Incidental Mutation 'R1509:Map1b'
| ID |
168168 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Map1b
|
| Ensembl Gene |
ENSMUSG00000052727 |
| Gene Name |
microtubule-associated protein 1B |
| Synonyms |
Mtap1b, Mtap-5, MAP5, Mtap5, LC1 |
| MMRRC Submission |
039556-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1509 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
99557954-99653048 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 99568036 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 1562
(T1562A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000068374
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064762]
|
| AlphaFold |
P14873 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000064762
AA Change: T1562A
|
| SMART Domains |
Protein: ENSMUSP00000068374
Gene: ENSMUSG00000052727
AA Change: T1562A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
41 |
50 |
N/A |
INTRINSIC |
|
Blast:Lactamase_B
|
270 |
514 |
1e-56 |
BLAST |
|
low complexity region
|
578 |
595 |
N/A |
INTRINSIC |
|
low complexity region
|
597 |
617 |
N/A |
INTRINSIC |
|
SCOP:d1gkub2
|
633 |
735 |
8e-4 |
SMART |
|
low complexity region
|
771 |
813 |
N/A |
INTRINSIC |
|
low complexity region
|
855 |
866 |
N/A |
INTRINSIC |
|
low complexity region
|
889 |
913 |
N/A |
INTRINSIC |
|
low complexity region
|
935 |
956 |
N/A |
INTRINSIC |
|
low complexity region
|
1006 |
1030 |
N/A |
INTRINSIC |
|
low complexity region
|
1247 |
1261 |
N/A |
INTRINSIC |
|
low complexity region
|
1390 |
1404 |
N/A |
INTRINSIC |
|
low complexity region
|
1545 |
1557 |
N/A |
INTRINSIC |
|
low complexity region
|
1724 |
1735 |
N/A |
INTRINSIC |
|
Pfam:MAP1B_neuraxin
|
1891 |
1907 |
1.9e-10 |
PFAM |
|
Pfam:MAP1B_neuraxin
|
1908 |
1924 |
8.3e-11 |
PFAM |
|
Pfam:MAP1B_neuraxin
|
1942 |
1958 |
3.1e-9 |
PFAM |
|
Pfam:MAP1B_neuraxin
|
1959 |
1975 |
6.2e-9 |
PFAM |
|
Pfam:MAP1B_neuraxin
|
2027 |
2043 |
2.9e-10 |
PFAM |
|
Pfam:MAP1B_neuraxin
|
2044 |
2060 |
3.9e-9 |
PFAM |
|
low complexity region
|
2227 |
2257 |
N/A |
INTRINSIC |
|
low complexity region
|
2286 |
2307 |
N/A |
INTRINSIC |
|
low complexity region
|
2316 |
2343 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223693
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000224702
|
| Meta Mutation Damage Score |
0.0834 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.4%
- 20x: 93.1%
|
| Validation Efficiency |
99% (89/90) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to the microtubule-associated protein family. The proteins of this family are thought to be involved in microtubule assembly, which is an essential step in neurogenesis. The product of this gene is a precursor polypeptide that presumably undergoes proteolytic processing to generate the final MAP1B heavy chain and LC1 light chain. Gene knockout studies of the mouse microtubule-associated protein 1B gene suggested an important role in development and function of the nervous system. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for one knock-out allele die prior to E8.5. While mice homozygous for other knock-out alleles exhibit behavioral, visual system, and nervous system defects. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
