Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01654:Gm3327'

102905

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm3327

Ensembl Gene

ENSMUSG00000090594

Gene Name

predicted gene 3327

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.246) question?

Stock #

IGL01654

Quality Score

Status

Chromosome

Chromosomal Location

44361308-44366500 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 44362317 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 72 (E72G)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000168906
AA Change: E72G

SMART Domains

Protein: ENSMUSP00000130980
Gene: ENSMUSG00000090594
AA Change: E72G

Domain	Start	End	E-Value	Type
Pfam:Takusan	57	137	4.3e-27	PFAM
coiled coil region	164	186	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000226712

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700034J05Rik	T	A	6: 146,854,838 (GRCm39)	E68V	probably damaging	Het
Abcb1a	T	C	5: 8,765,065 (GRCm39)		probably null	Het
Abcg2	T	A	6: 58,660,306 (GRCm39)		probably null	Het
Adgrf5	T	C	17: 43,762,061 (GRCm39)	I1252T	possibly damaging	Het
Apol10b	A	T	15: 77,472,996 (GRCm39)	D19E	probably benign	Het
Bbs9	T	A	9: 22,402,238 (GRCm39)		probably null	Het
Bod1l	T	C	5: 41,975,519 (GRCm39)	T1932A	probably damaging	Het
C2cd5	A	G	6: 143,027,133 (GRCm39)	V124A	probably benign	Het
Cd151	T	A	7: 141,050,275 (GRCm39)	I170N	probably benign	Het
Ckap5	C	T	2: 91,407,954 (GRCm39)	H827Y	probably benign	Het
Clk3	C	T	9: 57,659,046 (GRCm39)	V572M	probably damaging	Het
Ddrgk1	T	C	2: 130,496,629 (GRCm39)	D245G	probably damaging	Het
Enpp5	A	G	17: 44,392,066 (GRCm39)	D165G	possibly damaging	Het
Epha6	A	C	16: 59,659,666 (GRCm39)	N817K	probably benign	Het
Fbxw14	T	C	9: 109,115,648 (GRCm39)		probably benign	Het
Fes	C	T	7: 80,036,558 (GRCm39)		probably null	Het
Gemin4	A	T	11: 76,104,224 (GRCm39)	L179H	probably damaging	Het
Gm4847	C	T	1: 166,465,917 (GRCm39)	R224Q	probably damaging	Het
Lonp2	T	C	8: 87,440,714 (GRCm39)	V357A	probably damaging	Het
Mc2r	A	G	18: 68,541,143 (GRCm39)	I50T	probably benign	Het
Mmp19	C	T	10: 128,634,389 (GRCm39)	A310V	probably damaging	Het
Naip6	C	T	13: 100,435,853 (GRCm39)	R890Q	probably benign	Het
Npdc1	T	C	2: 25,297,649 (GRCm39)	S101P	possibly damaging	Het
Phldb1	T	C	9: 44,629,654 (GRCm39)		probably null	Het
Pkd2l1	T	C	19: 44,142,662 (GRCm39)	N460S	probably damaging	Het
Pnpo	A	G	11: 96,834,555 (GRCm39)		probably null	Het
Prkcq	A	T	2: 11,288,654 (GRCm39)	T536S	probably damaging	Het
Rft1	T	A	14: 30,398,837 (GRCm39)	V269E	probably damaging	Het
Skint4	A	T	4: 111,977,254 (GRCm39)	I215F	probably damaging	Het
Slc12a5	G	A	2: 164,815,675 (GRCm39)	D41N	possibly damaging	Het
Srp68	T	C	11: 116,138,638 (GRCm39)		probably benign	Het
Wdr17	T	C	8: 55,115,914 (GRCm39)	T623A	probably damaging	Het
Zfand2a	A	G	5: 139,467,823 (GRCm39)		probably benign	Het
Zfp644	T	C	5: 106,783,796 (GRCm39)	Y917C	probably damaging	Het
Zmym6	C	T	4: 127,017,519 (GRCm39)	S1008L	probably damaging	Het

Other mutations in Gm3327

Allele	Source	Chr	Coord	Type	Predicted Effect
R2496:Gm3327	UTSW	14	44,363,720 (GRCm39)	missense	unknown
R5098:Gm3327	UTSW	14	44,362,292 (GRCm39)	missense	unknown
R7054:Gm3327	UTSW	14	44,363,732 (GRCm39)	missense
R7384:Gm3327	UTSW	14	44,362,334 (GRCm39)	missense
Z1177:Gm3327	UTSW	14	44,362,257 (GRCm39)	missense

Posted On

2014-01-21