Mutagenetix > Incidental Mutation

Incidental Mutation 'R0388:Dmbt1'

31413

Institutional Source

Beutler Lab

Gene Symbol

Dmbt1

Ensembl Gene

ENSMUSG00000047517

Gene Name

deleted in malignant brain tumors 1

Synonyms

CRP-[a], Crpd, gp300, vomeroglandin, CRP-[b], ebnerin, MUCLIN, hensin

MMRRC Submission

038594-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.194) question?

Stock #

R0388 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

131032053-131121630 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 131096049 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000148657 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000084509] [ENSMUST00000124096] [ENSMUST00000208311] [ENSMUST00000213064]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000084509

SMART Domains

Protein: ENSMUSP00000081556
Gene: ENSMUSG00000047517

Domain	Start	End	E-Value	Type
SR	37	137	5.54e-59	SMART
SR	186	286	3.6e-58	SMART
SR	324	424	1.21e-59	SMART
SR	463	563	2.97e-59	SMART
SR	602	702	3.36e-58	SMART
SR	741	841	5.17e-59	SMART
low complexity region	848	879	N/A	INTRINSIC
CUB	884	993	4.22e-41	SMART
CUB	1000	1109	7.35e-41	SMART
CUB	1126	1235	3.73e-42	SMART
CUB	1242	1351	2.02e-38	SMART
SR	1371	1471	3.92e-59	SMART
low complexity region	1476	1488	N/A	INTRINSIC
CUB	1494	1603	6.7e-44	SMART
ZP	1612	1860	8.11e-74	SMART
transmembrane domain	1906	1928	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000124096

SMART Domains

Protein: ENSMUSP00000130971
Gene: ENSMUSG00000030849

Domain	Start	End	E-Value	Type
Pfam:Pkinase	1	118	4.8e-19	PFAM
Pfam:Pkinase_Tyr	1	118	1.7e-50	PFAM
low complexity region	146	160	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000208311

Predicted Effect

probably benign
Transcript: ENSMUST00000213064

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.0%
3x: 98.0%
10x: 95.6%
20x: 90.7%

