Mutagenetix > Incidental Mutation

Incidental Mutation 'R0044:Fcho2'

32903

Institutional Source

Beutler Lab

Gene Symbol

Fcho2

Ensembl Gene

ENSMUSG00000041685

Gene Name

FCH domain only 2

Synonyms

5832424M12Rik

MMRRC Submission

038338-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0044 (G1)

Quality Score

183

Status

Validated (trace)

Chromosome

Chromosomal Location

98859911-98951957 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to G at 98892052 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000153477 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040340] [ENSMUST00000099277] [ENSMUST00000109403] [ENSMUST00000179563] [ENSMUST00000224992]

AlphaFold

Q3UQN2

Predicted Effect

probably benign
Transcript: ENSMUST00000040340

SMART Domains

Protein: ENSMUSP00000042959
Gene: ENSMUSG00000041685

Domain	Start	End	E-Value	Type
FCH	8	94	1.74e-19	SMART
low complexity region	341	351	N/A	INTRINSIC
low complexity region	433	456	N/A	INTRINSIC
low complexity region	485	501	N/A	INTRINSIC
low complexity region	503	520	N/A	INTRINSIC
Pfam:muHD	542	808	2.5e-71	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000099277

SMART Domains

Protein: ENSMUSP00000096883
Gene: ENSMUSG00000041685

Domain	Start	End	E-Value	Type
FCH	8	94	1.74e-19	SMART
low complexity region	342	352	N/A	INTRINSIC
low complexity region	434	457	N/A	INTRINSIC
low complexity region	486	502	N/A	INTRINSIC
low complexity region	504	521	N/A	INTRINSIC
Pfam:muHD	543	803	4.7e-68	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000109403

SMART Domains

Protein: ENSMUSP00000105030
Gene: ENSMUSG00000041685

Domain	Start	End	E-Value	Type
FCH	8	94	1.74e-19	SMART
low complexity region	341	351	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000179563

SMART Domains

Protein: ENSMUSP00000137422
Gene: ENSMUSG00000041685

Domain	Start	End	E-Value	Type
FCH	8	94	1.74e-19	SMART
low complexity region	341	351	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000224992

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225094

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.6%
20x: 93.6%

Validation Efficiency

100% (77/77)

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
6430571L13Rik	A	C	9: 107,219,698 (GRCm39)	R50S	probably damaging	Het
Actn2	G	T	13: 12,290,013 (GRCm39)	T176N	possibly damaging	Het
Adamts7	T	C	9: 90,053,641 (GRCm39)	V62A	possibly damaging	Het
Adcy2	A	G	13: 68,876,018 (GRCm39)	S495P	possibly damaging	Het
Agbl3	A	T	6: 34,776,834 (GRCm39)	M447L	probably damaging	Het
Asxl1	C	T	2: 153,242,129 (GRCm39)	T893I	probably benign	Het
Atp11b	T	A	3: 35,866,401 (GRCm39)	I400N	probably damaging	Het
Bpifb2	C	T	2: 153,724,599 (GRCm39)		probably benign	Het
Capn1	T	A	19: 6,064,373 (GRCm39)	Y42F	probably benign	Het
Cdk5rap2	A	T	4: 70,279,138 (GRCm39)	L190H	probably damaging	Het
Cfap54	T	C	10: 92,871,295 (GRCm39)	I594V	probably null	Het
Cpsf1	A	G	15: 76,483,753 (GRCm39)	V830A	probably benign	Het
Cyp2c70	T	A	19: 40,153,815 (GRCm39)	N258I	possibly damaging	Het
Dctn1	T	G	6: 83,168,116 (GRCm39)	Y386D	probably damaging	Het
Degs2	T	C	12: 108,658,413 (GRCm39)	N189D	probably damaging	Het
Dido1	C	T	2: 180,303,612 (GRCm39)	A1431T	probably damaging	Het
Diras1	G	T	10: 80,857,972 (GRCm39)	S93*	probably null	Het
E130308A19Rik	T	A	4: 59,690,290 (GRCm39)	H41Q	possibly damaging	Het
Ebf2	C	T	14: 67,548,417 (GRCm39)		probably benign	Het
Gbe1	T	A	16: 70,358,020 (GRCm39)	Y681*	probably null	Het
Gm10036	A	C	18: 15,965,873 (GRCm39)	K8T	probably benign	Het
Herc1	T	A	9: 66,355,457 (GRCm39)	M2236K	probably benign	Het
Hmcn2	A	T	2: 31,302,520 (GRCm39)	Y2948F	probably damaging	Het
Jakmip2	A	T	18: 43,715,170 (GRCm39)	C119S	probably benign	Het
Kif1b	A	G	4: 149,348,058 (GRCm39)		probably benign	Het
Kif6	T	C	17: 50,139,284 (GRCm39)		probably benign	Het
Lpin1	A	T	12: 16,618,530 (GRCm39)		probably benign	Het
Lrp2	T	C	2: 69,357,899 (GRCm39)	I377V	probably benign	Het
Mavs	C	A	2: 131,083,944 (GRCm39)	T147N	probably damaging	Het
Mcoln2	C	T	3: 145,889,316 (GRCm39)	T374M	probably damaging	Het
Mreg	T	G	1: 72,201,534 (GRCm39)	T153P	probably damaging	Het
Naglu	T	C	11: 100,962,043 (GRCm39)	I172T	probably damaging	Het
Odad4	A	T	11: 100,457,827 (GRCm39)	I477F	probably damaging	Het
Ogdhl	T	C	14: 32,061,285 (GRCm39)	V492A	possibly damaging	Het
Or4a72	A	G	2: 89,405,974 (GRCm39)	I32T	possibly damaging	Het
Parvg	A	G	15: 84,222,083 (GRCm39)	E323G	probably benign	Het
Pgap1	A	G	1: 54,532,527 (GRCm39)	L664S	probably damaging	Het
Pgm2l1	A	G	7: 99,899,539 (GRCm39)	N51S	probably benign	Het
Pik3r6	A	G	11: 68,435,576 (GRCm39)	T609A	probably benign	Het
Plcb4	T	A	2: 135,813,776 (GRCm39)	V705E	probably damaging	Het
Plppr5	T	A	3: 117,465,538 (GRCm39)		probably null	Het
Prkg2	C	A	5: 99,120,989 (GRCm39)	D411Y	probably damaging	Het
Ptprd	A	G	4: 76,004,566 (GRCm39)	V63A	probably benign	Het
Ptprz1	T	A	6: 23,007,402 (GRCm39)	I1655N	probably damaging	Het
Raf1	T	A	6: 115,600,476 (GRCm39)	D10V	probably benign	Het
Rexo1	T	A	10: 80,380,212 (GRCm39)	Q928L	probably benign	Het
Rpl7l1	A	C	17: 47,089,456 (GRCm39)		probably null	Het
Rrm2b	A	G	15: 37,953,932 (GRCm39)	S39P	possibly damaging	Het
Scn5a	A	G	9: 119,321,113 (GRCm39)		probably null	Het
Sgtb	A	G	13: 104,265,768 (GRCm39)	T93A	probably benign	Het
Sigirr	G	T	7: 140,672,226 (GRCm39)		probably null	Het
Slc16a7	T	C	10: 125,063,951 (GRCm39)	D462G	probably benign	Het
Slc25a30	C	T	14: 76,007,089 (GRCm39)	A85T	probably benign	Het
Spata24	A	G	18: 35,789,887 (GRCm39)	S167P	probably damaging	Het
Spock3	C	T	8: 63,597,041 (GRCm39)	T115I	possibly damaging	Het
Srgap2	A	G	1: 131,247,289 (GRCm39)	I581T	possibly damaging	Het
Syn2	A	T	6: 115,112,108 (GRCm39)	M23L	unknown	Het
Synrg	G	A	11: 83,900,007 (GRCm39)	V839I	probably damaging	Het
Tmtc1	A	G	6: 148,314,327 (GRCm39)		probably benign	Het
Tnfaip3	C	A	10: 18,887,374 (GRCm39)	M50I	probably damaging	Het
Topbp1	T	A	9: 103,202,972 (GRCm39)	I721N	possibly damaging	Het
Ttc22	T	G	4: 106,494,003 (GRCm39)	V321G	probably benign	Het
Ubr2	A	G	17: 47,303,911 (GRCm39)		probably benign	Het
Ubr4	T	C	4: 139,164,369 (GRCm39)		probably benign	Het
Usp24	T	C	4: 106,269,281 (GRCm39)		probably benign	Het
Vmn2r100	A	T	17: 19,742,441 (GRCm39)	I272L	possibly damaging	Het
Vrtn	T	A	12: 84,695,379 (GRCm39)	L43H	probably damaging	Het
Wnk1	G	T	6: 120,014,110 (GRCm39)	R162S	probably damaging	Het
Xkr9	G	A	1: 13,754,286 (GRCm39)	W93*	probably null	Het
Zfp804b	G	T	5: 6,819,655 (GRCm39)	P1136H	probably damaging	Het

