Mutagenetix > Incidental Mutation

Incidental Mutation 'R6260:Tcerg1'

506663

Institutional Source

Beutler Lab

Gene Symbol

Tcerg1

Ensembl Gene

ENSMUSG00000024498

Gene Name

transcription elongation regulator 1 (CA150)

Synonyms

ca150, p144, Fbp28, 2900090C16Rik, Taf2s, 2410022J09Rik

MMRRC Submission

044377-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6260 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

42644552-42708858 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 42686530 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 696 (Y696N)

Ref Sequence

ENSEMBL: ENSMUSP00000134458 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025375] [ENSMUST00000173642]

AlphaFold

Q8CGF7

Predicted Effect

probably damaging
Transcript: ENSMUST00000025375
AA Change: Y696N

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

SMART Domains

Protein: ENSMUSP00000025375
Gene: ENSMUSG00000024498
AA Change: Y696N

Domain	Start	End	E-Value	Type
low complexity region	3	13	N/A	INTRINSIC
low complexity region	40	92	N/A	INTRINSIC
WW	132	164	8.27e-10	SMART
low complexity region	178	257	N/A	INTRINSIC
low complexity region	260	347	N/A	INTRINSIC
low complexity region	350	373	N/A	INTRINSIC
WW	432	464	2.65e-8	SMART
WW	531	563	1.2e-6	SMART
low complexity region	611	623	N/A	INTRINSIC
coiled coil region	629	654	N/A	INTRINSIC
FF	661	714	2.67e-13	SMART
FF	727	781	1.51e-12	SMART
FF	794	848	4.29e-17	SMART
FF	898	954	8.33e-15	SMART
FF	956	1012	1.47e-15	SMART
FF	1014	1079	1.3e-16	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000173642
AA Change: Y696N

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

SMART Domains

Protein: ENSMUSP00000134458
Gene: ENSMUSG00000024498
AA Change: Y696N

Domain	Start	End	E-Value	Type
low complexity region	3	13	N/A	INTRINSIC
low complexity region	40	92	N/A	INTRINSIC
WW	132	164	8.27e-10	SMART
low complexity region	178	257	N/A	INTRINSIC
low complexity region	260	347	N/A	INTRINSIC
low complexity region	350	373	N/A	INTRINSIC
WW	432	464	2.65e-8	SMART
WW	531	563	1.2e-6	SMART
low complexity region	611	623	N/A	INTRINSIC
coiled coil region	629	654	N/A	INTRINSIC
FF	661	714	2.67e-13	SMART
FF	727	781	1.51e-12	SMART
FF	794	848	4.29e-17	SMART
FF	898	954	8.33e-15	SMART
FF	956	1012	1.47e-15	SMART

