Mutagenetix > Incidental Mutation

Incidental Mutation 'R5023:Klf11'

391156

Institutional Source

Beutler Lab

Gene Symbol

Klf11

Ensembl Gene

ENSMUSG00000020653

Gene Name

Kruppel-like factor 11

Synonyms

Tieg2b, D12Ertd427e, Tieg3, Tieg2

MMRRC Submission

042614-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5023 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

24651274-24662789 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 24655359 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 271 (S271T)

Ref Sequence

ENSEMBL: ENSMUSP00000020982 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020982] [ENSMUST00000139940] [ENSMUST00000144046] [ENSMUST00000146894]

AlphaFold

Q8K1S5

Predicted Effect

probably benign
Transcript: ENSMUST00000020982
AA Change: S271T

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000020982
Gene: ENSMUSG00000020653
AA Change: S271T

Domain	Start	End	E-Value	Type
low complexity region	267	275	N/A	INTRINSIC
low complexity region	356	367	N/A	INTRINSIC
ZnF_C2H2	384	408	5.9e-3	SMART
ZnF_C2H2	414	438	9.22e-5	SMART
ZnF_C2H2	444	466	1.38e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000139940

Predicted Effect

probably benign
Transcript: ENSMUST00000144046

Predicted Effect

probably benign
Transcript: ENSMUST00000146894

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.2%

Validation Efficiency

98% (127/129)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a zinc finger transcription factor that binds to SP1-like sequences in epsilon- and gamma-globin gene promoters. This binding inhibits cell growth and causes apoptosis. Defects in this gene are a cause of maturity-onset diabetes of the young type 7 (MODY7). Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]
PHENOTYPE: Mice homozygous for a knock-out allele are viable and fertile, show normal hematopoiesis, growth and development, and display no evidence of increased tumor formation following gamma-irradiation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 124 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933427D14Rik	A	T	11: 72,166,755 (GRCm38)	H739Q	probably benign	Het
Abca3	C	T	17: 24,374,300 (GRCm38)	R224C	probably damaging	Het
Abca8b	A	G	11: 109,974,988 (GRCm38)		probably null	Het
Adam1b	C	T	5: 121,501,159 (GRCm38)	V608M	probably damaging	Het
Ank2	A	G	3: 126,941,871 (GRCm38)		probably benign	Het
Ankrd17	A	C	5: 90,282,868 (GRCm38)	L1019R	probably damaging	Het
Arih1	T	C	9: 59,486,232 (GRCm38)	N39S	unknown	Het
Best3	G	A	10: 116,988,742 (GRCm38)	V38I	probably benign	Het
Bicc1	A	G	10: 70,947,883 (GRCm38)	S393P	possibly damaging	Het
C1d	T	A	11: 17,266,674 (GRCm38)	N135K	probably benign	Het
Cage1	G	T	13: 38,011,411 (GRCm38)	S778*	probably null	Het
Capn7	T	A	14: 31,352,426 (GRCm38)	V262E	probably damaging	Het
Ccdc190	A	G	1: 169,933,087 (GRCm38)	R95G	probably damaging	Het
Cd163	C	T	6: 124,325,288 (GRCm38)	T937I	probably damaging	Het
Cdh18	G	A	15: 23,259,666 (GRCm38)	S194N	probably damaging	Het
Ceacam23	A	T	7: 17,902,706 (GRCm38)	D236V	probably damaging	Het
Clec4b2	A	T	6: 123,200,956 (GRCm38)	S77C	probably null	Het
Ctsw	T	A	19: 5,466,049 (GRCm38)	D237V	probably damaging	Het
Cyp2c68	G	A	19: 39,712,507 (GRCm38)	T289I	probably benign	Het
Cyp4f39	A	G	17: 32,481,104 (GRCm38)	Y133C	probably damaging	Het
Dlg5	T	C	14: 24,136,622 (GRCm38)	E1847G	probably damaging	Het
Dnah7a	C	A	1: 53,647,248 (GRCm38)	E248*	probably null	Het
Eef2kmt	T	A	16: 5,247,599 (GRCm38)	D248V	probably damaging	Het
Ewsr1	T	C	11: 5,088,054 (GRCm38)	T113A	possibly damaging	Het
Fbxo4	A	G	15: 3,977,756 (GRCm38)		probably null	Het
Fbxo43	A	T	15: 36,162,929 (GRCm38)	M44K	probably benign	Het
Fchsd1	A	G	18: 37,964,810 (GRCm38)	I340T	possibly damaging	Het
Fgf5	C	A	5: 98,262,015 (GRCm38)	A141E	probably damaging	Het
Gfm1	T	C	3: 67,473,544 (GRCm38)	V664A	probably damaging	Het
Glp2r	T	C	11: 67,741,032 (GRCm38)	T121A	possibly damaging	Het
Gm10803	A	C	2: 93,564,172 (GRCm38)	L96F	probably damaging	Het
Gm14569	T	C	X: 36,430,817 (GRCm38)	D1413G	probably benign	Het
Gm15455	T	C	1: 33,837,351 (GRCm38)		noncoding transcript	Het
Gm1818	G	C	12: 48,555,535 (GRCm38)		noncoding transcript	Het
Gm7030	A	G	17: 36,109,415 (GRCm38)		probably benign	Het
Gnb2	G	A	5: 137,529,940 (GRCm38)		probably null	Het
Gpc4	G	A	X: 52,074,563 (GRCm38)	R148C	probably damaging	Het
Gpx5	C	T	13: 21,288,745 (GRCm38)	V140I	probably damaging	Het
Gtpbp1	A	T	15: 79,719,221 (GRCm38)	Q637L	possibly damaging	Het
Herc1	A	T	9: 66,470,326 (GRCm38)	K3458M	possibly damaging	Het
Hhat	A	T	1: 192,727,339 (GRCm38)	L138Q	probably damaging	Het
Hipk1	G	T	3: 103,777,507 (GRCm38)	T264N	probably damaging	Het
Hjurp	A	T	1: 88,275,050 (GRCm38)	Y71N	possibly damaging	Het
Hnf4g	G	T	3: 3,644,587 (GRCm38)	A144S	probably damaging	Het
Hook3	TAGAG	TAG	8: 26,032,019 (GRCm38)		probably null	Het
Ifi204	G	A	1: 173,751,740 (GRCm38)	T513I	possibly damaging	Het
Ino80b	G	T	6: 83,125,042 (GRCm38)	S26R	probably damaging	Het
Ints9	T	A	14: 64,980,228 (GRCm38)	L68H	probably damaging	Het
Isx	C	T	8: 74,892,714 (GRCm38)	T178I	probably benign	Het
Kel	A	G	6: 41,688,111 (GRCm38)	L255P	probably damaging	Het
Klhl20	A	C	1: 161,109,220 (GRCm38)		probably null	Het
Lama2	G	A	10: 27,190,504 (GRCm38)	T1127I	probably damaging	Het
Larp1b	T	A	3: 41,033,985 (GRCm38)	N81K	possibly damaging	Het
Lsm11	T	C	11: 45,944,839 (GRCm38)	D25G	probably damaging	Het
Map3k20	T	A	2: 72,402,345 (GRCm38)		probably benign	Het
Mbd6	C	T	10: 127,286,441 (GRCm38)	V173I	probably benign	Het
Milr1	A	G	11: 106,766,965 (GRCm38)	D131G	possibly damaging	Het
Mybpc1	T	G	10: 88,543,774 (GRCm38)	D635A	probably damaging	Het
Myh7b	G	C	2: 155,632,373 (GRCm38)	R1669S	possibly damaging	Het
Ndufa7	A	G	17: 33,824,603 (GRCm38)		probably benign	Het
Ndufs3	C	A	2: 90,898,660 (GRCm38)	A161S	probably benign	Het
Neo1	T	C	9: 58,990,271 (GRCm38)	D134G	probably damaging	Het
Nme4	G	A	17: 26,093,668 (GRCm38)	T129I	probably benign	Het
Npffr2	A	T	5: 89,582,687 (GRCm38)	T159S	probably benign	Het
Nup153	A	T	13: 46,681,109 (GRCm38)		probably benign	Het
Or3a10	T	A	11: 74,045,055 (GRCm38)	D73V	probably damaging	Het
Or51ac3	A	C	7: 103,565,171 (GRCm38)	M36R	possibly damaging	Het
Pate2	T	C	9: 35,686,111 (GRCm38)		probably benign	Het
Pcca	A	G	14: 122,790,398 (GRCm38)	N73D	probably damaging	Het
Pip5k1c	G	A	10: 81,310,889 (GRCm38)		probably null	Het
Pkhd1l1	A	T	15: 44,528,191 (GRCm38)	H1551L	probably benign	Het
Pkhd1l1	G	A	15: 44,582,227 (GRCm38)	M3768I	probably benign	Het
Ppa2	A	G	3: 133,370,434 (GRCm38)	M275V	probably benign	Het
Ptpn23	G	A	9: 110,388,556 (GRCm38)	T744I	probably benign	Het
Ptprv	A	T	1: 135,124,506 (GRCm38)		noncoding transcript	Het
Rad17	A	T	13: 100,645,063 (GRCm38)	H75Q	possibly damaging	Het
Rbm44	T	C	1: 91,169,098 (GRCm38)		probably null	Het
Rbpj	C	T	5: 53,649,415 (GRCm38)	R201W	probably damaging	Het
Rbpjl	C	A	2: 164,410,289 (GRCm38)	L215I	probably damaging	Het
Ror1	A	G	4: 100,425,932 (GRCm38)	E398G	probably benign	Het
Scamp3	T	A	3: 89,182,293 (GRCm38)		probably benign	Het
Selenot	CATGTATG	CATGTATGTATG	3: 58,588,453 (GRCm38)		probably null	Het
Siglec15	A	G	18: 78,048,675 (GRCm38)	C104R	probably damaging	Het
Sis	T	C	3: 72,934,122 (GRCm38)	I787V	probably benign	Het
Slc17a8	T	C	10: 89,576,560 (GRCm38)	D521G	probably benign	Het
Slc7a10	T	A	7: 35,197,355 (GRCm38)	M172K	possibly damaging	Het
Slco4c1	G	A	1: 96,841,228 (GRCm38)	P303L	probably damaging	Het
Slitrk3	T	C	3: 73,050,648 (GRCm38)	T264A	probably benign	Het
Smg8	A	C	11: 87,086,137 (GRCm38)	V206G	probably damaging	Het
Smg9	A	G	7: 24,405,872 (GRCm38)	K137R	possibly damaging	Het
Srrm2	C	A	17: 23,819,317 (GRCm38)		probably benign	Het
Sult2a2	T	A	7: 13,734,860 (GRCm38)	Y84N	possibly damaging	Het
Syngr2	A	T	11: 117,812,510 (GRCm38)	I34F	probably benign	Het
Tank	G	A	2: 61,578,635 (GRCm38)		probably benign	Het
Tead4	T	C	6: 128,294,171 (GRCm38)		probably benign	Het
Tesl1	G	A	X: 23,907,241 (GRCm38)	G327E	probably damaging	Het
Tex36	A	T	7: 133,595,290 (GRCm38)	C33S	probably benign	Het
Timd5	T	A	11: 46,528,532 (GRCm38)	D58E	probably damaging	Het
Timm21	C	A	18: 84,949,414 (GRCm38)	V112L	possibly damaging	Het
Tmem240	T	A	4: 155,739,674 (GRCm38)	L92Q	probably damaging	Het
Tmem268	C	G	4: 63,568,540 (GRCm38)	S100C	probably damaging	Het
Tmod3	G	A	9: 75,511,206 (GRCm38)	P183S	probably damaging	Het
Trappc10	G	T	10: 78,217,160 (GRCm38)	F260L	possibly damaging	Het
Trim16	A	T	11: 62,836,812 (GRCm38)	Y233F	probably benign	Het
Trmt112	T	C	19: 6,910,753 (GRCm38)	V91A	probably benign	Het
Ttc3	A	G	16: 94,429,359 (GRCm38)	E450G	probably benign	Het
Ttk	A	G	9: 83,863,541 (GRCm38)	D647G	probably damaging	Het
Ubash3b	A	G	9: 41,037,459 (GRCm38)	C187R	possibly damaging	Het
Vmn1r29	T	A	6: 58,308,067 (GRCm38)	Y257*	probably null	Het
Vmn1r33	T	C	6: 66,612,105 (GRCm38)	N155S	probably benign	Het
Vmn2r28	T	A	7: 5,486,464 (GRCm38)	I459L	probably benign	Het
Vps16	A	G	2: 130,439,452 (GRCm38)	S235G	probably benign	Het
Vwde	T	C	6: 13,192,642 (GRCm38)	I421V	possibly damaging	Het
Xiap	T	C	X: 42,094,465 (GRCm38)	F23L	probably benign	Het
Xkr7	A	G	2: 153,054,380 (GRCm38)	T385A	probably benign	Het
Zbtb11	A	G	16: 56,006,065 (GRCm38)	Y819C	probably damaging	Het
Zfp112	A	G	7: 24,126,484 (GRCm38)	T624A	probably damaging	Het
Zfp592	A	G	7: 81,024,347 (GRCm38)	D353G	probably damaging	Het
Zfp62	T	A	11: 49,215,729 (GRCm38)	S216T	probably damaging	Het
Zfp677	A	T	17: 21,397,794 (GRCm38)	H371L	probably damaging	Het
Zfp780b	T	C	7: 27,963,448 (GRCm38)	K561E	possibly damaging	Het
Zfp936	G	A	7: 43,187,257 (GRCm38)	D31N	probably damaging	Het
Znfx1	T	C	2: 167,039,826 (GRCm38)	Y217C	probably damaging	Het
Zpbp	C	T	11: 11,415,248 (GRCm38)	E200K	probably benign	Het

