Mutagenetix > Incidental Mutation

Incidental Mutation 'R0666:Kng2'

62045

Institutional Source

Beutler Lab

Gene Symbol

Kng2

Ensembl Gene

ENSMUSG00000060459

Gene Name

kininogen 2

Synonyms

Kininogen-II

MMRRC Submission

038851-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0666 (G1)

Quality Score

120

Status

Validated

Chromosome

Chromosomal Location

22804602-22847851 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 22815872 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039338] [ENSMUST00000100046] [ENSMUST00000115349] [ENSMUST00000160243]

AlphaFold

Q6S9I3

Predicted Effect

probably benign
Transcript: ENSMUST00000039338

SMART Domains

Protein: ENSMUSP00000046867
Gene: ENSMUSG00000060459

Domain	Start	End	E-Value	Type
CY	18	126	3.72e-19	SMART
CY	140	248	2.57e-22	SMART
CY	262	370	2.06e-35	SMART
low complexity region	376	390	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000100046

SMART Domains

Protein: ENSMUSP00000097623
Gene: ENSMUSG00000060459

Domain	Start	End	E-Value	Type
CY	18	126	3.72e-19	SMART
CY	140	248	2.57e-22	SMART
CY	262	370	2.06e-35	SMART
low complexity region	376	390	N/A	INTRINSIC
low complexity region	478	506	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000115349

SMART Domains

Protein: ENSMUSP00000111006
Gene: ENSMUSG00000060459

Domain	Start	End	E-Value	Type
CY	18	126	3.72e-19	SMART
CY	140	248	2.57e-22	SMART
CY	262	370	2.06e-35	SMART
low complexity region	376	390	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000160243

SMART Domains

Protein: ENSMUSP00000124161
Gene: ENSMUSG00000060459

Domain	Start	End	E-Value	Type
CY	18	126	3.72e-19	SMART
Blast:CY	140	171	2e-15	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000231872

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.7%
20x: 95.7%

Validation Efficiency

100% (89/89)

