ZMP
cyr61l2
Ensembl ID:
ZFIN ID:
Description:
cysteine-rich, angiogenic inducer, 61 [Source:RefSeq peptide;Acc:NP_001074456]
Human Orthologue:
CYR61
Human Description:
cysteine-rich, angiogenic inducer, 61 [Source:HGNC Symbol;Acc:2654]
Mouse Orthologue:
Cyr61
Mouse Description:
cysteine rich protein 61 Gene [Source:MGI Symbol;Acc:MGI:88613]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34520 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41310 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34520
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 |
|---|---|---|---|---|---|
| ENSDART00000098226 | Nonsense | 14 | 373 | 1 | 6 |
| ENSDART00000124857 | Nonsense | 14 | 373 | 1 | 5 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 55072027)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 52633317 |
| GRCz11 | 8 | 52619610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTTGGAAATGCATTCTGGAAGAAATCAGAGGACGCGGACACACACTTG[G/A]GTTGTTTTGTTGTTCGTGGTTTGCTCTGCTGACGGAGAGGTGAGGAGATT
Long Flanking Sequence:
ATATTAGAGGAAATACTGTGAAAAATTCCTGAATCTGTTCAACATCATTCGGGAAATATTTGATGAAGAAATTAAAAAAATCACAGGAGGGCGAATAATTCTGACTTCAGCTGTGCACAAACAATAGAAGACCAGCTGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAGTCTCTATAAGGTGAGCTGCTCCGCCGTAAATGCTCTGTAACACTGACTAGCCCAGTGCTCAGGCTTTGGGTCTTGCTGTAATTCTAGTCTAGTATCTATAGTCTGACTGATGCACTTTGCAGATGCACTAGCTTTAAACCTGAAAGACACGCTCTGAAATCTTTGGAGTGATTTAGAAAGTGGATAAACCTGCTTGTTTTGCATTGGGGACTTACTTTAAATCTTGGTCAACGCTTGGAAATGCATTCTGGAAGAAATCAGAGGACGCGGACACACACTTG[G/A]GTTGTTTTGTTGTTCGTGGTTTGCTCTGCTGACGGAGAGGTGAGGAGATTTCACACACTACTGCACACTTCACAGTGTTTTCTGGTGAAGATCATATTTGGTAATCAATAATTGTGGATTCAATCATTCATAATACTGATTCATTTTATGTGTTTGTGCATTGAATATTTGCTTTTTATTTGATTTCAGCTTAAGTCATTTTAAATAAACTCATAACGTGCAAAAATGTTCATTAAAAGCCGTTAATGTAAATTGCATGTGGTTGTACTTATTTTTAATCTATTAAAAAGTCTAAATAAAAAGCCTAAAAGGAAATATACTCTAAATATATTAACTACATTAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATATATATATATATATATATATATATATATATATATATATATATATATATATATTAACTTGTTTATTTTTTATATAATTTAAAAAAAGTTTTAAAAATATATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41310
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 |
|---|---|---|---|---|---|
| ENSDART00000098226 | Nonsense | 165 | 373 | 3 | 6 |
| ENSDART00000124857 | Nonsense | 165 | 373 | 3 | 5 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 55066904)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 52638440 |
| GRCz11 | 8 | 52624733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCACACTGCACCAATCCTCGGCTGGAGACGCCGACTGGGCACTGCTGC[C/T]AGCGCTGGGTGTGTGACAGCGACAACAGCATCAGAGAGGAGGAGCCGCTG
Long Flanking Sequence:
GAGAAGAAAAAATTGTTTGCCCTTGTGATCTTTAATTGAAATCTGAAATGTTTCCTGTTTATGTTCAGTTAAACTCTCAGATTAGGTTGTGTCTGGTATTGAGCGTGGCTAACATCAGGGTTGCCACCTGCCCTTAAAATACTGCTTTTATTCTAGCCGAAATAAAACAAACAAGACTTTCTTCAGAAGAAAAAATATCATAGGAACTACTGTGAAAAATTTCTGAATCTGTTCAACATCATTTGAGAAATATTTGAAAAATAATGTGTGTGTGTGTGTCTGTGTCCTGTGTGTGTGTGTCAGCGGAGGCTCATGGTCGTCCGTGTGAGTTTTCTGGTCGTGTGTATCAACATGGTGAGGACTTCCAGACGGGCTGCGAGCACCAGTGCAGCTGTATTGATGGTGTGGTGGGCTGTGTGCCACTGTGCCCGCTCCTCGTCCCGCTGCCCGGCTCACACTGCACCAATCCTCGGCTGGAGACGCCGACTGGGCACTGCTGC[C/T]AGCGCTGGGTGTGTGACAGCGACAACAGCATCAGAGAGGAGGAGCCGCTGCCTAAACACACACCGCAGTACAACCACATCAGCAAACTCCTGCAGGAGCACCGCAGCAGACCCGCAGCTCAGGGTAACACAACAACACTCACACTGCTGTCAGAAATCACTCAGATATCACACTGGTTTAGTCTGACGTCACAGTTTCTGGTCATGAGCAGGTTTAGCATGGTTTAAGCTGGTCATGAGCTGGTTTTAGCTGGTTCTAGCTAGTCTTGAGTTGGTTTAAGCTGGTTCCTGCTTGTTTAAGATGGTTCTTACTGGTTCTTGCTGGTCATGAAATGGTTTAAACTGATTCTTTCTGGTCATAAGATGGTTCTTGCTGGTCCTGAGCTGGTCTTAGCTGGTTGTTGCTGGTCATGAGTTGGTTTAAGCTGGTTCCTGCTTGTTTAAGATGGTTCTTACTGGTTCTTGCTGGTCATGAAATGGTTTAAACTGGTTCTTTCTGGT
Associated Phenotype:
Not determined