ZMP

si:ch211-124n19.2

Ensembl ID:

ENSDARG00000060401

ZFIN ID:

ZDB-GENE-081104-105

Description:

Novel prptein similar to vertebrate SH3 domain containing ring finger 1 (SH3RF1) [Source:UniProtKB/T

Human Orthologue:

SH3RF3

Human Description:

SH3 domain containing ring finger 3 [Source:HGNC Symbol;Acc:24699]

Mouse Orthologue:

Sh3rf3

Mouse Description:

SH3 domain containing ring finger 3 Gene [Source:MGI Symbol;Acc:MGI:2444637]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14831	Nonsense	Mutation detected in F1 DNA	Not yet available
sa41560	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14831

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
ENSDART00000085042	Nonsense	11	675	1	17
ENSDART00000133366	Nonsense	8	138	1	2
ENSDART00000134648	None	None	164	None	2
ENSDART00000138876	None	None	57	None	1

Genomic Location (Zv9):

Chromosome 9 (position 57606795)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	56596617
GRCz11	9	55946279

KASP Assay ID:

1641-0506.1 (used for ordering genotyping assays)

KASP Sequence:

TGTGTTCATGTGTGYTYTCTCTCTCACAGGATGAGATTCTGACYGTCRTA[C/T]GAAGAGTRGACGATAACTGGGCAGAAGGCATGCTGGGAGATAAAATYGGG

Long Flanking Sequence:

TTGAACCTTTGCATTGTTTTGTTTGTTTAATCCTGTTTGCTGCCTGCCTCTGACCACTTGCCTATTGACCATGATTCTGGATTGCCTGTATACATCTGCGTGCCCCTGTGTTGGGCATTGCTGGCCTGACCTCGCTAATAACCCTGCATGTGGATCCGCATCTCTGTTGTCAGTGTCACTTCCCAGGTTACAGTTCTGCACAGAAATCTTCAAAATGAAGCTTGGTTTCTGTGAAATATTCCTTGACATCAGCCATGTGTAAACGACTCAAAAAGACTGTTTGTTTTACATATATTAAAAGGCTTTAGGAGATTGTACCTGAAATGATATTGTGGTGTTTTATTCATTTATTTCTGAATATGCAAATGAAGTGTGTTATACAGGTATCAGGGTTTTTAATCAGTAACTGTGAGTCTTTCTACAATGCCAGAATGAAGTGCTACATCTGCATGTGTTCATGTGTGTTTTCTCTCTCACAGGATGAGATTCTGACCGTCATA[C/T]GAAGAGTGGACGATAACTGGGCAGAAGGCATGCTGGGAGATAAAATCGGGATTTTTCCAATCTTATATGTGGAGGTGAGTGCCTGTAAATAAACTGCGATGGAGATTATGAACAATAACTAGCATGTACGTTTTCAGAAGAAAATGAGAGTCGTACTCGCCAAAACTCAGCACTGGGTTGATGCTAAGACATTGAGACATCAGACTGGTTGCTAGGTGGTTTCTAATGCTGCGTTCACACCAGACGCGGAACGCACGTCAAGAGTGAGTGATTTACATGTTAAGTCAATGCAAACACACAAATAGACATCCTGCGGCGCGATACACGTAAATGGTGCGGCGCGAATTATGCGAATTGCGCGAATGACGCAGTGCGAATTTTGTGCGAAGCTCTCGAGTTTGAAAATCTGAACTTCAGTGGACATTTGCGCCGCGTTAACCAATCAGGAGCTTGCTCTTGTGGGGGCGTTATTGTGACGTATCGCCGGGGATACGTCACAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41560

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085042	Essential Splice Site	158	675	3	17
ENSDART00000133366	None	None	138	None	2
ENSDART00000134648	None	None	164	None	2
ENSDART00000138876	None	None	57	None	1

Genomic Location (Zv9):

Chromosome 9 (position 57589619)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	56579441
GRCz11	9	55929103

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTGCGCCCCTGCCTCCAGCACAGCTGCTGCACAGGTACAGCACACATG[T/A]ATGTCTGCATCAAGCGGCAACCTCCTGGTCTCCCTTGGGTAGCCAATTCG

Long Flanking Sequence:

CGCAAAAAGGGGGTATGCAGTATATGCGGCGCATAGGGGCGCCACACATGGGGGGGGGGGCGCCATTGTGCCAAAACTATTTTTTAAATTACCCTTATTAAAAGTTTTAAATAATAAAAATAAATAAATATGTTTTGTTAAAAAAATTTATTTGGCATTTTATAAAAATATAACATTGTTATTGTTTAATTCAAAATCATTTAACACAATAACATGCAGTCCCACAGCCGAAAGTGTTCATGTAGATGTAACTGTTTAGATTTGTTTTATTTTTATCAAAATAAACTGTCAAATCATGCATAATGTCAAAAGTTATAAGGTTAATCTGAAAATTTGTCTTCATTTATTATTAATTTCCACTTAATTACTAATAATTAATTTAATTATTAGTTTGCCAAAATAAGAGGGATCCCACAAAATTTGAACCCGCATACCCCTCAGTAAATGTGTAGTTGCGCCCCTGCCTCCAGCACAGCTGCTGCACAGGTACAGCACACATG[T/A]ATGTCTGCATCAAGCGGCAACCTCCTGGTCTCCCTTGGGTAGCCAATTCGGAAGTAGCTAAAACTGCAATTCATCGACTCGCCTTTGGGGGGCTGGTGTAACGGAGGCCAGCCAAGTAGGTGCTGTGCAGGTAACCCTCACTCCTCTGACCTCTAAAGGTGCTCTAGTGACTGACGCTAGAGGCCATGGTCTTTAGCCTCCTTGTTAGAGCAACCGACTCCTATGCGGAAGGTCGCTGGTTCGATACCAGCTCGGAGCAGCTTCGGTGGCGTAGGACCAGCAGGGTTACGTTGGCTCCAGGAAATCCAACTGCAATGGTAAATTAGCCATTTTTACAGCTGATAAAAACATGTTTACAGCCTGATACAAAATATGGCTTTAGTGCATACAGCTAATATTACCCTTCATGACCCTAACCTGCCTGCCTAATTAACCTAGTGAAGCCTTTAAAGGGCAATGAGACCCCCTGTTTCAGCAGGGTGTTTTCACACCTCTAGTTT

Associated Phenotype:

Not determined