Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00418:Irgm1'

4612

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Irgm1

Ensembl Gene

ENSMUSG00000046879

Gene Name

immunity-related GTPase family M member 1

Synonyms

Iigp3, Irgm, Ifi1, LRG-47

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL00418

Quality Score

Status

Chromosome

Chromosomal Location

48756072-48762247 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 48756832 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 326 (Y326*)

Ref Sequence

ENSEMBL: ENSMUSP00000094870 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049519] [ENSMUST00000097271]

AlphaFold

Q60766

Predicted Effect

probably null
Transcript: ENSMUST00000049519
AA Change: Y342*

SMART Domains

Protein: ENSMUSP00000050446
Gene: ENSMUSG00000046879
AA Change: Y342*

Domain	Start	End	E-Value	Type
Pfam:IIGP	42	399	5.5e-169	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000097271
AA Change: Y326*

SMART Domains

Protein: ENSMUSP00000094870
Gene: ENSMUSG00000046879
AA Change: Y326*

Domain	Start	End	E-Value	Type
Pfam:IIGP	26	288	2.5e-131	PFAM
Pfam:MMR_HSR1	62	175	2.8e-6	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147151

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: In the absence of infection, mice show no overt phenotype. Resistance to protozoan parasitic infection and bacterial infection is impaired in homozygous mutant mice, whereas resistance to viral infection is normal. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700097O09Rik	A	G	12: 55,095,748 (GRCm39)	I238T	probably damaging	Het
Akap4	T	C	X: 6,942,729 (GRCm39)	V344A	possibly damaging	Het
Apex2	T	C	X: 149,355,048 (GRCm39)	K430E	probably benign	Het
Aqp9	C	T	9: 71,040,013 (GRCm39)	A90T	probably damaging	Het
Asb15	T	A	6: 24,558,642 (GRCm39)		probably benign	Het
Barhl2	C	T	5: 106,603,365 (GRCm39)	A265T	possibly damaging	Het
Bspry	G	T	4: 62,414,342 (GRCm39)	D312Y	probably benign	Het
Cdh16	G	A	8: 105,350,045 (GRCm39)	R5W	probably benign	Het
Ciz1	C	T	2: 32,262,400 (GRCm39)	R461C	probably damaging	Het
Cldn14	T	A	16: 93,716,189 (GRCm39)	D219V	probably benign	Het
Clpb	A	T	7: 101,436,952 (GRCm39)	T706S	probably benign	Het
Cyp2d11	A	T	15: 82,276,669 (GRCm39)	M90K	probably benign	Het
Cyp2j8	T	A	4: 96,332,853 (GRCm39)	I498F	possibly damaging	Het
Dnah2	A	G	11: 69,385,892 (GRCm39)		probably benign	Het
Dpyd	T	A	3: 118,737,891 (GRCm39)	F477L	probably damaging	Het
Dscaml1	C	A	9: 45,581,498 (GRCm39)	S439*	probably null	Het
Faxc	A	G	4: 21,958,490 (GRCm39)	K216E	possibly damaging	Het
Fmo1	C	T	1: 162,663,815 (GRCm39)	R238Q	probably damaging	Het
Gm14399	G	A	2: 174,973,315 (GRCm39)	R147*	probably null	Het
H2-Ab1	G	A	17: 34,486,549 (GRCm39)	V203M	probably damaging	Het
Heatr5b	T	C	17: 79,060,570 (GRCm39)	E2035G	probably damaging	Het
Hip1	A	G	5: 135,455,200 (GRCm39)	I786T	probably damaging	Het
Homer1	T	C	13: 93,524,196 (GRCm39)		probably benign	Het
Igkv9-120	A	G	6: 68,026,971 (GRCm39)	D2G	possibly damaging	Het
Kctd19	A	T	8: 106,115,095 (GRCm39)		probably null	Het
Large1	T	C	8: 73,550,469 (GRCm39)		probably null	Het
Mzf1	G	A	7: 12,778,543 (GRCm39)	A287V	possibly damaging	Het
Nes	A	T	3: 87,883,561 (GRCm39)	K607*	probably null	Het
Pars2	T	A	4: 106,511,247 (GRCm39)	V307E	probably damaging	Het
Pcsk5	T	A	19: 17,488,785 (GRCm39)	I1012F	possibly damaging	Het
Pole	T	C	5: 110,451,431 (GRCm39)		probably benign	Het
Rbm14	T	C	19: 4,852,576 (GRCm39)		probably benign	Het
Scn2a	A	T	2: 65,594,866 (GRCm39)	Q1905L	probably benign	Het
Slc26a2	A	G	18: 61,331,812 (GRCm39)	F540L	probably benign	Het
Slco2a1	T	C	9: 102,956,640 (GRCm39)		probably benign	Het
Tas2r106	T	C	6: 131,654,922 (GRCm39)		probably null	Het
Tmem175	T	A	5: 108,793,732 (GRCm39)	D287E	probably benign	Het
Trappc12	T	C	12: 28,787,835 (GRCm39)	K416R	probably damaging	Het
Trim2	A	G	3: 84,115,596 (GRCm39)	L86P	probably damaging	Het
Vps13c	T	A	9: 67,783,544 (GRCm39)	N240K	probably damaging	Het
Wdr90	A	C	17: 26,068,338 (GRCm39)	I1330S	probably damaging	Het
Wfdc6a	A	G	2: 164,426,914 (GRCm39)		probably null	Het
Zc3h12c	C	T	9: 52,027,965 (GRCm39)	V466M	probably damaging	Het
Zswim8	A	G	14: 20,768,543 (GRCm39)	T1025A	probably damaging	Het

Other mutations in Irgm1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01821:Irgm1	APN	11	48,757,353 (GRCm39)	missense	probably damaging	1.00
IGL02043:Irgm1	APN	11	48,757,642 (GRCm39)	missense	probably damaging	0.98
IGL02252:Irgm1	APN	11	48,756,981 (GRCm39)	missense	possibly damaging	0.92
IGL03153:Irgm1	APN	11	48,757,094 (GRCm39)	missense	probably damaging	1.00
igraine	UTSW	11	48,757,440 (GRCm39)	missense	probably benign	0.33
R0487:Irgm1	UTSW	11	48,757,154 (GRCm39)	missense	probably damaging	0.98
R1808:Irgm1	UTSW	11	48,757,259 (GRCm39)	missense	probably damaging	0.99
R1809:Irgm1	UTSW	11	48,757,440 (GRCm39)	missense	probably benign	0.33
R1878:Irgm1	UTSW	11	48,756,897 (GRCm39)	missense	probably benign	0.07
R2971:Irgm1	UTSW	11	48,757,417 (GRCm39)	nonsense	probably null
R4492:Irgm1	UTSW	11	48,756,955 (GRCm39)	synonymous	silent
R4962:Irgm1	UTSW	11	48,757,159 (GRCm39)	missense	possibly damaging	0.93
R5186:Irgm1	UTSW	11	48,757,044 (GRCm39)	missense	probably benign	0.00
R5794:Irgm1	UTSW	11	48,757,064 (GRCm39)	missense	probably damaging	0.99
R6224:Irgm1	UTSW	11	48,757,713 (GRCm39)	missense	probably benign	0.02
R6487:Irgm1	UTSW	11	48,756,777 (GRCm39)	missense	probably benign	0.21
R6752:Irgm1	UTSW	11	48,757,290 (GRCm39)	missense	probably damaging	1.00
R6766:Irgm1	UTSW	11	48,756,928 (GRCm39)	missense	possibly damaging	0.80
R8005:Irgm1	UTSW	11	48,757,217 (GRCm39)	missense	probably damaging	1.00
R8418:Irgm1	UTSW	11	48,757,166 (GRCm39)	missense	probably damaging	0.97
R8924:Irgm1	UTSW	11	48,756,698 (GRCm39)	missense	probably benign	0.35
R8947:Irgm1	UTSW	11	48,759,575 (GRCm39)	intron	probably benign

Posted On

2012-04-20