Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02164:Gpr107'

282569

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gpr107

Ensembl Gene

ENSMUSG00000000194

Gene Name

G protein-coupled receptor 107

Synonyms

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL02164

Quality Score

Status

Chromosome

Chromosomal Location

31042099-31106579 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to A at 31068298 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 253 (Y253*)

Ref Sequence

ENSEMBL: ENSMUSP00000056739 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056433]

AlphaFold

Q8BUV8

Predicted Effect

probably null
Transcript: ENSMUST00000056433
AA Change: Y253*

SMART Domains

Protein: ENSMUSP00000056739
Gene: ENSMUSG00000000194
AA Change: Y253*

Domain	Start	End	E-Value	Type
signal peptide	1	33	N/A	INTRINSIC
Pfam:Lung_7-TM_R	213	504	3e-100	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151991

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000172422

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Homozygous inactivation of this gene causes complete embryonic lethality during organogenesis, associated with reduced expression of genes implicated in the cubilin-megalin multi-ligand endocytic receptor complex. Homozygous null MEFs show defects in receptor-mediated endocytosis and recycling. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5730480H06Rik	T	A	5: 48,537,524 (GRCm39)	V187E	probably benign	Het
Abcc12	T	A	8: 87,254,033 (GRCm39)	D917V	probably damaging	Het
Abhd15	A	T	11: 77,406,840 (GRCm39)	E272D	probably benign	Het
Adat3	T	A	10: 80,442,461 (GRCm39)	S100T	probably benign	Het
Adgrg6	T	C	10: 14,399,299 (GRCm39)		probably benign	Het
Alpl	C	T	4: 137,481,290 (GRCm39)	V121M	probably damaging	Het
Ano1	A	T	7: 144,190,918 (GRCm39)	Y388N	possibly damaging	Het
Arrdc4	C	T	7: 68,389,285 (GRCm39)		probably benign	Het
Asxl2	A	G	12: 3,552,079 (GRCm39)	M1274V	probably benign	Het
Bmt2	G	T	6: 13,628,878 (GRCm39)	N268K	possibly damaging	Het
Bpifb2	C	A	2: 153,725,482 (GRCm39)	L176M	probably damaging	Het
Brd8	C	T	18: 34,735,780 (GRCm39)	S899N	probably damaging	Het
Cd14	T	C	18: 36,858,838 (GRCm39)	R206G	possibly damaging	Het
Cfap65	G	T	1: 74,967,304 (GRCm39)	T215K	possibly damaging	Het
Chd9	T	C	8: 91,659,849 (GRCm39)	S270P	possibly damaging	Het
Cidea	C	T	18: 67,499,581 (GRCm39)	S156L	probably damaging	Het
Col5a3	A	G	9: 20,703,939 (GRCm39)		probably null	Het
Cspg5	T	C	9: 110,080,104 (GRCm39)	V424A	probably damaging	Het
Ctc1	A	G	11: 68,916,922 (GRCm39)	H272R	probably damaging	Het
D5Ertd579e	A	T	5: 36,772,303 (GRCm39)	S697R	probably damaging	Het
Dennd3	T	C	15: 73,416,297 (GRCm39)	S516P	probably benign	Het
Dipk2b	T	A	X: 18,285,192 (GRCm39)	R421*	probably null	Het
Dlgap4	G	A	2: 156,553,059 (GRCm39)	R509H	probably damaging	Het
Dus3l	T	C	17: 57,074,943 (GRCm39)		probably benign	Het
Dync1h1	G	T	12: 110,628,993 (GRCm39)	W4183C	probably damaging	Het
Eif2s3x	A	T	X: 93,248,678 (GRCm39)	M152K	possibly damaging	Het
