Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01912:Gm3633'

179848

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm3633

Ensembl Gene

ENSMUSG00000095113

Gene Name

predicted gene 3633

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01912

Quality Score

Status

Chromosome

Chromosomal Location

42458509-42463864 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 42462743 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000126330 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000163102]

AlphaFold

F6YU13

Predicted Effect

probably benign
Transcript: ENSMUST00000100697

SMART Domains

Protein: ENSMUSP00000098262
Gene: ENSMUSG00000095113

Domain	Start	End	E-Value	Type
Pfam:Takusan	57	137	2.9e-26	PFAM
coiled coil region	164	186	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000163102

SMART Domains

Protein: ENSMUSP00000126330
Gene: ENSMUSG00000095113

Domain	Start	End	E-Value	Type
Pfam:Takusan	1	32	6.1e-9	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc8	A	T	7: 45,769,934 (GRCm39)	D860E	probably damaging	Het
Actl11	C	A	9: 107,806,844 (GRCm39)	P389Q	probably damaging	Het
Bsg	G	T	10: 79,545,974 (GRCm39)	G103W	probably null	Het
Camk2d	T	A	3: 126,604,281 (GRCm39)		probably null	Het
Clcn7	T	C	17: 25,371,983 (GRCm39)		probably benign	Het
Dctd	C	T	8: 48,564,697 (GRCm39)		probably benign	Het
Dpy19l1	C	T	9: 24,396,365 (GRCm39)	R117Q	probably damaging	Het
Esyt2	T	C	12: 116,303,229 (GRCm39)	I289T	probably damaging	Het
Exoc6b	A	C	6: 84,602,156 (GRCm39)	C753G	probably damaging	Het
Gm10718	A	T	9: 3,025,118 (GRCm39)	Y194F	probably benign	Het
Gm21738	G	A	14: 19,416,979 (GRCm38)	S144L	probably benign	Het
Hrh3	A	T	2: 179,743,169 (GRCm39)	V153D	probably damaging	Het
Krt77	T	A	15: 101,772,286 (GRCm39)		probably benign	Het
Nat3	T	A	8: 68,000,398 (GRCm39)	C92*	probably null	Het
Nckap1l	T	A	15: 103,382,573 (GRCm39)	L525M	probably benign	Het
Nrp2	T	A	1: 62,810,896 (GRCm39)	C646S	probably damaging	Het
Or10a3m	T	C	7: 108,313,465 (GRCm39)	Y290H	possibly damaging	Het
Or2ag16	T	A	7: 106,352,199 (GRCm39)	Y132F	probably damaging	Het
Or52n20	T	C	7: 104,320,440 (GRCm39)	I177T	possibly damaging	Het
Orc1	T	C	4: 108,447,941 (GRCm39)	Y63H	probably damaging	Het
Otud4	T	C	8: 80,400,466 (GRCm39)	V1059A	probably benign	Het
Ptprm	A	G	17: 67,353,113 (GRCm39)	V235A	probably benign	Het
Rab3ip	G	T	10: 116,742,997 (GRCm39)	Q443K	probably benign	Het
Tnc	C	A	4: 63,926,977 (GRCm39)	D850Y	probably damaging	Het
Ubxn2b	T	A	4: 6,203,767 (GRCm39)		probably null	Het
Vmn1r233	T	A	17: 21,214,467 (GRCm39)	Y161F	probably benign	Het
Vmn1r54	T	C	6: 90,246,442 (GRCm39)	S119P	probably damaging	Het

Other mutations in Gm3633

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01335:Gm3633	APN	14	42,462,595 (GRCm39)	unclassified	probably benign
IGL01640:Gm3633	APN	14	42,460,324 (GRCm39)	nonsense	probably null
IGL01875:Gm3633	APN	14	42,461,234 (GRCm39)	missense	probably damaging	1.00
R5039:Gm3633	UTSW	14	42,461,161 (GRCm39)	missense	possibly damaging	0.78
R6866:Gm3633	UTSW	14	42,462,579 (GRCm39)	unclassified	probably benign
R8298:Gm3633	UTSW	14	42,462,675 (GRCm39)	missense
R8687:Gm3633	UTSW	14	42,462,648 (GRCm39)	missense
R9214:Gm3633	UTSW	14	42,460,359 (GRCm39)	unclassified	probably benign
R9397:Gm3633	UTSW	14	42,460,400 (GRCm39)	missense

Posted On

2014-05-07