Mutagenetix > Incidental Mutation

Incidental Mutation 'R5092:Frmd4b'

387820

Institutional Source

Beutler Lab

Gene Symbol

Frmd4b

Ensembl Gene

ENSMUSG00000030064

Gene Name

FERM domain containing 4B

Synonyms

GRSP1, 6030440G05Rik

MMRRC Submission

042681-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5092 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

97263828-97594502 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 97272941 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 763 (D763V)

Ref Sequence

ENSEMBL: ENSMUSP00000108982 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032146] [ENSMUST00000113355] [ENSMUST00000113359]

AlphaFold

Q920B0

Predicted Effect

probably damaging
Transcript: ENSMUST00000032146
AA Change: D817V

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000032146
Gene: ENSMUSG00000030064
AA Change: D817V

Domain	Start	End	E-Value	Type
B41	55	260	7.4e-35	SMART
FERM_C	264	365	8.7e-26	SMART
Pfam:DUF3338	395	529	4.5e-55	PFAM
coiled coil region	534	558	N/A	INTRINSIC
low complexity region	571	592	N/A	INTRINSIC
low complexity region	731	742	N/A	INTRINSIC
low complexity region	941	958	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000113355
AA Change: D763V

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000108982
Gene: ENSMUSG00000030064
AA Change: D763V

Domain	Start	End	E-Value	Type
B41	1	206	4.5e-37	SMART
FERM_C	210	311	4.1e-30	SMART
Pfam:DUF3338	340	476	6.9e-58	PFAM
coiled coil region	480	504	N/A	INTRINSIC
low complexity region	517	538	N/A	INTRINSIC
low complexity region	677	688	N/A	INTRINSIC
low complexity region	887	904	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113359
AA Change: D771V

PolyPhen 2 Score 0.161 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000108986
Gene: ENSMUSG00000030064
AA Change: D771V

Domain	Start	End	E-Value	Type
B41	9	214	7.4e-35	SMART
FERM_C	218	319	8.7e-26	SMART
Pfam:DUF3338	348	484	8e-61	PFAM
coiled coil region	488	512	N/A	INTRINSIC
low complexity region	525	546	N/A	INTRINSIC
low complexity region	685	696	N/A	INTRINSIC
low complexity region	895	912	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143698

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203486

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a GRP1-binding protein which contains a FERM protein interaction domain as well as two coiled coil domains. This protein may play a role as a scaffolding protein. [provided by RefSeq, Mar 2014]

Allele List at MGI

All alleles(24) : Targeted(2) Gene trapped(22)

