Ensembl ID:
Human Orthologues:
BX248098.1, ZNF107, ZNF160, ZNF197, ZNF208, ZNF616, ZNF658, ZNF721, ZNF729, ZNF808, ZNF836, ZNF841, ZNF845, ZNF91, ZNF99
Human Descriptions:
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 658B [Source:UniProtKB/Swiss-Prot;Acc:Q4V348]
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:
expressed sequence AA987161 Gene [Source:MGI Symbol;Acc:MGI:2145180]
RIKEN cDNA A530054K11 gene Gene [Source:MGI Symbol;Acc:MGI:3036250]
zinc finger protein 748 Gene [Source:MGI Symbol;Acc:MGI:1916455]


There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa26356 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
We currently estimate that this allele will be available during 2018.
C > T
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108908 Nonsense 549 646 4 4
Genomic Location (Zv9):
Chromosome 4 (position 58770394)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 72048738
GRCz11 4 73690272
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
Flanking Sequence:
Associated Phenotype:
Not determined


If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below: