Mutagenetix > Incidental Mutation

Incidental Mutation 'R1678:Tcerg1'

188320

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

039714-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R1678 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

42644552-42708858 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 42657414 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 299 (S299P)

Ref Sequence

ENSEMBL: ENSMUSP00000134458 (fasta)

Gene Model

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

AlphaFold

Q8CGF7

Predicted Effect

unknown
Transcript: ENSMUST00000025375
AA Change: S299P

SMART Domains

Protein: ENSMUSP00000025375
Gene: ENSMUSG00000024498
AA Change: S299P

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

unknown
Transcript: ENSMUST00000173642
AA Change: S299P

SMART Domains

Protein: ENSMUSP00000134458
Gene: ENSMUSG00000024498
AA Change: S299P

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

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.2%

Validation Efficiency

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: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca17	A	C	17: 24,554,594 (GRCm39)	I120S	probably benign	Het
Abcb5	A	C	12: 118,929,064 (GRCm39)		probably benign	Het
Abcc4	T	A	14: 118,832,306 (GRCm39)	T775S	probably benign	Het
Acnat2	T	A	4: 49,380,568 (GRCm39)	Y270F	probably damaging	Het
Aif1	G	A	17: 35,391,127 (GRCm39)	P44L	probably benign	Het
Ankib1	A	G	5: 3,756,301 (GRCm39)	I548T	probably damaging	Het
Apbb1ip	A	T	2: 22,764,892 (GRCm39)		probably null	Het
Asb17	C	T	3: 153,550,004 (GRCm39)	S12F	probably damaging	Het
Atad2b	G	A	12: 5,015,899 (GRCm39)	V542I	possibly damaging	Het
Atxn7	T	C	14: 14,096,239 (GRCm38)	F515L	probably damaging	Het
Bicc1	A	G	10: 70,779,348 (GRCm39)	L680P	probably damaging	Het
Bpifb6	G	A	2: 153,750,562 (GRCm39)	R351H	probably damaging	Het
C4b	A	G	17: 34,962,624 (GRCm39)	F26S	probably benign	Het
Cadps	A	G	14: 12,517,802 (GRCm38)		probably null	Het
Capza1	G	T	3: 104,771,669 (GRCm39)	S9*	probably null	Het
Ccl11	C	T	11: 81,948,866 (GRCm39)	P25L	probably damaging	Het
Cdyl	A	T	13: 36,040,872 (GRCm39)	K306N	probably damaging	Het
Cnga3	T	C	1: 37,300,579 (GRCm39)	V471A	possibly damaging	Het
Col4a4	T	C	1: 82,464,380 (GRCm39)	K983E	unknown	Het
Cp	A	C	3: 20,026,881 (GRCm39)	K436N	probably damaging	Het
Csmd1	T	A	8: 15,968,252 (GRCm39)	D3125V	possibly damaging	Het
Daw1	A	T	1: 83,161,087 (GRCm39)	N143I	probably damaging	Het
Dmd	T	A	X: 84,018,368 (GRCm39)	I3067N	probably benign	Het
Dnaaf9	A	G	2: 130,656,193 (GRCm39)	V105A	probably damaging	Het
Dnah11	T	G	12: 117,897,580 (GRCm39)	N3550T	possibly damaging	Het
Dnm2	T	C	9: 21,378,828 (GRCm39)	V129A	possibly damaging	Het
Dync1h1	A	T	12: 110,632,096 (GRCm39)		probably null	Het
Dync2i1	A	G	12: 116,189,590 (GRCm39)	S640P	probably damaging	Het
Efemp1	G	A	11: 28,866,942 (GRCm39)	E325K	probably benign	Het
Enox1	A	G	14: 77,815,096 (GRCm39)	T85A	probably benign	Het
Faim2	C	A	15: 99,418,217 (GRCm39)	V123F	possibly damaging	Het
Fgfr2	T	C	7: 129,830,350 (GRCm39)		probably null	Het
Fign	T	C	2: 63,810,718 (GRCm39)	E184G	probably damaging	Het
Fnd3c2	T	C	X: 105,281,305 (GRCm39)	T799A	probably benign	Het
Frem2	T	C	3: 53,427,359 (GRCm39)	D2931G	probably damaging	Het
Fsip2	A	G	2: 82,816,689 (GRCm39)	T4141A	probably benign	Het
Gigyf2	T	A	1: 87,344,705 (GRCm39)	M546K	probably benign	Het
