Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02898:Gm9956'

363479

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm9956

Ensembl Gene

ENSMUSG00000054758

Gene Name

predicted gene 9956

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02898

Quality Score

Status

Chromosome

Chromosomal Location

56621230-56624350 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 56621350 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Leucine at position 4 (S4L)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000067972
AA Change: S4L

SMART Domains

Protein: ENSMUSP00000071080
Gene: ENSMUSG00000054758
AA Change: S4L

Domain	Start	End	E-Value	Type
transmembrane domain	94	116	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamtsl5	A	G	10: 80,178,065 (GRCm39)		probably benign	Het
Brd3	A	G	2: 27,349,753 (GRCm39)	S267P	possibly damaging	Het
Btaf1	A	G	19: 36,946,468 (GRCm39)	T425A	probably benign	Het
Caskin1	A	T	17: 24,721,383 (GRCm39)	E544D	probably benign	Het
Col20a1	C	T	2: 180,630,905 (GRCm39)	Q58*	probably null	Het
Eif2ak1	G	A	5: 143,826,270 (GRCm39)	V428I	probably damaging	Het
Fez2	A	G	17: 78,692,184 (GRCm39)	I345T	probably benign	Het
Focad	A	T	4: 88,310,234 (GRCm39)	M1388L	probably benign	Het
Gfer	T	C	17: 24,914,921 (GRCm39)	R41G	probably benign	Het
Krtap6-1	G	A	16: 88,828,643 (GRCm39)	G13D	unknown	Het
Megf8	A	G	7: 25,045,933 (GRCm39)	E1492G	possibly damaging	Het
Myh7	T	C	14: 55,221,197 (GRCm39)	I909V	probably damaging	Het
Or11g25	T	A	14: 50,723,643 (GRCm39)	S243T	probably damaging	Het
Or1e21	T	A	11: 73,344,561 (GRCm39)	H159L	probably damaging	Het
Otog	A	G	7: 45,959,562 (GRCm39)	E717G	probably damaging	Het
Pik3r4	A	G	9: 105,527,605 (GRCm39)	I319M	probably benign	Het
Piwil4	A	T	9: 14,617,583 (GRCm39)		probably benign	Het
Plekho1	T	A	3: 95,899,493 (GRCm39)	H100L	probably damaging	Het
Prr30	T	G	14: 101,435,917 (GRCm39)	D215A	probably benign	Het
Prss52	C	T	14: 64,351,115 (GRCm39)	A300V	possibly damaging	Het
Ralgps2	C	A	1: 156,645,314 (GRCm39)	K514N	probably benign	Het
Robo4	T	C	9: 37,319,472 (GRCm39)	I463T	probably damaging	Het
Sars1	A	T	3: 108,336,579 (GRCm39)	F268Y	probably damaging	Het
Sidt1	C	T	16: 44,102,858 (GRCm39)	R289Q	possibly damaging	Het
Slco1a8	T	A	6: 141,940,023 (GRCm39)	Y140F	probably benign	Het
Slco2a1	T	C	9: 102,956,805 (GRCm39)	V539A	probably damaging	Het
Snrnp200	A	G	2: 127,058,676 (GRCm39)		probably benign	Het
Spag17	A	G	3: 100,008,702 (GRCm39)	D1944G	probably benign	Het
Spata1	C	T	3: 146,181,094 (GRCm39)	R288Q	possibly damaging	Het
Tatdn3	T	C	1: 190,778,507 (GRCm39)	*233W	probably null	Het
Ttc3	T	A	16: 94,220,285 (GRCm39)	V536E	probably damaging	Het
V1rd19	A	C	7: 23,702,854 (GRCm39)	T107P	probably damaging	Het

Other mutations in Gm9956

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01702:Gm9956	APN	10	56,621,335 (GRCm39)	start gained
IGL02411:Gm9956	APN	10	56,621,388 (GRCm39)	missense	unknown
R0513:Gm9956	UTSW	10	56,621,291 (GRCm39)	start gained
R0731:Gm9956	UTSW	10	56,621,639 (GRCm39)	nonsense	probably null
R0841:Gm9956	UTSW	10	56,621,425 (GRCm39)	missense	unknown
R0841:Gm9956	UTSW	10	56,621,424 (GRCm39)	missense	unknown
R1289:Gm9956	UTSW	10	56,621,676 (GRCm39)	missense	probably damaging	0.99

Posted On

2015-12-18