Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03062:Fam98a'

409525

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fam98a

Ensembl Gene

ENSMUSG00000002017

Gene Name

family with sequence similarity 98, member A

Synonyms

2810405J04Rik

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.642) question?

Stock #

IGL03062

Quality Score

Status

Chromosome

Chromosomal Location

75844081-75858941 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 75847100 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000108126 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000112507]

AlphaFold

Q3TJZ6

Predicted Effect

probably benign
Transcript: ENSMUST00000112507

SMART Domains

Protein: ENSMUSP00000108126
Gene: ENSMUSG00000002017

Domain	Start	End	E-Value	Type
Pfam:DUF2465	11	328	1.1e-137	PFAM
low complexity region	334	396	N/A	INTRINSIC
low complexity region	401	441	N/A	INTRINSIC
low complexity region	448	481	N/A	INTRINSIC
low complexity region	485	501	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140729

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141969

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb10	C	T	8: 124,681,054 (GRCm39)	R714Q	possibly damaging	Het
Abcb5	T	A	12: 118,899,822 (GRCm39)	I282L	probably benign	Het
Aox1	A	T	1: 58,117,624 (GRCm39)	E835D	probably benign	Het
Arhgap17	C	T	7: 122,921,097 (GRCm39)		probably null	Het
Bltp1	T	C	3: 37,092,666 (GRCm39)		probably benign	Het
Calcr	C	T	6: 3,693,718 (GRCm39)	V359I	probably benign	Het
Chd9	T	A	8: 91,741,895 (GRCm39)		probably benign	Het
Col28a1	T	C	6: 8,017,029 (GRCm39)		probably benign	Het
Dnajc11	A	G	4: 152,055,318 (GRCm39)	E171G	possibly damaging	Het
Efhd1	T	C	1: 87,192,406 (GRCm39)	F79L	possibly damaging	Het
Fam83a	A	T	15: 57,856,473 (GRCm39)		probably null	Het
Ficd	A	G	5: 113,876,314 (GRCm39)	Y163C	probably damaging	Het
Filip1l	T	C	16: 57,327,167 (GRCm39)	S66P	probably damaging	Het
Fmo5	A	G	3: 97,542,909 (GRCm39)	Y73C	probably damaging	Het
Galnt12	C	A	4: 47,122,566 (GRCm39)	R574S	possibly damaging	Het
Klc3	C	A	7: 19,128,987 (GRCm39)	G461W	probably damaging	Het
Lmo7	A	T	14: 102,149,515 (GRCm39)	T973S	possibly damaging	Het
Loxl1	C	A	9: 58,219,193 (GRCm39)	G326V	possibly damaging	Het
Lrrc24	A	G	15: 76,602,504 (GRCm39)	V127A	probably benign	Het
Lyrm1	T	C	7: 119,515,354 (GRCm39)		probably benign	Het
Med28	G	A	5: 45,679,811 (GRCm39)	V65I	probably damaging	Het
Mgat4c	T	C	10: 102,224,322 (GRCm39)	Y179H	probably damaging	Het
Micall1	A	C	15: 78,998,881 (GRCm39)	N58T	probably damaging	Het
Mtcl3	T	A	10: 29,074,945 (GRCm39)	F911Y	probably damaging	Het
Ncoa4	T	A	14: 31,895,377 (GRCm39)	M72K	possibly damaging	Het
Nutm1	T	C	2: 112,079,278 (GRCm39)	Q879R	probably benign	Het
Or4d6	C	T	19: 12,086,512 (GRCm39)	V133I	probably benign	Het
Or8b12i	T	A	9: 20,082,463 (GRCm39)	I135F	probably damaging	Het
Or8g52	T	A	9: 39,631,331 (GRCm39)	D269E	probably benign	Het
Phf11b	T	C	14: 59,562,373 (GRCm39)	I177M	probably damaging	Het
Pin1rt1	T	G	2: 104,545,052 (GRCm39)	I27L	probably benign	Het
Plxna2	T	C	1: 194,444,858 (GRCm39)	V750A	possibly damaging	Het
Pou5f1	A	T	17: 35,820,936 (GRCm39)	N126I	possibly damaging	Het
Ptprn	A	T	1: 75,224,517 (GRCm39)	H946Q	possibly damaging	Het
Rnf43	G	T	11: 87,623,130 (GRCm39)	G744*	probably null	Het
Rsbn1	C	A	3: 103,860,945 (GRCm39)		probably benign	Het
Sars2	T	A	7: 28,446,206 (GRCm39)	I145N	possibly damaging	Het
Sh3tc2	A	T	18: 62,144,951 (GRCm39)	E1135V	probably damaging	Het
Shroom1	A	G	11: 53,354,206 (GRCm39)	D42G	probably benign	Het
Sidt2	A	G	9: 45,853,981 (GRCm39)		probably null	Het
Slc39a8	T	C	3: 135,592,558 (GRCm39)		probably benign	Het
Slc9c1	T	C	16: 45,420,121 (GRCm39)	S1059P	probably benign	Het
Socs6	A	T	18: 88,887,970 (GRCm39)	M315K	probably benign	Het
Speer2	T	C	16: 69,654,865 (GRCm39)	E200G	probably damaging	Het
Sult2a5	T	A	7: 13,358,107 (GRCm39)		probably null	Het
Tmbim1	A	T	1: 74,330,858 (GRCm39)	I168N	possibly damaging	Het
Trim38	T	C	13: 23,966,946 (GRCm39)	V131A	probably damaging	Het
Ube2o	A	G	11: 116,432,468 (GRCm39)	S833P	probably damaging	Het
Uggt2	T	C	14: 119,312,758 (GRCm39)	I350M	probably damaging	Het
Unc80	A	G	1: 66,548,648 (GRCm39)	D640G	probably damaging	Het
Vmn2r13	A	G	5: 109,304,148 (GRCm39)	F761S	probably damaging	Het
Vmn2r54	C	T	7: 12,366,355 (GRCm39)	C193Y	probably damaging	Het

