ZMP
slc35c2
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 35 member C2 [Source:RefSeq peptide;Acc:NP_997808]
Human Orthologue:
COL20A1
Human Description:
collagen, type XX, alpha 1 [Source:HGNC Symbol;Acc:14670]
Mouse Orthologue:
Col20a1
Mouse Description:
collagen, type XX, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1920618]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37676 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37677 | Nonsense | Available for shipment | Available now |
sa37678 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10366 | Nonsense | Available for shipment | Available now |
sa18513 | Nonsense | Available for shipment | Available now |
sa45794 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24303 | Missense, Nonsense | Available for shipment | Available now |
sa43958 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37676
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 |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 341 | 1816 | 10 | 51 |
ENSDART00000102963 | Nonsense | 341 | 1816 | 10 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 341 | 1897 | 10 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20739763)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20524870 |
GRCz11 | 23 | 20451213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACTAACACATTCACGATGGCCCACATCTCTCCTCTCGTCCTCCCAGAG[C/T]GAATGACAATCTTCCTGGTGACTGTTCTCCTGATACTGGTTTCTGAAGTT
Long Flanking Sequence:
CTTTGTTCTGTTGTAGAAAATAAATTAATTCTCTACAATTTGTTGTTTTTTAGTAAGATTATTTTGTGGATTCATATGTAATTGTGTAATTGGAACAAACTATTTGTAAAATTTTAATCTCTCTTTCTCTTTATTAAAATATATTAAAGGGTCAAGTAGCTTTCTTAGCCGGAAACAGAAAACAGCAGTCCACATTTAGCTCCCTTTGTGAGACTGAAATGCATTACCTTTTTTTCCATTAATTGAGGGAGAAGTGTAGCATTTTGTGTCGTTAAATTACTCCTGGTCCAATTTAATATTCAGATAATTAAAGAAAAAAAAAACAGCTATATGGTGCCAACTTCCATAATTACTCTTTATATTATGTTGATGACCTCTTCTTTGATGGTTTAGTGAAAATGAGTTGCACTCATTTTGTTTCGACCATTTTTTCTACAGGTTTTTTAATTGGTACTAACACATTCACGATGGCCCACATCTCTCCTCTCGTCCTCCCAGAG[C/T]GAATGACAATCTTCCTGGTGACTGTTCTCCTGATACTGGTTTCTGAAGTTCAAACACAAGGTAATATGCTGCCATTTTAGCTGTTTTTTAAATATTTACCAATACACTTTTTCTGGATAATGTCAAAAATGATCTTTACTATTACGAGAACTGAAAAAGGCTAATATATAAAACTTGATAAAGCTGTGGATGTCATTCAGTTTAATCACACATTTATTGTGAAATTAAACAGAGACTTTCTTACCATTTATTTTGTTGTGATTTGGTGATTTTTGAAGAACAATTTTTTTTTTACAAAACCTTTTATTTAAAGGTAACTGTTGGTGTTTTCCCATAATACAACAAAGAACAAAACCATTCAGAATATACAGTGTACAGTTTGGTACAGTGCAACCACTAGGATATTGTTTACATTTTAGACAAGTCAAGTTGCAATATCAAACAGGATCACATGAGATGCCCAAAACCCTAAAACAGACACCTTGACTTGATGGCATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37677
