Mutagenetix > Incidental Mutation

Incidental Mutation 'R1959:Frmd4a'

218098

Institutional Source

Beutler Lab

Gene Symbol

Frmd4a

Ensembl Gene

ENSMUSG00000026657

Gene Name

FERM domain containing 4A

Synonyms

Gm13190, 2700017I06Rik, C230040M21Rik

MMRRC Submission

039973-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.154) question?

Stock #

R1959 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

4017717-4614043 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 4535186 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 210 (V210M)

Ref Sequence

ENSEMBL: ENSMUSP00000134788 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075767] [ENSMUST00000091497] [ENSMUST00000175669] [ENSMUST00000175944] [ENSMUST00000176803] [ENSMUST00000177457]

AlphaFold

Q8BIE6

Predicted Effect

probably damaging
Transcript: ENSMUST00000075767
AA Change: V195M

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

SMART Domains

Protein: ENSMUSP00000075172
Gene: ENSMUSG00000026657
AA Change: V195M

Domain	Start	End	E-Value	Type
B41	1	206	3.24e-40	SMART
FERM_C	210	311	7.69e-27	SMART
Pfam:DUF3338	340	477	1.9e-63	PFAM
low complexity region	558	571	N/A	INTRINSIC
low complexity region	610	623	N/A	INTRINSIC
low complexity region	732	741	N/A	INTRINSIC
low complexity region	764	785	N/A	INTRINSIC
low complexity region	790	801	N/A	INTRINSIC
low complexity region	924	947	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000091497
AA Change: V206M

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000089079
Gene: ENSMUSG00000026657
AA Change: V206M

Domain	Start	End	E-Value	Type
B41	12	217	3.24e-40	SMART
FERM_C	221	322	7.69e-27	SMART
Pfam:DUF3338	352	487	6.3e-61	PFAM
low complexity region	569	582	N/A	INTRINSIC
low complexity region	621	634	N/A	INTRINSIC
low complexity region	743	752	N/A	INTRINSIC
low complexity region	775	796	N/A	INTRINSIC
low complexity region	801	812	N/A	INTRINSIC
low complexity region	935	958	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000115039

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147156

Predicted Effect

probably damaging
Transcript: ENSMUST00000175669
AA Change: V225M

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000135306
Gene: ENSMUSG00000026657
AA Change: V225M

Domain	Start	End	E-Value	Type
B41	31	236	3.24e-40	SMART
FERM_C	240	341	7.69e-27	SMART
low complexity region	371	387	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000175944
AA Change: V243M

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

SMART Domains

Protein: ENSMUSP00000135686
Gene: ENSMUSG00000026657
AA Change: V243M

Domain	Start	End	E-Value	Type
B41	49	254	3.24e-40	SMART
FERM_C	258	359	7.69e-27	SMART
Pfam:DUF3338	388	525	6.5e-64	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000176803

SMART Domains

Protein: ENSMUSP00000135432
Gene: ENSMUSG00000026657

Domain	Start	End	E-Value	Type
Pfam:FERM_N	10	89	5.5e-21	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000177457
AA Change: V210M

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

SMART Domains

Protein: ENSMUSP00000134788
Gene: ENSMUSG00000026657
AA Change: V210M

Domain	Start	End	E-Value	Type
B41	16	221	3.24e-40	SMART
FERM_C	225	326	7.69e-27	SMART
Pfam:DUF3338	355	492	3.9e-63	PFAM
low complexity region	573	586	N/A	INTRINSIC
low complexity region	625	638	N/A	INTRINSIC
low complexity region	747	756	N/A	INTRINSIC
low complexity region	779	800	N/A	INTRINSIC
low complexity region	805	816	N/A	INTRINSIC
low complexity region	939	962	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a FERM domain-containing protein that regulates epithelial cell polarity. It connects ADP ribosylation factor 6 (ARF6) with the Par protein complex, which regulates the remodeling of adherens junctions and linear actin cable formation during epithelial cell polarization. Polymorphisms in this gene are associated with Alzheimer's disease, and also with nicotine dependence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

