Mutagenetix > Incidental Mutation

Incidental Mutation 'R9253:Lilrb4b'

701663

Institutional Source

Beutler Lab

Gene Symbol

Lilrb4b

Ensembl Gene

ENSMUSG00000112023

Gene Name

leukocyte immunoglobulin-like receptor, subfamily B, member 4B

Synonyms

gp49, Lilr4b, Gp49a

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.146) question?

Stock #

R9253 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

51356757-51362417 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 51357863 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 186 (V186I)

Ref Sequence

ENSEMBL: ENSMUSP00000099958 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000102894] [ENSMUST00000217706] [ENSMUST00000218123] [ENSMUST00000218704] [ENSMUST00000219661] [ENSMUST00000219696] [ENSMUST00000219960]

AlphaFold

Q61450

Predicted Effect

probably damaging
Transcript: ENSMUST00000102894
AA Change: V186I

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000099958
Gene: ENSMUSG00000112023
AA Change: V186I

Domain	Start	End	E-Value	Type
signal peptide	1	23	N/A	INTRINSIC
SCOP:d1nkr_2	24	118	3e-14	SMART
Blast:IG_like	28	118	5e-49	BLAST
Pfam:Ig_3	123	200	6.5e-8	PFAM
Pfam:Ig_2	123	218	5.9e-8	PFAM
Pfam:ig	127	211	8.4e-9	PFAM
transmembrane domain	239	261	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000217706

Predicted Effect

probably benign
Transcript: ENSMUST00000218123

Predicted Effect

unknown
Transcript: ENSMUST00000218704
AA Change: C59Y

Predicted Effect

possibly damaging
Transcript: ENSMUST00000219661
AA Change: V91I

PolyPhen 2 Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)

Predicted Effect

probably benign
Transcript: ENSMUST00000219696

Predicted Effect

probably benign
Transcript: ENSMUST00000219960

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

100% (63/63)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts19	A	G	18: 59,103,013 (GRCm39)	N685D	probably damaging	Het
Adh4	A	T	3: 138,129,860 (GRCm39)	I229F	probably damaging	Het
Ajm1	T	C	2: 25,467,172 (GRCm39)	H913R	possibly damaging	Het
Aldh3b1	T	A	19: 3,965,315 (GRCm39)	S399C	probably damaging	Het
Arhgef28	C	T	13: 98,124,779 (GRCm39)	G501D	probably benign	Het
Asb1	C	A	1: 91,468,551 (GRCm39)	T6N	unknown	Het
Asb18	C	T	1: 89,882,185 (GRCm39)	V382I	probably benign	Het
AU041133	T	C	10: 81,987,220 (GRCm39)	I291T	probably benign	Het
B4galnt2	C	T	11: 95,759,176 (GRCm39)		silent	Het
Bcl7c	T	C	7: 127,306,403 (GRCm39)		probably benign	Het
Brinp1	T	C	4: 68,711,083 (GRCm39)	N375S	possibly damaging	Het
C6	A	G	15: 4,764,679 (GRCm39)	Q125R	probably benign	Het
Card14	T	C	11: 119,212,759 (GRCm39)	S108P	probably benign	Het
Clec4a2	C	A	6: 123,100,608 (GRCm39)	T21N	probably damaging	Het
Cntnap2	C	T	6: 45,978,112 (GRCm39)	L256F	probably benign	Het
Cobll1	G	A	2: 64,981,503 (GRCm39)	T29I	probably benign	Het
Coq4	A	T	2: 29,685,433 (GRCm39)	D149V	probably damaging	Het
Dync1i1	T	C	6: 5,769,698 (GRCm39)	L91S	probably benign	Het
Fat2	T	A	11: 55,201,397 (GRCm39)	D559V	probably damaging	Het
Gm4779	TGGCAGAGGCAGAGGCAGAGGCAGAGGCAGAGGCAG	TGGCAGAGGCAGAGGCAGAGGCAGAGGCAGAGGCAGAGGCAG	X: 100,836,917 (GRCm39)		probably benign	Het
Gsdmc	A	T	15: 63,676,407 (GRCm39)	V12E	probably damaging	Het
H2-Ab1	T	C	17: 34,486,378 (GRCm39)	S146P	probably damaging	Het
Heatr5b	A	G	17: 79,135,423 (GRCm39)	V236A	probably benign	Het
Hjv	T	C	3: 96,435,710 (GRCm39)	S323P	probably benign	Het
Hmgcr	C	T	13: 96,796,645 (GRCm39)	C215Y	probably damaging	Het
L3mbtl1	G	T	2: 162,789,632 (GRCm39)	A57S	probably benign	Het
Map1a	T	C	2: 121,132,823 (GRCm39)	V1213A	probably benign	Het
Marf1	T	C	16: 13,935,172 (GRCm39)	E1532G	probably damaging	Het
Mcm6	T	C	1: 128,279,264 (GRCm39)	Y174C	probably damaging	Het
Miga2	T	A	2: 30,261,239 (GRCm39)	V178E	probably benign	Het
Myh11	T	A	16: 14,074,359 (GRCm39)	I174F		Het
Ndufv1	G	T	19: 4,059,412 (GRCm39)	A211E	probably damaging	Het
Nicn1	C	T	9: 108,171,708 (GRCm39)	R163C	possibly damaging	Het
Nlgn3	T	C	X: 100,352,390 (GRCm39)	V179A	probably damaging	Het
Nrp1	T	C	8: 129,229,144 (GRCm39)	V874A	possibly damaging	Het
Nsf	C	T	11: 103,804,142 (GRCm39)	G197S	probably null	Het
Or10al2	A	T	17: 37,983,637 (GRCm39)	H241L	probably benign	Het
Or2t26	T	C	11: 49,039,822 (GRCm39)	M246T	probably damaging	Het
Pacs2	A	G	12: 113,014,137 (GRCm39)	D196G	probably benign	Het
Pbxip1	A	G	3: 89,351,012 (GRCm39)	D118G	probably benign	Het
Pcdhb11	A	T	18: 37,554,529 (GRCm39)		probably benign	Het
Pgk2	C	T	17: 40,519,233 (GRCm39)	G65D	probably damaging	Het
Plcd3	T	C	11: 102,970,460 (GRCm39)	D193G	probably benign	Het
Plcl2	T	G	17: 50,915,127 (GRCm39)	M712R	probably damaging	Het
Plxna1	G	A	6: 89,334,522 (GRCm39)	Q36*	probably null	Het
Plxnb2	A	G	15: 89,052,015 (GRCm39)	V68A	probably benign	Het
Polr2b	A	G	5: 77,493,224 (GRCm39)	I1069V	probably benign	Het
Rbfox1	A	G	16: 7,111,973 (GRCm39)	T200A	probably benign	Het
Rspry1	T	A	8: 95,349,621 (GRCm39)	V3D	probably damaging	Het
Serpinb6d	T	C	13: 33,855,205 (GRCm39)	M293T	probably damaging	Het
Slc4a8	A	G	15: 100,680,913 (GRCm39)	R72G	probably benign	Het
Smarca5	A	C	8: 81,446,344 (GRCm39)	L452W	probably damaging	Het
Srcin1	T	C	11: 97,416,377 (GRCm39)	K952E	probably damaging	Het
Synpo2l	G	T	14: 20,716,738 (GRCm39)	Q79K	possibly damaging	Het
Tmem174	T	C	13: 98,773,803 (GRCm39)	E9G	possibly damaging	Het
Tmem270	T	C	5: 134,930,644 (GRCm39)	T206A	probably damaging	Het
Ttn	T	A	2: 76,562,951 (GRCm39)	T28668S	possibly damaging	Het
Vmn1r118	A	T	7: 20,645,817 (GRCm39)	S152R	possibly damaging	Het
Vmn2r25	T	A	6: 123,816,960 (GRCm39)	Q207L	probably damaging	Het
Vmn2r81	T	A	10: 79,129,582 (GRCm39)	S824R	probably damaging	Het
Vps54	G	A	11: 21,258,771 (GRCm39)	V733I	probably benign	Het
Zfp518b	G	T	5: 38,829,601 (GRCm39)	D801E	probably benign	Het
Zgrf1	C	A	3: 127,392,428 (GRCm39)	P1316Q	probably damaging	Het
Zzef1	C	A	11: 72,739,463 (GRCm39)		probably benign	Het

