Mutagenetix > Incidental Mutation

Incidental Mutation 'R5517:Gspt1'

484526

Institutional Source

Beutler Lab

Gene Symbol

Gspt1

Ensembl Gene

ENSMUSG00000062203

Gene Name

G1 to S phase transition 1

Synonyms

Gst-1, G1st, Gst-1

MMRRC Submission

043076-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.962) question?

Stock #

R5517 (G1)

Quality Score

77.1

Status

Validated

Chromosome

Chromosomal Location

11037156-11072189 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 11071843 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Cysteine at position 7 (G7C)

Ref Sequence

ENSEMBL: ENSMUSP00000130583 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080030] [ENSMUST00000167571]

AlphaFold

Q8R050

Predicted Effect

unknown
Transcript: ENSMUST00000080030
AA Change: G7C

SMART Domains

Protein: ENSMUSP00000078940
Gene: ENSMUSG00000062203
AA Change: G7C

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
low complexity region	35	49	N/A	INTRINSIC
Pfam:PAM2	64	81	4.3e-8	PFAM
low complexity region	101	116	N/A	INTRINSIC
low complexity region	151	193	N/A	INTRINSIC
Pfam:GTP_EFTU	209	482	3.1e-47	PFAM
Pfam:GTP_EFTU_D2	451	518	1.2e-8	PFAM
Pfam:GTP_EFTU_D3	524	632	7.6e-33	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000157919

Predicted Effect

unknown
Transcript: ENSMUST00000167571
AA Change: G7C

SMART Domains

Protein: ENSMUSP00000130583
Gene: ENSMUSG00000062203
AA Change: G7C

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
low complexity region	35	49	N/A	INTRINSIC
Pfam:PAM2	64	81	7.1e-8	PFAM
low complexity region	101	116	N/A	INTRINSIC
low complexity region	150	192	N/A	INTRINSIC
Pfam:GTP_EFTU	208	476	4.3e-49	PFAM
Pfam:GTP_EFTU_D2	450	517	1.3e-7	PFAM
Pfam:GTP_EFTU_D3	523	631	2.2e-23	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000229660

Meta Mutation Damage Score

0.1520

Coding Region Coverage

1x: 98.5%
3x: 97.4%
10x: 95.2%
20x: 90.5%

Validation Efficiency

99% (67/68)

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcf1	C	T	17: 36,269,233 (GRCm39)	R675K	possibly damaging	Het
Aire	A	T	10: 77,875,525 (GRCm39)	S282T	probably benign	Het
Ak9	A	G	10: 41,216,887 (GRCm39)	E283G	probably benign	Het
Akap9	T	A	5: 4,051,665 (GRCm39)	D1477E	possibly damaging	Het
Ap2a1	T	C	7: 44,556,405 (GRCm39)	D273G	possibly damaging	Het
Apob	T	C	12: 8,040,906 (GRCm39)	L664P	probably damaging	Het
Arhgap35	A	T	7: 16,297,414 (GRCm39)	F550L	probably damaging	Het
Armc2	T	C	10: 41,839,846 (GRCm39)	E373G	probably benign	Het
Atp8b2	C	A	3: 89,853,338 (GRCm39)	A726S	probably benign	Het
C030048H21Rik	T	A	2: 26,145,899 (GRCm39)	Q87L	probably damaging	Het
Cd244a	T	A	1: 171,405,542 (GRCm39)		probably benign	Het
Cdk10	T	A	8: 123,957,326 (GRCm39)		probably null	Het
Cenpe	C	A	3: 134,929,026 (GRCm39)	P310Q	probably damaging	Het
Chuk	T	A	19: 44,085,972 (GRCm39)		probably null	Het
Crebl2	T	C	6: 134,828,139 (GRCm39)	S104P	probably benign	Het
Ddo	A	G	10: 40,523,726 (GRCm39)	K239E	probably benign	Het
Defb5	A	G	8: 19,300,868 (GRCm39)		probably null	Het
Dhx35	T	A	2: 158,676,832 (GRCm39)	M422K	probably damaging	Het
Fchsd1	C	T	18: 38,092,926 (GRCm39)		probably benign	Het
Gatm	G	A	2: 122,426,024 (GRCm39)	T409I	probably damaging	Het
Gdpd1	A	T	11: 86,950,332 (GRCm39)	D80E	probably damaging	Het
Hells	G	A	19: 38,943,244 (GRCm39)	S516N	probably benign	Het
Ints1	A	G	5: 139,738,542 (GRCm39)	S2069P	possibly damaging	Het
Kank4	G	A	4: 98,663,118 (GRCm39)	T690M	probably damaging	Het
Kcnq4	T	C	4: 120,573,006 (GRCm39)	N265S	possibly damaging	Het
Kif5b	C	A	18: 6,220,954 (GRCm39)	A385S	probably benign	Het
Map2	T	C	1: 66,454,415 (GRCm39)	S1102P	probably benign	Het
Mcm7	A	G	5: 138,163,133 (GRCm39)	S340P	possibly damaging	Het
Mcrs1	C	T	15: 99,144,876 (GRCm39)	R246H	possibly damaging	Het
Myo16	T	A	8: 10,610,226 (GRCm39)	M1189K	probably benign	Het
Or4d2	A	T	11: 87,783,892 (GRCm39)	I286N	probably damaging	Het
Or4k52	G	T	2: 111,610,804 (GRCm39)	M46I	probably benign	Het
Or7g29	G	A	9: 19,287,063 (GRCm39)	T38I	probably damaging	Het
Otog	A	G	7: 45,923,995 (GRCm39)	N1118S	probably damaging	Het
Pakap	T	C	4: 57,855,987 (GRCm39)	Y439H	probably damaging	Het
Pcdhb7	G	T	18: 37,474,846 (GRCm39)		probably benign	Het
Picalm	C	T	7: 89,819,806 (GRCm39)	T189I	possibly damaging	Het
Ptx4	T	A	17: 25,343,760 (GRCm39)	S337T	possibly damaging	Het
Rad51ap2	C	T	12: 11,508,313 (GRCm39)	S745L	probably benign	Het
Rspry1	G	A	8: 95,363,388 (GRCm39)		probably null	Het
Scn5a	T	G	9: 119,324,779 (GRCm39)	I1350L	probably damaging	Het
Sgk2	T	C	2: 162,839,755 (GRCm39)	L121P	probably damaging	Het
Slc17a1	A	T	13: 24,056,575 (GRCm39)		probably benign	Het
Slc6a12	A	G	6: 121,331,298 (GRCm39)	N183S	probably benign	Het
Smg9	C	A	7: 24,114,338 (GRCm39)		probably benign	Het
Spred1	G	A	2: 117,008,195 (GRCm39)	S367N	probably damaging	Het
Srpra	T	C	9: 35,122,646 (GRCm39)	V21A	probably benign	Het
Taar2	A	T	10: 23,816,627 (GRCm39)	I56F	possibly damaging	Het
Taf1a	T	G	1: 183,177,323 (GRCm39)	L67R	probably damaging	Het
Tbc1d10b	C	A	7: 126,797,779 (GRCm39)	R787S	possibly damaging	Het
Topbp1	T	A	9: 103,213,313 (GRCm39)	N1044K	probably benign	Het
Usp24	A	G	4: 106,232,871 (GRCm39)	T886A	probably benign	Het
Vmn2r26	A	G	6: 124,027,676 (GRCm39)	D472G	probably damaging	Het
Zyg11a	T	C	4: 108,061,943 (GRCm39)	N286S	possibly damaging	Het

