Incidental Mutation 'R7310:Map1b'
| ID |
567532 |
| 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 |
045409-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7310 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
13 |
| Chromosomal Location |
99557954-99653048 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 99570163 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Serine
at position 853
(P853S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000068374
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064762]
|
| AlphaFold |
P14873 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000064762
AA Change: P853S
|
| SMART Domains |
Protein: ENSMUSP00000068374
Gene: ENSMUSG00000052727
AA Change: P853S
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
|
| 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 |
|---|
| 2810021J22Rik |
A |
T |
11: 58,771,094 (GRCm39) |
Q192L |
possibly damaging |
Het |
| Abat |
G |
A |
16: 8,423,457 (GRCm39) |
R250Q |
probably null |
Het |
| Abcg3 |
A |
C |
5: 105,114,632 (GRCm39) |
F295C |
probably benign |
Het |
| Abl1 |
T |
C |
2: 31,690,604 (GRCm39) |
S708P |
possibly damaging |
Het |
| Acap2 |
A |
T |
16: 30,926,972 (GRCm39) |
Y489* |
probably null |
Het |
| Akr1c6 |
A |
T |
13: 4,486,354 (GRCm39) |
M54L |
probably benign |
Het |
| Arhgap5 |
A |
T |
12: 52,589,270 (GRCm39) |
|
probably null |
Het |
| Asap1 |
A |
G |
15: 63,971,379 (GRCm39) |
|
probably null |
Het |
| Atrnl1 |
A |
T |
19: 57,630,856 (GRCm39) |
N208Y |
possibly damaging |
Het |
| BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
| BC028528 |
GTTCTGTGGTCACTG |
GTTCTGTGGTCACTGATTCTGTGGTCACTG |
3: 95,795,485 (GRCm39) |
|
probably benign |
Het |
| BC028528 |
G |
GGGGTCACTGGTTCTT |
3: 95,795,460 (GRCm39) |
|
probably benign |
Het |
| BC028528 |
ACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
ACTGGTTCTGTGGTCCCTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
3: 95,795,451 (GRCm39) |
|
probably benign |
Het |
| Bmi1 |
T |
C |
2: 18,689,230 (GRCm39) |
S305P |
probably benign |
Het |
| Bpifc |
T |
A |
10: 85,798,891 (GRCm39) |
I431F |
probably damaging |
Het |
| C130050O18Rik |
A |
T |
5: 139,400,993 (GRCm39) |
M349L |
probably benign |
Het |
| Cacna2d1 |
A |
T |
5: 16,519,914 (GRCm39) |
D428V |
probably damaging |
Het |
| Card14 |
A |
C |
11: 119,217,005 (GRCm39) |
Q363P |
probably null |
Het |
| Cdca2 |
A |
T |
14: 67,950,673 (GRCm39) |
L86H |
probably damaging |
Het |
| Cdh22 |
G |
T |
2: 164,954,214 (GRCm39) |
S769* |
probably null |
Het |
| Cdhr17 |
A |
G |
5: 17,075,246 (GRCm39) |
Y872C |
possibly damaging |
Het |
| Cep164 |
T |
C |
9: 45,686,664 (GRCm39) |
E690G |
probably damaging |
Het |
| Cluh |
A |
G |
11: 74,560,285 (GRCm39) |
H1304R |
probably benign |
Het |
| Daxx |
C |
A |
17: 34,129,435 (GRCm39) |
D5E |
possibly damaging |
Het |
| Dnah7c |
A |
G |
1: 46,636,127 (GRCm39) |
M1117V |
possibly damaging |
Het |
| Entpd3 |
T |
A |
9: 120,389,821 (GRCm39) |
|
probably null |
Het |
| Esr1 |
G |
A |
10: 4,889,259 (GRCm39) |
A386T |
probably damaging |
Het |
| Etv5 |
G |
A |
16: 22,220,487 (GRCm39) |
P300L |
probably benign |
Het |
| Exoc3l |
A |
T |
8: 106,020,340 (GRCm39) |
L195Q |
probably damaging |
Het |
| Exog |
T |
C |
9: 119,274,069 (GRCm39) |
L18P |
unknown |
Het |
| Fgfr1 |
T |
A |
8: 26,052,331 (GRCm39) |
V219D |
probably benign |
Het |
| Gna14 |
A |
T |
19: 16,511,113 (GRCm39) |
Q54L |
|
Het |
| Gnb5 |
T |
C |
9: 75,221,570 (GRCm39) |
L48P |
probably benign |
Het |
| Gpbp1 |
A |
G |
13: 111,589,924 (GRCm39) |
I57T |
probably benign |
Het |
| Hnrnpa1 |
T |
A |
15: 103,149,884 (GRCm39) |
D48E |
probably damaging |
Het |
| Hrc |
T |
A |
7: 44,985,227 (GRCm39) |
L126* |
probably null |
Het |
| Hspa8 |
T |
G |
9: 40,714,704 (GRCm39) |
D333E |
probably benign |
Het |
| Igsf3 |
T |
A |
3: 101,338,895 (GRCm39) |
V403D |
probably benign |
Het |
| Itga10 |
C |
A |
3: 96,555,475 (GRCm39) |
A143D |
probably damaging |
Het |
| Kdr |
