Mutagenetix > Incidental Mutation

Incidental Mutation 'R6088:Tns4'

486104

Institutional Source

Beutler Lab

Gene Symbol

Tns4

Ensembl Gene

ENSMUSG00000017607

Gene Name

tensin 4

Synonyms

9930017A07Rik

MMRRC Submission

044245-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.362) question?

Stock #

R6088 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

98956504-98980132 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 98964546 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 522 (S522P)

Ref Sequence

ENSEMBL: ENSMUSP00000017751 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000017751]

AlphaFold

Q8BZ33

Predicted Effect

probably damaging
Transcript: ENSMUST00000017751
AA Change: S522P

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000017751
Gene: ENSMUSG00000017607
AA Change: S522P

Domain	Start	End	E-Value	Type
low complexity region	63	72	N/A	INTRINSIC
low complexity region	271	304	N/A	INTRINSIC
SH2	427	527	6.95e-18	SMART
Pfam:PTB	562	695	1.6e-31	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000107465

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153351

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.7%
20x: 92.9%

Validation Efficiency

98% (59/60)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts19	G	T	18: 59,035,174 (GRCm39)	V360F	probably damaging	Het
Ankrd17	C	T	5: 90,401,547 (GRCm39)	E1605K	possibly damaging	Het
Arid4a	A	G	12: 71,069,010 (GRCm39)	D54G	probably damaging	Het
Baz2a	TCTCCTC	TCTC	10: 127,950,511 (GRCm39)		probably benign	Het
Bltp3a	G	A	17: 28,103,579 (GRCm39)		probably null	Het
Card6	A	T	15: 5,134,501 (GRCm39)	V234E	possibly damaging	Het
Cd1d1	G	T	3: 86,906,009 (GRCm39)	Q89K	probably benign	Het
Ciita	G	A	16: 10,329,795 (GRCm39)	R693K	probably damaging	Het
Cox7a2l	G	T	17: 83,811,401 (GRCm39)	L77I	probably benign	Het
Crybg2	A	T	4: 133,803,101 (GRCm39)		probably null	Het
Cts8	T	C	13: 61,401,780 (GRCm39)	N39S	probably benign	Het
Def8	G	T	8: 124,186,787 (GRCm39)	E456*	probably null	Het
Dld	A	G	12: 31,390,988 (GRCm39)	F153L	probably benign	Het
Elf1	C	T	14: 79,804,701 (GRCm39)	T122I	probably benign	Het
Emilin2	T	C	17: 71,562,119 (GRCm39)	N961S	probably benign	Het
Esp24	A	G	17: 39,350,901 (GRCm39)	I34V	probably benign	Het
Fam184b	C	A	5: 45,741,354 (GRCm39)	K292N	probably damaging	Het
Gabrg3	T	A	7: 56,634,826 (GRCm39)	N119I	probably damaging	Het
Gucy1b1	T	C	3: 81,942,187 (GRCm39)	H524R	probably damaging	Het
Kcp	A	T	6: 29,502,631 (GRCm39)	S205T	probably benign	Het
Klb	C	T	5: 65,506,356 (GRCm39)	T201M	probably benign	Het
Lamp3	A	T	16: 19,492,148 (GRCm39)	F365L	probably damaging	Het
Mad1l1	T	A	5: 140,179,718 (GRCm39)	H390L	probably benign	Het
Mlxipl	T	C	5: 135,162,884 (GRCm39)	Y711H	possibly damaging	Het
Myo5b	T	A	18: 74,853,969 (GRCm39)	L1196Q	possibly damaging	Het
Ndufb8	A	G	19: 44,543,464 (GRCm39)	S70P	probably benign	Het
Neb	T	C	2: 52,099,354 (GRCm39)	D4832G	probably damaging	Het
Niban2	T	C	2: 32,813,135 (GRCm39)	V540A	probably damaging	Het
Nr5a1	T	C	2: 38,592,007 (GRCm39)	D322G	probably benign	Het
Or1e1d-ps1	A	T	11: 73,819,649 (GRCm39)	T273S	probably benign	Het
Or5ak20	T	A	2: 85,183,698 (GRCm39)	S191C	probably damaging	Het
Oscar	G	A	7: 3,614,311 (GRCm39)	P143S	probably benign	Het
Oxa1l	T	A	14: 54,605,151 (GRCm39)		probably null	Het
Pafah2	A	G	4: 134,140,692 (GRCm39)	I221V	probably benign	Het
Pibf1	T	A	14: 99,416,794 (GRCm39)	F456I	probably benign	Het
Pla2g4d	C	T	2: 120,100,487 (GRCm39)	G615D	probably damaging	Het
Plekhg2	C	T	7: 28,060,438 (GRCm39)	V964I	probably benign	Het
Ppip5k1	C	A	2: 121,167,944 (GRCm39)	V770L	probably benign	Het
Ppl	A	T	16: 4,922,852 (GRCm39)	L213Q	possibly damaging	Het
Ptprf	G	A	4: 118,067,952 (GRCm39)	T1785I	possibly damaging	Het
Pycr2	G	A	1: 180,733,801 (GRCm39)	G131E	probably damaging	Het
Rbpj	C	T	5: 53,808,710 (GRCm39)		probably null	Het
Rcc1	G	T	4: 132,060,153 (GRCm39)	D430E	probably benign	Het
Rhbdf1	A	G	11: 32,162,007 (GRCm39)	V525A	possibly damaging	Het
Samd7	G	A	3: 30,810,632 (GRCm39)	M216I	probably benign	Het
Ska3	A	T	14: 58,054,151 (GRCm39)	D266E	probably benign	Het
Slc1a7	G	A	4: 107,869,641 (GRCm39)	V569M	probably damaging	Het
Slc26a1	C	T	5: 108,821,872 (GRCm39)	E6K	possibly damaging	Het
Slc4a4	T	A	5: 89,345,563 (GRCm39)	V741E	probably benign	Het
St6galnac3	C	T	3: 152,912,352 (GRCm39)	G164S	probably damaging	Het
Tgs1	T	A	4: 3,595,383 (GRCm39)	N517K	probably benign	Het
Trpm1	A	T	7: 63,917,724 (GRCm39)	M355L	probably damaging	Het
Trpm8	G	A	1: 88,234,400 (GRCm39)		probably benign	Het
V1ra8	T	C	6: 90,180,082 (GRCm39)	F95S	probably damaging	Het
Zfp521	A	C	18: 13,979,166 (GRCm39)	S416A	possibly damaging	Het
Zfp574	T	A	7: 24,779,764 (GRCm39)	V262E	probably benign	Het
Zfp740	T	A	15: 102,117,243 (GRCm39)	I77N	probably damaging	Het
Zscan18	A	T	7: 12,509,125 (GRCm39)		probably benign	Het