Other mutations in Fam98a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00337:Fam98a	APN	17	75,858,742 (GRCm39)	missense	probably damaging	1.00
IGL00548:Fam98a	APN	17	75,845,813 (GRCm39)	missense	probably damaging	1.00
IGL02170:Fam98a	APN	17	75,847,187 (GRCm39)	critical splice acceptor site	probably null
IGL02399:Fam98a	APN	17	75,845,936 (GRCm39)	splice site	probably benign
IGL03246:Fam98a	APN	17	75,845,848 (GRCm39)	missense	probably damaging	0.99
R0584:Fam98a	UTSW	17	75,851,772 (GRCm39)	missense	probably damaging	1.00
R0594:Fam98a	UTSW	17	75,845,482 (GRCm39)	nonsense	probably null
R1121:Fam98a	UTSW	17	75,845,529 (GRCm39)	missense	unknown
R1366:Fam98a	UTSW	17	75,846,381 (GRCm39)	splice site	probably benign
R1387:Fam98a	UTSW	17	75,845,264 (GRCm39)	missense	unknown
R1424:Fam98a	UTSW	17	75,847,173 (GRCm39)	missense	probably damaging	1.00
R1533:Fam98a	UTSW	17	75,848,276 (GRCm39)	missense	probably damaging	1.00
R1651:Fam98a	UTSW	17	75,854,710 (GRCm39)	missense	probably benign	0.16
R2211:Fam98a	UTSW	17	75,845,940 (GRCm39)	critical splice donor site	probably null
R4295:Fam98a	UTSW	17	75,848,342 (GRCm39)	missense	probably damaging	1.00
R4350:Fam98a	UTSW	17	75,848,220 (GRCm39)	missense	probably damaging	1.00
R4963:Fam98a	UTSW	17	75,845,977 (GRCm39)	missense	probably damaging	0.99
R5320:Fam98a	UTSW	17	75,845,810 (GRCm39)	missense	probably damaging	1.00
R5383:Fam98a	UTSW	17	75,845,576 (GRCm39)	missense	unknown
R6031:Fam98a	UTSW	17	75,846,427 (GRCm39)	missense	probably damaging	0.98
R6031:Fam98a	UTSW	17	75,846,427 (GRCm39)	missense	probably damaging	0.98
R7058:Fam98a	UTSW	17	75,845,384 (GRCm39)	missense	unknown
R7182:Fam98a	UTSW	17	75,846,013 (GRCm39)	nonsense	probably null
R7505:Fam98a	UTSW	17	75,845,233 (GRCm39)	missense	unknown
R7554:Fam98a	UTSW	17	75,854,670 (GRCm39)	nonsense	probably null
R7566:Fam98a	UTSW	17	75,854,657 (GRCm39)	missense	probably damaging	1.00
R8095:Fam98a	UTSW	17	75,845,766 (GRCm39)	missense	probably damaging	1.00
R8467:Fam98a	UTSW	17	75,851,830 (GRCm39)	missense	probably damaging	1.00
R8790:Fam98a	UTSW	17	75,854,684 (GRCm39)	missense	possibly damaging	0.93
R8827:Fam98a	UTSW	17	75,851,824 (GRCm39)	missense	possibly damaging	0.74
R9375:Fam98a	UTSW	17	75,848,330 (GRCm39)	missense	possibly damaging	0.55
R9625:Fam98a	UTSW	17	75,845,474 (GRCm39)	missense	unknown

Posted On

2016-08-02