Incidental Mutation 'R4690:Map1b'
ID |
354867 |
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 |
041941-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4690 (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 99567576 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 1715
(E1715G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000068374
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064762]
|
AlphaFold |
P14873 |
Predicted Effect |
unknown
Transcript: ENSMUST00000064762
AA Change: E1715G
|
SMART Domains |
Protein: ENSMUSP00000068374 Gene: ENSMUSG00000052727 AA Change: E1715G
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 |
0.0741 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.5%
|
Validation Efficiency |
98% (89/91) |
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: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,039,706 (GRCm39) |
F436L |
probably damaging |
Het |
Adam28 |
G |
T |
14: 68,879,497 (GRCm39) |
Q184K |
probably benign |
Het |
Adh6a |
A |
G |
3: 138,031,932 (GRCm39) |
T275A |
possibly damaging |
Het |
Agap2 |
A |
G |
10: 126,927,244 (GRCm39) |
D1082G |
possibly damaging |
Het |
Alox5 |
A |
T |
6: 116,400,150 (GRCm39) |
V263E |
probably damaging |
Het |
Arhgef16 |
C |
T |
4: 154,372,420 (GRCm39) |
|
probably null |
Het |
Bspry |
G |
A |
4: 62,404,762 (GRCm39) |
R186Q |
probably damaging |
Het |
Ccdc188 |
T |
A |
16: 18,036,159 (GRCm39) |
H111Q |
probably damaging |
Het |
Cd40 |
T |
C |
2: 164,911,615 (GRCm39) |
F209S |
possibly damaging |
Het |
Cfap43 |
C |
A |
19: 47,736,298 (GRCm39) |
V1398L |
probably benign |
Het |
Cln3 |
A |
T |
7: 126,174,565 (GRCm39) |
I286N |
possibly damaging |
Het |
Col9a1 |
T |
C |
1: 24,263,787 (GRCm39) |
|
probably null |
Het |
Cpne9 |
A |
G |
6: 113,279,016 (GRCm39) |
E470G |
probably damaging |
Het |
Cul5 |
A |
T |
9: 53,534,171 (GRCm39) |
W654R |
probably damaging |
Het |
Cyp2a22 |
T |
A |
7: 26,638,634 (GRCm39) |
K51* |
probably null |
Het |
Dcaf10 |
G |
A |
4: 45,372,769 (GRCm39) |
R394Q |
possibly damaging |
Het |
Dot1l |
C |
A |
10: 80,622,016 (GRCm39) |
S556* |
probably null |
Het |
Eif3d |
A |
T |
15: 77,851,516 (GRCm39) |
M98K |
probably benign |
Het |
Fiz1 |
A |
G |
7: 5,012,167 (GRCm39) |
V117A |
probably benign |
Het |
Fryl |
A |
G |
5: 73,257,636 (GRCm39) |
V722A |
probably benign |
Het |
Ftdc1 |
G |
A |
16: 58,434,333 (GRCm39) |
T128I |
probably benign |
Het |
Gm3095 |
G |
T |
14: 3,964,471 (GRCm38) |
R63I |
probably benign |
Het |
Gm7133 |
A |
T |
1: 97,197,224 (GRCm39) |
|
noncoding transcript |
Het |
Hoxb8 |
A |
T |
11: 96,175,286 (GRCm39) |
D241V |
probably benign |
Het |
Hrnr |
A |
G |
3: 93,230,959 (GRCm39) |
Q399R |
unknown |
Het |
Itpk1 |
A |
T |
12: 102,572,434 (GRCm39) |
V93D |
probably damaging |
Het |
Kars1 |
C |
T |
8: 112,729,216 (GRCm39) |
A164T |
probably benign |
Het |
Kcnq4 |
A |
T |
4: 120,574,208 (GRCm39) |
I150N |
probably damaging |
Het |
Kcnrg |
A |
T |
14: 61,849,176 (GRCm39) |
L212F |
probably damaging |
Het |
Kif5b |
A |
T |
18: 6,216,759 (GRCm39) |
D521E |
probably benign |
Het |
Klf11 |
C |
T |
12: 24,705,071 (GRCm39) |
T158M |
probably damaging |
Het |
Klhl6 |
T |
C |
16: 19,776,034 (GRCm39) |
I175V |
probably benign |
Het |
Lsm1 |
A |
G |
8: 26,283,708 (GRCm39) |
N40S |
probably damaging |
Het |
Mecom |
C |
A |
3: 30,292,459 (GRCm39) |
A4S |
probably benign |
Het |
Muc5b |
G |
A |
7: 141,396,031 (GRCm39) |
V96M |
unknown |
Het |
Mug2 |
A |
T |
6: 122,013,255 (GRCm39) |
I341L |
probably benign |
Het |
Mxra7 |
A |
T |
11: 116,707,078 (GRCm39) |
|
probably null |
Het |
Myo5a |
T |
C |
9: 75,061,105 (GRCm39) |
L537P |
probably damaging |
Het |
Myo5b |
A |
T |
18: 74,855,533 (GRCm39) |
N1241Y |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,582,497 (GRCm39) |
