Mutagenetix > Incidental Mutation

Incidental Mutation 'FR4340:Lrit3'

511103

Institutional Source

Beutler Lab

Gene Symbol

Lrit3

Ensembl Gene

ENSMUSG00000093865

Gene Name

leucine-rich repeat, immunoglobulin-like and transmembrane domains 3

Synonyms

LOC242235

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

FR4340 ()

Quality Score

203.468

Status

Not validated

Chromosome

Chromosomal Location

129787881-129804030 bp(-) (GRCm38)

Type of Mutation

small insertion (1 aa in frame mutation)

DNA Base Change (assembly)

CTG to CTGTTG at 129788808 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000140184 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000179187] [ENSMUST00000185462]

AlphaFold

W8DXL4

Predicted Effect

probably benign
Transcript: ENSMUST00000179187

SMART Domains

Protein: ENSMUSP00000136912
Gene: ENSMUSG00000093865

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
LRRNT	20	61	2.7e-1	SMART
LRR	80	103	6.96e0	SMART
LRR	104	127	3.27e1	SMART
LRR_TYP	128	151	4.47e-3	SMART
LRR_TYP	152	175	7.37e-4	SMART
LRRCT	201	252	4.65e-2	SMART
Blast:IG	260	297	9e-13	BLAST
low complexity region	298	311	N/A	INTRINSIC
FN3	364	443	1.85e0	SMART
transmembrane domain	462	484	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000185462

SMART Domains

Protein: ENSMUSP00000140184
Gene: ENSMUSG00000093865

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
LRRNT	20	61	1.3e-3	SMART
LRR	80	103	2.9e-2	SMART
LRR	104	127	1.4e-1	SMART
LRR_TYP	128	151	1.9e-5	SMART
LRR_TYP	152	175	3.2e-6	SMART
LRRCT	201	252	2.3e-4	SMART
IGc2	266	335	4.7e-11	SMART
low complexity region	340	352	N/A	INTRINSIC
low complexity region	362	376	N/A	INTRINSIC
low complexity region	408	432	N/A	INTRINSIC
FN3	485	564	9e-3	SMART
transmembrane domain	583	605	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000188978

