Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01021:Eif1ad9'

53917

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Eif1ad9

Ensembl Gene

ENSMUSG00000069276

Gene Name

eukaryotic translation initiation factor 1A domain containing 9

Synonyms

Gm10264, EG271022

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01021

Quality Score

Status

Chromosome

Chromosomal Location

88296024-88296452 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 88296042 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Arginine at position 7 (G7R)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000091715
AA Change: G7R

SMART Domains

Protein: ENSMUSP00000137429
Gene: ENSMUSG00000069276
AA Change: G7R

Domain	Start	End	E-Value	Type
low complexity region	2	17	N/A	INTRINSIC
eIF1a	26	108	2.51e-44	SMART
low complexity region	123	141	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220589

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222597

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
4930533L02Rik	T	C	7: 124,917,848 (GRCm39)	V80A	unknown	Het
Adam28	A	G	14: 68,879,563 (GRCm39)	S162P	probably benign	Het
Adamts14	G	T	10: 61,061,152 (GRCm39)	S426Y	probably damaging	Het
Ankrd24	A	G	10: 81,470,995 (GRCm39)		probably null	Het
B3galt5	C	A	16: 96,116,923 (GRCm39)	H185Q	probably benign	Het
Bod1l	A	G	5: 41,995,516 (GRCm39)		probably benign	Het
Ddx46	T	A	13: 55,814,145 (GRCm39)	Y700*	probably null	Het
Dph7	T	G	2: 24,861,935 (GRCm39)		probably null	Het
Fcho1	A	T	8: 72,166,167 (GRCm39)	Y354*	probably null	Het
Fnbp4	A	G	2: 90,608,013 (GRCm39)	M912V	probably benign	Het
Fpgt	T	A	3: 154,797,129 (GRCm39)	E42V	possibly damaging	Het
Frmd3	A	G	4: 73,992,357 (GRCm39)	I75V	possibly damaging	Het
Gm3278	G	T	14: 16,082,261 (GRCm39)	V159L	possibly damaging	Het
Gmds	T	C	13: 32,311,013 (GRCm39)	I205V	possibly damaging	Het
Gprin1	T	A	13: 54,888,182 (GRCm39)	S31C	probably damaging	Het
Igkv4-68	T	C	6: 69,281,865 (GRCm39)	E102G	probably damaging	Het
Itga1	T	A	13: 115,133,536 (GRCm39)	Y458F	probably benign	Het
Kif20b	T	C	19: 34,915,660 (GRCm39)	V479A	possibly damaging	Het
Megf8	T	A	7: 25,037,799 (GRCm39)	W772R	probably benign	Het
Muc6	T	A	7: 141,217,075 (GRCm39)	I2533F	possibly damaging	Het
Npas3	T	C	12: 54,050,343 (GRCm39)	S258P	probably damaging	Het
Padi3	T	C	4: 140,523,645 (GRCm39)		probably benign	Het
Pmfbp1	G	T	8: 110,264,625 (GRCm39)	R897L	possibly damaging	Het
Rims1	A	T	1: 22,525,701 (GRCm39)	W407R	probably damaging	Het
Scnn1b	G	T	7: 121,517,259 (GRCm39)	D632Y	probably damaging	Het
Tas2r123	G	A	6: 132,824,369 (GRCm39)	A89T	probably benign	Het
Tbk1	T	C	10: 121,387,177 (GRCm39)	E706G	probably benign	Het
Thra	A	G	11: 98,653,754 (GRCm39)	D195G	possibly damaging	Het
Tpp2	T	A	1: 43,973,347 (GRCm39)	Y33*	probably null	Het
Usp6nl	T	A	2: 6,429,198 (GRCm39)	M220K	probably damaging	Het
Vmn2r112	C	T	17: 22,837,885 (GRCm39)	T782I	probably damaging	Het
Zbtb43	T	C	2: 33,343,771 (GRCm39)	T485A	probably benign	Het
Zfat	T	C	15: 68,042,015 (GRCm39)	I840V	possibly damaging	Het

Other mutations in Eif1ad9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0562:Eif1ad9	UTSW	12	88,296,436 (GRCm39)	missense	unknown
R1158:Eif1ad9	UTSW	12	88,296,438 (GRCm39)	missense	unknown
R1840:Eif1ad9	UTSW	12	88,296,181 (GRCm39)	missense	probably benign	0.06
R5217:Eif1ad9	UTSW	12	88,296,196 (GRCm39)	missense	probably benign	0.08

Posted On

2013-06-28