ZMP
grin2ca
Ensembl ID:
ZFIN ID:
Human Orthologue:
GRIN2C
Human Description:
glutamate receptor, ionotropic, N-methyl D-aspartate 2C [Source:HGNC Symbol;Acc:4587]
Mouse Orthologue:
Grin2c
Mouse Description:
glutamate receptor, ionotropic, NMDA2C (epsilon 3) Gene [Source:MGI Symbol;Acc:MGI:95822]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40036 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14471 | Nonsense | Available for shipment | Available now |
| sa19980 | Essential Splice Site | Available for shipment | Available now |
| sa31320 | Essential Splice Site | Available for shipment | Available now |
| sa26037 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31319 | Nonsense | Available for shipment | Available now |
| sa31318 | Essential Splice Site | Available for shipment | Available now |
| sa40035 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40036
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Nonsense | 31 | 1400 | 1 | 12 |
| ENSDART00000145215 | Nonsense | 31 | 1400 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18912832)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18941194 |
| GRCz11 | 3 | 19090934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCGGTGCTGCTGCTGCTGTCTGTCTGCTCCGTGCCCTGCTGCCAGTGC[C/T]GACCGTTCGGGATGGTGGAGCCCACCGTCAACGTGGCGGTGGTGTTCAGT
Long Flanking Sequence:
AAAGGCTTAACTAGGTTAATTACAGTAGGTTAACTAGGCAGGTTAGGGTAAAAAGGCAAGTTATTGTATAATATATATATAGCTTAAAGGGCCTAATAATTTTGTCCTTAAAATGGTTTTTAAAAAATGAAAAACTGGTTTTATTCTTGCCTAAATAAATCATATAAGACTTTCTCCAGAAGAAAAAATGTGATCATACTGTGAAACATACTGTGAAAATTTACTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAAGAAAAATAATTCAAAGGGGAGGGACTTCAACTGTGTTTGTGTATTATTTTTGCATAACTCTTTCCACCTCTGACTAAACCTCAGCATCTCCTTGTAACTCCTGCCCATTTGTGTGTGCTTTCCTGCCCCCAGGCAGTAGGCGACTGAGATGGGCGTTCATCTAGGCTGTCTCAGCGACACACTGTGGCTGCCGGTGCTGCTGCTGCTGTCTGTCTGCTCCGTGCCCTGCTGCCAGTGC[C/T]GACCGTTCGGGATGGTGGAGCCCACCGTCAACGTGGCGGTGGTGTTCAGTGGCTCCGCCTACCAGACGGAGATCAAGGGCCGACTGAGCCGCGAGAACTTCCTGGACCTGCCGCTGGAGGTGAACCCCATCACTGTGCTGGTCAACAACACCAACCCGCGCACTCTACTGACGCGCATCTGCGACACGCTGGCTGCTAACAGAGTGCACGGGGTGGTCTTTGAAGATAACATTGGCTCTGAGGCCGTGGCGCAGATCCTGGACTTCATCTCCACGCAGACAGCCGTGCCCATCGTAGGCATCAGTGGGGGGTCGGCTGTCGTCCTGCCTCACAAGGTCAGAGTCGAGCACTGTGCCAGTTCCGCTTGACCTACATGGTTAAACTCTTGATTTCTGGGTGTTCACACTGAGATAAGATTCCCTCAGAGTTCTTTCATAGTCTGCATTAAAGATTGGTAAGAGGTAATGTACAGTCAGCATGTAAATAAACCCTGACAGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14471
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Nonsense | 245 | 1400 | 2 | 12 |
| ENSDART00000145215 | Nonsense | 245 | 1400 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18890892)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18919254 |