Epb41l1	C	T	2: 156,336,869 (GRCm39)		probably benign	Het
Ephx2	A	G	14: 66,341,169 (GRCm39)		probably benign	Het
Fabp12	T	A	3: 10,311,075 (GRCm39)	Y129F	probably damaging	Het
Fat3	A	G	9: 15,942,720 (GRCm39)		probably benign	Het
Fat4	T	C	3: 39,050,354 (GRCm39)		probably null	Het
Gnb1	T	A	4: 155,641,631 (GRCm39)		probably null	Het
Grb10	C	T	11: 11,893,962 (GRCm39)	E320K	probably damaging	Het
Gucy2g	G	T	19: 55,226,455 (GRCm39)	H154N	probably benign	Het
H2bl1	T	C	13: 99,120,715 (GRCm39)	K104E	probably damaging	Het
Hemk1	T	A	9: 107,208,735 (GRCm39)	H154L	probably benign	Het
Hk2	A	T	6: 82,720,920 (GRCm39)		probably null	Het
Htr5a	A	G	5: 28,047,463 (GRCm39)	N6S	probably damaging	Het
Htra3	T	C	5: 35,810,410 (GRCm39)	D424G	probably benign	Het
Ift52	A	G	2: 162,867,384 (GRCm39)		probably null	Het
Igdcc4	A	G	9: 65,032,064 (GRCm39)		probably benign	Het
Itpr1	A	G	6: 108,366,444 (GRCm39)	K124E	probably benign	Het
Kcnc2	T	A	10: 112,291,590 (GRCm39)	N259K	possibly damaging	Het
Kics2	A	G	10: 121,586,675 (GRCm39)	Y194C	probably damaging	Het
Lmod2	A	T	6: 24,603,909 (GRCm39)	I295F	possibly damaging	Het
Lrp1	T	C	10: 127,399,536 (GRCm39)	E2324G	probably benign	Het
Lss	T	C	10: 76,372,094 (GRCm39)	S150P	probably damaging	Het
Macf1	T	C	4: 123,374,065 (GRCm39)	N1515S	probably benign	Het
Mapk11	T	C	15: 89,029,651 (GRCm39)		probably null	Het
Mc3r	T	A	2: 172,091,314 (GRCm39)	F179I	probably damaging	Het
Mtmr9	T	A	14: 63,767,737 (GRCm39)	N291Y	probably damaging	Het
Myo1h	T	C	5: 114,472,157 (GRCm39)	F396L	probably damaging	Het
Nek2	A	G	1: 191,559,416 (GRCm39)	K307R	probably benign	Het
Or12d2	C	A	17: 37,624,578 (GRCm39)	M232I	probably benign	Het
Osmr	G	A	15: 6,871,529 (GRCm39)	T296I	probably damaging	Het
Pcdhb11	T	G	18: 37,556,412 (GRCm39)	S581A	probably benign	Het
Pfkp	C	T	13: 6,647,951 (GRCm39)	V542M	probably damaging	Het
Pmpca	C	T	2: 26,285,581 (GRCm39)	S519L	probably benign	Het
Ptgds	A	T	2: 25,359,124 (GRCm39)	Y44N	probably damaging	Het
Raly	T	A	2: 154,701,849 (GRCm39)	Y116*	probably null	Het
Rock2	A	G	12: 17,015,530 (GRCm39)	D809G	probably damaging	Het
Sgsm2	T	G	11: 74,756,242 (GRCm39)	N369T	possibly damaging	Het
Slc6a15	A	G	10: 103,254,083 (GRCm39)	D673G	probably benign	Het
Spire2	A	T	8: 124,059,703 (GRCm39)	D67V	probably damaging	Het
St7l	T	C	3: 104,829,597 (GRCm39)		probably null	Het
Stau2	A	G	1: 16,416,052 (GRCm39)	L469P	probably damaging	Het
Tefm	A	G	11: 80,030,915 (GRCm39)	L107S	probably damaging	Het
Ticam1	A	T	17: 56,577,019 (GRCm39)	V692D	unknown	Het
Tipin	T	A	9: 64,201,631 (GRCm39)	D143E	probably damaging	Het
Tmem132c	C	A	5: 127,613,441 (GRCm39)	T448K	probably damaging	Het
Trav8-1	A	T	14: 53,707,213 (GRCm39)	M1L	unknown	Het
Ttn	C	A	2: 76,569,141 (GRCm39)	V27251F	probably damaging	Het
Uvrag	A	T	7: 98,653,896 (GRCm39)	C31*	probably null	Het
Zap70	T	C	1: 36,810,267 (GRCm39)	Y126H	probably damaging	Het
Zfp644	A	G	5: 106,785,965 (GRCm39)	V194A	probably benign	Het
Zfp663	C	T	2: 165,200,968 (GRCm39)	W22*	probably null	Het

