Mutagenetix > Incidental Mutation

Incidental Mutation 'R4844:Islr2'

372055

Institutional Source

Beutler Lab

Gene Symbol

Islr2

Ensembl Gene

ENSMUSG00000051243

Gene Name

immunoglobulin superfamily containing leucine-rich repeat 2

Synonyms

mbu-3, B930052A04Rik, Linx

MMRRC Submission

042457-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4844 (G1)

Quality Score

147

Status

Validated

Chromosome

Chromosomal Location

58103580-58111602 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

C to T at 58115517 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000150316 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000114144] [ENSMUST00000214649] [ENSMUST00000217578]

AlphaFold

Q5RKR3

Predicted Effect

probably benign
Transcript: ENSMUST00000114144

SMART Domains

Protein: ENSMUSP00000109781
Gene: ENSMUSG00000051243

Domain	Start	End	E-Value	Type
LRRNT	19	55	1.1e-1	SMART
LRR	49	73	8.24e0	SMART
LRR	98	121	1.91e1	SMART
LRR	122	145	3.07e-1	SMART
LRR_TYP	146	169	1.58e-3	SMART
LRRCT	181	231	2.36e-12	SMART
IG	245	374	2.99e-2	SMART
low complexity region	510	535	N/A	INTRINSIC
transmembrane domain	591	613	N/A	INTRINSIC
low complexity region	662	682	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000178259

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000179787

Predicted Effect

probably benign
Transcript: ENSMUST00000214649

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000217158

Predicted Effect

probably benign
Transcript: ENSMUST00000217578

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.7%
20x: 93.6%

Validation Efficiency

97% (68/70)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit perinatal lethality, absent tail pinch response, and defective peroneal and tibial nerve morphology and branch extension. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc9	T	C	6: 142,634,824 (GRCm39)	T147A	probably benign	Het
Acvrl1	T	C	15: 101,033,409 (GRCm39)	S99P	probably damaging	Het
Adamts3	T	A	5: 89,825,675 (GRCm39)	S1055C	probably damaging	Het
Aftph	T	C	11: 20,658,667 (GRCm39)		probably benign	Het
Aldh1a1	A	G	19: 20,611,764 (GRCm39)	K363E	probably benign	Het
Astn2	A	G	4: 65,562,967 (GRCm39)	V886A	possibly damaging	Het
Atad5	G	A	11: 80,005,137 (GRCm39)		probably null	Het
C9orf72	A	G	4: 35,213,565 (GRCm39)	V31A	possibly damaging	Het
Ccnf	G	T	17: 24,449,331 (GRCm39)	Y482*	probably null	Het
Cfap97	A	G	8: 46,622,712 (GRCm39)	D34G	possibly damaging	Het
Chst11	G	T	10: 83,026,923 (GRCm39)	E117*	probably null	Het
Cobl	A	T	11: 12,204,740 (GRCm39)	L572Q	probably benign	Het
Coch	G	A	12: 51,649,477 (GRCm39)	G263S	probably damaging	Het
Coq4	T	C	2: 29,686,026 (GRCm39)	I205T	possibly damaging	Het
Cyp3a13	A	T	5: 137,915,813 (GRCm39)	I62K	probably benign	Het
Cyp7a1	A	G	4: 6,273,655 (GRCm39)	S84P	probably damaging	Het
Dennd10	GTCT	GT	19: 60,823,435 (GRCm39)		probably null	Het
G6pc3	G	A	11: 102,084,057 (GRCm39)		probably null	Het
Gm10576	T	C	4: 100,911,707 (GRCm39)		noncoding transcript	Het
Gm17511	G	A	7: 126,885,454 (GRCm39)		noncoding transcript	Het
Gnat2	T	C	3: 108,002,831 (GRCm39)	S80P	probably damaging	Het
Gpaa1	C	T	15: 76,216,508 (GRCm39)		probably benign	Het
Gpr107	T	A	2: 31,078,686 (GRCm39)		probably null	Het
Hormad1	T	C	3: 95,478,242 (GRCm39)	Y103H	probably damaging	Het
Ighv14-1	T	G	12: 113,895,622 (GRCm39)	Q101P	probably damaging	Het
Igsf9	A	G	1: 172,324,737 (GRCm39)	D885G	probably benign	Het
Il15ra	G	A	2: 11,723,082 (GRCm39)		probably benign	Het
Jak3	A	T	8: 72,134,299 (GRCm39)	N467I	possibly damaging	Het
Jarid2	T	C	13: 45,067,248 (GRCm39)	V1023A	probably damaging	Het
Kcnn2	A	T	18: 45,816,187 (GRCm39)	T333S	possibly damaging	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Kmt2c	T	C	5: 25,520,111 (GRCm39)	T2000A	probably benign	Het
Lpxn	A	G	19: 12,810,536 (GRCm39)	T327A	probably damaging	Het
Mxra8	A	G	4: 155,927,151 (GRCm39)	T362A	probably benign	Het
Myh6	A	G	14: 55,184,651 (GRCm39)	I1560T	possibly damaging	Het
Ndufv1	A	G	19: 4,062,574 (GRCm39)	S17P	probably benign	Het
Nwd1	A	T	8: 73,393,742 (GRCm39)	H335L	probably damaging	Het
Or1a1	A	G	11: 74,086,902 (GRCm39)	D191G	probably damaging	Het
Or2f1b	T	A	6: 42,739,394 (GRCm39)	M136K	probably damaging	Het
Otop2	G	A	11: 115,214,201 (GRCm39)		probably null	Het
Pwwp2b	C	A	7: 138,835,502 (GRCm39)	S314R	probably benign	Het
Rfx7	C	T	9: 72,500,524 (GRCm39)	Q95*	probably null	Het
Serpine2	A	T	1: 79,777,241 (GRCm39)	L192*	probably null	Het
Smpdl3b	T	C	4: 132,465,369 (GRCm39)	I322M	probably damaging	Het
Spata31d1b	C	T	13: 59,866,169 (GRCm39)	R1106C	possibly damaging	Het
Sprr2k	T	G	3: 92,336,732 (GRCm39)		probably null	Het
St8sia1	T	A	6: 142,774,996 (GRCm39)	R194S	possibly damaging	Het
Sv2a	T	A	3: 96,095,695 (GRCm39)	V337D	probably damaging	Het
Tars1	G	A	15: 11,385,281 (GRCm39)	R637W	possibly damaging	Het
Tcp11l2	G	T	10: 84,449,555 (GRCm39)	V507L	probably benign	Het
Tpr	T	C	1: 150,321,630 (GRCm39)	Y2262H	possibly damaging	Het
Vars1	A	G	17: 35,230,588 (GRCm39)	E529G	probably damaging	Het
Vash2	C	T	1: 190,710,691 (GRCm39)		probably benign	Het
Vmn1r194	T	C	13: 22,429,223 (GRCm39)	V280A	probably benign	Het
Vti1a	A	G	19: 55,380,297 (GRCm39)	T142A	probably damaging	Het
Zfp111	C	T	7: 23,898,801 (GRCm39)	C270Y	probably damaging	Het
Zfp518a	T	A	19: 40,903,340 (GRCm39)	Y1090N	probably damaging	Het
Zfp616	A	T	11: 73,975,225 (GRCm39)	Y498F	probably benign	Het

