Mutagenetix > Incidental Mutation

Incidental Mutation 'R1769:Farsb'

194651

Institutional Source

Beutler Lab

Gene Symbol

Farsb

Ensembl Gene

ENSMUSG00000026245

Gene Name

phenylalanyl-tRNA synthetase, beta subunit

Synonyms

Farsl, Frsb, PheRS alpha, Farslb

MMRRC Submission

039800-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.971) question?

Stock #

R1769 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

78417975-78488897 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 78466983 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Isoleucine at position 196 (K196I)

Ref Sequence

ENSEMBL: ENSMUSP00000139933 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000068333] [ENSMUST00000170217] [ENSMUST00000188247] [ENSMUST00000189529]

AlphaFold

Q9WUA2

Predicted Effect

probably benign
Transcript: ENSMUST00000068333
AA Change: K295I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000069508
Gene: ENSMUSG00000026245
AA Change: K295I

Domain	Start	End	E-Value	Type
Blast:B3_4	56	95	6e-14	BLAST
B3_4	117	279	3.29e-29	SMART
B5	304	374	6.31e-17	SMART
SCOP:d1jjcb5	377	586	1e-36	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000170217
AA Change: K295I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000129828
Gene: ENSMUSG00000026245
AA Change: K295I

Domain	Start	End	E-Value	Type
Blast:B3_4	56	95	6e-14	BLAST
B3_4	117	279	3.29e-29	SMART
B5	304	374	6.31e-17	SMART
SCOP:d1jjcb5	377	586	1e-36	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000188247
AA Change: K196I

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000139933
Gene: ENSMUSG00000026245
AA Change: K196I

Domain	Start	End	E-Value	Type
B3_4	18	180	2.5e-33	SMART
SCOP:d1jjcb2	204	237	3e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000189529

SMART Domains

Protein: ENSMUSP00000140001
Gene: ENSMUSG00000026245

Domain	Start	End	E-Value	Type
PDB:3L4G\|P	1	38	3e-20	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000189931

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000195509

Meta Mutation Damage Score

0.2651

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.5%

Validation Efficiency

100% (91/91)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a highly conserved enzyme that belongs to the aminoacyl-tRNA synthetase class IIc subfamily. This enzyme comprises the regulatory beta subunits that form a tetramer with two catalytic alpha subunits. In the presence of ATP, this tetramer is responsible for attaching L-phenylalanine to the terminal adenosine of the appropriate tRNA. A pseudogene located on chromosome 10 has been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

Allele List at MGI

All alleles(15) : Targeted(2) Gene trapped(13)

