Mutagenetix > Incidental Mutation

Incidental Mutation 'R2018:Arid1a'

223379

Institutional Source

Beutler Lab

Gene Symbol

Arid1a

Ensembl Gene

ENSMUSG00000007880

Gene Name

AT-rich interaction domain 1A

Synonyms

Smarcf1, 1110030E03Rik, Osa1, BAF250a

MMRRC Submission

040027-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R2018 (G1)

Quality Score

215

Status

Not validated

Chromosome

Chromosomal Location

133406319-133484080 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 133409145 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 1787 (D1787E)

Ref Sequence

ENSEMBL: ENSMUSP00000122354 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000008024] [ENSMUST00000105897] [ENSMUST00000145664]

AlphaFold

A2BH40

Predicted Effect

unknown
Transcript: ENSMUST00000008024
AA Change: D1402E

SMART Domains

Protein: ENSMUSP00000008024
Gene: ENSMUSG00000007880
AA Change: D1402E

Domain	Start	End	E-Value	Type
low complexity region	17	42	N/A	INTRINSIC
low complexity region	86	110	N/A	INTRINSIC
low complexity region	113	211	N/A	INTRINSIC
low complexity region	226	237	N/A	INTRINSIC
low complexity region	274	290	N/A	INTRINSIC
low complexity region	310	323	N/A	INTRINSIC
internal_repeat_3	329	402	4.13e-5	PROSPERO
low complexity region	410	426	N/A	INTRINSIC
low complexity region	429	442	N/A	INTRINSIC
internal_repeat_1	443	563	4.59e-6	PROSPERO
internal_repeat_2	461	595	1.38e-5	PROSPERO
low complexity region	604	626	N/A	INTRINSIC
ARID	630	720	3.56e-25	SMART
BRIGHT	634	725	3.76e-31	SMART
low complexity region	739	751	N/A	INTRINSIC
low complexity region	756	770	N/A	INTRINSIC
internal_repeat_3	778	872	4.13e-5	PROSPERO
internal_repeat_2	781	928	1.38e-5	PROSPERO
internal_repeat_1	825	940	4.59e-6	PROSPERO
low complexity region	962	987	N/A	INTRINSIC
low complexity region	1014	1045	N/A	INTRINSIC
low complexity region	1187	1200	N/A	INTRINSIC
low complexity region	1380	1404	N/A	INTRINSIC
low complexity region	1500	1518	N/A	INTRINSIC
Pfam:DUF3518	1592	1848	1.8e-146	PFAM
low complexity region	1849	1859	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000105897
AA Change: D1783E

SMART Domains

Protein: ENSMUSP00000101517
Gene: ENSMUSG00000007880
AA Change: D1783E

Domain	Start	End	E-Value	Type
low complexity region	2	10	N/A	INTRINSIC
low complexity region	24	52	N/A	INTRINSIC
low complexity region	74	96	N/A	INTRINSIC
low complexity region	118	148	N/A	INTRINSIC
low complexity region	161	169	N/A	INTRINSIC
low complexity region	233	266	N/A	INTRINSIC
low complexity region	273	295	N/A	INTRINSIC
low complexity region	308	332	N/A	INTRINSIC
low complexity region	367	373	N/A	INTRINSIC
low complexity region	402	427	N/A	INTRINSIC
low complexity region	471	495	N/A	INTRINSIC
low complexity region	498	596	N/A	INTRINSIC
low complexity region	611	622	N/A	INTRINSIC
low complexity region	659	675	N/A	INTRINSIC
low complexity region	695	708	N/A	INTRINSIC
low complexity region	795	811	N/A	INTRINSIC
low complexity region	814	827	N/A	INTRINSIC
internal_repeat_2	828	948	9.26e-7	PROSPERO
internal_repeat_1	831	980	9.26e-7	PROSPERO
low complexity region	989	1011	N/A	INTRINSIC
ARID	1015	1105	3.56e-25	SMART
BRIGHT	1019	1110	3.76e-31	SMART
low complexity region	1124	1136	N/A	INTRINSIC
low complexity region	1141	1155	N/A	INTRINSIC
internal_repeat_1	1159	1314	9.26e-7	PROSPERO
internal_repeat_2	1211	1326	9.26e-7	PROSPERO
low complexity region	1343	1368	N/A	INTRINSIC
low complexity region	1395	1426	N/A	INTRINSIC
low complexity region	1568	1581	N/A	INTRINSIC
low complexity region	1761	1785	N/A	INTRINSIC
low complexity region	1881	1899	N/A	INTRINSIC
Pfam:DUF3518	1973	2229	1.4e-146	PFAM
low complexity region	2230	2240	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000145664
AA Change: D1787E

