Mutagenetix > Incidental Mutation

Incidental Mutation 'R3743:1700013G24Rik'

270444

Institutional Source

Beutler Lab

Gene Symbol

1700013G24Rik

Ensembl Gene

ENSMUSG00000041399

Gene Name

RIKEN cDNA 1700013G24 gene

Synonyms

MMRRC Submission

040729-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.049) question?

Stock #

R3743 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

137180607-137182772 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 137182348 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 168 (R168G)

Ref Sequence

ENSEMBL: ENSMUSP00000043461 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048893]

AlphaFold

Q9DAC6

Predicted Effect

probably damaging
Transcript: ENSMUST00000048893
AA Change: R168G

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000043461
Gene: ENSMUSG00000041399
AA Change: R168G

Domain	Start	End	E-Value	Type
low complexity region	44	65	N/A	INTRINSIC
low complexity region	181	203	N/A	INTRINSIC
SCOP:d1i50b_	216	261	3e-3	SMART

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.0%

Validation Efficiency

98% (43/44)

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700030K09Rik	A	G	8: 73,199,013 (GRCm39)	H140R	probably benign	Het
Adamts10	A	G	17: 33,747,686 (GRCm39)	I41V	probably damaging	Het
Arnt	T	C	3: 95,382,016 (GRCm39)	V198A	possibly damaging	Het
Atg3	A	G	16: 44,998,591 (GRCm39)		probably null	Het
Atmin	T	C	8: 117,683,312 (GRCm39)	V324A	probably benign	Het
Ccdc88c	G	A	12: 100,914,843 (GRCm39)	R464C	probably damaging	Het
Ccr7	G	T	11: 99,036,033 (GRCm39)	S296R	possibly damaging	Het
Cdh12	T	A	15: 21,537,745 (GRCm39)	S415R	probably damaging	Het
Cep162	A	T	9: 87,099,230 (GRCm39)		probably benign	Het
Chd3	G	A	11: 69,254,876 (GRCm39)	R61*	probably null	Het
Cr2	A	G	1: 194,832,274 (GRCm39)		probably benign	Het
Csf1r	T	C	18: 61,247,846 (GRCm39)	S305P	probably benign	Het
Cyp4a31	A	C	4: 115,423,716 (GRCm39)	Q140P	possibly damaging	Het
Dhx40	A	T	11: 86,661,985 (GRCm39)	W691R	probably damaging	Het
Dlgap1	G	A	17: 71,025,221 (GRCm39)		probably null	Het
Entr1	A	G	2: 26,278,655 (GRCm39)		probably benign	Het
Exoc5	T	C	14: 49,251,806 (GRCm39)	I582V	probably benign	Het
Exoc5	A	T	14: 49,270,864 (GRCm39)	L387*	probably null	Het
Fbxw8	A	G	5: 118,251,704 (GRCm39)	S270P	probably damaging	Het
Fgf14	C	A	14: 124,914,032 (GRCm39)	G33V	probably benign	Het
Hoxd9	T	A	2: 74,528,710 (GRCm39)	V104E	probably damaging	Het
Igsf10	T	C	3: 59,233,546 (GRCm39)	H1729R	possibly damaging	Het
Irf8	C	T	8: 121,480,310 (GRCm39)	R274C	probably damaging	Het
Itgb4	G	A	11: 115,894,496 (GRCm39)	M1350I	probably damaging	Het
Lrrn4	A	G	2: 132,711,786 (GRCm39)		probably null	Het
Map3k6	C	T	4: 132,972,384 (GRCm39)	T320I	probably benign	Het
Morc2a	A	G	11: 3,633,700 (GRCm39)	E604G	possibly damaging	Het
Mtmr6	T	C	14: 60,537,747 (GRCm39)	I582T	probably benign	Het
Ninl	A	G	2: 150,792,168 (GRCm39)	V785A	probably benign	Het
Obscn	T	C	11: 58,969,911 (GRCm39)	E77G	probably damaging	Het
Or2b11	T	C	11: 59,462,335 (GRCm39)	Y77C	probably damaging	Het
Or2n1	T	G	17: 38,486,793 (GRCm39)	F273V	probably damaging	Het
Or4f61	A	G	2: 111,922,965 (GRCm39)	L27P	probably benign	Het
Pcdhb2	A	G	18: 37,429,470 (GRCm39)	D124G	probably damaging	Het
Pfkl	G	A	10: 77,832,179 (GRCm39)	T304M	probably damaging	Het
Ppil4	T	A	10: 7,696,935 (GRCm39)	S483T	unknown	Het
Slc7a10	C	T	7: 34,898,325 (GRCm39)	T332I	probably damaging	Het
Spats2	T	C	15: 99,108,795 (GRCm39)	S382P	probably benign	Het
Stpg1	T	A	4: 135,242,197 (GRCm39)	D70E	probably benign	Het
Tmprss11e	G	A	5: 86,857,315 (GRCm39)	Q333*	probably null	Het
Trpv1	A	T	11: 73,145,128 (GRCm39)	D430V	probably damaging	Het
Ttc23l	G	A	15: 10,537,652 (GRCm39)	S206L	probably benign	Het
Ttc23l	CT	CTTGGATT	15: 10,537,648 (GRCm39)		probably benign	Het
Zc3h6	A	G	2: 128,839,712 (GRCm39)	Y175C	probably damaging	Het

Other mutations in 1700013G24Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01547:1700013G24Rik	APN	4	137,182,573 (GRCm39)	missense	possibly damaging	0.82
IGL02646:1700013G24Rik	APN	4	137,182,101 (GRCm39)	nonsense	probably null
R0526:1700013G24Rik	UTSW	4	137,182,535 (GRCm39)	missense	possibly damaging	0.92
R1449:1700013G24Rik	UTSW	4	137,182,666 (GRCm39)	missense	possibly damaging	0.94
R5357:1700013G24Rik	UTSW	4	137,182,463 (GRCm39)	missense	possibly damaging	0.90
R6265:1700013G24Rik	UTSW	4	137,181,986 (GRCm39)	missense	probably damaging	1.00
R6586:1700013G24Rik	UTSW	4	137,182,639 (GRCm39)	missense	possibly damaging	0.90
R6720:1700013G24Rik	UTSW	4	137,181,997 (GRCm39)	missense	possibly damaging	0.94
R6988:1700013G24Rik	UTSW	4	137,181,890 (GRCm39)	missense	probably damaging	1.00
R7640:1700013G24Rik	UTSW	4	137,181,905 (GRCm39)	missense	probably damaging	0.99
R7825:1700013G24Rik	UTSW	4	137,182,654 (GRCm39)	missense	probably damaging	1.00
R8905:1700013G24Rik	UTSW	4	137,182,553 (GRCm39)	missense	probably benign
R9536:1700013G24Rik	UTSW	4	137,182,623 (GRCm39)	missense	probably damaging	0.99
Z1176:1700013G24Rik	UTSW	4	137,182,303 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTAGAGACGAGTCACCTGAC -3'
(R):5'- TTCAAACCAGTGGAACCCAGG -3'

Sequencing Primer
(F):5'- GTGGTCAAAAAGCCCACCTGTC -3'
(R):5'- AGGCACTGCAGGCTCTTG -3'

Posted On

2015-03-18