ZMP

c1qtnf4

Ensembl ID:

ENSDARG00000024299

ZFIN ID:

ZDB-GENE-050417-198

Description:

complement C1q tumor necrosis factor-related protein 4 [Source:RefSeq peptide;Acc:NP_001017702]

Human Orthologue:

C1QTNF4

Human Description:

C1q and tumor necrosis factor related protein 4 [Source:HGNC Symbol;Acc:14346]

Mouse Orthologue:

C1qtnf4

Mouse Description:

C1q and tumor necrosis factor related protein 4 Gene [Source:MGI Symbol;Acc:MGI:1914695]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1474	Nonsense	F2 line generated	Not yet available
sa40958	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa1474

Status:

F2 line generated
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
ENSDART00000035006	Nonsense	266	339	2	2
ENSDART00000137424	Nonsense	308	381	2	2

Genomic Location (Zv9):

Chromosome 7 (position 39994490)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	38331130
GRCz11	7	38602388

KASP Assay ID:

554-1399.1 (used for ordering genotyping assays)

KASP Sequence:

TGCCCCATAAGACCCTGTCAGTGAAGCTGATGAAGAATCATTTGGAGGTA[C/T]AGACCATGATCTACGATGACAGTGACACTGAGAAGGCCCTGCAGAGCCAG

Long Flanking Sequence:

ACCCTCGATACGCCATCTACAGCAACACGGGCCACTACACCACCTTCAACGGTTACCTGATCTACCCTGATGTGTATGGCTACCAAGAGCACACACACAAAGAACACGACAGTGCACACCAGCCCCCGAAAATCACTGATCACTTGCCATCTGAGCAAGAAAATACAATTACCAAAGACACTGCTGTGCGTATGAAGGAGGAGAGACGGGACGAGGAGGTAAAAGAGGAGGACAGCAGAGATGGAGAGGAGGAAGACGATGACCAAAGGTCAGCATTTTCAGTGGGCCGCACGCAAAGCATTGTAGGTGTGGATCAAGGACACCCTGAGCACCAGCCCATCATCTTTGACACAGAGTTCGTCAACATCGGCAACGACTTCAACTTGAGCTCGGGTGTTTTCAAATGCAGAGTAGCGGGGGCCTATTACTTCTCCTTCAATGCTGGCAAGCTGCCCCATAAGACCCTGTCAGTGAAGCTGATGAAGAATCATTTGGAGGTA[C/T]AGACCATGATCTACGATGACAGTGACACTGAGAAGGCCCTGCAGAGCCAGAGTCTGATGTTGTCTCTGCAAGATGGAGACACTGTGTGGCTTTACAGCCACCAGAGGGATGGGTTTGGGGCTTACAGTAATCACGCCAAGTATATCACTTTCACTGGCTTCCTGGTGTATCCTGAGCTGCACCTCAGCCTTCCTCAGCCGCAGAAACAGGATAAGACACTGTAGGCCTGTCAGGGAGACAGTCTGTCTGTGGGTCTGGAAGAAGGGCAAGAGTTTGGAGGAGAATTTATGTGGAAAAATTTGGAGTTCCCTATATGTAATCTTCTATGCTCTAGAAAATCATCACTCCCTTCATTTGCTTTTTATGATTCATTATTACACAATTTCTCCTGCTCGTCCCATGTGTAAACAAAATGTCTGATTTTGGAACATTTTCATGTAAAAAAAAAAGAGAGAGAAAAAGGTGATCAAATAATCACGTTTTATATTTTACATCAAAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40958

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
ENSDART00000035006	Nonsense	335	339	2	2
ENSDART00000137424	Nonsense	377	381	2	2

Genomic Location (Zv9):

Chromosome 7 (position 39994283)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	38330923
GRCz11	7	38602181

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTTCCTGGTGTATCCTGAGCTGCACCTCAGCCTTCCTCAGCCGCAGAAA[C/T]AGGATAAGACACTGTAGGCCTGTCAGGGAGACAGTCTGTCTGTGGGTCTG

Long Flanking Sequence:

GGGACGAGGAGGTAAAAGAGGAGGACAGCAGAGATGGAGAGGAGGAAGACGATGACCAAAGGTCAGCATTTTCAGTGGGCCGCACGCAAAGCATTGTAGGTGTGGATCAAGGACACCCTGAGCACCAGCCCATCATCTTTGACACAGAGTTCGTCAACATCGGCAACGACTTCAACTTGAGCTCGGGTGTTTTCAAATGCAGAGTAGCGGGGGCCTATTACTTCTCCTTCAATGCTGGCAAGCTGCCCCATAAGACCCTGTCAGTGAAGCTGATGAAGAATCATTTGGAGGTACAGACCATGATCTACGATGACAGTGACACTGAGAAGGCCCTGCAGAGCCAGAGTCTGATGTTGTCTCTGCAAGATGGAGACACTGTGTGGCTTTACAGCCACCAGAGGGATGGGTTTGGGGCTTACAGTAATCACGCCAAGTATATCACTTTCACTGGCTTCCTGGTGTATCCTGAGCTGCACCTCAGCCTTCCTCAGCCGCAGAAA[C/T]AGGATAAGACACTGTAGGCCTGTCAGGGAGACAGTCTGTCTGTGGGTCTGGAAGAAGGGCAAGAGTTTGGAGGAGAATTTATGTGGAAAAATTTGGAGTTCCCTATATGTAATCTTCTATGCTCTAGAAAATCATCACTCCCTTCATTTGCTTTTTATGATTCATTATTACACAATTTCTCCTGCTCGTCCCATGTGTAAACAAAATGTCTGATTTTGGAACATTTTCATGTAAAAAAAAAAGAGAGAGAAAAAGGTGATCAAATAATCACGTTTTATATTTTACATCAAAATTTCGCAAAACCCCAAAAATGTTTCACATGTGATTGAACACTTTTACCCAGTTCATCTGCTTTACGAGGAATTATACAACCAAGAAATAACCTGAAATAACAAAGCCTCTTCTTGGCATCTTTAAAGTTGCAATGAAACAGAGAATGTGAACATTTTTTTCTCTGTTGTGATCAGTGAGATGGCTCTATGATACGATCTCGGGACTGA

Associated Phenotype:

Not determined