Mutagenetix > Incidental Mutation

Incidental Mutation 'R0106:Firrm'

17856

Institutional Source

Beutler Lab

Gene Symbol

Firrm

Ensembl Gene

ENSMUSG00000041406

Gene Name

FIGNL1 interacting regulator of recombination and mitosis

Synonyms

BC055324

MMRRC Submission

038392-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0106 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

163773562-163822365 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 163810380 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000124826 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045876] [ENSMUST00000097493] [ENSMUST00000160926]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000045876

SMART Domains

Protein: ENSMUSP00000043143
Gene: ENSMUSG00000041406

Domain	Start	End	E-Value	Type
low complexity region	10	23	N/A	INTRINSIC
Pfam:DUF4487	233	779	2.3e-209	PFAM
low complexity region	877	889	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000097493

SMART Domains

Protein: ENSMUSP00000095101
Gene: ENSMUSG00000041406

Domain	Start	End	E-Value	Type
low complexity region	10	23	N/A	INTRINSIC
Pfam:DUF4487	233	779	1.3e-186	PFAM
low complexity region	877	889	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000160926

SMART Domains

Protein: ENSMUSP00000124826
Gene: ENSMUSG00000041406

Domain	Start	End	E-Value	Type
low complexity region	10	23	N/A	INTRINSIC

Coding Region Coverage

1x: 87.6%
3x: 83.1%
10x: 68.0%
20x: 43.0%

Validation Efficiency

97% (89/92)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933415A04Rik	A	T	11: 43,478,200 (GRCm39)		probably benign	Het
A730018C14Rik	A	T	12: 112,381,628 (GRCm39)		noncoding transcript	Het
Abca5	A	T	11: 110,210,651 (GRCm39)	L176Q	probably damaging	Het
Aspm	C	A	1: 139,404,614 (GRCm39)	Q1315K	probably benign	Het
Bpifb4	A	G	2: 153,782,888 (GRCm39)	D31G	probably benign	Het
Brf1	A	G	12: 112,937,083 (GRCm39)		probably benign	Het
Card19	A	C	13: 49,361,621 (GRCm39)	D3E	probably benign	Het
Chd6	A	G	2: 160,809,822 (GRCm39)	F1480L	probably damaging	Het
Cldn25	A	G	9: 48,958,933 (GRCm39)		noncoding transcript	Het
Col11a2	A	G	17: 34,276,249 (GRCm39)	N799D	probably damaging	Het
Cpb1	T	C	3: 20,320,697 (GRCm39)		probably null	Het
Cyp2g1	T	A	7: 26,513,607 (GRCm39)	I182N	probably damaging	Het
Dntt	A	T	19: 41,044,185 (GRCm39)		probably benign	Het
Dscc1	C	A	15: 54,946,966 (GRCm39)	C253F	probably benign	Het
Dysf	C	A	6: 84,090,318 (GRCm39)	F956L	probably benign	Het
Ephb6	T	C	6: 41,596,528 (GRCm39)		probably benign	Het
Fkbp6	C	T	5: 135,368,858 (GRCm39)	R234Q	probably benign	Het
Gda	T	C	19: 21,374,920 (GRCm39)	D332G	probably benign	Het
Ggt7	C	T	2: 155,336,813 (GRCm39)	A560T	possibly damaging	Het
Glis3	A	T	19: 28,509,268 (GRCm39)	S239T	possibly damaging	Het
Glyctk	G	A	9: 106,033,168 (GRCm39)	P124L	probably benign	Het
Gm10845	T	A	14: 80,100,644 (GRCm39)		noncoding transcript	Het
H13	A	G	2: 152,528,176 (GRCm39)	K175R	probably benign	Het
Igsf6	T	A	7: 120,673,677 (GRCm39)	I18F	probably benign	Het
Immt	A	G	6: 71,828,828 (GRCm39)	S128G	probably benign	Het
Isy1	G	A	6: 87,796,167 (GRCm39)	R257W	probably damaging	Het
Kif13a	G	T	13: 46,978,823 (GRCm39)		probably benign	Het
L2hgdh	A	T	12: 69,752,563 (GRCm39)	Y239*	probably null	Het
Lamp1	A	G	8: 13,224,550 (GRCm39)	T405A	probably damaging	Het
Lpin1	A	T	12: 16,590,980 (GRCm39)	N817K	possibly damaging	Het
Macf1	G	A	4: 123,302,357 (GRCm39)	T715I	probably benign	Het
Mapk12	T	C	15: 89,017,187 (GRCm39)		probably benign	Het
Mdga2	A	T	12: 66,763,480 (GRCm39)	N205K	probably damaging	Het
Nat10	A	G	2: 103,587,550 (GRCm39)	V55A	probably damaging	Het
Nlrp10	T	C	7: 108,524,529 (GRCm39)	E317G	possibly damaging	Het
Nolc1	T	A	19: 46,068,528 (GRCm39)		probably benign	Het
Nomo1	T	C	7: 45,687,056 (GRCm39)	I72T	probably damaging	Het
Or5b98	A	G	19: 12,931,720 (GRCm39)	I256V	probably benign	Het
Pappa2	C	T	1: 158,542,547 (GRCm39)	C1780Y	probably damaging	Het
Pgm2l1	A	G	7: 99,899,580 (GRCm39)	M65V	probably benign	Het
Pnisr	T	C	4: 21,874,617 (GRCm39)		probably benign	Het
Prss34	A	T	17: 25,517,700 (GRCm39)	D25V	probably damaging	Het
Ptpn1	T	C	2: 167,818,338 (GRCm39)		probably benign	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Pygb	A	G	2: 150,648,123 (GRCm39)	D119G	probably benign	Het
Racgap1	T	C	15: 99,540,839 (GRCm39)	T4A	possibly damaging	Het
Rap1gap2	A	G	11: 74,326,570 (GRCm39)	C166R	probably benign	Het
Rbm28	C	A	6: 29,127,802 (GRCm39)	V705L	probably benign	Het
Rgs1	C	T	1: 144,124,287 (GRCm39)	V50M	probably benign	Het
Rgs12	C	T	5: 35,124,008 (GRCm39)	T597I	probably benign	Het
Ros1	T	C	10: 52,018,363 (GRCm39)	N765S	possibly damaging	Het
Ruvbl1	A	G	6: 88,450,182 (GRCm39)	R58G	probably damaging	Het
Slc6a7	A	G	18: 61,135,295 (GRCm39)	V411A	probably benign	Het
Slco1a6	A	T	6: 142,103,116 (GRCm39)		probably benign	Het
Smc1b	A	T	15: 84,955,020 (GRCm39)	D1077E	probably damaging	Het
Srek1	G	A	13: 103,880,131 (GRCm39)	H476Y	unknown	Het
Strn3	A	G	12: 51,668,571 (GRCm39)	V673A	probably benign	Het
Tepsin	T	C	11: 119,982,637 (GRCm39)		probably null	Het
Tmem131l	C	T	3: 83,842,122 (GRCm39)		probably benign	Het
Tmem132c	T	C	5: 127,631,733 (GRCm39)	V664A	possibly damaging	Het
Tmprss15	T	C	16: 78,800,277 (GRCm39)	D602G	probably damaging	Het
Trbv15	T	C	6: 41,118,199 (GRCm39)		probably benign	Het
Trpm4	A	G	7: 44,968,664 (GRCm39)		probably null	Het
Wdr70	A	T	15: 8,049,068 (GRCm39)		probably null	Het