T |
C |
13: 77,340,766 (GRCm39) |
S132P |
probably benign |
Het |
| AC153895.1 |
T |
C |
6: 50,020,451 (GRCm39) |
R54G |
unknown |
Het |
| Acot12 |
G |
A |
13: 91,919,994 (GRCm39) |
|
probably null |
Het |
| Adhfe1 |
T |
A |
1: 9,623,671 (GRCm39) |
D98E |
probably benign |
Het |
| Ago2 |
A |
G |
15: 72,988,213 (GRCm39) |
F594S |
probably damaging |
Het |
| Aldh18a1 |
A |
G |
19: 40,545,927 (GRCm39) |
I620T |
probably damaging |
Het |
| Aspscr1 |
C |
A |
11: 120,592,342 (GRCm39) |
A294D |
probably damaging |
Het |
| Bod1l |
C |
G |
5: 41,976,883 (GRCm39) |
R1477T |
probably damaging |
Het |
| Ccdc18 |
C |
A |
5: 108,336,844 (GRCm39) |
A741D |
possibly damaging |
Het |
| Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
| Cfap52 |
C |
T |
11: 67,829,819 (GRCm39) |
V317I |
probably benign |
Het |
| Cgn |
A |
T |
3: 94,681,568 (GRCm39) |
L509Q |
probably benign |
Het |
| Crb2 |
A |
G |
2: 37,676,631 (GRCm39) |
H204R |
probably benign |
Het |
| Cspg4b |
A |
G |
13: 113,504,790 (GRCm39) |
N431S |
probably damaging |
Het |
| Ddx39a |
G |
A |
8: 84,446,527 (GRCm39) |
V99M |
probably damaging |
Het |
| Dis3l2 |
T |
A |
1: 86,948,808 (GRCm39) |
C582S |
possibly damaging |
Het |
| Dmbt1 |
G |
A |
7: 130,676,061 (GRCm39) |
|
probably benign |
Het |
| Dnah6 |
T |
C |
6: 73,004,425 (GRCm39) |
E3846G |
probably damaging |
Het |
| Dstyk |
A |
G |
1: 132,384,084 (GRCm39) |
E655G |
probably damaging |
Het |
| Epha4 |
T |
C |
1: 77,357,523 (GRCm39) |
Y825C |
probably damaging |
Het |
| Esp36 |
T |
A |
17: 38,728,173 (GRCm39) |
N36I |
probably damaging |
Het |
| Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
| Fem1c |
A |
G |
18: 46,657,280 (GRCm39) |
S145P |
probably benign |
Het |
| Galnt13 |
T |
C |
2: 54,623,094 (GRCm39) |
I80T |
probably damaging |
Het |
| Gm5698 |
T |
C |
1: 31,016,728 (GRCm39) |
T108A |
probably benign |
Het |
| Hipk3 |
A |
G |
2: 104,271,607 (GRCm39) |
S442P |
probably benign |
Het |
| Hmcn2 |
T |
A |
2: 31,204,491 (GRCm39) |
V22D |
possibly damaging |
Het |
| Hspg2 |
C |
T |
4: 137,238,552 (GRCm39) |
|
probably benign |
Het |
| Ide |
A |
G |
19: 37,262,603 (GRCm39) |
|
probably null |
Het |
| Ifnar1 |
C |
A |
16: 91,300,384 (GRCm39) |
P462Q |
probably damaging |
Het |
| Itgb2l |
T |
A |
16: 96,228,049 (GRCm39) |
I485F |
probably benign |
Het |
| Jakmip3 |
C |
T |
7: 138,629,505 (GRCm39) |
R549W |
possibly damaging |
Het |
| Lrrc36 |
A |
G |
8: 106,187,761 (GRCm39) |
Q680R |
probably damaging |
Het |
| Lysmd3 |
T |
G |
13: 81,817,390 (GRCm39) |
H122Q |
probably benign |
Het |
| Macf1 |
C |
A |
4: 123,577,802 (GRCm39) |
V61L |
possibly damaging |
Het |
| Map3k20 |
A |
T |
2: 72,194,968 (GRCm39) |
|
probably benign |
Het |
| Mroh8 |
A |
G |
2: 157,075,125 (GRCm39) |
V457A |
probably benign |
Het |
| Mrpl40 |
T |
A |
16: 18,694,159 (GRCm39) |
|
probably null |
Het |
| Ms4a10 |
C |
T |
19: 10,941,472 (GRCm39) |
V166I |
probably benign |
Het |
| Mycl |
A |
G |
4: 122,894,100 (GRCm39) |