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Akap6	T	A	12: 52,958,591 (GRCm39)	V782E	probably damaging	Het
Atg9a	A	G	1: 75,161,734 (GRCm39)	L604P	probably damaging	Het
Atp1a3	T	C	7: 24,689,974 (GRCm39)	I482V	probably benign	Het
Bltp2	T	G	11: 78,178,813 (GRCm39)	M2026R	probably damaging	Het
Bltp2	T	A	11: 78,168,038 (GRCm39)	L1491*	probably null	Het
Ccdc18	T	G	5: 108,311,530 (GRCm39)	V412G	probably benign	Het
Ccn6	T	C	10: 39,027,285 (GRCm39)	R316G	probably benign	Het
Cct6a	A	G	5: 129,871,449 (GRCm39)		noncoding transcript	Het
Clpx	A	G	9: 65,217,507 (GRCm39)	N25S	probably damaging	Het
Cnpy2	T	A	10: 128,162,894 (GRCm39)	C171*	probably null	Het
Cntnap3	C	T	13: 64,905,211 (GRCm39)	D857N	probably damaging	Het
Col5a1	A	G	2: 27,922,697 (GRCm39)	Y255C	probably damaging	Het
Coro7	A	T	16: 4,449,775 (GRCm39)	F638Y	possibly damaging	Het
Cpd	A	G	11: 76,673,153 (GRCm39)	F1331L	probably damaging	Het
Csmd1	A	T	8: 16,119,063 (GRCm39)	I1842N	possibly damaging	Het
Dgkg	T	A	16: 22,381,480 (GRCm39)	D490V	probably damaging	Het
Dnah9	A	T	11: 65,976,284 (GRCm39)	M1255K	probably benign	Het
E2f1	A	G	2: 154,402,849 (GRCm39)	V306A	probably benign	Het
Entpd1	A	G	19: 40,648,350 (GRCm39)		probably benign	Het
Esrrb	T	A	12: 86,552,676 (GRCm39)	I222N	probably benign	Het
Flt4	G	T	11: 49,516,274 (GRCm39)	A126S	possibly damaging	Het
Galnt11	C	T	5: 25,457,145 (GRCm39)	T237I	possibly damaging	Het
Galnt2l	A	T	8: 122,997,727 (GRCm39)		probably benign	Het
Gbf1	A	G	19: 46,250,983 (GRCm39)		probably benign	Het
H2-T9	T	C	17: 36,438,726 (GRCm39)	T222A	possibly damaging	Het
Herc1	T	A	9: 66,392,170 (GRCm39)		probably benign	Het
Hsph1	T	C	5: 149,554,967 (GRCm39)	Y105C	probably damaging	Het
Il23r	T	C	6: 67,411,664 (GRCm39)	T358A	probably benign	Het
Il2ra	C	T	2: 11,647,884 (GRCm39)		probably benign	Het
Kbtbd4	G	T	2: 90,744,459 (GRCm39)		probably benign	Het
Kcnt1	A	G	2: 25,781,255 (GRCm39)		probably benign	Het
Lap3	C	T	5: 45,669,270 (GRCm39)	T473I	possibly damaging	Het
Lrrk2	T	C	15: 91,641,273 (GRCm39)		probably null	Het
Map1s	A	G	8: 71,366,696 (GRCm39)	N534D	possibly damaging	Het
Mtg1	G	A	7: 139,724,257 (GRCm39)	V122I	probably benign	Het
Myadm	T	A	7: 3,345,865 (GRCm39)	I209K	probably damaging	Het
Ntsr2	G	A	12: 16,703,981 (GRCm39)	V75I	probably benign	Het
Or4b1b	A	T	2: 90,112,212 (GRCm39)	S236T	probably damaging	Het
Or8u10	G	A	2: 85,915,557 (GRCm39)	A188V	probably benign	Het
Pfn1	T	C	11: 70,545,192 (GRCm39)	T39A	probably benign	Het
Pipox	T	A	11: 77,774,651 (GRCm39)	K144M	probably benign	Het
Plekhh1	G	A	12: 79,115,889 (GRCm39)	E811K	probably damaging	Het
Pnpla3	T	A	15: 84,063,506 (GRCm39)	W295R	probably benign	Het
Prkacb	T	A	3: 146,457,273 (GRCm39)	T136S	probably damaging	Het
Ralbp1	T	A	17: 66,161,124 (GRCm39)	N473I	probably benign	Het
Rbp4	G	A	19: 38,106,908 (GRCm39)	T127M	probably damaging	Het
Rif1	GCCACCA	GCCA	2: 52,000,336 (GRCm39)		probably benign	Het
Rps3a1	G	A	3: 86,045,424 (GRCm39)		probably benign	Het
Scg3	G	T	9: 75,551,222 (GRCm39)	Y429*	probably null	Het
Shisal2b	G	T	13: 104,994,862 (GRCm39)	T95K	possibly damaging	Het
Spag5	T	C	11: 78,204,222 (GRCm39)	S492P	probably damaging	Het
St7	T	A	6: 17,934,238 (GRCm39)	M540K	probably damaging	Het
Stxbp3	C	A	3: 108,712,618 (GRCm39)	V281F	possibly damaging	Het
Sun5	A	G	2: 153,700,968 (GRCm39)	V242A	possibly damaging	Het
Susd5	G	T	9: 113,924,852 (GRCm39)	R245L	possibly damaging	Het
Syne2	A	G	12: 75,969,787 (GRCm39)	E954G	probably damaging	Het
Synpo2	A	T	3: 122,907,708 (GRCm39)	V536E	probably damaging	Het
Tas2r140	T	C	6: 133,032,405 (GRCm39)	I118V	probably benign	Het
Tbx18	C	A	9: 87,606,462 (GRCm39)	V228L	probably benign	Het
Tdrd9	T	A	12: 111,974,014 (GRCm39)		probably benign	Het
Tektl1	C	A	10: 78,586,381 (GRCm39)	L223F	probably benign	Het
Tg	T	C	15: 66,609,370 (GRCm39)	M310T	probably benign	Het
Ticam2	T	A	18: 46,693,718 (GRCm39)	D123V	probably damaging	Het
Timm23	A	G	14: 31,920,993 (GRCm39)		probably benign	Het
Tinag	C	T	9: 76,912,969 (GRCm39)	R280H	probably benign	Het
Topbp1	G	A	9: 103,186,011 (GRCm39)	R51K	probably benign	Het
Tor1b	A	G	2: 30,843,925 (GRCm39)	I121V	probably damaging	Het
Tpmt	C	A	13: 47,185,930 (GRCm39)	G148V	probably damaging	Het
Tubb1	A	G	2: 174,299,548 (GRCm39)	E410G	probably damaging	Het
Ubash3b	C	A	9: 40,958,360 (GRCm39)	V7L	possibly damaging	Het
Ube2o	C	T	11: 116,433,661 (GRCm39)	E686K	probably damaging	Het
Unc13d	T	A	11: 115,960,318 (GRCm39)		probably benign	Het
Vmn1r183	A	T	7: 23,754,601 (GRCm39)	M135L	probably benign	Het
Xkr8	T	C	4: 132,459,649 (GRCm39)	Y43C	probably damaging	Het
Zc3h4	T	A	7: 16,168,697 (GRCm39)	N935K	unknown	Het
Zc3h7a	G	A	16: 10,974,167 (GRCm39)		probably benign	Het
Zfp84	C	T	7: 29,476,276 (GRCm39)	H323Y	probably damaging	Het
Zfp873	G	T	10: 81,896,595 (GRCm39)	S442I	possibly damaging	Het
Zfp938	A	G	10: 82,061,606 (GRCm39)	L338P	probably damaging	Het