Meta Mutation Damage Score

0.9548

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.6%

Validation Efficiency

99% (77/78)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear protein that regulates transcriptional elongation and pre-mRNA splicing. The encoded protein interacts with the hyperphosphorylated C-terminal domain of RNA polymerase II via multiple FF domains, and with the pre-mRNA splicing factor SF1 via a WW domain. Alternative splicing results in multiple transcripts variants encoding different isoforms. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca7	T	A	10: 79,844,821 (GRCm39)	N1514K	probably damaging	Het
Abcb4	G	T	5: 8,984,219 (GRCm39)	G650*	probably null	Het
Acsbg1	T	A	9: 54,535,751 (GRCm39)		probably null	Het
Alms1	A	T	6: 85,605,717 (GRCm39)	K2456*	probably null	Het
Alppl2	A	T	1: 87,016,184 (GRCm39)	M225K	probably damaging	Het
Ank2	C	T	3: 126,737,206 (GRCm39)	V2806I	probably benign	Het
Atxn10	A	T	15: 85,346,612 (GRCm39)	I457F	probably benign	Het
Cad	G	T	5: 31,224,144 (GRCm39)	M800I	probably null	Het
Carmil3	T	A	14: 55,737,889 (GRCm39)	L815Q	probably damaging	Het
Ccz1	A	G	5: 143,940,859 (GRCm39)		probably null	Het
Cdc73	G	A	1: 143,567,211 (GRCm39)	T104I	probably benign	Het
Cfap52	A	T	11: 67,829,780 (GRCm39)	C330S	possibly damaging	Het
Clec16a	C	T	16: 10,512,712 (GRCm39)		probably benign	Het
Cntn3	A	G	6: 102,254,178 (GRCm39)		probably null	Het
Crocc2	A	G	1: 93,141,360 (GRCm39)	K1171R	possibly damaging	Het
Ctsa	T	C	2: 164,676,281 (GRCm39)	V86A	probably damaging	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Ddhd2	A	G	8: 26,242,144 (GRCm39)	F244L	probably benign	Het
Ddn	A	G	15: 98,703,735 (GRCm39)	V519A	possibly damaging	Het
Dip2b	G	T	15: 100,060,583 (GRCm39)	V253L	probably benign	Het
Dnah17	C	A	11: 118,017,148 (GRCm39)	W197C	probably damaging	Het
Dnah17	A	T	11: 118,017,150 (GRCm39)	W197R	probably damaging	Het
Dnah17	C	T	11: 118,017,149 (GRCm39)	W197*	probably null	Het
Ercc6	T	A	14: 32,279,813 (GRCm39)	D609E	probably benign	Het
Erg	C	A	16: 95,181,100 (GRCm39)	R147L	probably damaging	Het
Fbxo41	A	T	6: 85,455,537 (GRCm39)	L549H	probably damaging	Het
Foxd4	A	G	19: 24,876,968 (GRCm39)	S411P	probably benign	Het
Gaa	C	A	11: 119,171,997 (GRCm39)	A700D	probably benign	Het
Galntl6	T	A	8: 58,337,515 (GRCm39)	D135V	probably damaging	Het
Gm1043	G	C	5: 37,331,816 (GRCm39)	G832A	probably benign	Het
Gm21103	C	T	14: 17,484,841 (GRCm39)	E68K	probably damaging	Het
Gpam	A	G	19: 55,071,838 (GRCm39)	V301A	probably benign	Het
H2-M10.1	T	A	17: 36,634,994 (GRCm39)	I304F	unknown	Het
Itgb4	C	T	11: 115,874,983 (GRCm39)	R447W	probably benign	Het
Jak3	C	A	8: 72,131,954 (GRCm39)	Q177K	probably benign	Het