D300G |
probably damaging |
Het |
| Naca |
T |
A |
10: 127,879,266 (GRCm39) |
|
probably benign |
Het |
| Ncoa4 |
T |
C |
14: 31,895,391 (GRCm39) |
S172P |
probably damaging |
Het |
| Nfatc3 |
T |
C |
8: 106,810,486 (GRCm39) |
F421L |
possibly damaging |
Het |
| Nucb1 |
C |
A |
7: 45,144,649 (GRCm39) |
K301N |
probably benign |
Het |
| Or1af1 |
A |
G |
2: 37,109,966 (GRCm39) |
H155R |
probably damaging |
Het |
| Or52ae9 |
A |
T |
7: 103,390,243 (GRCm39) |
M68K |
probably benign |
Het |
| Or5b99 |
T |
A |
19: 12,976,815 (GRCm39) |
I155N |
possibly damaging |
Het |
| Panx1 |
A |
T |
9: 14,921,341 (GRCm39) |
V178E |
possibly damaging |
Het |
| Pkd1l3 |
G |
A |
8: 110,367,402 (GRCm39) |
V1210I |
probably damaging |
Het |
| Polr2a |
A |
T |
11: 69,638,039 (GRCm39) |
H143Q |
possibly damaging |
Het |
| Potefam1 |
A |
T |
2: 111,048,972 (GRCm39) |
M269K |
probably benign |
Het |
| Prdm12 |
G |
A |
2: 31,544,186 (GRCm39) |
R263H |
probably damaging |
Het |
| Prkdc |
A |
C |
16: 15,549,430 (GRCm39) |
K1998T |
probably damaging |
Het |
| Rab11fip1 |
A |
T |
8: 27,643,051 (GRCm39) |
S583T |
probably damaging |
Het |
| Rnf157 |
T |
A |
11: 116,237,921 (GRCm39) |
T567S |
probably benign |
Het |
| Rp1 |
T |
C |
1: 4,417,917 (GRCm39) |
K1065R |
probably damaging |
Het |
| Rp1 |
A |
G |
1: 4,418,760 (GRCm39) |
I784T |
probably benign |
Het |
| Rps10 |
A |
C |
17: 27,850,182 (GRCm39) |
F150V |
probably benign |
Het |
| Rrp12 |
A |
T |
19: 41,870,639 (GRCm39) |
F499I |
probably damaging |
Het |
| Sez6l2 |
G |
A |
7: 126,562,535 (GRCm39) |
R604H |
probably damaging |
Het |
| Slc25a21 |
G |
T |
12: 56,904,864 (GRCm39) |
Q57K |
probably benign |
Het |
| Slc27a2 |
A |
G |
2: 126,395,234 (GRCm39) |
T54A |
possibly damaging |
Het |
| Slc9a9 |
T |
A |
9: 95,111,011 (GRCm39) |
S610T |
probably benign |
Het |
| Smc1b |
A |
T |
15: 84,970,335 (GRCm39) |
S973T |
probably benign |
Het |
| Smc6 |
G |
A |
12: 11,329,734 (GRCm39) |
S164N |
possibly damaging |
Het |
| Sp1 |
A |
G |
15: 102,316,314 (GRCm39) |
T32A |
possibly damaging |
Het |
| Spen |
T |
C |
4: 141,202,946 (GRCm39) |
I1894V |
probably benign |
Het |
| Spen |
T |
C |
4: 141,203,011 (GRCm39) |
K1872R |
possibly damaging |
Het |
| Stab1 |
C |
A |
14: 30,873,541 (GRCm39) |
|
probably benign |
Het |
| Taar7d |
T |
G |
10: 23,904,102 (GRCm39) |
F328C |
probably damaging |
Het |
| Ticam1 |
A |
T |
17: 56,578,113 (GRCm39) |
S327R |
probably benign |
Het |
| Tmem248 |
C |
T |
5: 130,258,295 (GRCm39) |
|
probably benign |
Het |
| Tom1 |
T |
C |
8: 75,781,259 (GRCm39) |
S83P |
probably damaging |
Het |
| Txk |
T |
A |
5: 72,856,453 (GRCm39) |
Y446F |
probably damaging |
Het |
| Ubap1l |
T |
A |
9: 65,279,237 (GRCm39) |
C179S |
probably benign |
Het |
| Utrn |
T |
C |
10: 12,331,185 (GRCm39) |
E474G |
possibly damaging |
Het |
| Vmn2r14 |
T |
C |
5: 109,363,862 (GRCm39) |
M685V |
probably benign |
Het |
| Vmn2r7 |
A |
T |
3: 64,623,881 (GRCm39) |
Y146* |
probably null |
Het |
| Wdr1 |
G |
A |
5: 38,697,905 (GRCm39) |
T220M |
probably damaging |
Het |
| Xpo7 |
T |
C |
14: 70,915,582 (GRCm39) |
D726G |
