Mutagenetix > Incidental Mutation

Incidental Mutation 'R6419:Ints7'

517986

Institutional Source

Beutler Lab

Gene Symbol

Ints7

Ensembl Gene

ENSMUSG00000037461

Gene Name

integrator complex subunit 7

Synonyms

5930412E23Rik

MMRRC Submission

044561-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.952) question?

Stock #

R6419 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

191307748-191355800 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 191334414 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 313 (S313T)

Ref Sequence

ENSEMBL: ENSMUSP00000036277 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045450] [ENSMUST00000193569] [ENSMUST00000194785] [ENSMUST00000194877]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000045450
AA Change: S313T

PolyPhen 2 Score 0.686 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000036277
Gene: ENSMUSG00000037461
AA Change: S313T

Domain	Start	End	E-Value	Type
SCOP:d1gw5a_	76	530	1e-10	SMART
low complexity region	937	960	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000193569

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000193961

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194205

Predicted Effect

probably benign
Transcript: ENSMUST00000194785

Predicted Effect

probably benign
Transcript: ENSMUST00000194877

Meta Mutation Damage Score

0.1636

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.3%

Validation Efficiency

96% (67/70)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a subunit of the integrator complex. The integrator complex associates with the C-terminal domain of RNA polymerase II and mediates 3'-end processing of the small nuclear RNAs U1 and U2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930578G10Rik	T	C	4: 42,812,473 (GRCm39)		probably benign	Het
Abcc2	T	A	19: 43,825,947 (GRCm39)		probably null	Het
Adamts12	C	T	15: 11,215,759 (GRCm39)	T260M	possibly damaging	Het
Adamts20	C	T	15: 94,231,556 (GRCm39)	V878I	possibly damaging	Het
Adgrl4	A	G	3: 151,144,953 (GRCm39)	E34G	probably damaging	Het
Asah1	A	T	8: 41,796,803 (GRCm39)	I293N	probably damaging	Het
Atosa	G	A	9: 74,916,619 (GRCm39)	S413N	probably benign	Het
B3galt2	A	T	1: 143,522,839 (GRCm39)	E325V	possibly damaging	Het
Baz1b	T	A	5: 135,271,348 (GRCm39)	H1310Q	probably benign	Het
Ccdc125	T	A	13: 100,826,834 (GRCm39)	N204K	probably damaging	Het
Cd36	C	T	5: 18,002,150 (GRCm39)	D284N	probably benign	Het
Cdh12	T	C	15: 21,520,483 (GRCm39)	L316S	probably damaging	Het
Cenpv	T	C	11: 62,416,008 (GRCm39)	K247R	probably benign	Het
Cldn18	T	C	9: 99,574,801 (GRCm39)	H257R	possibly damaging	Het
Cnot8	T	A	11: 58,004,891 (GRCm39)	Y197N	probably damaging	Het
Cog3	A	T	14: 75,962,178 (GRCm39)	C554*	probably null	Het
Col4a4	A	G	1: 82,444,207 (GRCm39)		probably null	Het
Cops5	G	A	1: 10,103,532 (GRCm39)	T158I	probably damaging	Het
Dhh	A	G	15: 98,792,282 (GRCm39)	F242S	probably damaging	Het
Dot1l	T	C	10: 80,627,315 (GRCm39)	V1512A	possibly damaging	Het
