Incidental Mutation 'R1201:Crh'
| ID |
101350 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Crh
|
| Ensembl Gene |
ENSMUSG00000049796 |
| Gene Name |
corticotropin releasing hormone |
| Synonyms |
LOC383938, corticotropin-releasing factor, corticotropin releasing factor, CRF |
| MMRRC Submission |
039271-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.572)
|
| Stock # |
R1201 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
19747565-19749560 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 19748090 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 184
(I184T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000061185
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029139]
[ENSMUST00000061294]
|
| AlphaFold |
Q8CIT0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000029139
|
| SMART Domains |
Protein: ENSMUSP00000029139
Gene: ENSMUSG00000060913
| Domain | Start | End | E-Value | Type |
|---|
|
RING
|
26 |
81 |
3.69e-8 |
SMART |
|
BBOX
|
119 |
161 |
3.58e-6 |
SMART |
|
Blast:BBC
|
168 |
294 |
2e-33 |
BLAST |
|
PDB:4M3L|D
|
215 |
272 |
2e-12 |
PDB |
|
low complexity region
|
329 |
355 |
N/A |
INTRINSIC |
|
low complexity region
|
384 |
398 |
N/A |
INTRINSIC |
|
low complexity region
|
474 |
485 |
N/A |
INTRINSIC |
|
low complexity region
|
514 |
526 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000061294
AA Change: I184T
PolyPhen 2
Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000061185
Gene: ENSMUSG00000049796
AA Change: I184T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
38 |
56 |
N/A |
INTRINSIC |
|
CRF
|
146 |
185 |
1.55e-16 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.0%
- 10x: 95.2%
- 20x: 89.4%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the corticotropin-releasing factor family and preproprotein that is proteolytically processed to generate a mature protein product. This protein product is a neuropeptide hormone that binds to the corticotropin releasing hormone receptors (CRHR1 and CRHR2) to stimulate the release of adrenocorticotropic hormone from the pituitary gland in response to stress. The encoded protein may also regulate angiogenesis and inflammation. Homozygous knockout mice for this gene exhibit reduced corticosterone levels while the offspring of these mice die perinatally. [provided by RefSeq, Aug 2015]
PHENOTYPE: Homozygous null mice have abnormal adrenal gland morphology, decreased corticosterone levels and abnormal corticosteroid responses to stress. Homozygous litters born from homozygous females display neonatal lethality, impaired lung maturation and delayedcornified and granular layer development. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932414N04Rik |
A |
G |
2: 68,546,626 (GRCm39) |
T103A |
possibly damaging |
Het |
| Acly |
A |
G |
11: 100,384,761 (GRCm39) |
I674T |
probably damaging |
Het |
| Aco2 |
C |
T |
15: 81,779,394 (GRCm39) |
S33L |
probably damaging |
Het |
| Actc1 |
A |
G |
2: 113,879,994 (GRCm39) |
|
probably null |
Het |
| Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
| Arhgap40 |
A |
C |
2: 158,376,689 (GRCm39) |
D275A |
probably damaging |
Het |
| Bltp1 |
A |
G |
3: 37,002,524 (GRCm39) |
S1490G |
probably benign |
Het |
| Car11 |
A |
G |
7: 45,352,904 (GRCm39) |
D221G |
probably benign |
Het |
| Catsperg1 |
A |
T |
7: 28,891,095 (GRCm39) |
H596Q |
possibly damaging |
Het |
| Ccm2 |
T |
C |
11: 6,543,682 (GRCm39) |
V231A |
probably benign |
Het |
| Csgalnact2 |
A |
G |
6: 118,091,393 (GRCm39) |
S424P |
probably damaging |
Het |
| Dbf4 |
A |
C |
5: 8,447,498 (GRCm39) |
L571V |
possibly damaging |
Het |
| Fancm |
A |
G |
12: 65,153,542 (GRCm39) |
K66E |
possibly damaging |
Het |
| Hydin |
T |
C |
8: 111,296,487 (GRCm39) |
V3672A |
probably benign |
Het |
| Kcnh2 |
