ZMP
zgc:92479
Ensembl ID:
ZFIN ID:
Description:
transmembrane 4 L6 family member 4 [Source:RefSeq peptide;Acc:NP_001003489]
Human Orthologue:
TM4SF4
Human Description:
transmembrane 4 L six family member 4 [Source:HGNC Symbol;Acc:11856]
Mouse Orthologue:
Tm4sf4
Mouse Description:
transmembrane 4 superfamily member 4 Gene [Source:MGI Symbol;Acc:MGI:2385173]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6716 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43885 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6716
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104528 | Nonsense | 34 | 198 | 1 | 5 |
The following transcripts of ENSDARG00000040747 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 41095857)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38184158 |
| GRCz11 | 22 | 38137305 |
KASP Assay ID:
554-5383.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCCATCATCTGCGTCCTCTGCAACATCCTGCTCTTTTTCCCCAGCGGG[A/T]AAGTGGCCGATCAGAGCCAAGACATCACCGACGAAGTCTTTTACCTGGGG
Long Flanking Sequence:
CTCGGACCCTATCTCTCTTTGTCCTGATAAGTTGAATAACACAAGTTACGGAAAGGAATTTCTTTAGCATAGTCATAAATATAAAAAAAAAAGATTTACATAAAATTGATAAGTATTTGTCTATAAAATGCTTCTTGATTTAGGAATTTCTAGATATTTGGACTAGAAACAAGACGAAAGCTCAAAGTAAAGTCATTTTTTTTTCTCAGTGTAGTCATAAAGATCCTCATGTTAAGGTGAGGCCGGTGTGACGCACTGATATCTGTTAGTGTCAATTGTTAGCAGTTACTGATTTACAGACAGCAGGTATAAAGTCCTGCCTCCACTCTCCTGCTCCAGCACAGCCGAACAAACTCAACTCCCGTCGGACTGTATTTCTTCTCCCCAGCAGAGACTCAATCATGTGCTCTGGAAATTTCGCCAAGTGTCTGGGCATCACGCTCATCCCGCTGGCCATCATCTGCGTCCTCTGCAACATCCTGCTCTTTTTCCCCAGCGGG[A/T]AAGTGGCCGATCAGAGCCAAGACATCACCGACGAAGTCTTTTACCTGGGGGGAATTTTGGGATCTGGAGTGCTGGTGAGGAAATAACAACTCAGAACGCCTTCGATATTACTGTTTTAATAATAAATGCACTTGAGAAGGAGATTGTATAATACTGATATTAATAATAATAAAAAACAACAACATTATTATTCTATTATTAGCATTATTGTTATATGCTGTGTTTTTATTCCTTTTTAGCACTGAAAAAACTGATGCACTGCTAAAAATCTGTTTCGTACTTAGTGTTTTTGTTTTGTTTCTAGTCCAAATATCTAAAAGTTGACATATATGACATATTGTGTTGAGTATTTCATTAAACAAGCCTAATAATCTGCCAATGAGTAAACATTTTTGTTCCAAGATTATTTTTCTGACCCCATTGTCAGATTATTTTGCTTGTTTTATGGAAAAACCCACTTTATTCGACTCATTATTTCTGAAAACAAGACAATATTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43885
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104528 | Essential Splice Site | 89 | 198 | None | 5 |
The following transcripts of ENSDARG00000040747 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 41088626)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38176927 |
| GRCz11 | 22 | 38130074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATTATCTTGGCTTGTTTCCACTTTAACGTTTAGTTCTTCTTTCCTGC[A/T]GATGTTCAGCTCTATTCTGTTTGCGGCGGCAGGAGCAGTGGGCGCTGGTT
Long Flanking Sequence:
GTTATCACTTTAACGTTTCGTTAAAAGGTCTTTGTGCTTTTGTTGTACGAATTTAACAAAATCAAATTCTTCAATGTATAAAATAGTTACGTGTTGCGAAATTCAATGTTTTACTTAGCGATTCTTTGTGATTGCCCGAACACTATTTTTCCTTCGCATTGTTTCCATTTTAACGTTTTATTAAAAGGTCTTTTTGCTTTTTTGTAAAATTTCAACAAATTTGAATTCCCGAATGCGTAAAGATGTTAATGTCTAATTCAATGTTGGACTCGACAATTTCTTGCAATTGTTTTAACACAATTTTTTGTTGTTGTTATCACTTTAACGTTTAATTAAAAGCTCTGTGTGCATTTTTTCTGCAAATTTAACAAATTCCAATGTGTAAAATAGTTACGTAAAATGTCGTGCAATGCAGTGTTTTACTTATTCACCCCCTGTATTTATTGCAACACCATTATCTTGGCTTGTTTCCACTTTAACGTTTAGTTCTTCTTTCCTGC[A/T]GATGTTCAGCTCTATTCTGTTTGCGGCGGCAGGAGCAGTGGGCGCTGGTTACTCCGTCATTGTGTCCTGTGTGGCTCTAAATCACGGACCCAAATGTTTTTTAAGCGACGGCAGCAATAACGCCACTTACCCATTCACCGACGGGTGAGTGTTTATTCACAGACCCTCAAATAAATCCAGATCCTTTGATCTAAATCGTGGTGTTTTGGTGACTGTCGCTTTACATTCAAATGAGATTGTGCTCTTTTTAAAAGAGGGCGGAGCTACAGATGCCTGAGTGTCAGCATAGTGGCAGGTTCAAAAATAAGACTGACGTCCTATGCTAATGAGGGAGAGATGGTCACTAGTGGGCGGGGCTTTCCTCCACTGATGACACATACAAAGGGAGAATGTCAATCAAAGTGTTTCTGCAGACTGATTTCATCAAGTCTGATCTCAACAAATATATTTAATTAAATGTTATCACTAGAGGCTGGTAGTAATACATAGAGAAATACATA
Associated Phenotype:
Not determined