Allele List at MGI

Other mutations in this stock

Total: 130 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700123L14Rik	A	G	6: 96,165,269 (GRCm38)	S265P	possibly damaging	Het
Abcc1	T	C	16: 14,396,393 (GRCm38)	Y191H	probably damaging	Het
Aco1	T	C	4: 40,167,193 (GRCm38)		probably null	Het
Adap1	A	G	5: 139,273,341 (GRCm38)	Y364H	probably benign	Het
Add2	T	C	6: 86,096,756 (GRCm38)	F209S	probably damaging	Het
Adgb	A	T	10: 10,395,249 (GRCm38)	D883E	probably benign	Het
Als2cr12	A	T	1: 58,659,278 (GRCm38)	V327D	possibly damaging	Het
Anapc1	C	A	2: 128,633,415 (GRCm38)	R1381S	probably benign	Het
Aoah	A	G	13: 20,794,394 (GRCm38)	M1V	probably null	Het
Arap1	C	A	7: 101,373,015 (GRCm38)	A8E	probably damaging	Het
Arhgap10	A	G	8: 77,409,626 (GRCm38)	F319S	possibly damaging	Het
Btrc	T	G	19: 45,527,343 (GRCm38)	I480S	probably damaging	Het
Cabin1	A	T	10: 75,735,090 (GRCm38)	V784E	possibly damaging	Het
Card9	T	A	2: 26,354,873 (GRCm38)		probably null	Het
Cdk18	A	G	1: 132,117,821 (GRCm38)	I238T	possibly damaging	Het
Clec12a	A	C	6: 129,350,481 (GRCm38)	T21P	possibly damaging	Het
Commd3	A	T	2: 18,673,963 (GRCm38)	I70F	probably benign	Het
Cspg5	G	A	9: 110,251,026 (GRCm38)	V340M	probably damaging	Het
Cyb5r4	G	A	9: 87,055,849 (GRCm38)	S307N	possibly damaging	Het
Cyp26c1	T	A	19: 37,687,377 (GRCm38)	F230I	probably damaging	Het
Ddx11	A	G	17: 66,130,728 (GRCm38)	M150V	probably benign	Het
Dennd4b	A	G	3: 90,268,773 (GRCm38)	Y190C	probably damaging	Het
Det1	A	G	7: 78,843,443 (GRCm38)	V271A	probably benign	Het
Dgkd	C	A	1: 87,929,827 (GRCm38)	P754T	possibly damaging	Het
Dhx36	T	C	3: 62,479,385 (GRCm38)	S649G	probably benign	Het
Dlgap5	A	G	14: 47,416,386 (GRCm38)	I62T	possibly damaging	Het
Dmgdh	A	G	13: 93,720,559 (GRCm38)	M724V	probably benign	Het
Dnah7a	A	G	1: 53,684,983 (GRCm38)	S108P	probably benign	Het
Dock4	A	T	12: 40,710,798 (GRCm38)	K495M	probably damaging	Het
Dse	A	G	10: 34,160,206 (GRCm38)	Y225H	probably damaging	Het
Emx1	G	A	6: 85,203,934 (GRCm38)	R211K	probably damaging	Het
Ergic2	A	G	6: 148,199,354 (GRCm38)		probably null	Het
Fbxo27	G	A	7: 28,698,372 (GRCm38)	C277Y	possibly damaging	Het
Fcrl1	T	C	3: 87,376,520 (GRCm38)	I9T	possibly damaging	Het
Fjx1	T	C	2: 102,450,807 (GRCm38)	E261G	probably benign	Het
Flnb	C	T	14: 7,884,735 (GRCm38)	Q445*	probably null	Het
Flrt2	G	A	12: 95,780,300 (GRCm38)	V471I	probably benign	Het
Fsip2	A	G	2: 82,991,550 (GRCm38)	K5876E	probably benign	Het
Galnt10	T	C	11: 57,765,617 (GRCm38)	L209P	probably damaging	Het
Gata5	A	T	2: 180,326,936 (GRCm38)	S382T	possibly damaging	Het
Glt6d1	C	A	2: 25,794,413 (GRCm38)	V194L	probably damaging	Het
Gm10803	T	G	2: 93,563,943 (GRCm38)	V20G	unknown	Het
