Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01625:Gm8127'

92776

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm8127

Ensembl Gene

ENSMUSG00000090713

Gene Name

predicted gene 8127

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01625

Quality Score

Status

Chromosome

Chromosomal Location

43145769-43151289 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to G at 43148520 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000127788 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000163655]

AlphaFold

E9Q0P0

Predicted Effect

probably benign
Transcript: ENSMUST00000163655

SMART Domains

Protein: ENSMUSP00000127788
Gene: ENSMUSG00000090713

Domain	Start	End	E-Value	Type
coiled coil region	52	74	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000228505

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000228840

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700018F24Rik	T	A	5: 144,979,957 (GRCm39)	H37Q	possibly damaging	Het
Akr1c19	T	A	13: 4,283,816 (GRCm39)	I16N	probably damaging	Het
Arpc1b	T	C	5: 145,058,555 (GRCm39)		probably null	Het
Bzw1	A	G	1: 58,440,599 (GRCm39)	T191A	probably benign	Het
Cacna1h	G	A	17: 25,604,686 (GRCm39)	T1209I	possibly damaging	Het
Cacna1h	T	C	17: 25,602,459 (GRCm39)	D1523G	probably damaging	Het
Cdc20b	T	C	13: 113,196,319 (GRCm39)	L148P	possibly damaging	Het
Cubn	A	G	2: 13,311,085 (GRCm39)	F3147L	possibly damaging	Het
Dagla	A	G	19: 10,228,566 (GRCm39)		probably benign	Het
Dnah9	T	C	11: 65,935,471 (GRCm39)	N1983D	probably damaging	Het
Fbxw10	G	A	11: 62,750,853 (GRCm39)	D479N	probably damaging	Het
Fer	A	T	17: 64,344,621 (GRCm39)	Q630L	probably damaging	Het
Gbp5	A	G	3: 142,208,789 (GRCm39)	N111D	probably damaging	Het
Heatr1	T	A	13: 12,428,409 (GRCm39)	N814K	probably damaging	Het
Iba57	G	A	11: 59,049,775 (GRCm39)	R191W	probably damaging	Het
Itgae	C	A	11: 73,010,263 (GRCm39)	F584L	probably benign	Het
Kdm5b	A	G	1: 134,545,706 (GRCm39)	K956E	possibly damaging	Het
Muc4	C	T	16: 32,575,918 (GRCm39)		probably benign	Het
Mybpc2	T	C	7: 44,166,337 (GRCm39)	K218E	possibly damaging	Het
Pcdh10	T	C	3: 45,333,832 (GRCm39)	S49P	probably damaging	Het
Prss3b	A	C	6: 41,009,882 (GRCm39)	S151A	probably benign	Het
Rai14	T	C	15: 10,572,460 (GRCm39)	D889G	probably benign	Het
Rbpjl	A	G	2: 164,249,705 (GRCm39)	K102R	possibly damaging	Het
Retreg2	A	G	1: 75,121,359 (GRCm39)		probably benign	Het
Rfc4	A	T	16: 22,934,573 (GRCm39)	L149Q	probably damaging	Het
Rft1	T	A	14: 30,398,853 (GRCm39)	D274E	possibly damaging	Het
Rlf	A	T	4: 121,045,457 (GRCm39)	S143R	possibly damaging	Het
Rptn	T	A	3: 93,305,201 (GRCm39)	S845T	probably benign	Het
Slamf8	C	A	1: 172,410,049 (GRCm39)	D267Y	probably damaging	Het
Smoc2	C	T	17: 14,545,876 (GRCm39)	S55L	probably damaging	Het
Sptan1	C	T	2: 29,916,126 (GRCm39)	A2038V	probably damaging	Het
Stx17	C	A	4: 48,181,526 (GRCm39)	P210T	probably damaging	Het
Tbc1d5	A	G	17: 51,224,601 (GRCm39)	Y317H	probably benign	Het
Tenm4	C	A	7: 96,534,565 (GRCm39)	T1737N	probably damaging	Het
Tesk2	T	C	4: 116,628,998 (GRCm39)	F116L	possibly damaging	Het
Tln2	T	C	9: 67,277,905 (GRCm39)	S370G	probably damaging	Het
Tm6sf2	G	T	8: 70,528,733 (GRCm39)	G162C	probably null	Het
Togaram2	A	C	17: 72,021,693 (GRCm39)	E718D	probably benign	Het
Ttn	A	C	2: 76,578,327 (GRCm39)	F15862V	probably damaging	Het
Uba6	T	A	5: 86,268,388 (GRCm39)	R916*	probably null	Het
Umodl1	A	G	17: 31,215,229 (GRCm39)	M1018V	probably benign	Het
Wdr26	G	A	1: 181,019,381 (GRCm39)	T332I	possibly damaging	Het
Xdh	A	T	17: 74,223,781 (GRCm39)		probably null	Het

Posted On

2013-12-09