Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02437:Leng8'

293307

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Leng8

Ensembl Gene

ENSMUSG00000035545

Gene Name

leukocyte receptor cluster (LRC) member 8

Synonyms

Accession Numbers

Essential gene?

Probably essential (E-score: 0.968) question?

Stock #

IGL02437

Quality Score

Status

Chromosome

Chromosomal Location

4140038-4151176 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 4145092 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Valine at position 164 (A164V)

Ref Sequence

ENSEMBL: ENSMUSP00000118832 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037472] [ENSMUST00000117274] [ENSMUST00000121270] [ENSMUST00000128756] [ENSMUST00000132086] [ENSMUST00000144248] [ENSMUST00000154571]

AlphaFold

Q8CBY3

Predicted Effect

probably benign
Transcript: ENSMUST00000037472
AA Change: A164V

PolyPhen 2 Score 0.387 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000046465
Gene: ENSMUSG00000035545
AA Change: A164V

Domain	Start	End	E-Value	Type
low complexity region	47	69	N/A	INTRINSIC
low complexity region	73	118	N/A	INTRINSIC
low complexity region	156	174	N/A	INTRINSIC
low complexity region	383	396	N/A	INTRINSIC
low complexity region	413	447	N/A	INTRINSIC
low complexity region	453	468	N/A	INTRINSIC
Pfam:SAC3_GANP	567	762	8.2e-66	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000117274

SMART Domains

Protein: ENSMUSP00000113223
Gene: ENSMUSG00000035545

Domain	Start	End	E-Value	Type
low complexity region	47	69	N/A	INTRINSIC
low complexity region	73	104	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000121270
AA Change: A164V

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000112428
Gene: ENSMUSG00000035545
AA Change: A164V

Domain	Start	End	E-Value	Type
low complexity region	47	69	N/A	INTRINSIC
low complexity region	73	118	N/A	INTRINSIC
low complexity region	156	174	N/A	INTRINSIC
low complexity region	383	396	N/A	INTRINSIC
low complexity region	413	447	N/A	INTRINSIC
low complexity region	453	468	N/A	INTRINSIC
Pfam:SAC3_GANP	567	764	7.4e-67	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127723

Predicted Effect

probably damaging
Transcript: ENSMUST00000128756
AA Change: A164V

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000118832
Gene: ENSMUSG00000035545
AA Change: A164V

Domain	Start	End	E-Value	Type
low complexity region	47	69	N/A	INTRINSIC
low complexity region	73	118	N/A	INTRINSIC
low complexity region	156	174	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000132086

SMART Domains

Protein: ENSMUSP00000121129
Gene: ENSMUSG00000035545

Domain	Start	End	E-Value	Type
low complexity region	29	51	N/A	INTRINSIC
low complexity region	63	71	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000144248
AA Change: A127V

SMART Domains

Protein: ENSMUSP00000120574
Gene: ENSMUSG00000035545
AA Change: A127V

Domain	Start	End	E-Value	Type
low complexity region	47	69	N/A	INTRINSIC
low complexity region	73	104	N/A	INTRINSIC
low complexity region	119	137	N/A	INTRINSIC
low complexity region	346	359	N/A	INTRINSIC
low complexity region	376	410	N/A	INTRINSIC
low complexity region	416	431	N/A	INTRINSIC
Pfam:SAC3_GANP	530	725	1e-65	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146434