Validation Efficiency

100% (67/67)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Loss of sequences from human chromosome 10q has been associated with the progression of human cancers. This gene was originally isolated based on its deletion in a medulloblastoma cell line. This gene is expressed with transcripts of 6.0, 7.5, and 8.0 kb in fetal lung and with one transcript of 8.0 kb in adult lung, although the 7.5 kb transcript has not been characterized. The encoded protein precursor is a glycoprotein containing multiple scavenger receptor cysteine-rich (SRCR) domains separated by SRCR-interspersed domains (SID). Transcript variant 2 (8.0 kb) has been shown to bind surfactant protein D independently of carbohydrate recognition. This indicates that DMBT1 may not be a classical tumor suppressor gene, but rather play a role in the interaction of tumor cells and the immune system. [provided by RefSeq, Mar 2016]
PHENOTYPE: Mice homozygous for one null allele display embryonic lethality and an abnormal inner cell mass. Mice homozygous for a different null allele are viable and fertile with an increased susceptibility to induced colitis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010315B03Rik	T	C	9: 124,295,159 (GRCm38)		probably benign	Het
Acsbg1	T	C	9: 54,609,063 (GRCm38)	K678R	probably damaging	Het
Adgrg6	A	G	10: 14,450,658 (GRCm38)	I410T	probably benign	Het
Afap1l2	A	C	19: 56,917,242 (GRCm38)		probably benign	Het
Aox2	T	C	1: 58,354,406 (GRCm38)	Y1242H	probably damaging	Het
Apoo-ps	T	C	13: 107,414,673 (GRCm38)		noncoding transcript	Het
Camta1	C	A	4: 151,075,140 (GRCm38)	R1614L	probably damaging	Het
Cdh3	C	A	8: 106,539,129 (GRCm38)	T268K	probably damaging	Het
Chd5	T	A	4: 152,371,644 (GRCm38)	H923Q	probably damaging	Het
Chd7	T	C	4: 8,854,560 (GRCm38)	V1967A	probably benign	Het
Cntn3	T	C	6: 102,277,316 (GRCm38)	M222V	probably damaging	Het
Dcaf17	A	G	2: 71,078,571 (GRCm38)	K277R	probably benign	Het
Dmpk	T	A	7: 19,084,077 (GRCm38)		probably benign	Het
Dzank1	A	T	2: 144,476,106 (GRCm38)	L714Q	possibly damaging	Het
Efcab3	A	G	11: 105,109,401 (GRCm38)	D272G	possibly damaging	Het
Erbb2	G	C	11: 98,427,351 (GRCm38)	R471P	possibly damaging	Het
Esf1	T	A	2: 140,120,871 (GRCm38)	Y760F	possibly damaging	Het
Fanci	C	A	7: 79,439,630 (GRCm38)	T938K	probably benign	Het
Gnai3	A	G	3: 108,115,757 (GRCm38)		probably benign	Het
Hspg2	T	A	4: 137,511,158 (GRCm38)	C319S	probably damaging	Het
Il12a	T	A	3: 68,695,187 (GRCm38)		probably null	Het
Inpp4a	A	G	1: 37,396,160 (GRCm38)	D837G	probably damaging	Het
Kcnj5	T	A	9: 32,317,863 (GRCm38)	E13V	probably damaging	Het