Other mutations in Gpr107

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00586:Gpr107	APN	2	31,062,006 (GRCm39)	missense	probably benign	0.00
IGL00828:Gpr107	APN	2	31,067,795 (GRCm39)	critical splice acceptor site	probably null
IGL01138:Gpr107	APN	2	31,062,028 (GRCm39)	missense	probably benign	0.06
IGL01589:Gpr107	APN	2	31,057,163 (GRCm39)	splice site	probably benign
IGL02176:Gpr107	APN	2	31,058,858 (GRCm39)	missense	probably benign	0.01
IGL02190:Gpr107	APN	2	31,068,332 (GRCm39)	missense	probably damaging	1.00
IGL02234:Gpr107	APN	2	31,067,845 (GRCm39)	missense	probably damaging	1.00
IGL02838:Gpr107	APN	2	31,104,329 (GRCm39)	missense	probably benign	0.01
PIT4142001:Gpr107	UTSW	2	31,057,083 (GRCm39)	missense	probably benign	0.18
R0613:Gpr107	UTSW	2	31,068,297 (GRCm39)	missense	probably damaging	1.00
R0630:Gpr107	UTSW	2	31,104,309 (GRCm39)	missense	possibly damaging	0.89
R0735:Gpr107	UTSW	2	31,062,006 (GRCm39)	missense	probably benign	0.00
R1263:Gpr107	UTSW	2	31,068,267 (GRCm39)	missense	possibly damaging	0.82
R1572:Gpr107	UTSW	2	31,057,037 (GRCm39)	missense	probably damaging	1.00
R1675:Gpr107	UTSW	2	31,057,063 (GRCm39)	missense	possibly damaging	0.77
R2421:Gpr107	UTSW	2	31,075,541 (GRCm39)	missense	probably damaging	1.00
R4569:Gpr107	UTSW	2	31,097,677 (GRCm39)	splice site	probably benign
R4647:Gpr107	UTSW	2	31,100,513 (GRCm39)	missense	probably damaging	1.00
R4656:Gpr107	UTSW	2	31,104,261 (GRCm39)	missense	probably damaging	1.00
R4844:Gpr107	UTSW	2	31,078,686 (GRCm39)	splice site	probably null
R5385:Gpr107	UTSW	2	31,104,263 (GRCm39)	missense	probably benign	0.01
R5416:Gpr107	UTSW	2	31,075,560 (GRCm39)	missense	probably damaging	1.00
R5562:Gpr107	UTSW	2	31,042,375 (GRCm39)	missense	probably damaging	1.00
R5564:Gpr107	UTSW	2	31,042,375 (GRCm39)	missense	probably damaging	1.00
R5652:Gpr107	UTSW	2	31,075,601 (GRCm39)	missense	probably benign	0.16
R6075:Gpr107	UTSW	2	31,042,384 (GRCm39)	missense	probably benign	0.05
R7186:Gpr107	UTSW	2	31,042,371 (GRCm39)	start codon destroyed	possibly damaging	0.59
R7511:Gpr107	UTSW	2	31,068,358 (GRCm39)	missense	probably benign	0.03
R7587:Gpr107	UTSW	2	31,058,838 (GRCm39)	missense	probably benign
R7946:Gpr107	UTSW	2	31,078,716 (GRCm39)	missense	probably damaging	1.00
R8108:Gpr107	UTSW	2	31,074,881 (GRCm39)	missense	probably damaging	1.00
R8518:Gpr107	UTSW	2	31,066,939 (GRCm39)	missense	probably benign
R9320:Gpr107	UTSW	2	31,078,728 (GRCm39)	missense	possibly damaging	0.93
R9661:Gpr107	UTSW	2	31,057,075 (GRCm39)	missense	probably benign	0.06

Posted On

2015-04-16