Mutagenetix > Incidental Mutation

Incidental Mutation 'R4728:Tmem181a'

358639

Institutional Source

Beutler Lab

Gene Symbol

Tmem181a

Ensembl Gene

ENSMUSG00000038141

Gene Name

transmembrane protein 181A

Synonyms

5930418K15Rik, C76977, Gpr178, Tmem181

MMRRC Submission

042020-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4728 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

6307135-6358589 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 6340874 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 141 (D141G)

Ref Sequence

ENSEMBL: ENSMUSP00000156382 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000088940] [ENSMUST00000232383]

AlphaFold

A0A338P7C9

Predicted Effect

probably benign
Transcript: ENSMUST00000088940
AA Change: D100G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000086333
Gene: ENSMUSG00000038141
AA Change: D100G

Domain	Start	End	E-Value	Type
transmembrane domain	17	36	N/A	INTRINSIC
Pfam:MIG-14_Wnt-bd	127	422	1e-100	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000228334

Predicted Effect

probably benign
Transcript: ENSMUST00000232383
AA Change: D141G

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)

Meta Mutation Damage Score

0.2377

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.3%

Validation Efficiency

94% (73/78)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The TMEM181 gene encodes a putative G protein-coupled receptor expressed on the cell surface (Carette et al., 2009 [PubMed 19965467]; Wollscheid et al., 2009 [PubMed 19349973]).[supplied by OMIM, Jan 2010]

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Bicc1	C	T	10: 70,771,661 (GRCm39)		probably null	Het
Bpifc	T	A	10: 85,827,063 (GRCm39)	H162L	possibly damaging	Het
Ccdc163	C	T	4: 116,566,209 (GRCm39)		probably benign	Het
Cldn12	A	G	5: 5,558,385 (GRCm39)	F14S	probably damaging	Het
Cyth4	G	A	15: 78,486,913 (GRCm39)	G14R	probably benign	Het
Ddhd2	C	T	8: 26,242,294 (GRCm39)	V194I	probably damaging	Het
Ddx23	A	T	15: 98,548,106 (GRCm39)	V433E	probably damaging	Het
Defb34	A	G	8: 19,176,434 (GRCm39)	N42D	possibly damaging	Het
Dennd6a	A	G	14: 26,348,575 (GRCm39)	E313G	probably null	Het
Dhx30	A	G	9: 109,916,718 (GRCm39)	F570S	probably damaging	Het
Dnah3	T	C	7: 119,658,589 (GRCm39)	E864G	probably damaging	Het
Eps8	G	A	6: 137,486,160 (GRCm39)	Q451*	probably null	Het
Fmo9	A	T	1: 166,490,880 (GRCm39)	Y533N	possibly damaging	Het
Fut8	T	A	12: 77,521,973 (GRCm39)	D537E	probably damaging	Het
Gm5407	T	C	16: 49,117,283 (GRCm39)		noncoding transcript	Het
Gm9916	A	G	3: 118,228,690 (GRCm39)		noncoding transcript	Het
Grm5	T	A	7: 87,624,496 (GRCm39)	F354L	probably damaging	Het
Hira	C	T	16: 18,741,654 (GRCm39)	A353V	probably damaging	Het
Ifna4	C	A	4: 88,760,519 (GRCm39)	T141K	probably benign	Het
Igf1r	T	C	7: 67,839,372 (GRCm39)	L628P	probably damaging	Het
Kcnh5	A	T	12: 75,054,555 (GRCm39)	I463N	probably damaging	Het
Kcnh8	C	A	17: 53,032,898 (GRCm39)	Q62K	probably damaging	Het
Kif3c	A	T	12: 3,415,873 (GRCm39)		probably benign	Het
Kmo	A	G	1: 175,484,329 (GRCm39)	D353G	possibly damaging	Het
Lrp1	T	C	10: 127,399,606 (GRCm39)	T2301A	probably damaging	Het
Lrrc7	GAAGTTGTTTGGAGATTCTTATCTTA	GA	3: 158,024,045 (GRCm39)		probably benign	Het
Map3k9	C	T	12: 81,769,147 (GRCm39)	R967Q	probably damaging	Het
Mcm8	A	G	2: 132,674,774 (GRCm39)	H414R	probably damaging	Het
Mier1	A	G	4: 102,997,402 (GRCm39)	E145G	probably damaging	Het
Mlc1	A	T	15: 88,862,234 (GRCm39)		probably null	Het
Napb	T	C	2: 148,551,245 (GRCm39)	D96G	probably damaging	Het
Nbas	T	A	12: 13,338,740 (GRCm39)	S193R	probably damaging	Het
Nlrp4a	T	C	7: 26,174,515 (GRCm39)	V967A	probably benign	Het
Nlrp4e	T	A	7: 23,020,989 (GRCm39)	I492K	probably benign	Het
Notch4	A	G	17: 34,789,179 (GRCm39)	T497A	probably benign	Het
Npdc1	G	A	2: 25,298,957 (GRCm39)	D284N	probably damaging	Het
Ogdh	T	A	11: 6,292,549 (GRCm39)	Y417N	probably damaging	Het
Or5w19	T	C	2: 87,698,779 (GRCm39)	V148A	probably benign	Het
Ovol1	A	T	19: 5,603,690 (GRCm39)	Y70*	probably null	Het
P2ry1	A	G	3: 60,911,641 (GRCm39)	Y260C	probably damaging	Het
Pcx	G	T	19: 4,653,124 (GRCm39)	R263L	probably damaging	Het
Pla2g4f	T	A	2: 120,131,402 (GRCm39)	T774S	probably benign	Het
Prdm15	T	G	16: 97,622,986 (GRCm39)	K289Q	probably benign	Het
Prl7c1	A	T	13: 27,960,268 (GRCm39)	H91Q	probably benign	Het
Prmt5	C	T	14: 54,745,364 (GRCm39)	R601H	probably benign	Het
Prrc2b	T	A	2: 32,120,637 (GRCm39)	D2192E	probably damaging	Het
Ptdss2	A	G	7: 140,734,372 (GRCm39)	I299V	probably benign	Het
Rbm28	A	G	6: 29,143,591 (GRCm39)	V354A	probably damaging	Het
Rps6kb1	G	C	11: 86,435,484 (GRCm39)		probably null	Het
Sema3f	A	G	9: 107,582,639 (GRCm39)	S35P	probably benign	Het
Serpina3n	A	T	12: 104,375,422 (GRCm39)	T165S	probably benign	Het
Serpinb13	C	T	1: 106,910,574 (GRCm39)	S66L	probably damaging	Het
Sh2d4b	T	A	14: 40,564,389 (GRCm39)	R267*	probably null	Het
Slc5a12	A	T	2: 110,474,769 (GRCm39)	K554*	probably null	Het
Snrnp200	T	C	2: 127,059,334 (GRCm39)	L409P	probably damaging	Het
Snrnp200	T	A	2: 127,069,798 (GRCm39)	V981E	possibly damaging	Het
Spon2	T	A	5: 33,374,682 (GRCm39)	R41S	probably benign	Het
Sptb	A	T	12: 76,630,153 (GRCm39)	M2279K	probably benign	Het
Srcap	T	G	7: 127,140,096 (GRCm39)		probably null	Het
Tctn3	A	G	19: 40,594,186 (GRCm39)	V409A	probably damaging	Het
Tg	A	C	15: 66,554,676 (GRCm39)	Q697P	probably damaging	Het
Tmem82	A	G	4: 141,341,963 (GRCm39)	S334P	probably benign	Het
Ubr4	A	G	4: 139,151,190 (GRCm39)	Y1875C	probably damaging	Het
Vmn1r63	C	A	7: 5,806,362 (GRCm39)	R90L	probably damaging	Het
Zfp330	A	C	8: 83,497,475 (GRCm39)	Y56D	probably damaging	Het

