Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01779:Gm11110'

153880

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm11110

Ensembl Gene

ENSMUSG00000079414

Gene Name

predicted gene 11110

Synonyms

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

IGL01779

Quality Score

Status

Chromosome

Chromosomal Location

57092035-57105942 bp(-) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

C to T at 57102087 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000040412 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039490] [ENSMUST00000112915]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000039490

SMART Domains

Protein: ENSMUSP00000040412
Gene: ENSMUSG00000035678

Domain	Start	End	E-Value	Type
transmembrane domain	83	105	N/A	INTRINSIC
TNF	147	302	1.16e-46	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000112915
AA Change: V72M

SMART Domains

Protein: ENSMUSP00000108537
Gene: ENSMUSG00000079414
AA Change: V72M

Domain	Start	End	E-Value	Type
low complexity region	66	78	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 28 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrl3	A	T	5: 81,387,870	I119F	probably damaging	Het
Akt1	C	T	12: 112,657,169	G286R	probably damaging	Het
Apof	A	G	10: 128,269,477	I167V	probably benign	Het
Arhgap15	A	G	2: 44,065,045	E220G	possibly damaging	Het
Clca3a2	T	A	3: 144,819,378	Y31F	possibly damaging	Het
Clmn	T	C	12: 104,782,140	I383V	probably benign	Het
Cntnap5b	A	G	1: 99,967,339	D112G	probably damaging	Het
Col8a1	A	T	16: 57,628,363	H261Q	unknown	Het
Csmd3	A	T	15: 47,857,894	V1551D	probably benign	Het
Ddx60	G	A	8: 62,017,823	V1450M	possibly damaging	Het
Ethe1	A	T	7: 24,595,009	H79L	probably damaging	Het
Fhdc1	G	A	3: 84,444,735	A1061V	possibly damaging	Het
Hs1bp3	C	T	12: 8,341,945	T349I	probably benign	Het
Ifna16	A	T	4: 88,676,645	I71N	probably damaging	Het
Il18bp	A	G	7: 102,016,795	Y59H	possibly damaging	Het
Kcnt1	T	A	2: 25,900,967	I511N	probably damaging	Het
Mlph	A	G	1: 90,942,950	M528V	probably benign	Het
Olfr646	A	G	7: 104,106,633	D118G	probably damaging	Het
Pprc1	T	A	19: 46,062,202	I52N	probably damaging	Het
Rfx1	T	A	8: 84,092,662		probably benign	Het
Rnf17	A	T	14: 56,462,063	I553F	probably benign	Het
Scaper	A	T	9: 55,892,240	H180Q	probably benign	Het
Slc26a4	C	T	12: 31,528,854		probably benign	Het
Slc30a10	A	T	1: 185,464,179	Q346L	possibly damaging	Het
Stambpl1	A	T	19: 34,240,027	H422L	possibly damaging	Het
Trim67	G	A	8: 124,828,121	G701R	probably damaging	Het
Vipr1	T	C	9: 121,664,630	F249S	probably damaging	Het
Vmn2r117	G	T	17: 23,477,241	D397E	probably benign	Het

Other mutations in Gm11110

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01874:Gm11110	APN	17	57092693	unclassified	probably benign
IGL02744:Gm11110	APN	17	57092693	unclassified	probably benign
R3423:Gm11110	UTSW	17	57103435	unclassified	probably benign
R6888:Gm11110	UTSW	17	57102143	unclassified	probably benign
R8111:Gm11110	UTSW	17	57103427	missense	probably null
R8904:Gm11110	UTSW	17	57103439	missense	unknown
R9687:Gm11110	UTSW	17	57103439	missense	unknown
R9732:Gm11110	UTSW	17	57103382	missense	unknown

Posted On

2014-02-04