ZMP
rev3l
Ensembl ID:
ZFIN ID:
Human Orthologues:
KIAA2022, REV3L
Human Descriptions:
KIAA2022 [Source:HGNC Symbol;Acc:29433]
REV3-like, catalytic subunit of DNA polymerase zeta (yeast) [Source:HGNC Symbol;Acc:9968]
REV3-like, catalytic subunit of DNA polymerase zeta (yeast) [Source:HGNC Symbol;Acc:9968]
Mouse Orthologues:
C77370, Rev3l
Mouse Descriptions:
REV3-like, catalytic subunit of DNA polymerase zeta RAD54 like (S. cerevisiae) Gene [Source:MGI Symb
expressed sequence C77370 Gene [Source:MGI Symbol;Acc:MGI:2148050]
expressed sequence C77370 Gene [Source:MGI Symbol;Acc:MGI:2148050]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25129 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19224 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11025 | Nonsense | Available for shipment | Available now |
sa32271 | Nonsense | Available for shipment | Available now |
sa36949 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43372 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32270 | Essential Splice Site | Available for shipment | Available now |
sa19223 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11290 | Nonsense | Available for shipment | Available now |
sa44931 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36948 | Essential Splice Site | Available for shipment | Available now |
sa43371 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25129
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 377 | 2953 | 10 | 32 |
ENSDART00000136987 | Nonsense | 47 | 2623 | 2 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3420262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3363916 |
GRCz11 | 20 | 3381417 |
KASP Assay ID:
554-7709.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTCTTCTCATCATATAGATACAAAAAGGGACAGTAGAAAAGATGAC[G/T]AAGTAGCAGTTGTTGATGAAGAGGCCATTTTGAGCATGTTGGAAAATAGT
Long Flanking Sequence:
ACAAACGGTTGTGATGTTTTGTGGATGTTCCCAGCTATGCTGACCAAGTCTATTCAAAATCTAAGATTTCAAGGACAAACGTTAAATCTTTCGCTCACGAGTCTGCTGTTGTGAAGAAGCTCAGCAGCAGAGAGAAAACTAGCACTGTTTAGCAGCTGTTGAACTCGTGCTCTCACACAACAGTGAAAGGACGGCTCTGGCAACTCCCATTCATAGCAGTTCCTGTAGTTACTACTGATGTTTGAGGGAAGCACATTTATTTTGAACTATGATAAAAAATCTGACTGGAACTACCAGTACAGTTTAACAAATCCATTGCACACTCGCCAACCTATCAGAGTCAAGAACTTTAACAGACCATGGAATAATACAGTATATGTATGGAGTCTGTTTGAGACTGTACAGTGAAACTTACAATTGGTCTCTGACTGTATTGAAAATAATGACCTTGTTTTTCTTCTCATCATATAGATACAAAAAGGGACAGTAGAAAAGATGAC[G/T]AAGTAGCAGTTGTTGATGAAGAGGCCATTTTGAGCATGTTGGAAAATAGTCAGTCTTTCCTCCAGCTCTCTCAGACATCCAGCCAATCAGCAATATTTGGTATGTGCATTGTTACAAGAAATATAACATTGATTTCCGAAAAAAAAGAAGCTAAAAGCGTTTACACTGTAGGATATTAATCAAGGTTTTAATACATTTTTGAGTAAAAAGGTGAAGTCTTAGTTAAAAGATTTGTTTTTCTTGAACTAAAATTGTGAGATGCAATGTGTTTACGTACGTTTTCATAATTTTAGTTTTTTCCTATTGTTTACTCTTTAGTTATATGCCCAGAATTACATTTTGTAGATGTAAAAAAAAAGAGTTTATTTGTAATGTATTTGATATTATACTGGAAAATAACAAAATGTTTTCTTTTTTGCATTTATGATTTTGTCAATTATAACCTTTGCTTATTCATAATATTTTTTGTATGTGTTCTGATATATGCTATTTAATACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19224
