Incidental Mutation 'R0479:Atrn'
ID |
43244 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Atrn
|
Ensembl Gene |
ENSMUSG00000027312 |
Gene Name |
attractin |
Synonyms |
Mgca |
MMRRC Submission |
038679-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0479 (G1)
|
Quality Score |
215 |
Status
|
Validated
(trace)
|
Chromosome |
2 |
Chromosomal Location |
130748415-130872253 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 130841085 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Stop codon
at position 1162
(Y1162*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000028781
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028781]
|
AlphaFold |
Q9WU60 |
Predicted Effect |
probably null
Transcript: ENSMUST00000028781
AA Change: Y1162*
|
SMART Domains |
Protein: ENSMUSP00000028781 Gene: ENSMUSG00000027312 AA Change: Y1162*
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
9 |
N/A |
INTRINSIC |
low complexity region
|
51 |
97 |
N/A |
INTRINSIC |
EGF
|
99 |
129 |
9.85e-5 |
SMART |
CUB
|
131 |
247 |
7.85e-18 |
SMART |
EGF
|
248 |
282 |
1.47e1 |
SMART |
Pfam:Kelch_1
|
339 |
382 |
1.1e-7 |
PFAM |
Pfam:Kelch_5
|
389 |
434 |
2.5e-7 |
PFAM |
Pfam:Kelch_6
|
390 |
439 |
3.3e-8 |
PFAM |
Pfam:Kelch_1
|
553 |
606 |
8.4e-8 |
PFAM |
PSI
|
646 |
693 |
7.41e-7 |
SMART |
PSI
|
702 |
747 |
8.64e-8 |
SMART |
PSI
|
754 |
799 |
2.11e-2 |
SMART |
CLECT
|
787 |
918 |
6.14e-20 |
SMART |
PSI
|
931 |
982 |
1.11e-5 |
SMART |
PSI
|
985 |
1060 |
1.2e-6 |
SMART |
EGF_Lam
|
1062 |
1105 |
1.97e-4 |
SMART |
EGF_like
|
1108 |
1154 |
3.9e0 |
SMART |
transmembrane domain
|
1278 |
1300 |
N/A |
INTRINSIC |
low complexity region
|
1310 |
1322 |
N/A |
INTRINSIC |
low complexity region
|
1373 |
1385 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132557
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134964
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151364
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.6%
|
Validation Efficiency |
98% (105/107) |
MGI Phenotype |
FUNCTION: This gene encodes a widely expressed transmembrane glycoprotein that plays important roles in diverse physiological processes such as regulation of hair pigmentation, monocyte-T cell interaction and control of energy homeostasis. The encoded preproprotein undergoes proteolytic processing to generate a mature, functional protein. Certain mutations in this gene are responsible for the mahogany mouse phenotype of dark brown or black coat on a normally agouti background. Mice with loss-of-function mutations in this gene exhibit black coat color, tremor, adiposity, higher basal metabolic rate, juvenile-onset hypomyelination and age-dependent spongiform neurodegeneration of the central nervous system. [provided by RefSeq, Jul 2016] PHENOTYPE: Some mutant homozygotes exhibit decreases in phaeomelanin synthesis, body weight, and adiposity; increases in locomotion, and abnormal myelination and vacuolation of the central nervous system resulting in tremors. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
A |
G |
