Mutagenetix > Incidental Mutations

Incidental Mutation 'R0112:Tmem131l'

20492

Institutional Source

Beutler Lab

Gene Symbol

Tmem131l

Ensembl Gene

ENSMUSG00000033767

Gene Name

transmembrane 131 like

Synonyms

D930015E06Rik

MMRRC Submission

038398-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.109) question?

Stock #

R0112 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

83897655-84040175 bp(-) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 83940587 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 324 (Q324*)

Ref Sequence

ENSEMBL: ENSMUSP00000141607 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052342] [ENSMUST00000191758] [ENSMUST00000192095]

AlphaFold

Q3U3D7

Predicted Effect

probably null
Transcript: ENSMUST00000052342
AA Change: Q324*

SMART Domains

Protein: ENSMUSP00000049808
Gene: ENSMUSG00000033767
AA Change: Q324*

Domain	Start	End	E-Value	Type
signal peptide	1	40	N/A	INTRINSIC
Pfam:TMEM131_like	91	174	5.8e-20	PFAM
low complexity region	464	477	N/A	INTRINSIC
low complexity region	612	630	N/A	INTRINSIC
low complexity region	904	917	N/A	INTRINSIC
low complexity region	990	997	N/A	INTRINSIC
low complexity region	1221	1239	N/A	INTRINSIC
low complexity region	1291	1324	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000191758
AA Change: Q324*

SMART Domains

Protein: ENSMUSP00000141438
Gene: ENSMUSG00000033767
AA Change: Q324*

Domain	Start	End	E-Value	Type
signal peptide	1	40	N/A	INTRINSIC
Pfam:DUF3651	155	228	9.2e-10	PFAM
Pfam:DUF3651	285	362	1.5e-9	PFAM
low complexity region	464	477	N/A	INTRINSIC
low complexity region	612	630	N/A	INTRINSIC
low complexity region	904	917	N/A	INTRINSIC
low complexity region	990	997	N/A	INTRINSIC
low complexity region	1221	1239	N/A	INTRINSIC
low complexity region	1291	1324	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000192095
AA Change: Q324*

SMART Domains

Protein: ENSMUSP00000141607
Gene: ENSMUSG00000033767
AA Change: Q324*

Domain	Start	End	E-Value	Type
signal peptide	1	40	N/A	INTRINSIC
Pfam:DUF3651	155	228	8.8e-10	PFAM
Pfam:DUF3651	285	362	1.4e-9	PFAM
low complexity region	464	477	N/A	INTRINSIC
low complexity region	612	630	N/A	INTRINSIC
low complexity region	904	917	N/A	INTRINSIC
low complexity region	989	996	N/A	INTRINSIC
low complexity region	1220	1238	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194432

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194522

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 96.0%
20x: 91.8%

Validation Efficiency

100% (86/86)