| GRCz11 | 3 | 19068994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCGACGCGCAAGTGCTGCTGGTTTACTGTTCTCACGATGAGGCCCAGTA[T/A]CTTTTCTCCATGGCCAGGGAAGTGGGTCTGGTTGGTCCAGGCTACATCTG
Long Flanking Sequence:
AATGTAATATATTAAGATATTTTGATCATAATATAAAACATCATTTGGGGGACTCTTGAATCCATTTTGTTTCAGCTGATTTCTAGAGCCAGTTAAATTGAGTGAAATTTCTCCAATCTTGAAGTGGATGTTTATTTGAAGTGTCTTATGTAGAAATGCTTCTGATCTCTGTTTGTCCCGTGTCTCTCGCAGGGTGACGGCTCTACTTTCCTCCAGCTGGGCTCCTCCATCGAACAGCAGATCAACGGCATGTTCAAGGTAATGGAGGAGTACAACTGGGACAGTTTTGTGGTGGTAACCAGTCTATACCCGGGCTATGACACCTATGTGGACTACATCCGCTCCTTCATCGACACCTCGTATTTCCTGTGGGAGCTGCAGGACACCTTGACGTTTGACATGTCGGCGGACGGCATGAATGATCTCCGTGCACGTCGGTTATTACAACAGATCGACGCGCAAGTGCTGCTGGTTTACTGTTCTCACGATGAGGCCCAGTA[T/A]CTTTTCTCCATGGCCAGGGAAGTGGGTCTGGTTGGTCCAGGCTACATCTGGTTTATCCCTAGCCTTGCGGTGGGAAACCCCAATATTGCGCCCCCAGACAGCTTCCCAGTGGGACTGATTAGCATCATCACCGACCGCTGGAAGATGAGCTTGAGGAACAGAGTCAGGGATGGAGTGGCAATCGTGGTGAAAGGAGTGGAGAGTTTTCGCAAACAGAGAGGCTTCATTCCTGATGGACACATGGACTGTTTGAGTCCCATCCGGCCGGCCAGCAATGGCACGCTCTACAGGTGGGTTTTACTTTTTTGGTGACACTAACACTACCGTGTAAGTTCTATAAGTGCTATAATTCTGGCTGAATAAATTCTGGCCAGTACTTCTTATTGTCATGGAGGTTTAGGTGCACTTACAGCATGTCTGAATTCACTTTTGCTATTTTAAAGACAGGAAAAATGGTTGGTGCATCTGGTGAATGGTGTAAAAGTGTTGTCTTTATTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19980
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Essential Splice Site | 342 | 1400 | 3 | 12 |
| ENSDART00000145215 | Essential Splice Site | 342 | 1400 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18877248)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18905610 |
| GRCz11 | 3 | 19055350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTGATATTCTACAAATATCATTTAGAAAACATCTGTCTGATTTTTTGC[A/T]GGCATATGCTGAATGTGTCGTGGGAGAACACTGATTTCTCCTTCAACAGT
Long Flanking Sequence:
ACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGGTCGTAGTGAGTGTGTGTGTGCGTGTGGATGTTTCCCAAAGATGGGTTGCAGCTGGAAGGGCATCCACTGTGTAAAAACGTGCTGGATAAGTTGGCGCTTCATTCCGCAGTGGCGACCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAATTAATGAATGAATATAATTACTCCACAATAGTTGAGAACTCACATACTGTATTTGTCATGAGCACTTTCTTTTGCATTCACGGGTATGCGTTGAACTCAACAGCCCCCAAAGAATGCACCTGCTTCAGTATAAATTACTGATTTAAAACGAGTCCGCTGCGGAAAAGTTGTTAGTTTAGTCTTTTATTTTGTGGTTGGTCATTTGTTCTGGGAGACTTGTATGCTTTCATCTGTGAATCATAATTGATTTGATGTTAATTAATTATTGATATTCTACAAATATCATTTAGAAAACATCTGTCTGATTTTTTGC[A/T]GGCATATGCTGAATGTGTCGTGGGAGAACACTGATTTCTCCTTCAACAGTGATGGATATCTGGTCAACCCTTCAATGATCATAATCACTCTGGACCGTGGGAGACAGTGGGATAAGGTAAGGATGTTTTTTGTGCTTGTACAATTGAATTTCCTTCTGCCATACTCTATTCAAAAGGTTGCACCTCCAATGGCATCATCAATTTTAACGCGCCTCCGCAGGTTTCATTGCCCTCAGGGTAGTTGTGAGTCAAAATGCCACAGACAAACAGCATGTGTACCTCAGTGTTATTCATCTGAAATATGTCAACTTCCACTTTTTATTTTCAGAAAATGGAACATAAAATTAAACATTTATGTTTCTTACCGGAGCTGGACGGCATCTTCTGTGCATCATCTGGTTTTATGACCAAAGCATTCTCTGATGGCCTGCATTTTTATTGTGGTCAACATAAATTATAGCATATAGTATATCTGCTGCATTTTTACATGTCAGTGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31320
