Mutagenetix > Incidental Mutation

Incidental Mutation 'R4994:Tmem57'

385085

Institutional Source

Beutler Lab

Gene Symbol

Tmem57

Ensembl Gene

ENSMUSG00000028826

Gene Name

transmembrane protein 57

Synonyms

1110007C24Rik, C61, 9230118A01Rik

MMRRC Submission

042588-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.494) question?

Stock #

R4994 (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 134828299 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 288 (Y288H)

Ref Sequence

ENSEMBL: ENSMUSP00000030628 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030628] [ENSMUST00000137707] [ENSMUST00000148595]

AlphaFold

Q7TQE6

Predicted Effect

probably damaging
Transcript: ENSMUST00000030628
AA Change: Y288H

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

SMART Domains

Protein: ENSMUSP00000030628
Gene: ENSMUSG00000028826
AA Change: Y288H

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

Predicted Effect

probably benign
Transcript: ENSMUST00000137707

SMART Domains

Protein: ENSMUSP00000124477
Gene: ENSMUSG00000028826

Domain	Start	End	E-Value	Type
Pfam:Macoilin	2	157	2.1e-112	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000148595

SMART Domains

Protein: ENSMUSP00000125440
Gene: ENSMUSG00000028826

Domain	Start	End	E-Value	Type
Pfam:Macoilin	2	78	7e-48	PFAM

Meta Mutation Damage Score

0.0966

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.0%

Validation Efficiency

100% (79/79)

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1190002N15Rik	C	A	9: 94,537,433	R148L	probably benign	Het
1700030K09Rik	A	G	8: 72,455,118	E364G	probably benign	Het
4930505A04Rik	C	T	11: 30,426,349	V173M	probably damaging	Het
Abcb4	A	G	5: 8,928,524	T557A	probably damaging	Het
Acadm	C	T	3: 153,929,584	E298K	probably damaging	Het
Adrb3	T	C	8: 27,227,827		probably null	Het
Aldh1b1	A	G	4: 45,803,128	Y222C	possibly damaging	Het
Ankrd6	A	G	4: 32,860,387	Y19H	probably damaging	Het
Arhgap21	T	A	2: 20,849,890	T1554S	probably benign	Het
BC043934	T	C	9: 96,437,120		noncoding transcript	Het
Birc6	A	G	17: 74,594,324		probably benign	Het
Blm	A	C	7: 80,458,825	F1357C	probably benign	Het
Cd209a	T	C	8: 3,747,713		probably null	Het
Cdk7	G	A	13: 100,717,595	H129Y	probably damaging	Het
Clec14a	G	T	12: 58,268,284	P184Q	probably damaging	Het
Cma1	T	A	14: 55,941,671	I243F	probably damaging	Het
Cntnap3	G	T	13: 64,761,984	T769K	possibly damaging	Het
Col5a1	A	C	2: 28,032,739	K273T	possibly damaging	Het
Csnk1e	A	G	15: 79,424,929	Y266H	probably damaging	Het
Cyb5d1	A	G	11: 69,393,771	L185S	probably damaging	Het
Dennd5b	T	C	6: 149,041,500		probably null	Het
Drp2	G	A	X: 134,441,316	R567H	probably damaging	Homo
Dzank1	T	G	2: 144,522,566	D37A	probably damaging	Het
Echdc2	A	G	4: 108,165,628	I34V	probably benign	Het
Esm1	A	T	13: 113,213,431	R128S	probably benign	Het
Fbrsl1	A	G	5: 110,447,951	S73P	probably damaging	Het
Fbxo18	T	A	2: 11,764,230	I251F	probably damaging	Het
Fbxo6	A	T	4: 148,149,491	S49R	probably damaging	Het
Gm13089	T	A	4: 143,698,369	Q168L	possibly damaging	Het
Gm17093	A	T	14: 44,519,322	Q82L	probably damaging	Het
Hmcn2	T	C	2: 31,458,055		probably null	Het
Hspa4l	C	A	3: 40,745,649		probably benign	Het
Il3ra	G	A	14: 14,351,080	A201T	probably benign	Het
Irx5	T	A	8: 92,360,781	V447E	probably damaging	Het
Kif14	G	T	1: 136,482,959	L668F	probably damaging	Het
Lag3	T	A	6: 124,904,453	R519W	unknown	Het
Lgr4	A	G	2: 110,011,938	N756S	probably damaging	Het
Lingo4	A	G	3: 94,402,541	H262R	probably benign	Het
Lingo4	T	A	3: 94,403,001	H415Q	probably benign	Het
Lkaaear1	C	A	2: 181,697,583	G25*	probably null	Het
Marf1	T	C	16: 14,114,231	K1641E	probably benign	Het
Mtfmt	T	C	9: 65,443,851		probably benign	Het
Mtif3	G	A	5: 146,956,788	T203M	probably benign	Het
Mycbp2	A	G	14: 103,169,994	I2740T	probably benign	Het
Nrd1	A	G	4: 109,046,612	T720A	probably benign	Het
Olfr715	T	C	7: 107,129,064	T110A	probably benign	Het
Peak1	T	A	9: 56,241,276	D32V	possibly damaging	Het
Pigr	G	A	1: 130,841,817	D122N	probably benign	Het
Plekhg3	A	G	12: 76,565,537	R391G	possibly damaging	Het
Ppfia3	T	C	7: 45,341,118	D919G	probably damaging	Het
Rnase2b	T	A	14: 51,162,751	D96E	possibly damaging	Het
Rsf1	G	GACGGCGGCT	7: 97,579,909		probably benign	Het
Rsf1	CGGCGGC	CGGCGGCCGCGGCGGC	7: 97,579,923		probably benign	Het
Serpina3f	A	G	12: 104,220,356	T394A	probably benign	Het
Six3	A	G	17: 85,621,292	N18S	possibly damaging	Het
Slc12a5	T	A	2: 164,983,365		probably null	Het
Slc35f6	A	G	5: 30,648,083	N21S	probably damaging	Het
Slc39a6	A	T	18: 24,596,294	I454N	probably damaging	Het
Slc40a1	T	A	1: 45,909,664	E485D	probably damaging	Het
Sort1	G	A	3: 108,328,069	C255Y	probably damaging	Het
Stab2	T	A	10: 86,949,907	T624S	probably benign	Het
Stk33	T	A	7: 109,340,398	I99L	probably benign	Het
Taf4b	T	A	18: 14,898,043	I828N	probably damaging	Het
Terf2	T	C	8: 107,076,478		probably benign	Het
Timd4	C	T	11: 46,815,517	R49C	probably damaging	Het
Tpte	T	C	8: 22,318,346	S166P	probably benign	Het
Trabd2b	T	C	4: 114,406,855	L13P	probably benign	Het
Trappc11	A	T	8: 47,522,441	Y247*	probably null	Het
Trnt1	C	T	6: 106,778,892	Q303*	probably null	Het
Tspyl5	T	A	15: 33,687,055	Q248L	possibly damaging	Het
Ubxn7	A	T	16: 32,381,504	K337N	probably damaging	Het
Unc13a	T	A	8: 71,643,172	I1234F	probably benign	Het
Vmn1r127	A	T	7: 21,319,018	F282I	probably damaging	Het
Wdhd1	A	T	14: 47,268,654		probably null	Het
Zfp605	A	G	5: 110,127,486	K157E	probably damaging	Het
Zhx2	T	A	15: 57,821,359	D41E	probably benign	Het