Other mutations in Lilrb4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00323:Lilrb4b	APN	10	51,357,347 (GRCm39)	missense	probably benign	0.00
IGL02457:Lilrb4b	APN	10	51,357,334 (GRCm39)	missense	probably benign	0.04
IGL03221:Lilrb4b	APN	10	51,357,524 (GRCm39)	splice site	probably benign
IGL03396:Lilrb4b	APN	10	51,357,253 (GRCm39)	missense	possibly damaging	0.71
R0145:Lilrb4b	UTSW	10	51,360,614 (GRCm39)	missense	probably benign	0.00
R0336:Lilrb4b	UTSW	10	51,357,389 (GRCm39)	missense	probably benign	0.28
R1313:Lilrb4b	UTSW	10	51,356,832 (GRCm39)	missense	probably benign	0.25
R1543:Lilrb4b	UTSW	10	51,357,517 (GRCm39)	missense	probably damaging	0.98
R1984:Lilrb4b	UTSW	10	51,357,831 (GRCm39)	missense	possibly damaging	0.68
R1985:Lilrb4b	UTSW	10	51,357,831 (GRCm39)	missense	possibly damaging	0.68
R2243:Lilrb4b	UTSW	10	51,357,704 (GRCm39)	missense	possibly damaging	0.88
R4094:Lilrb4b	UTSW	10	51,357,506 (GRCm39)	missense	probably damaging	0.99
R4887:Lilrb4b	UTSW	10	51,360,616 (GRCm39)	missense	possibly damaging	0.81
R5588:Lilrb4b	UTSW	10	51,357,422 (GRCm39)	missense	probably benign
R6404:Lilrb4b	UTSW	10	51,361,825 (GRCm39)	missense	probably damaging	0.99
R8347:Lilrb4b	UTSW	10	51,357,850 (GRCm39)	missense	probably damaging	1.00
R9158:Lilrb4b	UTSW	10	51,357,829 (GRCm39)	missense	possibly damaging	0.65
R9301:Lilrb4b	UTSW	10	51,356,801 (GRCm39)	start gained	probably benign
R9400:Lilrb4b	UTSW	10	51,357,319 (GRCm39)	missense	probably benign	0.12
R9673:Lilrb4b	UTSW	10	51,357,753 (GRCm39)	missense	probably benign	0.00
Z1177:Lilrb4b	UTSW	10	51,357,445 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCCAGCTCTAATGTGACCTCTG -3'
(R):5'- GCAACTCCTGTATCAAGGGGTG -3'

Sequencing Primer
(F):5'- AATGTGACCTCTGGAGTTTCC -3'
(R):5'- AACTCCTGTATCAAGGGGTGAATGTC -3'

Posted On

2022-03-25