Other mutations in Fcho2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01449:Fcho2	APN	13	98,926,315 (GRCm39)	missense	probably benign
IGL02058:Fcho2	APN	13	98,867,414 (GRCm39)	missense	probably damaging	0.98
IGL02516:Fcho2	APN	13	98,866,720 (GRCm39)	missense	probably benign	0.08
IGL02715:Fcho2	APN	13	98,932,843 (GRCm39)	missense	probably damaging	1.00
IGL03243:Fcho2	APN	13	98,913,892 (GRCm39)	splice site	probably benign
R0087:Fcho2	UTSW	13	98,871,594 (GRCm39)	missense	probably benign	0.00
R0472:Fcho2	UTSW	13	98,884,775 (GRCm39)	missense	probably benign	0.01
R0501:Fcho2	UTSW	13	98,901,023 (GRCm39)	missense	possibly damaging	0.92
R1022:Fcho2	UTSW	13	98,869,167 (GRCm39)	missense	probably damaging	1.00
R1024:Fcho2	UTSW	13	98,869,167 (GRCm39)	missense	probably damaging	1.00
R1130:Fcho2	UTSW	13	98,884,797 (GRCm39)	missense	probably damaging	1.00
R1495:Fcho2	UTSW	13	98,886,358 (GRCm39)	critical splice donor site	probably null
R1593:Fcho2	UTSW	13	98,921,315 (GRCm39)	missense	possibly damaging	0.92
R1608:Fcho2	UTSW	13	98,862,706 (GRCm39)	missense	probably benign	0.01
R1638:Fcho2	UTSW	13	98,882,403 (GRCm39)	missense	possibly damaging	0.83
R1643:Fcho2	UTSW	13	98,921,324 (GRCm39)	missense	probably benign	0.00
R2125:Fcho2	UTSW	13	98,912,406 (GRCm39)	missense	possibly damaging	0.83
R3117:Fcho2	UTSW	13	98,913,946 (GRCm39)	missense	probably damaging	1.00
R3968:Fcho2	UTSW	13	98,871,564 (GRCm39)	missense	probably benign	0.06
R3970:Fcho2	UTSW	13	98,871,564 (GRCm39)	missense	probably benign	0.06
R4079:Fcho2	UTSW	13	98,892,120 (GRCm39)	missense	probably damaging	0.99
R4816:Fcho2	UTSW	13	98,942,874 (GRCm39)	missense	probably damaging	1.00
R5338:Fcho2	UTSW	13	98,867,399 (GRCm39)	missense	probably damaging	1.00
R5437:Fcho2	UTSW	13	98,913,982 (GRCm39)	missense	possibly damaging	0.95
R5457:Fcho2	UTSW	13	98,926,275 (GRCm39)	missense	probably damaging	0.99
R5733:Fcho2	UTSW	13	98,926,310 (GRCm39)	missense	probably damaging	0.99
R6136:Fcho2	UTSW	13	98,926,275 (GRCm39)	missense	probably damaging	0.99
R6186:Fcho2	UTSW	13	98,951,591 (GRCm39)	missense	probably benign	0.01
R6365:Fcho2	UTSW	13	98,926,367 (GRCm39)	missense	probably benign	0.20
R7041:Fcho2	UTSW	13	98,921,334 (GRCm39)	missense	possibly damaging	0.72
R7168:Fcho2	UTSW	13	98,925,971 (GRCm39)	missense	probably benign
R7218:Fcho2	UTSW	13	98,890,121 (GRCm39)	splice site	probably null
R7243:Fcho2	UTSW	13	98,891,724 (GRCm39)	missense	possibly damaging	0.94
R7533:Fcho2	UTSW	13	98,921,307 (GRCm39)	missense	probably benign	0.00
R7757:Fcho2	UTSW	13	98,901,011 (GRCm39)	critical splice donor site	probably null
R7904:Fcho2	UTSW	13	98,932,871 (GRCm39)	missense	possibly damaging	0.54
R7993:Fcho2	UTSW	13	98,888,524 (GRCm39)	splice site	probably null
R8004:Fcho2	UTSW	13	98,926,013 (GRCm39)	missense	possibly damaging	0.80
R8358:Fcho2	UTSW	13	98,862,282 (GRCm39)	nonsense	probably null
R8512:Fcho2	UTSW	13	98,891,730 (GRCm39)	missense	possibly damaging	0.69
R8692:Fcho2	UTSW	13	98,882,382 (GRCm39)	frame shift	probably null
R8792:Fcho2	UTSW	13	98,951,769 (GRCm39)	unclassified	probably benign
R8954:Fcho2	UTSW	13	98,913,985 (GRCm39)	missense	probably benign	0.05
R8969:Fcho2	UTSW	13	98,891,604 (GRCm39)	nonsense	probably null
R9091:Fcho2	UTSW	13	98,925,869 (GRCm39)	critical splice donor site	probably null
R9092:Fcho2	UTSW	13	98,886,391 (GRCm39)	missense	probably benign	0.01
R9171:Fcho2	UTSW	13	98,891,607 (GRCm39)	missense	probably benign
R9270:Fcho2	UTSW	13	98,925,869 (GRCm39)	critical splice donor site	probably null
R9668:Fcho2	UTSW	13	98,913,965 (GRCm39)	missense	probably benign	0.12
R9672:Fcho2	UTSW	13	98,869,178 (GRCm39)	nonsense	probably null
R9717:Fcho2	UTSW	13	98,900,202 (GRCm39)	missense	probably damaging	1.00
X0018:Fcho2	UTSW	13	98,868,590 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTTCAGAGTCAGAGTCACTGGATGAGT -3'
(R):5'- CCTTGACAGTGTCTTGCCCTGAAA -3'

Sequencing Primer
(F):5'- CACTGGATGAGTAGAAATGGTTCTC -3'
(R):5'- tcctcccgtctctatcttcc -3'

Posted On

2013-05-09