Mutagenetix > Incidental Mutation

Incidental Mutation 'R2357:Kng1'

247468

Institutional Source

Beutler Lab

Gene Symbol

Kng1

Ensembl Gene

ENSMUSG00000022875

Gene Name

kininogen 1

Synonyms

L-kininogen, H-kininigen

MMRRC Submission

040339-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2357 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

22876970-22900828 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 22897815 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Phenylalanine at position 405 (Y405F)

Ref Sequence

ENSEMBL: ENSMUSP00000023589 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023589] [ENSMUST00000039492] [ENSMUST00000089902]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000023589
AA Change: Y405F

PolyPhen 2 Score 0.883 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000023589
Gene: ENSMUSG00000022875
AA Change: Y405F

Domain	Start	End	E-Value	Type
CY	18	126	3.61e-17	SMART
CY	140	248	6.46e-28	SMART
CY	262	370	2.96e-36	SMART
low complexity region	439	450	N/A	INTRINSIC
low complexity region	494	524	N/A	INTRINSIC
low complexity region	541	555	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000039492

SMART Domains

Protein: ENSMUSP00000040485
Gene: ENSMUSG00000022875

Domain	Start	End	E-Value	Type
CY	18	126	3.61e-17	SMART
CY	140	248	6.46e-28	SMART
CY	262	370	2.96e-36	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000089902

SMART Domains

Protein: ENSMUSP00000087346
Gene: ENSMUSG00000022875

Domain	Start	End	E-Value	Type
CY	18	126	3.61e-17	SMART
CY	140	248	6.46e-28	SMART
CY	262	370	2.96e-36	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136778

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.8%
20x: 93.3%

Validation Efficiency

97% (66/68)