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930568D16Rik	T	A	2: 35,354,803	Y179F	probably benign	Het
Abcd4	A	G	12: 84,612,899		probably benign	Het
Abhd12b	C	T	12: 70,181,017	T191M	probably benign	Het
Adcy5	A	G	16: 35,156,178	E27G	possibly damaging	Het
Adgb	G	A	10: 10,407,158		probably benign	Het
Afdn	T	C	17: 13,884,637	S1186P	probably damaging	Het
Atf6b	G	T	17: 34,651,626	R351L	probably damaging	Het
Axin2	T	C	11: 108,939,397	S348P	possibly damaging	Het
BC030499	T	C	11: 78,291,681		probably benign	Het
Bfsp1	A	C	2: 143,827,643		probably null	Het
Brd1	A	G	15: 88,730,383	V103A	probably benign	Het
Ccdc13	C	A	9: 121,813,481	K392N	probably damaging	Het
Ccdc18	A	G	5: 108,173,761	K577R	probably damaging	Het
Csmd2	G	T	4: 128,496,029	G2186C	probably damaging	Het
Cyp2j5	A	T	4: 96,629,523	M484K	probably benign	Het
Defb3	T	A	8: 19,293,407	L12Q	probably null	Het
Defb7	G	T	8: 19,495,170		probably null	Het
Dhx35	T	A	2: 158,840,620	M491K	probably damaging	Het
Dnah17	T	C	11: 118,074,434	S2261G	possibly damaging	Het
Dnah5	A	C	15: 28,263,679	E853D	probably benign	Het
Dner	C	A	1: 84,583,053	A23S	probably benign	Het
Dock5	A	C	14: 67,819,641	S539A	probably benign	Het
Dsg2	T	A	18: 20,583,042	F317I	probably benign	Het
Enox1	A	T	14: 77,699,198	I539F	possibly damaging	Het
Eogt	G	A	6: 97,135,284		probably benign	Het
Fbxo22	A	G	9: 55,223,346	T300A	probably benign	Het
Fes	T	C	7: 80,384,005	D166G	probably damaging	Het
Fn1	A	G	1: 71,609,653	S1366P	probably damaging	Het
Fndc3a	A	T	14: 72,540,495		probably benign	Het
Foxh1	T	C	15: 76,669,010	H168R	probably benign	Het
Galnt14	T	G	17: 73,574,984		probably benign	Het
Gdf6	A	G	4: 9,844,482	D2G	probably damaging	Het
Gp6	C	A	7: 4,370,184	A247S	probably benign	Het
Gp6	G	C	7: 4,371,627	P232A	probably benign	Het
Grin2c	A	G	11: 115,251,134	Y820H	probably damaging	Het
Gtf2h4	T	C	17: 35,670,448	T198A	possibly damaging	Het
Helz	T	C	11: 107,672,948		probably benign	Het
Htr1d	A	G	4: 136,443,000	E180G	probably benign	Het
Igsf10	A	G	3: 59,326,008	V1768A	probably benign	Het
Ints10	A	T	8: 68,827,302	T694S	probably damaging	Het
Krt81	C	A	15: 101,463,627	R24L	possibly damaging	Het
Lipc	T	A	9: 70,820,427	Y131F	probably damaging	Het
Litaf	G	T	16: 10,966,511	T45K	probably damaging	Het
Lmo7	A	T	14: 101,887,193	R363*	probably null	Het
Lrrc37a	A	T	11: 103,500,913	Y1229N	probably benign	Het
Man2a2	C	T	7: 80,358,276	A943T	probably damaging	Het
Mtor	A	G	4: 148,480,923	Y1030C	probably damaging	Het
Naalad2	G	T	9: 18,351,447	Y384*	probably null	Het
Nat2	C	T	8: 67,501,726	Q163*	probably null	Het
Nell2	A	G	15: 95,431,681		probably benign	Het
Nphp3	C	T	9: 104,037,348	H102Y	possibly damaging	Het
Olfr1383	A	T	11: 49,524,134	H137L	possibly damaging	Het
Olfr1442	C	T	19: 12,674,757	T184I	probably benign	Het
Olfr686	A	T	7: 105,203,659	M228K	probably benign	Het
Olr1	T	C	6: 129,488,906	S46G	possibly damaging	Het
Parg	C	A	14: 32,202,433	A63E	probably damaging	Het
Pik3cg	A	G	12: 32,195,715		probably benign	Het
Ripk4	A	G	16: 97,743,561	C629R	probably benign	Het
Rnf145	A	G	11: 44,564,151	T620A	probably benign	Het
Samd9l	T	G	6: 3,376,031	D410A	possibly damaging	Het
Serpinb9f	A	T	13: 33,327,951		probably benign	Het
Slc19a1	T	C	10: 77,042,165	I178T	probably benign	Het
Slco1b2	A	T	6: 141,671,111	Y390F	probably benign	Het
Speg	A	G	1: 75,385,032	E230G	possibly damaging	Het
Tbc1d9	C	A	8: 83,264,837		probably benign	Het
Trf	A	G	9: 103,226,956		probably benign	Het
Trp53	T	G	11: 69,588,679	Y202D	probably damaging	Het
Trpv1	T	A	11: 73,253,272	M618K	probably damaging	Het
Trrap	C	A	5: 144,822,761	Y2250*	probably null	Het
Ttc3	A	G	16: 94,385,322		probably benign	Het
Ubtfl1	T	G	9: 18,409,787	S204A	probably benign	Het
Uck2	A	T	1: 167,227,771	Y203N	probably damaging	Het
Utrn	A	T	10: 12,686,465	L1280*	probably null	Het
Vmn1r178	A	T	7: 23,894,184	H146L	possibly damaging	Het
Vmn2r100	C	A	17: 19,522,120	P252Q	possibly damaging	Het
Vmn2r108	T	C	17: 20,471,635	M209V	probably benign	Het
Vmn2r9	G	A	5: 108,843,125	T790I	probably damaging	Het
Vmn2r94	C	A	17: 18,243,604	R808L	probably benign	Het
Zbtb7c	A	T	18: 76,136,891	S17C	probably damaging	Het
Zfp811	C	T	17: 32,797,764	R434Q	probably damaging	Het
Zkscan6	A	T	11: 65,814,863		probably benign	Het