Other mutations in Kng2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00851:Kng2	APN	16	22,847,580 (GRCm39)	missense	probably damaging	1.00
IGL01319:Kng2	APN	16	22,847,584 (GRCm39)	missense	probably damaging	0.99
IGL01469:Kng2	APN	16	22,818,577 (GRCm39)	missense	probably damaging	1.00
IGL01681:Kng2	APN	16	22,815,767 (GRCm39)	splice site	probably benign
IGL01830:Kng2	APN	16	22,806,801 (GRCm39)	missense	probably damaging	0.97
IGL01903:Kng2	APN	16	22,806,540 (GRCm39)	missense	possibly damaging	0.80
IGL02146:Kng2	APN	16	22,806,582 (GRCm39)	missense	probably damaging	0.97
IGL02305:Kng2	APN	16	22,819,374 (GRCm39)	unclassified	probably benign
IGL02429:Kng2	APN	16	22,830,829 (GRCm39)	missense	probably damaging	0.99
FR4548:Kng2	UTSW	16	22,819,302 (GRCm39)	nonsense	probably null
R0020:Kng2	UTSW	16	22,816,046 (GRCm39)	missense	probably benign	0.02
R0047:Kng2	UTSW	16	22,806,313 (GRCm39)	missense	possibly damaging	0.83
R0245:Kng2	UTSW	16	22,830,931 (GRCm39)	splice site	probably benign
R0610:Kng2	UTSW	16	22,819,344 (GRCm39)	missense	possibly damaging	0.96
R0646:Kng2	UTSW	16	22,806,486 (GRCm39)	missense	probably benign	0.10
R1552:Kng2	UTSW	16	22,806,270 (GRCm39)	missense	probably damaging	1.00
R1765:Kng2	UTSW	16	22,806,993 (GRCm39)	critical splice donor site	probably null
R1833:Kng2	UTSW	16	22,830,802 (GRCm39)	missense	possibly damaging	0.95
R1997:Kng2	UTSW	16	22,843,626 (GRCm39)	missense	possibly damaging	0.84
R2025:Kng2	UTSW	16	22,819,325 (GRCm39)	missense	probably benign	0.15
R2056:Kng2	UTSW	16	22,806,703 (GRCm39)	intron	probably benign
R2137:Kng2	UTSW	16	22,816,076 (GRCm39)	intron	probably benign
R2517:Kng2	UTSW	16	22,807,065 (GRCm39)	missense	probably benign	0.24
R3438:Kng2	UTSW	16	22,830,821 (GRCm39)	missense	probably benign	0.23
R3439:Kng2	UTSW	16	22,830,821 (GRCm39)	missense	probably benign	0.23
R3551:Kng2	UTSW	16	22,830,745 (GRCm39)	critical splice donor site	probably null
R4389:Kng2	UTSW	16	22,843,618 (GRCm39)	missense	possibly damaging	0.91
R4538:Kng2	UTSW	16	22,806,813 (GRCm39)	missense	probably benign	0.00
R4684:Kng2	UTSW	16	22,806,391 (GRCm39)	missense	possibly damaging	0.93
R4978:Kng2	UTSW	16	22,806,666 (GRCm39)	missense	probably damaging	1.00
R5658:Kng2	UTSW	16	22,815,770 (GRCm39)	splice site	probably null
R6074:Kng2	UTSW	16	22,819,346 (GRCm39)	missense	probably benign	0.03
R6216:Kng2	UTSW	16	22,806,343 (GRCm39)	missense	probably damaging	1.00
R6271:Kng2	UTSW	16	22,822,698 (GRCm39)	missense	probably benign	0.33
R6459:Kng2	UTSW	16	22,830,865 (GRCm39)	missense	probably damaging	1.00
R7124:Kng2	UTSW	16	22,830,805 (GRCm39)	missense	probably damaging	1.00
R7310:Kng2	UTSW	16	22,806,522 (GRCm39)	missense	probably benign	0.00
R7532:Kng2	UTSW	16	22,845,794 (GRCm39)	splice site	probably null
R7667:Kng2	UTSW	16	22,806,982 (GRCm39)	missense	probably damaging	0.99
R7787:Kng2	UTSW	16	22,818,598 (GRCm39)	missense	probably damaging	1.00
R8092:Kng2	UTSW	16	22,806,672 (GRCm39)	missense	probably benign	0.00
R8165:Kng2	UTSW	16	22,806,246 (GRCm39)	missense	unknown
R8814:Kng2	UTSW	16	22,822,761 (GRCm39)	missense	probably benign	0.00
R9019:Kng2	UTSW	16	22,847,546 (GRCm39)	missense	probably damaging	0.99
R9048:Kng2	UTSW	16	22,806,522 (GRCm39)	missense	probably benign	0.00
R9531:Kng2	UTSW	16	22,830,907 (GRCm39)	missense	possibly damaging	0.81
R9708:Kng2	UTSW	16	22,815,801 (GRCm39)	missense	probably damaging	0.99
R9764:Kng2	UTSW	16	22,822,737 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CGGGTTTAAAAGAGCAGCCCCT -3'
(R):5'- ACTCAGTGAAGTAAGCTGACCCAACTA -3'

Sequencing Primer
(F):5'- CCCCCAGTTATTTCAGTAATGATTC -3'
(R):5'- TTAACTTTACAGGTGGTAGCAGGAAC -3'

Posted On

2013-07-30