Mutagenetix > Incidental Mutation

Incidental Mutation 'R7307:Gtf2f1'

567351

Institutional Source

Beutler Lab

Gene Symbol

Gtf2f1

Ensembl Gene

ENSMUSG00000002658

Gene Name

general transcription factor IIF, polypeptide 1

Synonyms

MMRRC Submission

Accession Numbers

Essential gene?

Probably essential (E-score: 0.955) question?

Stock #

R7307 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

57003405-57011288 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 57007833 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Asparagine at position 69 (S69N)

Ref Sequence

ENSEMBL: ENSMUSP00000002733 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000002733] [ENSMUST00000210548]

AlphaFold

Q3THK3

Predicted Effect

probably damaging
Transcript: ENSMUST00000002733
AA Change: S69N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000002733
Gene: ENSMUSG00000002658
AA Change: S69N

Domain	Start	End	E-Value	Type
Pfam:TFIIF_alpha	2	508	2.6e-200	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000210548

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (75/75)

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610318N02Rik	G	A	16: 17,118,395	P155L	probably benign	Het
Adamts12	G	T	15: 11,217,813	L285F	probably damaging	Het
Ankrd6	A	T	4: 32,816,949	Y393N	possibly damaging	Het
Arhgap45	A	G	10: 80,029,182	Q993R	probably benign	Het
Arhgef33	G	C	17: 80,347,120		probably null	Het
B4galnt3	T	C	6: 120,215,431	D448G	probably benign	Het
Capn1	C	G	19: 5,993,908	E564D	possibly damaging	Het
Ccdc85a	A	G	11: 28,399,384	S474P	probably benign	Het
Cdk12	T	A	11: 98,249,800	L1289*	probably null	Het
Cramp1l	A	T	17: 24,974,745	N920K	possibly damaging	Het
Cubn	C	T	2: 13,340,332	S2091N	probably damaging	Het
Ddx1	A	T	12: 13,223,959	I581N	probably damaging	Het
Dnm2	A	T	9: 21,485,687	N487Y	probably damaging	Het
Enc1	A	C	13: 97,245,093	N37T	probably damaging	Het
Ephb3	T	G	16: 21,222,226	I932S	probably benign	Het
Frk	T	A	10: 34,591,938	M316K	probably damaging	Het
Gdap2	C	T	3: 100,202,033	R25C	unknown	Het
Gm10436	A	C	12: 88,181,749	C32W	probably damaging	Het
Gpat2	T	A	2: 127,434,890	D671E	probably damaging	Het
Gpr179	C	T	11: 97,338,846	E828K	probably benign	Het
Greb1l	T	C	18: 10,538,142	Y1052H	probably damaging	Het
Hid1	A	C	11: 115,348,482	I785S	probably damaging	Het
Hmcn2	T	C	2: 31,343,081	I214T	probably damaging	Het
Hsd3b5	G	T	3: 98,619,769	F120L	probably damaging	Het
Kif16b	C	T	2: 142,712,931	R649Q	probably benign	Het
Kif17	A	T	4: 138,262,643	E47D	probably benign	Het
Kmt2b	T	C	7: 30,580,471	H1368R	probably damaging	Het
Kmt2d	A	T	15: 98,849,418	S3342T	unknown	Het
Krt82	A	G	15: 101,542,907	C356R	probably damaging	Het
Lrit2	A	G	14: 37,072,199	K407E	probably benign	Het
Malt1	T	A	18: 65,451,569	H325Q	possibly damaging	Het
Mccc2	T	G	13: 99,988,600	D187A	possibly damaging	Het
Mgll	T	A	6: 88,814,121		probably null	Het
Mindy2	T	G	9: 70,610,959	E449A	possibly damaging	Het
Muc5b	G	A	7: 141,842,294	V96M	unknown	Het
Nlrp4e	A	G	7: 23,321,528	E480G	probably benign	Het
Nup98	A	G	7: 102,134,795	I1093T	probably benign	Het
Olfr1288	A	T	2: 111,478,760		probably benign	Het
Olfr243	G	T	7: 103,716,966	R124L	probably damaging	Het
Olfr350	G	A	2: 36,850,125	M26I	probably benign	Het
Olfr541	G	A	7: 140,705,147	V299I	probably benign	Het
Pcdhb6	A	T	18: 37,335,478	H484L	probably benign	Het
Phldb1	T	C	9: 44,694,047	T604A	possibly damaging	Het
Pitpnm3	G	T	11: 72,070,964	A275D	probably damaging	Het
Polr2a	A	T	11: 69,747,292		probably null	Het
Polr3a	A	G	14: 24,459,987	C960R	probably benign	Het
Pou6f2	G	A	13: 18,239,713	A159V		Het
Pramef6	A	C	4: 143,896,775	Y276*	probably null	Het
Psmc4	A	G	7: 28,042,660	V303A	probably benign	Het
Ptdss2	A	G	7: 141,151,732	N151S	possibly damaging	Het
Ptprk	T	A	10: 28,589,008	Y1295*	probably null	Het
Rbm19	A	G	5: 120,186,218	K881E	possibly damaging	Het
Rcan2	T	A	17: 44,021,102	Y183*	probably null	Het
Rnd1	T	C	15: 98,670,799	E166G	probably damaging	Het
Rnf113a2	T	A	12: 84,418,179	C282S	probably damaging	Het
S100b	G	A	10: 76,257,092	G20R	probably benign	Het
Sae1	G	T	7: 16,368,544	Y168*	probably null	Het
Samd9l	C	A	6: 3,372,600	G1554*	probably null	Het
Samhd1	T	C	2: 157,135,020	S55G	probably benign	Het
Sgsm1	T	C	5: 113,273,646	D525G	probably benign	Het
Slc28a3	A	T	13: 58,563,172	M512K	probably damaging	Het
Slc9b2	T	A	3: 135,318,390	N67K	probably benign	Het
Smarca4	T	A	9: 21,638,800	I402N	probably damaging	Het
St7l	T	C	3: 104,889,353	F261L	probably benign	Het
Syde2	T	A	3: 146,015,798	V1140D	probably damaging	Het
Syt6	T	A	3: 103,587,472	I251N	probably damaging	Het
Taok2	T	C	7: 126,866,818	E916G	probably damaging	Het
Tecta	A	G	9: 42,377,992	S426P	probably damaging	Het
Thra	T	C	11: 98,764,308	I338T	probably damaging	Het
Trub1	A	T	19: 57,472,703	Y137F	probably damaging	Het
Vps13b	T	C	15: 35,841,545	F2574L	probably benign	Het
Ythdf3	T	C	3: 16,183,500	S2P	possibly damaging	Het
Zc3h13	T	A	14: 75,330,541	D1091E	probably damaging	Het
Zdhhc6	A	G	19: 55,313,250	Y100H	probably damaging	Het