1: 173,159,712 (GRCm39) |
V269A |
probably benign |
Het |
Acsl1 |
G |
A |
8: 46,984,109 (GRCm39) |
G543R |
probably damaging |
Het |
Adam18 |
T |
C |
8: 25,141,838 (GRCm39) |
N244D |
probably benign |
Het |
Adgra3 |
C |
T |
5: 50,147,607 (GRCm39) |
V478M |
probably benign |
Het |
Arhgap39 |
C |
T |
15: 76,619,086 (GRCm39) |
D833N |
probably damaging |
Het |
Arhgef10 |
A |
T |
8: 15,041,070 (GRCm39) |
E723V |
probably damaging |
Het |
Arid3a |
C |
A |
10: 79,787,128 (GRCm39) |
N519K |
possibly damaging |
Het |
Cacng5 |
T |
A |
11: 107,768,777 (GRCm39) |
N172Y |
probably benign |
Het |
Cct8 |
C |
T |
16: 87,284,594 (GRCm39) |
V198M |
probably damaging |
Het |
Cep192 |
G |
A |
18: 67,991,089 (GRCm39) |
S1857N |
probably damaging |
Het |
Cherp |
A |
T |
8: 73,216,991 (GRCm39) |
D657E |
possibly damaging |
Het |
Clca3a2 |
T |
G |
3: 144,796,610 (GRCm39) |
D199A |
probably damaging |
Het |
Cops7b |
A |
G |
1: 86,532,798 (GRCm39) |
T219A |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,126,352 (GRCm39) |
M1392I |
probably damaging |
Het |
Csf3r |
A |
C |
4: 125,937,616 (GRCm39) |
E833D |
probably damaging |
Het |
Cutc |
A |
G |
19: 43,756,655 (GRCm39) |
E247G |
probably damaging |
Het |
Cyp2c38 |
A |
G |
19: 39,451,449 (GRCm39) |
L17P |
probably damaging |
Het |
D5Ertd615e |
T |
A |
5: 45,320,796 (GRCm39) |
|
noncoding transcript |
Het |
Ddx60 |
G |
T |
8: 62,422,691 (GRCm39) |
G643W |
probably damaging |
Het |
Depdc1a |
C |
T |
3: 159,226,497 (GRCm39) |
T268I |
probably damaging |
Het |
Dgke |
T |
C |
11: 88,943,296 (GRCm39) |
E231G |
probably benign |
Het |
Dhrs7b |
T |
A |
11: 60,746,513 (GRCm39) |
|
probably benign |
Het |
Dll3 |
A |
G |
7: 28,000,974 (GRCm39) |
V27A |
probably damaging |
Het |
Dnmt3c |
T |
A |
2: 153,556,861 (GRCm39) |
|
probably null |
Het |
Duox1 |
T |
C |
2: 122,176,861 (GRCm39) |
F1461L |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,106,323 (GRCm39) |
V301A |
possibly damaging |
Het |
Eny2 |
T |
A |
15: 44,299,000 (GRCm39) |
|
probably null |
Het |
Esr1 |
A |
G |
10: 4,947,911 (GRCm39) |
D488G |
probably damaging |
Het |
Ets1 |
A |
G |
9: 32,641,476 (GRCm39) |
K110E |
probably damaging |
Het |
Eya2 |
T |
A |
2: 165,557,876 (GRCm39) |
Y157* |
probably null |
Het |
F830045P16Rik |
T |
G |
2: 129,314,608 (GRCm39) |
D223A |
possibly damaging |
Het |
Fbh1 |
A |
G |
2: 11,763,230 (GRCm39) |
Y475H |
probably damaging |
Het |
Fbxo39 |
T |
C |
11: 72,208,419 (GRCm39) |
I257T |
probably damaging |
Het |
Fkbp10 |
T |
C |
11: 100,306,740 (GRCm39) |
V23A |
probably damaging |
Het |
Foxp3 |
A |
G |
X: 7,453,583 (GRCm39) |
I128V |
possibly damaging |
Het |
Fzd7 |
T |
C |
1: 59,522,867 (GRCm39) |
F250S |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,172,062 (GRCm39) |
T722A |
possibly damaging |
Het |
Gemin5 |
A |
G |
11: 58,030,377 (GRCm39) |
V816A |
probably benign |
Het |
Glb1l3 |
T |
A |
9: 26,740,389 (GRCm39) |
T314S |
probably benign |
Het |
H2-Ab1 |
A |
G |
17: 34,483,942 (GRCm39) |
E101G |
possibly damaging |
Het |
Hydin |
A |
C |
8: 111,325,720 (GRCm39) |
T4710P |
