Mutagenetix > Incidental Mutations

Incidental Mutation 'R6526:Klra2'

521846

Institutional Source

Beutler Lab

Gene Symbol

Klra2

Ensembl Gene

ENSMUSG00000030187

Gene Name

killer cell lectin-like receptor, subfamily A, member 2

Synonyms

Ly49b

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.052) question?

Stock #

R6526 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

131219223-131247362 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 131221876 bp

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 234 (D234V)

Ref Sequence

ENSEMBL: ENSMUSP00000086252 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032306] [ENSMUST00000088867]

Predicted Effect

probably benign
Transcript: ENSMUST00000032306

SMART Domains

Protein: ENSMUSP00000032306
Gene: ENSMUSG00000030187

Domain	Start	End	E-Value	Type
CLECT	137	260	1.17e-7	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000088867
AA Change: D234V

PolyPhen 2 Score 0.213 (Sensitivity: 0.92; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000086252
Gene: ENSMUSG00000030187
AA Change: D234V

Domain	Start	End	E-Value	Type
CLECT	137	293	6.54e-6	SMART

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.4%
20x: 91.5%

Validation Efficiency

100% (72/72)

MGI Phenotype

FUNCTION: The gene is a member of the large lectin-like type 2 transmembrane receptor family of the natural killer gene complex. The gene is located distantly telomeric to its family's gene cluster on chromosome 6. The gene differs from the other genes in its cluster as its promoter region contains long and short interspersed repetitive elements suggesting a possible rearrangement or gene conversion. It is unknown whether this gene's encoded protein is involved with natural killer cell differentiation as are its other family members. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aamp	A	G	1: 74,284,172		probably null	Het
Abcc3	C	T	11: 94,359,372	G975D	probably benign	Het
Abhd13	G	A	8: 9,987,777	G125S	probably damaging	Het
Ache	T	A	5: 137,290,644	L204Q	probably damaging	Het
Acnat2	A	G	4: 49,383,497	S19P	probably benign	Het
Adprh	A	G	16: 38,447,276	Y216H	probably benign	Het
Anapc1	T	A	2: 128,672,135	K429*	probably null	Het
Anxa13	T	C	15: 58,344,957		noncoding transcript	Het
Aprt	A	C	8: 122,576,816	L6W	probably damaging	Het
Arhgef15	T	C	11: 68,949,994	T569A	probably damaging	Het
Atp11a	T	C	8: 12,864,999	L1139P	probably benign	Het
Atp2b4	A	G	1: 133,711,729	S1136P	probably damaging	Het
B9d1	T	A	11: 61,509,097	Y90*	probably null	Het
Btla	G	A	16: 45,239,094	A54T	probably damaging	Het
Cd63	T	C	10: 128,911,489	V35A	probably benign	Het
Chek2	T	C	5: 110,848,690	F173L	probably damaging	Het
Cntnap3	T	A	13: 64,781,888	N499I	possibly damaging	Het
Cog4	T	C	8: 110,881,786	L738P	probably damaging	Het
Cops6	T	C	5: 138,163,900		probably null	Het
Cpeb1	T	A	7: 81,361,669	I175F	probably benign	Het
Cyp3a16	C	T	5: 145,455,895	D174N	probably benign	Het
Dnah6	T	G	6: 73,074,704	I2984L	probably benign	Het
Dock10	A	T	1: 80,586,351	I540N	probably damaging	Het
Elf5	A	G	2: 103,439,233	Y53C	probably damaging	Het
Elmod2	T	C	8: 83,319,457	T164A	probably damaging	Het
Epn3	A	G	11: 94,494,932		probably null	Het
Fam151a	A	T	4: 106,734,004	I15F	possibly damaging	Het
Gm11115	T	A	5: 88,154,050		probably null	Het
Gm13103	A	G	4: 143,852,814	D323G	probably damaging	Het
Golga3	T	A	5: 110,204,895	I884N	probably damaging	Het
Gria2	A	T	3: 80,692,469	F703I	probably damaging	Het
Gtf2h3	C	T	5: 124,584,297	T121I	probably benign	Het
Gtpbp2	A	T	17: 46,164,111		probably null	Het
Herc2	T	C	7: 56,157,330	S2419P	probably damaging	Het
Ikbkap	T	C	4: 56,798,812		probably null	Het
Inpp5d	T	C	1: 87,676,250		probably benign	Het
Kdm2b	C	A	5: 122,961,469	V136F	probably damaging	Het
Lct	A	T	1: 128,300,478	S1093T	probably benign	Het
March9	A	G	10: 127,056,689	L310P	probably benign	Het
Morc1	G	T	16: 48,587,124	E668*	probably null	Het
Mum1	A	G	10: 80,232,279	T86A	probably benign	Het
Nbas	A	T	12: 13,405,425	L1213F	probably damaging	Het
Neto1	A	G	18: 86,498,748	T397A	possibly damaging	Het
Oit3	A	G	10: 59,429,640	C268R	probably damaging	Het
Olfr476	A	G	7: 107,967,462	T22A	probably benign	Het
Pcx	T	C	19: 4,604,495	F312L	probably benign	Het
Pitx2	T	C	3: 129,214,783		probably null	Het
Pkhd1l1	G	A	15: 44,498,089		probably null	Het
Polr1a	C	A	6: 71,929,443	D414E	possibly damaging	Het
Prkch	T	C	12: 73,702,775	Y381H	probably damaging	Het
Ptger3	T	A	3: 157,567,502	V162E	probably damaging	Het
Ptgr2	T	G	12: 84,313,952	M332R	probably damaging	Het
Ptprq	G	T	10: 107,542,653	S2009*	probably null	Het
Rangrf	C	T	11: 68,973,688	G11R	probably damaging	Het
Rbl2	A	T	8: 91,096,839	Q465L	probably benign	Het
Rhbdd1	A	T	1: 82,340,659	M88L	probably benign	Het
Setd2	G	A	9: 110,532,717	M13I	probably benign	Het
Sirpb1a	T	C	3: 15,379,020	Y384C	probably damaging	Het
Slc13a1	C	T	6: 24,097,612	G439S	probably damaging	Het
Slc41a1	T	A	1: 131,841,149	I239N	probably damaging	Het
Slit2	T	A	5: 48,304,167	C1502S	probably damaging	Het
Slit3	G	A	11: 35,661,292	E888K	probably benign	Het
Srrm3	G	T	5: 135,835,234	R62L	probably damaging	Het
Synm	A	G	7: 67,735,583	V777A	possibly damaging	Het
Trmt13	T	A	3: 116,592,215	N31I	probably damaging	Het
Trpm8	G	A	1: 88,361,998	E893K	probably damaging	Het
Uqcc1	A	G	2: 155,851,423	F197S	probably damaging	Het
Vmn1r67	T	A	7: 10,447,671	N287K	probably benign	Het
Vmn2r44	A	T	7: 8,378,099	M265K	probably benign	Het
Wwc1	C	T	11: 35,853,437	E853K	probably benign	Het
Xdh	C	A	17: 73,900,551	C937F	probably damaging	Het
Zfp846	T	A	9: 20,593,871	N342K	probably benign	Het