Other mutations in Gtf2f1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02737:Gtf2f1	APN	17	57003918	missense	possibly damaging	0.86
IGL02752:Gtf2f1	APN	17	57009682	unclassified	probably benign
IGL03022:Gtf2f1	APN	17	57010971	splice site	probably null
IGL03094:Gtf2f1	APN	17	57007049	missense	probably damaging	1.00
R0242:Gtf2f1	UTSW	17	57003802	missense	probably benign	0.26
R0242:Gtf2f1	UTSW	17	57003802	missense	probably benign	0.26
R0480:Gtf2f1	UTSW	17	57004307	critical splice donor site	probably null
R1255:Gtf2f1	UTSW	17	57010982	missense	probably damaging	1.00
R2270:Gtf2f1	UTSW	17	57003462	missense	probably null	0.00
R4209:Gtf2f1	UTSW	17	57011003	missense	probably benign	0.01
R4637:Gtf2f1	UTSW	17	57004534	missense	probably benign	0.20
R5102:Gtf2f1	UTSW	17	57003626	missense	probably damaging	1.00
R5103:Gtf2f1	UTSW	17	57004519	missense	probably damaging	0.97
R6167:Gtf2f1	UTSW	17	57004161	missense	probably damaging	1.00
R6707:Gtf2f1	UTSW	17	57007770	missense	probably benign	0.00
R7254:Gtf2f1	UTSW	17	57007101	missense	possibly damaging	0.85
R7259:Gtf2f1	UTSW	17	57004562	missense	probably damaging	0.96
R7683:Gtf2f1	UTSW	17	57005458	missense	possibly damaging	0.94
R9727:Gtf2f1	UTSW	17	57011005	missense	possibly damaging	0.75
R9765:Gtf2f1	UTSW	17	57011125	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- CCAACAGTATCTAGTTGATTTACCTCC -3'
(R):5'- AACAGGTGCTCACATCCCTG -3'

Sequencing Primer
(F):5'- GCCTCCAAAGTATGCATGTG -3'
(R):5'- ACATCCCTGGCCTTCATGC -3'

Posted On

2019-06-26