Mutagenetix > Incidental Mutation

Incidental Mutation 'R5814:Gm10142'

447696

Institutional Source

Beutler Lab

Gene Symbol

Gm10142

Ensembl Gene

ENSMUSG00000094146

Gene Name

predicted gene 10142

Synonyms

MMRRC Submission

043396-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R5814 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

77551641-77552003 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 77551957 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Asparagine at position 106 (T106N)

Ref Sequence

ENSEMBL: ENSMUSP00000135962 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075421] [ENSMUST00000092366] [ENSMUST00000092370] [ENSMUST00000179767]

AlphaFold

J3KMP7

Predicted Effect

probably benign
Transcript: ENSMUST00000075421

SMART Domains

Protein: ENSMUSP00000074876
Gene: ENSMUSG00000094012

Domain	Start	End	E-Value	Type
Pfam:Keratin_B2_2	1	53	2.6e-8	PFAM
Pfam:Keratin_B2_2	29	74	9.2e-10	PFAM
low complexity region	92	105	N/A	INTRINSIC

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: ENSMUST00000092370

SMART Domains

Protein: ENSMUSP00000090024
Gene: ENSMUSG00000069583

Domain	Start	End	E-Value	Type
Pfam:Keratin_B2_2	1	42	3.1e-6	PFAM
Pfam:Keratin_B2_2	20	68	3.1e-10	PFAM
Pfam:Keratin_B2_2	39	84	3.7e-9	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000179767
AA Change: T106N

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000135962
Gene: ENSMUSG00000094146
AA Change: T106N

Domain	Start	End	E-Value	Type
Pfam:Keratin_B2_2	1	53	1.7e-8	PFAM
Pfam:Keratin_B2_2	29	74	1.8e-9	PFAM
low complexity region	88	106	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218482

Meta Mutation Damage Score

0.6329

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.8%

Validation Efficiency

91% (52/57)

