Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03051:Odam'

409075

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Odam

Ensembl Gene

ENSMUSG00000009580

Gene Name

odontogenic, ameloblast asssociated

Synonyms

2310011G06Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.108) question?

Stock #

IGL03051

Quality Score

Status

Chromosome

Chromosomal Location

88032888-88042033 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

G to A at 88040335 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000117898 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000113274] [ENSMUST00000129757]

AlphaFold

A1E960

Predicted Effect

probably benign
Transcript: ENSMUST00000113274

SMART Domains

Protein: ENSMUSP00000108899
Gene: ENSMUSG00000009580

Domain	Start	End	E-Value	Type
Pfam:ODAM	16	273	1.4e-128	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000129757

SMART Domains

Protein: ENSMUSP00000117898
Gene: ENSMUSG00000009580

Domain	Start	End	E-Value	Type
Pfam:ODAM	16	273	5.1e-132	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 38 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aak1	G	T	6: 86,964,283 (GRCm39)		probably benign	Het
Abhd14a	A	T	9: 106,321,128 (GRCm39)	F76I	possibly damaging	Het
Acvr1b	A	G	15: 101,100,959 (GRCm39)	R374G	probably damaging	Het
Akap13	T	A	7: 75,260,233 (GRCm39)	C149*	probably null	Het
Appbp2	A	T	11: 85,082,565 (GRCm39)	D555E	possibly damaging	Het
Arhgap25	T	C	6: 87,472,896 (GRCm39)	Q87R	probably null	Het
Baz1b	T	A	5: 135,246,079 (GRCm39)	N509K	probably benign	Het
Ccn4	T	A	15: 66,778,399 (GRCm39)	C73*	probably null	Het
Ces5a	C	A	8: 94,255,226 (GRCm39)	G156C	probably damaging	Het
Chtf18	G	A	17: 25,939,938 (GRCm39)	R723W	probably damaging	Het
Clec4e	A	G	6: 123,266,692 (GRCm39)	S6P	probably benign	Het
Dennd4a	A	G	9: 64,769,696 (GRCm39)	I468V	probably damaging	Het
Epb41l4a	A	T	18: 34,007,825 (GRCm39)	Y233N	probably damaging	Het
Fam210b	C	T	2: 172,194,612 (GRCm39)	H155Y	probably benign	Het
Frmd4b	A	T	6: 97,272,943 (GRCm39)	C770*	probably null	Het
Gpa33	A	G	1: 165,992,790 (GRCm39)	H301R	probably benign	Het
Gpr39	T	A	1: 125,605,485 (GRCm39)	C138S	probably damaging	Het
Gtf2i	T	A	5: 134,271,768 (GRCm39)	K858*	probably null	Het
Ighv7-1	A	T	12: 113,860,576 (GRCm39)		probably benign	Het
Iglv1	T	C	16: 18,903,973 (GRCm39)	T49A	possibly damaging	Het
Kif17	A	C	4: 138,016,565 (GRCm39)	D416A	probably damaging	Het
Mib2	T	C	4: 155,741,747 (GRCm39)	T431A	probably damaging	Het
Mpz	G	A	1: 170,986,380 (GRCm39)	R98H	probably damaging	Het
Naa16	T	C	14: 79,606,522 (GRCm39)	E337G	probably benign	Het
Or1e1f	T	A	11: 73,855,860 (GRCm39)	L142H	probably benign	Het
Parp2	T	C	14: 51,056,805 (GRCm39)		probably benign	Het
Pcdh7	T	G	5: 58,286,415 (GRCm39)	S1164A	probably damaging	Het
Pkp4	G	T	2: 59,142,106 (GRCm39)	A470S	probably benign	Het
Plin4	A	T	17: 56,412,417 (GRCm39)	M538K	possibly damaging	Het
Prex2	T	C	1: 11,212,889 (GRCm39)	V624A	probably damaging	Het
Rps6ka5	A	C	12: 100,582,250 (GRCm39)		probably null	Het
Simc1	T	C	13: 54,674,036 (GRCm39)	S795P	probably benign	Het
Slc35b4	A	T	6: 34,137,406 (GRCm39)		probably null	Het
Stxbp2	A	T	8: 3,691,971 (GRCm39)	I538F	probably benign	Het
Syt14	T	C	1: 192,615,528 (GRCm39)	N486S	probably benign	Het
Trim59	T	C	3: 68,944,206 (GRCm39)	N378S	probably benign	Het
Wdr17	T	A	8: 55,104,349 (GRCm39)	D908V	probably damaging	Het
Wdr74	A	G	19: 8,716,875 (GRCm39)		probably benign	Het

Other mutations in Odam

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00970:Odam	APN	5	88,034,467 (GRCm39)	splice site	probably benign
IGL01339:Odam	APN	5	88,033,755 (GRCm39)	critical splice donor site	probably null
IGL01940:Odam	APN	5	88,035,192 (GRCm39)	missense	possibly damaging	0.87
IGL02895:Odam	APN	5	88,033,723 (GRCm39)	missense	probably benign	0.32
IGL03118:Odam	APN	5	88,033,613 (GRCm39)	missense	unknown
BB005:Odam	UTSW	5	88,035,269 (GRCm39)	missense	possibly damaging	0.95
BB015:Odam	UTSW	5	88,035,269 (GRCm39)	missense	possibly damaging	0.95
R1816:Odam	UTSW	5	88,037,329 (GRCm39)	splice site	probably null
R2033:Odam	UTSW	5	88,040,278 (GRCm39)	missense	probably benign
R4965:Odam	UTSW	5	88,037,967 (GRCm39)	nonsense	probably null
R7257:Odam	UTSW	5	88,035,404 (GRCm39)	missense	probably benign	0.14
R7682:Odam	UTSW	5	88,040,287 (GRCm39)	missense	possibly damaging	0.71
R7928:Odam	UTSW	5	88,035,269 (GRCm39)	missense	possibly damaging	0.95
R8099:Odam	UTSW	5	88,040,299 (GRCm39)	missense	possibly damaging	0.52
R8844:Odam	UTSW	5	88,037,322 (GRCm39)	missense	probably damaging	0.98
R8872:Odam	UTSW	5	88,035,797 (GRCm39)	critical splice acceptor site	probably null
R9006:Odam	UTSW	5	88,040,298 (GRCm39)	missense	probably benign	0.16
R9227:Odam	UTSW	5	88,034,457 (GRCm39)	missense	probably benign	0.32
R9230:Odam	UTSW	5	88,034,457 (GRCm39)	missense	probably benign	0.32
R9705:Odam	UTSW	5	88,037,228 (GRCm39)	missense	probably benign	0.06
R9779:Odam	UTSW	5	88,037,327 (GRCm39)	critical splice donor site	probably null

Posted On

2016-08-02