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted null mutation are viable and grossly unaffected with normal tail vein bleeding times, despite loss of detectable plasma kininogen. However, homozygotes show a significantly longer time to carotid artery occlusion after RoseBengal and laser-induced arterial injury. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932414N04Rik	C	A	2: 68,569,844 (GRCm39)	T520K	possibly damaging	Het
Abca13	T	C	11: 9,247,336 (GRCm39)	L2361P	probably damaging	Het
Acsl6	T	A	11: 54,218,106 (GRCm39)	M248K	probably damaging	Het
Adam11	G	T	11: 102,665,334 (GRCm39)	V467L	probably benign	Het
Afap1	C	T	5: 36,141,618 (GRCm39)	H501Y	probably damaging	Het
Ankrd28	A	T	14: 31,486,251 (GRCm39)	Y22*	probably null	Het
Ccdc124	A	T	8: 71,321,179 (GRCm39)	L187Q	probably damaging	Het
Cdc42bpa	G	A	1: 179,894,792 (GRCm39)	S324N	possibly damaging	Het
Cgnl1	T	A	9: 71,632,950 (GRCm39)	K134*	probably null	Het
Cnpy3	G	T	17: 47,062,909 (GRCm39)	S47R	probably damaging	Het
Cpne8	A	T	15: 90,503,877 (GRCm39)	L96Q	probably damaging	Het
Crisp3	A	T	17: 40,533,396 (GRCm39)	Y212N	probably damaging	Het
Cryba1	A	T	11: 77,613,427 (GRCm39)		probably benign	Het
Cyc1	A	G	15: 76,229,766 (GRCm39)	M288V	possibly damaging	Het
Dnah8	T	A	17: 30,990,846 (GRCm39)	D3296E	probably benign	Het
Dnah8	A	G	17: 31,093,909 (GRCm39)	T4668A	probably benign	Het
Dnajb6	T	A	5: 29,958,638 (GRCm39)	F113I	probably damaging	Het
Dync2h1	A	G	9: 7,081,053 (GRCm39)	I2881T	probably benign	Het
Eps8l1	T	C	7: 4,473,354 (GRCm39)	S179P	probably benign	Het
Esco2	C	A	14: 66,064,000 (GRCm39)	A395S	probably benign	Het
Evi5l	T	C	8: 4,243,113 (GRCm39)		probably benign	Het
Exoc6b	T	C	6: 84,966,321 (GRCm39)	T218A	possibly damaging	Het
Gde1	A	T	7: 118,290,814 (GRCm39)	F170L	probably benign	Het
Ggt5	A	C	10: 75,445,075 (GRCm39)	I361L	probably benign	Het
Golga3	C	T	5: 110,350,514 (GRCm39)	T683M	probably damaging	Het
Golgb1	A	G	16: 36,732,370 (GRCm39)	Q539R	probably damaging	Het
Grm2	A	G	9: 106,524,780 (GRCm39)	V645A	probably damaging	Het
Gtf2h4	A	T	17: 35,978,891 (GRCm39)	V408D	probably damaging	Het
Gucy1a2	A	T	9: 3,797,299 (GRCm39)	H583L	probably damaging	Het
Hivep2	C	T	10: 14,019,043 (GRCm39)	A1938V	probably benign	Het
Iars1	T	C	13: 49,841,679 (GRCm39)	Y56H	probably damaging	Het
Il17re	A	G	6: 113,445,431 (GRCm39)	I381V	possibly damaging	Het
Klrd1	T	A	6: 129,573,872 (GRCm39)	*71K	probably null	Het
Kptn	G	T	7: 15,859,709 (GRCm39)	C311F	probably damaging	Het
Lama5	T	C	2: 179,821,890 (GRCm39)	I2982V	probably benign	Het
Mamstr	G	T	7: 45,291,754 (GRCm39)	D35Y	probably damaging	Het
Mdc1	A	G	17: 36,158,337 (GRCm39)	D239G	probably benign	Het
Mindy3	T	G	2: 12,408,987 (GRCm39)		probably benign	Het
Mrpl39	A	T	16: 84,524,452 (GRCm39)	H204Q	probably benign	Het
Myo16	G	A	8: 10,644,905 (GRCm39)	D1746N	possibly damaging	Het
Myo5a	T	A	9: 75,108,647 (GRCm39)	M1476K	probably damaging	Het
Nol4	A	G	18: 23,172,967 (GRCm39)	S45P	probably benign	Het
Nol8	T	C	13: 49,807,980 (GRCm39)		probably null	Het
Or4f61	A	G	2: 111,922,743 (GRCm39)	I101T	possibly damaging	Het
Or5d18	A	T	2: 87,865,028 (GRCm39)	W152R	probably damaging	Het
Or6c207	C	A	10: 129,104,642 (GRCm39)	K183N	probably benign	Het
Or8b56	T	C	9: 38,739,634 (GRCm39)	S216P	probably benign	Het
Plau	T	A	14: 20,888,683 (GRCm39)	V100D	probably damaging	Het
Plpp7	T	C	2: 31,999,654 (GRCm39)	V6A	probably benign	Het
Prr14	T	C	7: 127,074,535 (GRCm39)	S356P	probably benign	Het
Rabl3	A	G	16: 37,362,293 (GRCm39)	D44G	probably null	Het
Rasa4	T	C	5: 136,120,101 (GRCm39)	V59A	probably damaging	Het
Rbm46	A	T	3: 82,771,765 (GRCm39)	D283E	probably benign	Het
Rictor	A	T	15: 6,813,043 (GRCm39)	N932I	probably damaging	Het
Rpl9-ps6	A	G	19: 32,443,743 (GRCm39)	V70A	probably benign	Het
S100a7l2	A	T	3: 90,995,733 (GRCm39)	S56R	probably benign	Het
St3gal1	A	G	15: 66,985,631 (GRCm39)	Y8H	probably benign	Het
Strn	G	A	17: 78,963,028 (GRCm39)	T745I	probably damaging	Het
Tbx15	C	T	3: 99,223,672 (GRCm39)		probably null	Het
Tbx20	T	A	9: 24,681,072 (GRCm39)	D140V	possibly damaging	Het
Ttn	A	C	2: 76,666,923 (GRCm39)	Y42*	probably null	Het
Usp9y	G	A	Y: 1,394,050 (GRCm39)	T560I	possibly damaging	Het
Vmn2r111	A	G	17: 22,778,151 (GRCm39)		probably benign	Het
Vps13d	GG	GGGGGG	4: 144,801,547 (GRCm39)		probably null	Het
Wfdc12	A	T	2: 164,032,170 (GRCm39)	I40N	probably damaging	Het
Zfp78	G	A	7: 6,382,056 (GRCm39)	G369R	probably damaging	Het