T |
A |
5: 76,104,985 (GRCm39) |
I1082F |
probably damaging |
Het |
| Klk1b11 |
A |
T |
7: 43,428,254 (GRCm39) |
I242F |
probably damaging |
Het |
| Kng2 |
G |
A |
16: 22,806,522 (GRCm39) |
T559I |
probably benign |
Het |
| Mmp13 |
T |
C |
9: 7,280,880 (GRCm39) |
I421T |
possibly damaging |
Het |
| Mpeg1 |
A |
T |
19: 12,439,615 (GRCm39) |
T358S |
probably damaging |
Het |
| Msantd5l |
A |
C |
11: 51,145,474 (GRCm39) |
W38G |
probably damaging |
Het |
| Mttp |
T |
C |
3: 137,800,783 (GRCm39) |
D759G |
probably damaging |
Het |
| Mup17 |
T |
A |
4: 61,511,929 (GRCm39) |
Y115F |
possibly damaging |
Het |
| Myo1a |
G |
T |
10: 127,541,697 (GRCm39) |
A79S |
probably damaging |
Het |
| Myo9a |
T |
A |
9: 59,778,436 (GRCm39) |
N1397K |
probably benign |
Het |
| Nadk2 |
T |
C |
15: 9,103,469 (GRCm39) |
|
probably null |
Het |
| Ncf1 |
A |
T |
5: 134,250,615 (GRCm39) |
S402T |
probably benign |
Het |
| Ndufb10 |
T |
C |
17: 24,941,188 (GRCm39) |
D145G |
probably damaging |
Het |
| Nlgn2 |
G |
A |
11: 69,721,409 (GRCm39) |
T163M |
possibly damaging |
Het |
| Nol4 |
A |
T |
18: 22,903,801 (GRCm39) |
H172Q |
|
Het |
| Nup205 |
T |
A |
6: 35,202,904 (GRCm39) |
D1370E |
possibly damaging |
Het |
| Or1e32 |
A |
C |
11: 73,705,112 (GRCm39) |
N265K |
probably damaging |
Het |
| Or51ab3 |
T |
A |
7: 103,201,892 (GRCm39) |
I300N |
probably damaging |
Het |
| Or5b97 |
A |
G |
19: 12,878,637 (GRCm39) |
F169S |
probably damaging |
Het |
| Pkd1l2 |
A |
G |
8: 117,750,773 (GRCm39) |
V1746A |
probably benign |
Het |
| Plin2 |
T |
A |
4: 86,586,628 (GRCm39) |
I68F |
probably benign |
Het |
| Proc |
A |
T |
18: 32,268,952 (GRCm39) |
M11K |
probably benign |
Het |
| Rif1 |
T |
C |
2: 51,995,631 (GRCm39) |
V950A |
probably benign |
Het |
| Rmc1 |
A |
G |
18: 12,317,972 (GRCm39) |
K362E |
probably benign |
Het |
| Rnf208 |
C |
A |
2: 25,133,587 (GRCm39) |
P94T |
probably damaging |
Het |
| Rundc3b |
A |
T |
5: 8,571,011 (GRCm39) |
Y269* |
probably null |
Het |
| Senp7 |
T |
C |
16: 56,006,445 (GRCm39) |
V950A |
probably benign |
Het |
| Sipa1l1 |
T |
C |
12: 82,419,269 (GRCm39) |
V649A |
probably damaging |
Het |
| Sipa1l3 |
G |
T |
7: 29,099,121 (GRCm39) |
H383N |
probably benign |
Het |
| Slc12a5 |
G |
A |
2: 164,834,360 (GRCm39) |
V794M |
probably damaging |
Het |
| Slc7a7 |
A |
G |
14: 54,616,482 (GRCm39) |
I200T |
probably damaging |
Het |
| Spdye4b |
A |
C |
5: 143,188,103 (GRCm39) |
I199L |
probably damaging |
Het |
| Styxl2 |
G |
A |
1: 165,926,300 (GRCm39) |
T1104I |
possibly damaging |
Het |
| Tle4 |
A |
T |
19: 14,495,155 (GRCm39) |
H191Q |
probably benign |
Het |
| Tnfsf13b |
C |
A |
8: 10,081,651 (GRCm39) |
S271* |
probably null |
Het |
| Tnks2 |
G |
A |
19: 36,856,839 (GRCm39) |
V855I |
probably benign |
Het |
| Trank1 |
T |
C |
9: 111,196,194 (GRCm39) |
L1406S |
probably damaging |
Het |
| Trhde |
T |
C |
10: 114,636,478 (GRCm39) |
E243G |
probably damaging |
Het |
| Trim25 |
A |
T |
11: 88,906,608 (GRCm39) |
N448I |
probably benign |
Het |
| Trim31 |
T |
A |
17: 37,218,194 (GRCm39) |
M308K |
probably benign |
Het |
| Ugt2b36 |
A |
T |
5: 87,214,138 (GRCm39) |
V502E |
possibly damaging |
Het |
| Usp10 |
A |
C |
8: 120,668,344 (GRCm39) |
D215A |
possibly damaging |
Het |
| Usp33 |
T |
G |
3: 152,066,026 (GRCm39) |
L102* |
probably null |
Het |
| Wdr12 |
A |
T |
1: 60,121,734 (GRCm39) |
C272* |
probably null |
Het |
| Xndc1 |
A |
C |
7: 101,727,938 (GRCm39) |
|
probably null |
Het |
| Zkscan2 |
T |
C |
7: 123,089,276 (GRCm39) |
I332V |
possibly damaging |
Het |
| Zswim5 |
A |
T |
4: 116,841,885 (GRCm39) |
T822S |
probably benign |
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 |
|
|
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 |
|
|
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'- TCAATGTCATCCACGCCCTG -3'
(R):5'- CTGCTGGGAAACTCAAGGAC -3'
Sequencing Primer
(F):5'- ACGCCCTGCTTCTCAACTGG -3'
(R):5'- TGCCACAGCTGTTGGCAC -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation