Mutagenetix > Incidental Mutation

Incidental Mutation 'R0316:Gm19668'

34203

Institutional Source

Beutler Lab

Gene Symbol

Gm19668

Ensembl Gene

ENSMUSG00000096380

Gene Name

predicted gene, 19668

Synonyms

MMRRC Submission

038526-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.255) question?

Stock #

R0316 (G1)

Quality Score

132

Status

Not validated

Chromosome

Chromosomal Location

77634221-77634967 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to T at 77634564 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000151514 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092366] [ENSMUST00000172205] [ENSMUST00000178581]

AlphaFold

J3QMD1

Predicted Effect

probably benign
Transcript: ENSMUST00000092366

SMART Domains

Protein: ENSMUSP00000090020
Gene: ENSMUSG00000069581

Domain	Start	End	E-Value	Type
Blast:TSPN	1	71	8e-40	BLAST
SCOP:d1c4ra_	2	67	2e-7	SMART
low complexity region	190	200	N/A	INTRINSIC
Pfam:EPTP	208	255	2.6e-22	PFAM
Pfam:EPTP	260	307	1.4e-21	PFAM
Pfam:EPTP	312	359	8.9e-14	PFAM
Pfam:EPTP	362	417	6.2e-13	PFAM
Pfam:EPTP	422	469	1.3e-20	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000172205

SMART Domains

Protein: ENSMUSP00000128285
Gene: ENSMUSG00000096131

Domain	Start	End	E-Value	Type
Pfam:Keratin_B2_2	8	57	1.6e-9	PFAM
Pfam:Keratin_B2_2	48	100	5.2e-6	PFAM
Pfam:Keratin_B2_2	97	138	1.1e-7	PFAM
Pfam:Keratin_B2_2	133	178	2e-6	PFAM
Pfam:Keratin_B2_2	170	210	4.3e-4	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000172205

Predicted Effect

unknown
Transcript: ENSMUST00000178581
AA Change: I135N

SMART Domains

Protein: ENSMUSP00000136230
Gene: ENSMUSG00000096380
AA Change: I135N

Domain	Start	End	E-Value	Type
Pfam:PMG	2	116	7.5e-11	PFAM
Pfam:Keratin_B2_2	135	179	8.2e-8	PFAM
Pfam:Keratin_B2_2	170	216	7.3e-4	PFAM

