ZMP
si:ch211-287b5.3
Ensembl ID:
ZFIN ID:
Description:
Protein FAM133 [Source:UniProtKB/Swiss-Prot;Acc:A1A5I1]
Human Orthologues:
AC021171.1, FAM133A, FAM133B
Human Descriptions:
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A6NGY4]
family with sequence similarity 133, member A [Source:HGNC Symbol;Acc:26748]
family with sequence similarity 133, member B [Source:HGNC Symbol;Acc:28629]
family with sequence similarity 133, member A [Source:HGNC Symbol;Acc:26748]
family with sequence similarity 133, member B [Source:HGNC Symbol;Acc:28629]
Mouse Orthologue:
Fam133b
Mouse Description:
family with sequence similarity 133, member B Gene [Source:MGI Symbol;Acc:MGI:1915402]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36896 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36896
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052952 | Nonsense | 247 | 248 | 12 | 12 |
ENSDART00000089547 | Nonsense | 258 | 259 | 11 | 11 |
ENSDART00000135648 | None | None | 226 | None | 8 |
ENSDART00000140857 | None | None | 216 | None | 9 |
The following transcripts of ENSDARG00000013863 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 41308016)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 40760554 |
GRCz11 | 19 | 40347674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATAAGAAACACAGCAAAAAGAAAAAGAGGAAGACCTCCAGCTCGGAGT[T/A]GGACTGAAGGTGCTAGCGGCGGCTGGATTTGTGAATGGTAACGGAAAAGA
Long Flanking Sequence:
AGTCACTTAAATCATTCTTTTCCCCCATTCTGATGCTCAGTTTGAACTGCAGCAGATCATTGGTGATTGGCTGATTAGAAATTTTTGTTAACAAGCAGTTGACCTGTTAGCGTATATGCTCATTCTCGTATATAATGATTAAACTTTCCTGCCATACCATGGCTGCAGCACGTGCAATGATAGGACATTGGCTGAATGCATAAAAATGGTAAAACTCAACAGTTTTAACTGTTTAAAGAAGTATAAAATGAGCCTATTACCAAAAAAAGTGCAGTGTTCATTTAAAGCGGATCATTGATGTGTGATTTGCCCAAATGAATGTGTAAATGTCTGAATGTGCTACCCGCACCACTCGCAGTAATGTTATCAGCAGTGGATTCACAAAACAGAACTTCATGATTGCTTTTTGTATTTACAGGATAAGTCTAAAAAGAAAAAGAAAAAGAAGAAGCATAAGAAACACAGCAAAAAGAAAAAGAGGAAGACCTCCAGCTCGGAGT[T/A]GGACTGAAGGTGCTAGCGGCGGCTGGATTTGTGAATGGTAACGGAAAAGACAGAGCTCTTGACAGACAGTGGAGAAATAAATCCATCAGAAAGCTGTCCAAGTGACTCTTAAAAGTGGGTGCTCTTTAGCATCGTGCAGCTGTAGTGGAGACTGGGATGAGAGGATCGTGGCGGGGGTGTTGAACAGGGCGTGGGGTTCATTACGTCAGGTTTGTGTTTGTTTTTTAAGCAGATGATTCTCAGTCCAAATAAAGACCATTTACACATCATCAGCGGCTCTGTGTTCAGTATCTGTGTCCTGATGAGGGTGGGAGTTGCTGCTGGTGGCAGTCGATTTGCATTAGATGTATTTAGAAAGCTAGTTTTTCGCCTTCGGAGCTGGCTAGGGTTTACTTTCTGTGACGTGTGACAGTGCACAGAACAACTAATAAATAAATGTATAAAGTAGTCAACATTTATAGTGGATCAAAAAGTTTTCAAAATTGTCTTTTTATATATAT
Associated Phenotype:
Not determined