Kcnq3	T	A	15: 66,000,038 (GRCm38)	Y594F	probably benign	Het
Kif16b	T	C	2: 142,740,937 (GRCm38)	E556G	probably damaging	Het
Kif28	T	C	1: 179,740,089 (GRCm38)	I39V	possibly damaging	Het
Lgi2	T	C	5: 52,554,549 (GRCm38)	E143G	probably damaging	Het
Mast1	T	G	8: 84,915,537 (GRCm38)	I1063L	probably benign	Het
Med12l	T	C	3: 59,093,504 (GRCm38)		probably benign	Het
Mmp19	G	T	10: 128,798,883 (GRCm38)	R456L	probably benign	Het
Mon1b	T	A	8: 113,639,078 (GRCm38)	V346E	probably damaging	Het
Mpv17l	A	T	16: 13,940,999 (GRCm38)	I96L	probably benign	Het
Mrgpra9	A	T	7: 47,252,794 (GRCm38)	M1K	probably null	Het
Mycbp2	A	T	14: 103,156,667 (GRCm38)	H2819Q	probably benign	Het
Nav1	A	C	1: 135,448,917 (GRCm38)		probably benign	Het
Neurl4	T	C	11: 69,911,733 (GRCm38)		probably benign	Het
Ntng2	G	C	2: 29,207,426 (GRCm38)	P341R	probably damaging	Het
Oas1d	A	T	5: 120,917,028 (GRCm38)	Y221F	probably damaging	Het
Olfr1040	A	G	2: 86,146,630 (GRCm38)	Y35H	probably damaging	Het
Olfr348	C	A	2: 36,786,862 (GRCm38)	D112E	probably benign	Het
Olfr365	A	C	2: 37,202,184 (GRCm38)		probably null	Het
Osbpl8	A	G	10: 111,272,282 (GRCm38)	M380V	probably benign	Het
Pank1	T	C	19: 34,821,706 (GRCm38)		probably benign	Het
Parn	T	C	16: 13,654,476 (GRCm38)	D169G	possibly damaging	Het
Pknox1	T	A	17: 31,603,192 (GRCm38)	I311N	probably damaging	Het
Pprc1	T	C	19: 46,062,775 (GRCm38)	V248A	possibly damaging	Het
Prkcq	T	C	2: 11,254,234 (GRCm38)	C322R	probably benign	Het
Ptpn13	T	A	5: 103,555,062 (GRCm38)	I1298N	probably benign	Het
Rab11fip3	A	G	17: 26,069,072 (GRCm38)	S36P	probably benign	Het
Rif1	GCCACCA	GCCA	2: 52,110,324 (GRCm38)		probably benign	Het
Sass6	C	A	3: 116,607,308 (GRCm38)		probably benign	Het
Shroom3	G	A	5: 92,951,293 (GRCm38)	G1463D	probably benign	Het
Slc35d1	A	T	4: 103,184,887 (GRCm38)	Y249*	probably null	Het
Slc9a3	C	T	13: 74,121,536 (GRCm38)	P8S	unknown	Het
Slc9a9	T	A	9: 94,939,563 (GRCm38)		probably null	Het
Syne2	T	A	12: 75,986,975 (GRCm38)	M3666K	probably benign	Het
Synpo2	A	G	3: 123,079,897 (GRCm38)	V1140A	probably benign	Het
Thada	A	G	17: 84,231,096 (GRCm38)	F1495L	probably benign	Het
Timeless	A	G	10: 128,241,425 (GRCm38)		probably null	Het
Tlr6	G	T	5: 64,955,205 (GRCm38)	H120N	possibly damaging	Het
Tmem173	A	G	18: 35,735,111 (GRCm38)		probably null	Het
Tns3	T	C	11: 8,445,703 (GRCm38)	I1234V	probably benign	Het
Ttll9	A	G	2: 153,000,179 (GRCm38)	S318G	probably benign	Het
Vps13c	T	C	9: 67,922,915 (GRCm38)		probably benign	Het
Zfp933	T	C	4: 147,826,442 (GRCm38)	I232M	probably benign	Het
Zfyve27	T	C	19: 42,189,585 (GRCm38)	S382P	probably damaging	Het

