Mutagenetix > Incidental Mutation

Incidental Mutation 'R5822:Ftdc1'

450002

Institutional Source

Beutler Lab

Gene Symbol

Ftdc1

Ensembl Gene

ENSMUSG00000075002

Gene Name

ferritin domain containing 1

Synonyms

Gm813, LOC328695, LOC385656

MMRRC Submission

044052-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.061) question?

Stock #

R5822 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

58434049-58437341 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

C to A at 58436075 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000097255 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099663] [ENSMUST00000099663]

AlphaFold

Q3UWK9

Predicted Effect

probably null
Transcript: ENSMUST00000099663

SMART Domains

Protein: ENSMUSP00000097255
Gene: ENSMUSG00000075002

Domain	Start	End	E-Value	Type
Pfam:Ferritin	14	152	7.4e-16	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000099663

SMART Domains

Protein: ENSMUSP00000097255
Gene: ENSMUSG00000075002

Domain	Start	End	E-Value	Type
Pfam:Ferritin	14	152	7.4e-16	PFAM

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.8%

Validation Efficiency

96% (54/56)

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930553M12Rik	T	C	4: 88,786,596 (GRCm39)	I7M	unknown	Het
Abca8a	C	T	11: 109,921,705 (GRCm39)	E1450K	probably damaging	Het
B4galnt2	T	C	11: 95,756,985 (GRCm39)	Y482C	probably damaging	Het
Bud23	A	G	5: 135,092,775 (GRCm39)	F9L	probably damaging	Het
Cacna1s	A	T	1: 136,039,816 (GRCm39)	E1214V	probably damaging	Het
Cdh20	T	C	1: 104,861,823 (GRCm39)	M1T	probably null	Het
Chkb	T	C	15: 89,313,715 (GRCm39)	E30G	probably benign	Het
Crp	A	C	1: 172,525,635 (GRCm39)		probably benign	Het
Cyp11b1	T	C	15: 74,708,670 (GRCm39)	R375G	probably null	Het
Ddx11	C	T	17: 66,436,976 (GRCm39)	S90L	probably benign	Het
Flnc	A	C	6: 29,459,429 (GRCm39)	I2510L	probably damaging	Het
Fyb1	T	A	15: 6,692,707 (GRCm39)		probably benign	Het
Gbp3	C	T	3: 142,272,239 (GRCm39)	P247L	probably benign	Het
Ggn	C	T	7: 28,871,981 (GRCm39)	P454S	probably damaging	Het
Herc1	T	A	9: 66,352,894 (GRCm39)	S2127T	probably benign	Het
Ipo11	A	G	13: 106,984,926 (GRCm39)		probably benign	Het
Kcnh7	G	A	2: 62,546,582 (GRCm39)	R1000W	probably benign	Het
Kdm5b	A	T	1: 134,516,511 (GRCm39)		probably benign	Het
Klc3	C	T	7: 19,129,724 (GRCm39)		probably null	Het
Lst1	A	T	17: 35,407,359 (GRCm39)	M3K	unknown	Het
Madd	C	T	2: 90,982,878 (GRCm39)	R1355Q	probably damaging	Het
Map3k10	A	G	7: 27,356,159 (GRCm39)	L920P	probably damaging	Het
Mdga2	A	G	12: 66,702,109 (GRCm39)	V423A	probably damaging	Het
Mogat2	T	C	7: 98,869,112 (GRCm39)	D302G	possibly damaging	Het
Nkapl	A	C	13: 21,652,593 (GRCm39)	S7A	unknown	Het
Npas2	A	G	1: 39,386,647 (GRCm39)	S639G	probably benign	Het
Nr1h5	T	G	3: 102,856,644 (GRCm39)	H260P	probably damaging	Het
Or2g25	T	C	17: 37,971,122 (GRCm39)	Y34C	probably damaging	Het
Or2t49	A	T	11: 58,392,464 (GRCm39)	L306Q	possibly damaging	Het
Or4c35	T	C	2: 89,808,787 (GRCm39)	S222P	probably damaging	Het
Or7a36	C	T	10: 78,820,023 (GRCm39)	T133I	possibly damaging	Het
Or8a1b	T	C	9: 37,623,087 (GRCm39)	M163V	probably benign	Het
Pan2	T	C	10: 128,156,249 (GRCm39)	L1142P	probably damaging	Het
Pdik1l	C	T	4: 134,014,474 (GRCm39)	E11K	possibly damaging	Het
Ppp1r15a	A	G	7: 45,172,727 (GRCm39)	V555A	probably damaging	Het
Ppp6c	G	A	2: 39,090,064 (GRCm39)	Q81*	probably null	Het
Pramel18	A	G	4: 101,767,440 (GRCm39)	M230V	probably damaging	Het
Ptprz1	A	T	6: 23,001,444 (GRCm39)	Y1178F	probably benign	Het
Relch	G	A	1: 105,646,581 (GRCm39)	V660M	probably damaging	Het
Rictor	G	A	15: 6,823,487 (GRCm39)	E1555K	probably benign	Het
Rims2	T	A	15: 39,339,886 (GRCm39)	L860Q	probably damaging	Het
Sdr39u1	A	G	14: 56,135,196 (GRCm39)	V249A	probably benign	Het
Serhl	T	C	15: 83,000,528 (GRCm39)	V305A	probably benign	Het
Slc5a11	T	C	7: 122,851,654 (GRCm39)	I201T	probably damaging	Het
Stk32a	A	T	18: 43,446,552 (GRCm39)	E334V	probably benign	Het
Tmem217	A	G	17: 29,745,529 (GRCm39)	L67P	probably damaging	Het
Tnnt1	A	T	7: 4,519,345 (GRCm39)	L12*	probably null	Het
Trim80	C	T	11: 115,338,747 (GRCm39)	R526C	probably damaging	Het
Unc5b	A	T	10: 60,608,306 (GRCm39)	F635I	possibly damaging	Het
Utp20	T	G	10: 88,653,147 (GRCm39)	N311T	probably benign	Het
Zfp276	A	G	8: 123,982,457 (GRCm39)	T74A	probably benign	Het

