Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01298:Gm11444'

73213

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm11444

Ensembl Gene

Gene Name

predicted gene 11444

Synonyms

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.128) question?

Stock #

IGL01298

Quality Score

Status

Chromosome

Chromosomal Location

85846790-85850333 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 85848094 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Tyrosine at position 58 (D58Y)

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000146433
AA Change: D58Y

SMART Domains

Protein: ENSMUSP00000116236
Gene: ENSMUSG00000069785
AA Change: D58Y

Domain	Start	End	E-Value	Type
low complexity region	130	143	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 29 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adora2a	G	T	10: 75,333,492	W263C	probably damaging	Het
Agtpbp1	G	A	13: 59,504,226	H424Y	possibly damaging	Het
Angpt2	T	G	8: 18,710,528	N186T	probably benign	Het
Ank2	A	G	3: 126,959,720	V304A	possibly damaging	Het
Atg3	T	C	16: 45,171,673	M88T	possibly damaging	Het
Baz1a	G	T	12: 54,954,809	P142Q	probably damaging	Het
Btbd1	G	T	7: 81,794,307		probably null	Het
Cacnb3	T	C	15: 98,639,853	Y70H	probably damaging	Het
Cd4	G	A	6: 124,879,378	T50I	probably benign	Het
Cyp7a1	A	T	4: 6,275,517	W19R	probably damaging	Het
Dock10	T	A	1: 80,531,245	I1610F	probably damaging	Het
Gm7168	A	T	17: 13,949,858	T496S	probably benign	Het
Gpc5	A	G	14: 115,399,188	S428G	probably benign	Het
Haus8	T	C	8: 71,253,113	E309G	probably damaging	Het
Ice1	A	G	13: 70,604,904	L1021P	possibly damaging	Het
Krtap14	A	T	16: 88,825,727	H121Q	probably benign	Het
Nwd1	T	C	8: 72,662,331	V170A	probably benign	Het
Olfr338	T	A	2: 36,377,448	M224K	probably benign	Het
Olfr803	T	C	10: 129,692,029	Y4C	probably damaging	Het
Olfr938	G	A	9: 39,078,724	T7I	possibly damaging	Het
Pfpl	T	C	19: 12,428,673	M96T	possibly damaging	Het
Pramel5	A	G	4: 144,271,162		probably benign	Het
Proc	T	C	18: 32,123,552	N354S	probably benign	Het
Prss40	T	G	1: 34,560,766	I47L	probably benign	Het
Tmprss7	T	C	16: 45,664,175	R541G	probably benign	Het
Togaram2	T	C	17: 71,716,513	V788A	possibly damaging	Het
Trbv19	T	C	6: 41,178,904	Y70H	probably damaging	Het
Ttk	C	T	9: 83,865,142	S678L	probably benign	Het
Vmn2r85	T	C	10: 130,418,821	T665A	probably benign	Het

Other mutations in Gm11444

Allele	Source	Chr	Coord	Type	Predicted Effect
R1958:Gm11444	UTSW	11	85848173	splice site	probably benign
R5199:Gm11444	UTSW	11	85848019	missense	unknown
R6283:Gm11444	UTSW	11	85846791	splice site	probably null
R7088:Gm11444	UTSW	11	85847036	missense
R7579:Gm11444	UTSW	11	85850243	missense	unknown
R8378:Gm11444	UTSW	11	85850249	missense
R8708:Gm11444	UTSW	11	85846897	missense

Posted On

2013-10-07