ZMP
hmcn2
Ensembl ID:
ZFIN ID:
Human Orthologues:
HMCN2, RP11-88G17.6
Human Descriptions:
Novel protein similar to hemicentin (LOC392395) [Source:UniProtKB/TrEMBL;Acc:A2A3K3]
hemicentin 2 [Source:HGNC Symbol;Acc:21293]
hemicentin 2 [Source:HGNC Symbol;Acc:21293]
Mouse Orthologue:
Hmcn2
Mouse Description:
hemicentin 2 Gene [Source:MGI Symbol;Acc:MGI:2677838]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16664 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16664
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 |
---|---|---|---|---|---|
ENSDART00000112067 | Nonsense | 2885 | 2925 | 56 | 56 |
ENSDART00000137897 | Nonsense | 775 | 815 | 15 | 15 |
ENSDART00000138117 | None | None | 89 | None | 3 |
ENSDART00000142824 | None | None | 122 | None | 2 |
ENSDART00000145362 | None | None | 158 | None | 4 |
ENSDART00000147594 | None | None | 294 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 33632787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 32775513 |
GRCz11 | 8 | 32784745 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCATTTGGCATCAAGGATGAAGCAGGAAGAGGCATCATTTTCACAGTR[A/T]AGCCTTTAGACTGGCCAGGCCTGGTGCGACTTSGGGTACAAGCCACAACT
Long Flanking Sequence:
CAAGTTAGTAAAATGCATAGCTAAGAACTTTAATTTCACAACTTAAAAGGGGATTTTCTCAGAGTTTAGACATTTTTGAACCCTTAGGCTCCAGATAATCAAATTGAGATGATGTATAAACAACAGATGAAATAGGTTTCAGTTGATGCAGTTGATGTTCCCCCTTCCCCCCTCAAAAAAAAAAAAAAAACATATGACTGGTTTTGTATGTAATTAACACACATCCATTTGCTTACTTTAACTCCAGCACCTGCTTCAGACCTTGCTCTTCCAGGCTGGACTGTGGCTCTGTGGGCTCTTTTCCTCTGCTCCAGTACAAGCTCCTTACTCTTCCTCTGGGCATCCCAGCCCACCACAATGTGGCCCGTTTATCTGCTTTCTCCGAATCAGGAGTCCTCCAAGACCACACGTCCTTCACCATCCTGGAGCAAGGAGGAGATGACGGAGAGAGGCCATTTGGCATCAAGGATGAAGCAGGAAGAGGCATCATTTTCACAGTG[A/T]AGCCTTTAGACTGGCCAGGCCTGGTGCGACTTCGGGTACAAGCCACAACTCTGTCAGAGCAGGGCCGCGTTACCTACCAGAGTATCTTTATTATCTACATCTCCATATCCAAATACCCCTACTAATGAACGGCTGCTTCATAGAACATTAGAGAGGCATTAGTAAATGAACTCAATTGCCAGCTATTTATGTGCCCTCTTGTGGAGTGGAACTATCTAATTTTGCAAAATTATGCTGATGTTTGAAAGCACCAAAAATGACACACACATAACCCAGCAGGACCTCGGCCTCATTTGAAATCTCTGCTATCATTACTAGATGAGTAATGTATGTTAGGACTACATAGTGTGTAAGTATTTTGGGATTTGGTTCGACACTATGGTCAAAACCTTTTTTCCTTCTTTTTTGTTTTGGCTTAGTGAACTTTTCCTTTAATATTACTATTATTTGAAAATATTGTAGTAGCTTTGAGATATTGCTTGGGCTCTTCTGTTTTCACT
Associated Phenotype:
Not determined