Coding Region Coverage

1x: 99.7%
3x: 99.4%
10x: 97.8%
20x: 94.3%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that has a fibronectin type III domain and a C-terminal transmembrane domain, as well as a leucine-rich repeat domain and immunoglobulin-like domain near the N-terminus. The encoded protein may regulate fibroblast growth factor receptors and affect the modification of these receptors, which are glycosylated differently in the Golgi and endoplasmic reticulum. Mutations in this gene are associated with congenital stationary night blindness, type 1F. [provided by RefSeq, May 2013]
PHENOTYPE: Mice homozygous for a targeted allele show a selective absence of the ERG b-wave with a normal a-wave component under scotopic conditions, as well as variable ERG responses with larger a-wave amplitudes, shorter b-wave amplitudes, and longer implicit times of both waves under photopic conditions. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 115 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	AACC	A	7: 40,993,055 (GRCm38)		probably benign	Het
4930548H24Rik	GAGAAG	GAG	5: 31,487,373 (GRCm38)		probably benign	Het
4930578G10Rik	G	T	4: 42,761,098 (GRCm38)		probably benign	Het
4932438A13Rik	TATTATTAT	TATTATTATTATTATCATTATTAT	3: 37,050,752 (GRCm38)		probably benign	Het
7530416G11Rik	T	A	15: 85,494,307 (GRCm38)	E45V	unknown	Homo
A530032D15Rik	A	C	1: 85,109,351 (GRCm38)	N6K	probably damaging	Het
A530064D06Rik	GTAGGAAGCTTAG	GTAG	17: 48,163,381 (GRCm38)		probably benign	Homo
Arpc1b	CC	CCTGGTC	5: 145,126,792 (GRCm38)		probably null	Het
Arrb2	C	T	11: 70,438,671 (GRCm38)	T269M	probably damaging	Homo
BC051142	GC	GCAAC	17: 34,460,077 (GRCm38)		probably benign	Het
BC051142	GCA	GCATCA	17: 34,460,068 (GRCm38)		probably benign	Het
BC051142	CAG	CAGTAG	17: 34,460,060 (GRCm38)		probably null	Het
Bcas3	G	A	11: 85,509,497 (GRCm38)	V431I	probably benign	Homo
Blm	TCCTCCTCCTCCTCCTCCTCCTCC	TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC	7: 80,512,910 (GRCm38)		probably benign	Het
Blm	TCCTCCTCCTCCTCCTCCTCCTCC	TCCTCCTCCTCCGCCTCCTCCTCCTCCTCCTCCTCC	7: 80,512,907 (GRCm38)		probably benign	Het
Blm	ACCT	ACCTGCCT	7: 80,463,767 (GRCm38)		probably benign	Het
Cacna1a	ACC	ACCGCC	8: 84,638,723 (GRCm38)		probably benign	Het
Cacna1f	AGG	AGGCGG	X: 7,620,067 (GRCm38)		probably benign	Het
Calhm1	CTCTGTGGCTGTGGCTGTGGCTGTG	CTCTGTGGCTGTGTCTGTGGCTGTGGCTGTGGCTGTG	19: 47,141,251 (GRCm38)		probably benign	Het
Casz1	ACCACAGCCACAGCCACAGCCAC	ACCACAGCCACAGCCAC	4: 148,952,302 (GRCm38)		probably benign	Homo
Cd164	G	T	10: 41,521,926 (GRCm38)	A59S	probably benign	Het
Cd22	C	T	7: 30,878,082 (GRCm38)	R2H	possibly damaging	Homo
Cd80	GAA	GAAAAA	16: 38,486,316 (GRCm38)		probably benign	Homo
Col2a1	C	A	15: 97,988,981 (GRCm38)		probably null	Het
Col6a5	A	T	9: 105,934,174 (GRCm38)	N715K	unknown	Homo
Crygc	A	T	1: 65,071,663 (GRCm38)	F155Y	probably benign	Het
Cul9	TCC	TCCCCC	17: 46,500,853 (GRCm38)		probably benign	Het
Cyp2d11	T	TGGGA	15: 82,390,022 (GRCm38)		probably null	Homo
