 111,440,750	D202G	probably damaging	Het
Gpd2	C	A	2: 57,307,013	Y193*	probably null	Het
Grhl2	G	T	15: 37,287,249	R229L	probably benign	Het
Gtf2a1	A	G	12: 91,575,749	F59L	possibly damaging	Het
Heatr1	G	T	13: 12,410,599	W640L	probably benign	Het
Kalrn	A	T	16: 34,357,415		probably null	Het
Keap1	T	C	9: 21,237,286	T142A	probably damaging	Het
Kpna2	G	A	11: 106,991,235	T255M	probably damaging	Het
Kpna3	A	G	14: 61,370,389	C456R	probably damaging	Het
Lama1	G	A	17: 67,767,566		probably null	Het
Mag	C	A	7: 30,909,156	E178*	probably null	Het
Map3k13	A	G	16: 21,911,019	I467V	probably benign	Het
Mga	A	G	2: 119,903,301	E210G	probably damaging	Het
Msi2	C	T	11: 88,366,784		probably null	Het
Naa16	A	T	14: 79,345,085	D521E	probably damaging	Het
Nav2	C	T	7: 49,304,540		probably benign	Het
Nek10	T	A	14: 14,860,986	L513M	possibly damaging	Het
Nek5	T	C	8: 22,096,799	K332R	probably benign	Het
Nek5	T	A	8: 22,079,088	I573L	probably benign	Het
Ntn1	CCTTCTTCT	CCTTCT	11: 68,213,026		probably benign	Het
Olfr111	A	T	17: 37,530,750	T258S	possibly damaging	Het
Olfr263	G	A	13: 21,133,344	V190I	probably benign	Het
Olfr773	T	A	10: 129,186,597	T275S	probably benign	Het
Olfr875	T	A	9: 37,773,064	M135K	probably damaging	Het
Orai1	T	G	5: 123,029,250	V162G	probably damaging	Het
P2rx6	T	C	16: 17,567,444	S134P	probably damaging	Het
Pappa2	G	A	1: 158,857,136	T811I	probably null	Het
Pcdhga10	T	C	18: 37,747,160		probably benign	Het
Pex16	C	T	2: 92,379,060	R241*	probably null	Het
Plxnb1	T	C	9: 109,114,836	F1969L	probably damaging	Het
Postn	A	G	3: 54,390,315		probably benign	Het
Prdm15	A	T	16: 97,806,077	I752N	probably damaging	Het
Rasgef1c	A	T	11: 49,979,512	K468M	probably damaging	Het
Rbfox1	A	G	16: 7,277,088	S111G	probably benign	Het
Rbm28	T	C	6: 29,138,598	D405G	probably damaging	Het
Rell1	A	G	5: 63,939,667		probably benign	Het
Rfx3	A	G	19: 27,830,672	S224P	probably damaging	Het
Scarb2	A	T	5: 92,454,777	I260K	probably damaging	Het
Slc15a4	A	G	5: 127,603,837	F72L	probably damaging	Het
Spg7	C	A	8: 123,090,171	R534S	probably damaging	Het
Stoml2	T	C	4: 43,029,589	T164A	probably benign	Het
Syt11	C	T	3: 88,762,283	G101S	possibly damaging	Het
Traj12	A	G	14: 54,206,556		probably benign	Het
Traj7	A	T	14: 54,211,524		probably benign	Het
Tysnd1	C	T	10: 61,702,076	T175I	possibly damaging	Het
Usp48	T	G	4: 137,606,693	Y139*	probably null	Het
Vmn2r72	A	G	7: 85,751,109	L244P	probably benign	Het
Wasf1	C	A	10: 40,936,190	P325Q	unknown	Het
Zc3h18	T	A	8: 122,410,900		probably benign	Het
Zfp712	A	G	13: 67,040,841	S541P	possibly damaging	Het

Other mutations in Birc2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00909:Birc2	APN	9	7833665	missense	probably damaging	1.00
IGL00972:Birc2	APN	9	7833715	missense	probably benign	0.36
IGL02888:Birc2	APN	9	7819558	missense	probably benign	0.22
IGL03399:Birc2	APN	9	7821087	missense	probably damaging	1.00
1mM(1):Birc2	UTSW	9	7819408	missense	probably damaging	0.98
R0409:Birc2	UTSW	9	7819384	missense	possibly damaging	0.61
R1617:Birc2	UTSW	9	7826951	missense	possibly damaging	0.66
R1864:Birc2	UTSW	9	7819517	missense	probably benign	0.06
R2156:Birc2	UTSW	9	7826938	missense	probably damaging	1.00
R2519:Birc2	UTSW	9	7821179	missense	possibly damaging	0.46
R2867:Birc2	UTSW	9	7834477	start codon destroyed	probably null	0.08
R2867:Birc2	UTSW	9	7834477	start codon destroyed	probably null	0.08
R4028:Birc2	UTSW	9	7819351	missense	probably benign	0.01
R4243:Birc2	UTSW	9	7834385	missense	probably benign	0.00
R4250:Birc2	UTSW	9	7818935	missense	probably benign	0.00
R4584:Birc2	UTSW	9	7833674	missense	probably damaging	1.00
R5017:Birc2	UTSW	9	7818885	nonsense	probably null
R6163:Birc2	UTSW	9	7819035	missense	probably benign	0.15
R6789:Birc2	UTSW	9	7836965	intron	probably benign
R6795:Birc2	UTSW	9	7833872	missense	possibly damaging	0.81
R6941:Birc2	UTSW	9	7819468	missense	probably benign	0.00
R7105:Birc2	UTSW	9	7819441	missense	probably damaging	1.00
R7135:Birc2	UTSW	9	7818761	missense	probably damaging	1.00
R7233:Birc2	UTSW	9	7827008	missense	probably damaging	1.00
R7460:Birc2	UTSW	9	7818761	missense	probably damaging	1.00
R7517:Birc2	UTSW	9	7819423	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ATGGAGAACACCTTTCCCAG -3'
(R):5'- TCAACAATCAGGCGCCTCTG -3'

Sequencing Primer
(F):5'- TGGAGAACACCTTTCCCAGTTAAAC -3'
(R):5'- TGAGTGCGGCTGCCTTC -3'

Posted On

2016-04-27