Other mutations in Dmbt1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00091:Dmbt1	APN	7	131,079,540 (GRCm38)	intron	probably benign
IGL00161:Dmbt1	APN	7	131,109,628 (GRCm38)	missense	probably damaging	1.00
IGL00331:Dmbt1	APN	7	131,099,290 (GRCm38)	missense	possibly damaging	0.46
IGL00769:Dmbt1	APN	7	131,082,500 (GRCm38)	missense	probably damaging	0.99
IGL00792:Dmbt1	APN	7	131,097,607 (GRCm38)	missense	possibly damaging	0.66
IGL00823:Dmbt1	APN	7	131,058,158 (GRCm38)	missense	probably benign	0.26
IGL01072:Dmbt1	APN	7	131,085,368 (GRCm38)	splice site	probably benign
IGL01317:Dmbt1	APN	7	131,041,191 (GRCm38)	missense	probably damaging	1.00
IGL01335:Dmbt1	APN	7	131,088,767 (GRCm38)	missense	possibly damaging	0.95
IGL01372:Dmbt1	APN	7	131,103,679 (GRCm38)	missense	possibly damaging	0.90
IGL01511:Dmbt1	APN	7	131,116,728 (GRCm38)	missense	possibly damaging	0.49
IGL01627:Dmbt1	APN	7	131,081,185 (GRCm38)	missense	probably benign	0.14
IGL01890:Dmbt1	APN	7	131,074,419 (GRCm38)	intron	probably benign
IGL02160:Dmbt1	APN	7	131,082,688 (GRCm38)	missense	probably damaging	1.00
IGL02186:Dmbt1	APN	7	131,093,256 (GRCm38)	splice site	probably benign
IGL02197:Dmbt1	APN	7	131,085,422 (GRCm38)	splice site	probably benign
IGL02332:Dmbt1	APN	7	131,066,613 (GRCm38)	intron	probably benign
IGL02427:Dmbt1	APN	7	131,088,085 (GRCm38)	splice site	probably null
IGL02726:Dmbt1	APN	7	131,074,410 (GRCm38)	intron	probably benign
IGL02967:Dmbt1	APN	7	131,071,189 (GRCm38)	missense	possibly damaging	0.70
IGL03003:Dmbt1	APN	7	131,082,679 (GRCm38)	missense	probably benign	0.05
IGL03089:Dmbt1	APN	7	131,111,049 (GRCm38)	missense	probably damaging	0.99
cavity	UTSW	7	131,112,236 (GRCm38)	missense	unknown
lacunar	UTSW	7	131,097,631 (GRCm38)	missense	probably damaging	0.97
BB005:Dmbt1	UTSW	7	131,037,890 (GRCm38)	missense	probably benign	0.16
BB015:Dmbt1	UTSW	7	131,037,890 (GRCm38)	missense	probably benign	0.16
H8562:Dmbt1	UTSW	7	131,112,076 (GRCm38)	nonsense	probably null
K3955:Dmbt1	UTSW	7	131,119,564 (GRCm38)	missense	probably damaging	0.98
R0051:Dmbt1	UTSW	7	131,119,496 (GRCm38)	missense	possibly damaging	0.79
R0051:Dmbt1	UTSW	7	131,119,496 (GRCm38)	missense	possibly damaging	0.79
R0257:Dmbt1	UTSW	7	131,106,393 (GRCm38)	missense	probably damaging	1.00
R0427:Dmbt1	UTSW	7	131,040,902 (GRCm38)	nonsense	probably null
R0478:Dmbt1	UTSW	7	131,041,187 (GRCm38)	missense	possibly damaging	0.93
R0502:Dmbt1	UTSW	7	131,097,673 (GRCm38)	splice site	probably null
R0538:Dmbt1	UTSW	7	131,049,901 (GRCm38)	splice site	probably benign
R0626:Dmbt1	UTSW	7	131,102,081 (GRCm38)	missense	probably damaging	0.97
R0631:Dmbt1	UTSW	7	131,097,653 (GRCm38)	missense	possibly damaging	0.90
R0948:Dmbt1	UTSW	7	131,093,117 (GRCm38)	missense	possibly damaging	0.95
R1169:Dmbt1	UTSW	7	131,074,524 (GRCm38)	critical splice donor site	probably null
R1413:Dmbt1	UTSW	7	131,050,214 (GRCm38)	missense	probably damaging	1.00
R1458:Dmbt1	UTSW	7	131,044,487 (GRCm38)	splice site	probably benign
R1463:Dmbt1	UTSW	7	131,109,637 (GRCm38)	critical splice donor site	probably null
R1509:Dmbt1	UTSW	7	131,074,331 (GRCm38)	intron	probably benign
R1990:Dmbt1	UTSW	7	131,058,288 (GRCm38)	missense	probably damaging	0.98
R2018:Dmbt1	UTSW	7	131,110,989 (GRCm38)	missense	possibly damaging	0.93
R2019:Dmbt1	UTSW	7	131,110,989 (GRCm38)	missense	possibly damaging	0.93
