ZMP
si:ch211-287b5.2
Ensembl ID:
ZFIN ID:
Description:
Si:ch211-287b5.2 [Source:UniProtKB/TrEMBL;Acc:A4JYQ6]
Human Orthologue:
HEPACAM2
Human Description:
HEPACAM family member 2 [Source:HGNC Symbol;Acc:27364]
Mouse Orthologue:
Hepacam2
Mouse Description:
HEPACAM family member 2 Gene [Source:MGI Symbol;Acc:MGI:2141520]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7462 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa43333 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7462
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087444 | Missense | 160 | 457 | 3 | 9 |
| ENSDART00000137752 | Missense | 162 | 362 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 41324317)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 40776855 |
| GRCz11 | 19 | 40363975 |
KASP Assay ID:
554-4331.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCCACTCCTGTTATCAGTAAAACCCCAGAATCTGAACTTGTTGAAGAY[C/T]GGGACAACGTAACGCTGACTTGTTCTGCTCWACAMGGGACGGAGATTCGG
Long Flanking Sequence:
TAAATTAGCAGTTTTCCATATTTTGTGATTCCTTTTTTAGGTTTACTTATGCTTTTGAATTGCATTATGGGACCTTGATATTTCTTTCGCCAAATTTTAACCTACTAAAGTTTTAAAAAAGTGACTTTTATTAACGTTTTTATATTGTCTGAGTTGCAGTTGTTTACCGTCTTGTAATAAACTGGCAGTTCATTGTCTGTTCATTTACAGACTTATTTCTCTCTATATTGTTTCTTAAACAATATATTATTCCAAAATACAAACATTTCAATAAATGTCACTATATTAAACTGTAGAGTTGAATTATTAACATCAAAAGTCGACAGAGCAAAGATCAAGGTCCAATAATGAAATTCACAACTGTAAATAAATGGAAAAACACTTTACACTAACAAAAATGAATAAGCAGCAGGGTTACATTTTAACATCTTTTCTGTTTTACAGTACCGGTCTCCACTCCTGTTATCAGTAAAACCCCAGAATCTGAACTTGTTGAAGAC[C/T]GGGACAACGTAACGCTGACTTGTTCTGCTCTACACGGGACGGAGATTCGGTACAAATGGCTAAAGGACAACATGTTGGTTAGTCCAAGCGACCGGCACACATTCTCTGAAGATAACGGGACGCTTTTCATAAACCCTGTTAGGAAAGAAGACATGGGCCAGTACATTTGCGAGGCTCATAACCAGATCAGCAGTGAACAAAGCCAACAGACTGATCTCAGTGTATTCTGTGAGTATCTGTCGTCGTTTACTGACCTCAAGCTCATTTATCATCTGTTATCATGGCTGGTGTCGTTATTGGACTCTGTTCCTCCCGCAGCCTGAGAATTGACTGCTGTTTGCATTGTTACTCAGACGTTAAACATGATCTGTGCATGACGTGTCATTTATAATAACTGAGAGATGAATGTGGGTTAAGTTATTAAAGGTTTTAAGTGTTGGTGTATACATCAAATTAACTTTACAGAAGGGAGACATGGATAGTGTGTCCAGAATGTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43333
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 |
|---|---|---|---|---|---|
| ENSDART00000087444 | Nonsense | 305 | 457 | 4 | 9 |
| ENSDART00000137752 | Nonsense | 307 | 362 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 41326242)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 40778780 |
| GRCz11 | 19 | 40365900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTGTCATGACGGGGCCAAGGTTGGAGGTGAAGACGTACGAGTTGCCA[C/T]AGGGGAAGGAGTTCTTGTGCAGAGCTTTCAATAACGCCACGAAGAAGCAG
Long Flanking Sequence:
TTTCTAGATATGATATAGACATCTAGGCATATTTTTTGAAATATGATATAGCTGGATAGGATATAGCTAGTCACATCTGTTCTTCTTTGGGGCTAAGTCCCTTATTCCTTTAGTGTTATTCAACCCTAGTGACGCCCCTGACGTAAGGTAAGCGATGCAGTAAGGTATTGGGTAGGTTTAGGTATATAAAATAAGATCATACTTTATAAGTATATAAAGTAAGGTTATAAGCCAGTAGTAAATGATGTGAATTGTTACCTAAACTAAAGTATTACCACACGTTTTGTTTTCCAGATGGGCCTTATAACCTGGCAGTAAATTGTGACCAAGCTCTGAAAACGGAAGGGGTTTTTACGGTAAACCCAGGGGAACTGGCGTTTTTTGAGTGTAATGCAGACTCGAATCCTCCAAACACCTTCCTTTGGATCTCAAAAACAGGTAATGGGACTGAGATTGTCATGACGGGGCCAAGGTTGGAGGTGAAGACGTACGAGTTGCCA[C/T]AGGGGAAGGAGTTCTTGTGCAGAGCTTTCAATAACGCCACGAAGAAGCAGGACGAGACCAAGTTCACACTGGTCGTGGCCAGACTGCACAGAGGTGAGTTGACAAGCATCTGCGGTTATAGATCTGGACATTATATATTCTTCATGCTCTGTGGAGATGTTGTAATGGTAAAAACTGACAAGACTTTGCTCAAAAAAGGGAGTAGTCCATTGTAACTTGGACTTGAATGGTTAATTTGAGTTAATTTTTATAATTCTGCACATAATTAATTAATTGATTGTAAAGCAAAAGGTTTACTAACTTTTTTTTTAACTCGACTAATAGCTTCACTATGCATATGACGTTTGTTAGTTAATTAAACATTTCTTTGACTTCCTAATTGAAATAAAAACAGGTGTTATTAAAGCTGAATAATTCTACTTATAATAAATTATATATTTAGTTATAATATATAATATTTTTTAACAACAATAAGAGACCTAAAACTAACATTATAAAAT
Associated Phenotype:
Not determined