Other mutations in Gspt1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00159:Gspt1	APN	16	11,040,476 (GRCm39)	missense	probably damaging	0.99
IGL00902:Gspt1	APN	16	11,050,443 (GRCm39)	missense	probably damaging	1.00
IGL00983:Gspt1	APN	16	11,048,861 (GRCm39)	splice site	probably benign
IGL01775:Gspt1	APN	16	11,041,159 (GRCm39)	missense	possibly damaging	0.92
IGL02079:Gspt1	APN	16	11,058,693 (GRCm39)	missense	probably benign	0.17
IGL02122:Gspt1	APN	16	11,047,080 (GRCm39)	missense	probably damaging	1.00
IGL02525:Gspt1	APN	16	11,048,854 (GRCm39)	missense	probably damaging	1.00
IGL03092:Gspt1	APN	16	11,056,763 (GRCm39)	missense	probably benign	0.11
goliad	UTSW	16	11,042,406 (GRCm39)	missense	probably benign	0.04
R0835:Gspt1	UTSW	16	11,056,802 (GRCm39)	missense	probably benign
R1519:Gspt1	UTSW	16	11,038,719 (GRCm39)	missense	probably damaging	1.00
R3410:Gspt1	UTSW	16	11,047,109 (GRCm39)	missense	probably damaging	1.00
R4834:Gspt1	UTSW	16	11,040,581 (GRCm39)	missense	probably damaging	1.00
R4866:Gspt1	UTSW	16	11,040,529 (GRCm39)	missense	possibly damaging	0.69
R5121:Gspt1	UTSW	16	11,041,165 (GRCm39)	missense	probably damaging	0.99
R5408:Gspt1	UTSW	16	11,071,719 (GRCm39)	missense	probably benign
R5410:Gspt1	UTSW	16	11,048,374 (GRCm39)	missense	probably benign	0.00
R5704:Gspt1	UTSW	16	11,046,057 (GRCm39)	missense	possibly damaging	0.89
R6224:Gspt1	UTSW	16	11,042,406 (GRCm39)	missense	probably benign	0.04
R6317:Gspt1	UTSW	16	11,041,072 (GRCm39)	splice site	probably null
R7069:Gspt1	UTSW	16	11,040,525 (GRCm39)	missense	probably damaging	1.00
R7151:Gspt1	UTSW	16	11,071,692 (GRCm39)	missense	probably benign	0.05
R7317:Gspt1	UTSW	16	11,040,521 (GRCm39)	missense	probably benign	0.01
R8137:Gspt1	UTSW	16	11,058,532 (GRCm39)	missense	probably benign	0.00
R9401:Gspt1	UTSW	16	11,050,535 (GRCm39)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- TTGAGTTGCCGGCTGAAAGC -3'
(R):5'- ATCCTTTCGCACACACGAG -3'

Sequencing Primer
(F):5'- AAAGCCGCGCTGAGGTTC -3'
(R):5'- TCGACCTGGTCTCGAGTGTAC -3'

Posted On

2017-08-08