Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00557:Gm12258'

332602

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm12258

Ensembl Gene

ENSMUSG00000072915

Gene Name

predicted gene 12258

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL00557

Quality Score

Status

Chromosome

Chromosomal Location

58737984-58752782 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 58746896 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 51 (D51G)

Ref Sequence

ENSEMBL: ENSMUSP00000117644 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093768] [ENSMUST00000139337]

AlphaFold

Q5NC63

Predicted Effect

probably benign
Transcript: ENSMUST00000093768

SMART Domains

Protein: ENSMUSP00000091282
Gene: ENSMUSG00000072915

Domain	Start	End	E-Value	Type
ZnF_C2H2	8	30	5.21e-4	SMART
ZnF_C2H2	36	58	1.03e-2	SMART
ZnF_C2H2	64	86	2.4e-3	SMART
ZnF_C2H2	92	114	4.17e-3	SMART
ZnF_C2H2	120	142	8.34e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000139337
AA Change: D51G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000117644
Gene: ENSMUSG00000072915
AA Change: D51G

Domain	Start	End	E-Value	Type
KRAB	56	116	1.8e-32	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143407

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 25 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Agpat3	A	T	10: 78,109,516 (GRCm39)		probably benign	Het
Arhgap35	T	C	7: 16,298,340 (GRCm39)	T242A	probably benign	Het
Asb15	C	A	6: 24,558,649 (GRCm39)	R55S	probably benign	Het
Brca2	C	T	5: 150,484,003 (GRCm39)	R2941W	probably benign	Het
Chrng	T	C	1: 87,134,469 (GRCm39)	V135A	probably damaging	Het
Corin	G	T	5: 72,462,231 (GRCm39)	H859Q	probably damaging	Het
Cul7	A	G	17: 46,963,434 (GRCm39)	E208G	probably damaging	Het
Dnah6	T	C	6: 73,172,603 (GRCm39)	N285S	possibly damaging	Het
Ell2	T	A	13: 75,904,409 (GRCm39)	I166N	probably damaging	Het
Fsip2	A	G	2: 82,821,657 (GRCm39)	R5797G	possibly damaging	Het
Galntl6	T	C	8: 59,364,451 (GRCm39)	I20V	possibly damaging	Het
Glra2	A	G	X: 164,072,633 (GRCm39)	F78L	possibly damaging	Het
Gsta2	T	A	9: 78,238,525 (GRCm39)	K185*	probably null	Het
Hmgcr	C	T	13: 96,795,786 (GRCm39)	D294N	probably benign	Het
Iglv2	A	G	16: 19,079,547 (GRCm39)		probably benign	Het
Myo10	T	A	15: 25,776,466 (GRCm39)	L63H	probably damaging	Het
P2ry10b	T	C	X: 106,215,243 (GRCm39)	V201A	probably benign	Het
Psmb2	A	G	4: 126,571,642 (GRCm39)		probably null	Het
Samd4	T	A	14: 47,290,355 (GRCm39)	L154H	probably damaging	Het
Sult2a4	A	T	7: 13,718,870 (GRCm39)	D124E	probably damaging	Het
Trav9-1	A	T	14: 53,725,815 (GRCm39)	Y43F	probably damaging	Het
Trpv2	A	G	11: 62,483,681 (GRCm39)	N506S	probably damaging	Het
Ube3c	T	C	5: 29,824,227 (GRCm39)	S474P	probably damaging	Het
Wdr87-ps	A	G	7: 29,235,227 (GRCm39)		noncoding transcript	Het
Zfp942	A	T	17: 22,148,042 (GRCm39)	C196S	probably benign	Het

Other mutations in Gm12258

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01391:Gm12258	APN	11	58,739,520 (GRCm39)	missense	probably benign	0.03
IGL03081:Gm12258	APN	11	58,749,085 (GRCm39)	missense	probably benign	0.07
R1521:Gm12258	UTSW	11	58,750,381 (GRCm39)	missense	probably damaging	1.00
R1653:Gm12258	UTSW	11	58,749,113 (GRCm39)	missense	possibly damaging	0.68
R3895:Gm12258	UTSW	11	58,749,375 (GRCm39)	nonsense	probably null
R4065:Gm12258	UTSW	11	58,749,352 (GRCm39)	missense	probably benign	0.08
R4066:Gm12258	UTSW	11	58,749,352 (GRCm39)	missense	probably benign	0.08
R4747:Gm12258	UTSW	11	58,750,422 (GRCm39)	missense	probably damaging	1.00
R4803:Gm12258	UTSW	11	58,749,856 (GRCm39)	missense	probably benign	0.06
R5554:Gm12258	UTSW	11	58,749,294 (GRCm39)	missense	possibly damaging	0.92
R5896:Gm12258	UTSW	11	58,750,457 (GRCm39)	missense	probably damaging	1.00
R5956:Gm12258	UTSW	11	58,750,285 (GRCm39)	missense	probably benign	0.02
R6277:Gm12258	UTSW	11	58,745,113 (GRCm39)	missense	probably damaging	1.00
R7166:Gm12258	UTSW	11	58,749,299 (GRCm39)	missense
R7728:Gm12258	UTSW	11	58,750,518 (GRCm39)	missense	unknown
R8161:Gm12258	UTSW	11	58,750,138 (GRCm39)	missense	unknown
R8268:Gm12258	UTSW	11	58,745,084 (GRCm39)	critical splice acceptor site	probably null
R8491:Gm12258	UTSW	11	58,745,122 (GRCm39)	missense
R8878:Gm12258	UTSW	11	58,750,112 (GRCm39)	missense	unknown
R9381:Gm12258	UTSW	11	58,750,007 (GRCm39)	missense	unknown
R9409:Gm12258	UTSW	11	58,745,119 (GRCm39)	missense
R9546:Gm12258	UTSW	11	58,749,922 (GRCm39)	missense	unknown
R9723:Gm12258	UTSW	11	58,750,448 (GRCm39)	missense	unknown
Z1186:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1186:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1186:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1186:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1186:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1186:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1186:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1186:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense
Z1187:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense
Z1187:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1187:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1187:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1187:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1187:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1187:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1187:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1188:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1188:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1188:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1188:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1188:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1188:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1188:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense
Z1188:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1189:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1189:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1189:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1189:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1189:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1189:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1189:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1189:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense
Z1190:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense
Z1190:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1190:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1190:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1190:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1190:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1190:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1190:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1191:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1191:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1191:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1191:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1191:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1191:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1191:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1191:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense
Z1192:Gm12258	UTSW	11	58,750,690 (GRCm39)	missense	unknown
Z1192:Gm12258	UTSW	11	58,750,014 (GRCm39)	unclassified	probably benign
Z1192:Gm12258	UTSW	11	58,750,013 (GRCm39)	unclassified	probably benign
Z1192:Gm12258	UTSW	11	58,749,833 (GRCm39)	missense	unknown
Z1192:Gm12258	UTSW	11	58,749,776 (GRCm39)	missense	unknown
Z1192:Gm12258	UTSW	11	58,749,764 (GRCm39)	missense	unknown
Z1192:Gm12258	UTSW	11	58,749,262 (GRCm39)	missense
Z1192:Gm12258	UTSW	11	58,749,126 (GRCm39)	missense

Posted On

2015-08-05