Gm44511	T	G	6: 128,820,271 (GRCm38)	T52P	probably damaging	Het
Gpat4	A	T	8: 23,182,936 (GRCm38)	L88Q	possibly damaging	Het
Gpr15	T	A	16: 58,718,007 (GRCm38)	I240L	probably benign	Het
Hivep2	A	T	10: 14,132,709 (GRCm38)	I1684F	probably benign	Het
Hmcn1	T	C	1: 150,649,676 (GRCm38)	T3366A	probably benign	Het
Hnmt	A	G	2: 24,003,882 (GRCm38)	V200A	possibly damaging	Het
Hps6	A	T	19: 46,004,335 (GRCm38)	H237L	probably benign	Het
Hspg2	C	T	4: 137,564,895 (GRCm38)	P4033S	probably damaging	Het
Irf9	T	A	14: 55,607,717 (GRCm38)	S297T	possibly damaging	Het
Kdm3b	T	C	18: 34,812,395 (GRCm38)	V753A	possibly damaging	Het
Kif21a	G	A	15: 90,970,848 (GRCm38)	A703V	probably damaging	Het
Kif27	T	G	13: 58,293,123 (GRCm38)	R1159S	probably benign	Het
Krtap4-16	A	G	11: 99,851,547 (GRCm38)	V9A	unknown	Het
Lama2	G	T	10: 27,422,618 (GRCm38)	P161T	probably damaging	Het
Ltbp4	G	A	7: 27,329,018 (GRCm38)	P273L	unknown	Het
Lvrn	T	A	18: 46,894,717 (GRCm38)	S866R	probably damaging	Het
Med13	A	G	11: 86,298,979 (GRCm38)	Y1035H	probably damaging	Het
Mertk	T	A	2: 128,759,090 (GRCm38)	N331K	probably damaging	Het
Mios	T	A	6: 8,215,437 (GRCm38)	F211Y	probably benign	Het
Mpeg1	G	A	19: 12,462,911 (GRCm38)	V578M	probably damaging	Het
Mphosph9	A	T	5: 124,315,701 (GRCm38)	S183T	possibly damaging	Het
Mrto4	A	T	4: 139,349,638 (GRCm38)	I56N	probably damaging	Het
Muc5b	T	C	7: 141,862,637 (GRCm38)	C3107R	possibly damaging	Het
Ncoa2	A	G	1: 13,160,252 (GRCm38)	Y1023H	probably damaging	Het
Nlrp2	T	C	7: 5,327,738 (GRCm38)	E553G	probably damaging	Het
Nlrp6	GAGAAGAAGAAGAAGAAGAAGA	GAGAAGAAGAAGAAGAAGA	7: 140,924,113 (GRCm38)		probably benign	Het
Nr2f1	T	C	13: 78,189,816 (GRCm38)	T237A	probably damaging	Het
Nup205	C	A	6: 35,233,366 (GRCm38)	Q1621K	probably benign	Het
Nxpe2	T	A	9: 48,319,726 (GRCm38)	S448C	probably benign	Het
Ogdh	T	A	11: 6,346,638 (GRCm38)	C498S	possibly damaging	Het
Olfr1176	T	C	2: 88,340,201 (GRCm38)	L212P	probably damaging	Het
Olfr281	T	C	15: 98,456,753 (GRCm38)	S148P	probably damaging	Het
Olfr294	A	T	7: 86,616,431 (GRCm38)	F71L	probably benign	Het
Olfr414	A	T	1: 174,430,905 (GRCm38)	K159M	probably damaging	Het
Olfr697	T	C	7: 106,741,394 (GRCm38)	E180G	probably damaging	Het
Olfr715	A	T	7: 107,128,510 (GRCm38)	D294E	possibly damaging	Het
Olfr994	T	C	2: 85,430,619 (GRCm38)	D70G	probably damaging	Het
Oplah	G	A	15: 76,297,464 (GRCm38)	T1119I	probably damaging	Het
Pcdhb9	T	A	18: 37,403,316 (GRCm38)	Y788N	probably damaging	Het
Pcsk5	T	C	19: 17,433,418 (GRCm38)	D1870G	unknown	Het
Pde6g	A	G	11: 120,448,136 (GRCm38)	L76P	probably damaging	Het
Peak1	A	T	9: 56,206,789 (GRCm38)	Y593N	probably damaging	Het
Pfas	C	T	11: 68,994,284 (GRCm38)	G16R	probably damaging	Het
Pkd1l2	A	T	8: 117,043,231 (GRCm38)		probably null	Het
