Mutagenetix > Incidental Mutation

Incidental Mutation 'R1183:Tmc2'

101693

Institutional Source

Beutler Lab

Gene Symbol

Tmc2

Ensembl Gene

ENSMUSG00000060332

Gene Name

transmembrane channel-like gene family 2

Synonyms

MMRRC Submission

039255-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.244) question?

Stock #

R1183 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

130195194-130264445 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 130247976 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 627 (M627K)

Ref Sequence

ENSEMBL: ENSMUSP00000125843 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077988] [ENSMUST00000166774]

AlphaFold

Q8R4P4

Predicted Effect

probably damaging
Transcript: ENSMUST00000077988
AA Change: M627K

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

SMART Domains

Protein: ENSMUSP00000077139
Gene: ENSMUSG00000060332
AA Change: M627K

Domain	Start	End	E-Value	Type
transmembrane domain	236	258	N/A	INTRINSIC
transmembrane domain	317	339	N/A	INTRINSIC
transmembrane domain	412	434	N/A	INTRINSIC
transmembrane domain	488	507	N/A	INTRINSIC
low complexity region	541	553	N/A	INTRINSIC
Pfam:TMC	556	671	8.6e-41	PFAM
transmembrane domain	676	698	N/A	INTRINSIC
transmembrane domain	735	757	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000166774
AA Change: M627K

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

SMART Domains

Protein: ENSMUSP00000125843
Gene: ENSMUSG00000060332
AA Change: M627K

Domain	Start	End	E-Value	Type
transmembrane domain	236	258	N/A	INTRINSIC
transmembrane domain	317	339	N/A	INTRINSIC
transmembrane domain	412	434	N/A	INTRINSIC
transmembrane domain	488	507	N/A	INTRINSIC
low complexity region	541	553	N/A	INTRINSIC
Pfam:TMC	556	671	1.2e-36	PFAM
transmembrane domain	676	698	N/A	INTRINSIC
transmembrane domain	735	757	N/A	INTRINSIC