Other mutations in Firrm

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02051:Firrm	APN	1	163,785,091 (GRCm39)	missense	probably benign	0.01
IGL02638:Firrm	APN	1	163,786,868 (GRCm39)	nonsense	probably null
IGL03337:Firrm	APN	1	163,818,328 (GRCm39)	missense	probably damaging	0.96
IGL03048:Firrm	UTSW	1	163,792,094 (GRCm39)	missense	probably benign	0.04
R0106:Firrm	UTSW	1	163,810,380 (GRCm39)	unclassified	probably benign
R0414:Firrm	UTSW	1	163,795,890 (GRCm39)	missense	probably benign	0.02
R0511:Firrm	UTSW	1	163,799,412 (GRCm39)	splice site	probably null
R1323:Firrm	UTSW	1	163,783,030 (GRCm39)	unclassified	probably benign
R1870:Firrm	UTSW	1	163,792,363 (GRCm39)	missense	probably damaging	1.00
R2129:Firrm	UTSW	1	163,794,026 (GRCm39)	missense	probably damaging	1.00
R3716:Firrm	UTSW	1	163,784,457 (GRCm39)	missense	probably damaging	1.00
R3783:Firrm	UTSW	1	163,815,252 (GRCm39)	missense	probably benign	0.27
R3872:Firrm	UTSW	1	163,814,533 (GRCm39)	missense	probably damaging	0.99
R4427:Firrm	UTSW	1	163,781,853 (GRCm39)	missense	probably benign
R5069:Firrm	UTSW	1	163,815,243 (GRCm39)	missense	possibly damaging	0.59
R5620:Firrm	UTSW	1	163,789,613 (GRCm39)	nonsense	probably null
R5681:Firrm	UTSW	1	163,789,654 (GRCm39)	missense	probably damaging	1.00
R5699:Firrm	UTSW	1	163,785,120 (GRCm39)	missense	probably benign	0.26
R5936:Firrm	UTSW	1	163,814,581 (GRCm39)	missense	probably benign	0.00
R6065:Firrm	UTSW	1	163,815,257 (GRCm39)	missense	probably damaging	1.00
R6065:Firrm	UTSW	1	163,786,957 (GRCm39)	missense	probably benign	0.08
R6075:Firrm	UTSW	1	163,805,656 (GRCm39)	missense	probably damaging	1.00
R6466:Firrm	UTSW	1	163,781,734 (GRCm39)	missense	probably benign	0.01
R6701:Firrm	UTSW	1	163,799,412 (GRCm39)	splice site	probably null
R6776:Firrm	UTSW	1	163,804,318 (GRCm39)	missense	probably damaging	1.00
R6851:Firrm	UTSW	1	163,792,336 (GRCm39)	missense	probably damaging	1.00
R6923:Firrm	UTSW	1	163,814,454 (GRCm39)	critical splice donor site	probably null
R7125:Firrm	UTSW	1	163,789,631 (GRCm39)	missense	probably benign	0.00
R7361:Firrm	UTSW	1	163,813,602 (GRCm39)	missense	possibly damaging	0.54
R7492:Firrm	UTSW	1	163,786,897 (GRCm39)	missense	probably benign	0.35
R8528:Firrm	UTSW	1	163,813,652 (GRCm39)	missense	probably damaging	1.00
R8755:Firrm	UTSW	1	163,786,895 (GRCm39)	missense	probably damaging	1.00
R8786:Firrm	UTSW	1	163,792,040 (GRCm39)	missense	probably damaging	1.00
R8938:Firrm	UTSW	1	163,789,541 (GRCm39)	missense	probably benign	0.01
R8957:Firrm	UTSW	1	163,792,335 (GRCm39)	missense	probably damaging	1.00
R9023:Firrm	UTSW	1	163,818,300 (GRCm39)	missense	possibly damaging	0.83
R9132:Firrm	UTSW	1	163,814,514 (GRCm39)	missense	probably damaging	0.99
R9159:Firrm	UTSW	1	163,814,514 (GRCm39)	missense	probably damaging	0.99
R9229:Firrm	UTSW	1	163,794,659 (GRCm39)	missense	probably damaging	1.00
R9310:Firrm	UTSW	1	163,792,089 (GRCm39)	missense	probably damaging	1.00
R9455:Firrm	UTSW	1	163,781,721 (GRCm39)	missense	probably benign	0.05
R9463:Firrm	UTSW	1	163,795,907 (GRCm39)	missense	probably benign	0.00
R9597:Firrm	UTSW	1	163,804,340 (GRCm39)	missense	probably null	1.00
R9646:Firrm	UTSW	1	163,822,195 (GRCm39)	missense	probably damaging	0.97
Z1177:Firrm	UTSW	1	163,792,086 (GRCm39)	missense	probably damaging	1.00

Posted On

2013-03-25