Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01589:Gm9912'

91538

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm9912

Ensembl Gene

Gene Name

predicted gene 9912

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01589

Quality Score

Status

Chromosome

Chromosomal Location

148889329-148891133 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 148890986 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 49 (D49G)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000066092
AA Change: D49G

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 30 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	A	G	11: 110,046,003 (GRCm39)	F307S	probably damaging	Het
Abcc6	A	T	7: 45,652,096 (GRCm39)		probably benign	Het
Adamts12	T	A	15: 11,311,323 (GRCm39)	D1193E	probably benign	Het
Akap6	T	A	12: 53,186,447 (GRCm39)	L1287H	probably damaging	Het
Ascl3	A	G	7: 109,327,245 (GRCm39)	S25P	probably benign	Het
Brd2	A	G	17: 34,336,016 (GRCm39)	S66P	probably damaging	Het
Cacna1i	C	A	15: 80,271,960 (GRCm39)		probably benign	Het
Cdc5l	T	C	17: 45,715,602 (GRCm39)	Y670C	probably damaging	Het
Clybl	T	A	14: 122,608,834 (GRCm39)	I142N	probably damaging	Het
Cyp2c66	T	C	19: 39,172,379 (GRCm39)		probably null	Het
Dck	C	T	5: 88,922,095 (GRCm39)		probably benign	Het
Dsg1b	T	C	18: 20,542,651 (GRCm39)	Y1053H	probably damaging	Het
Gpr107	T	C	2: 31,057,163 (GRCm39)		probably benign	Het
Hsd3b7	T	C	7: 127,402,036 (GRCm39)	F227S	probably damaging	Het
Lrrtm2	T	A	18: 35,345,851 (GRCm39)	N484Y	probably damaging	Het
Muc19	A	T	15: 91,754,699 (GRCm39)		noncoding transcript	Het
Nodal	G	A	10: 61,254,176 (GRCm39)	R33Q	probably benign	Het
Or1a1	T	C	11: 74,086,587 (GRCm39)	L86P	probably damaging	Het
Plcb4	A	G	2: 135,809,038 (GRCm39)	I569V	probably benign	Het
Plekhg1	T	C	10: 3,913,631 (GRCm39)	Y1118H	probably benign	Het
Polr2a	T	G	11: 69,632,020 (GRCm39)	E1015D	probably benign	Het
Recql5	A	G	11: 115,785,495 (GRCm39)	F667S	probably damaging	Het
Scube1	T	C	15: 83,496,754 (GRCm39)	Y749C	probably damaging	Het
Serpinb1c	C	A	13: 33,070,155 (GRCm39)	V136F	probably damaging	Het
Slain2	T	C	5: 73,098,789 (GRCm39)		probably benign	Het
Slc10a7	T	C	8: 79,456,369 (GRCm39)	S296P	probably damaging	Het
Sspo	C	T	6: 48,428,112 (GRCm39)	R320W	probably damaging	Het
Usp16	G	A	16: 87,276,071 (GRCm39)	A469T	probably benign	Het
Vmn2r102	A	T	17: 19,899,066 (GRCm39)	L469F	probably benign	Het
Zfp772	A	G	7: 7,208,523 (GRCm39)	F107S	possibly damaging	Het

Other mutations in Gm9912

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01759:Gm9912	APN	3	148,891,074 (GRCm39)	missense	unknown
IGL01995:Gm9912	APN	3	148,891,085 (GRCm39)	missense	unknown
R0219:Gm9912	UTSW	3	148,891,131 (GRCm39)	missense	unknown
R2062:Gm9912	UTSW	3	148,890,795 (GRCm39)	missense	unknown
R2064:Gm9912	UTSW	3	148,890,795 (GRCm39)	missense	unknown
R2066:Gm9912	UTSW	3	148,890,795 (GRCm39)	missense	unknown
R2067:Gm9912	UTSW	3	148,890,795 (GRCm39)	missense	unknown

Posted On

2013-12-09