ZMP
ENSDARG00000088302
Ensembl ID:
Human Orthologues:
AP005117.2, FAM38B
Human Descriptions:
Transmembrane protein C18orf30 [Source:UniProtKB/Swiss-Prot;Acc:Q8N787]
family with sequence similarity 38, member B [Source:HGNC Symbol;Acc:26270]
family with sequence similarity 38, member B [Source:HGNC Symbol;Acc:26270]
Mouse Orthologue:
Fam38b
Mouse Description:
family with sequence similarity 38, member B Gene [Source:MGI Symbol;Acc:MGI:1918781]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24422 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24422
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124243 | Essential Splice Site | 366 | 805 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 383904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 905188 |
GRCz11 | 24 | 901342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCATCGCATACAACGTCTTCGTGATCACCATGAAGAACATCCTCTCGG[T/A]GAGTACAGGCTGTCTTTAAAACTCTTCAAATTAAACCTAGCCATATTGAT
Long Flanking Sequence:
AGGAGGAGTGCGTGTCTCCCGTTCAGCTGTTAGCTGGTGATAATGTGGAGATCTGTCGAGATCTGGACGCCGCCACCTTCAGCCAGCACAACCCCGTCCCAGACTTCATCCACTGCAGGTCAGACATGTTAAACATGCATAATGAACGTGGACGTTCATCTGATCCGTGTGTCACATCAAAAACCGGAACTTTTCCAAACCTTTCCTCATGTCATGGCTAGCTGTGAATGTAAACGTTGTGTTTTGTGCGGTCAGGTCGTATCTGGACATGCTGAAGGTGATGGTGTTCAGTTATCTGTTCTGGTTTGTGCTGACCATCATCTTCATCACGGGCACCACGCGCATCAGCATCTTCTGCATGGGGTATCTGGTGGCCTGCTTCTACTTCCTGATCTTCGGCGGTGAGCTTTTACTCAAACCCATCAAGAGTATCCTGCATTACTGGGACTTCCTCATCGCATACAACGTCTTCGTGATCACCATGAAGAACATCCTCTCGG[T/A]GAGTACAGGCTGTCTTTAAAACTCTTCAAATTAAACCTAGCCATATTGATGCTGTTGGTTCACATTGCTAATTTTGTGCTGAACAATTCATCTGTGTCATTAAGAAACAAAAATGCCCTTGTAATGTTTAATTGAAATCTGAAGATGCACTTCCTGTTTGTTTTGAGTTGCATCCTCCGATTAAGTCAGTCTGAGGTATTGGACGTGGCTACATACTCAGCCACGCCCCTCCAGCTGTCAGTTCTGACATCAAAAAGAAATGGTGAGGAGGAGGAGGAGTCTGTTAGGTTGTAATAACCCTCCCCAAAACCTTTACTACATCTAATCAGCTCACAGTAAAAAAAAAACAAGCCACTCCCACCGTTTTCTTATTTAATATTCCGTTTCTTTAGGAACTGCGTCACAATAACAAAACAAAAACAATGGCAGCTTCCGGTTCATGCAGACTCTAAACTCACTAAACTATGAGGTTGTAGGTTTTAAATCGTTTTAACTGGGTC
Associated Phenotype:
Not determined