ZMP
si:dkey-93f15.3
Ensembl ID:
ZFIN ID:
Description:
ras GTPase-activating protein 4 [Source:RefSeq peptide;Acc:NP_001092921]
Human Orthologues:
RASA4, RASA4B
Human Descriptions:
RAS p21 protein activator 4 [Source:HGNC Symbol;Acc:23181]
RAS p21 protein activator 4B [Source:HGNC Symbol;Acc:35202]
RAS p21 protein activator 4B [Source:HGNC Symbol;Acc:35202]
Mouse Orthologue:
Rasa4
Mouse Description:
RAS p21 protein activator 4 Gene [Source:MGI Symbol;Acc:MGI:1858600]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5749 | Essential Splice Site | F2 line generated | Not yet available |
| sa2226 | Essential Splice Site | F2 line generated | Not yet available |
| sa18002 | Essential Splice Site | Available for shipment | Available now |
| sa33731 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18178 | Nonsense | Available for shipment | Available now |
| sa33732 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa11873 | Nonsense | Available for shipment | Available now |
| sa33733 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5749
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097374 | Essential Splice Site | 22 | 800 | 1 | 21 |
| ENSDART00000097374 | Essential Splice Site | 22 | 800 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 60976822)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58608949 |
| GRCz11 | 5 | 59278658 |
KASP Assay ID:
554-2897.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCTATTCATCAGGATTGTGGAAGGAAAGAACCTGCCAATCAAGGATAT[G/A]TAAGTGTTGATGACTTTATGGGATTATTTGAAGTTAAATTATTTAGAAAT
Long Flanking Sequence:
CTAAAAAATGACTTCAGCTCACTTGACTTCAATTTAAAAGACTTAAATTTACCCGTCGCTCGCATCTCGACGCCACAAAAGTACAATATTCAACAAAACCACCTGAAATCACGAACTTGCGGTTTAGCTGGATATGAAACTCGCGTTTGTTGTAGTTTGACGCGTCGCGTAATACCATCCCTCTTCCAGTGTGTATGTGTGAATCCAGTCAGTCACTCCTCATACAAACAGCCCACAGAGCTCAAACCAACCCGCCCGTGTTTAACGCGTGGACGACCGCTGGACAGACAGGCGGTGCTGCTTCTTAACACAGGATCTACCATAAGCTTTATTGATTCAATAGCCCGTTTTTCAATTCTGCATTGCTTATAAACATGCGTGTTATTGAAGGAACAAGAAGTGTCGGCGCTTGAGAGACAGTCACTGAATGACAGCATGGCTAAACGAAGCACTCTATTCATCAGGATTGTGGAAGGAAAGAACCTGCCAATCAAGGATAT[G/A]TAAGTGTTGATGACTTTATGGGATTATTTGAAGTTAAATTATTTAGAAATATGTGGGAATGCATTGGTTGGGCGGTATAGAAACTGAACGCAGCAGTATGGGATTTATAATCCAGATGTAGAACATCTCATTCAAATAAAGCCATACATAATAAAATGATAATCCATGTTGTGGGCAAAATAAACAAAGAACCAATAGGAACCCTTTTGTAATTTTAAATTGTTAAAATGGGAATTGTATTATTTATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCCTTACTCTGTAGATGCTAAAAACTCATCGTTCTAAGACTTTTATATTTTAATAATATTTATTATTTTAATAATATTTACTCTTATATTTTAGAACTTTTTTTTTCAATGCATACTTGTATTTTATTGCATGTTTGATTTCTCTTTTCTTGTAGCGCTTTGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2226
