Mutagenetix > Incidental Mutation

Incidental Mutation 'R7116:Gimap9'

551763

Institutional Source

Beutler Lab

Gene Symbol

Gimap9

Ensembl Gene

ENSMUSG00000051124

Gene Name

GTPase, IMAP family member 9

Synonyms

MMRRC Submission

045207-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.050) question?

Stock #

R7116 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

48653084-48656050 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 48654989 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Valine at position 192 (A192V)

Ref Sequence

ENSEMBL: ENSMUSP00000050330 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054050] [ENSMUST00000147936]

AlphaFold

G3X987

Predicted Effect

probably benign
Transcript: ENSMUST00000054050
AA Change: A192V

PolyPhen 2 Score 0.048 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000050330
Gene: ENSMUSG00000051124
AA Change: A192V

Domain	Start	End	E-Value	Type
Pfam:AIG1	9	219	8.5e-83	PFAM
Pfam:MMR_HSR1	10	157	3.4e-11	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000147936

SMART Domains

Protein: ENSMUSP00000122830
Gene: ENSMUSG00000051124

Domain	Start	End	E-Value	Type
Pfam:MMR_HSR1	1	123	7.3e-11	PFAM
Pfam:AIG1	1	138	5.6e-61	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actn1	A	G	12: 80,251,751 (GRCm39)	S109P	probably damaging	Het
Afg3l1	T	G	8: 124,216,601 (GRCm39)	L280R	probably damaging	Het
Akap13	T	A	7: 75,369,943 (GRCm39)	S129T	probably benign	Het
Ankrd11	A	G	8: 123,622,869 (GRCm39)	S328P	probably damaging	Het
Aox3	A	T	1: 58,192,689 (GRCm39)	E554D	probably benign	Het
Bcl11a	T	C	11: 24,113,839 (GRCm39)	V394A	probably damaging	Het
Cass4	A	G	2: 172,269,889 (GRCm39)	Y657C	unknown	Het
Ccdc88a	C	T	11: 29,454,051 (GRCm39)	A1738V	probably benign	Het
Cfap74	T	C	4: 155,539,518 (GRCm39)	F948L	unknown	Het
Chgb	A	T	2: 132,623,237 (GRCm39)		probably benign	Het
Coro1c	C	T	5: 113,990,267 (GRCm39)	W138*	probably null	Het
Dgkb	A	G	12: 38,031,989 (GRCm39)	Q17R	probably benign	Het
Esco2	A	G	14: 66,064,006 (GRCm39)	Y393H	probably damaging	Het
Eya3	T	A	4: 132,422,110 (GRCm39)	D228E	probably benign	Het
Fat2	T	C	11: 55,173,162 (GRCm39)	D2517G	probably damaging	Het
Fry	T	A	5: 150,319,334 (GRCm39)		probably null	Het
Gal3st2b	A	T	1: 93,868,498 (GRCm39)	Q243L	possibly damaging	Het
Glg1	T	A	8: 111,905,589 (GRCm39)	Q564L	probably benign	Het
H2-Aa	A	T	17: 34,502,601 (GRCm39)	Y188*	probably null	Het
Hira	T	C	16: 18,730,864 (GRCm39)	Y188H	probably damaging	Het
Ighv8-8	C	T	12: 115,257,814 (GRCm39)	D76N	probably benign	Het
Irf6	T	C	1: 192,849,905 (GRCm39)	F276L	probably damaging	Het
Itpr1	T	C	6: 108,458,229 (GRCm39)	C2000R	probably damaging	Het
Jakmip3	T	C	7: 138,621,979 (GRCm39)	V293A	possibly damaging	Het
Kcnh7	A	G	2: 62,707,614 (GRCm39)	V132A	probably benign	Het
Kcnj1	A	G	9: 32,308,277 (GRCm39)	T234A	possibly damaging	Het
Kpna3	T	A	14: 61,605,635 (GRCm39)	N470I	probably benign	Het
Lamb2	T	C	9: 108,364,522 (GRCm39)	F1121L	probably damaging	Het
Lingo1	T	C	9: 56,527,911 (GRCm39)	D232G	probably benign	Het
Lpxn	T	A	19: 12,788,622 (GRCm39)	N70K	probably benign	Het
Ltbp4	T	A	7: 27,004,852 (GRCm39)	H1657L	probably damaging	Het
Luzp2	C	A	7: 54,915,078 (GRCm39)	F334L	possibly damaging	Het
Mgat5b	A	T	11: 116,835,785 (GRCm39)	S142C	possibly damaging	Het
Mroh7	G	A	4: 106,568,517 (GRCm39)	T396I	probably benign	Het
Muc5b	T	C	7: 141,417,487 (GRCm39)	S3478P	probably benign	Het
Nfatc2	A	T	2: 168,349,269 (GRCm39)	M626K	probably benign	Het
Nlrp14	A	G	7: 106,782,255 (GRCm39)	D484G	possibly damaging	Het
Npc1	T	C	18: 12,344,601 (GRCm39)	Y423C	probably damaging	Het
Nrsn1	A	G	13: 25,437,388 (GRCm39)	I180T	probably damaging	Het
Or11g25	A	T	14: 50,723,025 (GRCm39)	I37F	probably benign	Het
Or51a8	T	A	7: 102,549,842 (GRCm39)	N89K	probably benign	Het
Osbpl6	A	T	2: 76,426,225 (GRCm39)	I935F	probably benign	Het
Otog	T	C	7: 45,947,689 (GRCm39)	F96L	probably damaging	Het
Pde1b	T	C	15: 103,436,745 (GRCm39)	L534P	possibly damaging	Het
Pdzd8	C	T	19: 59,288,125 (GRCm39)	E1092K	probably damaging	Het
Pfkl	T	C	10: 77,837,249 (GRCm39)	H108R	probably benign	Het
Pkhd1l1	G	A	15: 44,421,372 (GRCm39)	V3047I	probably benign	Het
Plag1	A	T	4: 3,904,812 (GRCm39)	C126*	probably null	Het
Pphln1	T	A	15: 93,353,406 (GRCm39)	S229T	probably benign	Het
Pramel5	C	T	4: 144,000,451 (GRCm39)	D42N	possibly damaging	Het
Psd3	A	G	8: 68,166,390 (GRCm39)	V915A	probably benign	Het
Ptdss1	T	A	13: 67,093,391 (GRCm39)	I77N	probably benign	Het
Rsbn1	T	A	3: 103,821,892 (GRCm39)	C3*	probably null	Het
Shank1	C	T	7: 43,976,585 (GRCm39)	A561V	unknown	Het
Stip1	C	T	19: 6,999,178 (GRCm39)	G467S	possibly damaging	Het
Sv2c	A	T	13: 96,113,152 (GRCm39)	V599E	probably damaging	Het
Vmn2r37	T	C	7: 9,220,898 (GRCm39)	T322A	probably benign	Het
Vmn2r60	T	A	7: 41,786,487 (GRCm39)	M430K	probably benign	Het
Wipf3	T	A	6: 54,458,904 (GRCm39)		probably null	Het

