Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02961:Gm7247'

365338

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm7247

Ensembl Gene

ENSMUSG00000068399

Gene Name

predicted gene 7247

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.135) question?

Stock #

IGL02961

Quality Score

Status

Chromosome

Chromosomal Location

51601678-51765127 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 51602812 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 49 (N49K)

Ref Sequence

ENSEMBL: ENSMUSP00000125409 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000162998]

AlphaFold

Q6UY52

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162079

Predicted Effect

probably damaging
Transcript: ENSMUST00000162998
AA Change: N49K

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000125409
Gene: ENSMUSG00000068399
AA Change: N49K

Domain	Start	End	E-Value	Type
Pfam:Takusan	35	115	2.2e-25	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrv1	A	G	13: 81,671,731 (GRCm39)	V2288A	probably damaging	Het
Agbl4	T	A	4: 110,437,318 (GRCm39)	N76K	probably damaging	Het
AI182371	A	T	2: 34,976,124 (GRCm39)	V258E	possibly damaging	Het
Alg1	T	A	16: 5,052,861 (GRCm39)	N80K	probably benign	Het
Ambra1	A	G	2: 91,741,793 (GRCm39)	M963V	possibly damaging	Het
Avil	C	A	10: 126,844,175 (GRCm39)	Q245K	probably benign	Het
Caml	A	G	13: 55,779,695 (GRCm39)	N256S	probably benign	Het
Ccdc102a	A	C	8: 95,629,978 (GRCm39)	I521S	possibly damaging	Het
Ccm2l	A	G	2: 152,920,521 (GRCm39)	T393A	probably benign	Het
Cdh16	A	G	8: 105,341,837 (GRCm39)	V91A	probably damaging	Het
Chd7	A	G	4: 8,751,542 (GRCm39)	D13G	probably damaging	Het
Chsy1	T	A	7: 65,821,530 (GRCm39)	D588E	probably benign	Het
Cilp	T	A	9: 65,185,891 (GRCm39)	V662E	possibly damaging	Het
Cog8	A	G	8: 107,782,885 (GRCm39)		probably benign	Het
Cpb2	T	C	14: 75,502,823 (GRCm39)	V134A	probably benign	Het
Ctcfl	T	A	2: 172,943,712 (GRCm39)	H546L	possibly damaging	Het
Dclre1c	A	G	2: 3,438,070 (GRCm39)	D136G	probably damaging	Het
Dnah2	T	A	11: 69,409,240 (GRCm39)	E379D	probably damaging	Het
Extl3	A	G	14: 65,294,408 (GRCm39)	Y808H	possibly damaging	Het
Insr	T	C	8: 3,308,785 (GRCm39)	I84V	probably benign	Het
Ipo7	C	T	7: 109,646,223 (GRCm39)	P541S	probably benign	Het
Kcnc3	T	C	7: 44,240,916 (GRCm39)	S203P	probably damaging	Het
Myo5a	A	G	9: 75,122,402 (GRCm39)	D1732G	probably benign	Het
Or10q3	T	A	19: 11,847,695 (GRCm39)	N295I	probably damaging	Het
Or52d1	C	A	7: 103,756,357 (GRCm39)	Y290*	probably null	Het
Or5p68	T	C	7: 107,945,334 (GRCm39)	I285V	probably benign	Het
Or5w22	A	G	2: 87,363,028 (GRCm39)	Y217C	probably damaging	Het
Or6x1	T	C	9: 40,098,897 (GRCm39)	V162A	probably benign	Het
Pde3a	T	A	6: 141,405,426 (GRCm39)	L426*	probably null	Het
Pkd1	T	A	17: 24,797,089 (GRCm39)	D8E	possibly damaging	Het
Polr3a	A	T	14: 24,517,108 (GRCm39)	Y714*	probably null	Het
Pramel16	T	C	4: 143,675,717 (GRCm39)	T370A	probably damaging	Het
Prb1c	A	T	6: 132,338,371 (GRCm39)	F282L	unknown	Het
Rasgrf1	T	C	9: 89,863,702 (GRCm39)	V556A	possibly damaging	Het
Rev3l	T	C	10: 39,703,941 (GRCm39)	Y1996H	possibly damaging	Het
Rttn	T	C	18: 89,071,697 (GRCm39)	L1248P	probably damaging	Het
Slc11a1	T	C	1: 74,416,332 (GRCm39)	L53P	probably damaging	Het
Slc22a27	T	C	19: 7,903,886 (GRCm39)	R84G	probably damaging	Het
Sptbn4	A	G	7: 27,097,392 (GRCm39)	L1302P	probably damaging	Het
Srm	T	C	4: 148,678,586 (GRCm39)	V271A	possibly damaging	Het
Sycp2	A	G	2: 178,022,655 (GRCm39)	I492T	probably benign	Het
Tmprss13	A	G	9: 45,256,301 (GRCm39)	T472A	probably damaging	Het
Togaram1	A	G	12: 65,013,484 (GRCm39)	D245G	probably damaging	Het
Vmn1r184	A	T	7: 25,967,075 (GRCm39)	I274L	probably benign	Het
Vmn1r21	T	C	6: 57,820,974 (GRCm39)	M157V	probably benign	Het
Wdr90	C	A	17: 26,067,649 (GRCm39)	E1420*	probably null	Het
Zfp518a	A	T	19: 40,903,462 (GRCm39)	R1130S	probably benign	Het