Pla2g3	C	T	11: 3,490,983 (GRCm38)	T316I	probably benign	Het
Ptpru	T	A	4: 131,803,477 (GRCm38)	I489F	probably damaging	Het
Rere	T	G	4: 150,468,790 (GRCm38)	H146Q	probably benign	Het
Rundc1	A	T	11: 101,431,496 (GRCm38)	Q272L	probably damaging	Het
Scml4	T	C	10: 42,956,021 (GRCm38)	L305P	probably damaging	Het
Sec16a	A	T	2: 26,430,132 (GRCm38)	H1431Q	probably benign	Het
Serpina1a	G	A	12: 103,853,800 (GRCm38)	Q373*	probably null	Het
Shank1	A	T	7: 44,325,377 (GRCm38)	N377I	unknown	Het
Shc2	T	C	10: 79,626,791 (GRCm38)		probably null	Het
Slc22a29	C	A	19: 8,169,193 (GRCm38)	R415M	probably benign	Het
Slc7a2	A	T	8: 40,914,965 (GRCm38)	I589F	probably damaging	Het
Smim8	C	T	4: 34,771,316 (GRCm38)	R26Q	probably damaging	Het
Smox	C	A	2: 131,520,464 (GRCm38)	A221D	probably damaging	Het
Sox5	A	G	6: 143,874,105 (GRCm38)	S62P	possibly damaging	Het
Spg21	A	C	9: 65,484,492 (GRCm38)	K240N	probably damaging	Het
Sv2c	C	T	13: 95,976,645 (GRCm38)	V599M	probably damaging	Het
Tanc2	T	A	11: 105,910,295 (GRCm38)	H1112Q	probably damaging	Het
Tbata	T	C	10: 61,175,844 (GRCm38)	I58T	possibly damaging	Het
Tbc1d2	T	G	4: 46,606,419 (GRCm38)	Y842S	probably benign	Het
Tctn1	A	T	5: 122,241,840 (GRCm38)		probably null	Het
Tenm1	T	C	X: 42,827,201 (GRCm38)	D402G	probably benign	Het
Tfcp2l1	T	C	1: 118,669,389 (GRCm38)	V400A	probably benign	Het
Tm9sf2	T	A	14: 122,126,164 (GRCm38)	L99I	probably benign	Het
Top2a	T	C	11: 98,995,977 (GRCm38)		probably null	Het
Traf7	C	A	17: 24,513,281 (GRCm38)	G191C	probably damaging	Het
Trpm1	T	A	7: 64,230,230 (GRCm38)	L661Q	probably damaging	Het
Ttc30b	C	T	2: 75,937,099 (GRCm38)	E437K	probably benign	Het
Ttn	T	C	2: 76,750,623 (GRCm38)	I23309V	probably benign	Het
Usp50	T	C	2: 126,777,961 (GRCm38)	K199E	possibly damaging	Het
Vmn1r218	T	C	13: 23,136,513 (GRCm38)	F10S	probably damaging	Het
Vmn2r89	C	A	14: 51,457,440 (GRCm38)	T459K	probably benign	Het
Vps13a	T	G	19: 16,677,938 (GRCm38)	S1909R	possibly damaging	Het
Vwa5b2	T	C	16: 20,602,191 (GRCm38)		probably null	Het
Vwa8	A	G	14: 78,982,360 (GRCm38)	H516R	possibly damaging	Het
Wnk1	T	C	6: 119,969,247 (GRCm38)	I648M	probably damaging	Het
Zfat	G	C	15: 68,146,543 (GRCm38)	P974R	probably benign	Het
Zfc3h1	T	A	10: 115,423,253 (GRCm38)	I1601K	probably benign	Het
Zfp239	A	G	6: 117,871,817 (GRCm38)	K172R	probably benign	Het
Zfp335	C	T	2: 164,894,802 (GRCm38)	G971D	probably damaging	Het
Zfp532	A	T	18: 65,624,492 (GRCm38)	I499F	probably damaging	Het
Zfp647	T	C	15: 76,911,114 (GRCm38)	T449A	possibly damaging	Het
Zfp938	C	T	10: 82,225,631 (GRCm38)	G385D	probably damaging	Het
Zfp959	T	G	17: 55,897,404 (GRCm38)	V147G	probably damaging	Het
Znfx1	A	T	2: 167,050,350 (GRCm38)	C649S	probably damaging	Het