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 394 | 2953 | 10 | 32 |
ENSDART00000136987 | Nonsense | 64 | 2623 | 2 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
ENSDART00000092264 | Nonsense | 394 | 2953 | 10 | 32 |
ENSDART00000136987 | Nonsense | 64 | 2623 | 2 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3420211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3363865 |
GRCz11 | 20 | 3381366 |
KASP Assay ID:
2261-3903.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTAGCAGTTGTTGATGAAGAGGCCATTTTGAGCATGTTGGAAAATAGT[C/T]AGTCTTTCCTCCAGCTCTCTCAGACATCCAGCCAATCAGCAATATTTGGT
Long Flanking Sequence:
ATTCAAAATCTAAGATTTCAAGGACAAACGTTAAATCTTTCGCTCACGAGTCTGCTGTTGTGAAGAAGCTCAGCAGCAGAGAGAAAACTAGCACTGTTTAGCAGCTGTTGAACTCGTGCTCTCACACAACAGTGAAAGGACGGCTCTGGCAACTCCCATTCATAGCAGTTCCTGTAGTTACTACTGATGTTTGAGGGAAGCACATTTATTTTGAACTATGATAAAAAATCTGACTGGAACTACCAGTACAGTTTAACAAATCCATTGCACACTCGCCAACCTATCAGAGTCAAGAACTTTAACAGACCATGGAATAATACAGTATATGTATGGAGTCTGTTTGAGACTGTACAGTGAAACTTACAATTGGTCTCTGACTGTATTGAAAATAATGACCTTGTTTTTCTTCTCATCATATAGATACAAAAAGGGACAGTAGAAAAGATGACGAAGTAGCAGTTGTTGATGAAGAGGCCATTTTGAGCATGTTGGAAAATAGT[C/T]AGTCTTTCCTCCAGCTCTCTCAGACATCCAGCCAATCAGCAATATTTGGTATGTGCATTGTTACAAGAAATATAACATTGATTTCCGAAAAAAAAGAAGCTAAAAGCGTTTACACTGTAGGATATTAATCAAGGTTTTAATACATTTTTGAGTAAAAAGGTGAAGTCTTAGTTAAAAGATTTGTTTTTCTTGAACTAAAATTGTGAGATGCAATGTGTTTACGTACGTTTTCATAATTTTAGTTTTTTCCTATTGTTTACTCTTTAGTTATATGCCCAGAATTACATTTTGTAGATGTAAAAAAAAAGAGTTTATTTGTAATGTATTTGATATTATACTGGAAAATAACAAAATGTTTTCTTTTTTGCATTTATGATTTTGTCAATTATAACCTTTGCTTATTCATAATATTTTTTGTATGTGTTCTGATATATGCTATTTAATACATTCAAGTTCATCCTAATAGTGTCGACTCTGTTCTAACAGACGGCAGTCAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11025
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 394 | 2953 | 10 | 32 |
ENSDART00000136987 | Nonsense | 64 | 2623 | 2 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
ENSDART00000092264 | Nonsense | 394 | 2953 | 10 | 32 |
ENSDART00000136987 | Nonsense | 64 | 2623 | 2 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3420211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3363865 |
GRCz11 | 20 | 3381366 |
KASP Assay ID:
2261-3903.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTAGCAGTTGTTGATGAAGAGGCCATTTTGAGCATGTTGGAAAATAGT[C/T]AGTCTKTCCTCCAGCTCTCTCAGACATCCAGCCAATCAGCAATATTTGGT
Long Flanking Sequence:
ATTCAAAATCTAAGATTTCAAGGACAAACGTTAAATCTTTCGCTCACGAGTCTGCTGTTGTGAAGAAGCTCAGCAGCAGAGAGAAAACTAGCACTGTTTAGCAGCTGTTGAACTCGTGCTCTCACACAACAGTGAAAGGACGGCTCTGGCAACTCCCATTCATAGCAGTTCCTGTAGTTACTACTGATGTTTGAGGGAAGCACATTTATTTTGAACTATGATAAAAAATCTGACTGGAACTACCAGTACAGTTTAACAAATCCATTGCACACTCGCCAACCTATCAGAGTCAAGAACTTTAACAGACCATGGAATAATACAGTATATGTATGGAGTCTGTTTGAGACTGTACAGTGAAACTTACAATTGGTCTCTGACTGTATTGAAAATAATGACCTTGTTTTTCTTCTCATCATATAGATACAAAAAGGGACAGTAGAAAAGATGACGAAGTAGCAGTTGTTGATGAAGAGGCCATTTTGAGCATGTTGGAAAATAGT[C/T]AGTCTTTCCTCCAGCTCTCTCAGACATCCAGCCAATCAGCAATATTTGGTATGTGCATTGTTACAAGAAATATAACATTGATTTCCGAAAAAAAAGAAGCTAAAAGCGTTTACACTGTAGGATATTAATCAAGGTTTTAATACATTTTTGAGTAAAAAGGTGAAGTCTTAGTTAAAAGATTTGTTTTTCTTGAACTAAAATTGTGAGATGCAATGTGTTTACGTACGTTTTCATAATTTTAGTTTTTTCCTATTGTTTACTCTTTAGTTATATGCCCAGAATTACATTTTGTAGATGTAAAAAAAAAGAGTTTATTTGTAATGTATTTGATATTATACTGGAAAATAACAAAATGTTTTCTTTTTTGCATTTATGATTTTGTCAATTATAACCTTTGCTTATTCATAATATTTTTTGTATGTGTTCTGATATATGCTATTTAATACATTCAAGTTCATCCTAATAGTGTCGACTCTGTTCTAACAGACGGCAGTCAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32271
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 976 | 2953 | 13 | 32 |
ENSDART00000136987 | Nonsense | 646 | 2623 | 5 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3417768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3361422 |
GRCz11 | 20 | 3378923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTCAGTTCTGATGAAACTCACACAGTTTTAACACCGGAAAAGCTTGCT[G/T]GATATGAACAGCTTGCTCCTCTCAAAAAATTCTGGCCCAAAATTCCAGAG
Long Flanking Sequence:
CATTAGATCAAAAACGGGAACTTCCTGTAAAGACACATTCTCCTACGAAAGAAGAACCTCCAGCCCTTCTTTCCATCACTCCAGGCTCTCACAATCAGAACGAAGTGAGCAAGGAGGTTGACATGGAAACTTCAGGATCGTTAATTGAGAGTTCGGGAAAGGGCGATTTTGCAGATATTCCAACAAACATCTCTTGTACCAAGGTGGCAAGTTTGCCAGGCAGCAAATATACCTTGCGGACCAAAAGAAAAAGGATTTATGAAAAAGGAGATCATCCAAGATCTGGTTCCTCCAAACAAGCCTCAGTACATCATGATGACCCTAAAGGAAGTGATCATGTCTTCAGTCAAAAAAAGAGGAAAGTGACTAAAAAAGAGCCACCGGTTATCATCAAATACATAATCATTAACAGATTTAAAGGTCAGAAGAACATGTTAGTAAAGATTTCTAAAGTCAGTTCTGATGAAACTCACACAGTTTTAACACCGGAAAAGCTTGCT[G/T]GATATGAACAGCTTGCTCCTCTCAAAAAATTCTGGCCCAAAATTCCAGAGTCTACAGCAGAGAAGTACCCGTCGCTTGAGCCAAAAGTAAAGAAATGTCCCAAACGGAAAGCGAAGATCAACCCAGTGGTAAAAAGGATGACCACCTTCCCAAAATCCAAGTGTCCACGAGTTGGCCAGACTAGAGGGGAAAGGCGTGCTAAAGCAATGTTGCCTGTGCAAACATTAGCCCCTCCATGGCCTTCCTATAATGATTTTACAGATGACACTTGTACAGAGTATTGCGATGTCATGATGAAGTTGGGTTACTTGTCAGAAAGAGCCCCCAGTCCTACTGACTCAACCCCACCTAGATGTTGGTCTCCTACAGAGCACTTGCATGGATCAAATTCAAATGATCATTTTATAAATCCTCATAATGATCCATGTCTAGGTTCTTCTTGTGAAGCCCTGACTCCAAAACCATCCCAAAGTGGTCTTTTGAATAGAAGCAGAATGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36949
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 1208 | 2953 | 13 | 32 |
ENSDART00000136987 | Nonsense | 878 | 2623 | 5 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3417070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3360724 |
GRCz11 | 20 | 3378225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAAAGGCCAATGTTTGTAGATGTCACATCTACTTCTCAGAAAGGATG[G/A]ATGCGCAATGAGAAGCAATTACTTCAAAGAAAGCAGGATCATGGCAAGGG
Long Flanking Sequence:
GCTAAAGCAATGTTGCCTGTGCAAACATTAGCCCCTCCATGGCCTTCCTATAATGATTTTACAGATGACACTTGTACAGAGTATTGCGATGTCATGATGAAGTTGGGTTACTTGTCAGAAAGAGCCCCCAGTCCTACTGACTCAACCCCACCTAGATGTTGGTCTCCTACAGAGCACTTGCATGGATCAAATTCAAATGATCATTTTATAAATCCTCATAATGATCCATGTCTAGGTTCTTCTTGTGAAGCCCTGACTCCAAAACCATCCCAAAGTGGTCTTTTGAATAGAAGCAGAATGCAGAGACCTAAGAAGACTTCTGGGACCAGCCAAAAAAGAAAATCGAATAGCTTAACAACAGCAACAAACAAGGGTTCTCTGAAAACTGAGGATTCTAAATGGAAAAGTATTCCAGCAGCTTCAAGGAAGCATAAGAAATATTGTGATGGAATTGAAAGGCCAATGTTTGTAGATGTCACATCTACTTCTCAGAAAGGATG[G/A]ATGCGCAATGAGAAGCAATTACTTCAAAGAAAGCAGGATCATGGCAAGGGAAGCAATAATTCACAGGGCCTGAATTCATCTGACAATTTACCTGTTACTCAATTATCTGATTATCTAACTCCTTTCCAATGTCCCAGTTTTCTAAAAAGCAACCCGGAGGACCTTGCTCTCGGTTGTTCAGACTCTAAAACTGAGGTTCATAGTTTCTTTGATTCTATTGCTTCAAATAACTCTCAGAAAGACTTACGAATTGCTCCCAATTCCACTATTGAAAAGTCTTTTAGTATTCTTTCCCAACCCACAAAGACTGTAGGACATCCATGTTCTGTCATTACATATGGAAGTTCTAATTCAAAATCCAAAAATACAAGTCAGGATGGGACTAAAACAAAAAACCATGATGTCATATCAGTGGTCTCTGGCCATGAAGAAAGATCTGGTACTGTACAGCAATCACAGTTACCCATAACATCGAGAAGGCCGCAAGCGAGAAAGAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43372
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 1428 | 2953 | 13 | 32 |
ENSDART00000136987 | Nonsense | 1098 | 2623 | 5 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3416412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3360066 |
GRCz11 | 20 | 3377567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTAAGAATAGGGAAATGTGTGTTTTGAAGGAACTTCTCCAGAAGAGG[C/T]AGCTTAAGGAAGAACAGGAAGCAAATAAAAGTGATGGTTTGACTGAGGCG
Long Flanking Sequence:
AGGACCTTGCTCTCGGTTGTTCAGACTCTAAAACTGAGGTTCATAGTTTCTTTGATTCTATTGCTTCAAATAACTCTCAGAAAGACTTACGAATTGCTCCCAATTCCACTATTGAAAAGTCTTTTAGTATTCTTTCCCAACCCACAAAGACTGTAGGACATCCATGTTCTGTCATTACATATGGAAGTTCTAATTCAAAATCCAAAAATACAAGTCAGGATGGGACTAAAACAAAAAACCATGATGTCATATCAGTGGTCTCTGGCCATGAAGAAAGATCTGGTACTGTACAGCAATCACAGTTACCCATAACATCGAGAAGGCCGCAAGCGAGAAAGAAAGACACTGGGACAGCTTTATTGAAGCCTGTTGATTCTATATCTTCTCCTACTTCCTCTACTAAGAGTGCAGCTATATATGAATCAAACACAGATCTCACATTGTCCTCCGATTTTAAGAATAGGGAAATGTGTGTTTTGAAGGAACTTCTCCAGAAGAGG[C/T]AGCTTAAGGAAGAACAGGAAGCAAATAAAAGTGATGGTTTGACTGAGGCGGTTTCTTCCACCAGTCAAAATACTGATGTTGCCAAAAGGGCAAAATCTAAGAGAACTCTGTCATCACCATCAAGAAAACCAAGGGGTGCAAGAACAAAAGTGCAAACCAGATGTAAGAAAAATAAACAAGATGACCAGAGAAATGATTGTCTTTCCTCAGATGGCAGTCCTGTGTTTTTTTCTGATCCTGGCTTTGACAGCTGTTGCTCTGTTGAGGATAGCTTGTCCCCAGAACTTCCAGATAATTACAGATTTGATATCAATGTCATCGGCCAAACAGAGTTCTCCAGTCTTTATTCTGGTAACCAGTTTGTGTTAACTGACAAGATCTTGCCTCAGAAGTTCCTCAGTGATGTCAGTCAAGAGGCAGCGAATGCGCTGGTTGGGTTGGGGAACAGGACACAAAAGATGTTTGATGTTGATGATGACTTCAATCATGGAAACGATCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32270
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092264 | Essential Splice Site | 1757 | 2953 | 13 | 32 |
ENSDART00000136987 | Essential Splice Site | 1427 | 2623 | 5 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3415422)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3359076 |
GRCz11 | 20 | 3376577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGGAACCATTCTACAGTGACCCGTCAGATGTGCCATTGAAGCCAAGG[T/C]AAGGTACACAAGTCTGTGTTGTAATTTTTTCTTGTTTAAAAGTTGCATTT
Long Flanking Sequence:
GAAACGATCGGAATAAATCTGGTGCTCTTAGTCCAGAATTGTTTGATAAGGTGTCTTGTGAAAATGGCAGAGTTTTTCCCAATAAGGTATCCCTGTCTCTGCTGGATTCAGAAAAGATCTTTAGCACTAATTGGGCTGGTTCTTTAGGTAAAATTCATGGCCTCAGCCACTTTCGGGACTTTCACTGTGAGAAGAGAGATGTGCTGCTTGACCCAGAGCCCAAATCCCCCATTATGTCAGCTTCTTTTGCTTACGGTGTTTCCCCAAATAGTGATCTCCTAGATGGCAGTTCACTAACACCGAGCAGTTCACCACGGTCAATCAACTCTCTGTCTCAGCTGAAGACTTCAAGGACTGGTGGAACTCGCATTCTCAAACCTTTGATGTCTCCACCTGCTCGAGAAGAAATCTTAGCTAATTTGATGGATCTGGACTTTTCAGAAGCTACAAAACAGGAACCATTCTACAGTGACCCGTCAGATGTGCCATTGAAGCCAAGG[T/C]AAGGTACACAAGTCTGTGTTGTAATTTTTTCTTGTTTAAAAGTTGCATTTGCGTGGTTTTGGATTCAAGTGTCTGTTTATCTGTGTATTTTCAAGTTGGACTATGAAATTATCAAATAAAATAATAAGTAAACAGTCACTGTTTTTTCAGGGAGGTTGGTGGACGAAAGTTGATTTTGGAAACCAGGCAGGCAAGCAGACTAGTTGAATTCCATGGGGACTTATCTCAAAATGGTTTGCAGTTTTGGAAAGTCGCATTTTCTGCAATGACAAATCAGGCCTCTGCTCCAACTCAAGGATGTAAATCCTCCAAACTGATCAAGAACCAAAGCCCATCTTCTGTCAGTGACCCAAAAGTTATCATCCTTCCCTGCAAGTGTGCCCCTAGCCGAGAGCAGGTGCAGCTTTGGGCGCAGGCCAAAAAACAGTATGAGTGCCTTCAGAGAGGTAGGATACAAATGGGTGGCCATGAGATTTCAGAGCTGAAGCAGAGTACATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19223
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 1850 | 2953 | 14 | 32 |
ENSDART00000136987 | Nonsense | 1520 | 2623 | 6 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
ENSDART00000092264 | Nonsense | 1850 | 2953 | 14 | 32 |
ENSDART00000136987 | Nonsense | 1520 | 2623 | 6 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3414992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3358646 |
GRCz11 | 20 | 3376147 |
