Mutagenetix > Incidental Mutations

Incidental Mutation 'R0011:Tmem202'

8069

Institutional Source

Beutler Lab

Gene Symbol

Tmem202

Ensembl Gene

ENSMUSG00000049526

Gene Name

transmembrane protein 202

Synonyms

4930425N13Rik

MMRRC Submission

038306-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R0011 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

59518685-59539847 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 59524801 bp

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Isoleucine at position 81 (N81I)

Ref Sequence

ENSEMBL: ENSMUSP00000053782 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055345]

Predicted Effect

probably benign
Transcript: ENSMUST00000055345
AA Change: N81I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000053782
Gene: ENSMUSG00000049526
AA Change: N81I

Domain	Start	End	E-Value	Type
Pfam:PMP22_Claudin	50	206	2.2e-9	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000214580

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000216061

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 78.3%
3x: 67.8%
10x: 41.6%
20x: 22.3%

Validation Efficiency

92% (85/92)

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5430419D17Rik	T	A	7: 131,229,993	L389Q	probably damaging	Het
Ank3	A	G	10: 69,979,451		probably benign	Het
Art3	T	A	5: 92,403,612	Y17N	probably damaging	Het
Asic3	C	T	5: 24,417,492		probably benign	Het
Brip1	C	A	11: 86,186,998	K201N	possibly damaging	Het
Casc1	T	A	6: 145,179,055	M515L	probably damaging	Het
Ccdc88a	T	C	11: 29,374,364	F6S	probably damaging	Het
Cfap54	A	T	10: 93,065,225	C156S	probably damaging	Het
Chia1	A	G	3: 106,130,974		probably benign	Het
Cops4	C	A	5: 100,527,981	Q28K	probably benign	Het
Epha7	G	A	4: 28,962,564	D961N	probably benign	Het
Grin2c	T	C	11: 115,255,750	Y476C	probably damaging	Het
Igf2bp1	T	C	11: 96,005,584	D17G	probably damaging	Het
Kidins220	T	A	12: 24,999,352	V322E	probably damaging	Het
Krt35	T	A	11: 100,093,676	Q331L	probably benign	Het
Miox	C	T	15: 89,336,274	L189F	possibly damaging	Het
Mrc1	T	C	2: 14,261,337		probably null	Het
Msh2	T	C	17: 87,680,093		probably benign	Het
Ncoa1	A	C	12: 4,322,896	F57L	possibly damaging	Het
Npy4r	C	T	14: 34,146,723	V203M	probably damaging	Het
Pcdhgb8	T	C	18: 37,764,282	S802P	probably benign	Het
Ralgapa1	A	G	12: 55,786,263	S152P	probably damaging	Het
Rasgef1b	T	C	5: 99,232,354	Y344C	probably damaging	Het
Rdh19	T	A	10: 127,856,911	L149Q	probably damaging	Het
Shtn1	A	G	19: 59,032,218	S191P	possibly damaging	Het
Trim58	A	T	11: 58,643,120	T167S	probably benign	Het
Trp53i11	A	T	2: 93,199,353		probably benign	Het
Ttc30a2	T	A	2: 75,976,217	R650S	probably damaging	Het
Ttn	T	C	2: 76,810,355	H5356R	probably damaging	Het
Tyrp1	C	T	4: 80,840,793	T301I	probably damaging	Het
Wdr17	A	T	8: 54,672,501	I448K	possibly damaging	Het
Wscd1	T	C	11: 71,788,828	V509A	probably damaging	Het
Zfp251	A	G	15: 76,854,554	V108A	probably benign	Het

Other mutations in Tmem202

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03344:Tmem202	APN	9	59519068	missense	possibly damaging	0.53
R0011:Tmem202	UTSW	9	59524801	missense	probably benign	0.00
R0711:Tmem202	UTSW	9	59525372	missense	probably damaging	0.99
R1690:Tmem202	UTSW	9	59519108	missense	possibly damaging	0.93
R2127:Tmem202	UTSW	9	59520200	missense	probably benign	0.41
R4747:Tmem202	UTSW	9	59519194	missense	possibly damaging	0.47
R4998:Tmem202	UTSW	9	59524846	missense	probably damaging	0.99
R6916:Tmem202	UTSW	9	59525474	start gained	probably benign
R6929:Tmem202	UTSW	9	59519221	missense	probably benign	0.20

Posted On

2012-11-20