Other mutations in Klra2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02271:Klra2	APN	6	131230217	missense	probably benign	0.11
IGL02280:Klra2	APN	6	131245293	missense	probably damaging	1.00
IGL02503:Klra2	APN	6	131230094	missense	probably benign	0.10
IGL03120:Klra2	APN	6	131220217	missense	probably benign	0.00
FR4449:Klra2	UTSW	6	131221846	frame shift	probably null
FR4548:Klra2	UTSW	6	131221851	frame shift	probably null
FR4737:Klra2	UTSW	6	131221852	frame shift	probably null
R0082:Klra2	UTSW	6	131220247	missense	possibly damaging	0.90
R0597:Klra2	UTSW	6	131220185	missense	probably benign	0.00
R0606:Klra2	UTSW	6	131220224	missense	probably damaging	1.00
R0636:Klra2	UTSW	6	131220104	splice site	probably benign
R0800:Klra2	UTSW	6	131230174	nonsense	probably null
R1645:Klra2	UTSW	6	131243894	critical splice donor site	probably null
R1655:Klra2	UTSW	6	131220211	missense	probably damaging	0.96
R1950:Klra2	UTSW	6	131230115	missense	probably benign	0.02
R2088:Klra2	UTSW	6	131242826	missense	probably damaging	0.99
R2402:Klra2	UTSW	6	131243901	missense	probably benign	0.01
R3776:Klra2	UTSW	6	131242963	missense	probably benign	0.06
R4131:Klra2	UTSW	6	131228217	missense	probably benign	0.03
R4570:Klra2	UTSW	6	131243937	missense	probably damaging	1.00
R4585:Klra2	UTSW	6	131230157	missense	probably benign	0.11
R4586:Klra2	UTSW	6	131230157	missense	probably benign	0.11
R4884:Klra2	UTSW	6	131230202	missense	probably damaging	1.00
R4982:Klra2	UTSW	6	131220189	missense	probably benign	0.25
R5043:Klra2	UTSW	6	131220172	missense	probably benign	0.06
R5457:Klra2	UTSW	6	131221889	missense	possibly damaging	0.92
R6538:Klra2	UTSW	6	131242990	missense	probably damaging	0.99
R7393:Klra2	UTSW	6	131230202	missense	probably damaging	1.00
R7785:Klra2	UTSW	6	131245290	missense	possibly damaging	0.95
R8394:Klra2	UTSW	6	131245310	missense	possibly damaging	0.94
RF020:Klra2	UTSW	6	131221838	frame shift	probably null
RF059:Klra2	UTSW	6	131221838	frame shift	probably null
RF064:Klra2	UTSW	6	131221839	frame shift	probably null
Z1088:Klra2	UTSW	6	131228290	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGCCATTGTCTTAATAGCCAGG -3'
(R):5'- TGTGGAATTCTAGATGGTCTTCACC -3'

Sequencing Primer
(F):5'- GCCATTGTCTTAATAGCCAGGAAAAG -3'
(R):5'- GTTCAACACACTGCTTTATTGATTG -3'

Posted On

2018-06-06