Other mutations in Gm7247

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00162:Gm7247	APN	14	51,760,962 (GRCm39)	missense	possibly damaging	0.73
IGL01776:Gm7247	APN	14	51,759,356 (GRCm39)	missense	possibly damaging	0.86
IGL01836:Gm7247	APN	14	51,602,853 (GRCm39)	missense	probably damaging	1.00
IGL02270:Gm7247	APN	14	51,759,341 (GRCm39)	missense	probably benign	0.10
IGL03390:Gm7247	APN	14	51,760,914 (GRCm39)	missense	probably benign
R0054:Gm7247	UTSW	14	51,807,057 (GRCm39)	utr 3 prime	probably benign
R0413:Gm7247	UTSW	14	51,760,929 (GRCm39)	missense	probably benign	0.33
R1143:Gm7247	UTSW	14	51,760,875 (GRCm39)	missense	probably benign	0.33
R2018:Gm7247	UTSW	14	51,602,804 (GRCm39)	missense	possibly damaging	0.60
R2019:Gm7247	UTSW	14	51,602,804 (GRCm39)	missense	possibly damaging	0.60
R2117:Gm7247	UTSW	14	51,602,792 (GRCm39)	missense	probably damaging	0.99
R3971:Gm7247	UTSW	14	51,602,841 (GRCm39)	missense	probably damaging	1.00
R4649:Gm7247	UTSW	14	51,807,051 (GRCm39)	critical splice acceptor site	probably null
R5109:Gm7247	UTSW	14	51,602,774 (GRCm39)	missense	probably damaging	0.98
R5773:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R5775:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R5776:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R5994:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R5995:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R5996:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R6008:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R6009:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R6010:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R6011:Gm7247	UTSW	14	51,601,805 (GRCm39)	missense	probably benign	0.01
R6193:Gm7247	UTSW	14	51,759,299 (GRCm39)	missense	possibly damaging	0.89
R6986:Gm7247	UTSW	14	51,602,832 (GRCm39)	missense	possibly damaging	0.95
R7226:Gm7247	UTSW	14	51,602,808 (GRCm39)	missense	probably damaging	0.97
R7331:Gm7247	UTSW	14	51,601,792 (GRCm39)	missense	probably damaging	0.98
R8878:Gm7247	UTSW	14	51,666,210 (GRCm39)	intron	probably benign
RF021:Gm7247	UTSW	14	51,601,781 (GRCm39)	small deletion	probably benign
RF046:Gm7247	UTSW	14	51,601,781 (GRCm39)	small deletion	probably benign

Posted On

2015-12-18