probably damaging |
Het |
| Zbtb14 |
C |
G |
17: 69,694,759 (GRCm39) |
I152M |
probably benign |
Het |
| Zbtb3 |
A |
G |
19: 8,780,771 (GRCm39) |
D128G |
probably damaging |
Het |
| Zeb1os1 |
A |
G |
18: 5,583,794 (GRCm39) |
|
noncoding transcript |
Het |
| Zfp462 |
T |
A |
4: 55,007,667 (GRCm39) |
D35E |
probably damaging |
Het |
| Zfp467 |
A |
G |
6: 48,415,621 (GRCm39) |
S344P |
possibly damaging |
Het |
| Zfpm1 |
A |
T |
8: 123,034,285 (GRCm39) |
D73V |
possibly damaging |
Het |
|
| Other mutations in Map1b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00508:Map1b
|
APN |
13 |
99,565,741 (GRCm39) |
missense |
unknown |
|
|
IGL00533:Map1b
|
APN |
13 |
99,569,112 (GRCm39) |
missense |
unknown |
|
|
IGL00801:Map1b
|
APN |
13 |
99,566,605 (GRCm39) |
missense |
unknown |
|
|
IGL01141:Map1b
|
APN |
13 |
99,571,269 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01418:Map1b
|
APN |
13 |
99,568,338 (GRCm39) |
missense |
unknown |
|
|
IGL01464:Map1b
|
APN |
13 |
99,569,251 (GRCm39) |
missense |
unknown |
|
|
IGL01690:Map1b
|
APN |
13 |
99,571,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01991:Map1b
|
APN |
13 |
99,566,077 (GRCm39) |
missense |
unknown |
|
|
IGL02245:Map1b
|
APN |
13 |
99,568,036 (GRCm39) |
missense |
unknown |
|
|
IGL02376:Map1b
|
APN |
13 |
99,572,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02380:Map1b
|
APN |
13 |
99,567,651 (GRCm39) |
missense |
unknown |
|
|
IGL02442:Map1b
|
APN |
13 |
99,644,706 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02465:Map1b
|
APN |
13 |
99,569,914 (GRCm39) |
missense |
unknown |
|
|
IGL02816:Map1b
|
APN |
13 |
99,578,263 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02859:Map1b
|
APN |
13 |
99,569,544 (GRCm39) |
missense |
unknown |
|
|
IGL02934:Map1b
|
APN |
13 |
99,571,639 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02970:Map1b
|
APN |
13 |
99,567,242 (GRCm39) |
nonsense |
probably null |
|
|
IGL03148:Map1b
|
APN |
13 |
99,578,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03401:Map1b
|
APN |
13 |
99,563,776 (GRCm39) |
missense |
unknown |
|
|
IGL03138:Map1b
|
UTSW |
13 |
99,562,334 (GRCm39) |
missense |
unknown |
|
|
R0006:Map1b
|
UTSW |
13 |
99,571,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0006:Map1b
|
UTSW |
13 |
99,571,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0035:Map1b
|
UTSW |
13 |
99,571,846 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0069:Map1b
|
UTSW |
13 |
99,566,356 (GRCm39) |
missense |
unknown |
|
|
R0315:Map1b
|
UTSW |
13 |
99,567,624 (GRCm39) |
missense |
unknown |
|
|
R0539:Map1b
|
UTSW |
13 |
99,570,526 (GRCm39) |
missense |
unknown |
|
|
R0548:Map1b
|
UTSW |
13 |
99,568,191 (GRCm39) |
missense |
unknown |
|
|
R0613:Map1b
|
UTSW |
13 |
99,578,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0730:Map1b
|
UTSW |
13 |
99,566,274 (GRCm39) |
nonsense |
probably null |
|
|
R1103:Map1b
|
UTSW |
13 |
99,563,974 (GRCm39) |
splice site |
probably benign |
|
|
R1300:Map1b
|
UTSW |
13 |
99,569,029 (GRCm39) |
missense |
unknown |
|
|
R1353:Map1b
|
UTSW |
13 |
99,563,834 (GRCm39) |