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Essential Splice Site | 451 | 1400 | 5 | 12 |
| ENSDART00000145215 | Essential Splice Site | 451 | 1400 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18845308)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18873670 |
| GRCz11 | 3 | 19023410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTATGATCGACTTGCATGAAATGATCAATTTTCCATTGTGTTCCCACA[G/A]TATAGTCGGACACACAGAGCCTTACACCAAACTCTGCTGCAAAGGCTTCT
Long Flanking Sequence:
TTTATTTTAAAAATATATCCTAATAGTTTCTTTAATTTGTGATTTGCAGGTTTTGTTTTAATTTATCTACCGTTTTTACAAATGTCTTTTATTGACATTTCTAAACTTTCCAACATCAAAACTTGTTGGAAGAAAGATCAAGATCTCATAATGCAATAAAACAAAAACATGAATTACAAAATACATTTATTCATAATATTCCTTTGGCTTAGTCCCTTATTTTTCAGGGGTGGCCACAGCGAAATGAATCGACAACTATTCTGGCATAATTTTTTTACAAAGCAGATGCCCGTTCAGCCGCAACCCAGTACTCGGAAACATTACAAAATACAGTAAACTGTTAATTTGCAGACATTTTTGTACAGCACCTAAGTTAAACTAGCAGTGTGCAGATTGATGACATCTGAAATTAAACATTTATTTTGAAATGATATTTAATGTTTTTATTGCTATTATGATCGACTTGCATGAAATGATCAATTTTCCATTGTGTTCCCACA[G/A]TATAGTCGGACACACAGAGCCTTACACCAAACTCTGCTGCAAAGGCTTCTGCATAGACATCCTGAAAAAGCTCTCTCGCAACATCAAGTTCTCCTATGACCTCTACCTGGTCACCAACGGCAAACATGGCAAACTGGTACGAGGAATCTGGAACGGGATGATCGGAGAGGTAAGACAACATTTCAGTTTAGTTTTCAAGTCAACAAAAAGACTTTATTTACTTCTTTAAAGGGACACAAAAATCTGTTGAACACAAAAGAAGATATTTTAAGGAATGTTGGAAACCGGTAACTTTCTAACGGGTATTTTTTTAAACAATAGATTTCAACATTCTTCAAAATATCTTCTTTTATGATCAACAGAAATGAAAAACTCACATTTTCGTAACCACTTGAATGCAAAAGGAAAATTATAATTTTGGCTTGGCATTTCTGGCCTGGTCTTGCTGCACTACAACACGTTCTTATTTATTTATTTACGTTGCTCCACCAACAAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26037
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Nonsense | 473 | 1400 | 5 | 12 |
| ENSDART00000145215 | Nonsense | 473 | 1400 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18845243)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18873605 |
| GRCz11 | 3 | 19023345 |
KASP Assay ID:
2259-3274.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGCCTTACACCAAACTCTGCTGCAAAGGCTTCTGCATAGACATCCTG[A/T]AAAAGCTCTCTCGCAACATCAAGTTCTCCTATGACCTCTACCTGGTCACC
Long Flanking Sequence:
TCTACCGTTTTTACAAATGTCTTTTATTGACATTTCTAAACTTTCCAACATCAAAACTTGTTGGAAGAAAGATCAAGATCTCATAATGCAATAAAACAAAAACATGAATTACAAAATACATTTATTCATAATATTCCTTTGGCTTAGTCCCTTATTTTTCAGGGGTGGCCACAGCGAAATGAATCGACAACTATTCTGGCATAATTTTTTTACAAAGCAGATGCCCGTTCAGCCGCAACCCAGTACTCGGAAACATTACAAAATACAGTAAACTGTTAATTTGCAGACATTTTTGTACAGCACCTAAGTTAAACTAGCAGTGTGCAGATTGATGACATCTGAAATTAAACATTTATTTTGAAATGATATTTAATGTTTTTATTGCTATTATGATCGACTTGCATGAAATGATCAATTTTCCATTGTGTTCCCACAGTATAGTCGGACACACAGAGCCTTACACCAAACTCTGCTGCAAAGGCTTCTGCATAGACATCCTG[A/T]AAAAGCTCTCTCGCAACATCAAGTTCTCCTATGACCTCTACCTGGTCACCAACGGCAAACATGGCAAACTGGTACGAGGAATCTGGAACGGGATGATCGGAGAGGTAAGACAACATTTCAGTTTAGTTTTCAAGTCAACAAAAAGACTTTATTTACTTCTTTAAAGGGACACAAAAATCTGTTGAACACAAAAGAAGATATTTTAAGGAATGTTGGAAACCGGTAACTTTCTAACGGGTATTTTTTTAAACAATAGATTTCAACATTCTTCAAAATATCTTCTTTTATGATCAACAGAAATGAAAAACTCACATTTTCGTAACCACTTGAATGCAAAAGGAAAATTATAATTTTGGCTTGGCATTTCTGGCCTGGTCTTGCTGCACTACAACACGTTCTTATTTATTTATTTACGTTGCTCCACCAACAAAATATCATTACATACAACTTCTCACTGTCCAGTCATTTTGGGTTGCAGAAAAAAAATGTTTATTTACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31319
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Nonsense | 614 | 1400 | 8 | 12 |
| ENSDART00000145215 | Nonsense | 614 | 1400 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18835448)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18863810 |
| GRCz11 | 3 | 19013550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCATTTCAGATCCAGGTGGTCCGACGTTCACCATTGGGAAGTCGGTCTG[G/A]CTGCTGTGGGGGATCGTCTTCAACAACTCAGTGCCCATCGAAAACCCCAA
Long Flanking Sequence:
AACAAATGTATATGATAATTTTCATTACTACAGTAAAGATAAAATAAATCAATTATACGAAATGAGTCATTAAATCTGTTCATAAATGTGTTGAAAAAAAATCTTCTCTTCGTTAAACAGAAATTGACAAAATTAAAACAAAATTCAGGGGGGCTAATAATTCTGACTTTAACTCTACGTTTGTTCTGTAGACAATCGAAAAAGTTATTGTTTTAGGGGGCTAATAATTTAGACCTTAAAATGTTTTTTTTTTTTTTTTTTACTAAAAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCTGAAGAAAAAAAAACTTAGCGAAAATACTTTGAAAGTATCCTAGCTCCATTAAAAATCATTTGAGAAACATGTTTTTTAACAGAATAAATATTTCAGAGAAGGGCTAATAAATTTACCCTCAACTGTATGTCATGACTTCCATTTCAGATCCAGGTGGTCCGACGTTCACCATTGGGAAGTCGGTCTG[G/A]CTGCTGTGGGGGATCGTCTTCAACAACTCAGTGCCCATCGAAAACCCCAAAGGCACCACCAGCAAGATAATGGTGCTGGTGTGGGCCTTCTTTGCTGTGATCTTCCTGGCAAGTTACACAGCCAACCTGGCAGCCTTCATGATCCAGGAGCAGTACATTGACACGGTTTCTGGACTCAGTGACAAGAAGGTAAGAGCTGCCAGAGTCTCTCACAGCCAAGTGGCCATTCAAGGGCAGCGGTTTTAATTAAACTCATCACCAGGCTGAACTACAAGGCAGTTTCACGCTGATATGATATATGGTTGCACTGGCATGATGGAATGCCGTGACGCTAATCGCTAATTTGTGTAACTTTAAAGAGACATTAATTGACTATTTGAAATATTAAGCCAGTTTTAGATGTTGCCAACATGACAAAGAGGTGTAAATCTAGGAAATGGTTTGGAATTTTAGTTTTTTCACTTTAATAAATGCTTGCTGACTTAATTTTTGTAGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31318
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Essential Splice Site | 731 | 1400 | 9 | 12 |
| ENSDART00000145215 | Essential Splice Site | 731 | 1400 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18831600)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18859962 |
| GRCz11 | 3 | 19009702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACAACCAAAAAGGTGTGGAGGATGCTCTCAACAGCCTCAAAACTGGG[T/A]GCGTTTACTGTAAATTCTCACCTGAAACTCTAAAACAAATCCTTCCCTGA