SMART Domains

Protein: ENSMUSP00000122354
Gene: ENSMUSG00000007880
AA Change: D1787E

Domain	Start	End	E-Value	Type
low complexity region	2	10	N/A	INTRINSIC
low complexity region	24	52	N/A	INTRINSIC
low complexity region	74	96	N/A	INTRINSIC
low complexity region	118	148	N/A	INTRINSIC
low complexity region	161	169	N/A	INTRINSIC
low complexity region	233	266	N/A	INTRINSIC
low complexity region	273	295	N/A	INTRINSIC
low complexity region	308	332	N/A	INTRINSIC
low complexity region	367	373	N/A	INTRINSIC
low complexity region	402	427	N/A	INTRINSIC
low complexity region	471	495	N/A	INTRINSIC
low complexity region	498	596	N/A	INTRINSIC
low complexity region	611	622	N/A	INTRINSIC
low complexity region	659	675	N/A	INTRINSIC
low complexity region	695	708	N/A	INTRINSIC
internal_repeat_3	714	787	9.49e-6	PROSPERO
low complexity region	795	811	N/A	INTRINSIC
low complexity region	814	827	N/A	INTRINSIC
internal_repeat_1	828	948	8.73e-7	PROSPERO
internal_repeat_2	846	980	2.88e-6	PROSPERO
low complexity region	989	1011	N/A	INTRINSIC
ARID	1015	1105	3.56e-25	SMART
BRIGHT	1019	1110	3.76e-31	SMART
low complexity region	1124	1136	N/A	INTRINSIC
low complexity region	1141	1155	N/A	INTRINSIC
internal_repeat_3	1163	1257	9.49e-6	PROSPERO
internal_repeat_2	1166	1313	2.88e-6	PROSPERO
internal_repeat_1	1210	1325	8.73e-7	PROSPERO
low complexity region	1347	1372	N/A	INTRINSIC
low complexity region	1399	1430	N/A	INTRINSIC
low complexity region	1572	1585	N/A	INTRINSIC
low complexity region	1765	1789	N/A	INTRINSIC
low complexity region	1885	1903	N/A	INTRINSIC
Pfam:DUF3518	1978	2233	1.3e-117	PFAM
low complexity region	2234	2244	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 93.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the SWI/SNF family, whose members have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. It possesses at least two conserved domains that could be important for its function. First, it has a DNA-binding domain that can specifically bind an AT-rich DNA sequence known to be recognized by a SNF/SWI complex at the beta-globin locus. Second, the C-terminus of the protein can stimulate glucocorticoid receptor-dependent transcriptional activation. It is thought that the protein encoded by this gene confers specificity to the SNF/SWI complex and may recruit the complex to its targets through either protein-DNA or protein-protein interactions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Embryos with homozygous null alleles arrest development at E6.5 with failure to form a mesoderm layer. Mice homozygous for an allele lacking exon 2 and 3 die shortly after birth and exhibit an increase in the hematopoietic stem cell population of the fetal liver at E14.5. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 111 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610028H24Rik	C	A	10: 76,293,899 (GRCm39)	F252L	possibly damaging	Het
4930447A16Rik	T	G	15: 37,440,742 (GRCm39)		probably benign	Het
Abca14	A	T	7: 119,815,408 (GRCm39)	M219L	probably benign	Het
Abi3bp	A	G	16: 56,498,159 (GRCm39)	T918A	probably damaging	Het
Acss3	C	T	10: 106,772,068 (GRCm39)	S669N	probably benign	Het
Adamts16	G	A	13: 70,927,637 (GRCm39)		probably benign	Het
Adamtsl4	A	G	3: 95,588,412 (GRCm39)	Y559H	probably damaging	Het
Adgrg5	T	A	8: 95,661,108 (GRCm39)	M106K	probably damaging	Het
Akt1	T	C	12: 112,626,059 (GRCm39)	N71S	probably damaging	Het
Amer2	A	C	14: 60,615,894 (GRCm39)	K30Q	probably damaging	Het
Anapc5	T	C	5: 122,938,587 (GRCm39)	K383E	probably damaging	Het
Ano1	A	G	7: 144,207,987 (GRCm39)	L258P	probably damaging	Het
Arb2a	A	G	13: 78,147,756 (GRCm39)	T321A	possibly damaging	Het
Arhgef10l	A	G	4: 140,271,695 (GRCm39)	S560P	probably damaging	Het
Arhgef40	T	A	14: 52,241,162 (GRCm39)	L1395Q	probably damaging	Het
Ces2h	T	C	8: 105,745,030 (GRCm39)	L388P	probably damaging	Het
Cfap54	T	A	10: 92,852,466 (GRCm39)	N880I	probably benign	Het
Cryz	T	C	3: 154,327,320 (GRCm39)	V116A	probably damaging	Het
Csrp1	G	A	1: 135,678,366 (GRCm39)	A159T	probably damaging	Het
Cttnbp2	A	G	6: 18,434,517 (GRCm39)	F447S	probably damaging	Het
Cyp4a12a	A	T	4: 115,184,702 (GRCm39)	I328F	probably damaging	Het
Cyth4	T	G	15: 78,492,371 (GRCm39)	H133Q	probably damaging	Het
Ddah2	A	G	17: 35,279,402 (GRCm39)	I88V	possibly damaging	Het
Dmbt1	T	G	7: 130,712,718 (GRCm39)	I1563S	possibly damaging	Het
Dnajc22	T	C	15: 98,999,114 (GRCm39)	S100P	probably benign	Het
Fancl	T	A	11: 26,372,459 (GRCm39)	D123E	probably damaging	Het
Fbxo30	A	G	10: 11,166,772 (GRCm39)	Q498R	probably damaging	Het
Fgd4	T	C	16: 16,253,824 (GRCm39)	H581R	probably benign	Het
Gm2663	T	C	6: 40,974,900 (GRCm39)	Q57R	probably benign	Het
Gm7247	A	T	14: 51,602,804 (GRCm39)	M47L	possibly damaging	Het
Gsdmc2	T	A	15: 63,699,975 (GRCm39)		probably null	Het
Hc	A	C	2: 34,903,540 (GRCm39)	F1038C	probably damaging	Het
