Mutagenetix > Incidental Mutation

Incidental Mutation 'R6611:1810009J06Rik'

523567

Institutional Source

Beutler Lab

Gene Symbol

1810009J06Rik

Ensembl Gene

ENSMUSG00000094808

Gene Name

RIKEN cDNA 1810009J06 gene

Synonyms

MMRRC Submission

044734-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.162) question?

Stock #

R6611 (G1)

Quality Score

93.0077

Status

Not validated

Chromosome

Chromosomal Location

40941706-40945361 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 40943713 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 126 (T126S)

Ref Sequence

ENSEMBL: ENSMUSP00000075935 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076638]

AlphaFold

Q9CPN7

Predicted Effect

probably benign
Transcript: ENSMUST00000076638
AA Change: T126S

PolyPhen 2 Score 0.085 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000075935
Gene: ENSMUSG00000094808
AA Change: T126S

Domain	Start	End	E-Value	Type
Tryp_SPc	23	240	4.94e-97	SMART

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.1%
20x: 94.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Bex6	A	G	16: 32,005,483 (GRCm39)	K97R	probably benign	Het
Brca2	T	C	5: 150,459,658 (GRCm39)	L311P	probably damaging	Het
Ccng2	C	G	5: 93,421,202 (GRCm39)	S237R	probably benign	Het
Cdc16	C	A	8: 13,831,512 (GRCm39)	P582T	probably benign	Het
Cep112	T	C	11: 108,397,377 (GRCm39)	I280T	possibly damaging	Het
Cfhr4	A	G	1: 139,660,128 (GRCm39)	Y666H	probably damaging	Het
Chd2	A	G	7: 73,143,313 (GRCm39)	F527L	probably damaging	Het
Drc3	G	T	11: 60,255,773 (GRCm39)	R120L	probably damaging	Het
Efcab6	T	A	15: 83,777,036 (GRCm39)	R1133S	possibly damaging	Het
Fer1l5	T	C	1: 36,445,735 (GRCm39)	V834A	probably benign	Het
Flnb	A	G	14: 7,915,318 (GRCm38)	Y1483C	probably damaging	Het
Fstl4	A	T	11: 53,077,552 (GRCm39)	M770L	probably benign	Het
Gm10428	A	T	11: 62,644,115 (GRCm39)		probably benign	Het
Hmbs	C	A	9: 44,252,988 (GRCm39)	R15L	probably damaging	Het
Irx3	T	C	8: 92,526,631 (GRCm39)	T358A	probably damaging	Het
Kmt2a	T	A	9: 44,760,569 (GRCm39)	I460L	probably damaging	Het
Mob2	G	T	7: 141,563,293 (GRCm39)	F55L	probably damaging	Het
Muc6	G	C	7: 141,226,700 (GRCm39)		probably benign	Het
Ntrk2	T	C	13: 59,202,228 (GRCm39)	L612P	probably damaging	Het
Obscn	A	G	11: 58,955,056 (GRCm39)		probably null	Het
Or4d5	T	C	9: 40,012,316 (GRCm39)	I157V	probably benign	Het
Or5j1	A	T	2: 86,879,577 (GRCm39)	M1K	probably null	Het
Or8b44	A	T	9: 38,410,534 (GRCm39)	T190S	probably damaging	Het
Oxct2a	T	C	4: 123,216,640 (GRCm39)	E247G	probably damaging	Het
Phykpl	G	T	11: 51,489,181 (GRCm39)	A336S	probably damaging	Het
Pik3r4	T	G	9: 105,521,476 (GRCm39)	L14R	probably damaging	Het
Pnpla1	A	G	17: 29,100,021 (GRCm39)	N296S	probably benign	Het
Pramel7	A	G	2: 87,320,393 (GRCm39)	I300T	probably damaging	Het
Rictor	T	G	15: 6,780,140 (GRCm39)	C132G	probably damaging	Het
Rsf1	G	GACGGCGGCT	7: 97,229,116 (GRCm39)		probably benign	Homo
Slc9a9	G	T	9: 94,821,531 (GRCm39)	R306L	probably benign	Het
Smc5	A	G	19: 23,206,283 (GRCm39)	V681A	probably benign	Het
Snap91	C	T	9: 86,672,180 (GRCm39)	S646N	probably benign	Het
Ssh3	T	C	19: 4,314,450 (GRCm39)	N368S	probably damaging	Het
Syne1	A	T	10: 4,995,273 (GRCm39)	N8326K	probably benign	Het
Traf3	T	G	12: 111,204,074 (GRCm39)	L21R	possibly damaging	Het
Ubxn11	C	A	4: 133,850,910 (GRCm39)	T254K	probably damaging	Het

Other mutations in 1810009J06Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00741:1810009J06Rik	APN	6	40,941,768 (GRCm39)	splice site	probably benign
IGL00952:1810009J06Rik	APN	6	40,941,733 (GRCm39)	missense	probably benign	0.00
IGL01146:1810009J06Rik	APN	6	40,943,217 (GRCm39)	missense	probably damaging	1.00
IGL02815:1810009J06Rik	APN	6	40,941,729 (GRCm39)	missense	probably benign
R1543:1810009J06Rik	UTSW	6	40,945,138 (GRCm39)	missense	probably damaging	1.00
R1708:1810009J06Rik	UTSW	6	40,941,732 (GRCm39)	missense	probably benign
R1964:1810009J06Rik	UTSW	6	40,945,141 (GRCm39)	missense	probably damaging	1.00
R5786:1810009J06Rik	UTSW	6	40,945,122 (GRCm39)	missense	probably damaging	1.00
R7057:1810009J06Rik	UTSW	6	40,945,181 (GRCm39)	missense	probably benign	0.00
R9371:1810009J06Rik	UTSW	6	40,943,663 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TAATGCAGAAGACTCCAGGTTC -3'
(R):5'- GTGAAGCAATGTTCTGGCCTAC -3'

Sequencing Primer
(F):5'- CGCCTTGGTGAACACAATATTG -3'
(R):5'- TCTACAAGTATCTCTCACAGTGAC -3'

Posted On

2018-06-22