Other mutations in Kng1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01460:Kng1	APN	16	22,897,944 (GRCm39)	missense	probably benign	0.26
IGL01754:Kng1	APN	16	22,898,364 (GRCm39)	missense	probably benign	0.10
IGL02049:Kng1	APN	16	22,892,187 (GRCm39)	missense	probably damaging	0.99
IGL02138:Kng1	APN	16	22,886,558 (GRCm39)	missense	probably damaging	0.99
IGL02216:Kng1	APN	16	22,877,283 (GRCm39)	missense	probably damaging	0.98
IGL02230:Kng1	APN	16	22,879,244 (GRCm39)	critical splice donor site	probably null
IGL02630:Kng1	APN	16	22,898,595 (GRCm39)	utr 3 prime	probably benign
IGL03024:Kng1	APN	16	22,893,442 (GRCm39)	missense	possibly damaging	0.92
R0518:Kng1	UTSW	16	22,879,232 (GRCm39)	missense	possibly damaging	0.70
R0521:Kng1	UTSW	16	22,879,232 (GRCm39)	missense	possibly damaging	0.70
R1352:Kng1	UTSW	16	22,886,444 (GRCm39)	critical splice acceptor site	probably null
R1396:Kng1	UTSW	16	22,897,730 (GRCm39)	missense	probably benign	0.00
R1514:Kng1	UTSW	16	22,898,510 (GRCm39)	missense	probably damaging	0.97
R1753:Kng1	UTSW	16	22,897,869 (GRCm39)	missense	possibly damaging	0.68
R2048:Kng1	UTSW	16	22,877,354 (GRCm39)	missense	probably damaging	0.98
R2290:Kng1	UTSW	16	22,897,875 (GRCm39)	missense	possibly damaging	0.79
R3014:Kng1	UTSW	16	22,898,120 (GRCm39)	missense	possibly damaging	0.72
R3607:Kng1	UTSW	16	22,886,552 (GRCm39)	missense	probably damaging	1.00
R4322:Kng1	UTSW	16	22,898,270 (GRCm39)	missense	probably benign
R4334:Kng1	UTSW	16	22,898,370 (GRCm39)	missense	possibly damaging	0.88
R4388:Kng1	UTSW	16	22,898,068 (GRCm39)	missense	possibly damaging	0.63
R4558:Kng1	UTSW	16	22,896,168 (GRCm39)	splice site	probably null
R4887:Kng1	UTSW	16	22,886,448 (GRCm39)	missense	possibly damaging	0.71
R5115:Kng1	UTSW	16	22,888,032 (GRCm39)	missense	possibly damaging	0.87
R5288:Kng1	UTSW	16	22,897,842 (GRCm39)	missense	probably damaging	0.96
R5461:Kng1	UTSW	16	22,897,887 (GRCm39)	missense	probably benign	0.19
R5894:Kng1	UTSW	16	22,892,113 (GRCm39)	missense	probably benign	0.08
R6137:Kng1	UTSW	16	22,893,395 (GRCm39)	missense	possibly damaging	0.56
R6260:Kng1	UTSW	16	22,877,371 (GRCm39)	missense	possibly damaging	0.66
R6291:Kng1	UTSW	16	22,898,475 (GRCm39)	missense	probably damaging	1.00
R6620:Kng1	UTSW	16	22,900,232 (GRCm39)	missense	possibly damaging	0.74
R6947:Kng1	UTSW	16	22,896,124 (GRCm39)	missense	probably benign	0.21
R7142:Kng1	UTSW	16	22,898,170 (GRCm39)	missense	probably benign	0.25
R7166:Kng1	UTSW	16	22,898,428 (GRCm39)	missense	probably benign	0.00
R7168:Kng1	UTSW	16	22,898,391 (GRCm39)	missense	probably benign	0.26
R7347:Kng1	UTSW	16	22,886,537 (GRCm39)	missense	possibly damaging	0.46
R9005:Kng1	UTSW	16	22,898,146 (GRCm39)	missense	probably damaging	0.99
R9388:Kng1	UTSW	16	22,898,388 (GRCm39)	missense	possibly damaging	0.84
R9563:Kng1	UTSW	16	22,879,170 (GRCm39)	missense	probably damaging	1.00
R9689:Kng1	UTSW	16	22,879,224 (GRCm39)	missense	probably damaging	0.98
Z1176:Kng1	UTSW	16	22,898,366 (GRCm39)	missense	probably benign	0.00
Z1177:Kng1	UTSW	16	22,892,139 (GRCm39)	missense	probably benign	0.31

Predicted Primers

PCR Primer
(F):5'- GAAAGACTCACCCCATTTTGATG -3'
(R):5'- GACCAAGGCCATGTGGTTTC -3'

Sequencing Primer
(F):5'- ACCCCATTTTGATGCGGCATG -3'
(R):5'- TTCTGGTGTCCATGACCAAGGC -3'

Posted On

2014-11-11