Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03390:Gm7367'

421016

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm7367

Ensembl Gene

ENSMUSG00000047370

Gene Name

predicted pseudogene 7367

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.211) question?

Stock #

IGL03390

Quality Score

Status

Chromosome

Chromosomal Location

59805357-59805848 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 59805517 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: ENSMUST00000057611

SMART Domains

Protein: ENSMUSP00000053975
Gene: ENSMUSG00000047370

Domain	Start	End	E-Value	Type
Pfam:UBA_4	11	53	1e-11	PFAM

Meta Mutation Damage Score

0.0690

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 34 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810004N23Rik	A	G	8: 125,566,564 (GRCm39)		probably benign	Het
Ccdc18	A	G	5: 108,359,997 (GRCm39)	Y1127C	probably damaging	Het
Cdnf	T	A	2: 3,524,863 (GRCm39)	L134*	probably null	Het
Col11a1	A	G	3: 113,883,902 (GRCm39)	D257G	unknown	Het
Cthrc1	T	A	15: 38,940,529 (GRCm39)	I44N	probably benign	Het
Dlec1	T	C	9: 118,952,288 (GRCm39)	Y545H	probably benign	Het
Drosha	T	G	15: 12,885,069 (GRCm39)		probably null	Het
Ebf2	A	G	14: 67,661,558 (GRCm39)	N562S	probably benign	Het
Fem1b	G	A	9: 62,704,246 (GRCm39)	A338V	probably benign	Het
Gga3	A	T	11: 115,477,820 (GRCm39)		probably null	Het
Gm7247	A	T	14: 51,760,914 (GRCm39)	H161L	probably benign	Het
Inpp5a	T	G	7: 139,105,664 (GRCm39)	V213G	probably benign	Het
Kcns3	T	C	12: 11,141,233 (GRCm39)	T489A	probably benign	Het
Kifc3	G	A	8: 95,835,241 (GRCm39)	A211V	probably damaging	Het
Krt71	T	C	15: 101,642,987 (GRCm39)	D507G	possibly damaging	Het
Lama5	T	C	2: 179,849,011 (GRCm39)	Y224C	probably damaging	Het
Lrrc37a	A	G	11: 103,386,857 (GRCm39)	L2421P	unknown	Het
Mtch2	C	T	2: 90,689,894 (GRCm39)	T205I	probably benign	Het
Or1o11	T	C	17: 37,757,255 (GRCm39)	V281A	probably benign	Het
Prkdc	T	A	16: 15,488,490 (GRCm39)	C537*	probably null	Het
Prl2a1	T	C	13: 27,985,699 (GRCm39)	V5A	probably benign	Het
Prob1	T	C	18: 35,787,192 (GRCm39)	Y354C	probably benign	Het
Rimklb	C	T	6: 122,433,280 (GRCm39)	S347N	possibly damaging	Het
Rnase2a	T	C	14: 51,492,945 (GRCm39)	D140G	probably damaging	Het
Ryr2	G	A	13: 11,787,302 (GRCm39)	P1017S	probably benign	Het
Slc3a1	A	G	17: 85,340,205 (GRCm39)	D209G	probably damaging	Het
Sntn	T	A	14: 13,682,205 (GRCm38)		probably benign	Het
Tal2	G	T	4: 53,785,994 (GRCm39)	L58F	probably damaging	Het
Trim39	T	C	17: 36,571,463 (GRCm39)	K432E	probably damaging	Het
Trmt5	A	T	12: 73,329,501 (GRCm39)	M219K	probably benign	Het
Vmn2r3	T	A	3: 64,182,767 (GRCm39)	I311L	possibly damaging	Het
Wfdc17	A	T	11: 83,595,611 (GRCm39)		probably benign	Het
Zbtb6	T	G	2: 37,319,584 (GRCm39)	I115L	probably damaging	Het
Zfp750	A	T	11: 121,402,770 (GRCm39)	C659*	probably null	Het

Other mutations in Gm7367

Allele	Source	Chr	Coord	Type	Predicted Effect
R4214:Gm7367	UTSW	7	59,805,517 (GRCm39)	exon	noncoding transcript
R4332:Gm7367	UTSW	7	59,805,364 (GRCm39)	exon	noncoding transcript
R5700:Gm7367	UTSW	7	59,805,510 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02