Other mutations in Tmem57

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00793:Tmem57	APN	4	134828206	missense	probably damaging	0.96
IGL01062:Tmem57	APN	4	134833297	missense	probably damaging	0.97
IGL02249:Tmem57	APN	4	134828312	missense	possibly damaging	0.50
IGL02850:Tmem57	APN	4	134828386	missense	probably benign	0.12
subtle	UTSW	4	134828299	missense	probably damaging	1.00
R0400:Tmem57	UTSW	4	134828116	missense	probably benign	0.25
R0548:Tmem57	UTSW	4	134806660	missense	probably damaging	1.00
R0589:Tmem57	UTSW	4	134828217	missense	probably benign	0.30
R1536:Tmem57	UTSW	4	134804507	missense	probably damaging	1.00
R2063:Tmem57	UTSW	4	134828279	missense	possibly damaging	0.95
R2151:Tmem57	UTSW	4	134811223	missense	probably benign	0.00
R2509:Tmem57	UTSW	4	134804388	missense	probably damaging	1.00
R2510:Tmem57	UTSW	4	134804388	missense	probably damaging	1.00
R2511:Tmem57	UTSW	4	134804388	missense	probably damaging	1.00
R3806:Tmem57	UTSW	4	134830580	missense	probably benign	0.00
R3946:Tmem57	UTSW	4	134804481	missense	probably damaging	1.00
R4999:Tmem57	UTSW	4	134828133	missense	probably benign	0.23
R5169:Tmem57	UTSW	4	134828463	missense	probably benign	0.23
R5310:Tmem57	UTSW	4	134837019	intron	probably benign
R5443:Tmem57	UTSW	4	134833308	nonsense	probably null
R5554:Tmem57	UTSW	4	134828134	missense	probably benign
R5712:Tmem57	UTSW	4	134828058	missense	probably benign	0.06
R6627:Tmem57	UTSW	4	134836343	missense	probably damaging	0.98
R7100:Tmem57	UTSW	4	134806660	missense	probably damaging	1.00
R7448:Tmem57	UTSW	4	134828279	missense	possibly damaging	0.95
R8059:Tmem57	UTSW	4	134828048	nonsense	probably null
R8300:Tmem57	UTSW	4	134828451	missense	probably benign
R9246:Tmem57	UTSW	4	134837931	missense	possibly damaging	0.50
R9786:Tmem57	UTSW	4	134830682	nonsense	probably null
X0062:Tmem57	UTSW	4	134836347	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTAGACGAGGAAGGAATGCTTC -3'
(R):5'- TTGGTACTGTAGCAGCCAAGG -3'

Sequencing Primer
(F):5'- GAATGCTTCCATTTGTAGCGC -3'
(R):5'- ATTGCCGGACATGGATTCC -3'

Posted On

2016-05-10