Meta Mutation Damage Score

0.5526

Coding Region Coverage

1x: 98.9%
3x: 97.9%
10x: 95.0%
20x: 88.8%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a transmembrane protein that is necesssary for mechanotransduction in cochlear hair cells of the inner ear. Mutations in this gene may underlie hereditary disorders of balance and hearing. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for a null allele display normal hearing and motor behavior. Cochlear hair cells show partial resistance to gentamicin induced toxicity. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438A13Rik	T	A	3: 36,895,303 (GRCm38)	L366Q	possibly damaging	Het
Aars	T	G	8: 111,041,574 (GRCm38)	Y192*	probably null	Het
Abcc6	T	C	7: 45,985,253 (GRCm38)	Y1100C	probably damaging	Het
Adamtsl2	T	C	2: 27,084,080 (GRCm38)	W132R	probably damaging	Het
Adgra2	T	A	8: 27,114,388 (GRCm38)	V497E	probably damaging	Het
Adtrp	T	G	13: 41,828,337 (GRCm38)		probably benign	Het
Alg9	T	A	9: 50,789,533 (GRCm38)	L201Q	possibly damaging	Het
Ap4e1	T	A	2: 127,014,201 (GRCm38)	I84K	probably damaging	Het
Atrnl1	T	C	19: 57,650,293 (GRCm38)	S288P	probably damaging	Het
Cacna1a	A	G	8: 84,580,217 (GRCm38)	D1367G	probably damaging	Het
Card19	C	T	13: 49,205,251 (GRCm38)	R82Q	probably damaging	Het
Cep128	T	C	12: 91,325,598 (GRCm38)	I226V	possibly damaging	Het
Ces1f	A	C	8: 93,268,005 (GRCm38)	D259E	probably benign	Het
Ckap5	T	A	2: 91,586,266 (GRCm38)	M1072K	probably benign	Het
Dcpp2	T	A	17: 23,900,494 (GRCm38)	V94D	probably benign	Het
Dnah2	T	C	11: 69,446,648 (GRCm38)	D3209G	possibly damaging	Het
Dsg1c	A	G	18: 20,283,198 (GRCm38)	T719A	probably damaging	Het
Dsp	G	A	13: 38,191,740 (GRCm38)	W1167*	probably null	Het
Eml5	T	C	12: 98,792,046 (GRCm38)	I1874V	probably benign	Het
Epg5	A	G	18: 77,960,711 (GRCm38)	T645A	probably damaging	Het
F2rl2	T	C	13: 95,701,113 (GRCm38)	L222S	probably damaging	Het
Fam114a1	T	A	5: 65,034,388 (GRCm38)	C495S	probably damaging	Het
Fbn1	A	T	2: 125,321,617 (GRCm38)	D2106E	probably benign	Het
Fgf14	T	A	14: 124,676,524 (GRCm38)	N65I	probably benign	Het
Fip1l1	T	C	5: 74,595,102 (GRCm38)	Y497H	probably damaging	Het
Fn1	A	C	1: 71,586,245 (GRCm38)	D2376E	probably damaging	Het
Foxd2	T	C	4: 114,907,465 (GRCm38)	T453A	possibly damaging	Het
Galnt1	G	T	18: 24,271,590 (GRCm38)	W328L	probably damaging	Het
Gapt	A	G	13: 110,353,838 (GRCm38)	V97A	possibly damaging	Het
Gatad1	A	G	5: 3,643,707 (GRCm38)	V154A	possibly damaging	Het
Gdf15	A	G	8: 70,631,552 (GRCm38)	F21L	probably benign	Het
Igdcc4	T	C	9: 65,121,900 (GRCm38)	F273S	possibly damaging	Het
Invs	A	T	4: 48,421,725 (GRCm38)	R786W	possibly damaging	Het
Itfg1	T	G	8: 85,780,523 (GRCm38)	E236A	probably benign	Het
Jak3	A	T	8: 71,684,550 (GRCm38)	I752F	probably damaging	Het
Kcnip3	C	A	2: 127,465,065 (GRCm38)	G144W	probably damaging	Het
Kctd19	T	C	8: 105,382,966 (GRCm38)	H925R	probably benign	Het
Kdr	C	T	5: 75,946,851 (GRCm38)	A1011T	probably damaging	Het
Kif13b	C	A	14: 64,782,377 (GRCm38)	H1398Q	probably benign	Het
Lrp4	A	T	2: 91,477,519 (GRCm38)		probably null	Het
Lrtm2	T	C	6: 119,320,885 (GRCm38)	D65G	probably benign	Het
Lyz1	A	G	10: 117,292,810 (GRCm38)	L10P	probably damaging	Het
Metap2	A	T	10: 93,870,184 (GRCm38)	N245K	probably damaging	Het
Mms19	T	C	19: 41,954,831 (GRCm38)	D297G	possibly damaging	Het
Mocs3	A	G	2: 168,231,653 (GRCm38)	D340G	possibly damaging	Het
Mtfr1l	A	G	4: 134,529,125 (GRCm38)	L243P	probably damaging	Het
Mtss1	A	G	15: 58,971,048 (GRCm38)	I105T	probably damaging	Het
Myo18a	T	C	11: 77,857,745 (GRCm38)	S1967P	probably damaging	Het
Ncor2	T	C	5: 125,023,521 (GRCm38)	N2248S	possibly damaging	Het
Nfatc2	T	C	2: 168,590,088 (GRCm38)	D35G	possibly damaging	Het
Nup210l	T	A	3: 90,159,945 (GRCm38)	M764K	probably benign	Het
Olfr519	A	G	7: 108,893,741 (GRCm38)	L222P	probably damaging	Het
Otof	T	C	5: 30,371,912 (GRCm38)	S1753G	probably damaging	Het
Otog	G	A	7: 46,289,755 (GRCm38)	V2070I	probably benign	Het
Piezo2	A	G	18: 63,086,753 (GRCm38)	V961A	probably damaging	Het
Pofut1	C	T	2: 153,261,238 (GRCm38)	S169L	probably benign	Het
Ppp1r10	T	A	17: 35,929,443 (GRCm38)	S542T	possibly damaging	Het
Prpf8	T	C	11: 75,490,330 (GRCm38)	Y219H	possibly damaging	Het
Ptges3l	T	C	11: 101,421,905 (GRCm38)	D113G	possibly damaging	Het
Pycrl	G	A	15: 75,918,798 (GRCm38)	L71F	probably benign	Het
Ramp3	A	G	11: 6,674,867 (GRCm38)	K54E	possibly damaging	Het
Rbpms	C	A	8: 33,804,072 (GRCm38)	Q214H	possibly damaging	Het
Rif1	GCCACCA	GCCA	2: 52,110,324 (GRCm38)		probably benign	Het
Robo4	C	A	9: 37,408,052 (GRCm38)	D565E	probably damaging	Het
S100a1	C	T	3: 90,511,334 (GRCm38)	V58I	probably benign	Het
Setx	T	A	2: 29,180,092 (GRCm38)	D2636E	probably benign	Het
Sun2	A	T	15: 79,728,468 (GRCm38)	V417E	probably damaging	Het
Tbccd1	T	C	16: 22,841,769 (GRCm38)	N99S	probably benign	Het
Tex15	A	G	8: 33,574,865 (GRCm38)	D1441G	probably benign	Het
Trim32	A	G	4: 65,614,391 (GRCm38)	Y395C	probably benign	Het
Trpm2	A	G	10: 77,923,564 (GRCm38)	Y1129H	probably damaging	Het
Trpm8	A	T	1: 88,348,091 (GRCm38)	R470S	probably damaging	Het
Tsg101	G	T	7: 46,889,624 (GRCm38)	D389E	probably benign	Het
Ubn1	T	C	16: 5,064,542 (GRCm38)	L46P	probably damaging	Het
Ubr5	T	C	15: 37,997,175 (GRCm38)	I1745V	possibly damaging	Het
Usp20	T	C	2: 31,011,785 (GRCm38)	Y521H	probably benign	Het
Vmn1r159	A	T	7: 22,843,594 (GRCm38)	H4Q	probably null	Het
Vmn2r27	T	A	6: 124,200,532 (GRCm38)	E504D	probably benign	Het
Wdr72	A	T	9: 74,179,585 (GRCm38)	I612F	probably benign	Het
Zbtb8a	T	C	4: 129,357,727 (GRCm38)	H317R	possibly damaging	Het
Zfp507	T	C	7: 35,794,890 (GRCm38)	S243G	probably damaging	Het
Zfp764	A	G	7: 127,406,247 (GRCm38)	W73R	probably damaging	Het
Zmym4	A	T	4: 126,925,839 (GRCm38)	D90E	probably damaging	Het

Other mutations in Tmc2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00465:Tmc2	APN	2	130,261,304 (GRCm38)	missense	possibly damaging	0.94
IGL00966:Tmc2	APN	2	130,264,012 (GRCm38)	missense	probably benign	0.02
IGL01094:Tmc2	APN	2	130,260,166 (GRCm38)	splice site	probably benign
IGL01331:Tmc2	APN	2	130,232,356 (GRCm38)	missense	probably damaging	1.00
IGL01660:Tmc2	APN	2	130,260,224 (GRCm38)	nonsense	probably null
IGL01926:Tmc2	APN	2	130,260,240 (GRCm38)	missense	possibly damaging	0.68
IGL02150:Tmc2	APN	2	130,240,153 (GRCm38)	missense	probably damaging	0.98
IGL02273:Tmc2	APN	2	130,229,206 (GRCm38)	missense	probably damaging	0.99
IGL03137:Tmc2	APN	2	130,240,130 (GRCm38)	missense	probably damaging	1.00
IGL03179:Tmc2	APN	2	130,229,187 (GRCm38)	missense	probably damaging	1.00
FR4449:Tmc2	UTSW	2	130,240,196 (GRCm38)	missense	probably damaging	1.00
H8786:Tmc2	UTSW	2	130,226,262 (GRCm38)	missense	probably damaging	1.00
PIT4418001:Tmc2	UTSW	2	130,248,651 (GRCm38)	missense	probably damaging	0.96
R0364:Tmc2	UTSW	2	130,202,103 (GRCm38)	missense	probably benign	0.00
R1446:Tmc2	UTSW	2	130,248,730 (GRCm38)	missense	probably damaging	0.97
R1458:Tmc2	UTSW	2	130,248,762 (GRCm38)	missense	probably damaging	1.00
R1589:Tmc2	UTSW	2	130,247,960 (GRCm38)	missense	probably damaging	0.99
R1656:Tmc2	UTSW	2	130,247,934 (GRCm38)	missense	possibly damaging	0.93
R1686:Tmc2	UTSW	2	130,256,116 (GRCm38)	missense	possibly damaging	0.71
R1765:Tmc2	UTSW	2	130,260,225 (GRCm38)	missense	probably benign	0.34
R1776:Tmc2	UTSW	2	130,234,869 (GRCm38)	missense	probably damaging	1.00
R1873:Tmc2	UTSW	2	130,248,756 (GRCm38)	missense	possibly damaging	0.68
R1972:Tmc2	UTSW	2	130,214,664 (GRCm38)	splice site	probably benign
R2020:Tmc2	UTSW	2	130,232,385 (GRCm38)	missense	probably damaging	1.00
R2208:Tmc2	UTSW	2	130,214,563 (GRCm38)	splice site	probably null
R3968:Tmc2	UTSW	2	130,202,071 (GRCm38)	missense	probably benign	0.02
R4732:Tmc2	UTSW	2	130,261,397 (GRCm38)	splice site	probably null
R4733:Tmc2	UTSW	2	130,261,397 (GRCm38)	splice site	probably null
R4989:Tmc2	UTSW	2	130,202,041 (GRCm38)	missense	possibly damaging	0.88
R5143:Tmc2	UTSW	2	130,234,818 (GRCm38)	missense	probably damaging	0.98
R5411:Tmc2	UTSW	2	130,240,115 (GRCm38)	missense	probably damaging	1.00
R5514:Tmc2	UTSW	2	130,241,644 (GRCm38)	missense	possibly damaging	0.94
R5690:Tmc2	UTSW	2	130,232,386 (GRCm38)	missense	probably damaging	1.00
R5983:Tmc2	UTSW	2	130,247,976 (GRCm38)	missense	probably damaging	1.00
R6451:Tmc2	UTSW	2	130,264,203 (GRCm38)	missense	probably damaging	0.99
R6927:Tmc2	UTSW	2	130,261,380 (GRCm38)	missense	probably benign
R7132:Tmc2	UTSW	2	130,232,409 (GRCm38)	missense	possibly damaging	0.82
R7240:Tmc2	UTSW	2	130,234,804 (GRCm38)	missense	possibly damaging	0.80
R7353:Tmc2	UTSW	2	130,196,577 (GRCm38)	critical splice donor site	probably null
R8167:Tmc2	UTSW	2	130,241,568 (GRCm38)	missense	probably benign	0.04
R8554:Tmc2	UTSW	2	130,264,164 (GRCm38)	missense	probably benign	0.00
R9134:Tmc2	UTSW	2	130,232,401 (GRCm38)	missense	probably benign	0.21
R9169:Tmc2	UTSW	2	130,241,596 (GRCm38)	missense	probably damaging	1.00
R9209:Tmc2	UTSW	2	130,261,397 (GRCm38)	splice site	probably null
R9232:Tmc2	UTSW	2	130,243,129 (GRCm38)	missense	probably damaging	1.00
R9725:Tmc2	UTSW	2	130,247,961 (GRCm38)	missense	probably damaging	0.99
X0019:Tmc2	UTSW	2	130,208,285 (GRCm38)	missense	possibly damaging	0.59
X0052:Tmc2	UTSW	2	130,201,972 (GRCm38)	missense	probably benign	0.00
Z1177:Tmc2	UTSW	2	130,208,296 (GRCm38)	missense	possibly damaging	0.56

Predicted Primers

PCR Primer
(F):5'- GTTGTCTTGACTTGACAGGCTCCAG -3'
(R):5'- TCCTATCGGCAGATCACATGGTCTC -3'

Sequencing Primer
(F):5'- CCCTCATATGCCGAGTTTGA -3'
(R):5'- ccttccttccctctcactttc -3'

Posted On

2014-01-15