Mutagenetix > Incidental Mutation

Incidental Mutation 'R3946:Tmem57'

307697

Institutional Source

Beutler Lab

Gene Symbol

Tmem57

Ensembl Gene

ENSMUSG00000028826

Gene Name

transmembrane protein 57

Synonyms

1110007C24Rik, C61, 9230118A01Rik

MMRRC Submission

040827-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.698) question?

Stock #

R3946 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

134802759-134853345 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 134804481 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 626 (Y626H)

Ref Sequence

ENSEMBL: ENSMUSP00000030628 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030628]

AlphaFold

Q7TQE6

Predicted Effect

probably damaging
Transcript: ENSMUST00000030628
AA Change: Y626H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000030628
Gene: ENSMUSG00000028826
AA Change: Y626H

Domain	Start	End	E-Value	Type
Pfam:Macoilin	2	662	N/A	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150031

Meta Mutation Damage Score

0.4659

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.0%
20x: 94.1%

Validation Efficiency

98% (60/61)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aaed1	T	C	13: 64,309,098 (GRCm38)	I104V	probably damaging	Het
Abi2	A	G	1: 60,453,754 (GRCm38)	Q328R	probably damaging	Het
Agr3	C	A	12: 35,947,513 (GRCm38)		probably benign	Het
Brca2	T	A	5: 150,536,704 (GRCm38)	S481R	probably damaging	Het
Cabin1	T	G	10: 75,745,259 (GRCm38)	Q411P	probably damaging	Het
Calr3	A	G	8: 72,443,620 (GRCm38)	Y22H	probably damaging	Het
Caprin1	T	A	2: 103,796,766 (GRCm38)	I59F	probably damaging	Het
Cdk5rap1	T	C	2: 154,348,716 (GRCm38)	T442A	probably damaging	Het
Chn2	T	C	6: 54,269,426 (GRCm38)		probably benign	Het
Cic	C	A	7: 25,272,346 (GRCm38)	R501S	possibly damaging	Het
Coch	A	G	12: 51,601,812 (GRCm38)		probably null	Het
Defa25	G	A	8: 21,084,490 (GRCm38)	V17I	probably null	Het
Dglucy	T	C	12: 100,838,700 (GRCm38)		probably null	Het
Dtx1	T	G	5: 120,681,286 (GRCm38)	T616P	possibly damaging	Het
Eef1g	T	C	19: 8,969,977 (GRCm38)	L171P	probably benign	Het
Fam135a	A	G	1: 24,030,394 (GRCm38)	S465P	probably damaging	Het
Gm14025	A	G	2: 129,039,601 (GRCm38)	L135P	probably damaging	Het
Gm14412	A	T	2: 177,314,685 (GRCm38)	C472*	probably null	Het
Gm7104	T	C	12: 88,286,042 (GRCm38)		noncoding transcript	Het
Got2	A	G	8: 95,888,230 (GRCm38)	S26P	probably benign	Het
H2-M11	A	G	17: 36,549,231 (GRCm38)	I329M	probably damaging	Het
Hmcn2	T	A	2: 31,382,394 (GRCm38)	D1295E	possibly damaging	Het
Hoxd12	G	T	2: 74,675,427 (GRCm38)	R114L	probably damaging	Het
Ilkap	A	C	1: 91,387,250 (GRCm38)	D124E	probably damaging	Het
Med6	T	C	12: 81,581,851 (GRCm38)	Y88C	probably damaging	Het
Mep1a	A	T	17: 43,475,041 (GRCm38)	L719*	probably null	Het
Mmp23	T	C	4: 155,652,023 (GRCm38)	Y187C	probably damaging	Het
Myo1g	A	G	11: 6,520,760 (GRCm38)	M32T	possibly damaging	Het
Ncstn	T	C	1: 172,067,494 (GRCm38)	E614G	probably benign	Het
Nr2c2	C	T	6: 92,163,138 (GRCm38)	R464W	probably damaging	Het
Olfr1309	G	A	2: 111,983,297 (GRCm38)	T259M	possibly damaging	Het
Otub2	T	A	12: 103,392,826 (GRCm38)	L58*	probably null	Het
Pcdhga12	G	A	18: 37,767,629 (GRCm38)	V505I	probably benign	Het
Pcdhga9	T	A	18: 37,737,844 (GRCm38)	V242D	probably damaging	Het
Pex1	C	T	5: 3,626,084 (GRCm38)	L891F	probably damaging	Het
Pgm1	C	T	5: 64,112,061 (GRCm38)	T497I	probably benign	Het
Pikfyve	T	C	1: 65,196,681 (GRCm38)	F171L	probably damaging	Het
Pilrb1	T	G	5: 137,857,392 (GRCm38)	K79T	probably benign	Het
Pin1	C	T	9: 20,655,364 (GRCm38)	R21W	probably damaging	Het
Ptprq	A	G	10: 107,686,392 (GRCm38)		probably benign	Het
Rad17	G	A	13: 100,622,863 (GRCm38)	A552V	possibly damaging	Het
Rbbp8	A	G	18: 11,718,868 (GRCm38)	T249A	probably benign	Het
Rtkn	A	T	6: 83,135,976 (GRCm38)	I10F	probably benign	Het
Scube2	T	A	7: 109,857,590 (GRCm38)	I103F	possibly damaging	Het
Sec23b	A	G	2: 144,581,973 (GRCm38)	H514R	probably benign	Het
Serbp1	T	A	6: 67,272,220 (GRCm38)	D223E	probably benign	Het
Slc14a1	C	A	18: 78,111,392 (GRCm38)	V260L	probably benign	Het
Slc22a23	A	G	13: 34,183,126 (GRCm38)	I633T	probably damaging	Het
Stk19	A	T	17: 34,824,747 (GRCm38)		probably benign	Het
Svs2	T	C	2: 164,237,127 (GRCm38)	M287V	probably benign	Het
Syne3	T	A	12: 104,958,066 (GRCm38)	Q358L	probably damaging	Het
Synj1	A	G	16: 91,010,096 (GRCm38)	F58L	possibly damaging	Het
Tg	T	C	15: 66,674,023 (GRCm38)	V198A	probably damaging	Het
Tle4	A	T	19: 14,597,388 (GRCm38)	Y9N	probably damaging	Het
Tmx3	G	A	18: 90,524,335 (GRCm38)	A186T	possibly damaging	Het
Traf3	G	A	12: 111,255,245 (GRCm38)	S280N	possibly damaging	Het
Trmt13	A	G	3: 116,581,518 (GRCm38)	F447S	probably damaging	Het
Trp53bp1	T	A	2: 121,228,626 (GRCm38)	H918L	probably damaging	Het
Ush2a	T	G	1: 188,728,504 (GRCm38)	V2654G	probably benign	Het
Vmn2r25	A	G	6: 123,840,098 (GRCm38)	Y175H	probably damaging	Het
Zfp335	T	C	2: 164,892,189 (GRCm38)	D1330G	probably damaging	Het