missense |
unknown |
|
|
R1387:Map1b
|
UTSW |
13 |
99,569,158 (GRCm39) |
missense |
unknown |
|
|
R1481:Map1b
|
UTSW |
13 |
99,567,679 (GRCm39) |
missense |
unknown |
|
|
R1521:Map1b
|
UTSW |
13 |
99,569,247 (GRCm39) |
missense |
unknown |
|
|
R1604:Map1b
|
UTSW |
13 |
99,566,080 (GRCm39) |
missense |
unknown |
|
|
R1649:Map1b
|
UTSW |
13 |
99,652,986 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1651:Map1b
|
UTSW |
13 |
99,569,091 (GRCm39) |
missense |
unknown |
|
|
R1661:Map1b
|
UTSW |
13 |
99,568,437 (GRCm39) |
missense |
unknown |
|
|
R1665:Map1b
|
UTSW |
13 |
99,568,437 (GRCm39) |
missense |
unknown |
|
|
R1770:Map1b
|
UTSW |
13 |
99,567,001 (GRCm39) |
missense |
unknown |
|
|
R1926:Map1b
|
UTSW |
13 |
99,567,200 (GRCm39) |
missense |
unknown |
|
|
R1928:Map1b
|
UTSW |
13 |
99,567,454 (GRCm39) |
missense |
unknown |
|
|
R2093:Map1b
|
UTSW |
13 |
99,566,178 (GRCm39) |
missense |
unknown |
|
|
R2110:Map1b
|
UTSW |
13 |
99,567,629 (GRCm39) |
missense |
unknown |
|
|
R2116:Map1b
|
UTSW |
13 |
99,567,152 (GRCm39) |
missense |
unknown |
|
|
R2164:Map1b
|
UTSW |
13 |
99,565,846 (GRCm39) |
missense |
unknown |
|
|
R2207:Map1b
|
UTSW |
13 |
99,567,591 (GRCm39) |
missense |
unknown |
|
|
R2273:Map1b
|
UTSW |
13 |
99,568,592 (GRCm39) |
missense |
unknown |
|
|
R2443:Map1b
|
UTSW |
13 |
99,566,919 (GRCm39) |
missense |
unknown |
|
|
R3054:Map1b
|
UTSW |
13 |
99,569,250 (GRCm39) |
missense |
unknown |
|
|
R3766:Map1b
|
UTSW |
13 |
99,570,595 (GRCm39) |
missense |
unknown |
|
|
R3911:Map1b
|
UTSW |
13 |
99,567,580 (GRCm39) |
missense |
unknown |
|
|
R4005:Map1b
|
UTSW |
13 |
99,566,415 (GRCm39) |
missense |
unknown |
|
|
R4130:Map1b
|
UTSW |
13 |
99,568,188 (GRCm39) |
missense |
unknown |
|
|
R4513:Map1b
|
UTSW |
13 |
99,580,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4613:Map1b
|
UTSW |
13 |
99,566,810 (GRCm39) |
nonsense |
probably null |
|
|
R4633:Map1b
|
UTSW |
13 |
99,571,450 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4646:Map1b
|
UTSW |
13 |
99,568,977 (GRCm39) |
missense |
unknown |
|
|
R4690:Map1b
|
UTSW |
13 |
99,567,576 (GRCm39) |
missense |
unknown |
|
|
R4704:Map1b
|
UTSW |
13 |
99,566,983 (GRCm39) |
missense |
unknown |
|
|
R4836:Map1b
|
UTSW |
13 |
99,567,562 (GRCm39) |
missense |
unknown |
|
|
R4916:Map1b
|
UTSW |
13 |
99,569,808 (GRCm39) |
missense |
unknown |
|
|
R4951:Map1b
|
UTSW |
13 |
99,568,935 (GRCm39) |
missense |
unknown |
|
|
R4960:Map1b
|
UTSW |
13 |
99,568,720 (GRCm39) |
missense |
probably benign |
0.23 |
|
R4961:Map1b
|
UTSW |
13 |
99,572,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5030:Map1b
|
UTSW |
13 |
99,570,682 (GRCm39) |
missense |
unknown |
|
|
R5090:Map1b
|
UTSW |
13 |
99,566,534 (GRCm39) |
nonsense |
probably null |
|
|
R5469:Map1b
|
UTSW |
13 |
99,565,846 (GRCm39) |
missense |
unknown |
|
|
R5820:Map1b
|
UTSW |
13 |
99,569,332 (GRCm39) |
missense |
unknown |
|
|
R5885:Map1b
|
UTSW |
13 |
99,566,589 (GRCm39) |
missense |
unknown |
|
|
R5915:Map1b
|
UTSW |
13 |
99,566,839 (GRCm39) |
missense |
unknown |
|
|
R5923:Map1b
|
UTSW |
13 |
99,569,661 (GRCm39) |
