ZMP
zgc:109953
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein KIAA1310 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q499B3]
Human Orthologue:
KIAA1310
Human Description:
KIAA1310 [Source:HGNC Symbol;Acc:25473]
Mouse Orthologue:
4632411B12Rik
Mouse Description:
RIKEN cDNA 4632411B12 gene Gene [Source:MGI Symbol;Acc:MGI:1918055]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41304 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1367 | Essential Splice Site | F2 line generated | Not yet available |
| sa34509 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41304
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060633 | Nonsense | 291 | 835 | 7 | 20 |
The following transcripts of ENSDARG00000029556 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 53608905)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 51344264 |
| GRCz11 | 8 | 51330793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTATTGCTCCATCTGGACCAACCAACCCTGCCTTTCCTACATCCCGA[C/T]GAATGAGATTCTGGCAATCTCAGCTGTCCTGTCTTGGGAAGGTATGCAGC
Long Flanking Sequence:
TGTTTCAGCAGGCTGTTTTCACACCTCTAGTTTGAAAACAGTCAGGACAGTGGCTCACAGTCAGTCCAGCTTTGTTTAGGTGGGAGTGTCAAGTGGCGAAAGAGGGAAGGATTTGCATTTAAAGGGGAGTTTCTGTTCGAGCACGCGCTGATTTTTCACTGAGGCAAAACAACACACAGACACAGGGGAGAAAGACAGTGTATTTACATGGACATCTATCATCTGAATTATTTGCCAAATTCTTAATTTGTCGACTTTAACTGCAGTTTGGCTCTTTCACTTTCATCCAGGAACATTTCATGCATGCCCCCCATGACAAACGATGCACAGATATAATCACATCAGAGTTCATTCAATGTGAATGCATCTGTAGTATAATGCACTTTCAGTGTACTTCATCTTTTCTCTCATGTTTGTATTTTCAGAGTAAACTTCCTGGATCCCCGCTGATCCTTATTGCTCCATCTGGACCAACCAACCCTGCCTTTCCTACATCCCGA[C/T]GAATGAGATTCTGGCAATCTCAGCTGTCCTGTCTTGGGAAGGTATGCAGCATCATAAGCGTAACGCTTTTAATTTATCAATCTCACCGATGATTTTTGAATTGTGGCTTGATTACTGTGAGATTTACCTAGGGCTGGGCGATATTGCAAAAAAATGTATCACGATATCATCTTTCATATTAATCTATATCAATAATTATTGAATATTTTTTATTAACAGTACATTTAGGAGTAGTAGGACTTTTAATTTTTATTTATTATTTTAATTTACCAACATTACTAAGGCAAATAGTTTTAATATTCATTCATTTTCTTTTCGGTTTAGTCCCTTTTTGTAGTTTTAATAGTCAAAAATAAAAATATTTAAACTGAATATCTGATGTCTTAATAATAAAATTAACGTAAGTGTTAAAGAGACTCTTCAACTTTATAAATAAAATCTTACAAAGTGAGTGCAATGGTAAAGCGTAAATACTGAACAATCCGAGCCAACCTTAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1367
Status:
F2 line generated
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060633 | Essential Splice Site | 361 | 835 | 9 | 20 |
The following transcripts of ENSDARG00000029556 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 53606550)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 51341909 |
| GRCz11 | 8 | 51328438 |
KASP Assay ID:
554-1279.1 (used for ordering genotyping assays)
KASP Sequence:
ACCGATCATCTTGGTGGGCTGGAATGTAGGATCATTGATGGCTTGTCATG[T/G]AAGTCTTGCATTAATTAAANNNNATGATTAATTCTTTGATTAGTTGTCTGTGTT
