Mutagenetix > Incidental Mutation

Incidental Mutation 'R7274:Rassf8'

565449

Institutional Source

Beutler Lab

Gene Symbol

Rassf8

Ensembl Gene

ENSMUSG00000030259

Gene Name

Ras association (RalGDS/AF-6) domain family (N-terminal) member 8

Synonyms

5133400D11Rik, mHoj-1

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably essential (E-score: 0.752) question?

Stock #

R7274 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

145746748-145821079 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 145815569 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 207 (V207A)

Ref Sequence

ENSEMBL: ENSMUSP00000032388 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032388] [ENSMUST00000058538] [ENSMUST00000111704] [ENSMUST00000140966]

AlphaFold

Q8CJ96

Predicted Effect

probably benign
Transcript: ENSMUST00000032388
AA Change: V207A

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000032388
Gene: ENSMUSG00000030259
AA Change: V207A

Domain	Start	End	E-Value	Type
RA	1	82	4.17e-11	SMART
coiled coil region	161	354	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000058538

Predicted Effect

probably benign
Transcript: ENSMUST00000111704
AA Change: V207A

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000107333
Gene: ENSMUSG00000030259
AA Change: V207A

Domain	Start	End	E-Value	Type
RA	1	82	4.17e-11	SMART
coiled coil region	161	354	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000140966

SMART Domains

Protein: ENSMUSP00000122684
Gene: ENSMUSG00000030259

Domain	Start	End	E-Value	Type
RA	1	80	7.85e-7	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

100% (61/61)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1190005I06Rik	T	C	8: 120,611,266	S69G	possibly damaging	Het
Alg12	G	A	15: 88,806,707	S337F	probably damaging	Het
Bcl11a	T	C	11: 24,163,985	S443P	probably damaging	Het
C1qtnf4	T	C	2: 90,889,541	Y53H	probably damaging	Het
Cacna1d	T	A	14: 30,142,643	E454V	probably damaging	Het
Cacna1h	A	G	17: 25,378,837	F1761S	probably damaging	Het
Cacna1i	A	T	15: 80,376,822	I1344F	possibly damaging	Het
Cat	T	C	2: 103,476,890	N33D	probably benign	Het
Cdh17	C	T	4: 11,783,174	Q172*	probably null	Het
Chrna2	A	G	14: 66,149,226	I274V	probably benign	Het
Cog2	T	G	8: 124,535,519	S299A	possibly damaging	Het
Cpa6	C	A	1: 10,409,299	M236I	probably damaging	Het
Crym	T	A	7: 120,190,519	Q242L	probably benign	Het
Ddx60	T	C	8: 61,940,108		probably null	Het
Epdr1	A	T	13: 19,593,288	I180N	possibly damaging	Het
Fancd2os	G	A	6: 113,597,890	L52F	probably benign	Het
Fbxo16	C	A	14: 65,321,267	R292S	probably benign	Het
Fn1	T	C	1: 71,628,113	Q820R	probably benign	Het
Gm4131	T	A	14: 62,466,852	Y140F	possibly damaging	Het
Gm8994	A	G	6: 136,329,398	T286A	possibly damaging	Het
Grin2a	T	C	16: 9,579,122	R1034G	possibly damaging	Het
Hypk	A	G	2: 121,454,324		probably benign	Het
Ighmbp2	A	G	19: 3,264,951	V823A	probably benign	Het
Irf5	A	G	6: 29,534,040	N95S	probably damaging	Het
Kdr	A	T	5: 75,964,700	M379K	probably benign	Het
Kif19a	G	T	11: 114,765,455		probably benign	Het
Klhdc4	T	C	8: 121,799,658		probably null	Het
Lama2	A	T	10: 27,119,980	I1717N	probably damaging	Het
Lama4	A	T	10: 39,092,299	Q1479L	probably benign	Het
Lgr5	T	A	10: 115,452,505	T745S	probably damaging	Het
Lifr	T	A	15: 7,167,059		probably null	Het
Llgl1	C	T	11: 60,705,986	R138C	possibly damaging	Het
Mccc1	A	T	3: 35,989,856	V246E	probably damaging	Het
Mdn1	T	A	4: 32,725,944	L2621H	probably benign	Het
Mecr	C	A	4: 131,853,778	A80D	probably damaging	Het
Mia2	A	G	12: 59,108,119	E206G	probably damaging	Het
Nubpl	A	G	12: 52,132,420		probably benign	Het
Obscn	C	T	11: 59,133,227	R539H	probably damaging	Het
Olfr1100	A	G	2: 86,978,523	V91A	probably benign	Het
Olfr733	T	A	14: 50,298,422	T296S	probably benign	Het
Pde5a	A	T	3: 122,855,246	K838*	probably null	Het
Pgm3	A	G	9: 86,562,597	L295P	probably damaging	Het
Pkp2	T	C	16: 16,246,929	L439P	possibly damaging	Het
Polr1a	T	A	6: 71,920,516	C205*	probably null	Het
Rab3gap1	T	A	1: 127,927,512	I429K	probably benign	Het
Sacs	T	A	14: 61,214,081	D4525E	possibly damaging	Het
Sec24a	A	T	11: 51,707,255	L864Q	probably damaging	Het
Spats2l	C	A	1: 57,879,513	Y35*	probably null	Het
Sptlc2	A	T	12: 87,341,606	D367E	probably benign	Het
Ssc4d	T	C	5: 135,967,956	D97G	possibly damaging	Het
Tjp1	A	G	7: 65,527,652	Y3H	possibly damaging	Het
Tkt	T	A	14: 30,569,145		probably null	Het
Trim60	T	A	8: 65,000,481	N372I	possibly damaging	Het
Trpm2	T	C	10: 77,923,555	N1132D	probably benign	Het
Tsc22d1	T	C	14: 76,416,714	I211T	probably damaging	Het
Ttc39b	T	C	4: 83,261,851	K132E	possibly damaging	Het
Ttn	C	T	2: 76,723,588	V30924I	probably damaging	Het
Tubgcp6	G	A	15: 89,102,970	Q1267*	probably null	Het
Zfp30	C	A	7: 29,792,618	T180N	probably benign	Het
Zp2	A	G	7: 120,132,391	*714R	probably null	Het

