ZMP
nexn
Ensembl ID:
ZFIN IDs:
Description:
nexilin [Source:RefSeq peptide;Acc:NP_001077324]
Human Orthologues:
AC026150.5, AC091304.2, AC100756.2, AC135983.4, AC138749.1, GOLGA6L1, GOLGA6L2, GOLGA6L6, NEXN
Human Descriptions:
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:C9IYW0]
golgin A6 family-like 1 [Source:HGNC Symbol;Acc:37444]
golgin A6 family-like 2 [Source:HGNC Symbol;Acc:26695]
golgin A6 family-like 6 [Source:HGNC Symbol;Acc:37225]
nexilin (F actin binding protein) [Source:HGNC Symbol;Acc:29557]
golgin A6 family-like 1 [Source:HGNC Symbol;Acc:37444]
golgin A6 family-like 2 [Source:HGNC Symbol;Acc:26695]
golgin A6 family-like 6 [Source:HGNC Symbol;Acc:37225]
nexilin (F actin binding protein) [Source:HGNC Symbol;Acc:29557]
Mouse Orthologue:
Nexn
Mouse Description:
nexilin Gene [Source:MGI Symbol;Acc:MGI:1916060]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21252 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21252
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 |
---|---|---|---|---|---|
ENSDART00000079936 | Nonsense | 423 | 861 | 7 | 14 |
ENSDART00000100558 | None | None | 176 | 8 | 15 |
ENSDART00000100562 | Nonsense | 423 | 845 | 7 | 13 |
ENSDART00000122471 | Nonsense | 423 | 612 | 8 | 12 |
ENSDART00000128203 | Nonsense | 423 | 598 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 19043470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18488358 |
GRCz11 | 8 | 18524070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAATTCAGACCAGGAAAACTTCGACTCAGTTTTGAAGAGCTGGAAAGA[C/T]AGAGGCTGGAAGACGAACATAAGCGGGTTGAGGAAGAGAGGAAAAGACGC
Long Flanking Sequence:
CTGTGGCTCGTGGGAACGGTGGGCGGAGATAACCACAGTAGCTCATTTGCATTCAAGTATACAGCAAACAAAAACAGCTATATATGTCAATATACAATAATATGTCCTAACAGCTCAAATATCCCAGATTCAGAAAGATATAATAAATAATCTGATAGGTATTTTGAGCTGAAACTGTACAGACTCATTCTGGAAACACAAAAGACTTAAATCTTGAAAAAGGTAAATAGGTGCCCTTTAAGTTAGTTCTGAGGGAAGCTCTAACATTTGATTGCGTACATACACTTTGTTTTCTATGTATTAATTTACTTGAAAATGAAACATATATATGTGACGCTTATGCTAATTGAGCAAATTGTGTGCACTGCTAATGTGTATTTTGAATAATAATGCACTGTTAATCACAGGGTCAGGAAGATGAGGACACTCAGGACACACATGGAGAGAAGGAAGAATTCAGACCAGGAAAACTTCGACTCAGTTTTGAAGAGCTGGAAAGA[C/T]AGAGGCTGGAAGACGAACATAAGCGGGTTGAGGAAGAGAGGAAAAGACGCATTGAAGAAGAAAGAAAGGCCTTTGCTGAGGCCAGAAAGAGCATGGTCAGTTTGTGTGCTCGTAAAAAGTTACAATAGTAAAATGATGATTAGTTGATTGTTTGTTCAGTGGCTAAGAGGGTAGCACTTCCACCTCACAGACAGAAGGTCGCTGGTTCGAATCCCGGCTTGAACCAGTTAGCATTTTTGTGTGGAGTTTGAATGTTCTCCATGTATTCGCATGGGTCTTCTATGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCTGTATAGGTGAAGTGAATGAACTAGTGGATGTGTGTGAATGTGAGAGTGTATGGGTGTTTCCCAGTACTGGGTTGTGGCTGAAAGGGCATCCGCTGCATGAAACAAATGCCAGAATAGTTGCACTCATTTCGCTGTGGTGACCTCTGACAATAGAGACTAAGCCGAAAGAAAATAAATGTTTG
Associated Phenotype:
Not determined