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155881

Predicted Effect

probably benign
Transcript: ENSMUST00000154571

SMART Domains

Protein: ENSMUSP00000123328
Gene: ENSMUSG00000035545

Domain	Start	End	E-Value	Type
low complexity region	47	69	N/A	INTRINSIC
low complexity region	73	118	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A930011G23Rik	A	G	5: 99,377,236 (GRCm39)	S404P	probably damaging	Het
A930011G23Rik	G	A	5: 99,377,241 (GRCm39)	P402L	probably damaging	Het
Abca16	T	G	7: 120,132,952 (GRCm39)	C1294G	probably benign	Het
Abca7	T	A	10: 79,844,223 (GRCm39)	S1410T	probably damaging	Het
Abhd12	T	C	2: 150,676,289 (GRCm39)	D356G	probably benign	Het
BC004004	T	C	17: 29,517,671 (GRCm39)	L295P	probably damaging	Het
Bpifc	T	C	10: 85,824,595 (GRCm39)	S215G	probably damaging	Het
Bptf	C	T	11: 106,965,521 (GRCm39)	M1109I	probably benign	Het
Brat1	C	T	5: 140,698,563 (GRCm39)	A245V	possibly damaging	Het
Cask	G	A	X: 13,403,860 (GRCm39)	T16I	probably damaging	Het
Cemip2	T	C	19: 21,789,342 (GRCm39)		probably null	Het
Cibar2	T	C	8: 120,901,525 (GRCm39)	E60G	probably damaging	Het
Clic6	A	T	16: 92,327,817 (GRCm39)	I541F	probably damaging	Het
Clnk	C	T	5: 38,931,909 (GRCm39)		probably null	Het
Cntnap1	T	A	11: 101,077,677 (GRCm39)	I1113N	probably damaging	Het
Csgalnact1	C	A	8: 68,854,144 (GRCm39)	G219V	probably damaging	Het
Cyp26a1	T	C	19: 37,686,943 (GRCm39)	S132P	probably benign	Het
Cyp4f13	G	T	17: 33,149,582 (GRCm39)	H85N	probably benign	Het
Dcaf15	C	T	8: 84,828,445 (GRCm39)	G215D	probably damaging	Het
Dip2a	T	C	10: 76,134,101 (GRCm39)	T500A	probably benign	Het
Gbe1	T	A	16: 70,231,546 (GRCm39)		probably benign	Het
Gli2	T	A	1: 118,763,733 (GRCm39)	I1473F	probably damaging	Het
Gm5129	A	T	5: 29,940,861 (GRCm39)		probably benign	Het
Hdgf	C	T	3: 87,821,792 (GRCm39)	R168C	probably damaging	Het
Heph	A	G	X: 95,516,633 (GRCm39)	T342A	probably benign	Het
Kdelr3	T	C	15: 79,409,988 (GRCm39)	Y158H	probably damaging	Het
Lamb3	C	T	1: 193,010,253 (GRCm39)	R289C	probably damaging	Het
Ltn1	T	C	16: 87,194,889 (GRCm39)	T1337A	probably benign	Het
Mast3	C	A	8: 71,233,202 (GRCm39)	R316L	possibly damaging	Het
Nampt	A	G	12: 32,880,215 (GRCm39)	Y36C	probably damaging	Het
Ncapd3	T	A	9: 26,975,264 (GRCm39)		probably benign	Het
Nipbl	T	C	15: 8,388,558 (GRCm39)	D354G	probably damaging	Het
Nsd1	A	T	13: 55,461,254 (GRCm39)	R2494W	probably damaging	Het
Nt5c1a	A	G	4: 123,108,034 (GRCm39)	N239S	probably benign	Het
Ogfr	A	G	2: 180,231,329 (GRCm39)	E19G	possibly damaging	Het
Or11h4b	A	T	14: 50,918,657 (GRCm39)	S145T	probably benign	Het
Or4c58	A	G	2: 89,675,128 (GRCm39)	L63P	probably damaging	Het
Pcna	A	T	2: 132,093,155 (GRCm39)		probably benign	Het
Pdia3	T	A	2: 121,264,129 (GRCm39)	V326E	probably damaging	Het
Phf8	T	A	X: 150,414,356 (GRCm39)	L1002Q	possibly damaging	Het
Rhobtb2	T	C	14: 70,033,365 (GRCm39)	E535G	probably damaging	Het
Rusc2	G	T	4: 43,415,545 (GRCm39)	D284Y	probably damaging	Het
Samd8	A	G	14: 21,825,491 (GRCm39)	Y212C	probably benign	Het
Sash3	C	A	X: 47,247,672 (GRCm39)	Q169K	probably benign	Het
Scyl1	C	T	19: 5,816,224 (GRCm39)	G324S	probably damaging	Het
Sec62	G	A	3: 30,872,996 (GRCm39)	G360R	unknown	Het
Sis	T	C	3: 72,826,947 (GRCm39)		probably null	Het
Slc6a1	T	A	6: 114,285,578 (GRCm39)	I338N	probably damaging	Het
Snrnp200	A	G	2: 127,058,030 (GRCm39)	D264G	probably damaging	Het
Tgm3	G	T	2: 129,871,961 (GRCm39)		probably null	Het
Tnrc6b	T	G	15: 80,764,658 (GRCm39)	L720R	probably damaging	Het
Tspyl4	A	T	10: 34,174,228 (GRCm39)	Q240L	probably damaging	Het
Tube1	G	A	10: 39,016,846 (GRCm39)	V80I	probably damaging	Het
Uap1l1	C	T	2: 25,253,945 (GRCm39)	V304M	probably damaging	Het
Wtap	T	C	17: 13,186,620 (GRCm39)	N309S	probably benign	Het
Zfp518a	G	A	19: 40,903,061 (GRCm39)	G997R	probably damaging	Het
Zfyve26	T	C	12: 79,315,621 (GRCm39)	D1285G	probably benign	Het
Zscan20	G	A	4: 128,482,210 (GRCm39)	T484I	probably damaging	Het

Other mutations in Leng8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01599:Leng8	APN	7	4,148,481 (GRCm39)	missense	probably benign	0.03
Coolhand	UTSW	7	4,147,932 (GRCm39)	nonsense	probably null
R0104:Leng8	UTSW	7	4,146,807 (GRCm39)	missense	probably damaging	0.99
R0774:Leng8	UTSW	7	4,145,135 (GRCm39)	missense	probably damaging	1.00
R1696:Leng8	UTSW	7	4,148,135 (GRCm39)	missense	probably damaging	1.00
R2001:Leng8	UTSW	7	4,148,073 (GRCm39)	missense	probably damaging	1.00
R2012:Leng8	UTSW	7	4,146,609 (GRCm39)	missense	probably damaging	1.00
R2054:Leng8	UTSW	7	4,147,289 (GRCm39)	nonsense	probably null
R3433:Leng8	UTSW	7	4,145,131 (GRCm39)	missense	probably benign	0.22
R4335:Leng8	UTSW	7	4,150,037 (GRCm39)	missense	probably damaging	0.99
R4607:Leng8	UTSW	7	4,147,796 (GRCm39)	missense	probably damaging	1.00
R4608:Leng8	UTSW	7	4,147,796 (GRCm39)	missense	probably damaging	1.00
R4886:Leng8	UTSW	7	4,147,930 (GRCm39)	splice site	probably null
R5307:Leng8	UTSW	7	4,148,472 (GRCm39)	missense	probably damaging	1.00
R5339:Leng8	UTSW	7	4,148,285 (GRCm39)	missense	possibly damaging	0.96
R5368:Leng8	UTSW	7	4,142,987 (GRCm39)	missense	probably damaging	0.97
R5370:Leng8	UTSW	7	4,148,433 (GRCm39)	missense	possibly damaging	0.48
R5615:Leng8	UTSW	7	4,147,957 (GRCm39)	nonsense	probably null
R5645:Leng8	UTSW	7	4,148,273 (GRCm39)	missense	probably damaging	1.00
R5750:Leng8	UTSW	7	4,145,119 (GRCm39)	missense	probably benign	0.04
R6041:Leng8	UTSW	7	4,148,568 (GRCm39)	missense	probably benign	0.01
R6054:Leng8	UTSW	7	4,148,522 (GRCm39)	splice site	probably null
R6481:Leng8	UTSW	7	4,148,412 (GRCm39)	missense	probably damaging	1.00
R6826:Leng8	UTSW	7	4,148,319 (GRCm39)	missense	probably damaging	1.00
R6919:Leng8	UTSW	7	4,146,625 (GRCm39)	missense	possibly damaging	0.82
R7313:Leng8	UTSW	7	4,142,525 (GRCm39)	missense	possibly damaging	0.73
R7357:Leng8	UTSW	7	4,147,932 (GRCm39)	nonsense	probably null
R7428:Leng8	UTSW	7	4,146,572 (GRCm39)	missense	probably damaging	1.00
R7686:Leng8	UTSW	7	4,146,504 (GRCm39)	nonsense	probably null
R8027:Leng8	UTSW	7	4,145,855 (GRCm39)	frame shift	probably null
R8198:Leng8	UTSW	7	4,147,170 (GRCm39)	missense	possibly damaging	0.82
R9048:Leng8	UTSW	7	4,146,931 (GRCm39)	unclassified	probably benign
R9103:Leng8	UTSW	7	4,146,897 (GRCm39)	missense	probably damaging	1.00
R9234:Leng8	UTSW	7	4,145,247 (GRCm39)	missense	probably damaging	1.00

Posted On

2015-04-16