C |
T |
5: 24,527,670 (GRCm39) |
R894H |
probably damaging |
Het |
| Krt36 |
T |
C |
11: 99,994,883 (GRCm39) |
N230D |
probably benign |
Het |
| Nlrp4b |
G |
T |
7: 10,449,363 (GRCm39) |
R522L |
possibly damaging |
Het |
| Ntn1 |
T |
C |
11: 68,104,052 (GRCm39) |
D532G |
probably damaging |
Het |
| Numb |
A |
T |
12: 83,848,059 (GRCm39) |
V215D |
probably damaging |
Het |
| Or1x2 |
T |
A |
11: 50,917,937 (GRCm39) |
M36K |
probably damaging |
Het |
| Or4k15 |
T |
A |
14: 50,364,813 (GRCm39) |
W260R |
probably damaging |
Het |
| Or5k8 |
A |
G |
16: 58,644,226 (GRCm39) |
I282T |
probably damaging |
Het |
| Or6b2b |
T |
G |
1: 92,418,875 (GRCm39) |
I201L |
probably benign |
Het |
| Or7a39 |
A |
T |
10: 78,715,311 (GRCm39) |
M102L |
probably benign |
Het |
| Otulinl |
G |
A |
15: 27,658,259 (GRCm39) |
Q84* |
probably null |
Het |
| Pidd1 |
A |
G |
7: 141,020,187 (GRCm39) |
F580L |
probably benign |
Het |
| Plekhg4 |
A |
G |
8: 106,108,305 (GRCm39) |
D1116G |
probably damaging |
Het |
| Prss33 |
G |
T |
17: 24,054,084 (GRCm39) |
S74* |
probably null |
Het |
| Rab34 |
T |
A |
11: 78,081,222 (GRCm39) |
|
probably null |
Het |
| Rims2 |
A |
C |
15: 39,479,720 (GRCm39) |
T1251P |
possibly damaging |
Het |
| Skint5 |
A |
G |
4: 113,413,342 (GRCm39) |
S1152P |
unknown |
Het |
| Slc6a17 |
T |
A |
3: 107,400,388 (GRCm39) |
Q206L |
possibly damaging |
Het |
| Tmem59l |
C |
T |
8: 70,937,037 (GRCm39) |
W310* |
probably null |
Het |
| Tnrc6c |
T |
G |
11: 117,612,500 (GRCm39) |
N379K |
probably damaging |
Het |
| Vmn1r76 |
A |
C |
7: 11,664,252 (GRCm39) |
F286V |
probably benign |
Het |
| Xdh |
T |
C |
17: 74,225,413 (GRCm39) |
D463G |
probably benign |
Het |
| Zfp251 |
C |
T |
15: 76,738,436 (GRCm39) |
R219Q |
possibly damaging |
Het |
| Zfp263 |
T |
A |
16: 3,567,294 (GRCm39) |
H536Q |
probably damaging |
Het |
| Zfp607a |
T |
A |
7: 27,578,736 (GRCm39) |
F602Y |
probably damaging |
Het |
|
| Other mutations in Crh |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02698:Crh
|
APN |
3 |
19,748,354 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R0047:Crh
|
UTSW |
3 |
19,748,201 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0697:Crh
|
UTSW |
3 |
19,748,241 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0835:Crh
|
UTSW |
3 |
19,748,528 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2034:Crh
|
UTSW |
3 |
19,748,262 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2233:Crh
|
UTSW |
3 |
19,748,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2234:Crh
|
UTSW |
3 |
19,748,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2235:Crh
|
UTSW |
3 |
19,748,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5045:Crh
|
UTSW |
3 |
19,748,153 (GRCm39) |
nonsense |
probably null |
|
|
R5191:Crh
|
UTSW |
3 |
19,748,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5283:Crh
|
UTSW |
3 |
19,748,171 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6481:Crh
|
UTSW |
3 |
19,748,501 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6790:Crh
|
UTSW |
3 |
19,748,459 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6865:Crh
|
UTSW |
3 |
19,748,304 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R7259:Crh
|
UTSW |
3 |
19,748,418 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R7758:Crh
|
UTSW |
3 |
19,748,453 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7981:Crh
|
UTSW |
3 |
19,748,216 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8247:Crh
|
UTSW |
3 |
19,748,291 (GRCm39) |
missense |
probably benign |
0.06 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAACAACTGGATGACTCCCATCTGC -3'
(R):5'- ATCTCAACAGAAGTCCCGCTGCTC -3'
Sequencing Primer
(F):5'- AACGCTGTTTTGTTACGACAC -3'
(R):5'- GCTAACTTTTTCCGCGTGTTG -3'
|
| Posted On |
2014-01-15 |
Incidental Mutation