Other mutations in Tmem131l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00229:Tmem131l	APN	3	83942500	missense	probably damaging	0.99
IGL00777:Tmem131l	APN	3	83899290	missense	probably damaging	1.00
IGL01400:Tmem131l	APN	3	83922122	missense	probably damaging	0.99
IGL01642:Tmem131l	APN	3	83938050	missense	possibly damaging	0.63
IGL01796:Tmem131l	APN	3	83938055	nonsense	probably null
IGL02055:Tmem131l	APN	3	83910366	splice site	probably null
IGL02269:Tmem131l	APN	3	83938050	missense	possibly damaging	0.63
IGL02806:Tmem131l	APN	3	83928816	splice site	probably benign
IGL03308:Tmem131l	APN	3	83940902	missense	probably benign	0.00
IGL03345:Tmem131l	APN	3	83961589	missense	probably damaging	1.00
R0106:Tmem131l	UTSW	3	83934815	splice site	probably benign
R0212:Tmem131l	UTSW	3	83913268	missense	probably benign	0.19
R0328:Tmem131l	UTSW	3	83921931	splice site	probably benign
R0412:Tmem131l	UTSW	3	84031648	missense	probably damaging	1.00
R0544:Tmem131l	UTSW	3	83898546	missense	probably damaging	1.00
R0676:Tmem131l	UTSW	3	83934815	splice site	probably benign
R0815:Tmem131l	UTSW	3	83940572	missense	probably benign	0.01
R0826:Tmem131l	UTSW	3	83898417	missense	probably damaging	1.00
R1432:Tmem131l	UTSW	3	83928714	missense	probably damaging	1.00
R1582:Tmem131l	UTSW	3	83931783	missense	probably damaging	0.99
R1591:Tmem131l	UTSW	3	83940889	critical splice donor site	probably null
R1804:Tmem131l	UTSW	3	83910479	missense	possibly damaging	0.72
R1875:Tmem131l	UTSW	3	83905076	nonsense	probably null
R1955:Tmem131l	UTSW	3	83961544	missense	probably damaging	1.00
R2049:Tmem131l	UTSW	3	83942788	missense	probably damaging	1.00
R2125:Tmem131l	UTSW	3	83942751	critical splice donor site	probably null
R2173:Tmem131l	UTSW	3	83926145	missense	probably damaging	1.00
R2321:Tmem131l	UTSW	3	83936023	missense	probably damaging	0.98
R2407:Tmem131l	UTSW	3	83922048	missense	probably benign	0.25
R2917:Tmem131l	UTSW	3	83937580	nonsense	probably null
R3082:Tmem131l	UTSW	3	83909150	critical splice donor site	probably null
R3086:Tmem131l	UTSW	3	83931739	missense	probably benign	0.00
R3773:Tmem131l	UTSW	3	83898586	missense	probably damaging	1.00
R3921:Tmem131l	UTSW	3	83940601	missense	possibly damaging	0.68
R3953:Tmem131l	UTSW	3	83910419	missense	probably damaging	1.00
R3954:Tmem131l	UTSW	3	83910419	missense	probably damaging	1.00
R3956:Tmem131l	UTSW	3	83910419	missense	probably damaging	1.00
