ZMP
grin2db
Ensembl ID:
ZFIN ID:
Human Orthologue:
GRIN2D
Human Description:
glutamate receptor, ionotropic, N-methyl D-aspartate 2D [Source:HGNC Symbol;Acc:4588]
Mouse Orthologue:
Grin2d
Mouse Description:
glutamate receptor, ionotropic, NMDA2D (epsilon 4) Gene [Source:MGI Symbol;Acc:MGI:95823]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25008 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15765 | Nonsense | Available for shipment | Available now |
sa9877 | Nonsense | Available for shipment | Available now |
sa19134 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44841 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22781 | Nonsense | Available for shipment | Available now |
sa36065 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32078 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25008
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 |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 166 | 1959 | 2 | 14 |
ENSDART00000144062 | Nonsense | 166 | 1016 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 15055693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13414152 |
GRCz11 | 16 | 13304272 |
KASP Assay ID:
554-7542.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCCCCATTGTTGCTGTGGGAGGGGGAGCAGCTCTGGGCAGGGTACCA[C/T]AGGTAATGCCGTTTACTGAATTGAAATGTGGTCATGTTTTTGTTGCTCTG
Long Flanking Sequence:
TTTGAAAAATTCTATAATAAACACTTAAAGTGTACTTTGTTTCCTCTAGATTGAAAAAAAAAACATATAAAAAGCCAAAAGCCTAAAATCTCAATAATAATAATATAAAAACCTAGGATTTTGCAGGGTAGACTGTGATTTTACTTTCAGTGTCTTACCTGAATGCTTTGTTAATTGTGATCTGAAGTGCGAACACAAAAGGAGAGACAAATATGCGCAATTAAGCATGAGCGTTCATTCATAACTGCAGGGGTCAATGTGGTGTGAATGTGAACATGAATGTGAATTGACTGCAGGTGAATGACAGCAGTCCCAGGACGCTGCTCTCTCAACTGTGTGACCTGCTGGCAGCCAGACCCCTTCAGGGACTTGTGTATGAGGATGAGAGACCCCTCCCGCTTGCCACCGGCCCCCTGGCACCGATGCTAGAGTTCGTCTCAGCCCAGACCGGCCTCCCCATTGTTGCTGTGGGAGGGGGAGCAGCTCTGGGCAGGGTACCA[C/T]AGGTAATGCCGTTTACTGAATTGAAATGTGGTCATGTTTTTGTTGCTCTGCAAGAATACTTTGTGAGATACAATACAGCAGTTCCCCAAGCAGAATTTTCAGTGTTTATGTTGGTCATGCAATTTTGCTGACTCGACTAAAAGCTAGCTCACTCTACAGGACTGCAAGGCTACATGAATCACTGTGGTTTTGCTACACAAGGTTTCTTGTAATTTTGTCAACTTCAAGTTATAAGCTTTTGTCTGACAGTTTTGTCATTATTGTGTTATTCACATATTCTTATTTTGTGCCACCTTATTATGTGATTTTATTTTATTTTTCTTTTGGTAAGGGGACCATTAGTTTAGAAAGCTAAAACTTTTTTATTCACAAAGTTAACTCCAAATTTAAAGTGCCAATCAGCATCTGAGAGACCAAGATGAGTGATATTATGGGCTCTATCATACAATAGTATTTCATATAAATAATAATACGCAAGATTTGTTTGGCATACTTTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15765
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 |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 193 | 1959 | 3 | 14 |
ENSDART00000144062 | Nonsense | 193 | 1016 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 15048749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13407208 |
GRCz11 | 16 | 13297328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTCCACCGCACTCCAATTGGAGGTGATCTTTGAGGWACTGGAGGAGTA[T/A]GATTGGACGGCCTTCTCGGTGGTGTCCACCCGTCACCATGGCTACCAGGA
Long Flanking Sequence:
TTCTTTTATAAAAACAAAATTAGATTTGTCCGCATGTTGTGTTTTGGAGACGTACTGTATGCGTCACCATTTGGGACATAAGAATGGGACGTGTGTTTGGACATACCTCAGTTGTTTGACCACACTTCATTATGATTGTTCATTTATTCGTTTGCTGGAAATTAGAACGGAATTTAGAAATTTTCAAAACAAATCTTTGCACTCAACAAACTAAATTAAATTTGTTGGCTAATTGTCTTCCGTGGAGTGCATACAACACCATTTCCTTGTCAACAAAAGTTAAGGAGCAAAGGAAAGAGTAAAAGGAAAGGGTCATCTTAGAGGTACAAACCTAAAATGATCTAAGTTTCCTCAGAAAAAAAAAAAAAAAGTATTTTTTCTTGGGAAATGTGGTTGTTTACCTTTTTAATTACTTCGCAGGAGTCCGGCTCAATCTTCCTGCAGTTCAGCTCTTCCACCGCACTCCAATTGGAGGTGATCTTTGAGGTACTGGAGGAGTA[T/A]GATTGGACGGCCTTCTCGGTGGTGTCCACCCGTCACCATGGCTACCAGGACTTTCTGTCGGTGGTGGAGGGTTTGACCGACGGGTCCTTCATCGGCTGGGAAAAGAAGAGCATAGTAATGCTGAATTTAACCGATGACCCGGGAGGAGTGCGCACACAGCGGTTGCTGAAGGAGAACGAAGCACAGGTAGAGAGGGAAGGTCAATGTGTTTCTGTCTCACTTATTTATTTAATCATTCACTTACTGTACTCTTCCACCTTCCCCCTTGACATCACTTCCTGTCCTTTAACCGTTTATTTGACTTTTCTTTTTTTTTTTGCTGTTGCTCGCATTCTCCACCACATCTTTCTGACCTCTCGCTGTCTTTCCATTCTAATTCTCGTTCTTCATCTCTACATATATATTTGTGTAATGCGTACGTGTGTGTATGTGTGTTGCAGGTTGTCCTCTGCCTCCCCCTGGCTCCAGGCTGTTATTGTTCTGTGTATGTGTGTGTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9877
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 737 | 1959 | 11 | 14 |
ENSDART00000144062 | Nonsense | 737 | 1016 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14952536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13310995 |
GRCz11 | 16 | 13201115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAACATCCGCAGTAACTATCCAGACATGCACCAATACATGGTCAAGTA[C/A]AACCAGAAGAGTGTGGAGGACGCCATCTCYCACCTCAAGACTGGGTCTGT
Long Flanking Sequence:
GCTATTTAGCACATGGTGGCTTTTGTTGGTTCTTGTTTCTAAGCGCCTTGTGTTCATTTTGTAAATCCCTTTTTAAATGAAAATAGTTTCCCCATCTGCTTCTTCGCCATTGTTCCCTTTTGTTAAAAGCAGAATGAACACAACGTGCATATCAGCATTGCTGCTTTGTATATTGTTCAGCGTTTATGATGTATTATATTTGGTTTTGACAGCTGCAGTGGCTGGAGACTCGTTTCTTACATGCATTCGCTGTCATATGTCATTCATGTTTTGTCTTGAAATATTTTTTTCATTGCGCTCTATTGTGAGTCCGCTAATTACTTAGAGAAAACAAATGCAACATCAGTTTCAATAAAACTTACATCCTGTGTTTCCCTCTCTCAGTTTCAGCACCCCACAGAGCAGTACCCCCCTCTGAAATTTGGAACGGTCCCCAACGGAAGCACAGAGAAAAACATCCGCAGTAACTATCCAGACATGCACCAATACATGGTCAAGTA[C/A]AACCAGAAGAGTGTGGAGGACGCCATCTCTCACCTCAAGACTGGGTCTGTGCTGGCTTTCTCACTCAATTGCCTTCATTCTGATTGTCACACAGCGTTTTCTGTTTCATTTTGTTTAACAATCTTCAGTTTAAGTTGTAATGAAGATTTTAAAAGATGTTAAATGAATACTAGTTTATTATTAGTAGTAGTTTATTAATAATAGTAGATTATAATAATAATAATAATAATTGTTATTATTATTATATTTATTATCATTATTATTATTGTTGTTGTTGTTATTGTTATTATTATTCATTCATTCATTTTCTTGTTGGCTTAGTCCATTTATTAATCCGGGGTTGCCACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTATTACGCAACGGATGTCCTTCCAGCTGCCACCCATCTCTGGGAAACATCCACACACACATTCACACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCACCTATACCACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19134