Long Flanking Sequence:
GGCAAAAACAGCCACAAACATAACGATTGACCAATATACAAGGGTTAACACATTTTGACAGTTAAATATTGCGTTAACTTAGTCATTTTTTACTTTCAAAGTCAAGGTTCAGAAATGTTTTTGTCTTGTTTTGTTGATTCAGGTCATTCCCATTAACGTTCATGTTGGCAGTGGAGCCAACGTTGGAATCACGCAGTGTTTGGAGCACATGATCGGCACAGTCAGAGGAAAAGTCATCGAGGTACAAAACAGCATGCTTTCACTTTACAGAAACCCCAGGACTATATTCGCTATGGATGTCAAAATTAATTGCTTCTTTGATGCACCGCGATGTAGACGTGAACAACTCTGTATCGATTCAGCAATAATCATAACCGGTTATTATGTACTGACGTCATTTATTTCAAATGCGCTATATTTGCTCTAGGTTCACAGTCACTTCCCTCACAAACCGATCATCTTGGTGGGCTGGAATGTAGGATCATTGATGGCTTGTCATG[T/G]AAGTCTTGCATTAATTAAAATGATTAATTCTTTGATTAGTTGTCTGTGTTTGGCTGTAAACAGATGAACTCACAGAGGCCTGTTTTTGCACACAGGTGTCTTTAATGGAGTACATGACTGCTGTTGTGTGTTTGGGTTTCCCTCTCCAAACGATCAGTGGGCCACGAGGGGTAAGAGCAAACACAGTCCATAGTTTCCTATCGATATCACAATGTAGTCATTTGCAATAGTCACATCGCAGGATATATAATGTTGAGTCTGTACAACCCCAAATCGTGTTGTGACCGTCTGGAAAATGCAAATAAAAAAGAAGGAAGTGATTCCTGAGTTTACTTTGACTTGTGCTTCATTGCAGACAATACAGCAAACATTATTTAATGTGTTCCTCATGATCGGTTTTAAACATTTCAATAATTCTCTTGCGTGTTTCTCGGCAAACTGTTGATCCTCCCCATTTTTTCTCCTAAAGGACCAGACCTTTCTTGGATGCTGCTTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34509
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060633 | Nonsense | 665 | 835 | 17 | 20 |
The following transcripts of ENSDARG00000029556 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 53591201)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 51326560 |
| GRCz11 | 8 | 51313089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGTTTACAGTGGGTTTGTCAGGAAAGCCTCTCGGTCTGACAGTGGGC[C/T]AGACGACAGTATCAGGGGCCAAAGAACTGTCTGAGCTTCTCAGTGCACAA
Long Flanking Sequence:
AGTAACAACTCGACCTCGTCGTTTGTCCACAAAAATACCTCTCTTGCTTTCTTTGCCATCGCATTCATTGTTCGACCGGCGTTTGTTGACTAACAATAACCAAATGTCGAGCGAGACACATGCTTCCTGTTTATACTAGAACGCGCATGCCCAGAGTGCGCGAATGGTCATGTGATATACGTTTTGGTGGCGTATTGTGGACGGAGATATGTTCAGAAATGCTAGGTGAACCGCTAGTGTGGATGCGGATCGTTTTTGATCTAAAACGCTGTTTTAAAACTAAAACACACTAGTGTAAACGGGGCCTGAGACCACTGTTTGATACATAGTTAAGCATTTGGGAAAGTTTTGATTCATGCAGGTAGATTTATGACTTTATTTGCTTCATGATTAAGTTATTTAATAGGAATTTTTTAATCGAAAATATCTGTAAACTAAGTTTTTTTGTCTTTGTGTTTACAGTGGGTTTGTCAGGAAAGCCTCTCGGTCTGACAGTGGGC[C/T]AGACGACAGTATCAGGGGCCAAAGAACTGTCTGAGCTTCTCAGTGCACAAAGGTACCTTTATCTTTCAACACCAGATTGTACAGTGTTCAAAAGAAAAAAGACTATCAACCTTTATAGGTTGCGCATGGTCACACCATGTGATTTTAAAGTTATGTCATCAGCTGCTAAATTCAAATCTTTTCACTGATGCTGAGGCATAGAAAGTGTCATAAATCACATATTATCAGGGTTTTCTAACAAACAACATTTATTTTAGATTTTAGACATACATTAGGATGGATACCGAAACTCTGTACTTTATCGGTATCGGTTCTATGTTATAAAAGGCCGAACTATCGACAAGCTCAGACGTTAACGGTTCTGCTGTCTGTACATTACTTACAGTAGCATAATAGAACTGACCAACCTTTTCTAATTGGAGATATTTGATATTCGTATGCAGAGTTGGCCATTTCACATGATGCAAAGGCTTGTGTTTCCAGCGAGCGCGTCAAGTATA
Associated Phenotype:
Not determined