D230025D16Rik	G	A	8: 105,241,098 (GRCm38)	G207E	probably benign	Homo
Dbr1	AGG	AGGAGGCGG	9: 99,583,701 (GRCm38)		probably benign	Het
Dnah12	G	T	14: 26,849,385 (GRCm38)	G2817V	probably damaging	Homo
Dnah8	ACACTGCC	AC	17: 30,635,463 (GRCm38)		probably benign	Het
Dthd1	C	CTTA	5: 62,843,026 (GRCm38)		probably benign	Homo
Fam166b	CAGAG	CAG	4: 43,427,384 (GRCm38)		probably null	Homo
Fam45a	CT	CTTTT	19: 60,814,621 (GRCm38)		probably benign	Homo
Frem3	CT	CTTTT	8: 80,615,241 (GRCm38)		probably benign	Homo
Frmpd2	G	T	14: 33,511,021 (GRCm38)	L399F	probably damaging	Homo
G530012D18Rik	CACACAGAGAGAGAGAGAGAGAGAGA	CA	1: 85,577,152 (GRCm38)		probably benign	Het
Gbp2b	A	G	3: 142,603,652 (GRCm38)	I175V	probably benign	Het
Gm14393	T	C	2: 175,061,634 (GRCm38)	E160G	possibly damaging	Het
Gm16519	A	AGAAC	17: 70,929,338 (GRCm38)		probably null	Homo
Gm4340	CAG	CAGTAG	10: 104,196,075 (GRCm38)		probably null	Het
Gm4340	GCAG	GCAACAG	10: 104,196,098 (GRCm38)		probably benign	Het
Gm4340	CAGAAG	CAGAAGAAG	10: 104,196,099 (GRCm38)		probably benign	Het
Gpatch11	AGGAAG	AGGAAGGGGAAG	17: 78,842,174 (GRCm38)		probably benign	Het
H2-Q4	G	A	17: 35,380,405 (GRCm38)	D155N	probably damaging	Het
Ifi208	ATGGTG	ATG	1: 173,677,698 (GRCm38)		probably benign	Homo
Ighv5-9	C	T	12: 113,661,877 (GRCm38)	S82N	probably benign	Homo
Ipo9	TCC	TCCCCC	1: 135,386,269 (GRCm38)		probably benign	Het
Ipo9	CTC	CTCTTC	1: 135,386,271 (GRCm38)		probably benign	Het
Isg20l2	AAG	AAGTAG	3: 87,931,712 (GRCm38)		probably null	Het
Kmt2b	TCCTCC	TCCTCCCCCTCC	7: 30,586,363 (GRCm38)		probably benign	Het
Kmt2b	TCCTCC	TCCTCCCCCTCC	7: 30,586,369 (GRCm38)		probably benign	Het
Kmt2b	TCCTCC	TCCTCCCCCTCC	7: 30,586,375 (GRCm38)		probably benign	Het
Krt10	CCTCCT	CCTCCTTCTCCT	11: 99,389,274 (GRCm38)		probably benign	Het
Krt10	ACCG	ACCGCCG	11: 99,386,203 (GRCm38)		probably benign	Homo
Krt10	CAC	CACGAC	11: 99,386,202 (GRCm38)		probably benign	Het
Las1l	TCCTC	TCCTCTACCTC	X: 95,940,622 (GRCm38)		probably benign	Het
Lce1a1	C	T	3: 92,646,844 (GRCm38)	G108S	unknown	Het
Lkaaear1	CCAGCTCCAG	CCAGCTCCAGCTGCAGCTCCAG	2: 181,697,594 (GRCm38)		probably benign	Het
Mamld1	CAG	CAGAAG	X: 71,118,846 (GRCm38)		probably benign	Het
Mapk7	TGCTGGCGCTGGTGCTGGCGCTGG	TGCTGGCGCTGGCGCTGGTGCTGGCGCTGG	11: 61,490,206 (GRCm38)		probably benign	Het
Mast4	TTTT	TTTTATTT	13: 102,734,857 (GRCm38)		probably null	Het
Mast4	GCA	GCAGTGTCA	13: 102,736,317 (GRCm38)		probably benign	Homo
Med12l	AGC	AGCCGC	3: 59,275,985 (GRCm38)		probably benign	Het
Mfsd5	G	A	15: 102,281,161 (GRCm38)	V323I	probably benign	Het
Nacad	GTC	GTCAGGATC	11: 6,599,761 (GRCm38)		probably benign	Het
Naip1	A	C	13: 100,423,076 (GRCm38)	M1140R	probably benign	Het
Nbea	TTTA	T	3: 56,009,212 (GRCm38)		probably benign	Homo
Nefh	ACTTGGCCTCACCTGGGG	ACTTGGCCTCACCTGGGGCCTTGGCCTCACCTGGGG	11: 4,941,033 (GRCm38)		probably benign	Het
Nefh	GCCTCACCTGGGGACTTGGCCTC	GCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC	11: 4,941,038 (GRCm38)		probably benign	Homo
