Busch Lab

ZMP

ENSDARG00000087249

Ensembl ID:
ENSDARG00000087249
Human Orthologues:
BX248098.1, ZNF107, ZNF160, ZNF197, ZNF208, ZNF616, ZNF658, ZNF721, ZNF729, ZNF808, ZNF836, ZNF841, ZNF845, ZNF91, ZNF99
Human Descriptions:
Zinc finger protein 658B [Source:UniProtKB/Swiss-Prot;Acc:Q4V348]
zinc finger protein 107 [Source:HGNC Symbol;Acc:12887]
zinc finger protein 160 [Source:HGNC Symbol;Acc:12948]
zinc finger protein 197 [Source:HGNC Symbol;Acc:12988]
zinc finger protein 208 [Source:HGNC Symbol;Acc:12999]
zinc finger protein 616 [Source:HGNC Symbol;Acc:28062]
zinc finger protein 658 [Source:HGNC Symbol;Acc:25226]
zinc finger protein 721 [Source:HGNC Symbol;Acc:29425]
zinc finger protein 729 [Source:HGNC Symbol;Acc:32464]
zinc finger protein 808 [Source:HGNC Symbol;Acc:33230]
zinc finger protein 836 [Source:HGNC Symbol;Acc:34333]
zinc finger protein 841 [Source:HGNC Symbol;Acc:27611]
zinc finger protein 845 [Source:HGNC Symbol;Acc:25112]
zinc finger protein 91 [Source:HGNC Symbol;Acc:13166]
zinc finger protein 99 [Source:HGNC Symbol;Acc:13175]
Mouse Orthologues:
A530054K11Rik, AA987161, Zfp748
Mouse Descriptions:
RIKEN cDNA A530054K11 gene Gene [Source:MGI Symbol;Acc:MGI:3036250]
expressed sequence AA987161 Gene [Source:MGI Symbol;Acc:MGI:2145180]
zinc finger protein 748 Gene [Source:MGI Symbol;Acc:MGI:1916455]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa35776 Nonsense Mutation detected in F1 DNA Not yet available
sa35775 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35776
Status:
Mutation detected in F1 DNA
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
ENSDART00000131040 Nonsense 455 865 2 2
Genomic Location (Zv9):
Chromosome 15 (position 749467)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 789770
GRCz11 15 750573
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACAGAACATATGAGGGTTCACACAGGAGAAAGGCCTTACCCTTGCCAA[C/T]AGTGTGGAAAGAGTTTCACCCAGAAACATAAACTTACAGATCATTTGAGG
Long Flanking Sequence:
AAATAAGTGGAGTAAAATCAGAACAGACAAAAACTGCTTCAGAAAGACCAGCCTGCAAGACCGAACCTAATACCTGCCATCAGTGTGGAAAGAGTTTCACTCGGAAGCAATCCTTTACAAAACACATGAGAATTCACACTGGAGAAAGACCTTACACTTGCCAACAGTGTGGAAAGAGTTTCACACAAAAACATGTACTTACAGAACATATGAAGATTCACACTGGAGAAAGGCCTCACACTTGCCAACAATGTGGAAAGAGTTTCACTCAGAAACATATACTTACAGAACATATGAGGGTTCACACTGGAGAAAAGCCTTACACTTGCAAACAGTGTGGAAAGGGTTTCACTCAGAAGCACATGCTTACAGAACATATGAGGATTCACACTGGAGAAAAGCCTTACACCTGCAATCATTGTGAAAAGGGTTTCACTTGTAAACGAAACCTTACAGAACATATGAGGGTTCACACAGGAGAAAGGCCTTACCCTTGCCAA[C/T]AGTGTGGAAAGAGTTTCACCCAGAAACATAAACTTACAGATCATTTGAGGGTTCATACTGGAGAAAAGCCCTTCACTTGCCAACAGTGTGAAATGAGTTTCACTTGTAAACGATACCTTACAGAACATATGAAGGTTCACACTGGAGAAAGGCCTTACACTTGCCATCTGTGTGGAAAGAGTTTCACCTGGAAACGATACCATACAGAACACATGAAGATTCACTCTGGAGAAAAGCCTTACACGTGTCAACAGTGTGGAAAGAGTTTCATTTGTAAACAAAAACTTCTAAATCACATGATGGTTCACACTGAAGAAAAGCCTAACGCTTGCGATCAGTGCGGAAAGAGTTTTACCCTGAAACATATACTTATAGAACATATGAGGGTTCATACTGGAGAAAAGCCTTTCACTTGCCAACAGTGTGGAAAGAGTTTCATTTGTAAACGATACCGCACAGAACATATGAAGGTTCACTCTGGAGAAAAGCCTTACACTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35775
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000131040 Nonsense 703 865 2 2
Genomic Location (Zv9):
Chromosome 15 (position 748721)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 789024
GRCz11 15 749827
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAAAACCTTCAAAACCACATGACGTTTCACACTGGTGGAAATCTTTA[C/A]ACTTGTCAGCACTGTGGAAAGAGTTTCACTCGAGAACAAAGGCTTACAGA
Long Flanking Sequence:
TGTCAACAGTGTGGAAAGAGTTTCATTTGTAAACAAAAACTTCTAAATCACATGATGGTTCACACTGAAGAAAAGCCTAACGCTTGCGATCAGTGCGGAAAGAGTTTTACCCTGAAACATATACTTATAGAACATATGAGGGTTCATACTGGAGAAAAGCCTTTCACTTGCCAACAGTGTGGAAAGAGTTTCATTTGTAAACGATACCGCACAGAACATATGAAGGTTCACTCTGGAGAAAAGCCTTACACTTGCCAACTCTGTGGAAAGAGTTTCACCTGGAAACGATACCATACAGAACATATGAGGATTCACACTGGAGAAAAGCCTTACACTTGTCAGCAGTGTGGAAAAAGTTTCATTTGTAAACAAAATCTTGTAAAACACATGAAGGTTCACTCTGGGGAAAAGCCTCACACTTGCGATCAGTGTGGAAAGAGTTTCACTTGTAAACAAAACCTTCAAAACCACATGACGTTTCACACTGGTGGAAATCTTTA[C/A]ACTTGTCAGCACTGTGGAAAGAGTTTCACTCGAGAACAAAGGCTTACAGAGCATACTAGGATTCACACTGGAGAAAAACCTTACACTTGCCAACAGTGCGGAAAGAGTTTCACTGGTGAACAAAACCTTAAAAACCACATGAAGATTCACACTGGAGAAAAGATGTACACTTGCAAACAGTGTGGAAAAAGTTTCACTTGGAAACAAAACCTTACGGAGCATATGAAGATTCACACTGGAGAAAAGCCGTACACTTGCCAAGAGTGTGGAAAGAGTTTCTTTTGGAAACAAACTCTTATAGAGCATACAAGGATTCACACCGGGGAAAAGCCTAACACCTGCTGTCAATGTGGAAAGAGTTTTACTTGGAAACAAAACCTTATTGATCATATGAGGATTCACACTGGAGAAAAGCCTCACAGTTGCCAACAGTGTGGAAAGAGTTTCGTTTGTACCCAAAGTCTTAAAAGGCATATGAGAGTTCACACTGGAGAAAAGCC
Associated Phenotype:
Not determined