R4118:Tmem131l	UTSW	3	83960767	missense	probably benign	0.00
R4700:Tmem131l	UTSW	3	83899212	missense	probably benign
R4862:Tmem131l	UTSW	3	83898210	splice site	probably benign
R4941:Tmem131l	UTSW	3	83899239	missense	probably benign	0.03
R5101:Tmem131l	UTSW	3	83937504	missense	probably damaging	0.96
R5290:Tmem131l	UTSW	3	83899265	missense	probably benign	0.30
R5501:Tmem131l	UTSW	3	83926128	missense	probably damaging	1.00
R5813:Tmem131l	UTSW	3	83940572	missense	probably benign	0.01
R5845:Tmem131l	UTSW	3	83940553	missense	probably damaging	0.99
R5973:Tmem131l	UTSW	3	83922246	missense	possibly damaging	0.95
R6119:Tmem131l	UTSW	3	83898382	missense	probably damaging	1.00
R6241:Tmem131l	UTSW	3	83922164	missense	probably benign	0.06
R6278:Tmem131l	UTSW	3	83942491	missense	possibly damaging	0.93
R6490:Tmem131l	UTSW	3	83913280	missense	possibly damaging	0.67
R6502:Tmem131l	UTSW	3	83922408	missense	probably damaging	1.00
R6503:Tmem131l	UTSW	3	83940944	missense	probably benign	0.26
R6868:Tmem131l	UTSW	3	83961631	missense	probably damaging	0.99
R7104:Tmem131l	UTSW	3	83919459	missense	possibly damaging	0.68
R7736:Tmem131l	UTSW	3	83940568	missense	probably damaging	0.97
R7885:Tmem131l	UTSW	3	83910417	missense	possibly damaging	0.89
R8085:Tmem131l	UTSW	3	83927131	missense	possibly damaging	0.81
R8478:Tmem131l	UTSW	3	83898462	missense	probably damaging	0.99
R8677:Tmem131l	UTSW	3	83928702	missense	probably damaging	1.00
R8942:Tmem131l	UTSW	3	83898486	missense	possibly damaging	0.66
R8943:Tmem131l	UTSW	3	83924172	missense	probably damaging	1.00
R8973:Tmem131l	UTSW	3	83928732	missense	probably damaging	1.00
R9068:Tmem131l	UTSW	3	83910468	missense	probably benign	0.05
R9096:Tmem131l	UTSW	3	83942815	missense	probably damaging	1.00
R9097:Tmem131l	UTSW	3	83942815	missense	probably damaging	1.00
R9143:Tmem131l	UTSW	3	83934913	missense	probably benign	0.14
R9273:Tmem131l	UTSW	3	83940937	missense	probably damaging	1.00
R9325:Tmem131l	UTSW	3	83910461	missense	probably benign	0.00
R9400:Tmem131l	UTSW	3	83922986	missense	possibly damaging	0.68
R9433:Tmem131l	UTSW	3	83938152	missense	probably benign	0.14
Z1177:Tmem131l	UTSW	3	84040093	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGGAGGCATCCACAGCCACTTTAG -3'
(R):5'- TTTGTGTGAAGACTGTCAGCGCCC -3'

Sequencing Primer
(F):5'- CCAATGGCTTTGGTTTACAGGAAC -3'
(R):5'- AGCGCCCCTTTCTGCTG -3'

Posted On

2013-04-11