Kcnu1	G	A	8: 26,341,919 (GRCm39)	R88H	probably damaging	Het
Kng1	A	T	16: 22,877,371 (GRCm39)	I60F	possibly damaging	Het
Krt77	A	T	15: 101,772,807 (GRCm39)	Y257*	probably null	Het
Lcor	A	T	19: 41,570,809 (GRCm39)	S1C	probably null	Het
Lcor	G	T	19: 41,570,810 (GRCm39)	S1I	possibly damaging	Het
Lgr6	C	T	1: 134,921,748 (GRCm39)	A199T	probably damaging	Het
Map4k5	C	A	12: 69,878,336 (GRCm39)	R355L	probably benign	Het
Mefv	C	T	16: 3,530,898 (GRCm39)	R498H	probably benign	Het
Mical3	A	T	6: 120,985,991 (GRCm39)	L150Q	probably damaging	Het
Mtcl1	T	A	17: 66,650,536 (GRCm39)	Q1340L	probably damaging	Het
Nfic	A	T	10: 81,256,351 (GRCm39)	C126*	probably null	Het
Nisch	T	A	14: 30,899,085 (GRCm39)		probably benign	Het
Nt5dc3	A	G	10: 86,647,395 (GRCm39)	Y130C	probably damaging	Het
Or2ag1b	A	T	7: 106,288,079 (GRCm39)	N286K	probably damaging	Het
Or4f15	C	T	2: 111,814,396 (GRCm39)	V8I	probably benign	Het
Or6c65	C	A	10: 129,603,389 (GRCm39)	T8K	probably benign	Het
Pcdhb12	T	C	18: 37,569,892 (GRCm39)	V346A	probably benign	Het
Pla2g4a	A	G	1: 149,733,238 (GRCm39)	S504P	probably benign	Het
Plin2	G	T	4: 86,575,526 (GRCm39)	A341D	probably damaging	Het
Plxnb2	A	T	15: 89,049,494 (GRCm39)	I575N	probably benign	Het
Pnma8b	T	G	7: 16,680,158 (GRCm39)	W381G	probably benign	Het
Psma8	A	G	18: 14,854,324 (GRCm39)	D68G	probably damaging	Het
Rcor3	G	A	1: 191,808,559 (GRCm39)	H207Y	probably benign	Het
Rwdd2b	C	A	16: 87,231,356 (GRCm39)	G266V	probably damaging	Het
Ryr3	A	G	2: 112,490,449 (GRCm39)	F3795S	probably damaging	Het
Slc28a2b	A	T	2: 122,353,963 (GRCm39)	I530F	probably damaging	Het
Sord	T	A	2: 122,089,613 (GRCm39)		probably null	Het
Spdl1	T	A	11: 34,710,713 (GRCm39)	N345I	probably damaging	Het
St8sia2	T	A	7: 73,626,441 (GRCm39)	R42S	possibly damaging	Het
Syt9	G	T	7: 107,035,717 (GRCm39)	V245F	possibly damaging	Het
Tbpl2	T	A	2: 23,984,898 (GRCm39)	N82I	possibly damaging	Het
Thsd7b	A	G	1: 129,595,655 (GRCm39)	T492A	probably benign	Het
Timm13	A	C	10: 80,736,135 (GRCm39)		probably benign	Het
Trdmt1	T	A	2: 13,524,870 (GRCm39)	Q195L	probably benign	Het
Ttc27	T	A	17: 75,165,086 (GRCm39)	V764D	probably damaging	Het
Ttc39d	C	A	17: 80,524,076 (GRCm39)	S245*	probably null	Het
Ttc41	A	G	10: 86,567,023 (GRCm39)	E563G	probably benign	Het
Ttc41	A	T	10: 86,569,571 (GRCm39)	T650S	probably benign	Het
U2surp	A	C	9: 95,358,210 (GRCm39)	L723R	probably damaging	Het
Ubqln3	G	A	7: 103,791,524 (GRCm39)	Q189*	probably null	Het
Vezf1	A	G	11: 87,972,326 (GRCm39)	N229S	probably damaging	Het
Vmn2r79	T	A	7: 86,686,365 (GRCm39)	M582K	probably benign	Het
Zfp518a	A	G	19: 40,902,567 (GRCm39)	D832G	probably benign	Het
Zfyve28	T	C	5: 34,356,216 (GRCm39)	N762D	probably damaging	Het