Gm21775	G	A	Y: 10,553,867 (GRCm39)	V139M	probably damaging	Het
Gpr83	G	T	9: 14,778,145 (GRCm39)	V172F	probably damaging	Het
Itprid1	G	T	6: 55,945,499 (GRCm39)	C740F	probably benign	Het
Jmjd4	A	G	11: 59,344,438 (GRCm39)	Y179C	probably damaging	Het
Kcnq3	A	G	15: 65,903,281 (GRCm39)	L143P	probably damaging	Het
Klhl41	T	C	2: 69,501,283 (GRCm39)	V248A	probably benign	Het
Lama1	T	C	17: 68,117,150 (GRCm39)	Y2482H	possibly damaging	Het
Lamb2	A	T	9: 108,360,885 (GRCm39)		probably null	Het
Lclat1	G	A	17: 73,503,715 (GRCm39)	G162R	probably damaging	Het
Map6	T	C	7: 98,917,305 (GRCm39)	V26A	probably damaging	Het
Mdn1	A	T	4: 32,663,050 (GRCm39)	D107V	probably damaging	Het
Metap1d	T	A	2: 71,355,121 (GRCm39)	V304D	possibly damaging	Het
Naca	A	G	10: 127,879,395 (GRCm39)		probably benign	Het
Napg	T	C	18: 63,117,143 (GRCm39)		probably null	Het
Nbeal1	T	A	1: 60,299,493 (GRCm39)	F7L	probably benign	Het
Ndst2	T	C	14: 20,774,582 (GRCm39)	T825A	probably benign	Het
Nsun2	T	C	13: 69,775,222 (GRCm39)	I353T	probably damaging	Het
Nt5c3b	T	A	11: 100,327,036 (GRCm39)	I87F	probably damaging	Het
Nxf3	T	C	X: 134,976,270 (GRCm39)	D407G	probably damaging	Het
Or51f2	T	A	7: 102,526,870 (GRCm39)	V181E	probably damaging	Het
Or8c13	A	T	9: 38,091,933 (GRCm39)	F62Y	possibly damaging	Het
Osbpl3	A	C	6: 50,313,193 (GRCm39)		probably null	Het
P2rx3	T	C	2: 84,852,811 (GRCm39)	T172A	possibly damaging	Het
Pcdh10	G	T	3: 45,336,316 (GRCm39)	E877*	probably null	Het
Pcdhb9	A	T	18: 37,534,682 (GRCm39)	K225N	probably damaging	Het
Plch1	A	G	3: 63,648,115 (GRCm39)	S419P	probably damaging	Het
Prex2	T	G	1: 11,355,313 (GRCm39)	I1538S	possibly damaging	Het
Prss59	C	A	6: 40,906,453 (GRCm39)		probably benign	Het
Rasl10a	A	G	11: 5,009,815 (GRCm39)	E121G	possibly damaging	Het
Rbbp8	A	G	18: 11,865,372 (GRCm39)	T754A	probably benign	Het
Rictor	T	C	15: 6,785,952 (GRCm39)	V156A	probably benign	Het
Ryr1	A	T	7: 28,815,579 (GRCm39)	Y104N	probably damaging	Het
Sctr	G	T	1: 119,964,169 (GRCm39)		probably null	Het
Sptbn2	T	C	19: 4,800,525 (GRCm39)	Y2247H	probably damaging	Het
Sqle	C	T	15: 59,196,358 (GRCm39)	R384W	probably damaging	Het
Srcin1	C	A	11: 97,409,470 (GRCm39)	R1163L	probably damaging	Het
Srp72	A	G	5: 77,128,154 (GRCm39)	Y125C	probably damaging	Het
Srrm2	T	C	17: 24,037,960 (GRCm39)	S1535P	probably benign	Het
Sumf2	A	G	5: 129,883,557 (GRCm39)	E125G	possibly damaging	Het
Tas2r144	A	T	6: 42,192,490 (GRCm39)	I77F	probably benign	Het
Tcp1	T	A	17: 13,139,310 (GRCm39)	N212K	probably benign	Het
Ttc7	G	T	17: 87,669,329 (GRCm39)	G659C	probably damaging	Het
Ttn	A	T	2: 76,691,903 (GRCm39)		probably null	Het
Ubtf	A	T	11: 102,199,804 (GRCm39)	D440E	probably benign	Het
Usp30	A	G	5: 114,259,207 (GRCm39)	D428G	probably damaging	Het
Vmn2r115	ATCTTCT	ATCT	17: 23,578,962 (GRCm39)		probably benign	Het
Vmn2r58	G	A	7: 41,513,480 (GRCm39)	H388Y	probably benign	Het
Zbtb49	T	C	5: 38,371,038 (GRCm39)	D281G	probably damaging	Het
Zfp248	A	G	6: 118,406,765 (GRCm39)	S174P	probably benign	Het
Zswim9	T	C	7: 13,011,337 (GRCm39)	T4A	probably benign	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
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
R6260: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'- ACTCGTGAATCTGCATGGACCAAG -3'
(R):5'- GGCACACATCTGTAATTCCCACAGC -3'

Sequencing Primer
(F):5'- tcaagcccaagcccaag -3'
(R):5'- ACATCTGTAATTCCCACAGCATTTG -3'

Posted On

2014-05-09