probably damaging |
Het |
Ica1 |
C |
T |
6: 8,754,627 (GRCm39) |
V48M |
probably damaging |
Het |
Ica1 |
T |
C |
6: 8,754,683 (GRCm39) |
Y29C |
probably damaging |
Het |
Ints7 |
T |
A |
1: 191,346,666 (GRCm39) |
|
probably null |
Het |
Iqub |
T |
C |
6: 24,505,809 (GRCm39) |
E33G |
probably benign |
Het |
Itgb1bp2 |
T |
A |
X: 100,492,806 (GRCm39) |
C10S |
probably damaging |
Het |
Katnip |
T |
C |
7: 125,442,518 (GRCm39) |
L809S |
probably benign |
Het |
Kcnd1 |
T |
A |
X: 7,697,461 (GRCm39) |
I391N |
possibly damaging |
Het |
Kdm8 |
T |
C |
7: 125,051,812 (GRCm39) |
L135P |
probably damaging |
Het |
Ksr1 |
T |
C |
11: 78,916,109 (GRCm39) |
D574G |
probably damaging |
Het |
Lama5 |
C |
T |
2: 179,826,250 (GRCm39) |
R2331H |
probably benign |
Het |
Larp1 |
C |
A |
11: 57,933,646 (GRCm39) |
N357K |
possibly damaging |
Het |
Lgi3 |
C |
T |
14: 70,771,992 (GRCm39) |
|
probably benign |
Het |
Lmbrd1 |
T |
A |
1: 24,785,878 (GRCm39) |
|
probably benign |
Het |
Methig1 |
A |
T |
15: 100,272,825 (GRCm39) |
K53* |
probably null |
Het |
Mfap3 |
T |
A |
11: 57,420,469 (GRCm39) |
I150N |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,817,186 (GRCm39) |
Q85L |
probably benign |
Het |
Npl |
A |
G |
1: 153,391,155 (GRCm39) |
V200A |
probably damaging |
Het |
Nuf2 |
A |
T |
1: 169,326,503 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
G |
11: 59,003,533 (GRCm39) |
V1255A |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or5h18 |
C |
T |
16: 58,847,491 (GRCm39) |
V260M |
possibly damaging |
Het |
Or8b51 |
T |
C |
9: 38,569,478 (GRCm39) |
D70G |
probably damaging |
Het |
P2rx1 |
T |
C |
11: 72,903,787 (GRCm39) |
V283A |
probably damaging |
Het |
Pex2 |
C |
A |
3: 5,626,355 (GRCm39) |
L151F |
probably damaging |
Het |
Pias1 |
A |
G |
9: 62,800,400 (GRCm39) |
|
probably benign |
Het |
Pmfbp1 |
A |
T |
8: 110,257,105 (GRCm39) |
|
probably benign |
Het |
Pogz |
A |
G |
3: 94,783,947 (GRCm39) |
K545E |
possibly damaging |
Het |
Ppp3cb |
T |
C |
14: 20,553,309 (GRCm39) |
|
probably null |
Het |
Prl |
G |
A |
13: 27,248,911 (GRCm39) |
D189N |
probably damaging |
Het |
Prpf6 |
A |
G |
2: 181,292,920 (GRCm39) |
N794S |
probably benign |
Het |
Prr36 |
G |
A |
8: 4,263,930 (GRCm39) |
Q579* |
probably null |
Het |
Ptprq |
A |
T |
10: 107,479,855 (GRCm39) |
Y1138* |
probably null |
Het |
Rabepk |
A |
T |
2: 34,675,592 (GRCm39) |
H179Q |
probably damaging |
Het |
Rest |
T |
C |
5: 77,430,598 (GRCm39) |
S1006P |
probably damaging |
Het |
Rimklb |
A |
C |
6: 122,441,175 (GRCm39) |
|
probably benign |
Het |
Rnpepl1 |
T |
C |
1: 92,846,587 (GRCm39) |
|
probably benign |
Het |
Ro60 |
A |
T |
1: 143,633,489 (GRCm39) |
D536E |
possibly damaging |
Het |
Sacs |
T |
A |
14: 61,428,928 (GRCm39) |
L329Q |
probably damaging |
Het |
Safb |
C |
T |
17: 56,913,025 (GRCm39) |
R914C |
probably damaging |
Het |
Setd5 |
A |
T |
6: 113,091,994 (GRCm39) |
I272F |
probably damaging |
Het |
Sgk1 |
G |
T |
10: 21,872,209 (GRCm39) |
A262S |
probably benign |
Het |
Skint2 |
G |
A |
4: 112,481,238 (GRCm39) |
V34I |
possibly damaging |
Het |