Other mutations in Frmd4a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00339:Frmd4a	APN	2	4,594,714 (GRCm38)	missense	probably benign	0.00
IGL00508:Frmd4a	APN	2	4,594,734 (GRCm38)	nonsense	probably null
IGL01331:Frmd4a	APN	2	4,602,225 (GRCm38)	missense	probably benign	0.32
IGL01774:Frmd4a	APN	2	4,535,236 (GRCm38)	splice site	probably benign
IGL01909:Frmd4a	APN	2	4,604,033 (GRCm38)	missense	probably benign	0.11
IGL02170:Frmd4a	APN	2	4,566,177 (GRCm38)	missense	probably damaging	0.99
IGL02269:Frmd4a	APN	2	4,604,234 (GRCm38)	missense	probably benign	0.19
IGL02377:Frmd4a	APN	2	4,534,574 (GRCm38)	missense	possibly damaging	0.47
IGL03308:Frmd4a	APN	2	4,498,026 (GRCm38)	missense	possibly damaging	0.95
R0066:Frmd4a	UTSW	2	4,473,152 (GRCm38)	missense	probably damaging	1.00
R0066:Frmd4a	UTSW	2	4,473,152 (GRCm38)	missense	probably damaging	1.00
R0081:Frmd4a	UTSW	2	4,572,441 (GRCm38)	critical splice donor site	probably null
R0128:Frmd4a	UTSW	2	4,604,092 (GRCm38)	missense	probably damaging	0.98
R0130:Frmd4a	UTSW	2	4,604,092 (GRCm38)	missense	probably damaging	0.98
R0376:Frmd4a	UTSW	2	4,572,387 (GRCm38)	missense	probably damaging	0.97
R0529:Frmd4a	UTSW	2	4,606,023 (GRCm38)	missense	probably damaging	1.00
R0549:Frmd4a	UTSW	2	4,603,967 (GRCm38)	missense	possibly damaging	0.76
R1593:Frmd4a	UTSW	2	4,473,188 (GRCm38)	missense	probably damaging	1.00
R2002:Frmd4a	UTSW	2	4,572,365 (GRCm38)	missense	probably damaging	1.00
R2100:Frmd4a	UTSW	2	4,606,023 (GRCm38)	missense	probably damaging	1.00
R2310:Frmd4a	UTSW	2	4,572,399 (GRCm38)	frame shift	probably null
R2340:Frmd4a	UTSW	2	4,586,376 (GRCm38)	missense	probably damaging	1.00
R2426:Frmd4a	UTSW	2	4,529,862 (GRCm38)	missense	probably damaging	1.00
R2680:Frmd4a	UTSW	2	4,534,553 (GRCm38)	missense	probably damaging	1.00
R3409:Frmd4a	UTSW	2	4,153,028 (GRCm38)	intron	probably benign
R3772:Frmd4a	UTSW	2	4,590,622 (GRCm38)	missense	probably damaging	0.99
R3773:Frmd4a	UTSW	2	4,590,622 (GRCm38)	missense	probably damaging	0.99
R3932:Frmd4a	UTSW	2	4,537,260 (GRCm38)	missense	probably damaging	1.00
R4094:Frmd4a	UTSW	2	4,611,032 (GRCm38)	missense	probably damaging	1.00
R4226:Frmd4a	UTSW	2	4,333,078 (GRCm38)	missense	probably benign	0.00
R4299:Frmd4a	UTSW	2	4,333,071 (GRCm38)	missense	probably benign	0.02
R4304:Frmd4a	UTSW	2	4,333,078 (GRCm38)	missense	probably benign	0.00
R4306:Frmd4a	UTSW	2	4,333,078 (GRCm38)	missense	probably benign	0.00
R4307:Frmd4a	UTSW	2	4,333,078 (GRCm38)	missense	probably benign	0.00
R4346:Frmd4a	UTSW	2	4,608,033 (GRCm38)	missense	possibly damaging	0.92
R4360:Frmd4a	UTSW	2	4,601,241 (GRCm38)	missense	probably damaging	1.00
R4384:Frmd4a	UTSW	2	4,594,563 (GRCm38)	nonsense	probably null
R4547:Frmd4a	UTSW	2	4,473,145 (GRCm38)	missense	probably damaging	1.00
R4575:Frmd4a	UTSW	2	4,603,679 (GRCm38)	missense	possibly damaging	0.83
R4577:Frmd4a	UTSW	2	4,603,679 (GRCm38)	missense	possibly damaging	0.83
R4578:Frmd4a	UTSW	2	4,603,679 (GRCm38)	missense	possibly damaging	0.83
R4688:Frmd4a	UTSW	2	4,537,311 (GRCm38)	missense	possibly damaging	0.81
R4764:Frmd4a	UTSW	2	4,603,448 (GRCm38)	missense	probably damaging	1.00
R4826:Frmd4a	UTSW	2	4,601,297 (GRCm38)	missense	probably damaging	1.00
R4879:Frmd4a	UTSW	2	4,529,817 (GRCm38)	missense	probably damaging	1.00
R5053:Frmd4a	UTSW	2	4,603,921 (GRCm38)	missense	probably damaging	1.00
R5392:Frmd4a	UTSW	2	4,594,573 (GRCm38)	missense	probably damaging	1.00
R5733:Frmd4a	UTSW	2	4,300,957 (GRCm38)	missense	possibly damaging	0.53
R5762:Frmd4a	UTSW	2	4,484,065 (GRCm38)	missense	probably damaging	1.00
R5920:Frmd4a	UTSW	2	4,333,116 (GRCm38)	missense	probably benign	0.02
R5932:Frmd4a	UTSW	2	4,529,839 (GRCm38)	missense	probably damaging	1.00
R6117:Frmd4a	UTSW	2	4,602,249 (GRCm38)	missense	possibly damaging	0.66
R6328:Frmd4a	UTSW	2	4,590,698 (GRCm38)	missense	probably damaging	0.99
R6622:Frmd4a	UTSW	2	4,606,062 (GRCm38)	missense	probably benign	0.00
R6903:Frmd4a	UTSW	2	4,586,456 (GRCm38)	missense	probably damaging	1.00
R7065:Frmd4a	UTSW	2	4,566,112 (GRCm38)
R7098:Frmd4a	UTSW	2	4,572,433 (GRCm38)	missense	probably damaging	1.00
R7258:Frmd4a	UTSW	2	4,300,953 (GRCm38)	missense	probably benign
R7336:Frmd4a	UTSW	2	4,473,214 (GRCm38)	missense	possibly damaging	0.92
R7582:Frmd4a	UTSW	2	4,594,597 (GRCm38)	frame shift	probably null
R7607:Frmd4a	UTSW	2	4,591,936 (GRCm38)	nonsense	probably null
R7697:Frmd4a	UTSW	2	4,484,081 (GRCm38)	missense	probably damaging	1.00
R7750:Frmd4a	UTSW	2	4,601,349 (GRCm38)	missense	probably benign	0.14
R7795:Frmd4a	UTSW	2	4,590,695 (GRCm38)	missense	probably damaging	1.00
R7848:Frmd4a	UTSW	2	4,591,917 (GRCm38)	intron	probably benign
R7899:Frmd4a	UTSW	2	4,604,089 (GRCm38)	missense	probably damaging	1.00
R8024:Frmd4a	UTSW	2	4,603,702 (GRCm38)	missense	probably damaging	1.00
R8399:Frmd4a	UTSW	2	4,572,433 (GRCm38)	missense	probably damaging	1.00
R8778:Frmd4a	UTSW	2	4,473,215 (GRCm38)	missense	probably damaging	1.00
R8876:Frmd4a	UTSW	2	4,601,300 (GRCm38)	missense	probably damaging	0.99
R9074:Frmd4a	UTSW	2	4,603,954 (GRCm38)	missense	probably damaging	1.00
R9075:Frmd4a	UTSW	2	4,603,954 (GRCm38)	missense	probably damaging	1.00
R9076:Frmd4a	UTSW	2	4,603,954 (GRCm38)	missense	probably damaging	1.00
R9105:Frmd4a	UTSW	2	4,535,183 (GRCm38)	missense	probably damaging	0.96
R9213:Frmd4a	UTSW	2	4,603,561 (GRCm38)	missense	probably damaging	1.00
R9227:Frmd4a	UTSW	2	4,608,033 (GRCm38)	missense	possibly damaging	0.92
R9230:Frmd4a	UTSW	2	4,608,033 (GRCm38)	missense	possibly damaging	0.92
R9235:Frmd4a	UTSW	2	4,594,555 (GRCm38)	missense	probably damaging	0.99
R9266:Frmd4a	UTSW	2	4,606,035 (GRCm38)	missense	probably damaging	0.99
R9301:Frmd4a	UTSW	2	4,153,093 (GRCm38)	missense	probably benign	0.27
R9307:Frmd4a	UTSW	2	4,604,233 (GRCm38)	missense	probably benign
R9365:Frmd4a	UTSW	2	4,602,162 (GRCm38)	missense	probably benign	0.01
R9476:Frmd4a	UTSW	2	4,603,513 (GRCm38)	missense	probably benign	0.32
R9484:Frmd4a	UTSW	2	4,604,215 (GRCm38)	missense	possibly damaging	0.49
R9510:Frmd4a	UTSW	2	4,603,513 (GRCm38)	missense	probably benign	0.32
R9513:Frmd4a	UTSW	2	4,603,900 (GRCm38)	missense	probably damaging	0.99
Z1176:Frmd4a	UTSW	2	4,498,021 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCACACAAGACGATGTTTGAGTG -3'
(R):5'- TCTTTCTGACCAAGCCAACC -3'

Sequencing Primer
(F):5'- AGGCCATATATCGAGGCTATTG -3'
(R):5'- TGACCAAGCCAACCTCCGTC -3'

Posted On

2014-08-01