Other mutations in Gimap9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01012:Gimap9	APN	6	48,654,851 (GRCm39)	critical splice donor site	probably null
IGL01568:Gimap9	APN	6	48,654,550 (GRCm39)	missense	probably benign	0.07
R0442:Gimap9	UTSW	6	48,655,000 (GRCm39)	nonsense	probably null
R1354:Gimap9	UTSW	6	48,654,982 (GRCm39)	missense	probably benign	0.24
R2276:Gimap9	UTSW	6	48,654,812 (GRCm39)	missense	probably benign	0.00
R6190:Gimap9	UTSW	6	48,655,285 (GRCm39)	missense	probably damaging	1.00
R6930:Gimap9	UTSW	6	48,654,601 (GRCm39)	missense	probably damaging	1.00
R8819:Gimap9	UTSW	6	48,654,821 (GRCm39)	missense	probably benign	0.09
R8820:Gimap9	UTSW	6	48,654,821 (GRCm39)	missense	probably benign	0.09
R9346:Gimap9	UTSW	6	48,654,492 (GRCm39)	missense	probably damaging	1.00
R9536:Gimap9	UTSW	6	48,654,416 (GRCm39)	start codon destroyed	probably null	1.00
R9559:Gimap9	UTSW	6	48,655,134 (GRCm39)	missense	probably benign	0.13

Predicted Primers

PCR Primer
(F):5'- AACGGTCGCTCTGATCAAGG -3'
(R):5'- AAACAATTTGTGCCGCCTTTC -3'

Sequencing Primer
(F):5'- CAGCCCTGAAGTACATGATCATCTTG -3'
(R):5'- GCCTTTCCTTTTTCTAATTTAGCAG -3'

Posted On

2019-05-15