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	C	T	7: 40,637,091 (GRCm39)		probably benign	Het
Abca13	T	A	11: 9,208,535 (GRCm39)	L236Q	probably damaging	Het
Acp2	A	T	2: 91,038,391 (GRCm39)	T255S	probably benign	Het
Acsf3	A	C	8: 123,544,131 (GRCm39)	R536S	probably benign	Het
Adgrb1	T	G	15: 74,401,664 (GRCm39)	V220G	probably benign	Het
Anks6	C	T	4: 47,030,795 (GRCm39)	G601S	probably damaging	Het
Atp5f1b	A	G	10: 127,919,854 (GRCm39)	Q74R	probably benign	Het
Bltp1	A	T	3: 37,054,234 (GRCm39)	M3118L	probably benign	Het
Brf1	G	A	12: 112,943,352 (GRCm39)	T166M	probably damaging	Het
Capn9	A	G	8: 125,324,264 (GRCm39)	K188R	probably damaging	Het
Casp8	A	T	1: 58,883,835 (GRCm39)	N381Y	possibly damaging	Het
Ccdc88b	A	G	19: 6,825,600 (GRCm39)	S1218P	probably damaging	Het
Cdc42bpg	C	T	19: 6,363,250 (GRCm39)	P403S	probably benign	Het
Cdkal1	T	A	13: 30,030,222 (GRCm39)	Y91F	probably damaging	Het
Cdyl2	T	C	8: 117,350,679 (GRCm39)	N151D	possibly damaging	Het
Cnot1	T	A	8: 96,479,396 (GRCm39)	R875S	possibly damaging	Het
Cpd	A	G	11: 76,702,530 (GRCm39)	S613P	possibly damaging	Het
Cyp2e1	G	T	7: 140,354,648 (GRCm39)	R492L	probably damaging	Het
D5Ertd579e	G	A	5: 36,760,047 (GRCm39)	T1371M	probably benign	Het
Dcaf8	A	G	1: 172,014,476 (GRCm39)	T394A	probably benign	Het
Dgka	T	C	10: 128,571,702 (GRCm39)	E117G	probably damaging	Het
Dock4	G	A	12: 40,894,440 (GRCm39)	V1867I	probably benign	Het
E2f2	G	T	4: 135,914,248 (GRCm39)	A333S	probably benign	Het
Eif3l	T	C	15: 78,968,354 (GRCm39)	S208P	probably benign	Het
Elovl3	A	T	19: 46,122,961 (GRCm39)	H179L	probably damaging	Het
Eml5	T	C	12: 98,758,875 (GRCm39)	D1766G	probably damaging	Het
Eno4	A	G	19: 58,934,023 (GRCm39)	T75A	probably benign	Het
Fam135a	C	T	1: 24,067,888 (GRCm39)	D94N	probably benign	Het
Fasn	G	T	11: 120,705,862 (GRCm39)	Q1136K	probably benign	Het
Fcer1a	T	G	1: 173,053,022 (GRCm39)	N58T	probably damaging	Het
Gm43518	A	G	5: 124,076,297 (GRCm39)	T115A	probably damaging	Het
Gria4	C	T	9: 4,472,176 (GRCm39)	E438K	probably benign	Het
Grin2d	T	C	7: 45,503,692 (GRCm39)	E681G	probably damaging	Het
Gtf3c5	G	T	2: 28,472,885 (GRCm39)	N35K	possibly damaging	Het
Hydin	A	G	8: 111,309,300 (GRCm39)	T4031A	probably benign	Het
Igfn1	G	T	1: 135,892,564 (GRCm39)	N2185K	probably benign	Het
Il17rb	T	C	14: 29,724,333 (GRCm39)	T174A	probably benign	Het
Kdm3b	T	A	18: 34,946,515 (GRCm39)	C835S	probably benign	Het
Lgi2	A	T	5: 52,695,429 (GRCm39)	I510N	probably damaging	Het
Map3k6	A	G	4: 132,979,054 (GRCm39)	E1164G	probably benign	Het
Mpv17l	T	A	16: 13,758,537 (GRCm39)	M1K	probably null	Het
Myoc	T	A	1: 162,467,203 (GRCm39)	L124Q	probably damaging	Het
Nbeal2	C	A	9: 110,455,796 (GRCm39)		probably null	Het
Nek10	A	G	14: 14,820,851 (GRCm38)	K13E	possibly damaging	Het
Nt5dc2	A	G	14: 30,860,989 (GRCm39)	H491R	possibly damaging	Het
Or4f61	A	C	2: 111,922,452 (GRCm39)	M198R	possibly damaging	Het
Or51b6	T	A	7: 103,556,406 (GRCm39)	Y250*	probably null	Het
Or8k21	T	C	2: 86,144,706 (GRCm39)	Q308R	probably benign	Het
Pclo	T	A	5: 14,727,322 (GRCm39)		probably benign	Het
Pgm2	A	T	5: 64,265,092 (GRCm39)	N371I	possibly damaging	Het
Phf20l1	T	A	15: 66,508,762 (GRCm39)	S873T	possibly damaging	Het
Plch1	T	C	3: 63,606,131 (GRCm39)	T1249A	probably benign	Het
Plekhn1	A	T	4: 156,309,222 (GRCm39)	I228N	possibly damaging	Het
Ppp1r12a	A	T	10: 108,103,263 (GRCm39)		probably null	Het
Ptchd3	T	C	11: 121,721,972 (GRCm39)	Y282H	probably damaging	Het
Ptprk	T	A	10: 28,468,769 (GRCm39)	N1396K	probably damaging	Het
Rap1gap2	T	C	11: 74,329,121 (GRCm39)	E81G	probably damaging	Het
Rpf2	T	C	10: 40,122,971 (GRCm39)	M1V	probably null	Het
Rpgrip1l	G	A	8: 91,948,012 (GRCm39)	Q1224*	probably null	Het
Rreb1	A	G	13: 38,112,254 (GRCm39)	D286G	probably benign	Het
Rufy4	T	C	1: 74,186,822 (GRCm39)	C537R	probably damaging	Het
Senp5	A	T	16: 31,807,960 (GRCm39)	N431K	probably benign	Het
Serpina1f	A	C	12: 103,659,809 (GRCm39)	S158A	probably damaging	Het
Sertad3	T	A	7: 27,176,145 (GRCm39)	I193N	probably damaging	Het
Slc22a8	T	A	19: 8,571,528 (GRCm39)	N86K	probably damaging	Het
Slc6a2	T	C	8: 93,721,347 (GRCm39)	V492A	possibly damaging	Het
Slf2	T	A	19: 44,940,523 (GRCm39)	D773E	probably benign	Het
Slmap	A	C	14: 26,184,744 (GRCm39)	L272R	probably damaging	Het
Smyd5	T	C	6: 85,422,185 (GRCm39)		probably benign	Het
Snx21	G	T	2: 164,628,666 (GRCm39)	R103L	probably damaging	Het
Sphk2	T	A	7: 45,361,777 (GRCm39)		probably null	Het
Stab1	T	C	14: 30,867,812 (GRCm39)	K1653E	probably benign	Het
Syde1	A	G	10: 78,425,252 (GRCm39)	V253A	probably benign	Het
Sympk	G	T	7: 18,776,584 (GRCm39)	R492L	probably benign	Het
Taar7f	T	C	10: 23,925,451 (GRCm39)	I15T	probably benign	Het
Tas2r140	A	G	6: 40,468,200 (GRCm39)	D10G	probably benign	Het
Tbcc	A	G	17: 47,202,600 (GRCm39)	S329G	probably benign	Het
Teddm3	G	A	16: 20,971,900 (GRCm39)	T223M	probably benign	Het
Tex14	G	T	11: 87,405,668 (GRCm39)	C860F	probably benign	Het
Thada	A	T	17: 84,751,896 (GRCm39)	L360Q	probably damaging	Het
Thop1	C	A	10: 80,916,412 (GRCm39)	H473Q	probably damaging	Het
Tln2	T	C	9: 67,163,310 (GRCm39)	D1075G	probably benign	Het
Tmem130	G	A	5: 144,680,528 (GRCm39)	T292I	probably benign	Het
Tmem198b	T	C	10: 128,637,305 (GRCm39)	N278S	probably benign	Het
Ttc21a	A	T	9: 119,771,731 (GRCm39)	T177S	probably benign	Het
Ubr2	A	T	17: 47,280,173 (GRCm39)	C659S	probably damaging	Het
Vmn2r4	T	C	3: 64,298,373 (GRCm39)	K585R	probably benign	Het
Vmn2r86	A	G	10: 130,282,456 (GRCm39)	I720T	probably damaging	Het
Wdr35	G	T	12: 9,037,327 (GRCm39)	W311L	probably damaging	Het
Zfp39	A	T	11: 58,782,028 (GRCm39)	F245I	possibly damaging	Het
Zftraf1	A	T	15: 76,530,512 (GRCm39)	F269L	probably benign	Het
Zmym5	G	A	14: 57,034,236 (GRCm39)	T325I	probably benign	Het
Zng1	A	T	19: 24,898,383 (GRCm39)		probably null	Het