Other mutations in Ftdc1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02701:Ftdc1	APN	16	58,436,170 (GRCm39)	missense	probably benign	0.00
IGL02839:Ftdc1	APN	16	58,436,210 (GRCm39)	missense	probably damaging	1.00
IGL03275:Ftdc1	APN	16	58,436,119 (GRCm39)	missense	probably damaging	1.00
R0946:Ftdc1	UTSW	16	58,435,075 (GRCm39)	missense	probably damaging	1.00
R1323:Ftdc1	UTSW	16	58,437,278 (GRCm39)	missense	possibly damaging	0.65
R1323:Ftdc1	UTSW	16	58,437,278 (GRCm39)	missense	possibly damaging	0.65
R1548:Ftdc1	UTSW	16	58,436,202 (GRCm39)	missense	probably benign	0.06
R2382:Ftdc1	UTSW	16	58,436,239 (GRCm39)	splice site	probably null
R2871:Ftdc1	UTSW	16	58,434,342 (GRCm39)	missense	probably benign	0.39
R2871:Ftdc1	UTSW	16	58,434,342 (GRCm39)	missense	probably benign	0.39
R2873:Ftdc1	UTSW	16	58,434,342 (GRCm39)	missense	probably benign	0.39
R2874:Ftdc1	UTSW	16	58,434,342 (GRCm39)	missense	probably benign	0.39
R4690:Ftdc1	UTSW	16	58,434,333 (GRCm39)	missense	probably benign	0.00
R5097:Ftdc1	UTSW	16	58,434,227 (GRCm39)	missense	probably benign	0.15
R6234:Ftdc1	UTSW	16	58,435,034 (GRCm39)	missense	probably benign	0.01
R6382:Ftdc1	UTSW	16	58,434,273 (GRCm39)	missense	possibly damaging	0.73
R7170:Ftdc1	UTSW	16	58,436,091 (GRCm39)	nonsense	probably null
R8119:Ftdc1	UTSW	16	58,437,211 (GRCm39)	missense	probably benign	0.00
R9082:Ftdc1	UTSW	16	58,437,294 (GRCm39)	missense	probably benign	0.04
R9360:Ftdc1	UTSW	16	58,434,234 (GRCm39)	missense	probably benign	0.00
R9718:Ftdc1	UTSW	16	58,434,974 (GRCm39)	missense	probably benign	0.02
RF016:Ftdc1	UTSW	16	58,437,230 (GRCm39)	missense	probably damaging	1.00
X0026:Ftdc1	UTSW	16	58,434,322 (GRCm39)	missense	probably benign	0.08

Predicted Primers

PCR Primer
(F):5'- TGGTTGGCTGATTGAGAAAAGC -3'
(R):5'- CCTCTTCTAGATGACCACTGAGAC -3'

Sequencing Primer
(F):5'- CCAGACAGGTATTTAATGGACATG -3'
(R):5'- GACCACTGAGACAAGAAACTCTTTTC -3'

Posted On

2016-12-20