Mutagenetix > Incidental Mutations

Incidental Mutation 'R7115:Gm10428'

551737

Institutional Source

Beutler Lab

Gene Symbol

Gm10428

Ensembl Gene

ENSMUSG00000096083

Gene Name

predicted gene 10428

Synonyms

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.145) question?

Stock #

R7115 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

62753100-62753498 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 62753380 bp

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Tyrosine at position 94 (C94Y)

Ref Sequence

ENSEMBL: ENSMUSP00000136979 (fasta)

Predicted Effect

unknown
Transcript: ENSMUST00000178750
AA Change: C94Y

Predicted Effect

probably benign
Transcript: ENSMUST00000207597

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc1	T	A	16: 14,437,725	I636N	probably benign	Het
Adam5	A	G	8: 24,781,696	I565T	possibly damaging	Het
Amd2	C	A	10: 35,711,637		probably benign	Het
Ap5m1	T	A	14: 49,086,270	Y472*	probably null	Het
Apcdd1	T	C	18: 62,936,953	F97S	probably damaging	Het
Axdnd1	T	C	1: 156,380,876	K267R		Het
BC067074	T	G	13: 113,320,776	S1119A		Het
Carf	G	T	1: 60,148,150	L637F	probably damaging	Het
Ccdc103	A	T	11: 102,883,810	S95C	possibly damaging	Het
Cfap20	T	C	8: 95,421,246	I156V	probably benign	Het
Csn1s2a	T	C	5: 87,781,805	C96R	probably benign	Het
Ctif	CGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACAC	CGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACAC	18: 75,471,803		probably benign	Het
Dennd2a	G	A	6: 39,506,711	T405M	probably damaging	Het
Dennd5a	A	G	7: 109,894,754	Y1248H	probably damaging	Het
Dnah14	A	T	1: 181,720,145	K2504N	probably damaging	Het
Dnajb2	G	A	1: 75,243,662	G275D		Het
Elf3	T	G	1: 135,257,118	D110A	probably damaging	Het
Eomes	A	G	9: 118,484,489	N534S	probably benign	Het
Fry	A	T	5: 150,386,067	R659W	probably damaging	Het
Gm2696	T	A	10: 77,836,299	C111S	unknown	Het
Gpt2	G	A	8: 85,518,052	E325K	probably benign	Het
Lrp1b	T	A	2: 40,998,235	N2338Y		Het
Map2k1	A	G	9: 64,212,606	I139T	probably damaging	Het
Olfr44	T	C	9: 39,484,648	I202V	probably benign	Het
Olfr964-ps1	T	C	9: 39,686,707	Y79C	probably benign	Het
Pxylp1	G	A	9: 96,825,010	T373I	probably benign	Het
Ranbp9	T	C	13: 43,406,671	N484S	probably benign	Het
Rassf5	A	G	1: 131,181,249	V293A	probably benign	Het
Ring1	A	G	17: 34,023,446	I29T	probably damaging	Het
Scn1a	G	A	2: 66,324,618	Q666*	probably null	Het
Spice1	G	A	16: 44,379,275	G697R	probably benign	Het
Tas2r131	A	G	6: 132,957,604	F81L	probably benign	Het
Tenm2	G	A	11: 36,163,817	S572L	probably damaging	Het
Tfr2	A	G	5: 137,571,715	T128A	probably benign	Het
Trim56	T	A	5: 137,113,660	Q334L	probably damaging	Het
Vmn2r44	T	A	7: 8,367,528	R840*	probably null	Het

Other mutations in Gm10428

Allele	Source	Chr	Coord	Type	Predicted Effect
R0630:Gm10428	UTSW	11	62753430	utr 3 prime	probably benign
R1925:Gm10428	UTSW	11	62753353	utr 3 prime	probably benign
R5466:Gm10428	UTSW	11	62753106	utr 3 prime	probably benign
R5761:Gm10428	UTSW	11	62753343	utr 3 prime	probably benign
R5788:Gm10428	UTSW	11	62753281	utr 3 prime	probably benign
R5939:Gm10428	UTSW	11	62753462	utr 3 prime	probably benign
R6611:Gm10428	UTSW	11	62753289	utr 3 prime	probably benign
R8398:Gm10428	UTSW	11	62753347	missense	unknown

Predicted Primers

PCR Primer
(F):5'- TCACATGTGCCTACATCTATAGGG -3'
(R):5'- AGAAGATCGCTGTACTGGGG -3'

Sequencing Primer
(F):5'- GTCTTCTGTATCCTTGACG -3'
(R):5'- TCCAGAATGGAAGGCCTGAG -3'

Posted On

2019-05-15