Other mutations in Tcerg1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00701:Tcerg1	APN	18	42,669,407 (GRCm39)	missense	probably benign	0.34
IGL00708:Tcerg1	APN	18	42,704,190 (GRCm39)	missense	probably benign	0.38
IGL00741:Tcerg1	APN	18	42,701,518 (GRCm39)	missense	possibly damaging	0.94
IGL01314:Tcerg1	APN	18	42,706,374 (GRCm39)	missense	probably damaging	1.00
IGL01358:Tcerg1	APN	18	42,657,342 (GRCm39)	missense	unknown
IGL01832:Tcerg1	APN	18	42,707,620 (GRCm39)	missense	probably damaging	0.99
IGL01985:Tcerg1	APN	18	42,663,721 (GRCm39)	missense	unknown
IGL02937:Tcerg1	APN	18	42,657,414 (GRCm39)	missense	unknown
IGL02953:Tcerg1	APN	18	42,681,535 (GRCm39)	missense	probably damaging	1.00
IGL03082:Tcerg1	APN	18	42,706,422 (GRCm39)	missense	probably damaging	1.00
P0031:Tcerg1	UTSW	18	42,706,367 (GRCm39)	missense	probably benign	0.07
R0060:Tcerg1	UTSW	18	42,657,073 (GRCm39)	missense	unknown
R0138:Tcerg1	UTSW	18	42,701,679 (GRCm39)	splice site	probably benign
R0482:Tcerg1	UTSW	18	42,697,305 (GRCm39)	splice site	probably benign
R0502:Tcerg1	UTSW	18	42,656,021 (GRCm39)	missense	unknown
R0731:Tcerg1	UTSW	18	42,704,905 (GRCm39)	missense	probably damaging	0.99
R1117:Tcerg1	UTSW	18	42,707,717 (GRCm39)	missense	probably damaging	0.99
R1542:Tcerg1	UTSW	18	42,686,495 (GRCm39)	missense	probably damaging	0.99
R1571:Tcerg1	UTSW	18	42,657,357 (GRCm39)	missense	unknown
R1673:Tcerg1	UTSW	18	42,685,646 (GRCm39)	missense	possibly damaging	0.91
R1678:Tcerg1	UTSW	18	42,657,414 (GRCm39)	missense	unknown
R1799:Tcerg1	UTSW	18	42,694,012 (GRCm39)	missense	possibly damaging	0.92
R2094:Tcerg1	UTSW	18	42,697,210 (GRCm39)	missense	possibly damaging	0.92
R2231:Tcerg1	UTSW	18	42,657,309 (GRCm39)	missense	unknown
R2989:Tcerg1	UTSW	18	42,652,540 (GRCm39)	missense	unknown
R3831:Tcerg1	UTSW	18	42,701,554 (GRCm39)	missense	probably damaging	1.00
R4009:Tcerg1	UTSW	18	42,697,201 (GRCm39)	frame shift	probably null
R4034:Tcerg1	UTSW	18	42,652,598 (GRCm39)	missense	unknown
R4826:Tcerg1	UTSW	18	42,668,180 (GRCm39)	missense	unknown
R4858:Tcerg1	UTSW	18	42,657,046 (GRCm39)	missense	unknown
R5371:Tcerg1	UTSW	18	42,652,600 (GRCm39)	missense	unknown
R5865:Tcerg1	UTSW	18	42,669,413 (GRCm39)	missense	probably damaging	0.98
R6128:Tcerg1	UTSW	18	42,644,563 (GRCm39)	splice site	probably null
R6258:Tcerg1	UTSW	18	42,686,530 (GRCm39)	missense	probably damaging	1.00
R6516:Tcerg1	UTSW	18	42,663,957 (GRCm39)	critical splice donor site	probably null
R6825:Tcerg1	UTSW	18	42,681,542 (GRCm39)	missense	probably damaging	0.98
R7147:Tcerg1	UTSW	18	42,683,128 (GRCm39)	missense	probably benign	0.22
R7714:Tcerg1	UTSW	18	42,694,000 (GRCm39)	missense	possibly damaging	0.77
R7739:Tcerg1	UTSW	18	42,657,039 (GRCm39)	missense	unknown
R7838:Tcerg1	UTSW	18	42,670,002 (GRCm39)	missense	probably benign	0.01
R8204:Tcerg1	UTSW	18	42,707,618 (GRCm39)	missense	probably damaging	1.00
R8293:Tcerg1	UTSW	18	42,694,020 (GRCm39)	missense	probably benign	0.03
R8300:Tcerg1	UTSW	18	42,683,137 (GRCm39)	missense	probably benign	0.22
R8426:Tcerg1	UTSW	18	42,681,466 (GRCm39)	missense	possibly damaging	0.68
R8514:Tcerg1	UTSW	18	42,697,187 (GRCm39)	missense	probably damaging	0.98
R8672:Tcerg1	UTSW	18	42,686,559 (GRCm39)	missense	probably damaging	1.00
R9367:Tcerg1	UTSW	18	42,685,573 (GRCm39)	missense	possibly damaging	0.93
R9715:Tcerg1	UTSW	18	42,706,413 (GRCm39)	missense	probably damaging	0.99
R9718:Tcerg1	UTSW	18	42,663,836 (GRCm39)	missense	unknown
R9781:Tcerg1	UTSW	18	42,701,030 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAATTTGCTGTTGCTAGCCTCC -3'
(R):5'- GCGACAGTGGCTTAGTCTGAATAG -3'

Sequencing Primer
(F):5'- GTTGCTAGCCTCCCACTG -3'
(R):5'- GTATGTTTTTACTGCAGAGAGAGAC -3'

Posted On

2018-03-15