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 733 | 1816 | 18 | 51 |
ENSDART00000102963 | Nonsense | 733 | 1816 | 18 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 733 | 1897 | 18 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20767496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20552603 |
GRCz11 | 23 | 20478946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCAGAGTTGAGGCAGGTGGCGTCTGAACCTCTGGAGCTGAATGTGTA[T/G]AAGGTGAATGATTTTCCTCTGCTCAGTAAACTGGTGGGAAAACTAGCACG
Long Flanking Sequence:
GTTTAGTTTCAAGTGTTGTTGACTCATTTAAAAGTACAAATTTCAAGCTTATTTGTATATATTTCTTATGTCTGTGAAGCAAGTATTCGCTGAGATTGCAGTGTGTTTGTTGACCACAAAAACTGTTGTAAAAGCACACGCCTGGTCCAAGATTCTCCTCTGGAGAAACATCAGTCTATAGCGATCAATGATTGGTTCTTGTTTTAGTAGGCGGGGCTTCATTCGCAATATTGACCATTACATTTTTCACCATTCAAAACTGTATGAGTGACATATCTTGTGTATTCTATAGTTTTCGCTATTACATACACTACAGGCCATACCATATAAATAGAGAATTTAAAGCCCAATATTTGGAATATAAAAGCCCAACTTTATTGTGTTTTTTTTTTATCTAAGTTTTCTGTTTGTTTGCTTGTTTGCTCTTGTCCAGGTGTGAAAAATGCAGATGAGGCAGAGTTGAGGCAGGTGGCGTCTGAACCTCTGGAGCTGAATGTGTA[T/G]AAGGTGAATGATTTTCCTCTGCTCAGTAAACTGGTGGGAAAACTAGCACGCATCCTCTGTGGCAAGATTGAAGACCGTATTAAAGCCAAGAGTAGGTCAATCACAAATTTGTTTTCATTAAATTGGCGAATCTGTACCGTACACTCACATTAAAACTAAAAACTGTGTCTTTTGTGAGAAGGAATGGAGCATCCAACTCAGGAACCAGTTCTGTCATTTCCCAGCCCAACTGATCTGCAGTATGTAGGACTGGGCTCCAGAGAGTTGCGTCTGCGCTGGACCGTCCCCAGCAGAAATCCCCAGCAATACAGAGTGGTTTACCACACCGCTGAAGGACAGAGCCTTAATGAGGTGAGACGGAGGTCTAGCATTATCATGGACATTATTTGGTGTTATTTCTCTCACTATTTATTCAATCATGAGCTTTTAAATGCTGCATTTTTACATTTAAATTCTAGTATGTGCTGTGTTATCTTGTCCATATAATGTGCTAGCTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37678
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 |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 805 | 1816 | 19 | 51 |
ENSDART00000102963 | Nonsense | 805 | 1816 | 19 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 805 | 1897 | 19 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20767800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20552907 |
GRCz11 | 23 | 20479250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCAGAGAGTTGCGTCTGCGCTGGACCGTCCCCAGCAGAAATCCCCAG[C/T]AATACAGAGTGGTTTACCACACCGCTGAAGGACAGAGCCTTAATGAGGTG
Long Flanking Sequence:
CATACACTACAGGCCATACCATATAAATAGAGAATTTAAAGCCCAATATTTGGAATATAAAAGCCCAACTTTATTGTGTTTTTTTTTTATCTAAGTTTTCTGTTTGTTTGCTTGTTTGCTCTTGTCCAGGTGTGAAAAATGCAGATGAGGCAGAGTTGAGGCAGGTGGCGTCTGAACCTCTGGAGCTGAATGTGTATAAGGTGAATGATTTTCCTCTGCTCAGTAAACTGGTGGGAAAACTAGCACGCATCCTCTGTGGCAAGATTGAAGACCGTATTAAAGCCAAGAGTAGGTCAATCACAAATTTGTTTTCATTAAATTGGCGAATCTGTACCGTACACTCACATTAAAACTAAAAACTGTGTCTTTTGTGAGAAGGAATGGAGCATCCAACTCAGGAACCAGTTCTGTCATTTCCCAGCCCAACTGATCTGCAGTATGTAGGACTGGGCTCCAGAGAGTTGCGTCTGCGCTGGACCGTCCCCAGCAGAAATCCCCAG[C/T]AATACAGAGTGGTTTACCACACCGCTGAAGGACAGAGCCTTAATGAGGTGAGACGGAGGTCTAGCATTATCATGGACATTATTTGGTGTTATTTCTCTCACTATTTATTCAATCATGAGCTTTTAAATGCTGCATTTTTACATTTAAATTCTAGTATGTGCTGTGTTATCTTGTCCATATAATGTGCTAGCTTTTTGATGCAGCAAAAATATTTCTTTTAATTTGATTACATTGCTTAGCATAATATCTCACTGCTTAAGTATTTATTAACAATATGTATTTAAATATTGTTTTGAGAGTTGTGTTTTAAAACTGTATATAATGTTGTTCAAAACAAAAAGAATGAGGATTTTCAGGGCCTGAGGTTTCAGAGCTTGAAAAGCAGTTTCCTGTAGAGTAGAATGAGTTTTTCAAGCTCCCTCAGGTCACTTGATTTTTACTTGAAACTAAATTAAAAGTTTTGTAAAAAGGAATATTAAATGTTGCGGGGAAATACCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10366
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 |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 1051 | 1816 | 25 | 51 |
ENSDART00000102963 | Nonsense | 1051 | 1816 | 25 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 1051 | 1897 | 25 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
ENSDART00000054641 | Nonsense | 1051 | 1816 | 25 | 51 |
ENSDART00000102963 | Nonsense | 1051 | 1816 | 25 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 1051 | 1897 | 25 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20776106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20561213 |
GRCz11 | 23 | 20487556 |
KASP Assay ID:
2261-7594.1 (used for ordering genotyping assays)
KASP Sequence:
AGACTGCTGCTCACATGTGTTTGATCTTTCAGTRAGGGTTCCAGCTCCAT[C/A]AGATCTGAGGGTCACTAACTTCACCGGCAGTGAGATAACAGTACGATGGG
Long Flanking Sequence:
TTGTTAAGCCTTTAAATTGCGCTTTAAGCTGAATACTAGCATCTTGTAAAATACGATGTGCTGTCATCATGGCAATGACAAAAGAAATGAGATGTTATAAATTATTTATTAAAATTATTACCTTTAAAAATGTGATGACAGACTCTCTCTATTAAACAGCACTTGGGAAATATTAGGAAAAGAAATGCAATATTTATTTAAATAATCTAATAATTTTGTCTTCCAATGTATATTAGATGTTCTACCCAAACATCATTGTGCATAGTTATCTGTATTTCTCAGGTGGAAGTCAGAGGTGTGAACACAGTGTTGCTGCAGAATCTGTCATCCCTCTCCAGGTATCTCGTGTCAGTCCATTCACTCTACGAGAAGGGCCTGTCCAGCCCGGTCACGGCCAATGTTACTACCTGTAAGTCTGTGACGCATATAACTCTGTGACTCTGATTTGGAAGACTGCTGCTCACATGTGTTTGATCTTTCAGTAAGGGTTCCAGCTCCAT[C/A]AGATCTGAGGGTCACTAACTTCACCGGCAGTGAGATAACAGTACGATGGGAAGCTGCAGCTGATGATGTGGTCTTTTATCTCATCAAATGGATCTCGCTCAATGGAGGAGACCTCAGCCAGGTTAGCTCCAACTCAAGTACTTCCTGTGTTCAGTCAAGATTGAAATTCAGTGGTGATCAAATCATCATTTTTTCTGTCGTCTTGTTCAATTTGTCTTACATGAACGACTAAACATTGGGGGACTTGAAATGTCAGATTTGCAATGGCTAGATTCTCTTATTATAAAAAGGAAATCATCTCTCTTTGGATTTAATCTGGACAGCATGCTTTTAAAGGGTTTAATTTATTTTAAAACAGCTCGTCCACTTACAAAGTCGGTAAAAACTGGAAAGTTTAGCCTGTGTCACACTAAAGATTGAGTATGTGGAATTTGGTCAGATGGTGCTCCGAATATAGGCTGGATAATTTGCTTTTTATTTGAAATTTCTAGCACGTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18513
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 |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 1051 | 1816 | 25 | 51 |
ENSDART00000102963 | Nonsense | 1051 | 1816 | 25 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 1051 | 1897 | 25 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
ENSDART00000054641 | Nonsense | 1051 | 1816 | 25 | 51 |
ENSDART00000102963 | Nonsense | 1051 | 1816 | 25 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 1051 | 1897 | 25 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20776106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20561213 |
GRCz11 | 23 | 20487556 |
KASP Assay ID:
2261-7594.1 (used for ordering genotyping assays)
KASP Sequence:
AGACTGCTGCTCAYATGTGTTTGATCTTTCAGTRAGGGTTCCAGCTCCAT[C/A]AGATCTKAGGGTCACTAACTTCACCGGCAGTGAGATAACAGTACGATGGG
Long Flanking Sequence:
TTGTTAAGCCTTTAAATTGCGCTTTAAGCTGAATACTAGCATCTTGTAAAATACGATGTGCTGTCATCATGGCAATGACAAAAGAAATGAGATGTTATAAATTATTTATTAAAATTATTACCTTTAAAAATGTGATGACAGACTCTCTCTATTAAACAGCACTTGGGAAATATTAGGAAAAGAAATGCAATATTTATTTAAATAATCTAATAATTTTGTCTTCCAATGTATATTAGATGTTCTACCCAAACATCATTGTGCATAGTTATCTGTATTTCTCAGGTGGAAGTCAGAGGTGTGAACACAGTGTTGCTGCAGAATCTGTCATCCCTCTCCAGGTATCTCGTGTCAGTCCATTCACTCTACGAGAAGGGCCTGTCCAGCCCGGTCACGGCCAATGTTACTACCTGTAAGTCTGTGACGCATATAACTCTGTGACTCTGATTTGGAAGACTGCTGCTCACATGTGTTTGATCTTTCAGTAAGGGTTCCAGCTCCAT[C/A]AGATCTGAGGGTCACTAACTTCACCGGCAGTGAGATAACAGTACGATGGGAAGCTGCAGCTGATGATGTGGTCTTTTATCTCATCAAATGGATCTCGCTCAATGGAGGAGACCTCAGCCAGGTTAGCTCCAACTCAAGTACTTCCTGTGTTCAGTCAAGATTGAAATTCAGTGGTGATCAAATCATCATTTTTTCTGTCGTCTTGTTCAATTTGTCTTACATGAACGACTAAACATTGGGGGACTTGAAATGTCAGATTTGCAATGGCTAGATTCTCTTATTATAAAAAGGAAATCATCTCTCTTTGGATTTAATCTGGACAGCATGCTTTTAAAGGGTTTAATTTATTTTAAAACAGCTCGTCCACTTACAAAGTCGGTAAAAACTGGAAAGTTTAGCCTGTGTCACACTAAAGATTGAGTATGTGGAATTTGGTCAGATGGTGCTCCGAATATAGGCTGGATAATTTGCTTTTTATTTGAAATTTCTAGCACGTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45794
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 |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 1722 | 1816 | 45 | 51 |
