Mutagenetix > Incidental Mutation

Incidental Mutation 'R0674:Gml'

61573

Institutional Source

Beutler Lab

Gene Symbol

Gml

Ensembl Gene

ENSMUSG00000068349

Gene Name

glycosylphosphatidylinositol anchored molecule like

Synonyms

EG625599

MMRRC Submission

038859-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R0674 (G1)

Quality Score

138

Status

Validated

Chromosome

Chromosomal Location

74685301-74690664 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 74685709 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 92 (T92I)

Ref Sequence

ENSEMBL: ENSMUSP00000128174 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096400] [ENSMUST00000164026] [ENSMUST00000185253]

AlphaFold

E9PX31

Predicted Effect

probably damaging
Transcript: ENSMUST00000096400
AA Change: T92I

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000094131
Gene: ENSMUSG00000068349
AA Change: T92I

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
LU	47	141	2.3e-5	SMART
low complexity region	162	175	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000164026
AA Change: T92I

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000128174
Gene: ENSMUSG00000068349
AA Change: T92I

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
LU	47	141	2.3e-5	SMART
low complexity region	162	175	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000185253
AA Change: T92I

PolyPhen 2 Score 0.777 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000140245
Gene: ENSMUSG00000068349
AA Change: T92I

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:UPAR_LY6	49	104	3.8e-3	PFAM

Meta Mutation Damage Score

0.2759

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.3%
20x: 90.4%

Validation Efficiency

97% (124/128)

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adar	A	G	3: 89,657,130 (GRCm39)		probably benign	Het
Adgrl2	A	T	3: 148,543,315 (GRCm39)	M803K	possibly damaging	Het
Atp13a5	T	C	16: 29,067,102 (GRCm39)		probably benign	Het
Atp2a3	T	C	11: 72,872,711 (GRCm39)	I753T	probably damaging	Het
Bace2	G	A	16: 97,237,949 (GRCm39)	V467M	possibly damaging	Het
Bltp1	T	A	3: 37,098,775 (GRCm39)	V1134E	possibly damaging	Het
Ccser2	A	G	14: 36,640,548 (GRCm39)	C11R	possibly damaging	Het
Cd2ap	T	A	17: 43,156,283 (GRCm39)	I85F	possibly damaging	Het
Cd2bp2	C	T	7: 126,794,008 (GRCm39)	E94K	probably damaging	Het
Chrna3	C	A	9: 54,922,456 (GRCm39)	A451S	probably damaging	Het
Cmya5	C	A	13: 93,229,299 (GRCm39)	V1930F	probably damaging	Het
Csmd1	T	C	8: 16,050,550 (GRCm39)	T2229A	probably benign	Het
Csrnp2	A	T	15: 100,385,872 (GRCm39)	L122H	probably damaging	Het
Cyp11b2	G	A	15: 74,727,393 (GRCm39)	P96L	probably damaging	Het
Ddr1	G	T	17: 36,000,561 (GRCm39)	S368*	probably null	Het
E2f1	T	C	2: 154,406,029 (GRCm39)	K115E	probably damaging	Het
Erlec1	A	T	11: 30,885,073 (GRCm39)		probably benign	Het
Fus	T	A	7: 127,571,948 (GRCm39)		probably benign	Het
Herc1	T	C	9: 66,408,474 (GRCm39)	S4567P	probably damaging	Het
Iglc2	A	G	16: 19,017,591 (GRCm39)	S5P	probably benign	Het
Itgam	T	C	7: 127,715,390 (GRCm39)	V1028A	possibly damaging	Het
Krt222	T	A	11: 99,127,086 (GRCm39)	N178I	probably benign	Het
Krt81	C	A	15: 101,361,508 (GRCm39)	R24L	possibly damaging	Het
Luzp1	C	T	4: 136,270,768 (GRCm39)	T997I	possibly damaging	Het
Maml1	G	T	11: 50,148,885 (GRCm39)	Q952K	probably benign	Het
Map2	A	G	1: 66,452,361 (GRCm39)	E499G	probably damaging	Het
Map4k4	A	T	1: 40,042,975 (GRCm39)	H118L	probably damaging	Het
Myzap	T	C	9: 71,422,426 (GRCm39)	D382G	probably damaging	Het
Naip5	T	C	13: 100,359,707 (GRCm39)	T510A	probably benign	Het
Nek6	G	C	2: 38,448,916 (GRCm39)	G95R	possibly damaging	Het
Nphp3	T	C	9: 103,913,481 (GRCm39)		probably null	Het
Nr1d2	T	C	14: 18,215,086 (GRCm38)	S309G	probably benign	Het
Nrcam	A	T	12: 44,611,105 (GRCm39)	I570F	probably benign	Het
Oas1d	T	C	5: 121,058,049 (GRCm39)	I331T	probably benign	Het
Or2h2c	G	C	17: 37,422,347 (GRCm39)	L176V	probably benign	Het
Or4f14	A	T	2: 111,743,018 (GRCm39)	F86I	probably benign	Het
Or51b6	T	C	7: 103,556,462 (GRCm39)	V272A	probably benign	Het
Pex5l	A	T	3: 33,006,765 (GRCm39)	W535R	probably damaging	Het
Pisd	C	T	5: 32,931,781 (GRCm39)	R202H	probably benign	Het
Plxna2	A	G	1: 194,331,783 (GRCm39)	N403S	probably benign	Het
Prdm12	A	G	2: 31,533,924 (GRCm39)	I180M	probably benign	Het
Prpf6	A	G	2: 181,273,767 (GRCm39)	T304A	probably benign	Het
Ptprm	G	A	17: 67,498,336 (GRCm39)	T35I	possibly damaging	Het
Ptx3	T	A	3: 66,132,148 (GRCm39)	I223N	probably damaging	Het
Pygb	G	A	2: 150,657,054 (GRCm39)		probably null	Het
Qrsl1	A	G	10: 43,771,997 (GRCm39)		probably benign	Het
Rad51ap2	T	C	12: 11,508,818 (GRCm39)		probably null	Het
Ralbp1	C	T	17: 66,159,748 (GRCm39)	R505H	probably benign	Het
Rimbp3	T	C	16: 17,030,601 (GRCm39)	S1342P	probably benign	Het
Slc22a14	C	A	9: 119,007,608 (GRCm39)	R267L	probably damaging	Het
Slco6c1	T	A	1: 97,032,498 (GRCm39)		probably benign	Het
Tcp1	T	C	17: 13,142,131 (GRCm39)	I375T	probably damaging	Het
Tiparp	T	C	3: 65,460,586 (GRCm39)	I525T	probably benign	Het
Tjp2	A	G	19: 24,108,680 (GRCm39)	L144P	probably benign	Het
Tssk2	A	G	16: 17,716,930 (GRCm39)	D111G	probably benign	Het
Ttn	T	C	2: 76,775,823 (GRCm39)	T1740A	possibly damaging	Het
Vmn2r102	T	A	17: 19,898,129 (GRCm39)	D381E	probably benign	Het
Vsig10	C	T	5: 117,481,911 (GRCm39)	T367M	probably damaging	Het
Wnt11	T	C	7: 98,495,735 (GRCm39)	C80R	probably damaging	Het
Zar1	T	A	5: 72,737,643 (GRCm39)		probably null	Het
Zfp52	A	T	17: 21,782,108 (GRCm39)	H652L	probably damaging	Het
Zpr1	T	A	9: 46,186,747 (GRCm39)	L194Q	probably damaging	Het

Other mutations in Gml

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01113:Gml	APN	15	74,685,576 (GRCm39)	missense	probably benign	0.00
IGL01161:Gml	APN	15	74,685,688 (GRCm39)	missense	probably damaging	1.00
IGL02415:Gml	APN	15	74,688,289 (GRCm39)	nonsense	probably null
R1716:Gml	UTSW	15	74,685,665 (GRCm39)	missense	possibly damaging	0.81
R1757:Gml	UTSW	15	74,685,462 (GRCm39)	unclassified	probably benign
R1827:Gml	UTSW	15	74,688,280 (GRCm39)	missense	probably benign	0.00
R1941:Gml	UTSW	15	74,689,020 (GRCm39)	missense	probably damaging	0.99
R3783:Gml	UTSW	15	74,685,521 (GRCm39)	missense	probably damaging	0.98
R4007:Gml	UTSW	15	74,685,548 (GRCm39)	missense	possibly damaging	0.59
R5326:Gml	UTSW	15	74,688,299 (GRCm39)	missense	probably damaging	1.00
R7378:Gml	UTSW	15	74,688,970 (GRCm39)	missense	possibly damaging	0.89
R7790:Gml	UTSW	15	74,685,462 (GRCm39)	unclassified	probably benign
R8298:Gml	UTSW	15	74,685,541 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAGGTCAGTATGATGCTGGAGAGG -3'
(R):5'- TGGGCACAGAGCCAAAACTCAGTC -3'

Sequencing Primer
(F):5'- TCACAGCTCTAGCAATTACCTC -3'
(R):5'- TTCGTGAGTCTAAGAAGTCAACTGG -3'

Posted On

2013-07-30