Other mutations in this stock

Total: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921507P07Rik	A	G	6: 50,591,821 (GRCm38)		probably benign	Het
A430033K04Rik	A	G	5: 138,646,257 (GRCm38)	I135V	probably benign	Het
Abca1	T	A	4: 53,074,325 (GRCm38)	K1119N	probably damaging	Het
Abcb10	C	T	8: 123,962,052 (GRCm38)	G495D	probably damaging	Het
Abcc9	T	C	6: 142,627,468 (GRCm38)		probably benign	Het
Akap3	A	G	6: 126,865,846 (GRCm38)	E476G	possibly damaging	Het
Aldh3b1	A	G	19: 3,918,740 (GRCm38)	F271S	probably damaging	Het
Alkbh2	C	T	5: 114,124,226 (GRCm38)	E148K	probably damaging	Het
Ascc3	T	C	10: 50,700,490 (GRCm38)	V847A	probably damaging	Het
Best3	A	G	10: 117,023,978 (GRCm38)	N381S	probably benign	Het
Blm	A	T	7: 80,513,370 (GRCm38)	S78T	probably benign	Het
Bmpr2	T	A	1: 59,868,361 (GRCm38)	L871Q	probably damaging	Het
Car13	T	A	3: 14,650,735 (GRCm38)	H104Q	probably benign	Het
Ccdc39	T	C	3: 33,826,480 (GRCm38)	K446R	probably damaging	Het
Ccnb1ip1	T	C	14: 50,792,111 (GRCm38)	M165V	probably benign	Het
Cd4	A	T	6: 124,866,655 (GRCm38)	M431K	possibly damaging	Het
Cdh7	C	T	1: 110,052,876 (GRCm38)	T178I	probably damaging	Het
Ceacam3	C	T	7: 17,158,376 (GRCm38)	T348I	probably damaging	Het
Cfap54	C	T	10: 92,904,263 (GRCm38)		probably null	Het
Clcn6	A	T	4: 148,014,301 (GRCm38)		probably null	Het
Csf3	A	G	11: 98,702,420 (GRCm38)	Y121C	probably damaging	Het
Csmd3	C	T	15: 47,704,109 (GRCm38)		probably benign	Het
Cyp2c69	A	G	19: 39,876,371 (GRCm38)	I221T	probably benign	Het
Dgcr2	T	C	16: 17,857,251 (GRCm38)		probably benign	Het
Dhcr7	T	C	7: 143,847,513 (GRCm38)	F474S	probably damaging	Het
Dnah1	T	C	14: 31,310,882 (GRCm38)	I399V	probably null	Het
Efcab14	T	A	4: 115,752,991 (GRCm38)	L183Q	probably damaging	Het
Elmsan1	G	A	12: 84,158,350 (GRCm38)		probably benign	Het
Evx2	A	G	2: 74,659,157 (GRCm38)	V88A	probably benign	Het
Exph5	A	G	9: 53,373,809 (GRCm38)	N730S	probably benign	Het
Fbln7	C	T	2: 128,893,762 (GRCm38)		probably benign	Het
Fhdc1	A	G	3: 84,448,778 (GRCm38)	F453S	probably damaging	Het
Gast	T	A	11: 100,336,858 (GRCm38)	W89R	probably damaging	Het
Gata2	A	G	6: 88,205,255 (GRCm38)	S402G	probably benign	Het
Gin1	T	A	1: 97,792,437 (GRCm38)	S386T	probably benign	Het
Golgb1	A	G	16: 36,916,001 (GRCm38)	E1870G	probably damaging	Het
Hivep3	T	A	4: 120,097,571 (GRCm38)	V1028E	possibly damaging	Het
Ifi203	G	A	1: 173,928,760 (GRCm38)	R486*	probably null	Het
Ifi209	G	A	1: 173,641,162 (GRCm38)	S186N	probably benign	Het
Ifih1	C	T	2: 62,606,394 (GRCm38)	A562T	probably damaging	Het
Itch	T	C	2: 155,172,561 (GRCm38)	L106S	probably damaging	Het
Itga4	T	A	2: 79,315,706 (GRCm38)		probably null	Het
Kdm4c	A	G	4: 74,280,997 (GRCm38)	S141G	possibly damaging	Het
Kirrel	C	T	3: 87,089,151 (GRCm38)	M380I	probably null	Het
Klra3	T	C	6: 130,330,263 (GRCm38)		probably null	Het
Lama2	G	C	10: 27,208,407 (GRCm38)	F922L	probably benign	Het
Lama2	A	T	10: 27,208,406 (GRCm38)	S923T	probably damaging	Het
Llgl1	G	A	11: 60,707,047 (GRCm38)	V331M	probably damaging	Het
Lrrc30	T	C	17: 67,631,681 (GRCm38)	*301W	probably null	Het
Map1lc3b	C	T	8: 121,593,487 (GRCm38)		probably benign	Het
Mbd2	A	G	18: 70,616,619 (GRCm38)	I302V	probably benign	Het
Med27	A	G	2: 29,500,295 (GRCm38)	Y78C	probably damaging	Het
Mei1	C	T	15: 82,112,570 (GRCm38)		probably null	Het
Miga1	T	C	3: 152,287,554 (GRCm38)	E346G	probably damaging	Het
Myef2	A	G	2: 125,115,443 (GRCm38)	S131P	probably damaging	Het
Myocd	T	C	11: 65,178,701 (GRCm38)	H899R	probably benign	Het
Ncam1	A	G	9: 49,545,256 (GRCm38)		probably benign	Het
Ngf	T	A	3: 102,520,197 (GRCm38)	N87K	possibly damaging	Het
Nol10	T	A	12: 17,416,708 (GRCm38)		probably benign	Het
Nrip2	A	G	6: 128,408,268 (GRCm38)	I221V	probably benign	Het
Nup205	G	A	6: 35,205,431 (GRCm38)	G777D	probably damaging	Het
Olfr1446	A	G	19: 12,889,683 (GRCm38)	V298A	probably damaging	Het
Olfr199	A	G	16: 59,215,981 (GRCm38)	F211L	probably benign	Het
Olfr802	T	A	10: 129,682,212 (GRCm38)	T176S	probably benign	Het
Olfr855	A	T	9: 19,585,386 (GRCm38)	Q283L	probably damaging	Het
Olfr974	G	T	9: 39,942,955 (GRCm38)	D232Y	probably benign	Het
Oxt	A	T	2: 130,576,300 (GRCm38)	R31W	probably damaging	Het
Pde4dip	A	G	3: 97,695,930 (GRCm38)	S2248P	probably benign	Het
Pias1	A	G	9: 62,952,178 (GRCm38)	V16A	probably damaging	Het
Pkp2	T	C	16: 16,262,697 (GRCm38)	S616P	probably damaging	Het
Plch2	T	C	4: 155,000,083 (GRCm38)	Y379C	probably damaging	Het
Pnpt1	A	G	11: 29,154,159 (GRCm38)	N540D	probably benign	Het
Ptpn23	G	A	9: 110,391,678 (GRCm38)	H255Y	possibly damaging	Het
Rad21	T	C	15: 51,972,307 (GRCm38)	N237D	probably benign	Het
Ryr3	A	C	2: 112,751,768 (GRCm38)		probably null	Het
Sgk1	C	A	10: 21,997,108 (GRCm38)		probably benign	Het
Slc1a5	G	T	7: 16,797,539 (GRCm38)	A490S	probably damaging	Het
Slc5a8	T	A	10: 88,919,466 (GRCm38)	Y478*	probably null	Het
Slc5a8	T	C	10: 88,919,464 (GRCm38)	Y478H	probably benign	Het
Slc9a3	A	T	13: 74,163,071 (GRCm38)	M562L	probably benign	Het
Thsd7a	G	A	6: 12,555,715 (GRCm38)	R57*	probably null	Het
Tiam1	T	C	16: 89,860,279 (GRCm38)	R690G	probably damaging	Het
Tmem150b	A	G	7: 4,724,366 (GRCm38)	S47P	probably damaging	Het
Trim39	C	T	17: 36,263,940 (GRCm38)	R190Q	probably damaging	Het
Ttc32	A	T	12: 9,035,073 (GRCm38)	I98L	possibly damaging	Het
Vps13c	A	G	9: 67,965,721 (GRCm38)	T3304A	probably benign	Het
Wdr35	A	C	12: 9,012,728 (GRCm38)	D638A	probably damaging	Het
Wwc1	G	T	11: 35,861,844 (GRCm38)	P797T	probably benign	Het
Zan	T	A	5: 137,464,518 (GRCm38)	T800S	unknown	Het
Zbbx	A	G	3: 75,083,619 (GRCm38)		probably benign	Het
Zufsp	T	C	10: 33,935,176 (GRCm38)	M291V	probably damaging	Het