Other mutations in Tmem181a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02071:Tmem181a	APN	17	6,347,531 (GRCm39)	missense	probably damaging	1.00
IGL03027:Tmem181a	APN	17	6,348,494 (GRCm39)	missense	probably damaging	1.00
a_team	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
abraham	UTSW	17	6,340,874 (GRCm39)	missense	probably benign	0.03
PIT4651001:Tmem181a	UTSW	17	6,351,170 (GRCm39)	missense	probably benign
R1966:Tmem181a	UTSW	17	6,353,501 (GRCm39)	missense	probably benign
R2139:Tmem181a	UTSW	17	6,348,481 (GRCm39)	missense	probably damaging	1.00
R2323:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R2324:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3001:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3002:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3003:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3034:Tmem181a	UTSW	17	6,330,901 (GRCm39)	missense	possibly damaging	0.50
R3425:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3426:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3427:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3428:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3499:Tmem181a	UTSW	17	6,330,894 (GRCm39)	nonsense	probably null
R3683:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R3893:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4226:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4227:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4428:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4429:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4430:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4465:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4466:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4467:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4496:Tmem181a	UTSW	17	6,346,061 (GRCm39)	missense	probably damaging	0.99
R4822:Tmem181a	UTSW	17	6,330,940 (GRCm39)	missense	probably benign	0.00
R5301:Tmem181a	UTSW	17	6,346,070 (GRCm39)	missense	possibly damaging	0.52
R5991:Tmem181a	UTSW	17	6,339,312 (GRCm39)	missense	probably damaging	1.00
R6052:Tmem181a	UTSW	17	6,330,890 (GRCm39)	missense	probably damaging	1.00
R6222:Tmem181a	UTSW	17	6,351,192 (GRCm39)	missense	probably benign	0.29
R7131:Tmem181a	UTSW	17	6,348,247 (GRCm39)	missense	probably damaging	0.98
R7231:Tmem181a	UTSW	17	6,348,195 (GRCm39)	missense	possibly damaging	0.81
R7374:Tmem181a	UTSW	17	6,354,533 (GRCm39)	missense	possibly damaging	0.85
R7437:Tmem181a	UTSW	17	6,353,540 (GRCm39)	missense	possibly damaging	0.70
R7592:Tmem181a	UTSW	17	6,339,295 (GRCm39)	missense	probably benign	0.00
R8175:Tmem181a	UTSW	17	6,346,075 (GRCm39)	missense	probably benign	0.00
R8327:Tmem181a	UTSW	17	6,351,680 (GRCm39)	missense	probably damaging	1.00
R8385:Tmem181a	UTSW	17	6,339,274 (GRCm39)	missense	probably benign	0.10
R9144:Tmem181a	UTSW	17	6,346,048 (GRCm39)	missense	possibly damaging	0.94
R9221:Tmem181a	UTSW	17	6,307,265 (GRCm39)	missense	probably damaging	0.99
R9327:Tmem181a	UTSW	17	6,346,048 (GRCm39)	missense	possibly damaging	0.94
RF010:Tmem181a	UTSW	17	6,330,978 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TGCAGGTTTGACATAGCACAGG -3'
(R):5'- ATGAATGCGAGCCAAGTGTG -3'

Sequencing Primer
(F):5'- GGAGGTAGCAGAGCCTTCTCAG -3'
(R):5'- CCAAGTGTGTGTGCAAATTGC -3'

Posted On

2015-11-11