ZMP
chn2
Ensembl ID:
ZFIN ID:
Human Orthologue:
CHN2
Human Description:
chimerin (chimaerin) 2 [Source:HGNC Symbol;Acc:1944]
Mouse Orthologue:
Chn2
Mouse Description:
chimerin (chimaerin) 2 Gene [Source:MGI Symbol;Acc:MGI:1917243]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22814 | Essential Splice Site | Available for shipment | Available now |
sa22813 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22814
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 |
---|---|---|---|---|---|
ENSDART00000014769 | Essential Splice Site | 245 | 466 | None | 13 |
ENSDART00000139776 | Essential Splice Site | 229 | 450 | None | 12 |
The following transcripts of ENSDARG00000011845 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 22442197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 20548640 |
GRCz11 | 16 | 20354459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCTAACTTCATGTGGGGTCTCATCGCTCAGGGCGTCCGTTGTTCAGG[T/C]AACCCTCCACCAAACACACACAAATGAGTTATAGCATTGTCTATCGAATT
Long Flanking Sequence:
AGTAATACGCAAGGGTGAAGAAGCTGAGCTAGAGCTGTTATATTGCATGGCTATCAGCAATAATCAGATTCTAGAACCAGACAGAACTTTTGTTGTGAAATAAGTATGTTTTGAACGATTTTTTACTGTTTGACTCAAACTGAAAGAATTAAAAGTGTAATGTCTGTTGCGTATGCATTGAGATTAATATGGATTTTACATAGTTATCAAATGACTTATTGTGTAATTAACTTTCCTTTAAGACAAAGTAATTAGAAAAGTTATTTAAATAAAATTTTAATGATGTAATCAGTAATTAGGTTTTTGTAACAAACCTACACAACAATTTGAGCCATTAGTTTTTATTTACACAAAAACTTGGTGTATATATAGTCTGTGTTTTGACTTTCAGTTATTGCTGTGTTTTTGGTGCAGGTGCACACGTTCAGGGGGCCGCACTGGTGTGAATACTGCGCTAACTTCATGTGGGGTCTCATCGCTCAGGGCGTCCGTTGTTCAGG[T/C]AACCCTCCACCAAACACACACAAATGAGTTATAGCATTGTCTATCGAATTTCGACTAAAAGCTTTTGTCTTGCAACAATGCCTGAAGAAATTCAGCAGAAAGTGCTGTGGAAACCTGCGGCCAAATACTGAAAGTGAGAAGCAGGACAATAAGGGTTTTAACTATTATGCTGATTTGTGGGTATTTTGCATTCCTGAATGACACCTGGTCCAAACCAGTCAAGTGTCTTTTGTTGAGTGTTGACTATTTATAGTGGTGCACACTGTATACACTATTAAGTGCTGTGAGACAGACACACCCAGGTACACATAAACACACATCAACACATGCACTGTGCACACACAACCTGCACTTAATGTTCAAAAAGTATTGGTTGTTGTCACGGTAAGTAGGAGTGATGCAGATGAGTTATATAAAATATTGAATATCTATAATATTGAAGCTGCAAGCAGGAATGAAAGGGACCTCACGCCCGGTGGCCTTTTGATGACAGAGAACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22813
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 |
---|---|---|---|---|---|
ENSDART00000014769 | Nonsense | 311 | 466 | 10 | 13 |
ENSDART00000139776 | Nonsense | 295 | 450 | 9 | 12 |
The following transcripts of ENSDARG00000011845 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 22412949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 20519392 |
GRCz11 | 16 | 20325211 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTCATACTGTTCTTCTTCTTCCAGGTTTGAAATCAGAGGGTCTGTAC[A/T]GAGTGTCAGGCTTCACAGAACACATAGAAGATGTCCGACTGTCCTTCGAT
Long Flanking Sequence:
GAATTCAATCGTCCGGTTTGTAATGCGTACCGAACCGAAAGTCTCGTACCGAACGGTTCAATACTAATTCGCGTATCGTTACACCCTTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTGTGTGTGTGTGTGTGTGTGTGTATTGAAGACTTTCTTTAAAGCAACTGCAGTTGCAGTCCAGACCATTCAGAATTTGTGAGGATCCCTGGTCTAAATTAAGTAAAGATAATCAGCAGATGATAGATGCACTGTGCTATGTGCAGATTATCCAATTTATCAAAGGAACAACCAGCAGATGAATTGATTATTCACTTAAAGTTGTTGGCTGCAGTCCTAGTTTGATCAATTTTAATTTACATGTCCACTTCCCCACCATTGACCGCATAGTTTATGTAAATTCATACTGTTCTTCTTCTTCCAGGTTTGAAATCAGAGGGTCTGTAC[A/T]GAGTGTCAGGCTTCACAGAACACATAGAAGATGTCCGACTGTCCTTCGATAGAGGTGGGTATTAGAAACACTCTTCATGCTGTACTGGCACAGTTATTGGTAGATCAAACAAATAGGAAGCGATTAGTCTTTTCACATTTGCTTGCATGCTTGAAATAGTCATGGATGTCATTGTTATTCTATCAACATTCAGTCTGGATGGAAAAAACTCAGCTTTTCCATCCAAAACACTGCATTATTGGTACAATATGGTGATTCACCTTGTATTTTTAACAGATGGTGAGAAGGCAGACATCAGTGCCAACATCTACCCAGACATTAATATAATTGCTGGTGCTCTGAAGCTGTATTTGCGAGATCTGCCCATTCCAGTTATCACATACGACGTCTACTCCAGATTCATCCAAGCAGCGAGTAAGAAATTTCACATTTGATTGTATTGTAACTGGGTCTTGTAATCTGTGTTTTAATGATCCTTAATAATGTCTATTTGGGCTGCA
Associated Phenotype:
Not determined