Mutagenetix > Incidental Mutation

Incidental Mutation 'R6666:Myct1'

526980

Institutional Source

Beutler Lab

Gene Symbol

Myct1

Ensembl Gene

ENSMUSG00000046916

Gene Name

myc target 1

Synonyms

MT-MC1, Mtmc1, 1110020B04Rik

MMRRC Submission

044786-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6666 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

5543728-5556789 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 5554333 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 67 (S67P)

Ref Sequence

ENSEMBL: ENSMUSP00000050430 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051809]

AlphaFold

Q8R411

Predicted Effect

probably damaging
Transcript: ENSMUST00000051809
AA Change: S67P

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000050430
Gene: ENSMUSG00000046916
AA Change: S67P

Domain	Start	End	E-Value	Type
Pfam:Myc_target_1	1	187	2.5e-80	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.3%
20x: 95.2%

Validation Efficiency

100% (46/46)

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700020N01Rik	C	A	10: 21,469,228 (GRCm39)		probably null	Het
Arhgap24	A	G	5: 102,700,163 (GRCm39)		probably null	Het
Atp12a	G	T	14: 56,610,821 (GRCm39)	V322L	probably benign	Het
Capza1	A	C	3: 104,735,922 (GRCm39)		probably null	Het
Cela3a	A	T	4: 137,131,175 (GRCm39)	S188T	probably benign	Het
Cplx1	G	T	5: 108,668,031 (GRCm39)	Y123*	probably null	Het
Ddias	A	T	7: 92,507,289 (GRCm39)	D875E	probably benign	Het
Dnah3	T	C	7: 119,670,172 (GRCm39)	E715G	probably benign	Het
Fam83e	A	G	7: 45,376,426 (GRCm39)	T380A	probably benign	Het
Fancd2	T	C	6: 113,562,470 (GRCm39)	V1270A	probably damaging	Het
Foxh1	A	G	15: 76,552,613 (GRCm39)	F367S	probably damaging	Het
Gpat2	G	C	2: 127,273,838 (GRCm39)	G294R	possibly damaging	Het
Gprc5a	A	G	6: 135,056,473 (GRCm39)	I307V	probably benign	Het
Gtpbp3	A	G	8: 71,943,582 (GRCm39)	D212G	possibly damaging	Het
Helb	A	G	10: 119,920,856 (GRCm39)	V1029A	probably damaging	Het
Il22ra1	A	T	4: 135,477,772 (GRCm39)	H281L	probably damaging	Het
Il2rb	TAGTCA	TAGTCAGTCA	15: 78,366,034 (GRCm39)		probably null	Het
Itga3	T	C	11: 94,956,652 (GRCm39)	T170A	probably benign	Het
Kdm3a	T	C	6: 71,588,974 (GRCm39)	E345G	probably benign	Het
Kif11	T	C	19: 37,398,214 (GRCm39)	I680T	probably benign	Het
Klhl28	C	T	12: 64,990,301 (GRCm39)	D547N	probably benign	Het
Limk2	T	A	11: 3,310,493 (GRCm39)	E49D	probably damaging	Het
Lmbrd2	T	A	15: 9,151,656 (GRCm39)	F120I	probably benign	Het
Mefv	T	A	16: 3,525,862 (GRCm39)	N802Y	possibly damaging	Het
Ms4a2	C	T	19: 11,595,787 (GRCm39)	S168N	probably benign	Het
Myh4	A	G	11: 67,142,638 (GRCm39)	E933G	probably damaging	Het
Naif1	C	A	2: 32,344,863 (GRCm39)	T189K	probably damaging	Het
Nppb	A	G	4: 148,070,463 (GRCm39)	I11V	probably benign	Het
Nr3c1	T	C	18: 39,620,200 (GRCm39)	D29G	probably damaging	Het
Nrcam	A	G	12: 44,618,338 (GRCm39)	Y782C	probably damaging	Het
Or1af1	A	T	2: 37,110,331 (GRCm39)	I277F	probably damaging	Het
Or51e1	T	C	7: 102,359,135 (GRCm39)		probably null	Het
Or9m1	T	A	2: 87,733,852 (GRCm39)	H56L	probably damaging	Het
Parp1	A	G	1: 180,413,516 (GRCm39)	T375A	probably benign	Het
Pcdhgb1	G	T	18: 37,814,546 (GRCm39)	E346*	probably null	Het
Pds5b	G	T	5: 150,701,631 (GRCm39)	S754I	probably damaging	Het
Scnn1g	G	A	7: 121,366,611 (GRCm39)	D603N	probably benign	Het
Slitrk5	A	G	14: 111,917,534 (GRCm39)	D386G	probably damaging	Het
Trmt1	T	C	8: 85,425,083 (GRCm39)	L493P	probably damaging	Het
Vrk1	A	G	12: 106,024,910 (GRCm39)	E262G	probably damaging	Het
Wfs1	T	C	5: 37,124,963 (GRCm39)	T567A	possibly damaging	Het
Zbtb11	A	T	16: 55,826,615 (GRCm39)	K846I	probably damaging	Het
Zfp318	A	G	17: 46,720,140 (GRCm39)	T1113A	probably benign	Het
Zfp654	A	T	16: 64,606,596 (GRCm39)	S535R	probably benign	Het

Other mutations in Myct1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02668:Myct1	APN	10	5,554,513 (GRCm39)	missense	probably damaging	1.00
R0677:Myct1	UTSW	10	5,554,261 (GRCm39)	missense	probably benign	0.02
R5991:Myct1	UTSW	10	5,554,426 (GRCm39)	nonsense	probably null
R7122:Myct1	UTSW	10	5,554,492 (GRCm39)	missense	probably damaging	1.00
R7239:Myct1	UTSW	10	5,554,601 (GRCm39)	missense	possibly damaging	0.72
R8886:Myct1	UTSW	10	5,554,208 (GRCm39)	missense	probably damaging	0.99
R8887:Myct1	UTSW	10	5,554,208 (GRCm39)	missense	probably damaging	0.99
R8954:Myct1	UTSW	10	5,554,208 (GRCm39)	missense	probably damaging	0.99
R8956:Myct1	UTSW	10	5,554,208 (GRCm39)	missense	probably damaging	0.99
R8957:Myct1	UTSW	10	5,554,208 (GRCm39)	missense	probably damaging	0.99
R9323:Myct1	UTSW	10	5,554,195 (GRCm39)	missense	probably benign	0.01
Z1177:Myct1	UTSW	10	5,554,361 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAGGGCTATCGTTTACTGGC -3'
(R):5'- CTCAGGAATCGGGAAATGCC -3'

Sequencing Primer
(F):5'- CTGATTCTTTGTTTCAGAGGACC -3'
(R):5'- CTCAGGAATCGGGAAATGCCTTTATG -3'

Posted On

2018-07-23