Mutagenetix > Incidental Mutation

Incidental Mutation 'R8398:Gm10428'

647725

Institutional Source

Beutler Lab

Gene Symbol

Gm10428

Ensembl Gene

ENSMUSG00000096083

Gene Name

predicted gene 10428

Synonyms

MMRRC Submission

067761-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.146) question?

Stock #

R8398 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

62643926-62644324 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 62644173 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 83 (I83T)

Ref Sequence

ENSEMBL: ENSMUSP00000136979 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000178750] [ENSMUST00000207597]

AlphaFold

J3QNV7

Predicted Effect

unknown
Transcript: ENSMUST00000178750
AA Change: I83T

Predicted Effect

probably benign
Transcript: ENSMUST00000207597

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.8%
20x: 99.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrv1	T	C	13: 81,330,797 (GRCm39)	D6086G	probably damaging	Het
Amh	T	C	10: 80,641,394 (GRCm39)	S105P	probably benign	Het
Arap2	A	T	5: 62,906,252 (GRCm39)	Y256N	probably damaging	Het
Asap3	G	A	4: 135,961,704 (GRCm39)	M271I	probably benign	Het
Bbof1	T	C	12: 84,475,188 (GRCm39)	L459P	probably damaging	Het
Ccl21a	T	C	4: 42,773,412 (GRCm39)	T109A	probably benign	Het
Cnot6	C	T	11: 49,593,445 (GRCm39)	R12Q	probably damaging	Het
D5Ertd579e	G	A	5: 36,771,621 (GRCm39)	Q925*	probably null	Het
Dbh	G	A	2: 27,064,910 (GRCm39)	V374M	probably damaging	Het
Dvl2	T	A	11: 69,899,128 (GRCm39)	L462Q	probably damaging	Het
Fchsd1	G	A	18: 38,099,577 (GRCm39)	R206C	probably damaging	Het
Gjd4	C	T	18: 9,280,326 (GRCm39)	V251M	possibly damaging	Het
Glud1	A	G	14: 34,033,228 (GRCm39)	D125G	probably benign	Het
Gm10985	A	C	3: 53,752,674 (GRCm39)	Y19S	probably damaging	Het
Gm3045	A	G	13: 56,577,280 (GRCm39)	T143A	possibly damaging	Het
Heatr6	A	C	11: 83,672,164 (GRCm39)	E1057D	probably benign	Het
Hoxa9	T	C	6: 52,201,403 (GRCm39)	T213A	probably damaging	Het
Hsd3b5	T	A	3: 98,526,720 (GRCm39)	D242V	possibly damaging	Het
Lama5	A	G	2: 179,838,827 (GRCm39)		probably null	Het
Lrp1b	C	T	2: 40,591,819 (GRCm39)	C3827Y		Het
Mast2	A	T	4: 116,165,946 (GRCm39)	S1261T	probably damaging	Het
Mex3b	T	A	7: 82,518,842 (GRCm39)	F386I	probably benign	Het
Mta1	T	A	12: 113,095,242 (GRCm39)	M465K	possibly damaging	Het
Mtmr12	T	A	15: 12,265,695 (GRCm39)	F470L	probably damaging	Het
Myot	A	G	18: 44,487,883 (GRCm39)	N400S	probably benign	Het
Ndnf	T	C	6: 65,681,362 (GRCm39)	V547A	probably damaging	Het
Noc3l	A	T	19: 38,783,554 (GRCm39)	D607E	probably benign	Het
Or5w14	A	G	2: 87,542,175 (GRCm39)	V25A	probably benign	Het
Pcdha11	G	A	18: 37,146,116 (GRCm39)	G736R	possibly damaging	Het
Pcgf3	A	G	5: 108,647,509 (GRCm39)	N205S	probably damaging	Het
Pkd1l3	C	T	8: 110,350,520 (GRCm39)	P455L	possibly damaging	Het
Psg27	T	C	7: 18,295,837 (GRCm39)	T203A	probably benign	Het
Ptch1	T	C	13: 63,672,939 (GRCm39)	T889A	probably benign	Het
Sars1	C	T	3: 108,335,489 (GRCm39)		probably null	Het
Scrn2	G	T	11: 96,921,730 (GRCm39)	V67L	probably benign	Het
Slc1a4	T	C	11: 20,257,982 (GRCm39)	D380G	probably damaging	Het
Slc9a1	A	T	4: 133,146,814 (GRCm39)	Q516L	probably benign	Het
Smc4	T	C	3: 68,933,184 (GRCm39)	Y627H	probably damaging	Het
Spon2	G	T	5: 33,374,154 (GRCm39)	H76Q	probably damaging	Het
Sppl2b	TGTCACAGGT	TGT	10: 80,701,903 (GRCm39)		probably null	Het
Sppl2b	CTGTCACA	C	10: 80,701,902 (GRCm39)		probably null	Het
Sugp1	A	G	8: 70,523,783 (GRCm39)	Y550C	probably damaging	Het
Sun1	A	G	5: 139,222,408 (GRCm39)	D558G	probably damaging	Het
Syne1	T	C	10: 5,074,923 (GRCm39)	E1134G	probably damaging	Het
Thbd	C	T	2: 148,248,600 (GRCm39)	V423I	probably benign	Het
V1rd19	C	A	7: 23,703,374 (GRCm39)	S280*	probably null	Het
Zfp947	A	T	17: 22,365,102 (GRCm39)	C191S	probably benign	Het

Other mutations in Gm10428

Allele	Source	Chr	Coord	Type	Predicted Effect
R0630:Gm10428	UTSW	11	62,644,256 (GRCm39)	utr 3 prime	probably benign
R1925:Gm10428	UTSW	11	62,644,179 (GRCm39)	utr 3 prime	probably benign
R5466:Gm10428	UTSW	11	62,643,932 (GRCm39)	utr 3 prime	probably benign
R5761:Gm10428	UTSW	11	62,644,169 (GRCm39)	utr 3 prime	probably benign
R5788:Gm10428	UTSW	11	62,644,107 (GRCm39)	utr 3 prime	probably benign
R5939:Gm10428	UTSW	11	62,644,288 (GRCm39)	utr 3 prime	probably benign
R6611:Gm10428	UTSW	11	62,644,115 (GRCm39)	utr 3 prime	probably benign
R7115:Gm10428	UTSW	11	62,644,206 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- AGGCCTTTCCGAATTCATTACATTC -3'
(R):5'- TTCAAGAGCATCACCCGAGTC -3'

Sequencing Primer
(F):5'- GACCTCTTCATGTTGAATGAGCAG -3'
(R):5'- TCACCCGAGTCAGAGACTAGTAAG -3'

Posted On

2020-09-02