Skint5 |
G |
C |
4: 113,512,869 (GRCm39) |
Q888E |
unknown |
Het |
Slc4a3 |
T |
C |
1: 75,528,472 (GRCm39) |
|
probably benign |
Het |
Sox10 |
T |
C |
15: 79,047,519 (GRCm39) |
E133G |
probably damaging |
Het |
Spryd3 |
G |
A |
15: 102,038,835 (GRCm39) |
R129* |
probably null |
Het |
Stag1 |
T |
A |
9: 100,810,144 (GRCm39) |
N782K |
probably benign |
Het |
Stam |
T |
C |
2: 14,122,306 (GRCm39) |
L132P |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,528,077 (GRCm39) |
S1445T |
probably damaging |
Het |
Syt5 |
C |
T |
7: 4,546,108 (GRCm39) |
R94Q |
probably benign |
Het |
Tbc1d23 |
A |
T |
16: 56,992,177 (GRCm39) |
H594Q |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,249,235 (GRCm39) |
I1871F |
probably damaging |
Het |
Tek |
A |
G |
4: 94,692,549 (GRCm39) |
D219G |
probably benign |
Het |
Thrb |
T |
C |
14: 18,033,643 (GRCm38) |
F469L |
probably damaging |
Het |
Tyr |
T |
C |
7: 87,142,429 (GRCm39) |
S44G |
possibly damaging |
Het |
Usp20 |
T |
A |
2: 30,907,487 (GRCm39) |
V673E |
probably benign |
Het |
Usp28 |
T |
C |
9: 48,948,513 (GRCm39) |
S873P |
probably damaging |
Het |
Usp43 |
C |
T |
11: 67,788,100 (GRCm39) |
V306M |
possibly damaging |
Het |
Wdr17 |
G |
T |
8: 55,104,456 (GRCm39) |
|
probably null |
Het |
Wsb2 |
T |
G |
5: 117,514,744 (GRCm39) |
|
probably benign |
Het |
Xkrx |
A |
T |
X: 133,051,715 (GRCm39) |
L312Q |
probably damaging |
Het |
|
Other mutations in Atrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Atrn
|
APN |
2 |
130,799,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00571:Atrn
|
APN |
2 |
130,836,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01092:Atrn
|
APN |
2 |
130,789,556 (GRCm39) |
nonsense |
probably null |
|
IGL01572:Atrn
|
APN |
2 |
130,844,715 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01924:Atrn
|
APN |
2 |
130,777,485 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02116:Atrn
|
APN |
2 |
130,800,009 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02372:Atrn
|
APN |
2 |
130,844,674 (GRCm39) |
splice site |
probably benign |
|
IGL02390:Atrn
|
APN |
2 |
130,862,897 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02548:Atrn
|
APN |
2 |
130,814,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02749:Atrn
|
APN |
2 |
130,789,654 (GRCm39) |
splice site |
probably benign |
|
IGL02749:Atrn
|
APN |
2 |
130,812,064 (GRCm39) |
nonsense |
probably null |
|
BB010:Atrn
|
UTSW |
2 |
130,836,986 (GRCm39) |
missense |
probably damaging |
1.00 |
BB020:Atrn
|
UTSW |
2 |
130,836,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Atrn
|
UTSW |
2 |
130,799,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R0403:Atrn
|
UTSW |
2 |
130,748,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Atrn
|
UTSW |
2 |
130,828,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Atrn
|
UTSW |
2 |
130,822,054 (GRCm39) |
missense |
probably benign |
0.01 |
R0606:Atrn
|
UTSW |
2 |
130,748,776 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0617:Atrn
|
UTSW |
2 |
130,837,005 (GRCm39) |
critical splice donor site |
