Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02940:Gm9944'

364462

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm9944

Ensembl Gene

ENSMUSG00000095213

Gene Name

predicted gene 9944

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.075) question?

Stock #

IGL02940

Quality Score

Status

Chromosome

Chromosomal Location

144177790-144180211 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 144179709 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000101375 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000105749] [ENSMUST00000177649]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000105749

SMART Domains

Protein: ENSMUSP00000101375
Gene: ENSMUSG00000078507

Domain	Start	End	E-Value	Type
transmembrane domain	2	24	N/A	INTRINSIC
Pfam:Abhydrolase_3	116	263	1.8e-33	PFAM
Pfam:Abhydrolase_3	302	382	6.9e-12	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000177649
AA Change: N60S

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
Adgrg3	T	A	8: 95,760,084 (GRCm39)	V101D	possibly damaging	Het
Brca1	T	C	11: 101,380,738 (GRCm39)	D1765G	probably benign	Het
Cadps2	T	C	6: 23,496,808 (GRCm39)	K450R	probably benign	Het
Cc2d2a	A	T	5: 43,885,636 (GRCm39)		probably null	Het
Dbh	A	G	2: 27,058,321 (GRCm39)	Y163C	probably damaging	Het
Drc7	T	A	8: 95,800,925 (GRCm39)	I649N	probably damaging	Het
Dst	G	A	1: 34,328,668 (GRCm39)	A7097T	probably benign	Het
Fbxo46	A	G	7: 18,869,537 (GRCm39)	H52R	probably benign	Het
Lsm14a	G	T	7: 34,070,596 (GRCm39)	S100*	probably null	Het
Mrc2	C	T	11: 105,231,997 (GRCm39)	R850C	probably damaging	Het
Musk	A	G	4: 58,373,364 (GRCm39)	D763G	probably damaging	Het
Ncan	C	T	8: 70,562,735 (GRCm39)	V508I	probably benign	Het
Or4k35	A	T	2: 111,100,073 (GRCm39)	L213Q	probably damaging	Het
Pgls	C	T	8: 72,046,741 (GRCm39)	S18L	probably damaging	Het
Phf20l1	A	G	15: 66,467,000 (GRCm39)	T98A	probably damaging	Het
Ppp1r36dn	A	C	12: 76,497,944 (GRCm39)		noncoding transcript	Het
Prdm13	T	A	4: 21,683,421 (GRCm39)	K180*	probably null	Het
Rai1	T	C	11: 60,077,844 (GRCm39)	V636A	probably benign	Het
Setd5	T	C	6: 113,091,899 (GRCm39)	F240S	possibly damaging	Het
Slco1a5	A	G	6: 142,187,731 (GRCm39)	L536P	probably damaging	Het
Stk39	C	T	2: 68,051,243 (GRCm39)		probably null	Het
Tenm2	T	C	11: 35,932,471 (GRCm39)	T1707A	probably damaging	Het
Tlr2	A	T	3: 83,743,781 (GRCm39)	D767E	probably benign	Het
Tlr7	C	T	X: 166,090,830 (GRCm39)	V219I	probably benign	Het
Tmprss7	A	G	16: 45,476,818 (GRCm39)	S815P	probably damaging	Het
Trav12-1	T	A	14: 53,776,017 (GRCm39)	W57R	probably damaging	Het
Uxt	T	C	X: 20,826,025 (GRCm39)	E66G	possibly damaging	Het
Vmn2r45	A	T	7: 8,475,369 (GRCm39)	M553K	probably damaging	Het
Vmn2r67	A	G	7: 84,785,951 (GRCm39)	W685R	probably benign	Het
Vstm5	A	C	9: 15,168,962 (GRCm39)	D144A	probably damaging	Het
Zfp592	A	G	7: 80,674,575 (GRCm39)	H513R	probably damaging	Het
Zfp830	T	A	11: 82,656,295 (GRCm39)		probably benign	Het
Zfp990	A	G	4: 145,261,492 (GRCm39)		probably null	Het

Other mutations in Gm9944

Allele	Source	Chr	Coord	Type	Predicted Effect
R1378:Gm9944	UTSW	4	144,179,773 (GRCm39)	unclassified	probably benign
R1707:Gm9944	UTSW	4	144,179,833 (GRCm39)	unclassified	probably benign
R3552:Gm9944	UTSW	4	144,179,613 (GRCm39)	unclassified	probably benign
R4986:Gm9944	UTSW	4	144,179,760 (GRCm39)	unclassified	probably benign
R5988:Gm9944	UTSW	4	144,179,775 (GRCm39)	unclassified	probably benign
R8728:Gm9944	UTSW	4	144,179,601 (GRCm39)	missense	unknown
R9129:Gm9944	UTSW	4	144,179,763 (GRCm39)	missense	unknown

Posted On

2015-12-18