ZMP
ENSDARG00000076722
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 are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33056 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14724 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33056
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111325 | Nonsense | 1050 | 2444 | 21 | 43 |
Genomic Location (Zv9):
Chromosome 2 (position 54878512)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 54562007 |
GRCz11 | 2 | 54287886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGAAACTGACAGTGAAGAGGAGGAGGAAGAGGAGGAGAAAAAAGAC[G/T]AAGAGCCTCCCAAAAGATCAGCCTTTCAGGTGTGTGAAACCATGCAGTTC
Long Flanking Sequence:
CTGTTTTAAAGAGGAAAAAATTCCTTATTTTTTACTTTTTGTTTCTGAAATCTTAATATTTCTTACTCGTCTAAAAAGGCTTTTTGATTTAAGAATCTTTAGATTTTTGGACTAGGAACAAGGCAAAAACTCTAAATAAGAATTTTTTTTTTTTTTGTGCAGTTTAATCTTGTACTTTAGTATTATTTTACAAATGATGTATGCTAATATGATATGCCTTACAAGCACAATTTGACTGTGTGTTTTTCAGATTGAGGTAAGTTTGGTTTGAGATTGTTTGGTATTTTCTCAGGAGGCGTATGGGGATGCGCAAAACTGATTTTATCAATGACAAGCTTGTGAATAATCAAAAGCATACTGTGTTATTCTACTGTTTTCTGTTTTGATGTCATTGTTTTTTGCTCAACGCTCTCCATATTTTCTCAGTGGTTAGAAGTGGTGATTATTACCTGTTTGAAACTGACAGTGAAGAGGAGGAGGAAGAGGAGGAGAAAAAAGAC[G/T]AAGAGCCTCCCAAAAGATCAGCCTTTCAGGTGTGTGAAACCATGCAGTTCAGCTCATTCTGTATTCAGGTCATTGGTCCTCTGTGTGGAAAGGAAGTAACTTTTATTGTTACACAATAAGGCTTGACGTATATCTTTTTTCAACAGATTTAATAATTCTTTTATATAAGTTAATTTATTTTATCTTTGTCATGATGACAGTGCACAATATTTGACTAGATATTTTTCGAGATACTAGTATTCAGCTTAAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGCAGGTCAGGATAATTTTGCAAGTCATTGGACAACGGTGGTTTGTTCTGTAGATAATCTAAACAAATATTGTATAAGGGGGCTAATACTATTGACCTTAAAACGGTGTTAAAAAATTAGAAACTGCTCTTATTCTAGCCAAAATAAAACGAAAAAGACTTTCTCCAGAAGAAAAAAAAATATTATAGGAAATACTTACGCTCTGTTAAACGTCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14724
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111325 | Nonsense | 2172 | 2444 | 38 | 43 |
Genomic Location (Zv9):
Chromosome 2 (position 54930745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 54614150 |
GRCz11 | 2 | 54338820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATATCAAATCCGTCACTGGGGCAGAATTTAAGAAGTTCACAGATCACTA[C/A]AAGTCTAAYGCAGTAAGTGYCTGTTGTCAAATTACAGYMGATACTATGTG
Long Flanking Sequence:
GCTAGGTGGTTGCTAAAGAGTTCTAGGTCATTGCTAAAGTATTGCTAGGTTTTTGCTAGGGTTTTCTGAGTGGTTGCTAGGTGATTGCTAAGACATTGCTATGTGGTTGCTATGGTGTTCTAGGTAGCTGCTAATGCATTGCTATGGGTTTGCTAGAGTGTTTTGAGTGATTGCTAGGCAGTTGCTAGGGCATTGCTAGGTGGTTGCTAAGGTATTCTAGGTCATTGCTAAGGTGTTGCTAGGTGGTTGGCTTTCTCAAGCCACCATAGTTATCCAGTCGTTCTTCAATTATTCTCTGTGGAACTGATGTTGTGTATGTCTTTCCTATGGGATTTGTTCTAACCTCAAGTTGTTTACAGTTTGTATACTAACAAGGCTCTCTTTTCCTCCTCCTTGTGTGTTTGACATTCTGTCCTCCAGCCGATCTTCACAATGAGTGCCCAGCAGAACCATATCAAATCCGTCACTGGGGCAGAATTTAAGAAGTTCACAGATCACTA[C/A]AAGTCTAACGCAGTAAGTGCCTGTTGTCAAATTACAGCCGATACTATGTGTTTTAGGACAGTGTTTCTCAACCACATTCCTTGAGGACCACCAGCACTGCATGTTTTGGATGTCTCCTTCACAGCTTTAAGGCACTGCAGTGTCCCTGTATCTGCAGTTACACGCAGTAAACAGCTGTTCGGTGAACTGATGACTTTTAGAGTCATTTCAATTGAGCACATGAACTTAATGGTAAATCAGCGCAGTTTAAGAATGCGATCAAATGTTAGCAGGAAATGGACGTTTTTAAAATTTCAGTACAGATTGGTATGGAATTCCTGTATCGTGACAACACTACCAGTATCGTCCGAACAGTTGATGCTCACCATTGACTTCTATATTACCATTACCAGTTGTTTTTGCTCTGTTTACCTTTTGGTCCATCTAGACCAGGGGTCACCAAACTTGTTCCTGGAGGGCCGGTGTCCTGCAGATTTTAGCTCCAACCCTAATCAAACACA
Associated Phenotype:
Not determined