Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL03309:Glipr1l1'

416506

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Glipr1l1

Ensembl Gene

ENSMUSG00000020213

Gene Name

GLI pathogenesis-related 1 like 1

Synonyms

1700011E04Rik

Accession Numbers

Is this an essential gene?

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

Stock #

IGL03309

Quality Score

Status

Chromosome

Chromosomal Location

112060189-112078510 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 112072236 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000073302 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073617]

Predicted Effect

probably benign
Transcript: ENSMUST00000073617

SMART Domains

Protein: ENSMUSP00000073302
Gene: ENSMUSG00000020213

Domain	Start	End	E-Value	Type
SCP	40	186	6.52e-50	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadac	A	G	3: 60,039,882	T334A	possibly damaging	Het
Armc9	A	G	1: 86,274,433	E771G	possibly damaging	Het
Cd207	G	T	6: 83,677,753	T16K	possibly damaging	Het
Cd44	C	T	2: 102,814,177	E421K	probably damaging	Het
Cfap221	A	G	1: 119,934,601	Y584H	probably damaging	Het
Clock	A	G	5: 76,231,394		probably null	Het
Clpx	T	G	9: 65,322,692	L474R	probably damaging	Het
Cntd1	T	C	11: 101,284,764	V143A	probably damaging	Het
Cttnbp2	A	G	6: 18,381,036	V877A	probably damaging	Het
Dlx6	G	T	6: 6,867,289	M158I	possibly damaging	Het
Fank1	A	G	7: 133,862,173	T33A	probably damaging	Het
Fbf1	A	G	11: 116,147,811	L828P	probably damaging	Het
Fh1	A	T	1: 175,604,043	S426T	probably benign	Het
Gabrg3	G	T	7: 56,982,685	Q172K	probably damaging	Het
Hypk	T	A	2: 121,458,192	L113*	probably null	Het
Hypk	G	T	2: 121,458,193	L113F	probably damaging	Het
Ipo5	G	A	14: 120,920,004	V85I	probably benign	Het
Kif1a	A	T	1: 93,058,857	Y575*	probably null	Het
Morf4l1	T	A	9: 90,103,745	E60V	probably benign	Het
Olfr655	A	G	7: 104,597,041	F47L	probably benign	Het
Olfr782	A	T	10: 129,351,309	T249S	probably benign	Het
Parp4	A	T	14: 56,587,808	T130S	probably benign	Het
Prkd1	A	G	12: 50,388,424	Y507H	probably damaging	Het
Psme2b	A	C	11: 48,945,799		probably null	Het
Rbm44	T	C	1: 91,168,840		probably null	Het
Rngtt	C	A	4: 33,339,091	R299S	probably damaging	Het
Ros1	A	G	10: 52,118,261	S1308P	possibly damaging	Het
Rpl3l	A	G	17: 24,736,024	K398E	possibly damaging	Het
Scube3	C	T	17: 28,164,357	R374*	probably null	Het
Srcap	A	G	7: 127,530,793	T616A	probably damaging	Het
Stk3	G	A	15: 35,099,551		probably benign	Het
Tas2r124	A	T	6: 132,754,935	D69V	probably benign	Het
Zbtb41	T	A	1: 139,432,078		probably null	Het

Other mutations in Glipr1l1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00467:Glipr1l1	APN	10	112078381	missense	probably benign	0.02
IGL01660:Glipr1l1	APN	10	112072279	missense	probably damaging	0.97
IGL01893:Glipr1l1	APN	10	112076169	missense	probably benign	0.06
IGL02576:Glipr1l1	APN	10	112060319	missense	possibly damaging	0.77
P0031:Glipr1l1	UTSW	10	112060387	missense	probably benign
R0987:Glipr1l1	UTSW	10	112078435	missense	probably benign
R0992:Glipr1l1	UTSW	10	112062325	missense	probably benign
R2136:Glipr1l1	UTSW	10	112060476	missense	probably damaging	1.00
R2248:Glipr1l1	UTSW	10	112062287	missense	probably benign	0.09
R4297:Glipr1l1	UTSW	10	112062347	missense	probably benign	0.05
R4298:Glipr1l1	UTSW	10	112062347	missense	probably benign	0.05
R4569:Glipr1l1	UTSW	10	112062412	missense	probably benign	0.00
R5015:Glipr1l1	UTSW	10	112078374	missense	probably benign	0.00
R5552:Glipr1l1	UTSW	10	112062338	missense	probably benign	0.00
R5629:Glipr1l1	UTSW	10	112078403	missense	possibly damaging	0.90
R6061:Glipr1l1	UTSW	10	112076170	missense	probably benign	0.32
R6237:Glipr1l1	UTSW	10	112060427	nonsense	probably null
R6519:Glipr1l1	UTSW	10	112062248	missense	probably benign	0.02
R6913:Glipr1l1	UTSW	10	112062434	critical splice donor site	probably null
R7621:Glipr1l1	UTSW	10	112060395	missense	probably benign	0.00
R8171:Glipr1l1	UTSW	10	112078384	missense	probably benign	0.01
X0023:Glipr1l1	UTSW	10	112078439	missense	probably damaging	0.98
Z1177:Glipr1l1	UTSW	10	112078390	missense	probably benign	0.00

Posted On

2016-08-02