Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01388:Gm6802'

79127

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm6802

Ensembl Gene

ENSMUSG00000059229

Gene Name

predicted gene 6802

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.149) question?

Stock #

IGL01388

Quality Score

Status

Chromosome

Chromosomal Location

19540309-19542291 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to G at 19540546 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000167843

SMART Domains

Protein: ENSMUSP00000132665
Gene: ENSMUSG00000059229

Domain	Start	End	E-Value	Type
low complexity region	45	62	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000186566

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
Arhgap28	T	G	17: 68,160,034 (GRCm39)		probably benign	Het
Ces2b	A	C	8: 105,561,236 (GRCm39)		probably benign	Het
Col20a1	T	A	2: 180,645,264 (GRCm39)	M924K	probably benign	Het
Commd4	G	A	9: 57,063,273 (GRCm39)		probably benign	Het
Ctnna3	A	G	10: 63,339,886 (GRCm39)	E24G	possibly damaging	Het
Cyp2a22	C	T	7: 26,637,217 (GRCm39)	R189H	probably benign	Het
Gapdhrt	T	C	14: 11,281,836 (GRCm38)	D33G	probably damaging	Het
Gm20426	T	C	6: 90,155,694 (GRCm39)		probably benign	Het
Igkv8-21	A	G	6: 70,292,153 (GRCm39)	S30P	probably benign	Het
Lig4	A	G	8: 10,023,586 (GRCm39)	Y65H	probably damaging	Het
Mpzl1	T	C	1: 165,433,336 (GRCm39)	D105G	probably benign	Het
Myo10	A	G	15: 25,736,703 (GRCm39)	I451V	possibly damaging	Het
Nos2	G	T	11: 78,848,278 (GRCm39)	V1062L	probably damaging	Het
Oas2	A	G	5: 120,886,657 (GRCm39)	S170P	probably damaging	Het
Or1j19	G	T	2: 36,677,367 (GRCm39)	V277L	probably benign	Het
Or5w11	T	A	2: 87,458,973 (GRCm39)	H55Q	probably benign	Het
Or8b3b	A	T	9: 38,584,379 (GRCm39)	Y120*	probably null	Het
Or8g37	A	G	9: 39,731,298 (GRCm39)	D121G	probably damaging	Het
Pcdh7	T	C	5: 57,877,546 (GRCm39)	L367P	probably damaging	Het
Pde3a	A	G	6: 141,405,464 (GRCm39)	T439A	probably damaging	Het
Plekhm2	T	C	4: 141,369,312 (GRCm39)	Y124C	probably damaging	Het
Ppp4r4	T	A	12: 103,543,108 (GRCm39)	W155R	probably damaging	Het
Prl7c1	C	A	13: 27,960,198 (GRCm39)	A115S	probably damaging	Het
Psg25	T	C	7: 18,263,590 (GRCm39)	I78V	possibly damaging	Het
Ptpn9	T	A	9: 56,944,002 (GRCm39)	V292E	probably benign	Het
Ptprs	G	A	17: 56,728,261 (GRCm39)	R908C	probably damaging	Het
Rps6ka1	C	T	4: 133,599,275 (GRCm39)	V51I	probably damaging	Het
Scube1	T	C	15: 83,504,332 (GRCm39)	I492V	probably benign	Het
Trappc2	G	A	X: 165,232,775 (GRCm39)		probably benign	Het
Ubr4	T	C	4: 139,187,554 (GRCm39)	V739A	possibly damaging	Het
Unc79	T	C	12: 103,136,018 (GRCm39)		probably benign	Het
Vmn2r27	G	A	6: 124,200,791 (GRCm39)	P389S	possibly damaging	Het
Wipi2	T	A	5: 142,646,798 (GRCm39)	F212I	possibly damaging	Het

Other mutations in Gm6802

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R3411:Gm6802	UTSW	12	19,540,621 (GRCm39)	exon	noncoding transcript

Posted On

2013-11-05