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097374 | Essential Splice Site | 22 | 800 | 1 | 21 |
| ENSDART00000097374 | Essential Splice Site | 22 | 800 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 60976822)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58608949 |
| GRCz11 | 5 | 59278658 |
KASP Assay ID:
554-2897.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCTATTCATCAGGATTGTGGAAGGAAAGAACCTGCCAATCAAGGATAT[G/A]TAAGTGTTGATGACTTTATGGGATTATTTGAAGTTAAATTATTTAGAAAT
Long Flanking Sequence:
CTAAAAAATGACTTCAGCTCACTTGACTTCAATTTAAAAGACTTAAATTTACCCGTCGCTCGCATCTCGACGCCACAAAAGTACAATATTCAACAAAACCACCTGAAATCACGAACTTGCGGTTTAGCTGGATATGAAACTCGCGTTTGTTGTAGTTTGACGCGTCGCGTAATACCATCCCTCTTCCAGTGTGTATGTGTGAATCCAGTCAGTCACTCCTCATACAAACAGCCCACAGAGCTCAAACCAACCCGCCCGTGTTTAACGCGTGGACGACCGCTGGACAGACAGGCGGTGCTGCTTCTTAACACAGGATCTACCATAAGCTTTATTGATTCAATAGCCCGTTTTTCAATTCTGCATTGCTTATAAACATGCGTGTTATTGAAGGAACAAGAAGTGTCGGCGCTTGAGAGACAGTCACTGAATGACAGCATGGCTAAACGAAGCACTCTATTCATCAGGATTGTGGAAGGAAAGAACCTGCCAATCAAGGATAT[G/A]TAAGTGTTGATGACTTTATGGGATTATTTGAAGTTAAATTATTTAGAAATATGTGGGAATGCATTGGTTGGGCGGTATAGAAACTGAACGCAGCAGTATGGGATTTATAATCCAGATGTAGAACATCTCATTCAAATAAAGCCATACATAATAAAATGATAATCCATGTTGTGGGCAAAATAAACAAAGAACCAATAGGAACCCTTTTGTAATTTTAAATTGTTAAAATGGGAATTGTATTATTTATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCCTTACTCTGTAGATGCTAAAAACTCATCGTTCTAAGACTTTTATATTTTAATAATATTTATTATTTTAATAATATTTACTCTTATATTTTAGAACTTTTTTTTTCAATGCATACTTGTATTTTATTGCATGTTTGATTTCTCTTTTCTTGTAGCGCTTTGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18002
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 |
|---|---|---|---|---|---|
| ENSDART00000097374 | Essential Splice Site | 22 | 800 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 60976823)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58608950 |
| GRCz11 | 5 | 59278659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTATTCATCAGGATTGTGGAAGGAAAGAACCTGCCAATCAAGGATATR[T/A]AAGTGTTKATGACTTTATGGGATTATTTGAAGTTAAATTATTTAGAAATA
Long Flanking Sequence:
TAAAAAATGACTTCAGCTCACTTGACTTCAATTTAAAAGACTTAAATTTACCCGTCGCTCGCATCTCGACGCCACAAAAGTACAATATTCAACAAAACCACCTGAAATCACGAACTTGCGGTTTAGCTGGATATGAAACTCGCGTTTGTTGTAGTTTGACGCGTCGCGTAATACCATCCCTCTTCCAGTGTGTATGTGTGAATCCAGTCAGTCACTCCTCATACAAACAGCCCACAGAGCTCAAACCAACCCGCCCGTGTTTAACGCGTGGACGACCGCTGGACAGACAGGCGGTGCTGCTTCTTAACACAGGATCTACCATAAGCTTTATTGATTCAATAGCCCGTTTTTCAATTCTGCATTGCTTATAAACATGCGTGTTATTGAAGGAACAAGAAGTGTCGGCGCTTGAGAGACAGTCACTGAATGACAGCATGGCTAAACGAAGCACTCTATTCATCAGGATTGTGGAAGGAAAGAACCTGCCAATCAAGGATATG[T/A]AAGTGTTGATGACTTTATGGGATTATTTGAAGTTAAATTATTTAGAAATATGTGGGAATGCATTGGTTGGGCGGTATAGAAACTGAACGCAGCAGTATGGGATTTATAATCCAGATGTAGAACATCTCATTCAAATAAAGCCATACATAATAAAATGATAATCCATGTTGTGGGCAAAATAAACAAAGAACCAATAGGAACCCTTTTGTAATTTTAAATTGTTAAAATGGGAATTGTATTATTTATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCCTTACTCTGTAGATGCTAAAAACTCATCGTTCTAAGACTTTTATATTTTAATAATATTTATTATTTTAATAATATTTACTCTTATATTTTAGAACTTTTTTTTTCAATGCATACTTGTATTTTATTGCATGTTTGATTTCTCTTTTCTTGTAGCGCTTTGGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33731
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 |
|---|---|---|---|---|---|
| ENSDART00000097374 | Nonsense | 117 | 800 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 61024481)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58656608 |
| GRCz11 | 5 | 59326317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGACGGATGGATGAACCTAACAGAGATTGACCCAGATGAGGAGGTG[C/T]AAGGGGAGATTCACCTCCAGATCTCAGTGCTGGGAGATGGAGATATCCCA
Long Flanking Sequence:
GTCCTTCATATCGTAATGCACATTGTTGGAACATTTATCATGTTAGTGAATGTTCTCGGTCTGCCGTAAGCTTATTCTGTAGAAATACAGCAAGGCCATTAATTCTATTAACCTAAGCCTCTTAAAGCTAGAGTTCCTGTGGAGGGGCACAATATATTACATTTATCCCAGCTGTAGGCCTTCCCGCTGTGGGTTTGTGTATGTGTGTATGTACTTACTGACCTTCCCTTATCAGGTCGCCTGTGTGTGTTTGCAGATATACGAAAATGTTCTGGATCAGTGGAAGCCATAATAACACTCCTAGCCCTGTGCACTAGACCGCTTTAGGGTCTCTGTCCTTGAACTTAGCCCACCGCCATAACTTGATTGCCTGCTAAATTATTCATTTGAACATCAGAGGCGGACATATGAGCTCTTCTTTTTTTCAGCTTCTTGTCATTTTGTGTTTAGGTGTTGACGGATGGATGAACCTAACAGAGATTGACCCAGATGAGGAGGTG[C/T]AAGGGGAGATTCACCTCCAGATCTCAGTGCTGGGAGATGGAGATATCCCACGGAAACTGTGCTGCCAGGTCCTAGAGGCAAGGTGAGGAGTTGGATTAGCTATATATACTGTATAAACAAGTTAGGTTTCAGATTTCAGGTCATTAAATAAACAAGTAAATAAGTAAAAACGCACATAAATCACAAAAATACAAAGATTTGGTTGGATTGCAGCACCAAATTTTTCTGCTTAATGAAATTCATTCATTCATTCGTTTTCTTTTCAGCTTAGTCCCTTTATTAATTCAGGTTTGCCACAGCGGAATGAACCACCAACTTATCCAGCACTAAGTGTTTTACAGCTAAATTATTAAATGAGGGCTAAAAGACAAACAAAGCACCTTTAACGCTGAAAAAAAAATTATTAATTACTGATTTTTTTAAGGTAAGTGGTTGAAAACAATTTATATTGGCTGAATTTGAACAAAGTATGATCAAAGTTGAACATTACTAAATTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18178
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097374 | Nonsense | 210 | 800 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 61026895)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58659022 |
| GRCz11 | 5 | 59328731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACTGACAGTCTACTGAGTGTGGAGGTGTGGGACTGGGATCTGRTCAGC[A/T]GAAATGACTTCCTGGGAAAGGTGAAGTACATTTCCTGCATGGAGCAYTAA
Long Flanking Sequence:
GAGGCCTAATTATTTTTATTTCATCTGCAGTCACGATTAGTGTTGTGTGTTATTCAAACATAAAGAAACAGATATAACCAGCCATGCACAAAAATAAAATGTCCTCAGTGTATGTGAATCAGGCATGGACTGCTGAAATGGGGATTGGGAGATTTCATCTTCATAAGCTGTGTTTGGATTTGTGTTTAATAGCTTCATGTACTTTCGGCTTTATTTCTAGAGATCTTGCGAAAAAGGATCGCAACGGGGCCTCTGATCCTTTTGTCCGAGTGAGATACAATGGGAAAACGTATGAGAGCTCGGTAAGGATGTAGTACTTCTGTAAGCCTCTCATTTGATCTGCCACACTAGAAAGGTCTGTTAACCTTGATTCTGCTTCCCTCCAGGTGGTTAAAAAGTCCTGTTATCCTCGCTGGAACGAGAGTTTTGAGTTTGAACTGGACGAGGCGCTGACTGACAGTCTACTGAGTGTGGAGGTGTGGGACTGGGATCTGGTCAGC[A/T]GAAATGACTTCCTGGGAAAGGTGAAGTACATTTCCTGCATGGAGCACTAAGAGATTTGGATTAGAAGATGTTTTGGACTTCGCCTTTGCCTTATTTAACATAAAATATAAAAGATTAAAATAAGTAGTACAAAAAAAGGTGTGTTTTAAAGGGAAGTTCACCTAAATGTCATCATGTTTTTACTGTAAGATTAGTACACACGTGATTTCTGTGGGACACAAAAATATACAGCACTGTACAAAAGTCCTAAGCACTATACCAGCTTTGGTGGCTTAAGACTTTTGCACAAGATACTATCAAGCAGTTTTTTTATTAAAAACAAATTTAAATAAAAAGAAAATAGCAAATAGGTACAAAAAACCAACAACAGCACAACATTTCATCTTCAAGCTGAAGTCTATGTTTAATGTGGCTTCCCTTGGCACCAAGCAAAACGTTCGAGGTTACAGAAGTAACCCTTCGTTCCCCGAGGAGGGGAACGGAAGTGCCATAGAGTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33732
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097374 | Essential Splice Site | 247 | 800 | 8 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 61039901)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58672028 |
| GRCz11 | 5 | 59341737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCTGGTTCCGCCTGGGGCCTGACAAATCTAAACACAGCGAATATGAG[T/A]GAGTCTATTTGAAAAATAAAGCGGAGAGCAAATTAAAGAACAGATAATGT
Long Flanking Sequence:
AAAAGAACCTGTTTTTGCGATAAAAGTGGATTTACTGAACATACAAACGGGAGTTTGCAAAAAATGCTCATTTTAGAAGAAAGTTTCAGATGGCATTTAGGTTTTTGCATCTGAACTCTTCAATATTAGTACCAACAAGCAAAACTAATTTTTAAAAAATATTTATAAAATATATAATTGATGAAATATTTCTTACTTGTCAATTCAGCGTATCCTGAAGTTGCCTAAATAATTGAAGCGTAGTCAGTGTTTCATTGTATTTCATTTGTTCTCTGTTTGACAGATGTTCACTGTGACATTGCCTTTGTCGCCCAATAATAAGTGTCCCAATTGCTGTGTTTAGCTTCGGTTGCTTTGACAGCTAATTGTCACGTCGATTGACGTGTGCTGCTTCTGTTTTCCTTCAGGTCCTGTTCAACATCAATAAGCTTCAGTCTGCACTGCAAGAGGAGGGCTGGTTCCGCCTGGGGCCTGACAAATCTAAACACAGCGAATATGAG[T/A]GAGTCTATTTGAAAAATAAAGCGGAGAGCAAATTAAAGAACAGATAATGTAATCTTTATAGCTTTAAAACTTCACTCCACCTTTCTTGTAAATAGAATCATTTAACTTTTTACAAAAAGTCCTTTACAGTTACAAAGATTTTAATATTTTTGAATCCATTCAGCCAATTTCCAGGTCTGGCGGGAACACTTTTAGCATAGCTCAGTATAAATCATTCAATTGGATTAGACCATTAGCATCTCTCGCAAAAAAATTAAAAAGAGTTTATATATTTTCCTATTTTCAGTGATAGATTCTTCTGTGGTTACATTATGTACTAAGAGTGACGGAAAATAAAAAGTTCCTATTTTCTAGGTGATAAGAGTAGGAACTATACTCACATTTGGGCATACTAATCTATCCACTTTGCTGCTATACCATGGCTGCAGCAGGCACAATCATATTACTCAGCACCTGAAAATAGTCCCTAGTTAACAGCACTGCTGACAATTTGCACTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11873
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 |
|---|---|---|---|---|---|
| ENSDART00000097374 | Nonsense | 556 | 800 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 61076441)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58708568 |
| GRCz11 | 5 | 59378277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTWCTTGTGTTTACTTTATTTTGAATCCAGATCTTGAACTTCAGACA[C/T]GAATGAGCCTCCAGTGCGGCACTATGGAGAAAGAGGGTTTTCTCTTCCTG
Long Flanking Sequence:
TATGGACCCATTTTATAAGACTCTTTTTATATTCGTGGGTTTCTCAGTAGCGGAAGTCATCATAGTTGGAAAAACTTGGAGCTCAGTGAATGGGAGAGTACGACAAATCATTTTTTACACTCCTGTATCACAATTTGCTGAAACGAATAAAGAAAAACTCCACAATGGTGTTGGCAAGACTTTCAGAAAAAGAAAACAAATAGTGTGAGACTGACAACGGCAGCCAGAAAAGAGAACAAGGTCAAATTTACTGTCCTGCTCCTAGACGCTGTATTAGAAATGCCTCCCACAAGCGATAATTAGTTTTTTTGTAATTTGATAGATTTTTAAGACCGTTAATTGCTTCATAATAGTCTTGTGAAAAGGGTTCATTGTATTTCTTTTTTTTTAATGGAAGTATATTAAGTCACACTTCACGCTTCTCCAGTCTTCAAATAATCACTTATCTTGCTGTTTCTTGTGTTTACTTTATTTTGAATCCAGATCTTGAACTTCAGACA[C/T]GAATGAGCCTCCAGTGCGGCACTATGGAGAAAGAGGGTTTTCTCTTCCTGCACAGGACCAAGGACAAGTGTATGCCAATGACTTCTCCCTTTAAGAAGTACTATGTGACGCTCAGTAAGGACACGCTGTCTTATTCCAGGACTCTGCACTCTAAGGTGGGCAGCAGTAATGGCTTGTTTTTTTTTGTTTTTTTTTTCATCAAATATATATATTTTCAGCAACAAGCTGCAAGGAAACAACTAACATGTACAGTACATACAGAGAGATATGTTGCATATGGTTGTACATGAATGTCATGGGATTTTTTCGTTGCTATAATTTACTGTTGTATCTTATGAATACCTGTTTTAAAGGCTAGATTTATTAGTATACTTTTGTCCAAGACCTAGACTTTCTTTCTTTAAACTGACAAAAACCCATGAATATTTTTTGATTATATGTATTTTTAAACTGACTTGTTGTTTTTGTATTATTTAAAGATGTCTGTAGTTTTAATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33733
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 |
|---|---|---|---|---|---|
| ENSDART00000097374 | Essential Splice Site | 699 | 800 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 61079060)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58711187 |
| GRCz11 | 5 | 59380896 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTACAAAGCAGACAGATGGAGCTGCTGCCATCAGAAGGAGAAATCAGG[T/C]ACTGCAAAATATTACACTGTGTTTTAGCTAGTATTGAGCTAATGTTTTTT
Long Flanking Sequence:
ATATTATGTTGATAAAAACCCTTAAAGCTATATTAACCGGGCGTTTGGTCTTTGACTCTATAGAAGAGCTCATCTATTTCCCTGCCAAAGATCCGTGCGGTAGAGAAGGTGGAGGAGAAGTGTTTCGGCAGTGCCAACGTCATGCAGATCATCTCCAGTGAAGACTCAGGCCAGCAGGAGACCCTATACCTCGACTGCAAAGTTAGTGCTTCACTCCATATACAAACAAATCCTCAATGAGGCTTTTCATAGGCACTGATTCTCAGACACTTGTTTGTTGTTTGGCGAGACTGTAAGAATGGGGCCTGAAAAAGCTAAAAGGGCTTATTTGATGTTTCATTGTTTAAAACTCTTTGTCTGCAGAGTGTAAATGAGTTGAATCACTGGCTGTCGGCTCTCAGAAAAGCCTGCAGTCACAACACAAACACTATGAGCTGCTTTCATCCCGGCATCTACAAAGCAGACAGATGGAGCTGCTGCCATCAGAAGGAGAAATCAGG[T/C]ACTGCAAAATATTACACTGTGTTTTAGCTAGTATTGAGCTAATGTTTTTTTCCGTAGGCTGCATTTATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGCACAATTTTAATATAATTTAAAATGATATTCCTATTTTAATGTATTTTAAATGTACAGTGCTCATCATAAATGTGTACACCCCATTTTAATATCCTTTCTCGGAAAATTTAGGCAATAAATGTTGTGTGTTTAAACAAAACTGATTTATTAAAGAGATATTTTTATTAGGGCTGTCAAATAATTAAAAAAATTAACATAATTAATCACACTTTTTTATTATTAATCATGATTAATTACAAAACGTAACTATTATTAAATGTATTAACTATTAAATTTAAGTGGATTATACATATATAAAACAATTAGGATATCCAAAAAAGCCTCAGGAATTGTGTCGATT
Associated Phenotype:
Not determined