Mutagenetix > Incidental Mutation

Incidental Mutation 'R1745:Ttc38'

193950

Institutional Source

Beutler Lab

Gene Symbol

Ttc38

Ensembl Gene

ENSMUSG00000035944

Gene Name

tetratricopeptide repeat domain 38

Synonyms

MMRRC Submission

039777-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R1745 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

85716545-85743023 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 85717373 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 16 (L16P)

Ref Sequence

ENSEMBL: ENSMUSP00000114504 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000124011] [ENSMUST00000146088]

AlphaFold

A3KMP2

Predicted Effect

probably damaging
Transcript: ENSMUST00000124011
AA Change: L16P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133158

Predicted Effect

probably damaging
Transcript: ENSMUST00000146088
AA Change: L16P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000114504
Gene: ENSMUSG00000035944
AA Change: L16P

Domain	Start	End	E-Value	Type
SCOP:d1ld8a_	105	272	1e-7	SMART
low complexity region	342	354	N/A	INTRINSIC

Meta Mutation Damage Score

0.9541

Coding Region Coverage

1x: 97.4%
3x: 96.9%
10x: 95.3%
20x: 92.5%

Validation Efficiency

98% (54/55)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc10	A	T	17: 46,623,359 (GRCm39)	V851E	probably benign	Het
Adam28	A	G	14: 68,870,620 (GRCm39)	I351T	probably benign	Het
Agrp	G	T	8: 106,293,467 (GRCm39)	T106K	probably damaging	Het
Anpep	C	T	7: 79,488,004 (GRCm39)	E518K	probably benign	Het
Ap2a1	T	C	7: 44,556,369 (GRCm39)	E285G	probably damaging	Het
Arfgef1	A	C	1: 10,243,480 (GRCm39)	I1023R	probably damaging	Het
Atp2c2	G	A	8: 120,451,833 (GRCm39)	V133I	probably benign	Het
Bpifb6	A	G	2: 153,753,403 (GRCm39)	T401A	possibly damaging	Het
Capn3	G	A	2: 120,320,170 (GRCm39)	V283M	possibly damaging	Het
Chd6	A	T	2: 160,823,587 (GRCm39)	V1261E	probably damaging	Het
Col22a1	C	T	15: 71,878,636 (GRCm39)	A174T	probably damaging	Het
Crnn	T	C	3: 93,054,198 (GRCm39)	V27A	probably benign	Het
Dclk2	C	T	3: 86,712,946 (GRCm39)	R503Q	possibly damaging	Het
Dgkd	T	C	1: 87,859,766 (GRCm39)		probably null	Het
Diaph3	A	G	14: 87,203,996 (GRCm39)	L554P	probably damaging	Het
Ephb4	A	T	5: 137,358,696 (GRCm39)	H293L	probably benign	Het
Erbin	G	T	13: 103,975,957 (GRCm39)	H646N	probably damaging	Het
Faiml	T	C	9: 99,116,511 (GRCm39)	N60D	probably benign	Het
Fem1al	A	G	11: 29,774,723 (GRCm39)	S245P	probably benign	Het
Flot1	A	G	17: 36,135,552 (GRCm39)	E102G	probably damaging	Het
Fryl	G	A	5: 73,190,204 (GRCm39)		probably benign	Het
Gad1-ps	A	T	10: 99,281,386 (GRCm39)		noncoding transcript	Het
Gtf3c3	A	G	1: 54,473,371 (GRCm39)	S81P	probably damaging	Het
Hs1bp3	C	T	12: 8,371,690 (GRCm39)	Q91*	probably null	Het
Igf1r	T	C	7: 67,819,661 (GRCm39)	C324R	probably damaging	Het
Il23r	G	A	6: 67,443,275 (GRCm39)	T276I	probably damaging	Het
Ip6k1	G	A	9: 107,918,195 (GRCm39)	E77K	possibly damaging	Het
Kctd1	A	T	18: 15,196,263 (GRCm39)		probably benign	Het
Kmt2b	A	T	7: 30,285,275 (GRCm39)	M539K	possibly damaging	Het
Man2b1	T	A	8: 85,820,563 (GRCm39)	F617I	probably damaging	Het
Med15	G	A	16: 17,473,570 (GRCm39)		probably benign	Het
Myo9b	A	G	8: 71,806,691 (GRCm39)	K1543R	probably damaging	Het
N4bp2	A	G	5: 65,948,165 (GRCm39)	Y265C	probably benign	Het
N4bp2l2	A	T	5: 150,585,424 (GRCm39)	N185K	probably benign	Het
Nkx2-1	A	G	12: 56,580,529 (GRCm39)	M137T	probably benign	Het
Or51q1c	A	G	7: 103,653,270 (GRCm39)	T269A	probably benign	Het
Prickle2	A	T	6: 92,353,574 (GRCm39)	Y631N	probably damaging	Het
Ptpro	A	G	6: 137,377,643 (GRCm39)	T698A	probably benign	Het
Rapgef3	T	C	15: 97,648,059 (GRCm39)	I690V	probably benign	Het
Rnf44	G	A	13: 54,830,005 (GRCm39)	R271W	probably damaging	Het
Rundc3a	GAGCC	GAGCCAGCC	11: 102,291,739 (GRCm39)		probably null	Het
Ryr2	A	G	13: 11,805,153 (GRCm39)	Y904H	probably damaging	Het
Suz12	T	C	11: 79,912,922 (GRCm39)	L322P	probably damaging	Het
Tnfsf13	G	A	11: 69,575,973 (GRCm39)	A38V	probably benign	Het
Topbp1	G	A	9: 103,186,044 (GRCm39)	R62H	probably benign	Het
Tor1aip1	G	T	1: 155,906,180 (GRCm39)		probably null	Het
Trpv4	A	T	5: 114,771,215 (GRCm39)	V438E	probably damaging	Het
Tsku	A	T	7: 98,001,386 (GRCm39)	V315E	possibly damaging	Het
Vmn1r170	A	G	7: 23,305,759 (GRCm39)	I54V	probably damaging	Het
Vmn1r71	T	C	7: 10,482,196 (GRCm39)	D98G	probably benign	Het
Wdfy3	A	T	5: 102,096,795 (GRCm39)	D334E	probably damaging	Het
Zfhx3	T	A	8: 109,682,494 (GRCm39)	F3311Y	unknown	Het
Zswim9	A	G	7: 13,003,482 (GRCm39)	S123P	probably damaging	Het

Other mutations in Ttc38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00899:Ttc38	APN	15	85,728,663 (GRCm39)	missense	possibly damaging	0.76
IGL01596:Ttc38	APN	15	85,720,274 (GRCm39)	missense	possibly damaging	0.89
IGL03221:Ttc38	APN	15	85,718,742 (GRCm39)	missense	probably benign	0.00
hairy	UTSW	15	85,735,802 (GRCm39)	splice site	probably null
Stubble	UTSW	15	85,728,716 (GRCm39)	nonsense	probably null
PIT4431001:Ttc38	UTSW	15	85,720,328 (GRCm39)	missense	probably benign
R0040:Ttc38	UTSW	15	85,725,690 (GRCm39)	missense	probably damaging	1.00
R0040:Ttc38	UTSW	15	85,725,690 (GRCm39)	missense	probably damaging	1.00
R0081:Ttc38	UTSW	15	85,740,673 (GRCm39)	missense	probably benign	0.04
R0143:Ttc38	UTSW	15	85,737,920 (GRCm39)	missense	possibly damaging	0.51
R0764:Ttc38	UTSW	15	85,730,604 (GRCm39)	splice site	probably benign
R1837:Ttc38	UTSW	15	85,735,764 (GRCm39)	missense	probably damaging	1.00
R2069:Ttc38	UTSW	15	85,722,989 (GRCm39)	missense	probably damaging	1.00
R2086:Ttc38	UTSW	15	85,722,928 (GRCm39)	missense	probably benign
R2151:Ttc38	UTSW	15	85,735,802 (GRCm39)	splice site	probably null
R2228:Ttc38	UTSW	15	85,728,704 (GRCm39)	missense	probably benign	0.01
R4641:Ttc38	UTSW	15	85,728,659 (GRCm39)	missense	possibly damaging	0.87
R4705:Ttc38	UTSW	15	85,737,164 (GRCm39)	missense	probably benign	0.00
R4721:Ttc38	UTSW	15	85,722,947 (GRCm39)	missense	probably benign
R5037:Ttc38	UTSW	15	85,728,741 (GRCm39)	missense	probably benign	0.16
R6208:Ttc38	UTSW	15	85,725,698 (GRCm39)	missense	possibly damaging	0.56
R6454:Ttc38	UTSW	15	85,723,023 (GRCm39)	missense	probably damaging	1.00
R7326:Ttc38	UTSW	15	85,737,062 (GRCm39)	missense	probably benign	0.00
R7809:Ttc38	UTSW	15	85,722,939 (GRCm39)	missense	possibly damaging	0.65
R8195:Ttc38	UTSW	15	85,728,716 (GRCm39)	nonsense	probably null
R9042:Ttc38	UTSW	15	85,720,310 (GRCm39)	missense	probably benign	0.00
R9631:Ttc38	UTSW	15	85,728,659 (GRCm39)	missense	possibly damaging	0.87

Predicted Primers

PCR Primer
(F):5'- GCTTCCTACCGTTCCTGGTAATGAC -3'
(R):5'- GCCTTTGTGGCAGCTCAACATTTC -3'

Sequencing Primer
(F):5'- GGTAATGACCCTCCTATTTGCTG -3'
(R):5'- GCAGAGATGCTTCCCATATTG -3'

Posted On

2014-05-23