Nefh	CTCACCTGGGGACTTGGCCTC	CTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC	11: 4,941,040 (GRCm38)		probably benign	Homo
Neu1	TCTTCTA	T	17: 34,932,558 (GRCm38)		probably benign	Het
Nutf2	G	T	8: 105,876,570 (GRCm38)	D78Y	probably damaging	Het
Olfr495	G	A	7: 108,395,898 (GRCm38)	M259I	probably benign	Het
Olfr495	A	G	7: 108,395,893 (GRCm38)	T258A	probably benign	Het
Olfr513	AT	ATGATATT	7: 108,754,954 (GRCm38)		probably benign	Homo
Olfr635	TCC	TCCC	7: 103,979,903 (GRCm38)		probably null	Het
Park2	G	A	17: 11,854,763 (GRCm38)	V323M	probably damaging	Homo
Pdik1l	ACCAC	ACCACCCCCAC	4: 134,279,512 (GRCm38)		probably benign	Het
Pik3c2g	AG	AGAGGG	6: 139,635,656 (GRCm38)		probably null	Homo
Plekhs1	TCCAGAC	TCCAGACCTCCCCCCAGAC	19: 56,479,858 (GRCm38)		probably benign	Homo
Prag1	C	CAGT	8: 36,103,886 (GRCm38)		probably benign	Homo
Pramef25	G	A	4: 143,949,742 (GRCm38)	T264M	probably damaging	Het
Raet1d	A	G	10: 22,371,559 (GRCm38)	Q178R	probably benign	Het
Serac1	T	A	17: 6,070,808 (GRCm38)	K70N	probably damaging	Homo
Serpina3i	CGG	CGGTGG	12: 104,265,164 (GRCm38)		probably benign	Het
Sfswap	ACTCAGCCC	ACTCAGCCCCCTCAGCCC	5: 129,569,751 (GRCm38)		probably benign	Het
Six3	CGG	CGGGGG	17: 85,621,356 (GRCm38)		probably benign	Het
Speer4a	C	A	5: 26,036,748 (GRCm38)	E127*	probably null	Het
Sry	GCTGCTGCTGCTG	GCTGCTGCTGCTGCTG	Y: 2,662,824 (GRCm38)		probably benign	Het
St5	CACCACACTGGGGCAGCCCACACTGGGGCAG	CCCCACACTGGGGCAG	7: 109,556,921 (GRCm38)		probably benign	Het
Tbr1	A	C	2: 61,806,347 (GRCm38)		probably benign	Het
Tdpoz2	T	TCC	3: 93,651,615 (GRCm38)		probably null	Homo
Tdpoz4	GAA	GA	3: 93,796,880 (GRCm38)		probably null	Het
Tgoln1	AAG	AAGCCTCAG	6: 72,616,351 (GRCm38)		probably benign	Homo
Tmbim7	C	T	5: 3,670,064 (GRCm38)	R100C	possibly damaging	Het
Tob1	CA	CAGAA	11: 94,214,477 (GRCm38)		probably benign	Het
Tob1	AGC	AGCCGC	11: 94,214,460 (GRCm38)		probably benign	Het
Tob1	AGC	AGCCGC	11: 94,214,454 (GRCm38)		probably benign	Het
Tomm5	GCATCTTCC	GCATCTTCCACATCTTCC	4: 45,107,973 (GRCm38)		probably benign	Het
Triobp	TCGG	TCGGCGG	15: 78,993,390 (GRCm38)		probably benign	Homo
Tsen2	AGG	AGGGGG	6: 115,560,069 (GRCm38)		probably benign	Homo
Tsen2	AGG	AGGGGG	6: 115,560,066 (GRCm38)		probably benign	Homo
Ubtf	TCC	TCCCCC	11: 102,306,950 (GRCm38)		probably benign	Het
Vmn2r87	C	T	10: 130,478,714 (GRCm38)	M334I	probably benign	Homo
Zc3h13	CGGGATGTGCG	CGGGATGTGCGGGATGTGCG	14: 75,323,592 (GRCm38)		probably benign	Homo
Zfp28	G	A	7: 6,394,863 (GRCm38)	G766R	probably damaging	Het
Zfp384	AAGCCCAGGCCCAGGCCCAGGCCCA	AAGCCCAGGCCCAAGCCCAGGCCCAGGCCCAGGCCCA	6: 125,036,463 (GRCm38)		probably benign	Het
Zfp428	G	A	7: 24,515,081 (GRCm38)	D41N	probably damaging	Homo
Zfp598	CCACAGGC	CC	17: 24,679,372 (GRCm38)		probably benign	Het
Zfp598	CCACCA	CCACCAACACCA	17: 24,680,783 (GRCm38)		probably benign	Het
Zfp831	TCC	TCCCCC	2: 174,645,480 (GRCm38)		probably benign	Het
Zfp933	GCTT	GCTTTTCTT	4: 147,825,729 (GRCm38)		probably null	Homo
Zfp936	G	A	7: 43,189,489 (GRCm38)	G127R	possibly damaging	Het