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 |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 783 | 1959 | 12 | 14 |
ENSDART00000144062 | Nonsense | 783 | 1016 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14946227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13304686 |
GRCz11 | 16 | 13194806 |
KASP Assay ID:
2260-9354.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGGCTCGTAAAGATGAAGGCTGTAAAGTAATGACCATCGGCTCAGGG[A/T]AAGTATTCGCCACGACTGGATATGGGATCGCCCTGATCAAGAACTCTCGC
Long Flanking Sequence:
TTTTAGTTTACCGAAGCTCAATTTCCTTTGCCAGCTCATTTATATTTCTGTTAGCAAAAATACTTCATCTGTGTTTATTTAGTTGTGGTCTCTGTAATAGTTTTCATAACAACAATAATAACCTTGTTTTCAACGTGTTATGTAACCTCTCTCACAGAAACAGGAGTTCCTTTACGATGTGTTTGCACTTTTTTTTTTTTTACCTCCTCCCACACTTCCTCTCTCTGCCCTGTACACCTCACACACTTTTCCTCCATTTATCATGAGAAGTTAATCCACACAGTGGTTTTCCTGAGCCTGTCATTTCCGTATCCATTTTTAGCCAAAGTGCTAACATAATGCAGAGTTTCCCCCATGCTATCTTTCTGTCACCTTTTCTAACTTGTACTCTTCCTGTCTGTGTTTGCAGTAAGCTGGATGCCTTCATCTACGACGCGGCCGTGTTGAACTACATGGCTCGTAAAGATGAAGGCTGTAAAGTAATGACCATCGGCTCAGGG[A/T]AAGTATTCGCCACGACTGGATATGGGATCGCCCTGATCAAGAACTCTCGCTGGAAACGGCCATTGGACCTGGCTTTATTGCAGCTGGTGGGCGACGGTGAGAGTTCTGCGCTATCAAAGTGCCAAAATTAGGAGATTGCATATTGCTGTGTTTGTGCTGTCGGGTTGGAGAAGATAAAAGCCTTTGGGAGATTAAAGTCTCTTTTTTATATGCATATTTAACAAGACTTCATTCATTAGCCTGCGCTGTTAGCTTCCAGCCATCTTCTCAGCGATCTTGGTCTAATCTAGTTTCCTTGACATGACGCAATACAGTGTGTGTATCTTTGCTGTCTGCCAGGTGACATTTGTCTTTGTGCTAGCAGGCTGTTTACCGACTTTAAGGAGATGATGGCAGCATTGATGCATAAAAGAGATGGGCATGTATCAAAGATTCAGTCTCGGGAATGACAGAAGTGGTGTGTGTGAAAGAGAAATAAAGAGGATAAGACAGTGCTGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44841
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 |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 883 | 1959 | 13 | 14 |
ENSDART00000144062 | Nonsense | 883 | 1016 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14933941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13292400 |
GRCz11 | 16 | 13182520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAACACCTGGTTTACTGGAGGCTGCGGCACTGCATGAGCAAAATGGGA[C/T]AGTCTGGCAAATTGGACTTCCTTCTCGCCTTCAGCAGGGTGAGAGAGTGA
Long Flanking Sequence:
