Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00595:Gm15130'

332750

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm15130

Ensembl Gene

ENSMUSG00000079169

Gene Name

predicted gene 15130

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

IGL00595

Quality Score

Status

Chromosome

Chromosomal Location

(GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 110969322 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 132 (D132V)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000132464
AA Change: D132V

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
2310057J18Rik	G	A	10: 28,849,954 (GRCm39)	R161*	probably null	Het
Adam20	T	A	8: 41,249,084 (GRCm39)	F398Y	probably benign	Het
Ano1	T	A	7: 144,192,250 (GRCm39)	I374F	probably damaging	Het
Apol10a	A	T	15: 77,369,135 (GRCm39)	N45Y	probably null	Het
Asnsd1	A	G	1: 53,386,647 (GRCm39)	S327P	probably damaging	Het
Ccdc83	T	A	7: 89,893,252 (GRCm39)	K168N	probably damaging	Het
Chmp1b2	A	G	X: 106,831,450 (GRCm39)	S189P	probably damaging	Het
Dpysl4	G	T	7: 138,676,092 (GRCm39)	V274F	probably damaging	Het
Fxr2	T	G	11: 69,540,018 (GRCm39)	S292A	probably benign	Het
Gpr161	A	G	1: 165,146,372 (GRCm39)	H436R	probably benign	Het
Jaml	C	T	9: 45,012,287 (GRCm39)		probably benign	Het
Kcnc2	A	T	10: 112,297,893 (GRCm39)	S606C	probably damaging	Het
Kcnc2	G	T	10: 112,297,892 (GRCm39)	E605D	probably benign	Het
Kcnrg	T	C	14: 61,845,359 (GRCm39)	I133T	probably damaging	Het
Kdm7a	A	G	6: 39,121,444 (GRCm39)	I837T	probably benign	Het
Lactb2	A	G	1: 13,700,350 (GRCm39)	L227S	probably benign	Het
Lats1	T	G	10: 7,578,069 (GRCm39)	S398A	probably benign	Het
Llgl2	T	A	11: 115,725,710 (GRCm39)	D19E	probably benign	Het
Nup107	A	T	10: 117,609,257 (GRCm39)	C365*	probably null	Het
Nup107	T	C	10: 117,609,273 (GRCm39)		probably null	Het
Plekhf2	T	C	4: 10,991,022 (GRCm39)	K107E	probably damaging	Het
Rnf139	A	T	15: 58,770,391 (GRCm39)	I139F	possibly damaging	Het
Rsbn1	A	G	3: 103,836,006 (GRCm39)	N348S	probably benign	Het
Rttn	A	T	18: 88,992,464 (GRCm39)	Q136H	probably benign	Het
Syne2	C	T	12: 75,972,420 (GRCm39)	T1052I	possibly damaging	Het
Tom1l1	A	T	11: 90,565,566 (GRCm39)	L101Q	probably damaging	Het
Tubal3	A	G	13: 3,983,015 (GRCm39)	N265S	probably damaging	Het
Zfp141	T	C	7: 42,126,079 (GRCm39)	N131S	probably benign	Het
Zfp944	T	C	17: 22,558,186 (GRCm39)	S354G	probably benign	Het
Zfp961	G	A	8: 72,722,272 (GRCm39)	A262T	probably damaging	Het

Other mutations in Gm15130

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL03176:Gm15130	APN	2	110,978,846 (GRCm39)	missense	unknown
R0066:Gm15130	UTSW	2	110,969,284 (GRCm39)	splice site	probably benign
R0066:Gm15130	UTSW	2	110,969,284 (GRCm39)	splice site	probably benign
R4716:Gm15130	UTSW	2	110,964,560 (GRCm39)	nonsense	probably null
R4754:Gm15130	UTSW	2	110,973,207 (GRCm39)	missense	unknown
R4816:Gm15130	UTSW	2	110,965,714 (GRCm39)	splice site	probably benign
R5283:Gm15130	UTSW	2	110,965,754 (GRCm39)	missense	unknown
R5973:Gm15130	UTSW	2	110,965,714 (GRCm39)	splice site	probably benign
R6152:Gm15130	UTSW	2	110,974,950 (GRCm39)	missense	unknown
R6398:Gm15130	UTSW	2	110,965,787 (GRCm39)	missense	unknown
R7708:Gm15130	UTSW	2	110,974,962 (GRCm39)	missense
R7813:Gm15130	UTSW	2	110,969,320 (GRCm39)	missense
R7934:Gm15130	UTSW	2	110,964,582 (GRCm39)	missense
R8490:Gm15130	UTSW	2	110,983,230 (GRCm39)	critical splice donor site	probably null
Z1176:Gm15130	UTSW	2	110,974,932 (GRCm39)	critical splice donor site	probably null

Posted On

2015-08-05