Other mutations in Tns4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00783:Tns4	APN	11	98,961,221 (GRCm39)	splice site	probably benign
IGL01940:Tns4	APN	11	98,959,047 (GRCm39)	missense	probably benign	0.43
IGL03130:Tns4	APN	11	98,959,095 (GRCm39)	missense	probably damaging	1.00
IGL03376:Tns4	APN	11	98,969,382 (GRCm39)	missense	probably benign	0.00
PIT4486001:Tns4	UTSW	11	98,962,161 (GRCm39)	missense	probably damaging	1.00
R0089:Tns4	UTSW	11	98,966,024 (GRCm39)	missense	probably damaging	1.00
R1598:Tns4	UTSW	11	98,961,243 (GRCm39)	missense	probably damaging	1.00
R1872:Tns4	UTSW	11	98,970,926 (GRCm39)	missense	probably damaging	1.00
R1903:Tns4	UTSW	11	98,966,401 (GRCm39)	missense	probably damaging	1.00
R1998:Tns4	UTSW	11	98,976,529 (GRCm39)	missense	probably benign
R2126:Tns4	UTSW	11	98,970,904 (GRCm39)	critical splice donor site	probably null
R4468:Tns4	UTSW	11	98,961,241 (GRCm39)	missense	probably benign	0.41
R4973:Tns4	UTSW	11	98,966,039 (GRCm39)	missense	probably damaging	1.00
R5048:Tns4	UTSW	11	98,969,605 (GRCm39)	missense	possibly damaging	0.95
R5918:Tns4	UTSW	11	98,964,497 (GRCm39)	critical splice donor site	probably null
R6151:Tns4	UTSW	11	98,966,376 (GRCm39)	missense	probably benign	0.11
R6586:Tns4	UTSW	11	98,971,093 (GRCm39)	missense	probably benign	0.00
R7543:Tns4	UTSW	11	98,963,079 (GRCm39)	missense	probably benign	0.38
R7667:Tns4	UTSW	11	98,962,296 (GRCm39)	missense	probably damaging	1.00
R7909:Tns4	UTSW	11	98,976,849 (GRCm39)	missense	probably damaging	0.99
R8206:Tns4	UTSW	11	98,976,627 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TAAATTCTCACAGGCGGGAAG -3'
(R):5'- TTCGGCCAAAGGAGTACATCTG -3'

Sequencing Primer
(F):5'- CTCACAGGCGGGAAGTGGAG -3'
(R):5'- AGGAGCCCTACTTTGGTAAGC -3'

Posted On

2017-08-16