probably null |
|
R0658:Atrn
|
UTSW |
2 |
130,812,147 (GRCm39) |
critical splice donor site |
probably null |
|
R1108:Atrn
|
UTSW |
2 |
130,799,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R1112:Atrn
|
UTSW |
2 |
130,841,081 (GRCm39) |
missense |
probably benign |
0.04 |
R1219:Atrn
|
UTSW |
2 |
130,862,927 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1422:Atrn
|
UTSW |
2 |
130,799,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R1524:Atrn
|
UTSW |
2 |
130,799,000 (GRCm39) |
missense |
probably benign |
0.15 |
R1653:Atrn
|
UTSW |
2 |
130,777,544 (GRCm39) |
missense |
probably benign |
|
R1795:Atrn
|
UTSW |
2 |
130,814,208 (GRCm39) |
missense |
probably benign |
|
R1807:Atrn
|
UTSW |
2 |
130,824,692 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1920:Atrn
|
UTSW |
2 |
130,836,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Atrn
|
UTSW |
2 |
130,836,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Atrn
|
UTSW |
2 |
130,799,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Atrn
|
UTSW |
2 |
130,812,142 (GRCm39) |
missense |
probably benign |
|
R2000:Atrn
|
UTSW |
2 |
130,777,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Atrn
|
UTSW |
2 |
130,799,916 (GRCm39) |
missense |
probably benign |
0.03 |
R2336:Atrn
|
UTSW |
2 |
130,799,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Atrn
|
UTSW |
2 |
130,803,595 (GRCm39) |
critical splice donor site |
probably null |
|
R3426:Atrn
|
UTSW |
2 |
130,862,876 (GRCm39) |
missense |
probably benign |
0.06 |
R3909:Atrn
|
UTSW |
2 |
130,836,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Atrn
|
UTSW |
2 |
130,806,850 (GRCm39) |
critical splice donor site |
probably null |
|
R4162:Atrn
|
UTSW |
2 |
130,836,148 (GRCm39) |
splice site |
probably benign |
|
R4195:Atrn
|
UTSW |
2 |
130,775,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4364:Atrn
|
UTSW |
2 |
130,812,128 (GRCm39) |
missense |
probably benign |
0.39 |
R4465:Atrn
|
UTSW |
2 |
130,802,388 (GRCm39) |
missense |
probably benign |
0.08 |
R4510:Atrn
|
UTSW |
2 |
130,777,497 (GRCm39) |
nonsense |
probably null |
|
R4511:Atrn
|
UTSW |
2 |
130,777,497 (GRCm39) |
nonsense |
probably null |
|
R4527:Atrn
|
UTSW |
2 |
130,815,424 (GRCm39) |
missense |
probably benign |
0.10 |
R4586:Atrn
|
UTSW |
2 |
130,823,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R4592:Atrn
|
UTSW |
2 |
130,841,050 (GRCm39) |
intron |
probably benign |
|
R4658:Atrn
|
UTSW |
2 |
130,775,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Atrn
|
UTSW |
2 |
130,862,910 (GRCm39) |
missense |
probably benign |
0.06 |
R4960:Atrn
|
UTSW |
2 |
130,836,967 (GRCm39) |
nonsense |
probably null |
|
R4999:Atrn
|
UTSW |
2 |
130,817,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R5066:Atrn
|
UTSW |
2 |
130,836,113 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5080:Atrn
|
UTSW |
2 |
130,812,044 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5141:Atrn
|
UTSW |
2 |
130,841,050 (GRCm39) |
intron |
probably benign |
|
R5256:Atrn
|
UTSW |
2 |
130,787,939 (GRCm39) |
missense |
