Mutagenetix > Incidental Mutation

Incidental Mutation 'R7086:Lnx2'

568474

Institutional Source

Beutler Lab

Gene Symbol

Lnx2

Ensembl Gene

ENSMUSG00000016520

Gene Name

ligand of numb-protein X 2

Synonyms

MMRRC Submission

045180-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.094) question?

Stock #

R7086 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

146953465-147013385 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 146956988 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000016664 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000016664]

AlphaFold

Q91XL2

Predicted Effect

probably null
Transcript: ENSMUST00000016664

SMART Domains

Protein: ENSMUSP00000016664
Gene: ENSMUSG00000016520

Domain	Start	End	E-Value	Type
RING	51	88	2.06e-6	SMART
low complexity region	103	114	N/A	INTRINSIC
PDZ	242	317	2.25e-17	SMART
PDZ	348	421	2.97e-17	SMART
PDZ	474	553	7.37e-13	SMART
PDZ	606	683	1.27e-16	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

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
Adam30	A	G	3: 98,068,635 (GRCm39)	H28R	probably damaging	Het
Adgre4	T	C	17: 56,127,649 (GRCm39)	I563T	probably benign	Het
Ankub1	A	T	3: 57,597,746 (GRCm39)	C75S	probably damaging	Het
Antxrl	G	A	14: 33,787,873 (GRCm39)	V299I	probably benign	Het
Arfgef2	T	A	2: 166,718,536 (GRCm39)	C1442S	probably damaging	Het
Atp13a3	T	C	16: 30,169,881 (GRCm39)	D399G	possibly damaging	Het
Cacna2d1	T	A	5: 16,554,414 (GRCm39)	Y666N	probably damaging	Het
Cenpo	C	T	12: 4,265,307 (GRCm39)	E238K	probably benign	Het
Cfap91	A	T	16: 38,127,219 (GRCm39)	F512L	possibly damaging	Het
Chrng	C	A	1: 87,138,735 (GRCm39)	R455S	probably benign	Het
Cimap1a	A	G	7: 140,429,402 (GRCm39)	H151R	probably benign	Het
Cluh	T	A	11: 74,558,166 (GRCm39)	H1155Q	possibly damaging	Het
Col16a1	G	A	4: 129,946,773 (GRCm39)		probably null	Het
Cpne5	G	A	17: 29,378,051 (GRCm39)	P576L	unknown	Het
Crocc	C	A	4: 140,774,368 (GRCm39)	V144L	possibly damaging	Het
Cubn	A	G	2: 13,324,669 (GRCm39)	V2781A	probably damaging	Het
Cyp8b1	A	G	9: 121,744,355 (GRCm39)	F326L	probably benign	Het
Dclk1	G	A	3: 55,395,333 (GRCm39)		probably null	Het
Dennd2b	A	G	7: 109,124,781 (GRCm39)	I1083T	probably damaging	Het
Dnah7c	A	G	1: 46,789,285 (GRCm39)	R3303G	probably benign	Het
Dnhd1	G	T	7: 105,357,739 (GRCm39)	R3191S	probably benign	Het
Fgfbp3	T	G	19: 36,896,103 (GRCm39)	S172R	possibly damaging	Het
Gpr158	G	A	2: 21,831,386 (GRCm39)	V829I	probably benign	Het
Gtse1	A	G	15: 85,759,750 (GRCm39)	D647G	probably damaging	Het
H2-Q7	T	A	17: 35,658,461 (GRCm39)	V33E	probably damaging	Het
Hydin	A	G	8: 111,326,877 (GRCm39)	T4739A	possibly damaging	Het
Kcnip1	G	T	11: 33,584,629 (GRCm39)	P175T	probably damaging	Het
Klhl10	T	C	11: 100,347,768 (GRCm39)	V608A	probably benign	Het
Klhl2	A	G	8: 65,275,664 (GRCm39)	Y80H	probably damaging	Het
Lst1	G	A	17: 35,404,262 (GRCm39)	H59Y	probably damaging	Het
Mphosph8	G	C	14: 56,905,980 (GRCm39)	V58L	possibly damaging	Het
Mpnd	C	A	17: 56,316,457 (GRCm39)	S45R	possibly damaging	Het
Myh8	A	G	11: 67,183,453 (GRCm39)		probably null	Het
Or12j4	A	G	7: 140,046,341 (GRCm39)	T76A	possibly damaging	Het
Or4c52	A	G	2: 89,845,594 (GRCm39)	I107V	probably benign	Het
Phox2a	A	G	7: 101,467,718 (GRCm39)	Y5C	probably damaging	Het
Pkdrej	A	G	15: 85,704,317 (GRCm39)	S540P	probably damaging	Het
Plcb4	A	G	2: 135,849,767 (GRCm39)	M1133V	probably benign	Het
Plxnc1	T	C	10: 94,667,297 (GRCm39)	M1126V	probably benign	Het
Ppm1l	A	G	3: 69,225,186 (GRCm39)	Y96C	probably damaging	Het
Prpsap1	T	C	11: 116,368,109 (GRCm39)	T234A	probably benign	Het
R3hcc1l	T	C	19: 42,570,409 (GRCm39)	V668A	probably damaging	Het
Rapgef2	A	G	3: 78,993,353 (GRCm39)	S712P	probably benign	Het
Rcc2	T	C	4: 140,435,280 (GRCm39)	C100R	probably benign	Het
Recql4	C	A	15: 76,589,753 (GRCm39)	G764V	unknown	Het
Rlbp1	A	G	7: 79,029,813 (GRCm39)	I140T	possibly damaging	Het
Samsn1	T	C	16: 75,667,794 (GRCm39)	T261A	probably benign	Het
Sgtb	T	C	13: 104,254,924 (GRCm39)	S65P	possibly damaging	Het
Spag9	T	C	11: 93,988,690 (GRCm39)	V920A	probably benign	Het
Spata31	T	A	13: 65,070,043 (GRCm39)	S730R	probably benign	Het
Spta1	C	T	1: 174,027,050 (GRCm39)	A841V	probably damaging	Het
Tnfaip1	T	C	11: 78,416,265 (GRCm39)	S273G	probably benign	Het
Vezf1	T	C	11: 87,969,364 (GRCm39)	V371A	probably benign	Het
Vmn1r67	G	A	7: 10,181,044 (GRCm39)	V103I	possibly damaging	Het
Vmn2r87	G	T	10: 130,333,178 (GRCm39)	T24K	probably benign	Het
Wdr43	G	A	17: 71,923,434 (GRCm39)	G60D	probably benign	Het
Xkr4	G	A	1: 3,287,185 (GRCm39)	T335I	probably damaging	Het
Zdhhc23	A	T	16: 43,791,873 (GRCm39)	I300N	probably damaging	Het
Zfp729b	T	C	13: 67,741,056 (GRCm39)	K403R	probably damaging	Het

