Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01528:Gm2832'

89633

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm2832

Ensembl Gene

ENSMUSG00000091110

Gene Name

predicted gene 2832

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01528

Quality Score

Status

Chromosome

Chromosomal Location

41000762-41010772 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 41003670 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 167 (V167A)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000172412
AA Change: V167A

SMART Domains

Protein: ENSMUSP00000131087
Gene: ENSMUSG00000091110
AA Change: V167A

Domain	Start	End	E-Value	Type
Pfam:Takusan	57	137	7.3e-26	PFAM
coiled coil region	156	185	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AB124611	T	A	9: 21,451,190 (GRCm39)		probably benign	Het
Cdc45	A	G	16: 18,630,311 (GRCm39)	F2S	probably damaging	Het
Cdon	A	G	9: 35,381,403 (GRCm39)	R598G	possibly damaging	Het
Cemip2	T	C	19: 21,812,909 (GRCm39)	V1038A	possibly damaging	Het
Dusp22	C	T	13: 30,889,611 (GRCm39)	T64I	probably benign	Het
Gfer	T	A	17: 24,914,903 (GRCm39)	T47S	probably benign	Het
Gfra2	T	C	14: 71,203,738 (GRCm39)	S296P	possibly damaging	Het
Gjb2	G	A	14: 57,338,125 (GRCm39)	L28F	probably damaging	Het
Gm17782	A	G	17: 36,472,682 (GRCm39)		probably benign	Het
Gpr155	A	G	2: 73,192,767 (GRCm39)		probably null	Het
Gpr45	A	G	1: 43,072,383 (GRCm39)	H342R	probably benign	Het
Gsdmd	A	T	15: 75,735,354 (GRCm39)	T33S	possibly damaging	Het
Hal	T	A	10: 93,333,455 (GRCm39)	L341Q	probably damaging	Het
Igfbp7	T	G	5: 77,499,179 (GRCm39)	D273A	probably damaging	Het
Kdm2a	T	C	19: 4,393,083 (GRCm39)	D424G	probably benign	Het
Kif13a	C	T	13: 47,018,313 (GRCm39)		probably benign	Het
Krt35	A	T	11: 99,985,420 (GRCm39)	L207Q	probably damaging	Het
Lrp1b	A	T	2: 40,809,194 (GRCm39)	D2572E	probably damaging	Het
Lrp2	A	G	2: 69,322,804 (GRCm39)	V1848A	probably damaging	Het
Myo9a	T	C	9: 59,686,957 (GRCm39)	Y21H	probably damaging	Het
Ncan	G	T	8: 70,562,731 (GRCm39)	A509E	probably benign	Het
Or2q1	T	C	6: 42,795,208 (GRCm39)	S268P	probably damaging	Het
Pde11a	G	A	2: 76,025,300 (GRCm39)		probably benign	Het
Phf19	G	T	2: 34,787,119 (GRCm39)	D448E	probably damaging	Het
Ptprj	A	T	2: 90,282,488 (GRCm39)	V799D	probably damaging	Het
Rpgrip1	T	A	14: 52,349,634 (GRCm39)	Y7*	probably null	Het
Sema3c	A	G	5: 17,919,413 (GRCm39)	H483R	probably benign	Het
Slc4a11	A	G	2: 130,527,328 (GRCm39)		probably benign	Het
St3gal1	C	A	15: 66,984,466 (GRCm39)	R103L	probably benign	Het
Tet2	A	T	3: 133,186,059 (GRCm39)	V1126E	possibly damaging	Het
Tmem117	A	T	15: 94,992,545 (GRCm39)	I402L	probably benign	Het
Ttc28	T	A	5: 111,249,826 (GRCm39)		probably benign	Het
Ttn	A	T	2: 76,702,182 (GRCm39)		probably benign	Het
Vmn1r7	T	A	6: 57,001,532 (GRCm39)	M243L	probably benign	Het
Wnt1	G	T	15: 98,689,714 (GRCm39)	W167L	probably damaging	Het
Zfp553	G	T	7: 126,835,387 (GRCm39)	S314I	probably damaging	Het
Zranb2	T	C	3: 157,250,602 (GRCm39)		probably benign	Het

Other mutations in Gm2832

Allele	Source	Chr	Coord	Type	Predicted Effect
R1997:Gm2832	UTSW	14	41,002,943 (GRCm39)	critical splice donor site	probably null
R4105:Gm2832	UTSW	14	41,002,856 (GRCm39)	missense	unknown
R7024:Gm2832	UTSW	14	41,001,696 (GRCm39)	missense
R7526:Gm2832	UTSW	14	41,002,919 (GRCm39)	missense
R8124:Gm2832	UTSW	14	41,000,894 (GRCm39)	missense
R8187:Gm2832	UTSW	14	41,000,915 (GRCm39)	missense
R8793:Gm2832	UTSW	14	41,003,726 (GRCm39)	missense
R9460:Gm2832	UTSW	14	41,000,843 (GRCm39)	missense

Posted On

2013-12-03