probably benign |
0.39 |
R5494:Atrn
|
UTSW |
2 |
130,864,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5678:Atrn
|
UTSW |
2 |
130,811,936 (GRCm39) |
missense |
probably damaging |
0.96 |
R5752:Atrn
|
UTSW |
2 |
130,748,464 (GRCm39) |
unclassified |
probably benign |
|
R5931:Atrn
|
UTSW |
2 |
130,775,356 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6023:Atrn
|
UTSW |
2 |
130,862,900 (GRCm39) |
missense |
probably benign |
0.25 |
R6176:Atrn
|
UTSW |
2 |
130,788,011 (GRCm39) |
missense |
probably benign |
0.31 |
R6377:Atrn
|
UTSW |
2 |
130,821,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Atrn
|
UTSW |
2 |
130,864,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7226:Atrn
|
UTSW |
2 |
130,828,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R7402:Atrn
|
UTSW |
2 |
130,789,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R7541:Atrn
|
UTSW |
2 |
130,803,491 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7587:Atrn
|
UTSW |
2 |
130,822,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R7872:Atrn
|
UTSW |
2 |
130,812,147 (GRCm39) |
critical splice donor site |
probably null |
|
R7910:Atrn
|
UTSW |
2 |
130,806,807 (GRCm39) |
missense |
probably benign |
0.04 |
R7913:Atrn
|
UTSW |
2 |
130,812,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Atrn
|
UTSW |
2 |
130,836,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R8044:Atrn
|
UTSW |
2 |
130,777,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Atrn
|
UTSW |
2 |
130,855,561 (GRCm39) |
missense |
probably null |
1.00 |
R8093:Atrn
|
UTSW |
2 |
130,817,908 (GRCm39) |
missense |
probably benign |
0.00 |
R8203:Atrn
|
UTSW |
2 |
130,802,469 (GRCm39) |
missense |
probably benign |
0.00 |
R8234:Atrn
|
UTSW |
2 |
130,864,920 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8462:Atrn
|
UTSW |
2 |
130,777,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Atrn
|
UTSW |
2 |
130,846,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Atrn
|
UTSW |
2 |
130,748,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R8831:Atrn
|
UTSW |
2 |
130,748,521 (GRCm39) |
missense |
probably benign |
0.22 |
R8937:Atrn
|
UTSW |
2 |
130,841,157 (GRCm39) |
missense |
probably benign |
0.00 |
R9161:Atrn
|
UTSW |
2 |
130,777,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Atrn
|
UTSW |
2 |
130,803,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R9786:Atrn
|
UTSW |
2 |
130,786,809 (GRCm39) |
missense |
probably damaging |
1.00 |
RF009:Atrn
|
UTSW |
2 |
130,748,842 (GRCm39) |
missense |
probably benign |
0.12 |
X0024:Atrn
|
UTSW |
2 |
130,800,059 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Atrn
|
UTSW |
2 |
130,815,319 (GRCm39) |
missense |
probably benign |
|
Z1176:Atrn
|
UTSW |
2 |
130,788,113 (GRCm39) |
missense |
probably benign |
0.27 |
Z1177:Atrn
|
UTSW |
2 |
130,787,962 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- CCTTGGGCAGGATAGACAGATGAGC -3'
(R):5'- AGGTCACAGGTTGAATATCATCAAGCAC -3'
Sequencing Primer
(F):5'- AGACAGATGAGCTAAGATTCCTTC -3'
(R):5'- ATATTCCCACCCTGATACTGTCTG -3'
|
Posted On |
2013-05-23 |