Other mutations in Rassf8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02973:Rassf8	APN	6	145817190	unclassified	probably benign
IGL03017:Rassf8	APN	6	145817198	splice site	probably null
IGL03091:Rassf8	APN	6	145815810	missense	probably benign	0.00
R0230:Rassf8	UTSW	6	145819974	unclassified	probably benign
R0967:Rassf8	UTSW	6	145819950	unclassified	probably benign
R1429:Rassf8	UTSW	6	145815190	missense	probably damaging	1.00
R1622:Rassf8	UTSW	6	145820103	unclassified	probably benign
R1738:Rassf8	UTSW	6	145815308	missense	probably benign	0.03
R1894:Rassf8	UTSW	6	145808473	missense	probably damaging	1.00
R2126:Rassf8	UTSW	6	145815182	missense	probably benign	0.00
R2238:Rassf8	UTSW	6	145817184	missense	probably damaging	1.00
R2439:Rassf8	UTSW	6	145815334	missense	probably damaging	1.00
R3699:Rassf8	UTSW	6	145820076	unclassified	probably benign
R4678:Rassf8	UTSW	6	145815082	missense	probably damaging	1.00
R4734:Rassf8	UTSW	6	145815540	missense	probably benign	0.34
R4826:Rassf8	UTSW	6	145816550	missense	probably damaging	1.00
R4910:Rassf8	UTSW	6	145815280	nonsense	probably null
R4988:Rassf8	UTSW	6	145817144	missense	possibly damaging	0.89
R5425:Rassf8	UTSW	6	145815542	missense	probably benign
R5620:Rassf8	UTSW	6	145820181	unclassified	probably benign
R5747:Rassf8	UTSW	6	145815815	missense	probably benign	0.00
R6136:Rassf8	UTSW	6	145815656	missense	probably benign	0.00
R6220:Rassf8	UTSW	6	145817133	missense	probably damaging	1.00
R7315:Rassf8	UTSW	6	145815751	missense	probably benign
R7480:Rassf8	UTSW	6	145820031	missense	unknown
R7593:Rassf8	UTSW	6	145815403	missense	probably benign	0.08
R7714:Rassf8	UTSW	6	145815247	missense	probably damaging	0.98
R7962:Rassf8	UTSW	6	145815943	critical splice donor site	probably null
R8222:Rassf8	UTSW	6	145820057	missense	unknown
R8374:Rassf8	UTSW	6	145815137	nonsense	probably null
R8409:Rassf8	UTSW	6	145815703	missense	probably benign
R9314:Rassf8	UTSW	6	145816570	missense	probably damaging	1.00
Z1088:Rassf8	UTSW	6	145815482	missense	probably benign
Z1088:Rassf8	UTSW	6	145816616	missense	probably benign	0.41
Z1176:Rassf8	UTSW	6	145816642	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AGTCTCTCACCTTCACAGGG -3'
(R):5'- ATTGACCTGTGCCTCCTGAAC -3'

Sequencing Primer
(F):5'- CAAAGGGCTGACGGACATTTTTG -3'
(R):5'- CAGTTTTTCTGCCTGGAGACCG -3'

Posted On

2019-06-26