Other mutations in Lrit3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
FR4304:Lrit3	UTSW	3	129,788,819 (GRCm38)	small insertion	probably benign
FR4548:Lrit3	UTSW	3	129,788,816 (GRCm38)	small insertion	probably benign
FR4548:Lrit3	UTSW	3	129,788,813 (GRCm38)	small insertion	probably benign
FR4589:Lrit3	UTSW	3	129,803,913 (GRCm38)	frame shift	probably null
FR4737:Lrit3	UTSW	3	129,803,913 (GRCm38)	frame shift	probably null
FR4737:Lrit3	UTSW	3	129,788,810 (GRCm38)	small insertion	probably benign
FR4737:Lrit3	UTSW	3	129,788,806 (GRCm38)	small insertion	probably benign
FR4976:Lrit3	UTSW	3	129,803,910 (GRCm38)	unclassified	probably benign
R0555:Lrit3	UTSW	3	129,791,296 (GRCm38)	missense	probably damaging	1.00
R0629:Lrit3	UTSW	3	129,788,302 (GRCm38)	missense	probably damaging	1.00
R0631:Lrit3	UTSW	3	129,788,555 (GRCm38)	missense	probably damaging	1.00
R1690:Lrit3	UTSW	3	129,800,745 (GRCm38)	missense	probably damaging	0.99
R1902:Lrit3	UTSW	3	129,791,246 (GRCm38)	missense	probably benign	0.17
R1955:Lrit3	UTSW	3	129,800,481 (GRCm38)	missense	probably benign	0.11
R3155:Lrit3	UTSW	3	129,791,395 (GRCm38)	missense	probably benign	0.00
R4005:Lrit3	UTSW	3	129,791,372 (GRCm38)	missense	probably benign	0.14
R4445:Lrit3	UTSW	3	129,788,531 (GRCm38)	nonsense	probably null
R4675:Lrit3	UTSW	3	129,788,472 (GRCm38)	missense	probably damaging	1.00
R5104:Lrit3	UTSW	3	129,788,391 (GRCm38)	missense	possibly damaging	0.86
R5147:Lrit3	UTSW	3	129,803,925 (GRCm38)	missense	possibly damaging	0.78
R5271:Lrit3	UTSW	3	129,788,301 (GRCm38)	missense	probably damaging	1.00
R5505:Lrit3	UTSW	3	129,791,438 (GRCm38)	missense	possibly damaging	0.83
R5587:Lrit3	UTSW	3	129,788,898 (GRCm38)	missense	probably benign	0.25
R6056:Lrit3	UTSW	3	129,789,355 (GRCm38)	missense	probably damaging	1.00
R6239:Lrit3	UTSW	3	129,800,346 (GRCm38)	missense	probably damaging	0.98
R6280:Lrit3	UTSW	3	129,788,763 (GRCm38)	missense	probably damaging	0.99
R6305:Lrit3	UTSW	3	129,800,460 (GRCm38)	missense	probably damaging	0.98
R6441:Lrit3	UTSW	3	129,800,360 (GRCm38)	missense	probably benign
R6947:Lrit3	UTSW	3	129,789,234 (GRCm38)	missense	probably benign	0.01
R6949:Lrit3	UTSW	3	129,789,285 (GRCm38)	missense	probably damaging	1.00
R7850:Lrit3	UTSW	3	129,800,803 (GRCm38)	missense	probably damaging	1.00
R8157:Lrit3	UTSW	3	129,800,635 (GRCm38)	missense	probably benign	0.00
R8405:Lrit3	UTSW	3	129,788,652 (GRCm38)	missense	probably benign	0.26
R8896:Lrit3	UTSW	3	129,791,483 (GRCm38)	missense	probably damaging	1.00
R8937:Lrit3	UTSW	3	129,800,544 (GRCm38)	missense	probably damaging	1.00
R9794:Lrit3	UTSW	3	129,800,424 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGATACACAGATCCTCCCGG -3'
(R):5'- GTGTACAAACCAGCATCTCAGG -3'

Sequencing Primer
(F):5'- GGGACCCACTCCTTTTGGACAG -3'
(R):5'- AGCATCTCAGGACGCACCG -3'

Posted On

2018-04-05