Other mutations in Islr2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00834:Islr2	APN	9	58,107,069 (GRCm39)	missense	probably benign	0.03
IGL01444:Islr2	APN	9	58,105,661 (GRCm39)	missense	probably damaging	1.00
R0346:Islr2	UTSW	9	58,105,626 (GRCm39)	nonsense	probably null
R0360:Islr2	UTSW	9	58,107,027 (GRCm39)	missense	possibly damaging	0.82
R0364:Islr2	UTSW	9	58,107,027 (GRCm39)	missense	possibly damaging	0.82
R0528:Islr2	UTSW	9	58,106,645 (GRCm39)	missense	probably damaging	0.97
R0693:Islr2	UTSW	9	58,107,027 (GRCm39)	missense	possibly damaging	0.82
R1854:Islr2	UTSW	9	58,107,099 (GRCm39)	missense	probably damaging	0.97
R2893:Islr2	UTSW	9	58,105,149 (GRCm39)	missense	probably damaging	1.00
R3747:Islr2	UTSW	9	58,106,925 (GRCm39)	missense	probably benign	0.00
R3914:Islr2	UTSW	9	58,105,666 (GRCm39)	nonsense	probably null
R4176:Islr2	UTSW	9	58,107,183 (GRCm39)	missense	probably damaging	1.00
R4212:Islr2	UTSW	9	58,106,603 (GRCm39)	missense	probably damaging	1.00
R5303:Islr2	UTSW	9	58,115,558 (GRCm39)	unclassified	probably benign
R5636:Islr2	UTSW	9	58,108,584 (GRCm39)	missense	probably benign	0.03
R5787:Islr2	UTSW	9	58,105,637 (GRCm39)	missense	probably damaging	0.97
R5883:Islr2	UTSW	9	58,105,998 (GRCm39)	missense	probably benign	0.01
R6406:Islr2	UTSW	9	58,107,263 (GRCm39)	missense	probably benign
R7105:Islr2	UTSW	9	58,105,097 (GRCm39)	missense	probably damaging	1.00
R7130:Islr2	UTSW	9	58,105,575 (GRCm39)	missense	probably damaging	1.00
R7316:Islr2	UTSW	9	58,105,250 (GRCm39)	missense	probably damaging	0.99
X0026:Islr2	UTSW	9	58,105,569 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCTACTCTCTTGACCCAGAAC -3'
(R):5'- TCACGTATGGGTTAATCCGGC -3'

Sequencing Primer
(F):5'- AAGGGTATGCATATCCGC -3'
(R):5'- TAATCCGGCCATGAGCTCTGTAG -3'

Posted On

2016-03-01