Busch Lab

ZMP

ENSDARG00000088302

Ensembl ID:
ENSDARG00000088302
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]
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
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Availability:
Order Allele From ZIRC
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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