ENSDART00000102963 | Nonsense | 1722 | 1816 | 45 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 1722 | 1897 | 45 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20796026)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20581133 |
GRCz11 | 23 | 20507476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATGTTATTTTTCCCTTTTCAAAGGGTCTTCCTGGAAGTAAAGGTGAA[C/T]GAGGAGAGAAGGTGTGTTACAAAATGGCATGTCTAAGGAATACAAACCTT
Long Flanking Sequence:
TAAAATGGATCCATTACTACACACTAGTTAGGACTAAAAATGTTGTTGCTGGAGATTTAAACTAAAACGTCAACAAAGGTGTCCTGTGTTGCCATGTCCAATCATTATCCACGCAAGCATCTTTACAGATAAGAGATGCTTTACTTTAGTAGTTTCTTAATTTTAAGATTTAATGCTATTATTAATTTAAACTAGCTTGTTGTAGGTTAAAACATTTGTGCTCTTTTGTTTTTCTAGCAAGATCTGGTAATACTGATAAAAACATCCCTCATTTATTGTGATGTCTTGCACTGTGAAAACAGAAGAAAGGGCCAGCCCTGATAAACAATTTAATGTTTCATCTAGCTGTTTATTTAGAAGGCTTCTGTACACACTGTACTGAATTTTGTGAAAGTAGTAGAGAATTTTTTGTTTATATAATTTTAAAAAATGATGTAGAAATTGGTAAATCACATGTTATTTTTCCCTTTTCAAAGGGTCTTCCTGGAAGTAAAGGTGAA[C/T]GAGGAGAGAAGGTGTGTTACAAAATGGCATGTCTAAGGAATACAAACCTTAAAAGAGGTAGTTTTGTTTCGTTGGTTTTAATTCTCTTTCTGTTTATTAGGGCGAGCCACAGTCTCTTGCAATGATCTACCAGCTTGTTTCACAGGCCTGTGAAAAGCTTGTCCACAGTATGTACTACATTACCTACATCCATTTTAATTACAGTAAAGCAGAATTTAAAAGCATCTTTAAATGTAAATCTTGGCCTGAGTAAGAGCCCTTCAATTATCAATTGTGTTATCTTAATTAATTGTGTTCTAGATGAAGTGCTGAAGATGGATGCTTTTCTAAACGAGCTGAATCGGAAGCCAGTGCCCATCCAGGAGCCAGTAGCACCTCCCGGAGAGCCGGGCATACCAGGGGGAAGAGGGGCACCCGGACCCCGGGGCCCTCAGGGTCGACTGGGAAGCAGAGGGATGCCTGGGAAACCTGGTTATCCTGGAGAGCAAGGTAACCCTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24303
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054641 | Nonsense | 1807 | 1816 | 48 | 51 |
ENSDART00000102963 | Nonsense | 1807 | 1816 | 47 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Missense | 1808 | 1897 | 47 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20796507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20581614 |
GRCz11 | 23 | 20507957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGGTCGACTGGGAAGCAGAGGGATGCCTGGGAAACCTGGTTATCCTG[G/A]AGAGCAAGGTAACCCTTGATACTTGCATTTCTTTGGAGATGCAGGCAAAC
Long Flanking Sequence:
TCCTGGAAGTAAAGGTGAACGAGGAGAGAAGGTGTGTTACAAAATGGCATGTCTAAGGAATACAAACCTTAAAAGAGGTAGTTTTGTTTCGTTGGTTTTAATTCTCTTTCTGTTTATTAGGGCGAGCCACAGTCTCTTGCAATGATCTACCAGCTTGTTTCACAGGCCTGTGAAAAGCTTGTCCACAGTATGTACTACATTACCTACATCCATTTTAATTACAGTAAAGCAGAATTTAAAAGCATCTTTAAATGTAAATCTTGGCCTGAGTAAGAGCCCTTCAATTATCAATTGTGTTATCTTAATTAATTGTGTTCTAGATGAAGTGCTGAAGATGGATGCTTTTCTAAACGAGCTGAATCGGAAGCCAGTGCCCATCCAGGAGCCAGTAGCACCTCCCGGAGAGCCGGGCATACCAGGGGGAAGAGGGGCACCCGGACCCCGGGGCCCTCAGGGTCGACTGGGAAGCAGAGGGATGCCTGGGAAACCTGGTTATCCTG[G/A]AGAGCAAGGTAACCCTTGATACTTGCATTTCTTTGGAGATGCAGGCAAACTCTGATGGTTTTTTACTTGTATCATGTAAGTAATTCTGGGATTAACATCTAGGACGCAGAGGCATGGCTGGTGAGAAGGGCTCTCCCGGAGCAAATGCAGTGGGACCACAGGGAATGAAGGGTTTTGGAGGTAAAAATGTCTTGTATATCACATAGCTGTCTTCACTTTTTTATTTTTTATTATTAGTTTAACATTTTTAGATTTTCCTGTAACAAATGTGACAAAAACATTGCACATTTCTATCATCTTAATCTGTATTTTATCTCATTTTGTAACAAATTTCTTACCATATTTAAACAATATAGCGCTCAGATGCACAATTGCATTGTAGTAATATTGTTTGAAATGTTAAGTACAATTTTTATTTATTTTTTTATTTGTAAGTTTCTTTAAGTTTTAAGTCCTCTGCTAACCAAGACTGCATTTATTTGAAAATGAATTAATAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43958
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054641 | None | None | 1816 | 50 | 51 |
ENSDART00000102963 | None | None | 1816 | 49 | 50 |
ENSDART00000109899 | None | None | 362 | None | 10 |
ENSDART00000132920 | Nonsense | 1883 | 1897 | 49 | 50 |
ENSDART00000140219 | None | None | 187 | None | 6 |
The following transcripts of ENSDARG00000037517 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 20798251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 20583358 |
GRCz11 | 23 | 20509701 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGGGAGAAATGGGACCCTCGGGTGTTTGTGACAGCAGTGGATGTTA[T/A]CAAGGGCCTCCTGCAGGTGAAAAAAAAAGCTATCCCAGATATTATTAAAG
Long Flanking Sequence:
CAGGTGTCCTGCAGGTTTTAACTCCAACTTGCCTCAAAACTCCTGCCTGGATGTTTCTAGAAAGTCTAGTAAGAGCTTGATTAGCTAGCCCAAGTATCTCTGATTGGGGTTTGAACTAAACTTTTGCAGGACATCTGAACTCTAGGACCGAGTTTGGCCACCCCTGGTTTAAAGAATGGCACACGTCATTGCCCTTGCTCGAGAGTATCTCAACTGGGCATGTGCTGTTGAAAATGTTTTTCATCACTTGTTTTCCTGTCCATGAAGAATATCCACTCTTTTATTACTGAGTGAGACCTGATGTATTTCTAGTATTTTAAGTGCTAACTAAGTGTGCCTTCATTTATTTCCACTTCACCAGGACCTCCAGGTGAAGCTAAAATAGGGGAACCAGGTCCCAAAGGTGAGGATGGTAAAGCAGGACCTACAGGTATTCCTGGAGCTGCAGGTCAACAGGGAGAAATGGGACCCTCGGGTGTTTGTGACAGCAGTGGATGTTA[T/A]CAAGGGCCTCCTGCAGGTGAAAAAAAAAGCTATCCCAGATATTATTAAAGGTCCAGTGAAGTGCTTTGAAATGTGCATTTTTATTAACAGTGTGACATAATCTCAACTGAAACAGGAACACAGGGCGGGACATAGAGTAGCCCCTTTTCCCCTTTTCAAAAACAGCCAATAGCATTTTGTTTGCATCATATCTCTGCTAATCAGAGCTGTTGAGCTCATGCTCATCAGACTCATGACAGAATATAATAGTAATACTGAGTCTGACTCACTCTTACTCTACGTTAAAATAGTTTTCTGCGTGATTTAAGTGGATTGAAGCGGTTCTCATCACATTAACATGAAAGCAGACTTCATGCACCCTAAAGGAAATCATATTTACGCTGTCTGTATCCCTATATGGTACTATTCACCAAGTAAAACTGGATTTTAAATCTTTGTTAAATCTCTTCAGATCTCTTGCTGAGTTTGTAGGTGTGTGTGTGAATAAATGACCAATTTCA
Associated Phenotype:
Not determined