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933402N03Rik	T	C	7: 130,740,811 (GRCm39)	D135G	probably benign	Het
Arrdc3	G	T	13: 81,038,698 (GRCm39)	R220L	possibly damaging	Het
Bace1	A	G	9: 45,771,562 (GRCm39)	D458G	probably damaging	Het
Cacna1s	A	G	1: 136,034,880 (GRCm39)	Y1360C	probably benign	Het
Ccnb1-ps	T	C	7: 41,756,522 (GRCm39)		noncoding transcript	Het
Cd209b	T	C	8: 3,973,348 (GRCm39)	E112G	probably damaging	Het
Cit	T	A	5: 116,117,478 (GRCm39)	L1176Q	probably damaging	Het
Clcn3	T	C	8: 61,387,607 (GRCm39)	Y214C	probably damaging	Het
Clvs2	G	T	10: 33,404,503 (GRCm39)	Q238K	probably benign	Het
Creb3l3	C	T	10: 80,921,496 (GRCm39)	V350M	probably benign	Het
Crot	A	C	5: 9,023,996 (GRCm39)	D373E	probably damaging	Het
Cyp4a12b	T	A	4: 115,289,694 (GRCm39)	I187N	probably damaging	Het
Degs1l	G	A	1: 180,882,663 (GRCm39)	V142I	probably damaging	Het
Dnhd1	C	A	7: 105,369,102 (GRCm39)	A4291D	possibly damaging	Het
Dnmt3b	A	T	2: 153,514,417 (GRCm39)	E403D	probably benign	Het
Ect2l	A	T	10: 18,075,757 (GRCm39)	I43K	probably damaging	Het
Efcab3	T	A	11: 104,626,940 (GRCm39)		probably benign	Het
Ep400	C	A	5: 110,843,444 (GRCm39)		probably null	Het
Erp27	A	T	6: 136,888,564 (GRCm39)	V138E	possibly damaging	Het
Gbp4	G	A	5: 105,267,785 (GRCm39)	A487V	probably benign	Het
Gxylt2	C	A	6: 100,710,196 (GRCm39)	H112Q	probably damaging	Het
Hexim2	G	A	11: 103,029,209 (GRCm39)	R87Q	probably damaging	Het
Hgf	A	G	5: 16,807,305 (GRCm39)	N399S	probably benign	Het
Ikbke	T	A	1: 131,199,516 (GRCm39)	I302F	probably damaging	Het
Itgb4	C	T	11: 115,874,983 (GRCm39)	R447W	probably benign	Het
Kdm1b	A	G	13: 47,216,622 (GRCm39)		probably null	Het
Krtap19-9a	T	C	16: 88,721,002 (GRCm39)		noncoding transcript	Het
Lin9	T	A	1: 180,496,763 (GRCm39)	L351I	probably benign	Het
Mmp10	G	A	9: 7,503,621 (GRCm39)	A164T	possibly damaging	Het
Myrip	G	A	9: 120,253,734 (GRCm39)	G269D	probably benign	Het
Or1e16	AGCGGTCGTAGGC	AGC	11: 73,286,480 (GRCm39)		probably null	Het
Paxbp1	G	T	16: 90,827,384 (GRCm39)	R420S	probably damaging	Het
Pcbp2	T	A	15: 102,391,597 (GRCm39)	S38R	probably damaging	Het
Pcf11	A	G	7: 92,306,922 (GRCm39)	V1082A	probably benign	Het
Pkhd1	T	C	1: 20,269,629 (GRCm39)	E3305G	probably damaging	Het
Pla2g4c	T	A	7: 13,074,543 (GRCm39)	W250R	probably damaging	Het
Prune2	A	G	19: 16,993,725 (GRCm39)		probably null	Het
Rpsa	A	G	9: 119,957,551 (GRCm39)		probably benign	Het
Sema3e	A	G	5: 14,275,680 (GRCm39)	I262V	probably benign	Het
Setd2	T	A	9: 110,396,826 (GRCm39)	L1663*	probably null	Het
Sh3d19	G	A	3: 86,033,911 (GRCm39)	V755I	probably benign	Het
Spag9	T	A	11: 93,973,654 (GRCm39)	V14E	possibly damaging	Het
Srsf11	C	T	3: 157,728,981 (GRCm39)		probably benign	Het
Sspo	A	T	6: 48,428,818 (GRCm39)	Q411L	probably damaging	Het
Sycp1	A	C	3: 102,803,213 (GRCm39)	S532R	probably benign	Het
Taf6l	C	A	19: 8,752,210 (GRCm39)	A493S	probably benign	Het
Tsnaxip1	A	G	8: 106,570,603 (GRCm39)	D574G	probably benign	Het
Ttll10	T	A	4: 156,132,084 (GRCm39)	K117N	possibly damaging	Het
Uqcc5	A	G	14: 30,846,477 (GRCm39)		probably null	Het
Utp4	T	A	8: 107,638,907 (GRCm39)	I405K	probably damaging	Het
Vmn2r45	T	A	7: 8,474,475 (GRCm39)	Y851F	probably benign	Het
Vps33a	T	C	5: 123,703,119 (GRCm39)	D168G	probably damaging	Het

Other mutations in Gm10142

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02369:Gm10142	APN	10	77,551,947 (GRCm39)	missense	probably benign	0.07
R0244:Gm10142	UTSW	10	77,551,848 (GRCm39)	splice site	probably null
R1293:Gm10142	UTSW	10	77,551,869 (GRCm39)	missense	probably benign	0.03
R1918:Gm10142	UTSW	10	77,551,821 (GRCm39)	missense	probably benign	0.32
R5047:Gm10142	UTSW	10	77,551,996 (GRCm39)	missense	probably damaging	1.00
R8248:Gm10142	UTSW	10	77,551,950 (GRCm39)	missense	probably damaging	0.96
R8279:Gm10142	UTSW	10	77,552,001 (GRCm39)	makesense	probably null
R9681:Gm10142	UTSW	10	77,551,880 (GRCm39)	nonsense	probably null
R9685:Gm10142	UTSW	10	77,551,762 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- CCATCTTGCTGTGTGTCCAG -3'
(R):5'- AGATAACGCTTCCATGTTCTCC -3'

Sequencing Primer
(F):5'- TGCCAGTCAGCATGCTG -3'
(R):5'- CCATGTTCTCCCCACTGAG -3'

Posted On

2016-12-15