R2042:Dmbt1	UTSW	7	131,106,359 (GRCm38)	missense	probably damaging	0.99
R2056:Dmbt1	UTSW	7	131,106,170 (GRCm38)	missense	possibly damaging	0.80
R2057:Dmbt1	UTSW	7	131,106,170 (GRCm38)	missense	possibly damaging	0.80
R2058:Dmbt1	UTSW	7	131,106,170 (GRCm38)	missense	possibly damaging	0.80
R2059:Dmbt1	UTSW	7	131,106,170 (GRCm38)	missense	possibly damaging	0.80
R2061:Dmbt1	UTSW	7	131,099,133 (GRCm38)	missense	possibly damaging	0.66
R2092:Dmbt1	UTSW	7	131,050,018 (GRCm38)	missense	probably damaging	1.00
R2102:Dmbt1	UTSW	7	131,102,032 (GRCm38)	missense	probably damaging	0.97
R2155:Dmbt1	UTSW	7	131,097,575 (GRCm38)	missense	possibly damaging	0.66
R2243:Dmbt1	UTSW	7	131,046,562 (GRCm38)	missense	probably benign	0.03
R2256:Dmbt1	UTSW	7	131,090,494 (GRCm38)	missense	probably benign	0.01
R2391:Dmbt1	UTSW	7	131,106,468 (GRCm38)	missense	probably damaging	1.00
R2394:Dmbt1	UTSW	7	131,094,734 (GRCm38)	nonsense	probably null
R3014:Dmbt1	UTSW	7	131,032,097 (GRCm38)	intron	probably benign
R3155:Dmbt1	UTSW	7	131,050,157 (GRCm38)	nonsense	probably null
R3176:Dmbt1	UTSW	7	131,088,071 (GRCm38)	missense	probably benign	0.19
R3276:Dmbt1	UTSW	7	131,088,071 (GRCm38)	missense	probably benign	0.19
R3442:Dmbt1	UTSW	7	131,106,249 (GRCm38)	missense	probably damaging	1.00
R3807:Dmbt1	UTSW	7	131,112,090 (GRCm38)	missense	possibly damaging	0.77
R4060:Dmbt1	UTSW	7	131,074,202 (GRCm38)	intron	probably benign
R4396:Dmbt1	UTSW	7	131,116,632 (GRCm38)	missense	probably damaging	0.98
R4453:Dmbt1	UTSW	7	131,040,934 (GRCm38)	missense	probably damaging	1.00
R5001:Dmbt1	UTSW	7	131,050,012 (GRCm38)	missense	probably damaging	1.00
R5051:Dmbt1	UTSW	7	131,094,742 (GRCm38)	missense	probably benign	0.01
R5156:Dmbt1	UTSW	7	131,097,670 (GRCm38)	critical splice donor site	probably null
R5225:Dmbt1	UTSW	7	131,094,735 (GRCm38)	missense	possibly damaging	0.84
R5281:Dmbt1	UTSW	7	131,082,619 (GRCm38)	missense	probably damaging	1.00
R5308:Dmbt1	UTSW	7	131,041,021 (GRCm38)	missense	probably damaging	1.00
R5447:Dmbt1	UTSW	7	131,119,511 (GRCm38)	missense	probably damaging	0.99
R5467:Dmbt1	UTSW	7	131,040,993 (GRCm38)	missense	probably damaging	1.00
R5497:Dmbt1	UTSW	7	131,063,403 (GRCm38)	intron	probably benign
R5526:Dmbt1	UTSW	7	131,041,190 (GRCm38)	missense	probably damaging	1.00
R5554:Dmbt1	UTSW	7	131,099,300 (GRCm38)	nonsense	probably null
R5566:Dmbt1	UTSW	7	131,106,273 (GRCm38)	missense	probably damaging	1.00
R5595:Dmbt1	UTSW	7	131,054,067 (GRCm38)	missense	probably benign	0.17
R6154:Dmbt1	UTSW	7	131,109,641 (GRCm38)	splice site	probably null
R6188:Dmbt1	UTSW	7	131,097,631 (GRCm38)	missense	probably damaging	0.97
R6214:Dmbt1	UTSW	7	131,066,733 (GRCm38)	missense	possibly damaging	0.95
R6215:Dmbt1	UTSW	7	131,066,733 (GRCm38)	missense	possibly damaging	0.95
R6391:Dmbt1	UTSW	7	131,058,254 (GRCm38)	missense	probably damaging	1.00
R6397:Dmbt1	UTSW	7	131,103,578 (GRCm38)	missense	possibly damaging	0.46
R6436:Dmbt1	UTSW	7	131,116,641 (GRCm38)	missense	probably benign	0.01
R6603:Dmbt1	UTSW	7	131,046,510 (GRCm38)	splice site	probably null
R6719:Dmbt1	UTSW	7	131,119,603 (GRCm38)	missense	possibly damaging	0.83
R6781:Dmbt1	UTSW	7	131,046,561 (GRCm38)	missense	probably benign	0.16
R7148:Dmbt1	UTSW	7	131,066,734 (GRCm38)	nonsense	probably null
R7191:Dmbt1	UTSW	7	131,044,520 (GRCm38)	missense	unknown