Other mutations in Frmd4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00849:Frmd4b	APN	6	97,285,021 (GRCm39)	missense	probably damaging	1.00
IGL01478:Frmd4b	APN	6	97,305,254 (GRCm39)	missense	probably damaging	1.00
IGL01760:Frmd4b	APN	6	97,285,663 (GRCm39)	missense	probably damaging	1.00
IGL01777:Frmd4b	APN	6	97,272,905 (GRCm39)	missense	probably benign	0.03
IGL01960:Frmd4b	APN	6	97,272,741 (GRCm39)	missense	possibly damaging	0.93
IGL02408:Frmd4b	APN	6	97,272,770 (GRCm39)	missense	probably damaging	1.00
IGL02429:Frmd4b	APN	6	97,302,390 (GRCm39)	splice site	probably benign
IGL02525:Frmd4b	APN	6	97,389,494 (GRCm39)	missense	probably damaging	1.00
IGL02618:Frmd4b	APN	6	97,285,066 (GRCm39)	nonsense	probably null
IGL03051:Frmd4b	APN	6	97,272,943 (GRCm39)	nonsense	probably null
IGL03120:Frmd4b	APN	6	97,373,206 (GRCm39)	missense	possibly damaging	0.88
IGL03218:Frmd4b	APN	6	97,285,075 (GRCm39)	missense	probably benign	0.01
IGL03260:Frmd4b	APN	6	97,373,185 (GRCm39)	missense	probably damaging	1.00
IGL02984:Frmd4b	UTSW	6	97,273,221 (GRCm39)	missense	probably damaging	0.96
P0031:Frmd4b	UTSW	6	97,330,991 (GRCm39)	missense	probably damaging	1.00
R0055:Frmd4b	UTSW	6	97,300,610 (GRCm39)	splice site	probably benign
R0055:Frmd4b	UTSW	6	97,300,610 (GRCm39)	splice site	probably benign
R0058:Frmd4b	UTSW	6	97,400,460 (GRCm39)	missense	probably damaging	1.00
R0255:Frmd4b	UTSW	6	97,285,047 (GRCm39)	missense	probably damaging	1.00
R0437:Frmd4b	UTSW	6	97,400,424 (GRCm39)	missense	probably damaging	1.00
R0594:Frmd4b	UTSW	6	97,302,387 (GRCm39)	splice site	probably benign
R1525:Frmd4b	UTSW	6	97,273,347 (GRCm39)	missense	probably damaging	0.97
R1640:Frmd4b	UTSW	6	97,285,634 (GRCm39)	missense	possibly damaging	0.91
R1768:Frmd4b	UTSW	6	97,283,725 (GRCm39)	missense	possibly damaging	0.68
R1923:Frmd4b	UTSW	6	97,265,415 (GRCm39)	missense	probably benign	0.33
R2056:Frmd4b	UTSW	6	97,389,448 (GRCm39)	critical splice donor site	probably null
R2192:Frmd4b	UTSW	6	97,464,577 (GRCm39)	missense	probably damaging	0.98
R3809:Frmd4b	UTSW	6	97,300,690 (GRCm39)	missense	possibly damaging	0.49
R3831:Frmd4b	UTSW	6	97,389,486 (GRCm39)	nonsense	probably null
R4466:Frmd4b	UTSW	6	97,300,614 (GRCm39)	critical splice donor site	probably null
R4536:Frmd4b	UTSW	6	97,287,693 (GRCm39)	missense	possibly damaging	0.57
R4652:Frmd4b	UTSW	6	97,272,716 (GRCm39)	missense	probably benign	0.38
R4679:Frmd4b	UTSW	6	97,272,627 (GRCm39)	missense	possibly damaging	0.94
R4735:Frmd4b	UTSW	6	97,436,220 (GRCm39)	start gained	probably benign
R4793:Frmd4b	UTSW	6	97,272,822 (GRCm39)	missense	probably damaging	0.99
R4940:Frmd4b	UTSW	6	97,275,051 (GRCm39)	missense	probably damaging	1.00
R4948:Frmd4b	UTSW	6	97,283,691 (GRCm39)	missense	probably benign	0.06
R5119:Frmd4b	UTSW	6	97,277,275 (GRCm39)	missense	probably benign	0.03
R5289:Frmd4b	UTSW	6	97,279,309 (GRCm39)	splice site	probably null
R5610:Frmd4b	UTSW	6	97,283,752 (GRCm39)	missense	probably benign
R5690:Frmd4b	UTSW	6	97,330,164 (GRCm39)	missense	possibly damaging	0.56
R6248:Frmd4b	UTSW	6	97,436,173 (GRCm39)	missense	probably benign	0.10
R6437:Frmd4b	UTSW	6	97,273,228 (GRCm39)	missense	probably damaging	1.00
R6459:Frmd4b	UTSW	6	97,464,601 (GRCm39)	missense	probably damaging	1.00
R6825:Frmd4b	UTSW	6	97,302,437 (GRCm39)	missense	possibly damaging	0.89
R6964:Frmd4b	UTSW	6	97,282,158 (GRCm39)	missense	probably damaging	1.00
R7110:Frmd4b	UTSW	6	97,273,192 (GRCm39)	nonsense	probably null
R7154:Frmd4b	UTSW	6	97,283,707 (GRCm39)	missense	probably damaging	1.00
R7764:Frmd4b	UTSW	6	97,272,891 (GRCm39)	missense	probably damaging	1.00
R8073:Frmd4b	UTSW	6	97,283,674 (GRCm39)	missense	probably benign	0.03
R8382:Frmd4b	UTSW	6	97,282,209 (GRCm39)	missense	probably benign
R8746:Frmd4b	UTSW	6	97,269,370 (GRCm39)	missense	probably benign
R8856:Frmd4b	UTSW	6	97,269,359 (GRCm39)	nonsense	probably null
R8881:Frmd4b	UTSW	6	97,272,735 (GRCm39)	missense	probably benign	0.00
R8885:Frmd4b	UTSW	6	97,389,480 (GRCm39)	missense	probably benign	0.01
R8907:Frmd4b	UTSW	6	97,273,046 (GRCm39)	missense	probably damaging	1.00
R8975:Frmd4b	UTSW	6	97,283,477 (GRCm39)	missense	possibly damaging	0.46
R9032:Frmd4b	UTSW	6	97,269,334 (GRCm39)	missense	probably benign	0.00
R9085:Frmd4b	UTSW	6	97,269,334 (GRCm39)	missense	probably benign	0.00
R9094:Frmd4b	UTSW	6	97,398,559 (GRCm39)	missense
R9429:Frmd4b	UTSW	6	97,279,252 (GRCm39)	missense	probably damaging	1.00
X0020:Frmd4b	UTSW	6	97,282,326 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- ATGTGCTCAGATTTCACGGC -3'
(R):5'- TATTACTGTGTGACGCCTGCTG -3'

Sequencing Primer
(F):5'- AGATTTCACGGCCGCCTTC -3'
(R):5'- GCTGCCAGCCCTTACTACAC -3'

Posted On

2016-06-06