Other mutations in Tmem57

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00793:Tmem57	APN	4	134,828,206 (GRCm38)	missense	probably damaging	0.96
IGL01062:Tmem57	APN	4	134,833,297 (GRCm38)	missense	probably damaging	0.97
IGL02249:Tmem57	APN	4	134,828,312 (GRCm38)	missense	possibly damaging	0.50
IGL02850:Tmem57	APN	4	134,828,386 (GRCm38)	missense	probably benign	0.12
subtle	UTSW	4	134,828,299 (GRCm38)	missense	probably damaging	1.00
R0400:Tmem57	UTSW	4	134,828,116 (GRCm38)	missense	probably benign	0.25
R0548:Tmem57	UTSW	4	134,806,660 (GRCm38)	missense	probably damaging	1.00
R0589:Tmem57	UTSW	4	134,828,217 (GRCm38)	missense	probably benign	0.30
R1536:Tmem57	UTSW	4	134,804,507 (GRCm38)	missense	probably damaging	1.00
R2063:Tmem57	UTSW	4	134,828,279 (GRCm38)	missense	possibly damaging	0.95
R2151:Tmem57	UTSW	4	134,811,223 (GRCm38)	missense	probably benign	0.00
R2509:Tmem57	UTSW	4	134,804,388 (GRCm38)	missense	probably damaging	1.00
R2510:Tmem57	UTSW	4	134,804,388 (GRCm38)	missense	probably damaging	1.00
R2511:Tmem57	UTSW	4	134,804,388 (GRCm38)	missense	probably damaging	1.00
R3806:Tmem57	UTSW	4	134,830,580 (GRCm38)	missense	probably benign	0.00
R4994:Tmem57	UTSW	4	134,828,299 (GRCm38)	missense	probably damaging	1.00
R4999:Tmem57	UTSW	4	134,828,133 (GRCm38)	missense	probably benign	0.23
R5169:Tmem57	UTSW	4	134,828,463 (GRCm38)	missense	probably benign	0.23
R5310:Tmem57	UTSW	4	134,837,019 (GRCm38)	intron	probably benign
R5443:Tmem57	UTSW	4	134,833,308 (GRCm38)	nonsense	probably null
R5554:Tmem57	UTSW	4	134,828,134 (GRCm38)	missense	probably benign
R5712:Tmem57	UTSW	4	134,828,058 (GRCm38)	missense	probably benign	0.06
R6627:Tmem57	UTSW	4	134,836,343 (GRCm38)	missense	probably damaging	0.98
R7100:Tmem57	UTSW	4	134,806,660 (GRCm38)	missense	probably damaging	1.00
R7448:Tmem57	UTSW	4	134,828,279 (GRCm38)	missense	possibly damaging	0.95
R8059:Tmem57	UTSW	4	134,828,048 (GRCm38)	nonsense	probably null
R8300:Tmem57	UTSW	4	134,828,451 (GRCm38)	missense	probably benign
R9246:Tmem57	UTSW	4	134,837,931 (GRCm38)	missense	possibly damaging	0.50
R9786:Tmem57	UTSW	4	134,830,682 (GRCm38)	nonsense	probably null
X0062:Tmem57	UTSW	4	134,836,347 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TATCTTGACTGCCAGAGACGC -3'
(R):5'- AAAGTGCTCTGATGTTGGGTAC -3'

Sequencing Primer
(F):5'- CAGAGACGCTGCTTTTCGAAG -3'
(R):5'- CAGGAAGCTTGCTCGCTC -3'

Posted On

2015-04-17