Other mutations in Farsb

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00092:Farsb	APN	1	78,462,993 (GRCm38)	missense	probably benign	0.08
IGL01328:Farsb	APN	1	78,471,092 (GRCm38)	missense	probably benign	0.02
IGL01801:Farsb	APN	1	78,458,579 (GRCm38)	missense	probably benign	0.38
R0054:Farsb	UTSW	1	78,462,374 (GRCm38)	nonsense	probably null
R0054:Farsb	UTSW	1	78,462,374 (GRCm38)	nonsense	probably null
R1051:Farsb	UTSW	1	78,443,650 (GRCm38)	missense	possibly damaging	0.49
R4332:Farsb	UTSW	1	78,469,266 (GRCm38)	missense	possibly damaging	0.61
R4664:Farsb	UTSW	1	78,443,765 (GRCm38)	missense	possibly damaging	0.90
R4796:Farsb	UTSW	1	78,425,196 (GRCm38)	makesense	probably null
R4859:Farsb	UTSW	1	78,467,972 (GRCm38)	missense	probably benign	0.01
R5484:Farsb	UTSW	1	78,476,196 (GRCm38)	missense	probably damaging	1.00
R5500:Farsb	UTSW	1	78,471,124 (GRCm38)	missense	probably damaging	1.00
R5557:Farsb	UTSW	1	78,469,251 (GRCm38)	critical splice donor site	probably null
R6109:Farsb	UTSW	1	78,463,270 (GRCm38)	critical splice donor site	probably null
R6368:Farsb	UTSW	1	78,466,965 (GRCm38)	critical splice donor site	probably null
R6720:Farsb	UTSW	1	78,472,497 (GRCm38)	missense	probably damaging	1.00
R7166:Farsb	UTSW	1	78,471,184 (GRCm38)	missense	probably benign
R7184:Farsb	UTSW	1	78,482,357 (GRCm38)	missense	possibly damaging	0.86
R7233:Farsb	UTSW	1	78,471,081 (GRCm38)	critical splice donor site	probably null
R7536:Farsb	UTSW	1	78,443,754 (GRCm38)	missense	possibly damaging	0.89
R7753:Farsb	UTSW	1	78,480,103 (GRCm38)	missense	probably benign	0.25
R7824:Farsb	UTSW	1	78,469,299 (GRCm38)	missense	probably benign
R7916:Farsb	UTSW	1	78,458,563 (GRCm38)	critical splice donor site	probably null
R8120:Farsb	UTSW	1	78,462,838 (GRCm38)	missense	probably benign	0.00
R8517:Farsb	UTSW	1	78,463,296 (GRCm38)	nonsense	probably null
R8794:Farsb	UTSW	1	78,425,041 (GRCm38)	unclassified	probably benign
R9131:Farsb	UTSW	1	78,483,314 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AGGCTCCTCCACTTAAATCCGCAG -3'
(R):5'- TGTACATCAGCACGGTGCAAGAG -3'

Sequencing Primer
(F):5'- CTTAAATCCGCAGCACTTACC -3'
(R):5'- CTTTGTACACTGCGAGTAAGC -3'

Posted On

2014-05-23