Other mutations in Klf11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01630:Klf11	APN	12	24,660,369 (GRCm38)	missense	probably benign	0.01
IGL02202:Klf11	APN	12	24,653,632 (GRCm38)	missense	probably benign	0.37
IGL02527:Klf11	APN	12	24,655,323 (GRCm38)	missense	probably benign	0.31
IGL02964:Klf11	APN	12	24,655,627 (GRCm38)	missense	probably damaging	1.00
R0254:Klf11	UTSW	12	24,653,583 (GRCm38)	missense	probably damaging	1.00
R0553:Klf11	UTSW	12	24,655,090 (GRCm38)	missense	probably benign	0.12
R0739:Klf11	UTSW	12	24,660,248 (GRCm38)	missense	probably damaging	1.00
R1584:Klf11	UTSW	12	24,655,305 (GRCm38)	missense	probably damaging	1.00
R1592:Klf11	UTSW	12	24,653,738 (GRCm38)	missense	probably damaging	1.00
R2356:Klf11	UTSW	12	24,653,583 (GRCm38)	missense	probably damaging	1.00
R3085:Klf11	UTSW	12	24,655,491 (GRCm38)	missense	probably benign
R4690:Klf11	UTSW	12	24,655,072 (GRCm38)	missense	probably damaging	0.97
R5483:Klf11	UTSW	12	24,655,411 (GRCm38)	nonsense	probably null
R5528:Klf11	UTSW	12	24,654,930 (GRCm38)	missense	probably benign	0.00
R6148:Klf11	UTSW	12	24,651,568 (GRCm38)	critical splice donor site	probably null
R6698:Klf11	UTSW	12	24,653,619 (GRCm38)	missense	probably damaging	1.00
R6799:Klf11	UTSW	12	24,655,639 (GRCm38)	missense	possibly damaging	0.59
R7317:Klf11	UTSW	12	24,655,519 (GRCm38)	missense	possibly damaging	0.59
R7384:Klf11	UTSW	12	24,653,743 (GRCm38)	missense	probably damaging	0.97
R7440:Klf11	UTSW	12	24,655,491 (GRCm38)	missense	probably benign
R7473:Klf11	UTSW	12	24,655,142 (GRCm38)	splice site	probably null
R7477:Klf11	UTSW	12	24,653,563 (GRCm38)	missense	probably benign	0.01
R7658:Klf11	UTSW	12	24,653,671 (GRCm38)	missense	probably damaging	1.00
R9378:Klf11	UTSW	12	24,655,044 (GRCm38)	missense	probably benign	0.01
R9479:Klf11	UTSW	12	24,655,030 (GRCm38)	missense	probably benign	0.10
R9663:Klf11	UTSW	12	24,655,732 (GRCm38)	missense	probably damaging	1.00
R9721:Klf11	UTSW	12	24,660,241 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTTGCTGGACCACCTCGAAG -3'
(R):5'- AGCATCACAGTTCCCTGAGG -3'

Sequencing Primer
(F):5'- ACGCTTGGCAAATGGCTTAC -3'
(R):5'- TCACAGTTCCCTGAGGCACAG -3'

Posted On

2016-06-06