Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01636:Fam210b'

93007

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fam210b

Ensembl Gene

ENSMUSG00000027495

Gene Name

family with sequence similarity 210, member B

Synonyms

2010011I20Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL01636

Quality Score

Status

Chromosome

Chromosomal Location

172187485-172197669 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 172193460 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 91 (F91S)

Ref Sequence

ENSEMBL: ENSMUSP00000028995 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028995] [ENSMUST00000028997] [ENSMUST00000109139] [ENSMUST00000109140]

AlphaFold

Q9D8B6

Predicted Effect

probably damaging
Transcript: ENSMUST00000028995
AA Change: F91S

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000028995
Gene: ENSMUSG00000027495
AA Change: F91S

Domain	Start	End	E-Value	Type
Pfam:DUF1279	85	172	4e-30	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000028997

SMART Domains

Protein: ENSMUSP00000028997
Gene: ENSMUSG00000027496

Domain	Start	End	E-Value	Type
S_TKc	146	396	2.25e-99	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109139

SMART Domains

Protein: ENSMUSP00000104767
Gene: ENSMUSG00000027496

Domain	Start	End	E-Value	Type
S_TKc	124	374	2.25e-99	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109140

SMART Domains

Protein: ENSMUSP00000104768
Gene: ENSMUSG00000027496

Domain	Start	End	E-Value	Type
S_TKc	124	374	2.25e-99	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam4	T	C	12: 81,466,723 (GRCm39)	T633A	possibly damaging	Het
Adgrd1	G	T	5: 129,219,516 (GRCm39)		probably benign	Het
Bmp7	T	C	2: 172,717,001 (GRCm39)		probably benign	Het
Ccdc54	A	G	16: 50,410,277 (GRCm39)	*330Q	probably null	Het
Chd5	A	T	4: 152,469,110 (GRCm39)	K1812*	probably null	Het
Cnga3	T	A	1: 37,299,874 (GRCm39)	I236N	possibly damaging	Het
Ddost	T	G	4: 138,036,707 (GRCm39)	D135E	possibly damaging	Het
Dicer1	T	C	12: 104,688,500 (GRCm39)	D359G	probably damaging	Het
Dnah17	A	C	11: 117,931,882 (GRCm39)	S3697A	probably benign	Het
Dnttip2	G	A	3: 122,076,123 (GRCm39)	G685D	possibly damaging	Het
Dst	T	G	1: 34,254,650 (GRCm39)	S4552R	probably damaging	Het
Ebf2	G	A	14: 67,476,927 (GRCm39)	E157K	probably damaging	Het
Ehbp1	C	T	11: 22,039,584 (GRCm39)	V839M	probably benign	Het
Ehmt1	G	T	2: 24,729,620 (GRCm39)	T639K	probably damaging	Het
Esyt2	T	C	12: 116,329,550 (GRCm39)		probably null	Het
Etv6	T	C	6: 134,225,350 (GRCm39)	S194P	probably benign	Het
Fam184b	T	C	5: 45,741,637 (GRCm39)	H198R	probably benign	Het
Fam81a	G	A	9: 70,006,434 (GRCm39)	Q193*	probably null	Het
Fto	A	G	8: 92,135,969 (GRCm39)	D79G	probably damaging	Het
Haspin	C	T	11: 73,028,231 (GRCm39)	R286H	possibly damaging	Het
Hmcn1	C	T	1: 150,455,984 (GRCm39)	C5312Y	probably damaging	Het
Ik	T	A	18: 36,884,254 (GRCm39)	D245E	possibly damaging	Het
Itga1	A	G	13: 115,143,484 (GRCm39)	V349A	possibly damaging	Het
Kdm8	T	C	7: 125,060,377 (GRCm39)	V400A	probably damaging	Het
Larp1b	G	T	3: 40,924,913 (GRCm39)	R177L	probably benign	Het
Lifr	T	G	15: 7,208,499 (GRCm39)		probably benign	Het
Lrrn2	T	C	1: 132,864,959 (GRCm39)	L8P	possibly damaging	Het
Marcksl1	T	A	4: 129,408,587 (GRCm39)	D55E	probably benign	Het
Med12	C	A	X: 100,318,795 (GRCm39)	S74R	probably damaging	Het
Mtarc2	T	C	1: 184,564,838 (GRCm39)	K231E	probably benign	Het
Or52s1	C	A	7: 102,861,384 (GRCm39)	R95S	probably benign	Het
Or6c35	A	T	10: 129,168,752 (GRCm39)	M1L	probably damaging	Het
Or7e170	A	G	9: 19,795,484 (GRCm39)	V39A	probably benign	Het
Or8k39	G	A	2: 86,563,945 (GRCm39)	Q4*	probably null	Het
Orc3	A	C	4: 34,595,096 (GRCm39)	L233R	probably damaging	Het
Pik3cd	A	G	4: 149,738,772 (GRCm39)	M715T	possibly damaging	Het
Prss43	T	A	9: 110,656,505 (GRCm39)	L64Q	possibly damaging	Het
Pyroxd2	C	A	19: 42,726,771 (GRCm39)	G209V	probably benign	Het
Rab3b	A	G	4: 108,797,916 (GRCm39)	D198G	possibly damaging	Het
Rrbp1	A	T	2: 143,789,815 (GRCm39)		probably benign	Het
Smg6	T	C	11: 74,825,929 (GRCm39)		probably null	Het
Ssrp1	T	C	2: 84,871,443 (GRCm39)		probably benign	Het
Strip2	C	A	6: 29,931,192 (GRCm39)	T381K	probably benign	Het
Svep1	A	T	4: 58,116,622 (GRCm39)	L876Q	possibly damaging	Het
Tle4	T	C	19: 14,429,897 (GRCm39)	I625V	probably damaging	Het
Tnfrsf23	T	C	7: 143,233,736 (GRCm39)	T81A	probably damaging	Het
Ttc41	A	G	10: 86,612,542 (GRCm39)	K1272E	probably benign	Het
Usp3	A	G	9: 66,469,834 (GRCm39)		probably null	Het
Vmn1r121	C	T	7: 20,832,282 (GRCm39)	V53M	probably benign	Het
Vmn1r65	A	T	7: 6,011,720 (GRCm39)	S171R	probably benign	Het
Vmn2r4	A	T	3: 64,313,657 (GRCm39)	D441E	probably benign	Het
Vps13d	A	T	4: 144,801,618 (GRCm39)	H2353Q	probably damaging	Het
Vwa8	T	C	14: 79,435,794 (GRCm39)	S1835P	possibly damaging	Het

Other mutations in Fam210b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02142:Fam210b	APN	2	172,194,497 (GRCm39)	unclassified	probably benign
IGL02152:Fam210b	APN	2	172,193,423 (GRCm39)	missense	probably benign	0.02
IGL02531:Fam210b	APN	2	172,194,675 (GRCm39)	missense	probably damaging	0.99
IGL03051:Fam210b	APN	2	172,194,612 (GRCm39)	missense	probably benign	0.21
R0597:Fam210b	UTSW	2	172,187,773 (GRCm39)	splice site	probably benign
R4117:Fam210b	UTSW	2	172,193,486 (GRCm39)	missense	probably benign	0.25
R4281:Fam210b	UTSW	2	172,193,468 (GRCm39)	missense	probably damaging	0.98
R4978:Fam210b	UTSW	2	172,187,585 (GRCm39)	missense	probably damaging	0.99
R4983:Fam210b	UTSW	2	172,187,585 (GRCm39)	missense	probably damaging	0.99
R5150:Fam210b	UTSW	2	172,193,468 (GRCm39)	missense	probably damaging	0.98
R9544:Fam210b	UTSW	2	172,194,633 (GRCm39)	missense	probably damaging	1.00

Posted On

2013-12-09