Long Flanking Sequence:
ATTTTAGTCATATTCCCACTTGGATTTATGTTGTATTTAATGTGGCGTTTGCAGATACAGAATCGTGAGAATCCTTGGAACAGGCCGAAGACAAAGGCTGAACCCTACAATAAATTCCCATGCAGAAATCCAGCTTAAAGAAAAATCAATCACACTTTCCAGCAGCGTAGCTTTCCCATGCAAAAAAAGCCATTACTGGCATATCTAGCGGAGCAGGAATCTATTAAAATGCTCTAATCCTTAACCAAGTTACTCAGATTTATTTCTTCCACTCAGACTGTGATTTGTTCATGAAGTTTAATTTAAACATGCTAACTTGTTGAAATGCTGCCTTTTAGTTCCAGAAACCGCAGGACCAATATCCCCCATTCCGGTTTGGGACTGTGCCCAATGGCAGCACGGAACGAAACATAAGGAGCAATTATCCCGAAATGCATTCCCACATGGTTAAATACAACCAAAAAGGTGTGGAGGATGCTCTCAACAGCCTCAAAACTGGG[T/A]GCGTTTACTGTAAATTCTCACCTGAAACTCTAAAACAAATCCTTCCCTGATGTATTAGCATTTATACATTCTGTTGTTGTTTTTGTATTGTTAACAGCAAGCTGGATGCCTTCATATATGATGCAGCCGTGCTTAACTACATGGCCGGTAAAGATGAAGGGTGTAAATTGGTGACCATTGGTAGCGGGAAGGTGTTTGCTACGACAGGCTACGGTATCGCCCTTCAGAAAGAATCTCGATGGAAGCGGCCGATTGACCTCGCTCTTCTCCAGTTCCTTGCTGACGGTAACTTCAGAAACTTACTTTTGCTAGAGGAGCTCTGCTTCACAAATCTGACCCAAATATATTATTTATCACAGGTGACACTCAGAAGCTGCAGACGGTGTGGCTCACTGGGATCTGTCGTAATGAGAAGAAGGAGGTGATGAGCTCTAAGCTGGACATTGACAACATGGCTGGAGTGTTTTACATGCTTCTGGTGGCTATGGGTCTCAGTCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40035
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110554 | Nonsense | 850 | 1400 | 11 | 12 |
| ENSDART00000145215 | Nonsense | 850 | 1400 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 18831071)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 18859433 |
| GRCz11 | 3 | 19009173 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCTATGGGTCTCAGTCTGCTGGTCTTTGCCTGGGAACATCTACTGTA[C/A]TGGAAGCTGCGGCATTCAGTCCGCAAGTCTGAGCGATTGGACTTCTTGCT
Long Flanking Sequence:
TCTAAAACAAATCCTTCCCTGATGTATTAGCATTTATACATTCTGTTGTTGTTTTTGTATTGTTAACAGCAAGCTGGATGCCTTCATATATGATGCAGCCGTGCTTAACTACATGGCCGGTAAAGATGAAGGGTGTAAATTGGTGACCATTGGTAGCGGGAAGGTGTTTGCTACGACAGGCTACGGTATCGCCCTTCAGAAAGAATCTCGATGGAAGCGGCCGATTGACCTCGCTCTTCTCCAGTTCCTTGCTGACGGTAACTTCAGAAACTTACTTTTGCTAGAGGAGCTCTGCTTCACAAATCTGACCCAAATATATTATTTATCACAGGTGACACTCAGAAGCTGCAGACGGTGTGGCTCACTGGGATCTGTCGTAATGAGAAGAAGGAGGTGATGAGCTCTAAGCTGGACATTGACAACATGGCTGGAGTGTTTTACATGCTTCTGGTGGCTATGGGTCTCAGTCTGCTGGTCTTTGCCTGGGAACATCTACTGTA[C/A]TGGAAGCTGCGGCATTCAGTCCGCAAGTCTGAGCGATTGGACTTCTTGCTCGCCATTAGCAGGGTAAGTTTCATATGATGTATACTTTTAAAAGAAATACATTTTAAATAGGGATACTAGGGGTGCACAGAATTTTCCGCTGTCAAAAATCATATGCAGAAAATGGCATCTTAGAGTTTTGTCTGAAAGAAACAGCCAAAAACACAAAAAGAGGCACACTGGACTTGGAAAGTACTATGCTATGAAACCCATTCATTTCAATGGCTTGTGCCAAGCAAGGGCAGTTTAATGTTAAGCCAATCAAAGGGCAAGAGCAGCAGAGTGCACTAGCAACTAGCTTGTATGCACACTGCAGTTAATGTTTAAATTAGGTTACTATTCCACTTTGTGGATATTCTGCATGTATACTTATCTATGCATGAACAACACATGCTCACTGGAATAGCAAAGTCCACTCAAATAATGCCACGACAGGACATTTCTGTGTAGTACTTTTTCTT
Associated Phenotype:
Not determined