missense |
unknown |
|
|
R6063:Map1b
|
UTSW |
13 |
99,567,645 (GRCm39) |
missense |
unknown |
|
|
R6102:Map1b
|
UTSW |
13 |
99,562,381 (GRCm39) |
missense |
unknown |
|
|
R6218:Map1b
|
UTSW |
13 |
99,569,714 (GRCm39) |
missense |
unknown |
|
|
R6435:Map1b
|
UTSW |
13 |
99,652,871 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6663:Map1b
|
UTSW |
13 |
99,566,530 (GRCm39) |
missense |
unknown |
|
|
R6765:Map1b
|
UTSW |
13 |
99,562,449 (GRCm39) |
missense |
unknown |
|
|
R6860:Map1b
|
UTSW |
13 |
99,571,275 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6997:Map1b
|
UTSW |
13 |
99,567,142 (GRCm39) |
missense |
unknown |
|
|
R7001:Map1b
|
UTSW |
13 |
99,567,101 (GRCm39) |
missense |
unknown |
|
|
R7310:Map1b
|
UTSW |
13 |
99,570,163 (GRCm39) |
missense |
unknown |
|
|
R7349:Map1b
|
UTSW |
13 |
99,570,148 (GRCm39) |
missense |
unknown |
|
|
R7448:Map1b
|
UTSW |
13 |
99,644,648 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7449:Map1b
|
UTSW |
13 |
99,644,648 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7452:Map1b
|
UTSW |
13 |
99,644,648 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7810:Map1b
|
UTSW |
13 |
99,568,390 (GRCm39) |
missense |
unknown |
|
|
R7820:Map1b
|
UTSW |
13 |
99,567,685 (GRCm39) |
missense |
unknown |
|
|
R8396:Map1b
|
UTSW |
13 |
99,570,621 (GRCm39) |
missense |
unknown |
|
|
R8470:Map1b
|
UTSW |
13 |
99,652,950 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8535:Map1b
|
UTSW |
13 |
99,571,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8777:Map1b
|
UTSW |
13 |
99,567,304 (GRCm39) |
missense |
unknown |
|
|
R8777-TAIL:Map1b
|
UTSW |
13 |
99,567,304 (GRCm39) |
missense |
unknown |
|
|
R8812:Map1b
|
UTSW |
13 |
99,569,323 (GRCm39) |
missense |
unknown |
|
|
R8903:Map1b
|
UTSW |
13 |
99,569,017 (GRCm39) |
nonsense |
probably null |
|
|
R8928:Map1b
|
UTSW |
13 |
99,568,624 (GRCm39) |
missense |
unknown |
|
|
R8954:Map1b
|
UTSW |
13 |
99,570,735 (GRCm39) |
missense |
unknown |
|
|
R9164:Map1b
|
UTSW |
13 |
99,568,816 (GRCm39) |
nonsense |
probably null |
|
|
R9164:Map1b
|
UTSW |
13 |
99,562,351 (GRCm39) |
missense |
unknown |
|
|
R9190:Map1b
|
UTSW |
13 |
99,571,914 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9334:Map1b
|
UTSW |
13 |
99,568,148 (GRCm39) |
missense |
unknown |
|
|
R9339:Map1b
|
UTSW |
13 |
99,567,570 (GRCm39) |
missense |
unknown |
|
|
R9357:Map1b
|
UTSW |
13 |
99,566,708 (GRCm39) |
nonsense |
probably null |
|
|
R9430:Map1b
|
UTSW |
13 |
99,570,616 (GRCm39) |
missense |
unknown |
|
|
RF003:Map1b
|
UTSW |
13 |
99,567,258 (GRCm39) |
missense |
unknown |
|
|
X0019:Map1b
|
UTSW |
13 |
99,568,920 (GRCm39) |
missense |
unknown |
|
|
X0019:Map1b
|
UTSW |
13 |
99,566,476 (GRCm39) |
missense |
unknown |
|
|
Z1088:Map1b
|
UTSW |
13 |
99,644,623 (GRCm39) |
missense |
probably benign |
0.07 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGATTCCTGGCCGAACTCAATAGAC -3'
(R):5'- AGAGAAAAGCACGGGCTTCATACC -3'
Sequencing Primer
(F):5'- CATAGAAGACTGTTCAGATCGGTG -3'
(R):5'- CAATCAGCTCTAGCTTTGGATG -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation