Mutagenetix > Incidental Mutation

Incidental Mutation 'R8932:Mllt10'

690198

Institutional Source

Beutler Lab

Gene Symbol

Mllt10

Ensembl Gene

ENSMUSG00000026743

Gene Name

myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10

Synonyms

B130021D15Rik, D630001B22Rik, Af10

MMRRC Submission

068776-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.704) question?

Stock #

R8932 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

18060048-18217199 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 18128617 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 199 (S199R)

Ref Sequence

ENSEMBL: ENSMUSP00000028076 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028076] [ENSMUST00000114669] [ENSMUST00000114671] [ENSMUST00000114680]

AlphaFold

O54826

Predicted Effect

probably benign
Transcript: ENSMUST00000028076
AA Change: S199R

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000028076
Gene: ENSMUSG00000026743
AA Change: S199R

Domain	Start	End	E-Value	Type
PHD	24	72	8.51e-8	SMART
PHD	136	195	2.92e-6	SMART
low complexity region	217	248	N/A	INTRINSIC
low complexity region	258	274	N/A	INTRINSIC
low complexity region	308	326	N/A	INTRINSIC
low complexity region	352	372	N/A	INTRINSIC
low complexity region	490	515	N/A	INTRINSIC
low complexity region	581	594	N/A	INTRINSIC
low complexity region	609	627	N/A	INTRINSIC
low complexity region	674	692	N/A	INTRINSIC
coiled coil region	741	782	N/A	INTRINSIC
low complexity region	836	879	N/A	INTRINSIC
low complexity region	941	952	N/A	INTRINSIC
low complexity region	966	986	N/A	INTRINSIC
low complexity region	997	1018	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114669

SMART Domains

Protein: ENSMUSP00000110317
Gene: ENSMUSG00000026743

Domain	Start	End	E-Value	Type
low complexity region	38	51	N/A	INTRINSIC
low complexity region	66	84	N/A	INTRINSIC
low complexity region	131	149	N/A	INTRINSIC
coiled coil region	198	239	N/A	INTRINSIC
low complexity region	293	336	N/A	INTRINSIC
low complexity region	398	409	N/A	INTRINSIC
low complexity region	423	443	N/A	INTRINSIC
low complexity region	454	475	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000114671
AA Change: S121R

PolyPhen 2 Score 0.940 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000110319
Gene: ENSMUSG00000026743
AA Change: S121R

Domain	Start	End	E-Value	Type
PHD	58	117	2.92e-6	SMART
low complexity region	139	170	N/A	INTRINSIC
low complexity region	180	196	N/A	INTRINSIC
low complexity region	230	248	N/A	INTRINSIC
low complexity region	274	294	N/A	INTRINSIC
low complexity region	412	437	N/A	INTRINSIC
low complexity region	503	516	N/A	INTRINSIC
low complexity region	531	549	N/A	INTRINSIC
low complexity region	596	614	N/A	INTRINSIC
coiled coil region	663	704	N/A	INTRINSIC
low complexity region	758	801	N/A	INTRINSIC
low complexity region	863	874	N/A	INTRINSIC
low complexity region	888	908	N/A	INTRINSIC
low complexity region	919	940	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114680
AA Change: S199R

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000110328
Gene: ENSMUSG00000026743
AA Change: S199R