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.5%
20x: 96.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9130401M01Rik	A	T	15: 57,888,765 (GRCm39)	F276I	probably damaging	Het
Ado	A	G	10: 67,384,548 (GRCm39)	L19P	possibly damaging	Het
Ago2	T	C	15: 73,002,725 (GRCm39)	H169R	probably damaging	Het
Asic1	G	A	15: 99,569,819 (GRCm39)	A47T	probably benign	Het
Atg16l2	A	T	7: 100,942,603 (GRCm39)	I364N	probably damaging	Het
C130050O18Rik	G	A	5: 139,400,313 (GRCm39)	R122Q	probably damaging	Het
Capn7	T	A	14: 31,069,766 (GRCm39)	C197S	probably benign	Het
Casp16	T	C	17: 23,771,066 (GRCm39)	D113G	probably damaging	Het
Cdh18	T	A	15: 23,366,999 (GRCm39)	V235D	probably damaging	Het
Clca4a	G	T	3: 144,659,525 (GRCm39)	T777K	probably damaging	Het
Col17a1	A	G	19: 47,673,972 (GRCm39)		probably null	Het
Col5a3	C	A	9: 20,686,621 (GRCm39)	D1335Y	unknown	Het
Cpxm1	T	C	2: 130,235,091 (GRCm39)	E576G	probably damaging	Het
Dcbld2	T	C	16: 58,253,808 (GRCm39)	S182P	probably damaging	Het
Dclk1	C	T	3: 55,410,313 (GRCm39)	S616L	probably damaging	Het
Dll4	C	A	2: 119,161,634 (GRCm39)	D405E	probably damaging	Het
Dnah1	G	A	14: 31,000,108 (GRCm39)	R2462C	probably benign	Het
Dnah3	A	T	7: 119,564,882 (GRCm39)	Y2594N	possibly damaging	Het
Ess2	G	A	16: 17,727,958 (GRCm39)	P103S	probably benign	Het
Fam110a	C	A	2: 151,812,006 (GRCm39)	A255S	probably benign	Het
Fbn2	G	A	18: 58,246,397 (GRCm39)	R502W	probably damaging	Het
Fgl2	A	G	5: 21,580,521 (GRCm39)	S288G	possibly damaging	Het
Gm1527	T	C	3: 28,969,923 (GRCm39)	S342P	probably damaging	Het
Gm5901	A	T	7: 105,026,522 (GRCm39)	T97S	probably damaging	Het
Greb1l	A	G	18: 10,547,420 (GRCm39)	Y1546C	probably damaging	Het
Impg1	A	T	9: 80,249,347 (GRCm39)	S619T	probably damaging	Het
Itih2	C	A	2: 10,110,057 (GRCm39)	Q565H	possibly damaging	Het
Kbtbd6	T	A	14: 79,690,464 (GRCm39)	N386K	probably benign	Het
Lama3	T	C	18: 12,652,934 (GRCm39)	M218T	probably benign	Het
Lipg	T	C	18: 75,094,012 (GRCm39)	S12G	probably benign	Het
Marf1	C	T	16: 13,960,398 (GRCm39)	A549T	probably damaging	Het
Mex3d	G	T	10: 80,217,505 (GRCm39)	P571T	probably damaging	Het
Neb	A	C	2: 52,085,482 (GRCm39)	Y1538D	possibly damaging	Het
Nsd1	T	C	13: 55,361,584 (GRCm39)	I184T	probably damaging	Het
Or2z8	C	T	8: 72,812,244 (GRCm39)	T240M	probably damaging	Het
Or5b99	T	A	19: 12,976,766 (GRCm39)	C139S	probably damaging	Het
Or5w18	T	C	2: 87,633,525 (GRCm39)	F264S	probably damaging	Het
Pacs1	T	C	19: 5,185,149 (GRCm39)		silent	Het
Pdcd11	T	C	19: 47,101,611 (GRCm39)	V932A	probably damaging	Het
Pkd2	A	G	5: 104,625,032 (GRCm39)	D276G	probably damaging	Het
Pkia	T	A	3: 7,502,499 (GRCm39)	D25E	probably damaging	Het
Plxna2	A	C	1: 194,326,458 (GRCm39)	S131R	probably damaging	Het
Prelid1	T	C	13: 55,472,220 (GRCm39)	V132A	possibly damaging	Het
Psma3	T	C	12: 71,030,163 (GRCm39)	Y59H	probably benign	Het
Ptchd3	A	C	11: 121,732,916 (GRCm39)	E602A	possibly damaging	Het
Ptpro	T	C	6: 137,353,987 (GRCm39)	V121A	possibly damaging	Het
Ptprt	A	G	2: 161,449,239 (GRCm39)	L878P	probably damaging	Het
Pxn	G	A	5: 115,692,027 (GRCm39)	G370S	probably damaging	Het
Rcn2	G	T	9: 55,949,453 (GRCm39)	A40S	probably benign	Het
Rnf215	A	G	11: 4,089,760 (GRCm39)	N258D	probably damaging	Het
Rnpc3	T	C	3: 113,423,622 (GRCm39)	T28A	probably damaging	Het
Rtel1	T	A	2: 180,997,795 (GRCm39)	V1100E	possibly damaging	Het
Scn3a	T	A	2: 65,291,173 (GRCm39)	I1858F	probably damaging	Het
Slc9c1	G	A	16: 45,400,595 (GRCm39)	R735Q	possibly damaging	Het
Snapc1	C	T	12: 74,021,806 (GRCm39)	R81C	probably damaging	Het
Spata13	A	G	14: 60,929,788 (GRCm39)	T449A	probably benign	Het
Svep1	A	G	4: 58,072,737 (GRCm39)	W2191R	probably damaging	Het
Thbs1	G	A	2: 117,948,055 (GRCm39)	R405H	probably damaging	Het
Tnn	A	G	1: 159,948,137 (GRCm39)	Y859H	possibly damaging	Het
Tonsl	A	G	15: 76,513,500 (GRCm39)	S1245P	possibly damaging	Het
Tpcn1	G	A	5: 120,677,324 (GRCm39)	T661M	probably damaging	Het
Trap1	A	G	16: 3,863,424 (GRCm39)	F533L	probably benign	Het
Ttc23	T	C	7: 67,328,821 (GRCm39)		probably null	Het
Vax2	T	C	6: 83,688,426 (GRCm39)	S50P	possibly damaging	Het
Vmn1r5	A	C	6: 56,962,784 (GRCm39)	E153A	probably benign	Het
Vmn2r14	G	T	5: 109,366,762 (GRCm39)	P486Q	probably benign	Het
Vmn2r96	T	A	17: 18,802,827 (GRCm39)	F246I	probably damaging	Het
Zc3h10	C	A	10: 128,380,624 (GRCm39)	E244D	probably damaging	Het
Zdhhc18	T	A	4: 133,340,966 (GRCm39)	K265*	probably null	Het

Other mutations in Gm19668

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01548:Gm19668	APN	10	77,634,242 (GRCm39)	nonsense	probably null
R7559:Gm19668	UTSW	10	77,634,572 (GRCm39)	nonsense	probably null
R7955:Gm19668	UTSW	10	77,634,630 (GRCm39)	missense	unknown
R8081:Gm19668	UTSW	10	77,634,420 (GRCm39)	missense	unknown
R8347:Gm19668	UTSW	10	77,634,221 (GRCm39)	makesense	probably null
R9143:Gm19668	UTSW	10	77,634,960 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- GTGTTCCTCTTTTGGGGAGACCATC -3'
(R):5'- AGTTGTGGCAACCGGATATGCTC -3'

Sequencing Primer
(F):5'- CCATCTATATCAGGTCAGGGTCAG -3'
(R):5'- CAATTGTCAGGAGAGCTACTGTG -3'

Posted On

2013-05-09