Dstn	T	G	2: 143,781,907 (GRCm39)	I116S	possibly damaging	Het
Egfem1	G	A	3: 29,711,398 (GRCm39)	D326N	probably damaging	Het
Enpp3	A	T	10: 24,684,089 (GRCm39)	Y52N	probably damaging	Het
Gabra2	A	G	5: 71,119,426 (GRCm39)	S359P	probably benign	Het
Gbp7	G	A	3: 142,252,214 (GRCm39)	G599E	probably benign	Het
Gcat	T	G	15: 78,920,264 (GRCm39)	I198S	probably damaging	Het
Gm8439	A	G	4: 120,466,755 (GRCm39)	K82R	unknown	Het
Grin2b	A	G	6: 135,717,965 (GRCm39)	F709S	probably damaging	Het
Grm3	T	C	5: 9,620,201 (GRCm39)	N348D	probably damaging	Het
Hdgfl1	G	A	13: 26,954,075 (GRCm39)		probably benign	Het
Hmgxb3	G	T	18: 61,285,296 (GRCm39)	D564E	possibly damaging	Het
Igkv4-61	C	A	6: 69,394,138 (GRCm39)	A31S	possibly damaging	Het
Impg1	A	G	9: 80,287,300 (GRCm39)	V305A	probably benign	Het
Knl1	T	A	2: 118,899,484 (GRCm39)	I395K	probably benign	Het
Lactb2	A	T	1: 13,708,459 (GRCm39)	Y196*	probably null	Het
Lad1	T	C	1: 135,759,630 (GRCm39)	S509P	possibly damaging	Het
Ltf	T	C	9: 110,860,090 (GRCm39)	F504L	possibly damaging	Het
Med4	A	T	14: 73,751,363 (GRCm39)	D104V	probably damaging	Het
Mrpl58	A	T	11: 115,301,073 (GRCm39)	N128Y	probably damaging	Het
Ndufs2	T	C	1: 171,068,668 (GRCm39)	T54A	probably benign	Het
Notch2	G	T	3: 98,007,705 (GRCm39)		probably null	Het
Ntng1	A	T	3: 109,690,169 (GRCm39)	N424K	possibly damaging	Het
Ntrk2	G	A	13: 59,009,113 (GRCm39)	W301*	probably null	Het
Or5b116	T	A	19: 13,423,131 (GRCm39)	S252T	probably benign	Het
Otud6b	A	G	4: 14,822,766 (GRCm39)	S113P	possibly damaging	Het
Pcdhb20	A	G	18: 37,638,608 (GRCm39)	N378S	probably damaging	Het
Polr3b	T	C	10: 84,473,975 (GRCm39)	S185P	possibly damaging	Het
Ptprn	G	A	1: 75,240,681 (GRCm39)	R31C	probably benign	Het
Rgsl1	C	T	1: 153,698,117 (GRCm39)	V478M	probably damaging	Het
Sema6b	A	T	17: 56,439,784 (GRCm39)	L19*	probably null	Het
Slfn8	A	G	11: 82,894,881 (GRCm39)		probably null	Het
Spen	A	T	4: 141,203,621 (GRCm39)	S1669T	unknown	Het
Syne2	T	C	12: 76,143,740 (GRCm39)	F1522L	probably damaging	Het
Tarbp1	C	T	8: 127,185,783 (GRCm39)	A470T	possibly damaging	Het
Tent4a	A	C	13: 69,658,785 (GRCm39)	M350R	possibly damaging	Het
Tiam1	C	A	16: 89,694,912 (GRCm39)	E182*	probably null	Het
Tmem231	G	A	8: 112,653,524 (GRCm39)		probably benign	Het
Trip12	C	T	1: 84,771,591 (GRCm39)	A186T	probably damaging	Het
Ufc1	C	T	1: 171,116,529 (GRCm39)	A147T	probably damaging	Het
Vmn1r199	A	G	13: 22,567,777 (GRCm39)	K314R	possibly damaging	Het
Vmn2r13	A	T	5: 109,323,085 (GRCm39)	I68K	possibly damaging	Het
Vmn2r77	A	T	7: 86,460,767 (GRCm39)	I698F	probably damaging	Het
Vmn2r86	T	C	10: 130,282,795 (GRCm39)	K607R	probably damaging	Het
Vwa3b	T	C	1: 37,196,457 (GRCm39)	V28A	probably benign	Het
Wdr19	A	G	5: 65,373,236 (GRCm39)	N166S	possibly damaging	Het
Wfdc17	G	A	11: 83,595,634 (GRCm39)	G33R	probably damaging	Het
Zfp330	T	G	8: 83,491,545 (GRCm39)	K209N	probably benign	Het
Zfp493	A	G	13: 67,934,526 (GRCm39)	T160A	probably benign	Het
Zfp974	A	T	7: 27,610,940 (GRCm39)	C262S	possibly damaging	Het