R7269:Dmbt1	UTSW	7	131,066,621 (GRCm38)	missense	unknown
R7288:Dmbt1	UTSW	7	131,083,789 (GRCm38)	nonsense	probably null
R7296:Dmbt1	UTSW	7	131,112,132 (GRCm38)	missense	unknown
R7349:Dmbt1	UTSW	7	131,041,124 (GRCm38)	missense	unknown
R7386:Dmbt1	UTSW	7	131,112,236 (GRCm38)	missense	unknown
R7428:Dmbt1	UTSW	7	131,108,463 (GRCm38)	missense	possibly damaging	0.53
R7481:Dmbt1	UTSW	7	131,079,511 (GRCm38)	critical splice acceptor site	probably null
R7486:Dmbt1	UTSW	7	131,066,462 (GRCm38)	missense	unknown
R7513:Dmbt1	UTSW	7	131,090,512 (GRCm38)	missense	unknown
R7553:Dmbt1	UTSW	7	131,104,867 (GRCm38)	missense	unknown
R7567:Dmbt1	UTSW	7	131,061,363 (GRCm38)	splice site	probably null
R7584:Dmbt1	UTSW	7	131,088,751 (GRCm38)	nonsense	probably null
R7736:Dmbt1	UTSW	7	131,116,896 (GRCm38)	missense	unknown
R7758:Dmbt1	UTSW	7	131,121,197 (GRCm38)	missense	unknown
R7928:Dmbt1	UTSW	7	131,037,890 (GRCm38)	missense	probably benign	0.16
R8080:Dmbt1	UTSW	7	131,088,770 (GRCm38)	missense	unknown
R8098:Dmbt1	UTSW	7	131,108,459 (GRCm38)	nonsense	probably null
R8125:Dmbt1	UTSW	7	131,099,223 (GRCm38)	missense	unknown
R8177:Dmbt1	UTSW	7	131,106,432 (GRCm38)	missense	possibly damaging	0.46
R8350:Dmbt1	UTSW	7	131,085,417 (GRCm38)	critical splice donor site	probably null
R8366:Dmbt1	UTSW	7	131,066,600 (GRCm38)	missense	unknown
R8378:Dmbt1	UTSW	7	131,106,465 (GRCm38)	missense	probably damaging	0.96
R8399:Dmbt1	UTSW	7	131,082,587 (GRCm38)	missense	unknown
R8400:Dmbt1	UTSW	7	131,082,587 (GRCm38)	missense	unknown
R8445:Dmbt1	UTSW	7	131,090,380 (GRCm38)	missense	unknown
R8450:Dmbt1	UTSW	7	131,085,417 (GRCm38)	critical splice donor site	probably null
R8511:Dmbt1	UTSW	7	131,102,012 (GRCm38)	missense	unknown
R8688:Dmbt1	UTSW	7	131,058,254 (GRCm38)	missense	unknown
R8850:Dmbt1	UTSW	7	131,090,404 (GRCm38)	missense	unknown
R8852:Dmbt1	UTSW	7	131,041,123 (GRCm38)	missense	unknown
R8871:Dmbt1	UTSW	7	131,116,868 (GRCm38)	missense	unknown
R8943:Dmbt1	UTSW	7	131,119,643 (GRCm38)	missense	possibly damaging	0.68
R8978:Dmbt1	UTSW	7	131,037,881 (GRCm38)	missense	possibly damaging	0.53
R9004:Dmbt1	UTSW	7	131,112,069 (GRCm38)	missense	unknown
R9020:Dmbt1	UTSW	7	131,111,058 (GRCm38)	missense	possibly damaging	0.86
R9088:Dmbt1	UTSW	7	131,116,689 (GRCm38)	missense	unknown
R9230:Dmbt1	UTSW	7	131,037,912 (GRCm38)	missense	probably benign	0.01
R9304:Dmbt1	UTSW	7	131,099,125 (GRCm38)	missense	unknown
R9377:Dmbt1	UTSW	7	131,093,102 (GRCm38)	missense	unknown
R9428:Dmbt1	UTSW	7	131,066,478 (GRCm38)	missense	unknown
R9474:Dmbt1	UTSW	7	131,074,257 (GRCm38)	missense	unknown
R9573:Dmbt1	UTSW	7	131,056,180 (GRCm38)	critical splice donor site	probably null
R9675:Dmbt1	UTSW	7	131,110,923 (GRCm38)	missense	probably damaging	0.98
R9689:Dmbt1	UTSW	7	131,058,285 (GRCm38)	missense	unknown
R9781:Dmbt1	UTSW	7	131,037,869 (GRCm38)	missense	probably benign	0.00
X0024:Dmbt1	UTSW	7	131,112,248 (GRCm38)	nonsense	probably null
X0062:Dmbt1	UTSW	7	131,094,851 (GRCm38)	missense	possibly damaging	0.81
Z1176:Dmbt1	UTSW	7	131,088,812 (GRCm38)	missense	unknown
Z1177:Dmbt1	UTSW	7	131,082,485 (GRCm38)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- ACTTTCAATGCGGCAGCAGGTG -3'
(R):5'- AACAATGATGTGGCCCTGACCTC -3'

Sequencing Primer
(F):5'- GGTGAATACAACTCAGACTGTTATGC -3'
(R):5'- GACAAGAACAGTTTCTGTTGCCC -3'

Posted On

2013-04-24