Mutagenetix > Incidental Mutation

Incidental Mutation 'R9047:Cramp1l'

688150

Institutional Source

Beutler Lab

Gene Symbol

Cramp1l

Ensembl Gene

ENSMUSG00000038002

Gene Name

cramped chromatin regulator homolog 1

Synonyms

5830477H08Rik, Tce4

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9047 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

24961228-25015230 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 24979629 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 773 (V773G)

Ref Sequence

ENSEMBL: ENSMUSP00000073060 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073337]

AlphaFold

Q6PG95

Predicted Effect

possibly damaging
Transcript: ENSMUST00000073337
AA Change: V773G

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000073060
Gene: ENSMUSG00000038002
AA Change: V773G

Domain	Start	End	E-Value	Type
low complexity region	11	20	N/A	INTRINSIC
low complexity region	29	43	N/A	INTRINSIC
low complexity region	51	64	N/A	INTRINSIC
low complexity region	100	126	N/A	INTRINSIC
low complexity region	134	147	N/A	INTRINSIC
SANT	159	219	3.68e-3	SMART
low complexity region	479	503	N/A	INTRINSIC
low complexity region	548	562	N/A	INTRINSIC
low complexity region	792	803	N/A	INTRINSIC
low complexity region	833	845	N/A	INTRINSIC
low complexity region	889	903	N/A	INTRINSIC
low complexity region	1069	1086	N/A	INTRINSIC
low complexity region	1113	1124	N/A	INTRINSIC
low complexity region	1141	1156	N/A	INTRINSIC
low complexity region	1171	1185	N/A	INTRINSIC

Coding Region Coverage

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

Validation Efficiency

100% (76/76)