Other mutations in Lnx2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02593:Lnx2	APN	5	146,969,825 (GRCm39)	missense	possibly damaging	0.81
IGL02657:Lnx2	APN	5	146,964,984 (GRCm39)	missense	probably damaging	1.00
IGL02820:Lnx2	APN	5	146,978,877 (GRCm39)	missense	probably damaging	0.98
R0051:Lnx2	UTSW	5	146,966,163 (GRCm39)	missense	probably damaging	0.96
R0389:Lnx2	UTSW	5	146,955,850 (GRCm39)	missense	possibly damaging	0.51
R0482:Lnx2	UTSW	5	146,955,771 (GRCm39)	missense	probably damaging	0.99
R1601:Lnx2	UTSW	5	146,970,329 (GRCm39)	missense	probably damaging	0.99
R1604:Lnx2	UTSW	5	146,966,135 (GRCm39)	missense	probably benign	0.02
R1647:Lnx2	UTSW	5	146,964,152 (GRCm39)	missense	probably benign	0.04
R3001:Lnx2	UTSW	5	146,955,825 (GRCm39)	missense	probably benign	0.00
R3002:Lnx2	UTSW	5	146,955,825 (GRCm39)	missense	probably benign	0.00
R4734:Lnx2	UTSW	5	146,965,947 (GRCm39)	missense	probably damaging	1.00
R4960:Lnx2	UTSW	5	146,955,850 (GRCm39)	missense	probably benign	0.09
R5387:Lnx2	UTSW	5	146,964,964 (GRCm39)	missense	probably benign	0.00
R5689:Lnx2	UTSW	5	146,965,961 (GRCm39)	missense	probably damaging	1.00
R5950:Lnx2	UTSW	5	146,961,160 (GRCm39)	critical splice donor site	probably null
R6161:Lnx2	UTSW	5	146,978,836 (GRCm39)	splice site	probably null
R6623:Lnx2	UTSW	5	146,961,297 (GRCm39)	missense	probably damaging	1.00
R7320:Lnx2	UTSW	5	146,956,943 (GRCm39)	missense	possibly damaging	0.71
R7701:Lnx2	UTSW	5	146,961,333 (GRCm39)	missense	probably damaging	1.00
R7887:Lnx2	UTSW	5	146,955,853 (GRCm39)	missense	probably damaging	1.00
R8153:Lnx2	UTSW	5	146,964,906 (GRCm39)	missense	probably benign
R8267:Lnx2	UTSW	5	146,965,901 (GRCm39)	missense	probably damaging	1.00
R8298:Lnx2	UTSW	5	146,961,327 (GRCm39)	missense	probably benign	0.05
R8384:Lnx2	UTSW	5	146,966,138 (GRCm39)	missense	probably benign	0.01
R8446:Lnx2	UTSW	5	146,970,169 (GRCm39)	missense	probably benign
R8971:Lnx2	UTSW	5	146,970,236 (GRCm39)	missense	probably benign
R9378:Lnx2	UTSW	5	146,961,180 (GRCm39)	missense	probably benign	0.16
R9468:Lnx2	UTSW	5	146,979,289 (GRCm39)	start gained	probably benign
R9711:Lnx2	UTSW	5	146,961,376 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCTGCACCGTTGACGAGAAC -3'
(R):5'- AGTCAGAGGGGTTACACTAGC -3'

Sequencing Primer
(F):5'- GACGAGAACGAGACTTACTTTAATC -3'
(R):5'- GGGGTTACACTAGCCTGTTTTTCAC -3'

Posted On

2019-07-31