KASP Assay ID:
2261-3902.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCCTAGCCGAGAGCAGGTGCAGCTTTGGGCGCAGGCCAAAAAACAGTA[T/A]GAGTGCCTTCAGAGAGGTAGGATACAAATGGGTGGCCATGAGATTTCAGA
Long Flanking Sequence:
GGACTTTTCAGAAGCTACAAAACAGGAACCATTCTACAGTGACCCGTCAGATGTGCCATTGAAGCCAAGGTAAGGTACACAAGTCTGTGTTGTAATTTTTTCTTGTTTAAAAGTTGCATTTGCGTGGTTTTGGATTCAAGTGTCTGTTTATCTGTGTATTTTCAAGTTGGACTATGAAATTATCAAATAAAATAATAAGTAAACAGTCACTGTTTTTTCAGGGAGGTTGGTGGACGAAAGTTGATTTTGGAAACCAGGCAGGCAAGCAGACTAGTTGAATTCCATGGGGACTTATCTCAAAATGGTTTGCAGTTTTGGAAAGTCGCATTTTCTGCAATGACAAATCAGGCCTCTGCTCCAACTCAAGGATGTAAATCCTCCAAACTGATCAAGAACCAAAGCCCATCTTCTGTCAGTGACCCAAAAGTTATCATCCTTCCCTGCAAGTGTGCCCCTAGCCGAGAGCAGGTGCAGCTTTGGGCGCAGGCCAAAAAACAGTA[T/A]GAGTGCCTTCAGAGAGGTAGGATACAAATGGGTGGCCATGAGATTTCAGAGCTGAAGCAGAGTACATGTGACAGGAGCACAACTCAGAAGACCTCGAATTCGCTTTTCTCAGAGAATCATGATAAAAGGCCTGAAAAAAATTCAGAATCGCAACATAACAGTCGGAATGACTTCTGTTCACCCATCCATTTTTCACCAGTTAAAGCAGCTTCATCTGACAGTAGCCCTAGCAGTGTGAAATGTGTCCAGGACATTGACAAAACAAAAGATTGCCGGATTACTTCTCCTCCAAACTCACCTGAGATTTCTACATGGCAAGATAGCCCAGACGAGGTTGAGCAAGATGAGGATAAGGAGAATCTGACTGGGGGGTTGCAACCCCTCTCCATGGATCAAAATTTGAATGAGACGTTACTTGAAAATGCGGAGTCAAAAGATCACTTGAGTCCGTCATTTTTTGGAATTAAAGGCCTAGTTTCAGATGTCAGATGCTCGCACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11290
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 1850 | 2953 | 14 | 32 |
ENSDART00000136987 | Nonsense | 1520 | 2623 | 6 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
ENSDART00000092264 | Nonsense | 1850 | 2953 | 14 | 32 |
ENSDART00000136987 | Nonsense | 1520 | 2623 | 6 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3414992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3358646 |
GRCz11 | 20 | 3376147 |
KASP Assay ID:
2261-3902.1 (used for ordering genotyping assays)
KASP Sequence:
GCCCCTAGCCGAGAGCAGGTGCAGCTTWGGGCGCAGGCCAAAAAACAGWA[T/A]GAGTGCCTTCAGAGAGGTAGGATACAAATGGGTGGCCATGWGATTTCAGA
Long Flanking Sequence:
GGACTTTTCAGAAGCTACAAAACAGGAACCATTCTACAGTGACCCGTCAGATGTGCCATTGAAGCCAAGGTAAGGTACACAAGTCTGTGTTGTAATTTTTTCTTGTTTAAAAGTTGCATTTGCGTGGTTTTGGATTCAAGTGTCTGTTTATCTGTGTATTTTCAAGTTGGACTATGAAATTATCAAATAAAATAATAAGTAAACAGTCACTGTTTTTTCAGGGAGGTTGGTGGACGAAAGTTGATTTTGGAAACCAGGCAGGCAAGCAGACTAGTTGAATTCCATGGGGACTTATCTCAAAATGGTTTGCAGTTTTGGAAAGTCGCATTTTCTGCAATGACAAATCAGGCCTCTGCTCCAACTCAAGGATGTAAATCCTCCAAACTGATCAAGAACCAAAGCCCATCTTCTGTCAGTGACCCAAAAGTTATCATCCTTCCCTGCAAGTGTGCCCCTAGCCGAGAGCAGGTGCAGCTTTGGGCGCAGGCCAAAAAACAGTA[T/A]GAGTGCCTTCAGAGAGGTAGGATACAAATGGGTGGCCATGAGATTTCAGAGCTGAAGCAGAGTACATGTGACAGGAGCACAACTCAGAAGACCTCGAATTCGCTTTTCTCAGAGAATCATGATAAAAGGCCTGAAAAAAATTCAGAATCGCAACATAACAGTCGGAATGACTTCTGTTCACCCATCCATTTTTCACCAGTTAAAGCAGCTTCATCTGACAGTAGCCCTAGCAGTGTGAAATGTGTCCAGGACATTGACAAAACAAAAGATTGCCGGATTACTTCTCCTCCAAACTCACCTGAGATTTCTACATGGCAAGATAGCCCAGACGAGGTTGAGCAAGATGAGGATAAGGAGAATCTGACTGGGGGGTTGCAACCCCTCTCCATGGATCAAAATTTGAATGAGACGTTACTTGAAAATGCGGAGTCAAAAGATCACTTGAGTCCGTCATTTTTTGGAATTAAAGGCCTAGTTTCAGATGTCAGATGCTCGCACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44931
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092264 | Essential Splice Site | 2043 | 2953 | 14 | 32 |
ENSDART00000136987 | Essential Splice Site | 1713 | 2623 | 6 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3414413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3358067 |
GRCz11 | 20 | 3375568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGCACTGACGATGAAGCCTCTAGCTGCAGTCCAGTGCGACATGAAGG[T/C]ATAGCTTTATGTAACCTTTCTCAAATCTTTTCAACTACAGTTTGTTTAGC
Long Flanking Sequence:
ACAACTCAGAAGACCTCGAATTCGCTTTTCTCAGAGAATCATGATAAAAGGCCTGAAAAAAATTCAGAATCGCAACATAACAGTCGGAATGACTTCTGTTCACCCATCCATTTTTCACCAGTTAAAGCAGCTTCATCTGACAGTAGCCCTAGCAGTGTGAAATGTGTCCAGGACATTGACAAAACAAAAGATTGCCGGATTACTTCTCCTCCAAACTCACCTGAGATTTCTACATGGCAAGATAGCCCAGACGAGGTTGAGCAAGATGAGGATAAGGAGAATCTGACTGGGGGGTTGCAACCCCTCTCCATGGATCAAAATTTGAATGAGACGTTACTTGAAAATGCGGAGTCAAAAGATCACTTGAGTCCGTCATTTTTTGGAATTAAAGGCCTAGTTTCAGATGTCAGATGCTCGCACCTACTCCATAGTACACCTGTTCAAAGGAGAAACAGCACTGACGATGAAGCCTCTAGCTGCAGTCCAGTGCGACATGAAGG[T/C]ATAGCTTTATGTAACCTTTCTCAAATCTTTTCAACTACAGTTTGTTTAGCTTTATGAATAACTGGTTTCCACATGGTTTTATGTTTGTAGCCTCATAGAGTTGTTAAAGGGCACCTATGATTCGAAATCATCTTTTGGAAGCTGTTTGGACCACTGTCCCATAGGACAAGAAGTCTCCTAAATAAAAATTCTGACCTTTAAATCCCTGCATTTTTGAGGCACGGTGTAACGTGATGTAGGAGTGTGGTTTTCCCCATCCACTGAATTGATTGACAGCTGCATATTAACATGTCTCTTTAGTGACGCATATAATCATATCCATAAGGTAGGACTTGCAAAGAAACTGAGATTAAAAAAATCTGTTCAACTCTGTGATCAGCTGCACCTCAAGAAAGAGTTTTACAAGTTTAAAACGTTTTTAAAATGGTGCATGTTTGTAATAATGTAGAGAAAACTGTAAAATCGCTGTTAATCATGCTGGAATCACCACAGCTGCATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36948
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Essential Splice Site | 2216 | 2953 | 18 | 32 |
ENSDART00000136987 | Essential Splice Site | 1886 | 2623 | 10 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3408144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3351798 |
GRCz11 | 20 | 3369299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGTGATGAGAAGGAGCTGTTTGAAGAGGTCTCTAACATAATTAGGAA[G/A]TAGGTTTTTTATTTTCCTTTTTTAATTACGCTGCTTTGTTTCTGTCGGTT
Long Flanking Sequence:
CGTAGTGTGGACTGATATATGATCAGAAACGCTAGTTGAACTGCAGATCGTTTTTTATCTAAAACGACGTTTTAAAACTAAAACGCACTTGTGTAAACGGGGCCTTAGTGATGGGTTTTAAACAATTGGTTACGCATGTGAAAGAGCACAGATTTGCTTGTGATTCAGGCATTAGTCAGCGGTTTCTCAAAACTCGTCATTGAGTCAAAATCAGGGCTAAAATCATGCAGTCTGAGCTCTGCATTAGGGGGTTTCATTCGTCTCGCTGAATGAGACATAAAGTTTGGTAAAAAGATTCAAACTTCTAATCACTATACAGTCTTGCGTGATGTTTTACATAATATTAAATGTGTCTGTTTCAACATTATAGCTTGTTGTATTTTTTCAGCTTCCAGAAGTTCGACACCTTTTCTTTTTAGGTGCGGTGTGACAGGACTGCCGGTGACCTACACCTGTGATGAGAAGGAGCTGTTTGAAGAGGTCTCTAACATAATTAGGAA[G/A]TAGGTTTTTTATTTTCCTTTTTTAATTACGCTGCTTTGTTTCTGTCGGTTATTCCTTCATGTTAATAATAGACAAGTTCTATTATCTCTACTATTCTAAATGATTAGAACGCTAGTATTTTCATCAACTAAAAATTATTCTGTTTTGATATTTATGTCAAAGCAGTTCACAGGGTATGCCACATTTCAGGGTAATGCTTATTAATTTAGTTTGAAGATCTTAATACAAAAGGATCTGCTATTTTGAAAAGTTTGGGTTGTTCAGATGTGACCATTACCCATATCTCCCAGCCTGACCAGCTAAAACCAGGCTGGAAATGGCTGGAAACTAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGCCTGGTTGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGATGTTTTTTTCAGTAGGGTAATGTATCTCAATACATAAAAGGCTTTCTTTTCTTACTGCACACTCATTCGTTCATTAATTTATTCATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43371
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 |
---|---|---|---|---|---|
ENSDART00000092264 | Nonsense | 2237 | 2953 | 19 | 32 |
ENSDART00000136987 | Nonsense | 1907 | 2623 | 11 | 24 |
ENSDART00000148235 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3407110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3350764 |
GRCz11 | 20 | 3368265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTCTTGTTGGCTATGAGGTCCAGATGCATTCTTGGGGCTATTTACTA[C/T]AGCGTGCTTCAACGCTTGGTGTGAACTTGTGCCAACAACTATCCCGTGTG
Long Flanking Sequence:
TGGTCATCACAACGGAATGAACCGACAACTTATCCAGCATATGTTTTACGCAGCTGCAACCCATCTCTGAGAAACATCCATTTACACTCATTCACACTCATACACTACGGAATTGGACTGTGGGGTAAACCAGAGCACCGGAAGGAAACTAACGCAAGCGCGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACTCAGCTGAGGCTCGAACCAGCAACCTTCTTGCTGCAAGGCTACAGCACTACCTACTGCATCACCGCGTCGACCATACTGCACACTTATCATTTGTTAGATAGTTCTTTTTTTTTTACTATTATAACTTTTATCATTGTATGTGATTTTACACCTGAAACAGTCAATATGGCTGTCCAGAAAGCATGCTAGTTTGTGAAGGTGAGTACTCCTGACTTGTCATAACAATCACCTTTTCAGGTATGACCCAGACATTCTTGTTGGCTATGAGGTCCAGATGCATTCTTGGGGCTATTTACTA[C/T]AGCGTGCTTCAACGCTTGGTGTGAACTTGTGCCAACAACTATCCCGTGTGCCAGGTAAGGTTATAGTTCACTTTCTTGCCCTGTACATTCTGACAATAGTTTCAAGTTGCAGTTGCAGATTTGGGAAATGCTAACTTTAGCCTGATAACATTGAAAACATGCATCCATCCCGACATTCAAACTGTTTTCCAAAACCACAATATATAAACATCTACTCAGTGTTGGGCAGTAGCGTCGCCCCAAGTACTGATGCTACTAGTTTAACCACATTTCTCAGTAGTGTGGTGGTAGCATCACTGCTTTATAAATCAAATAGCTTTTCAGTAGCAAAGCTATTTCTTTAAGGCTGATTTATACTTCTGCGTCAAACGCCGGCGTATGCTACGGCGCTGATGCATAGCCCTTCGCCGTGACCGTCGGCGTCGCTGACGTGCACCTCTCAAAAAATGTAACTACACGTCGCAACGACGCGTTGCGTAAGCTCTGTGATTGGTCGGCTT
Associated Phenotype:
Not determined