Heatr1	C	A	13: 12,429,359 (GRCm39)	Q890K	possibly damaging	Het
Hipk4	C	A	7: 27,228,429 (GRCm39)	T293K	probably damaging	Het
Hp1bp3	C	A	4: 137,948,943 (GRCm39)	A2E	probably damaging	Het
Il6	T	C	5: 30,219,945 (GRCm39)		probably null	Het
Itga6	A	G	2: 71,648,828 (GRCm39)	D104G	probably benign	Het
Krt24	A	G	11: 99,173,277 (GRCm39)	S293P	probably damaging	Het
Krt4	C	T	15: 101,829,086 (GRCm39)	R309Q	probably damaging	Het
Krt40	A	T	11: 99,430,913 (GRCm39)	W199R	probably damaging	Het
Lamc1	T	C	1: 153,118,378 (GRCm39)	E931G	probably benign	Het
Lamp3	A	T	16: 19,519,961 (GRCm39)	M74K	probably benign	Het
Lgalsl2	A	G	7: 5,362,573 (GRCm39)	D68G	probably benign	Het
Magel2	G	A	7: 62,028,844 (GRCm39)	V583I	unknown	Het
Marchf7	T	A	2: 60,059,384 (GRCm39)	Y37*	probably null	Het
Mrpl36	A	G	13: 73,479,687 (GRCm39)	K66E	probably damaging	Het
Mrps35	G	T	6: 146,962,982 (GRCm39)	E229*	probably null	Het
Mtmr6	T	C	14: 60,536,441 (GRCm39)	M557T	probably benign	Het
Myocd	A	T	11: 65,077,854 (GRCm39)	I647N	probably damaging	Het
Myom2	A	C	8: 15,181,151 (GRCm39)	L1350F	probably damaging	Het
Nhsl3	A	G	4: 129,116,148 (GRCm39)	S884P	probably damaging	Het
Nosip	T	A	7: 44,726,033 (GRCm39)	S197T	probably benign	Het
Npat	A	G	9: 53,473,791 (GRCm39)	K528E	probably benign	Het
Nyap2	A	G	1: 81,169,587 (GRCm39)	T115A	probably benign	Het
Obi1	T	A	14: 104,759,978 (GRCm39)	K24M	probably damaging	Het
Or10al6	A	G	17: 38,083,467 (GRCm39)	R317G	probably benign	Het
Or4a72	A	G	2: 89,405,737 (GRCm39)	V111A	probably damaging	Het
Or4c109	G	T	2: 88,818,489 (GRCm39)	P19Q	probably benign	Het
Or51b6	T	A	7: 103,556,249 (GRCm39)	V201D	possibly damaging	Het
Or5m3	A	T	2: 85,838,567 (GRCm39)	Y149F	probably damaging	Het
Or8g55	A	G	9: 39,785,354 (GRCm39)	Q261R	probably benign	Het
Orc1	T	C	4: 108,447,897 (GRCm39)	V48A	possibly damaging	Het
Pde6d	T	C	1: 86,474,438 (GRCm39)	E69G	probably damaging	Het
Pdgfrb	A	T	18: 61,216,406 (GRCm39)	D1088V	possibly damaging	Het
Peg12	A	G	7: 62,113,386 (GRCm39)	V237A	probably benign	Het
Phf8-ps	T	C	17: 33,285,941 (GRCm39)	N287S	probably benign	Het
Piezo1	A	G	8: 123,209,451 (GRCm39)	F2371L	probably benign	Het
Podn	T	A	4: 107,880,570 (GRCm39)	S27C	probably damaging	Het
Pom121l2	A	G	13: 22,166,904 (GRCm39)	M392V	possibly damaging	Het
Ppm1b	A	G	17: 85,301,630 (GRCm39)	K170R	probably damaging	Het
Rab18	A	T	18: 6,770,113 (GRCm39)		probably null	Het
Raet1d	G	A	10: 22,246,911 (GRCm39)	A80T	probably damaging	Het