Domain	Start	End	E-Value	Type
PHD	24	72	8.51e-8	SMART
PHD	136	195	2.92e-6	SMART
low complexity region	217	248	N/A	INTRINSIC
low complexity region	258	274	N/A	INTRINSIC
low complexity region	308	326	N/A	INTRINSIC
low complexity region	352	372	N/A	INTRINSIC
low complexity region	490	515	N/A	INTRINSIC
low complexity region	581	594	N/A	INTRINSIC
low complexity region	609	627	N/A	INTRINSIC
low complexity region	674	692	N/A	INTRINSIC
coiled coil region	741	782	N/A	INTRINSIC
low complexity region	836	879	N/A	INTRINSIC
low complexity region	941	952	N/A	INTRINSIC
low complexity region	966	986	N/A	INTRINSIC
low complexity region	997	1018	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (67/67)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a transcription factor and has been identified as a partner gene involved in several chromosomal rearrangements resulting in various leukemias. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam34	G	T	8: 44,105,192 (GRCm39)	T151K	probably benign	Het
Adnp2	C	T	18: 80,185,893 (GRCm39)	G27S	probably damaging	Het
Ank3	A	G	10: 69,660,292 (GRCm39)	M265V	probably benign	Het
Aoc1l1	G	A	6: 48,952,428 (GRCm39)	E118K	probably damaging	Het
Apoe	T	C	7: 19,430,597 (GRCm39)	D215G	possibly damaging	Het
Atp5f1b	A	G	10: 127,924,850 (GRCm39)	I438V	probably benign	Het
Bckdha	A	G	7: 25,330,436 (GRCm39)	S387P	probably damaging	Het
Camkk1	T	C	11: 72,924,734 (GRCm39)	F316L	probably damaging	Het
Carmil1	A	G	13: 24,197,179 (GRCm39)	Y158H		Het
Ccdc148	T	C	2: 58,894,054 (GRCm39)	R29G	probably benign	Het
Ccdc39	A	G	3: 33,884,274 (GRCm39)	V356A	probably benign	Het
Cdan1	G	A	2: 120,561,568 (GRCm39)	Q66*	probably null	Het
Ckap4	A	T	10: 84,364,290 (GRCm39)	S258T	probably benign	Het
Col5a2	T	C	1: 45,419,306 (GRCm39)	D1258G	probably benign	Het
Col6a1	G	A	10: 76,552,593 (GRCm39)	P431L	unknown	Het
Cplane1	A	G	15: 8,223,859 (GRCm39)	Y874C	probably damaging	Het
Csn1s2a	A	G	5: 87,933,164 (GRCm39)	I138V	probably benign	Het
Cyp19a1	C	T	9: 54,083,861 (GRCm39)	G176D	probably benign	Het
Dnah10	A	G	5: 124,878,015 (GRCm39)	E2700G	possibly damaging	Het
Eif3l	T	A	15: 78,960,006 (GRCm39)	Y23*	probably null	Het
Fam72a	A	G	1: 131,456,502 (GRCm39)	K22E	probably benign	Het
Golim4	A	G	3: 75,805,351 (GRCm39)	V258A	probably benign	Het
Gtf2ird2	C	T	5: 134,237,739 (GRCm39)	A272V	probably benign	Het
Hpse	T	C	5: 100,846,872 (GRCm39)	T186A	possibly damaging	Het
Ift140	A	T	17: 25,305,862 (GRCm39)	Q816H	probably benign	Het
Iqca1	A	T	1: 90,067,750 (GRCm39)	I167N	probably damaging	Het
Iqgap1	A	T	7: 80,401,141 (GRCm39)	F515L	probably benign	Het
Itgb4	G	A	11: 115,879,295 (GRCm39)	R558H	probably benign	Het
Kcna10	G	A	3: 107,101,419 (GRCm39)	D17N	probably damaging	Het
Kcnj16	A	G	11: 110,915,829 (GRCm39)	I164V	probably damaging	Het
Lrrc55	G	T	2: 85,026,615 (GRCm39)	N136K	probably damaging	Het
Mdm4	A	T	1: 132,940,382 (GRCm39)	M50K	probably benign	Het
Mfge8	A	G	7: 78,786,530 (GRCm39)	S290P	probably damaging	Het
Mindy4	G	A	6: 55,201,115 (GRCm39)	D267N	probably benign	Het
Mms22l	T	C	4: 24,533,029 (GRCm39)	S436P	probably damaging	Het
Mpped2	A	G	2: 106,697,395 (GRCm39)	N290S	possibly damaging	Het
Mrgpra2a	A	G	7: 47,076,445 (GRCm39)	L271P	probably benign	Het
Myrf	T	A	19: 10,200,931 (GRCm39)	E247D	probably benign	Het
Ndrg3	A	G	2: 156,782,299 (GRCm39)	I189T	possibly damaging	Het
Nenf	C	T	1: 191,050,148 (GRCm39)	E48K	probably benign	Het
Nlgn2	T	A	11: 69,718,994 (GRCm39)	N232Y	probably damaging	Het
Oog2	G	T	4: 143,920,685 (GRCm39)	M39I	probably benign	Het
Or9r7	A	T	10: 129,962,631 (GRCm39)	N98K	probably benign	Het
Osbpl3	A	T	6: 50,304,371 (GRCm39)	N461K	probably benign	Het
P4ha1	A	G	10: 59,175,130 (GRCm39)	D30G	possibly damaging	Het
Pappa2	A	T	1: 158,590,762 (GRCm39)	C1631S	probably damaging	Het
Pigk	A	G	3: 152,445,871 (GRCm39)	M161V	possibly damaging	Het
Prdm1	G	T	10: 44,317,335 (GRCm39)	S496Y	probably damaging	Het
Prkg2	T	C	5: 99,095,299 (GRCm39)	N624S	possibly damaging	Het
Rgs6	A	G	12: 83,112,733 (GRCm39)	D181G	probably damaging	Het
Sbf2	A	G	7: 110,040,155 (GRCm39)		probably null	Het
Sbno2	A	C	10: 79,898,042 (GRCm39)	L728W	probably damaging	Het
Selenbp2	A	T	3: 94,609,793 (GRCm39)	I310F	probably damaging	Het
Shank3	T	A	15: 89,432,986 (GRCm39)	W1244R	possibly damaging	Het
Slc34a1	A	C	13: 24,004,184 (GRCm39)	I395L	probably benign	Het
Slf1	A	T	13: 77,194,693 (GRCm39)	D877E	probably damaging	Het
Smtn	T	C	11: 3,472,908 (GRCm39)	S255G	probably benign	Het
Tbx2	T	A	11: 85,725,533 (GRCm39)	D161E	probably damaging	Het
Tex14	C	A	11: 87,324,675 (GRCm39)	L26M	possibly damaging	Het
Traf7	A	G	17: 24,731,286 (GRCm39)	F249S	probably damaging	Het
Trpm6	A	G	19: 18,815,366 (GRCm39)	K1151E	possibly damaging	Het
Ttc7b	A	G	12: 100,268,022 (GRCm39)	V773A	probably benign	Het
Ttn	G	A	2: 76,747,912 (GRCm39)	T4379I	probably benign	Het
Ttn	G	A	2: 76,602,854 (GRCm39)	T18456I	probably damaging	Het
Ttn	G	C	2: 76,709,171 (GRCm39)	L8703V	unknown	Het
Ubb	T	A	11: 62,442,979 (GRCm39)	I3N	probably damaging	Het
Vmn1r209	A	T	13: 22,990,343 (GRCm39)	W116R	probably damaging	Het
Vmn1r75	A	G	7: 11,614,838 (GRCm39)	D190G	probably damaging	Het
Wdr12	T	A	1: 60,130,202 (GRCm39)	M70L	probably benign	Het
Wdr48	C	A	9: 119,740,142 (GRCm39)	T317K	probably damaging	Het
Zbtb5	A	G	4: 44,993,962 (GRCm39)	V474A	probably benign	Het
Zfp128	C	T	7: 12,625,113 (GRCm39)	R494C	possibly damaging	Het

Other mutations in Mllt10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01646:Mllt10	APN	2	18,127,128 (GRCm39)	missense	probably damaging	1.00
IGL02366:Mllt10	APN	2	18,069,898 (GRCm39)	missense	probably damaging	0.99
IGL02990:Mllt10	APN	2	18,128,522 (GRCm39)	splice site	probably benign
IGL03034:Mllt10	APN	2	18,069,847 (GRCm39)	start codon destroyed	probably null	0.55
R0348:Mllt10	UTSW	2	18,167,424 (GRCm39)	missense	probably damaging	1.00
R0487:Mllt10	UTSW	2	18,211,948 (GRCm39)	missense	probably damaging	0.98
R0492:Mllt10	UTSW	2	18,151,698 (GRCm39)	splice site	probably benign
R0518:Mllt10	UTSW	2	18,076,017 (GRCm39)	critical splice donor site	probably null
R0720:Mllt10	UTSW	2	18,201,406 (GRCm39)	missense	probably benign
R0733:Mllt10	UTSW	2	18,208,577 (GRCm39)	intron	probably benign
R1532:Mllt10	UTSW	2	18,097,646 (GRCm39)	critical splice donor site	probably null
R1665:Mllt10	UTSW	2	18,213,601 (GRCm39)	missense	possibly damaging	0.93
R1768:Mllt10	UTSW	2	18,167,657 (GRCm39)	missense	probably damaging	1.00
R2098:Mllt10	UTSW	2	18,167,464 (GRCm39)	missense	possibly damaging	0.50
R2114:Mllt10	UTSW	2	18,167,380 (GRCm39)	missense	probably benign
R2116:Mllt10	UTSW	2	18,167,380 (GRCm39)	missense	probably benign
R2117:Mllt10	UTSW	2	18,167,380 (GRCm39)	missense	probably benign
R2179:Mllt10	UTSW	2	18,215,604 (GRCm39)	missense	probably damaging	1.00
R2192:Mllt10	UTSW	2	18,211,871 (GRCm39)	missense	probably benign	0.11
R2510:Mllt10	UTSW	2	18,069,935 (GRCm39)	missense	possibly damaging	0.94
R2511:Mllt10	UTSW	2	18,069,935 (GRCm39)	missense	possibly damaging	0.94
R4669:Mllt10	UTSW	2	18,208,444 (GRCm39)	missense	probably damaging	1.00
R5004:Mllt10	UTSW	2	18,175,079 (GRCm39)	missense	probably damaging	1.00
R5072:Mllt10	UTSW	2	18,114,685 (GRCm39)	missense	possibly damaging	0.72
R5187:Mllt10	UTSW	2	18,213,585 (GRCm39)	nonsense	probably null
R5561:Mllt10	UTSW	2	18,114,656 (GRCm39)	missense	probably damaging	0.98
R6141:Mllt10	UTSW	2	18,215,604 (GRCm39)	missense	probably damaging	1.00
R6352:Mllt10	UTSW	2	18,128,604 (GRCm39)	missense	probably damaging	1.00
R6844:Mllt10	UTSW	2	18,164,294 (GRCm39)	missense	probably benign	0.02
R7060:Mllt10	UTSW	2	18,164,371 (GRCm39)	missense	possibly damaging	0.64
R7464:Mllt10	UTSW	2	18,175,090 (GRCm39)	missense	probably benign
R7691:Mllt10	UTSW	2	18,208,423 (GRCm39)	missense	probably null	0.94
R7691:Mllt10	UTSW	2	18,208,422 (GRCm39)	missense	possibly damaging	0.94
R7937:Mllt10	UTSW	2	18,210,895 (GRCm39)	missense	probably damaging	1.00
R7956:Mllt10	UTSW	2	18,175,068 (GRCm39)	missense	probably benign	0.01
R7976:Mllt10	UTSW	2	18,167,214 (GRCm39)	missense	possibly damaging	0.94
R8079:Mllt10	UTSW	2	18,128,567 (GRCm39)	missense	probably damaging	0.99
R8084:Mllt10	UTSW	2	18,114,637 (GRCm39)	missense	probably damaging	0.99
R8518:Mllt10	UTSW	2	18,151,670 (GRCm39)	missense	probably damaging	0.99
R8768:Mllt10	UTSW	2	18,167,583 (GRCm39)	missense	probably damaging	1.00
R8826:Mllt10	UTSW	2	18,167,353 (GRCm39)	missense	probably benign	0.10
R8850:Mllt10	UTSW	2	18,201,469 (GRCm39)	missense	probably benign	0.33
R9009:Mllt10	UTSW	2	18,167,163 (GRCm39)	missense	probably damaging	0.96
R9129:Mllt10	UTSW	2	18,167,404 (GRCm39)	missense	probably benign	0.41
R9514:Mllt10	UTSW	2	18,164,322 (GRCm39)	missense	probably damaging	1.00
R9602:Mllt10	UTSW	2	18,211,850 (GRCm39)	missense	probably damaging	1.00
R9706:Mllt10	UTSW	2	18,151,655 (GRCm39)	missense	possibly damaging	0.50
Z1177:Mllt10	UTSW	2	18,175,887 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TATGCTGTCTTTCAGGTGCC -3'
(R):5'- CTGTCAATAAGGAACAGGCTAAATG -3'

Sequencing Primer
(F):5'- CTGTCTTTCAGGTGCCAAAAAGG -3'
(R):5'- CAGGCTAAATGTCTGCACTGG -3'

Posted On

2021-11-19