GGATTAACAAAGACCTTCACACTAATGTTTCCTTAACACCCAGAGGGAGCATTTTAAAGTACCTGACCTATGACCTATAATGCTTTAAAGATCTCAAAATAGCACCTGACACAACAGATTTATATTTAGTGTTAGCATCTGCTTCTTGCTACAGTAAGCGTGTGGGAAAGGCAAGTTACTACCATATTGCATTCATGCATGTTTCATTGACGCATCTGTGCCAAGGTATTGTATCACTTATTAAATAAGAAAGTGCATAATTTTAATGTCTTGTCTTTTTCTCTTCTCTCCACTCAGATGAGATAGAGATGCTAGAGCGTCTCTGGCTCTCAGGGATCTGTCACAATGATAAAATTGAGGTGATGAGCTCCAAACTAGACATAGACAACATGGCGGGTGTTTTCTACATGCTGCTGGTAGCCATGGGCCTAAGTCTCCTGGTCTTTGCCTGGGAACACCTGGTTTACTGGAGGCTGCGGCACTGCATGAGCAAAATGGGA[C/T]AGTCTGGCAAATTGGACTTCCTTCTCGCCTTCAGCAGGGTGAGAGAGTGAGAGTGTGAAGTGAGAGAATGAATGATTTCAGTTGACATTAAGTTTGGGTCTGGTATTACAGATGGCATGCAATTAAAACATTGTCCTTTTTGGAATCTGACTTGCCTTCATTTATTTTTGTACTCTTAGGGAATGTATAGCTGCTGCAGCTTTGAAGATGAAACCGCACAAGGTGGGGCTAAAGTCACAGTTTCTGGCCACCATCACACTGCCATGGTTCCTACTTCTTCCTCACATGTGGTCACTTCAGCTGTATCCAATCCAGCCATTGCCATGGTCCAGCAGCAGCAACAGCAGCAACCACAACAGCCTCAACCTCCTCAGTCTTACAAGACACCTCTTCCTGGATCCCCTCCACCAATTGTTCATTCTGGAGCAGCCTTGGGTCCTGCAAATACGCAACTTATAGGAGCTCCACTACCATGCACTACTTTCTTACCCCGGCCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22781
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 1075 | 1959 | 14 | 14 |
ENSDART00000144062 | None | None | 1016 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14933224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13291683 |
GRCz11 | 16 | 13181803 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTACTATGGACCTATTGATCCAGAGGGACTTGGGCCATGTGTGGACCAA[C/T]AGACAGGTTCTCAAACCCCTAAAACAATCCCCAGAGTCCATCAACAACCC
Long Flanking Sequence:
CACAAGGTGGGGCTAAAGTCACAGTTTCTGGCCACCATCACACTGCCATGGTTCCTACTTCTTCCTCACATGTGGTCACTTCAGCTGTATCCAATCCAGCCATTGCCATGGTCCAGCAGCAGCAACAGCAGCAACCACAACAGCCTCAACCTCCTCAGTCTTACAAGACACCTCTTCCTGGATCCCCTCCACCAATTGTTCATTCTGGAGCAGCCTTGGGTCCTGCAAATACGCAACTTATAGGAGCTCCACTACCATGCACTACTTTCTTACCCCGGCCAGATCGCAGGCTGGCAGTCGTAGACCGGTGGAGACTACCCAAAACTGCTGGTGCCACCACGTCGATGGGTGTAAGAGGACCCCTAGCGGAAACGGTACCCTTACCCCAAAAGGTGGCACCTGCTTGGGCAAGTGGTGGAGGTACTGGTAGTGGTCTAGATGGATATAAGCGCTACTATGGACCTATTGATCCAGAGGGACTTGGGCCATGTGTGGACCAA[C/T]AGACAGGTTCTCAAACCCCTAAAACAATCCCCAGAGTCCATCAACAACCCCAACCAACTGGTGTGGCTTTCTACCAGGAGAAGGGCATGGACCATGGCGTGGGGAAGAAGGTGGGAGTGGGTACTGGTGGAGGGGGTCAGGGTAGAGGGGTTAAATCTCTGGGGACCCCCAGGCTTCCTCCTAAAAGCCAAACCCCAGCCCCACTGACACCTAACCCCCCACTGCAGCACCCCTCTCCCCCTCTCCCTTCATCTTTCTGGAGGAAACGGCGACCAAAAAAGCCCAAAGAACCTGGTGGCCCACTGTACGAAAACATCCTGCCACTGGGCCGGAGAGGAGGAGGCAGGGAAGCGAGTCGAAGACCGAGACCCTCTCCTCCTCTCCCCATCCCTGTGCCAGTTACACTTTCCCCATCCTACACTCCTCCTTCACCCTCTCCCTCACTGCCATACACTTCCACATCATCAACCTCATCCACCACTAGCTCTTCAACCACATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36065
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 |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 1444 | 1959 | 14 | 14 |
ENSDART00000144062 | None | None | 1016 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14932117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13290576 |
GRCz11 | 16 | 13180696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTTCCGGTAAGCGGTCAGAGCCAGAGGAAGGTGATGTTGAAGCAGAC[A/T]GAGATGGAGAGGGGGATGGGGATAGAGAAGGAGAGTACTCATCATTTTCT
Long Flanking Sequence:
AGCTGACCGAAGAGTCAAGTCTTCTTCAGGGCCACAACAGATCTAGGGACAGAGAGCGGTCTATACTTTCCCCTAGATCTCTTACTCATGGACCTCCCCCTCCCATACCGCCACGCAAACCATGGGGCACCTTTGGTGACAGGGAACATAAAAAAGACAGAGAAAGAGAGAGAGGTGGAAGTCAACTAGCACAGCTCCAGGAATGGTGGGCAGGATGGGCAGAAAGAGAGAGGGACAGGGAGAGGAGTGGTGGAGCTCAAGGAGAAACAGAAAGGAAAAGAGAGAAGAAACGTAGGAAAGACAGGGAAAAGGAGAAAAAGAAGAAGAAGAAGAAAAACAAAAAAAGGAAAAAGAGGGAGGAGCGTGAAAGGGAAAGAGAAAGAGAGAGGAAGCGTCGTAAGGTAAAAAAGAAGAAAAAGAAGGCAATGAAAACAAAAAAGAAGAAGAAGATATCTTCCGGTAAGCGGTCAGAGCCAGAGGAAGGTGATGTTGAAGCAGAC[A/T]GAGATGGAGAGGGGGATGGGGATAGAGAAGGAGAGTACTCATCATTTTCTACTCAGCATCGCAGTGCATTTGTGGACAAAGGCAGCCTTTCAGCTTGGGAAGGAGAGAGAGAACGAGTGAGGAGAGATGGAGGTGAAGATGATGGGGATGAAAGAGAGGATGAGAGTGGGGGAGGCAGAGGTAGAGAGAGAAGACCCAAAAGCTCCCATTCGCGGCATAGACCTTCCAGTAAACGCTATCCTAACCTTAACAAACTCCCCTCTTCAGTCAAATTCTGGGTTAGTGGAGGAGAGGCAGGTGGCACGGAGGCCTCCGGACCCTCCCCTCCCTCATCTTTACATACTCTCCTCTCTTCGTCCAAGAGACGGAGGAGTAGTGGGACAGAGAGAGAGGCAGAAGGGAGAGTAGGAGAGCGCCGACCACTGCTTCTCCACTACGAAAGAGGGCGAGTTAGCACAAGAGAAGGACTGTCCTTTCATGAGTGGGACTCTGAGGATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32078
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 |
---|---|---|---|---|---|
ENSDART00000103882 | Nonsense | 1503 | 1959 | 14 | 14 |
ENSDART00000144062 | None | None | 1016 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14931940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13290399 |
GRCz11 | 16 | 13180519 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGTGAAGATGATGGGGATGAAAGAGAGGATGAGAGTGGGGGAGGC[A/T]GAGGTAGAGAGAGAAGACCCAAAAGCTCCCATTCGCGGCATAGACCTTCC
Long Flanking Sequence:
GAAGTCAACTAGCACAGCTCCAGGAATGGTGGGCAGGATGGGCAGAAAGAGAGAGGGACAGGGAGAGGAGTGGTGGAGCTCAAGGAGAAACAGAAAGGAAAAGAGAGAAGAAACGTAGGAAAGACAGGGAAAAGGAGAAAAAGAAGAAGAAGAAGAAAAACAAAAAAAGGAAAAAGAGGGAGGAGCGTGAAAGGGAAAGAGAAAGAGAGAGGAAGCGTCGTAAGGTAAAAAAGAAGAAAAAGAAGGCAATGAAAACAAAAAAGAAGAAGAAGATATCTTCCGGTAAGCGGTCAGAGCCAGAGGAAGGTGATGTTGAAGCAGACAGAGATGGAGAGGGGGATGGGGATAGAGAAGGAGAGTACTCATCATTTTCTACTCAGCATCGCAGTGCATTTGTGGACAAAGGCAGCCTTTCAGCTTGGGAAGGAGAGAGAGAACGAGTGAGGAGAGATGGAGGTGAAGATGATGGGGATGAAAGAGAGGATGAGAGTGGGGGAGGC[A/T]GAGGTAGAGAGAGAAGACCCAAAAGCTCCCATTCGCGGCATAGACCTTCCAGTAAACGCTATCCTAACCTTAACAAACTCCCCTCTTCAGTCAAATTCTGGGTTAGTGGAGGAGAGGCAGGTGGCACGGAGGCCTCCGGACCCTCCCCTCCCTCATCTTTACATACTCTCCTCTCTTCGTCCAAGAGACGGAGGAGTAGTGGGACAGAGAGAGAGGCAGAAGGGAGAGTAGGAGAGCGCCGACCACTGCTTCTCCACTACGAAAGAGGGCGAGTTAGCACAAGAGAAGGACTGTCCTTTCATGAGTGGGACTCTGAGGATGAGGACGAGGAAAGAGAAGAAGAAGAGAGAGAACGAGAGAGGGAGAGAATAGAGGAGAGAGTACGGCGGGCAGGGCGAGGGGCAGTGTCAGAGTCAGAACGAGACAGAATAAGAGCAGAGGAAAGCTTTTCTGATGAGGGGTCCTCAGGAGAATTTGGCTGTTTTGAGAGATATTGGGAG
Associated Phenotype:
Not determined