Rfx7	T	A	9: 72,524,967 (GRCm39)	V719E	probably benign	Het
Ror1	C	T	4: 100,265,038 (GRCm39)	Q171*	probably null	Het
Rufy4	G	A	1: 74,180,106 (GRCm39)	V454M	possibly damaging	Het
Ryr2	C	T	13: 11,866,074 (GRCm39)	G292D	possibly damaging	Het
Ryr3	G	T	2: 112,611,410 (GRCm39)	N2257K	probably benign	Het
Saal1	A	G	7: 46,348,913 (GRCm39)	F306S	possibly damaging	Het
Sap18	A	G	14: 58,036,021 (GRCm39)	N69S	probably damaging	Het
Sar1b	A	T	11: 51,670,514 (GRCm39)		probably null	Het
Serpina3n	G	T	12: 104,375,473 (GRCm39)	V182L	probably damaging	Het
Setd3	A	T	12: 108,084,513 (GRCm39)	H279Q	probably damaging	Het
Slc18a2	C	A	19: 59,264,937 (GRCm39)	A307E	possibly damaging	Het
Slc4a10	A	T	2: 62,064,725 (GRCm39)	D193V	probably damaging	Het
Spire2	T	C	8: 124,059,657 (GRCm39)	C52R	probably damaging	Het
Syne2	A	T	12: 76,121,353 (GRCm39)	I5940F	probably damaging	Het
Sytl1	C	T	4: 132,983,471 (GRCm39)	S355N	probably damaging	Het
Tarbp1	C	T	8: 127,154,853 (GRCm39)	V1424I	probably damaging	Het
Tatdn3	A	T	1: 190,781,477 (GRCm39)		probably null	Het
Tbpl1	T	A	10: 22,583,576 (GRCm39)	E131D	probably damaging	Het
Telo2	A	T	17: 25,324,382 (GRCm39)	M501K	probably damaging	Het
Terb1	A	G	8: 105,179,331 (GRCm39)	V619A	probably benign	Het
Tmem132e	A	G	11: 82,335,989 (GRCm39)	T1024A	probably benign	Het
Tmem30a	T	C	9: 79,681,500 (GRCm39)	D223G	probably damaging	Het
Tmprss11d	A	G	5: 86,487,413 (GRCm39)	V19A	probably damaging	Het
Tnks	A	T	8: 35,318,260 (GRCm39)	S872T	probably damaging	Het
Tnxb	A	G	17: 34,890,724 (GRCm39)	S356G	probably benign	Het
Tob2	T	C	15: 81,735,400 (GRCm39)	K190E	probably damaging	Het
Togaram1	T	C	12: 65,049,433 (GRCm39)	V1240A	possibly damaging	Het
Trim13	T	A	14: 61,842,335 (GRCm39)	C117*	probably null	Het
Trpv4	G	A	5: 114,772,666 (GRCm39)	R308C	probably damaging	Het
Ttn	C	G	2: 76,585,676 (GRCm39)	D21987H	probably damaging	Het
Ttn	C	A	2: 76,656,418 (GRCm39)		probably null	Het
Upp1	A	T	11: 9,083,240 (GRCm39)	M111L	possibly damaging	Het
Vmn1r206	A	T	13: 22,804,358 (GRCm39)	V283E	probably damaging	Het
Vmn2r79	G	T	7: 86,651,634 (GRCm39)	L344F	probably benign	Het
Vmn2r93	T	G	17: 18,546,324 (GRCm39)	I732S	probably damaging	Het
Vmn2r96	G	T	17: 18,804,263 (GRCm39)	M504I	probably benign	Het
Vps39	T	C	2: 120,173,708 (GRCm39)	Y147C	probably damaging	Het
Zbtb20	T	A	16: 43,398,015 (GRCm39)	C35S	possibly damaging	Het
Zfp871	A	T	17: 32,993,751 (GRCm39)	C475S	probably damaging	Het

Other mutations in Arid1a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00565:Arid1a	APN	4	133,412,793 (GRCm39)	missense	unknown
IGL01139:Arid1a	APN	4	133,421,308 (GRCm39)	missense	unknown
IGL01392:Arid1a	APN	4	133,408,348 (GRCm39)	missense	unknown
IGL01543:Arid1a	APN	4	133,409,033 (GRCm39)	missense	unknown
IGL01642:Arid1a	APN	4	133,409,155 (GRCm39)	missense	unknown
IGL01843:Arid1a	APN	4	133,408,765 (GRCm39)	missense	unknown
IGL02108:Arid1a	APN	4	133,407,827 (GRCm39)	missense	unknown
IGL02117:Arid1a	APN	4	133,420,126 (GRCm39)	missense	unknown
IGL02150:Arid1a	APN	4	133,414,568 (GRCm39)	missense	unknown
IGL02478:Arid1a	APN	4	133,408,585 (GRCm39)	missense	unknown
IGL02544:Arid1a	APN	4	133,409,059 (GRCm39)	missense	unknown
IGL03070:Arid1a	APN	4	133,422,064 (GRCm39)	missense	unknown
PIT4520001:Arid1a	UTSW	4	133,409,227 (GRCm39)	missense	unknown
R0023:Arid1a	UTSW	4	133,418,487 (GRCm39)	missense	unknown
R0023:Arid1a	UTSW	4	133,418,487 (GRCm39)	missense	unknown
R0419:Arid1a	UTSW	4	133,408,435 (GRCm39)	missense	unknown
R0452:Arid1a	UTSW	4	133,416,416 (GRCm39)	missense	unknown
R0631:Arid1a	UTSW	4	133,416,481 (GRCm39)	missense	unknown
R0648:Arid1a	UTSW	4	133,412,515 (GRCm39)	missense	unknown
R1004:Arid1a	UTSW	4	133,414,586 (GRCm39)	missense	unknown
R1225:Arid1a	UTSW	4	133,414,676 (GRCm39)	missense	unknown
R1229:Arid1a	UTSW	4	133,418,548 (GRCm39)	missense	unknown
R1435:Arid1a	UTSW	4	133,408,009 (GRCm39)	missense	unknown
R1480:Arid1a	UTSW	4	133,407,700 (GRCm39)	missense	unknown
R1491:Arid1a	UTSW	4	133,448,237 (GRCm39)	missense	unknown
R1674:Arid1a	UTSW	4	133,416,571 (GRCm39)	missense	unknown
R1909:Arid1a	UTSW	4	133,421,072 (GRCm39)	missense	unknown
R1960:Arid1a	UTSW	4	133,480,401 (GRCm39)	missense	possibly damaging	0.84
R2147:Arid1a	UTSW	4	133,408,677 (GRCm39)	missense	unknown
R2303:Arid1a	UTSW	4	133,414,562 (GRCm39)	missense	unknown
R2320:Arid1a	UTSW	4	133,407,840 (GRCm39)	missense	unknown
R3775:Arid1a	UTSW	4	133,414,075 (GRCm39)	missense	unknown
R3907:Arid1a	UTSW	4	133,420,223 (GRCm39)	splice site	probably benign
R4509:Arid1a	UTSW	4	133,423,010 (GRCm39)	intron	probably benign
R4510:Arid1a	UTSW	4	133,423,010 (GRCm39)	intron	probably benign
R4551:Arid1a	UTSW	4	133,423,010 (GRCm39)	intron	probably benign
R4552:Arid1a	UTSW	4	133,423,010 (GRCm39)	intron	probably benign
R4606:Arid1a	UTSW	4	133,414,634 (GRCm39)	missense	unknown
R4745:Arid1a	UTSW	4	133,480,417 (GRCm39)	missense	probably benign	0.33
R4851:Arid1a	UTSW	4	133,408,672 (GRCm39)	missense	unknown
R4867:Arid1a	UTSW	4	133,448,168 (GRCm39)	missense	probably benign	0.01
R5203:Arid1a	UTSW	4	133,409,314 (GRCm39)	missense	unknown
R5227:Arid1a	UTSW	4	133,407,716 (GRCm39)	missense	unknown
R5294:Arid1a	UTSW	4	133,418,366 (GRCm39)	splice site	probably benign
R5299:Arid1a	UTSW	4	133,414,537 (GRCm39)	missense	unknown
R5412:Arid1a	UTSW	4	133,446,913 (GRCm39)	unclassified	probably benign
R5540:Arid1a	UTSW	4	133,407,765 (GRCm39)	missense	unknown
R5704:Arid1a	UTSW	4	133,409,050 (GRCm39)	missense	unknown
R5870:Arid1a	UTSW	4	133,408,387 (GRCm39)	missense	unknown
R6092:Arid1a	UTSW	4	133,421,163 (GRCm39)	missense	unknown
R6151:Arid1a	UTSW	4	133,412,287 (GRCm39)	missense	unknown
R6240:Arid1a	UTSW	4	133,407,997 (GRCm39)	missense	unknown
R6379:Arid1a	UTSW	4	133,408,238 (GRCm39)	missense	unknown
R6427:Arid1a	UTSW	4	133,408,835 (GRCm39)	missense	unknown
R6739:Arid1a	UTSW	4	133,414,937 (GRCm39)	missense	unknown
R7159:Arid1a	UTSW	4	133,480,879 (GRCm39)	missense	unknown
R7186:Arid1a	UTSW	4	133,480,544 (GRCm39)
R7354:Arid1a	UTSW	4	133,421,258 (GRCm39)	missense	unknown
R7408:Arid1a	UTSW	4	133,408,391 (GRCm39)	missense	unknown
R7452:Arid1a	UTSW	4	133,480,438 (GRCm39)	missense	possibly damaging	0.86
R7471:Arid1a	UTSW	4	133,408,355 (GRCm39)	missense	unknown
R7478:Arid1a	UTSW	4	133,412,482 (GRCm39)	missense	unknown
R7581:Arid1a	UTSW	4	133,407,662 (GRCm39)	missense	unknown
R7614:Arid1a	UTSW	4	133,418,466 (GRCm39)	missense	unknown
R7712:Arid1a	UTSW	4	133,479,922 (GRCm39)	missense	probably benign	0.14
R7734:Arid1a	UTSW	4	133,408,679 (GRCm39)	missense	unknown
R7878:Arid1a	UTSW	4	133,414,582 (GRCm39)	missense	unknown
R7973:Arid1a	UTSW	4	133,480,381 (GRCm39)	missense	probably damaging	0.96
R8012:Arid1a	UTSW	4	133,420,174 (GRCm39)	missense	unknown
R8355:Arid1a	UTSW	4	133,448,174 (GRCm39)	missense	unknown
R8396:Arid1a	UTSW	4	133,479,973 (GRCm39)	missense	probably damaging	0.99
R8708:Arid1a	UTSW	4	133,409,145 (GRCm39)	missense	unknown
R8923:Arid1a	UTSW	4	133,412,304 (GRCm39)	missense	unknown
R8997:Arid1a	UTSW	4	133,421,343 (GRCm39)	missense	unknown
R9003:Arid1a	UTSW	4	133,411,799 (GRCm39)	missense	unknown
R9145:Arid1a	UTSW	4	133,421,214 (GRCm39)	missense	unknown
R9224:Arid1a	UTSW	4	133,409,167 (GRCm39)	missense	unknown
R9310:Arid1a	UTSW	4	133,413,625 (GRCm39)	missense	unknown
R9470:Arid1a	UTSW	4	133,413,057 (GRCm39)	missense	unknown
RF012:Arid1a	UTSW	4	133,480,131 (GRCm39)	small deletion	probably benign
RF015:Arid1a	UTSW	4	133,480,142 (GRCm39)	small deletion	probably benign
X0064:Arid1a	UTSW	4	133,416,571 (GRCm39)	missense	unknown
Z1176:Arid1a	UTSW	4	133,447,861 (GRCm39)	missense	probably null
Z1177:Arid1a	UTSW	4	133,408,227 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- GGATATGCTCAGTGGTATCCCC -3'
(R):5'- CTTGCTAGAGCTCCTTGTGG -3'

Sequencing Primer
(F):5'- AATCCGCCAGTGTAGCAG -3'
(R):5'- GCTAGAGCTCCTTGTGGAATATTTCC -3'

Posted On

2014-08-25