MGI Phenotype

PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit cleft palate. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410004B18Rik	T	A	3: 145,939,093	S156T	probably damaging	Het
4930522L14Rik	A	G	5: 109,737,554	L146P		Het
Adra1a	T	A	14: 66,638,185	M203K	probably damaging	Het
Adtrp	G	A	13: 41,816,160	T89I	possibly damaging	Het
Akt3	G	T	1: 177,059,389	T298K	probably damaging	Het
Aldh4a1	G	T	4: 139,623,200		probably benign	Het
Aplf	T	C	6: 87,663,797	T77A	possibly damaging	Het
Arid4b	T	A	13: 14,181,230	W618R	probably damaging	Het
Asxl3	C	A	18: 22,452,408	P130Q	probably damaging	Het
Asxl3	A	G	18: 22,452,414	K132R	probably damaging	Het
Atp11a	T	C	8: 12,828,483	M353T	probably damaging	Het
Atp11b	A	G	3: 35,806,889	D375G	probably damaging	Het
BC052040	A	G	2: 115,777,023	T286A	probably benign	Het
Cage1	C	T	13: 38,017,362	A656T	possibly damaging	Het
Casz1	C	T	4: 148,939,040	P801S	probably damaging	Het
Ccdc130	C	T	8: 84,263,898	R35Q	probably damaging	Het
Ccdc144b	A	G	3: 36,032,884	I187T	probably benign	Het
Cdc14b	A	T	13: 64,220,944		probably benign	Het
Cox6b2	A	G	7: 4,752,087	F63L	probably benign	Het
Cul7	A	G	17: 46,654,522	E542G	probably benign	Het
Cyp2c55	T	C	19: 39,031,346	Y243H	possibly damaging	Het
Dnah9	C	A	11: 66,072,099	D1797Y	possibly damaging	Het
Dpep2	C	A	8: 105,989,312	A298S		Het
Dvl3	G	A	16: 20,524,076		probably null	Het
Enpp3	T	C	10: 24,798,274	D376G	possibly damaging	Het
Ffar4	T	C	19: 38,113,784	I289T	possibly damaging	Het
Gm3417	A	G	17: 14,967,680	Y111H	probably damaging	Het
Gm5565	T	C	5: 146,158,039	Y299C	probably damaging	Het
Gm8765	C	T	13: 50,702,092	R589*	probably null	Het
Gpat3	A	T	5: 100,846,922	M39L	probably benign	Het
Gpr153	T	C	4: 152,280,207	L240P	probably damaging	Het
Gpr182	T	C	10: 127,750,648	I145V	probably benign	Het
H2-Q4	A	T	17: 35,379,993	T80S	possibly damaging	Het
Hnf1a	T	A	5: 114,950,823	T545S	probably benign	Het
Kif5b	A	C	18: 6,208,261	F946V	probably benign	Het
Krtap16-1	C	T	11: 99,986,341	C79Y	probably damaging	Het
Lama2	A	G	10: 27,006,701	V2622A	possibly damaging	Het
Lrrc37a	T	A	11: 103,500,549	Q1350L	probably damaging	Het
Map2k2	G	A	10: 81,119,664	V294I	probably benign	Het
Mtus1	G	A	8: 41,083,723	H319Y	possibly damaging	Het
Ncdn	T	C	4: 126,750,828	D67G	possibly damaging	Het
Ngef	G	A	1: 87,503,288	P269L	probably damaging	Het
Nlrp9b	A	G	7: 20,023,476	I213V	possibly damaging	Het
Nyap2	G	A	1: 81,298,088	R649H	possibly damaging	Het
Olfr1165-ps	T	G	2: 88,101,072	D305A	unknown	Het
Olfr1200	C	A	2: 88,767,955	R120L	probably damaging	Het
Olfr304	A	G	7: 86,386,040	S207P	probably benign	Het
Pi4kb	T	A	3: 94,993,117	L354Q	probably damaging	Het
Plekhh2	T	C	17: 84,590,762	S944P	probably damaging	Het
Podn	C	T	4: 108,021,546	V375M	probably damaging	Het
Pramef8	C	A	4: 143,419,103	Q381K	possibly damaging	Het
Psmb2	T	A	4: 126,706,102	H110Q	probably benign	Het
Rasip1	A	G	7: 45,632,642	E523G	possibly damaging	Het
Ripor1	T	G	8: 105,616,151	C219G	probably damaging	Het
Rps6ka2	G	C	17: 7,300,279	V714L	probably damaging	Het
Sass6	G	T	3: 116,613,998	L254F	probably damaging	Het
Scarf2	G	A	16: 17,806,406	G525E	probably damaging	Het
Sh3d21	T	A	4: 126,152,338		probably benign	Het
Sh3tc1	C	A	5: 35,706,483	A787S	probably benign	Het
Skint5	T	A	4: 113,655,722	N871I	unknown	Het
Slc48a1	T	G	15: 97,789,952	D62E	probably damaging	Het
Slc6a21	G	A	7: 45,286,974	M157I		Het
Slurp2	T	C	15: 74,743,112	D60G	probably benign	Het
Sparcl1	G	T	5: 104,093,113	N148K	possibly damaging	Het
Spsb2	T	A	6: 124,810,013	N236K	probably benign	Het
Sptb	G	T	12: 76,632,534		probably benign	Het
Ssc4d	A	T	5: 135,961,176	C41S	probably damaging	Het
Tecta	A	T	9: 42,375,079	D760E	probably benign	Het
Tesmin	G	T	19: 3,389,431		probably benign	Het
Tiam1	A	C	16: 89,804,888		probably benign	Het
Tldc1	T	C	8: 119,762,311	N411S	probably benign	Het
Tnrc6a	T	C	7: 123,179,723	L1219S	probably damaging	Het
Tram1	T	G	1: 13,569,606	I306L	probably benign	Het
Trank1	A	C	9: 111,362,432	D503A	probably damaging	Het
Ttc21b	T	C	2: 66,201,252	H1044R		Het
Ubac2	T	C	14: 121,908,214	F95L	probably benign	Het
Vmn2r91	A	T	17: 18,106,034	M194L	probably benign	Het
Zdhhc1	G	T	8: 105,478,901	H90Q	probably damaging	Het
Zfp169	C	T	13: 48,498,816	V42I	probably damaging	Het
Zfp81	A	G	17: 33,334,413	C476R	probably damaging	Het

Other mutations in Cramp1l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00566:Cramp1l	APN	17	24983951	missense	probably benign	0.11
IGL01360:Cramp1l	APN	17	24997573	missense	probably damaging	1.00
IGL01966:Cramp1l	APN	17	24982943	missense	probably benign	0.01
IGL02211:Cramp1l	APN	17	24977636	missense	possibly damaging	0.94
IGL02474:Cramp1l	APN	17	24985050	missense	probably damaging	0.98
IGL02798:Cramp1l	APN	17	24968920	splice site	probably benign
IGL03340:Cramp1l	APN	17	24973542	missense	probably damaging	1.00
R0106:Cramp1l	UTSW	17	24972376	missense	probably benign	0.30
R1054:Cramp1l	UTSW	17	24983177	missense	probably damaging	1.00
R1220:Cramp1l	UTSW	17	24982237	missense	probably damaging	1.00
R1341:Cramp1l	UTSW	17	24977540	missense	probably damaging	1.00
R1491:Cramp1l	UTSW	17	24972349	missense	probably benign	0.17
R1610:Cramp1l	UTSW	17	24983951	missense	probably benign	0.11
R1649:Cramp1l	UTSW	17	24983243	missense	probably damaging	1.00
R1795:Cramp1l	UTSW	17	24964910	missense	probably damaging	1.00
R1856:Cramp1l	UTSW	17	24968978	missense	probably damaging	1.00
R1881:Cramp1l	UTSW	17	24977682	splice site	probably benign
R1968:Cramp1l	UTSW	17	24964939	missense	probably damaging	1.00
R2047:Cramp1l	UTSW	17	25003215	nonsense	probably null
R2099:Cramp1l	UTSW	17	24973085	missense	probably benign	0.01
R2298:Cramp1l	UTSW	17	24997480	missense	probably damaging	0.96
R3752:Cramp1l	UTSW	17	24971558	missense	probably damaging	1.00
R3821:Cramp1l	UTSW	17	24974782	missense	probably damaging	1.00
R3861:Cramp1l	UTSW	17	24997614	splice site	probably benign
R4399:Cramp1l	UTSW	17	24979585	missense	probably damaging	1.00
R4847:Cramp1l	UTSW	17	24985089	missense	probably damaging	1.00
R4883:Cramp1l	UTSW	17	24982319	missense	probably benign
R5579:Cramp1l	UTSW	17	24973113	missense	possibly damaging	0.89
R5631:Cramp1l	UTSW	17	24985603	missense	possibly damaging	0.93
R5716:Cramp1l	UTSW	17	24974735	missense	probably damaging	0.99
R6589:Cramp1l	UTSW	17	24977492	splice site	probably null
R6631:Cramp1l	UTSW	17	24983957	missense	probably benign	0.40
R7307:Cramp1l	UTSW	17	24974745	missense	possibly damaging	0.94
R7323:Cramp1l	UTSW	17	24982405	missense	possibly damaging	0.90
R7672:Cramp1l	UTSW	17	24982466	missense	probably damaging	0.96
R7832:Cramp1l	UTSW	17	24983222	missense	probably damaging	0.96
R8071:Cramp1l	UTSW	17	24982700	missense	probably damaging	0.99
R8244:Cramp1l	UTSW	17	24971410	missense	probably damaging	1.00
R8430:Cramp1l	UTSW	17	24977562	missense	probably damaging	1.00
R8783:Cramp1l	UTSW	17	24974758	missense	probably damaging	0.99
R8890:Cramp1l	UTSW	17	24983140	missense	probably damaging	1.00
R8892:Cramp1l	UTSW	17	24983140	missense	probably damaging	1.00
R8894:Cramp1l	UTSW	17	24983140	missense	probably damaging	1.00
R8937:Cramp1l	UTSW	17	24983982	missense	probably damaging	0.99
R8941:Cramp1l	UTSW	17	24983140	missense	probably damaging	1.00
R9029:Cramp1l	UTSW	17	25013910	missense	probably damaging	1.00
R9149:Cramp1l	UTSW	17	24968946	missense	probably damaging	0.99
R9262:Cramp1l	UTSW	17	25013946	missense	probably damaging	0.99
R9460:Cramp1l	UTSW	17	25003307	missense	probably damaging	1.00
R9614:Cramp1l	UTSW	17	24982809	missense	probably damaging	1.00
R9615:Cramp1l	UTSW	17	24982809	missense	probably damaging	1.00
R9651:Cramp1l	UTSW	17	24982809	missense	probably damaging	1.00
R9652:Cramp1l	UTSW	17	24982809	missense	probably damaging	1.00
R9653:Cramp1l	UTSW	17	24982809	missense	probably damaging	1.00
R9665:Cramp1l	UTSW	17	24977571	missense	probably damaging	1.00
R9753:Cramp1l	UTSW	17	24972346	missense	possibly damaging	0.81

Predicted Primers

PCR Primer
(F):5'- CCAGAAACATCAGGATGCTCTTG -3'
(R):5'- CCTTAGTAATTTTACATCTCTGGGC -3'

Sequencing Primer
(F):5'- CAGGATGCTCTTGAAGTATACCTG -3'
(R):5'- TTGTTGCTTCCCAGAAGACCAGAG -3'

Posted On

2021-11-19