Other mutations in Ints7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00904:Ints7	APN	1	191,328,276 (GRCm39)	splice site	probably null
IGL01285:Ints7	APN	1	191,347,890 (GRCm39)	missense	probably benign	0.00
IGL01289:Ints7	APN	1	191,347,890 (GRCm39)	missense	probably benign	0.00
IGL01572:Ints7	APN	1	191,347,905 (GRCm39)	missense	possibly damaging	0.71
IGL01665:Ints7	APN	1	191,345,331 (GRCm39)	splice site	probably benign
IGL02059:Ints7	APN	1	191,347,872 (GRCm39)	missense	probably benign	0.23
IGL02684:Ints7	APN	1	191,345,749 (GRCm39)	critical splice acceptor site	probably null
IGL02686:Ints7	APN	1	191,318,704 (GRCm39)	missense	probably damaging	1.00
IGL02812:Ints7	APN	1	191,351,853 (GRCm39)	missense	probably damaging	1.00
IGL03119:Ints7	APN	1	191,342,477 (GRCm39)	missense	probably damaging	1.00
IGL03162:Ints7	APN	1	191,353,524 (GRCm39)	utr 3 prime	probably benign
PIT4810001:Ints7	UTSW	1	191,328,348 (GRCm39)	missense	probably damaging	0.99
R0294:Ints7	UTSW	1	191,344,003 (GRCm39)	missense	possibly damaging	0.91
R0479:Ints7	UTSW	1	191,346,666 (GRCm39)	splice site	probably null
R0698:Ints7	UTSW	1	191,326,576 (GRCm39)	missense	probably damaging	0.97
R1420:Ints7	UTSW	1	191,345,169 (GRCm39)	missense	possibly damaging	0.73
R1680:Ints7	UTSW	1	191,353,274 (GRCm39)	splice site	probably null
R1781:Ints7	UTSW	1	191,328,396 (GRCm39)	missense	possibly damaging	0.95
R2141:Ints7	UTSW	1	191,336,972 (GRCm39)	missense	possibly damaging	0.73
R2291:Ints7	UTSW	1	191,338,315 (GRCm39)	splice site	probably null
R4718:Ints7	UTSW	1	191,315,389 (GRCm39)	missense	possibly damaging	0.60
R4741:Ints7	UTSW	1	191,351,747 (GRCm39)	missense	probably benign	0.29
R4797:Ints7	UTSW	1	191,329,045 (GRCm39)	missense	probably damaging	1.00
R4812:Ints7	UTSW	1	191,326,542 (GRCm39)	missense	possibly damaging	0.73
R4826:Ints7	UTSW	1	191,344,018 (GRCm39)	missense	probably damaging	0.97
R4870:Ints7	UTSW	1	191,328,443 (GRCm39)	missense	probably damaging	0.97
R5169:Ints7	UTSW	1	191,345,202 (GRCm39)	missense	probably benign	0.00
R5281:Ints7	UTSW	1	191,347,883 (GRCm39)	missense	possibly damaging	0.90
R5694:Ints7	UTSW	1	191,318,730 (GRCm39)	missense	probably damaging	1.00
R5752:Ints7	UTSW	1	191,308,005 (GRCm39)	missense	probably benign	0.00
R6048:Ints7	UTSW	1	191,353,524 (GRCm39)	utr 3 prime	probably benign
R6341:Ints7	UTSW	1	191,345,239 (GRCm39)	missense	probably damaging	1.00
R7037:Ints7	UTSW	1	191,351,717 (GRCm39)	missense	probably benign	0.16
R7163:Ints7	UTSW	1	191,349,949 (GRCm39)	missense	possibly damaging	0.67
R7603:Ints7	UTSW	1	191,328,336 (GRCm39)	missense	probably damaging	1.00
R7801:Ints7	UTSW	1	191,347,859 (GRCm39)	missense	possibly damaging	0.84
R7899:Ints7	UTSW	1	191,353,427 (GRCm39)	missense	probably damaging	1.00
R8034:Ints7	UTSW	1	191,345,183 (GRCm39)	frame shift	probably null
R8034:Ints7	UTSW	1	191,345,180 (GRCm39)	frame shift	probably null
R8231:Ints7	UTSW	1	191,328,465 (GRCm39)	nonsense	probably null
R8251:Ints7	UTSW	1	191,353,545 (GRCm39)	missense	unknown
R8520:Ints7	UTSW	1	191,314,603 (GRCm39)	missense	probably damaging	1.00
R8966:Ints7	UTSW	1	191,351,717 (GRCm39)	missense	probably benign	0.16
R9198:Ints7	UTSW	1	191,351,872 (GRCm39)	missense	probably benign	0.42
R9382:Ints7	UTSW	1	191,351,793 (GRCm39)	missense	probably damaging	1.00
Z1177:Ints7	UTSW	1	191,342,570 (GRCm39)	missense	probably benign	0.06

Predicted Primers

PCR Primer
(F):5'- GCTGCCACACTGTGTGTTTC -3'
(R):5'- CAATAAACTCAAGCCATGTGGTC -3'

Sequencing Primer
(F):5'- TCTAGGACACCACATTATATCTGGC -3'
(R):5'- TGTGGTCATGAGAAGAACAAAGTAC -3'

Posted On

2018-05-24