R531G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,134,087 (GRCm39) |
M3299L |
probably benign |
Het |
Nlrp4b |
T |
A |
7: 10,453,130 (GRCm39) |
Y76N |
probably benign |
Het |
Nmral1 |
T |
C |
16: 4,534,205 (GRCm39) |
T79A |
probably damaging |
Het |
Noct |
C |
T |
3: 51,155,300 (GRCm39) |
Q23* |
probably null |
Het |
Nrxn1 |
A |
T |
17: 90,344,509 (GRCm39) |
V438D |
probably damaging |
Het |
Or5b109 |
A |
C |
19: 13,212,132 (GRCm39) |
N173H |
possibly damaging |
Het |
Or5m9 |
T |
A |
2: 85,877,242 (GRCm39) |
C139S |
probably damaging |
Het |
Oxct2a |
T |
C |
4: 123,216,836 (GRCm39) |
T182A |
probably benign |
Het |
Pank2 |
T |
C |
2: 131,115,945 (GRCm39) |
I121T |
probably damaging |
Het |
Pcdh1 |
T |
A |
18: 38,336,528 (GRCm39) |
T36S |
probably benign |
Het |
Pfdn1 |
A |
T |
18: 36,584,133 (GRCm39) |
M67K |
possibly damaging |
Het |
Plec |
T |
C |
15: 76,058,456 (GRCm39) |
E3849G |
probably damaging |
Het |
Polr3a |
A |
T |
14: 24,514,349 (GRCm39) |
S817T |
possibly damaging |
Het |
Pomgnt1 |
T |
A |
4: 116,012,707 (GRCm39) |
D401E |
probably damaging |
Het |
Ppp1r13b |
T |
A |
12: 111,798,992 (GRCm39) |
D891V |
probably damaging |
Het |
Prr14l |
A |
G |
5: 33,001,500 (GRCm39) |
|
probably benign |
Het |
Ptk2b |
A |
G |
14: 66,410,749 (GRCm39) |
|
probably null |
Het |
Rab13 |
G |
C |
3: 90,128,330 (GRCm39) |
|
probably null |
Het |
Rexo1 |
C |
T |
10: 80,382,255 (GRCm39) |
A751T |
probably benign |
Het |
Rfx1 |
T |
C |
8: 84,809,374 (GRCm39) |
V233A |
possibly damaging |
Het |
Rnf149 |
C |
T |
1: 39,616,295 (GRCm39) |
|
probably benign |
Het |
Rrm1 |
A |
G |
7: 102,097,086 (GRCm39) |
D122G |
probably benign |
Het |
Serpina1b |
A |
G |
12: 103,698,639 (GRCm39) |
F70S |
probably damaging |
Het |
Serpinb13 |
C |
T |
1: 106,910,574 (GRCm39) |
S66L |
probably damaging |
Het |
Sh3rf3 |
T |
C |
10: 58,649,526 (GRCm39) |
S44P |
possibly damaging |
Het |
Shroom1 |
A |
G |
11: 53,356,549 (GRCm39) |
T471A |
possibly damaging |
Het |
Slc6a1 |
A |
G |
6: 114,279,792 (GRCm39) |
Y152C |
probably damaging |
Het |
Spata31f3 |
T |
A |
4: 42,873,032 (GRCm39) |
|
probably null |
Het |
Spata6 |
A |
T |
4: 111,632,023 (GRCm39) |
T145S |
probably damaging |
Het |
Srcap |
G |
A |
7: 127,137,186 (GRCm39) |
G956D |
probably damaging |
Het |
Ssh2 |
A |
T |
11: 77,346,031 (GRCm39) |
I1339F |
possibly damaging |
Het |
Tardbp |
A |
T |
4: 148,697,078 (GRCm39) |
*99K |
probably null |
Het |
Tbc1d22a |
A |
G |
15: 86,196,037 (GRCm39) |
Y336C |
probably damaging |
Het |
Tmcc3 |
G |
A |
10: 94,381,419 (GRCm39) |
|
probably benign |
Het |
Tmem178b |
T |
G |
6: 40,222,547 (GRCm39) |
D87E |
probably benign |
Het |
Tmem184a |
A |
C |
5: 139,791,377 (GRCm39) |
S380A |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,411,682 (GRCm39) |
K84R |
possibly damaging |
Het |
Tpgs1 |
A |
G |
10: 79,511,235 (GRCm39) |
T126A |
probably benign |
Het |
Traf3ip1 |
A |
G |
1: 91,447,834 (GRCm39) |
E437G |
possibly damaging |
Het |
Trpc4ap |
C |
T |
2: 155,477,053 (GRCm39) |
C755Y |
probably damaging |
Het |
Tsfm |
A |
G |
10: 126,866,547 (GRCm39) |
|
probably benign |
Het |
Tulp1 |
A |
C |
17: 28,570,811 (GRCm39) |
|
probably benign |
Het |
Vmn1r23 |
A |
T |
6: 57,903,010 (GRCm39) |
M256K |
probably benign |
Het |
Zdhhc8 |
T |
C |
16: 18,044,605 (GRCm39) |
D305G |
probably damaging |
Het |
Zfp326 |
G |
A |
5: 106,054,942 (GRCm39) |
R282H |
probably 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 |
|
R1509:Map1b
|
UTSW |
13 |
99,568,036 (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 |
|
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'- ATAAAGGTGAGGACTCTCGTGG -3'
(R):5'- TAGTCGGCAGTCTCCAGATCAC -3'
Sequencing Primer
(F):5'- ATCAGATTTCGGAGAGAGCTTC -3'
(R):5'- AGTCTCCAGATCACCCTACTCTGG -3'
|
Posted On |
2015-10-21 |