Mutagenetix > Incidental Mutation

Incidental Mutation 'R2422:Tmem102'

249384

Institutional Source

Beutler Lab

Gene Symbol

Tmem102

Ensembl Gene

ENSMUSG00000089876

Gene Name

transmembrane protein 102

Synonyms

Tmem102-ps, Cbap

MMRRC Submission

040384-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.118) question?

Stock #

R2422 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

69803603-69805624 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 69804537 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Valine at position 203 (E203V)

Ref Sequence

ENSEMBL: ENSMUSP00000132164 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000011285] [ENSMUST00000051025] [ENSMUST00000102585]

AlphaFold

Q3UPR7

Predicted Effect

probably benign
Transcript: ENSMUST00000011285

SMART Domains

Protein: ENSMUSP00000011285
Gene: ENSMUSG00000042826

Domain	Start	End	E-Value	Type
FGF	69	172	6.95e-35	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000051025
AA Change: E203V

PolyPhen 2 Score 0.018 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000132164
Gene: ENSMUSG00000089876
AA Change: E203V

Domain	Start	End	E-Value	Type
low complexity region	6	20	N/A	INTRINSIC
low complexity region	33	44	N/A	INTRINSIC
Mab-21	191	494	3.31e-43	SMART
low complexity region	498	507	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000102585

SMART Domains

Protein: ENSMUSP00000099645
Gene: ENSMUSG00000042826

Domain	Start	End	E-Value	Type
FGF	69	200	3.43e-66	SMART

Meta Mutation Damage Score

0.0707

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.1%
20x: 94.5%

Validation Efficiency

99% (77/78)

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010300C02Rik	C	A	1: 37,613,475	V1084L	probably benign	Het
4933409G03Rik	A	T	2: 68,591,520	N47I	probably benign	Het
Actr5	T	C	2: 158,636,081	F457S	probably damaging	Het
Adamts3	A	G	5: 89,683,175	S1007P	probably damaging	Het
Adck2	C	T	6: 39,583,998	A440V	possibly damaging	Het
Birc6	T	A	17: 74,660,614	L301Q	probably damaging	Het
Ccdc18	A	C	5: 108,228,588	E1298D	probably damaging	Het
Ccdc77	A	G	6: 120,339,159	C186R	probably benign	Het
Cdk12	T	G	11: 98,219,074	S640R	probably benign	Het
Cdv3	T	C	9: 103,365,118		probably benign	Het
Celf2	G	A	2: 6,553,889	T364I	probably damaging	Het
Cmtr2	C	A	8: 110,222,781	S574R	probably benign	Het
Col14a1	T	C	15: 55,449,922	L56P	unknown	Het
Dctn1	C	T	6: 83,199,800	L1241F	possibly damaging	Het
Depdc5	T	C	5: 32,991,035	F1505S	probably damaging	Het
Dhcr24	G	T	4: 106,561,094		probably benign	Het
Dnajc21	A	G	15: 10,461,935	S127P	probably benign	Het
Entpd7	A	T	19: 43,728,088	Y507F	possibly damaging	Het
Fbp1	T	C	13: 62,871,306	K24E	probably benign	Het
Galr1	A	T	18: 82,405,923	N76K	probably damaging	Het
Glrb	A	G	3: 80,860,235	I226T	probably damaging	Het
Gm17421	T	A	12: 113,369,487		noncoding transcript	Het
Gm4950	T	A	18: 51,865,784	Q33L	probably benign	Het
Gm5415	C	T	1: 32,545,861	A323T	possibly damaging	Het
Gm6583	A	T	5: 112,355,118	V240D	probably damaging	Het
Gnat2	A	T	3: 108,095,539	M88L	probably damaging	Het
Gpr183	A	G	14: 121,954,177	Y311H	probably damaging	Het
H2-M10.5	A	G	17: 36,774,999	I308V	probably benign	Het
Hipk3	C	T	2: 104,471,485	G121R	probably benign	Het
Hjurp	A	G	1: 88,266,561		probably benign	Het
Homez	C	A	14: 54,857,574	V226F	probably benign	Het
Inf2	C	A	12: 112,610,824	A1034D	unknown	Het
Kcnc4	G	T	3: 107,445,547	P572T	probably benign	Het
Kmt2d	T	C	15: 98,862,266	E1037G	unknown	Het
Krt78	T	C	15: 101,947,264	E704G	probably damaging	Het
Lama1	A	T	17: 67,750,553	M541L	probably benign	Het
Lmbrd2	C	T	15: 9,194,765	T618M	possibly damaging	Het
Ly6g6e	G	A	17: 35,078,146	R121Q	probably benign	Het
Mettl22	T	C	16: 8,487,361	F293L	probably damaging	Het
Mib1	T	C	18: 10,751,906	S263P	probably damaging	Het
Ndufaf1	T	C	2: 119,655,737	E298G	probably damaging	Het
Nek1	T	C	8: 61,019,901	V152A	probably damaging	Het
Nlrp4d	T	A	7: 10,362,945	D876V	probably benign	Het
Olfr178	T	C	16: 58,889,965	E85G	probably benign	Het
Olfr235	A	T	19: 12,268,919	T230S	probably damaging	Het
Olfr740	T	C	14: 50,453,436	L128P	probably damaging	Het
Olfr975	A	G	9: 39,950,528	L81P	possibly damaging	Het
Pcdha11	G	T	18: 37,007,272	L651F	probably damaging	Het
Plekhg1	G	A	10: 3,958,048	M988I	probably benign	Het
Plxnb1	G	A	9: 109,108,438	R1169H	probably benign	Het
Ppp4r3a	A	G	12: 101,042,653		probably benign	Het
Pum2	A	T	12: 8,748,931	Q930L	possibly damaging	Het
Rbp4	T	C	19: 38,124,344	E67G	probably damaging	Het
Rgs9	C	A	11: 109,225,777		probably null	Het
Sipa1	A	T	19: 5,652,112	D923E	possibly damaging	Het
Smc1a	A	G	X: 152,047,975		probably benign	Het
Snx33	C	A	9: 56,918,538	M546I	probably benign	Het
Spag17	T	A	3: 100,027,619	W714R	probably benign	Het
Spata2	C	T	2: 167,484,206	R231Q	probably damaging	Het
Stard9	C	T	2: 120,700,284	R2341C	probably benign	Het
Tas2r116	A	T	6: 132,855,594	I53F	possibly damaging	Het
Tlk1	T	C	2: 70,770,005	E110G	probably damaging	Het
Top2b	T	G	14: 16,409,189	I777M	probably damaging	Het
Ttc23l	CT	CTTGGATT	15: 10,537,562		probably benign	Het
Ttc23l	G	A	15: 10,537,566	S206L	probably benign	Het
Tyw5	A	G	1: 57,396,748	I82T	possibly damaging	Het
Uba6	A	G	5: 86,132,616		probably null	Het
Ugcg	C	T	4: 59,207,798	P46S	probably benign	Het
Unc13c	T	C	9: 73,931,547	Y674C	probably damaging	Het
Vmn2r105	T	A	17: 20,227,835	R242S	probably benign	Het
Vmn2r12	A	G	5: 109,086,532	Y605H	probably benign	Het
Wdr77	A	T	3: 105,960,021	K62*	probably null	Het
Zfhx4	C	A	3: 5,390,405	A1153E	probably benign	Het
Zfp266	C	A	9: 20,499,262	V540L	possibly damaging	Het
Zfp638	C	A	6: 83,966,439		probably benign	Het
Zfp644	A	G	5: 106,637,244	M479T	possibly damaging	Het
Zfp951	G	A	5: 104,815,277	T141I	probably benign	Het

Other mutations in Tmem102

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02528:Tmem102	APN	11	69803706	splice site	probably null
R1109:Tmem102	UTSW	11	69804804	missense	probably damaging	1.00
R1396:Tmem102	UTSW	11	69804370	missense	probably damaging	1.00
R1958:Tmem102	UTSW	11	69804399	missense	probably benign	0.02
R2138:Tmem102	UTSW	11	69805114	missense	probably damaging	1.00
R4716:Tmem102	UTSW	11	69804196	missense	probably damaging	1.00
R4776:Tmem102	UTSW	11	69804802	missense	probably damaging	1.00
R5933:Tmem102	UTSW	11	69803680	missense	probably damaging	1.00
R6609:Tmem102	UTSW	11	69805114	missense	probably damaging	1.00
R7460:Tmem102	UTSW	11	69804123	missense	probably damaging	1.00
R7466:Tmem102	UTSW	11	69804885	missense	probably damaging	1.00
R7835:Tmem102	UTSW	11	69804345	missense	probably damaging	1.00
R8687:Tmem102	UTSW	11	69804615	missense	probably benign	0.00
R9381:Tmem102	UTSW	11	69804315	missense	probably benign	0.33
R9650:Tmem102	UTSW	11	69805043	missense	probably benign	0.16
Z1186:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1186:Tmem102	UTSW	11	69805101	missense	probably benign
Z1187:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1187:Tmem102	UTSW	11	69805101	missense	probably benign
Z1188:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1188:Tmem102	UTSW	11	69805101	missense	probably benign
Z1189:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1189:Tmem102	UTSW	11	69805101	missense	probably benign
Z1190:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1190:Tmem102	UTSW	11	69805101	missense	probably benign
Z1191:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1191:Tmem102	UTSW	11	69805101	missense	probably benign
Z1192:Tmem102	UTSW	11	69805076	missense	possibly damaging	0.48
Z1192:Tmem102	UTSW	11	69805101	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ACCAGGAAGTTACTTGGGTCG -3'
(R):5'- GATCTGGAATCCTGTTCTGCATG -3'

Sequencing Primer
(F):5'- GGCATAATGTGGGCCATGC -3'
(R):5'- GAATCCTGTTCTGCATGGCTCC -3'

Posted On

2014-11-12